@article { WOS:000917764200001,
	title = {Transport of hydroxyapatite nanoparticles coated with polyacrylic acid under unsaturated water flow in soil columns},
	journal = {SOIL SCIENCE AND PLANT NUTRITION},
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	doi = {10.1080/00380768.2022.2163457},
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}
@article { WOS:000906178600001,
	title = {Elucidation of the Charging Mechanisms and the Coupled Structural-Mechanical Behavior of Ti3C2Tx (MXenes) Electrodes by In Situ Techniques},
	journal = {ADVANCED ENERGY MATERIALS},
	year = {Submitted},
	issn = {1614-6832},
	doi = {10.1002/aenm.202203154},
	author = {Bergman, Gil and Ballas, Elad and Gao, Qiang and Nimkar, Amey and Gavriel, Bar and Levi, Mikhael D. and Sharon, Daniel and Malchik, Fyodor and Wang, Xuehang and Shpigel, Netanel and Mandler, Daniel and Aurbach, Doron}
}
@article { WOS:001661905200001,
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	journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
	year = {2026},
	month = {2026 JAN 15},
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	doi = {10.1002/anie.202524876},
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}
@article { WOS:001620175400001,
	title = {Symmetry breaking of single-atom catalysts in heterogeneous electrocatalysis: reactivity and configuration},
	journal = {CHEMICAL SOCIETY REVIEWS},
	volume = {55},
	number = {1},
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	issn = {0306-0012},
	doi = {10.1039/d5cs00209e},
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}
@article { WOS:001561137400001,
	title = {Anion-guided interphase formation stabilizes reversible iron electrodeposition in aqueous electrolytes},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {13},
	number = {38},
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}
@article { WOS:001566156500001,
	title = {Confined electrochemistry in nanocavities: Perspective and techniques},
	journal = {CURRENT OPINION IN ELECTROCHEMISTRY},
	volume = {54},
	year = {2025},
	month = {DEC},
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	issn = {2451-9103},
	doi = {10.1016/j.coelec.2025.101747},
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}
@article { WOS:001503525000001,
	title = {Electropolymerization-Induced NbOPO4 Nanoparticle Electrodeposition for Hybrid Supercapacitors},
	journal = {ACS APPLIED ENERGY MATERIALS},
	volume = {8},
	number = {12},
	year = {2025},
	month = {JUN 6},
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	doi = {10.1021/acsaem.5c00432},
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}
@article { WOS:001546614200001,
	title = {Establishing the Principles for Antithrombogenic Coatings Based on Sol-Gel Films},
	journal = {LANGMUIR},
	volume = {41},
	number = {32},
	year = {2025},
	month = {AUG 19},
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	doi = {10.1021/acs.langmuir.5c01529},
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}
@article { WOS:001607695400001,
	title = {A Hybrid Battery-Capacitor Based on CoNiP Nanoparticles Embedded in Graphene Oxide by Electrophoretic Deposition},
	journal = {ACS APPLIED ENERGY MATERIALS},
	volume = {8},
	number = {22},
	year = {2025},
	month = {NOV 24},
	pages = {16668-16678},
	issn = {2574-0962},
	doi = {10.1021/acsaem.5c02493},
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}
@article { WOS:001474230400001,
	title = {An improved battery-supercapacitor-hybrid by electrochemically deposition of Anthraquinone-2-sulfonate/NiMn-layered double hydroxide on a 3D exfoliated graphite},
	journal = {ELECTROCHIMICA ACTA},
	volume = {527},
	year = {2025},
	month = {JUL 1},
	pages = {146168},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2025.146168},
	author = {Roy, Atanu and Shpigel, Netanel and Hao, Qingli and Mandler, Daniel}
}
@article { WOS:001441423300001,
	title = {Industrially viable formate production with 50\% lower CO2 emissions},
	journal = {ENERGY \& ENVIRONMENTAL SCIENCE},
	volume = {18},
	number = {8},
	year = {2025},
	month = {APR 15},
	pages = {3680-3688},
	issn = {1754-5692},
	doi = {10.1039/d5ee00452g},
	author = {Meng, Fanxu and Shen, Zihan and Lin, Xinlong and Song, Pengfei and Wu, Tianze and Xi, Shibo and Wu, Chao and Ma, Zhenhui and Mandler, Daniel and Xu, Zhichuan J.}
}
@article { WOS:001471341400001,
	title = {Layered double hydroxide with interlayer defects and intralayer defects for high-performance supercapacitors},
	journal = {APPLIED SURFACE SCIENCE},
	volume = {700},
	year = {2025},
	month = {AUG 15},
	pages = {163140},
	issn = {0169-4332},
	doi = {10.1016/j.apsusc.2025.163140},
	author = {Gao, Haiwen and Lu, Keren and Zhao, Peng and Wu, Zongdeng and Guo, Qiubo and Mandler, Daniel and Lei, Wu and Hao, Qingli}
}
@article { WOS:001420103300001,
	title = {A new {\textquoteleft}{\textquoteleft}tailor-made{\textquoteright}{\textquoteright} protocol for operational latent fingermarks{\textquoteright} development on unfired ammunition},
	journal = {FORENSIC CHEMISTRY},
	volume = {42},
	year = {2025},
	month = {MAR},
	pages = {100645},
	issn = {2468-1709},
	doi = {10.1016/j.forc.2025.100645},
	author = {Bengiat, Ravell and Dahan, Adi and Levin-Elad, Michal and Atar, Nurit and Liptz, Yakir and Mandler, Daniel and Almog, Joseph}
}
@article { WOS:001483235700001,
	title = {Optimization of Core-Shell Ternary Electrodes for High-Performance Ionic Actuator in Soft Gripper},
	journal = {ADVANCED MATERIALS},
	volume = {37},
	number = {26, SI},
	year = {2025},
	month = {JUL},
	issn = {0935-9648},
	doi = {10.1002/adma.202503297},
	author = {Zhang, Yufei and Gupta, Adit and Lu, Qiuchun and Lv, Jian and Chen, Shaohua and Hu, Tan and Yu, Jian and Mandler, Daniel and Lee, Pooi See}
}
@article { WOS:001357142600001,
	title = {Stretchable Energy Storage with Eutectic Gallium Indium Alloy},
	journal = {ADVANCED ENERGY MATERIALS},
	volume = {15},
	number = {11},
	year = {2025},
	month = {MAR},
	issn = {1614-6832},
	doi = {10.1002/aenm.202403760},
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}
@article { WOS:001477064000001,
	title = {Studying the Ingress of Ag Nanoparticles into Imprinted Nanocavities by Nanoimpact Electrochemistry},
	journal = {CHEMELECTROCHEM},
	volume = {12},
	number = {15},
	year = {2025},
	month = {JUL 24},
	issn = {2196-0216},
	doi = {10.1002/celc.202500022},
	author = {Sagi-Cohen, Hila and Savchenko, Pavel and Mandler, Daniel}
}
@article { WOS:001551473200001,
	title = {Suppression of Halide Ion Crossover in Zn-Halide Batteries by 2D MXene Membranes},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {17},
	number = {35},
	year = {2025},
	month = {SEP 3},
	pages = {49400-49408},
	issn = {1944-8244},
	doi = {10.1021/acsami.5c06056},
	author = {Roy, Atanu and Chakraborty, Arup and Valurouthu, Geetha and Zhang, Yuan and Bergman, Gil and Shpigel, Netanel and Islam, M. Saiful and Mandler, Daniel and Gogotsi, Yury}
}
@article { WOS:001446417500001,
	title = {Theoretical mechanisms and experimental validation of hard vs soft carbon coatings for enhanced silicon anode performance},
	journal = {CHEMICAL ENGINEERING JOURNAL},
	volume = {509},
	year = {2025},
	month = {APR 1},
	pages = {161385},
	issn = {1385-8947},
	doi = {10.1016/j.cej.2025.161385},
	author = {Zhao, Peng and Liu, Cai and Liu, Boyuan and Lu, Keren and Jing, Haiyan and Xia, Xifeng and Xia, Mingzhu and Han, Shuai and Mandler, Daniel and Lei, Wu and Guo, Qiubo and Hao, Qingli}
}
@article { WOS:001372058600001,
	title = {Tuning the local chemistry of SPAN to realize the development of room-temperature sodium-sulfur pouch cells},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {13},
	number = {2},
	year = {2025},
	month = {JAN 2},
	pages = {1420-1429},
	issn = {2050-7488},
	doi = {10.1039/d4ta05581k},
	author = {Sanjaykumar, C. and Chandra, Mahesh and Soni, Chhail Bihari and Vineeth, S. K. and Das, Sweta and Cohen, Nevo and Kumar, Hemant and Mandler, Daniel and Kumar, Vipin}
}
@article { WOS:001341714900001,
	title = {Continuous Material Deposition on Filaments in Fused Deposition Modeling},
	journal = {POLYMERS},
	volume = {16},
	number = {20},
	year = {2024},
	month = {OCT},
	pages = {2904},
	doi = {10.3390/polym16202904},
	author = {Naim, Guy and Magdassi, Shlomo and Mandler, Daniel}
}
@article { WOS:001341714900001,
	title = {Continuous Material Deposition on Filaments in Fused Deposition Modeling},
	journal = {POLYMERS},
	volume = {16},
	number = {20},
	year = {2024},
	month = {OCT},
	pages = {2904},
	doi = {10.3390/polym16202904},
	author = {Naim, Guy and Magdassi, Shlomo and Mandler, Daniel}
}
@article { WOS:001347996100020,
	title = {Differentiation of adsorption and degradation in steroid hormone micropollutants removal using electrochemical carbon nanotube membrane},
	journal = {NATURE COMMUNICATIONS},
	volume = {15},
	number = {1},
	year = {2024},
	month = {NOV 4},
	pages = {9524},
	doi = {10.1038/s41467-024-52730-7},
	author = {Liu, Siqi and Jassby, David and Mandler, Daniel and Schaefer, Andrea I.}
}
@article { WOS:001136823800001,
	title = {Editorial to the special topical issue {\textquoteleft}{\textquoteleft}Electrochemistry in Emerging Human Health{\textquoteright}{\textquoteright}},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {28},
	number = {2, SI},
	year = {2024},
	month = {FEB},
	pages = {335-336},
	issn = {1432-8488},
	doi = {10.1007/s10008-023-05793-3},
	author = {Mandler, Daniel and Domenech-Carbo, Antonio}
}
@article { WOS:001136823800001,
	title = {Editorial to the special topical issue {\textquoteleft}{\textquoteleft}Electrochemistry in Emerging Human Health{\textquoteright}{\textquoteright}},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {28},
	number = {2, SI},
	year = {2024},
	month = {FEB},
	pages = {335-336},
	issn = {1432-8488},
	doi = {10.1007/s10008-023-05793-3},
	author = {Mandler, Daniel and Domenech-Carbo, Antonio}
}
@article { WOS:001265529000001,
	title = {The Effect of the Capping Agents of Nanoparticles on Their Redox Potential},
	journal = {JOURNAL OF THE AMERICAN CHEMICAL SOCIETY},
	volume = {146},
	number = {32},
	year = {2024},
	month = {JUL 3},
	pages = {22208-22219},
	issn = {0002-7863},
	doi = {10.1021/jacs.4c02524},
	author = {Savchenko, Pavel and Zelikovich, Din and Sinai, Hadassah Elgavi and Baer, Roi and Mandler, Daniel}
}
@article { WOS:001265529000001,
	title = {The Effect of the Capping Agents of Nanoparticles on Their Redox Potential},
	journal = {JOURNAL OF THE AMERICAN CHEMICAL SOCIETY},
	volume = {146},
	number = {32},
	year = {2024},
	month = {JUL 3},
	pages = {22208-22219},
	issn = {0002-7863},
	doi = {10.1021/jacs.4c02524},
	author = {Savchenko, Pavel and Zelikovich, Din and Sinai, Hadassah Elgavi and Baer, Roi and Mandler, Daniel}
}
@article { WOS:001109029300001,
	title = {Efficient electrocatalytic H<sub>2</sub>O<sub>2</sub> activation over nitrogen-doped carbon encapsulated Co<sub>3</sub>O<sub>4</sub> for drinking water disinfection},
	journal = {APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY},
	volume = {342},
	year = {2024},
	month = {MAR},
	pages = {123437},
	issn = {0926-3373},
	doi = {10.1016/j.apcatb.2023.123437},
	author = {Wen, Xue and Zhang, Xiangcheng and Wang, Meng and Yuan, Congli and Lang, Junyu and Li, Xue and Wei, Hao and Mandler, Daniel and Long, Mingce}
}
@article { WOS:001202191400001,
	title = {Manipulating oxygen vacancy for controlling the kinetics of Nb2O5-based anode in Li-ion capacitor},
	journal = {CHEMICAL ENGINEERING JOURNAL},
	volume = {485},
	year = {2024},
	month = {APR 1},
	pages = {150046},
	issn = {1385-8947},
	doi = {10.1016/j.cej.2024.150046},
	author = {Song, Juanjuan and Zhang, Chao and Zhao, Peng and Liu, Boyuan and Liu, Cai and Du, Ping and Mandler, Daniel and Lei, Wu and Guo, Qiubo and Hao, Qingli}
}
@article { WOS:001202191400001,
	title = {Manipulating oxygen vacancy for controlling the kinetics of Nb2O5-based anode in Li-ion capacitor},
	journal = {CHEMICAL ENGINEERING JOURNAL},
	volume = {485},
	year = {2024},
	month = {APR 1},
	pages = {150046},
	issn = {1385-8947},
	doi = {10.1016/j.cej.2024.150046},
	author = {Song, Juanjuan and Zhang, Chao and Zhao, Peng and Liu, Boyuan and Liu, Cai and Du, Ping and Mandler, Daniel and Lei, Wu and Guo, Qiubo and Hao, Qingli}
}
@article { WOS:001225347800001,
	title = {Selective detection of nanomaterials: Gold nanorod imprinted matrices},
	journal = {SENSORS AND ACTUATORS B-CHEMICAL},
	volume = {410},
	year = {2024},
	month = {JUL 1},
	pages = {135544},
	doi = {10.1016/j.snb.2024.135544},
	author = {Sagi-Cohen, Hila and Savchenko, Pavel and Mandler, Daniel}
}
@article { WOS:001225347800001,
	title = {Selective detection of nanomaterials: Gold nanorod imprinted matrices},
	journal = {SENSORS AND ACTUATORS B-CHEMICAL},
	volume = {410},
	year = {2024},
	month = {JUL 1},
	pages = {135544},
	doi = {10.1016/j.snb.2024.135544},
	author = {Sagi-Cohen, Hila and Savchenko, Pavel and Mandler, Daniel}
}
@article { WOS:001241311800001,
	title = {Self-discharge in flowless Zn-Br2 batteries and its mitigation},
	journal = {ENERGY STORAGE MATERIALS},
	volume = {70},
	year = {2024},
	month = {JUN},
	pages = {103461},
	issn = {2405-8297},
	doi = {10.1016/j.ensm.2024.103461},
	author = {Ballas, Elad and Nimkar, Amey and Bergman, Gil and Elazari, Ran and Wakshlak, Racheli and Sharon, Daniel and Levi, Mikhael D. and Major, Dan Thomas and Mandler, Daniel and Shpigel, Netanel and Aurbach, Doron}
}
@article { WOS:001241311800001,
	title = {Self-discharge in flowless Zn-Br2 batteries and its mitigation},
	journal = {ENERGY STORAGE MATERIALS},
	volume = {70},
	year = {2024},
	month = {JUN},
	pages = {103461},
	issn = {2405-8297},
	doi = {10.1016/j.ensm.2024.103461},
	author = {Ballas, Elad and Nimkar, Amey and Bergman, Gil and Elazari, Ran and Wakshlak, Racheli and Sharon, Daniel and Levi, Mikhael D. and Major, Dan Thomas and Mandler, Daniel and Shpigel, Netanel and Aurbach, Doron}
}
@article { WOS:001228730100001,
	title = {To what extent do anions affect the electrodeposition of Zn?},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {12},
	number = {24},
	year = {2024},
	month = {JUN 18},
	pages = {14456-14466},
	issn = {2050-7488},
	doi = {10.1039/d4ta01466a},
	author = {Bergman, Gil and Bruchiel-Spanier, Netta and Bluman, Omer and Levi, Noam and Harpaz, Sara and Malchick, Fyodor and Wu, Langyuan and Sonoo, Masato and Chae, Munseok S. and Wang, Guoxiu and Mandler, Daniel and Aurbach, Doron and Zhang, Yong and Shpigel, Netanel and Sharon, Daniel}
}
@article { WOS:001228730100001,
	title = {To what extent do anions affect the electrodeposition of Zn?},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {12},
	number = {24},
	year = {2024},
	month = {JUN 18},
	pages = {14456-14466},
	issn = {2050-7488},
	doi = {10.1039/d4ta01466a},
	author = {Bergman, Gil and Bruchiel-Spanier, Netta and Bluman, Omer and Levi, Noam and Harpaz, Sara and Malchick, Fyodor and Wu, Langyuan and Sonoo, Masato and Chae, Munseok S. and Wang, Guoxiu and Mandler, Daniel and Aurbach, Doron and Zhang, Yong and Shpigel, Netanel and Sharon, Daniel}
}
@article { WOS:001048505500001,
	title = {Boosting the capacity of MXene electrodes in neutral aqueous electrolytes},
	journal = {CELL REPORTS PHYSICAL SCIENCE},
	volume = {4},
	number = {7},
	year = {2023},
	month = {JUL 19},
	pages = {101507},
	doi = {10.1016/j.xcrp.2023.101507},
	author = {Malchik, Fyodor and Maldybayev, Kairgali and Kan, Tatyana and Kokhmetova, Saule and Chae, Munseok S. and Kurbatov, Andrey and Galeyeva, Alina and Kaupbay, Olzhas and Nimkar, Amey and Bergman, Gil and Levi, Noam and Zhang, Hui and Jin, Qianqian and Lin, Zifeng and Shpigel, Netanel and Mandler, Daniel}
}
@article { WOS:001048505500001,
	title = {Boosting the capacity of MXene electrodes in neutral aqueous electrolytes},
	journal = {CELL REPORTS PHYSICAL SCIENCE},
	volume = {4},
	number = {7},
	year = {2023},
	month = {JUL 19},
	doi = {10.1016/j.xcrp.2023.101507},
	author = {Malchik, Fyodor and Maldybayev, Kairgali and Kan, Tatyana and Kokhmetova, Saule and Chae, Munseok S. and Kurbatov, Andrey and Galeyeva, Alina and Kaupbay, Olzhas and Nimkar, Amey and Bergman, Gil and Levi, Noam and Zhang, Hui and Jin, Qianqian and Lin, Zifeng and Shpigel, Netanel and Mandler, Daniel}
}
@article { WOS:000894567700001,
	title = {Double-carbon coated MnO nanoparticles as high-performance anode materials for lithium-ion storage},
	journal = {IONICS},
	volume = {29},
	number = {2},
	year = {2023},
	month = {FEB},
	pages = {483-496},
	issn = {0947-7047},
	doi = {10.1007/s11581-022-04825-8},
	author = {Chen, Ziyu and Song, Juanjuan and Zhang, Bin and Wu, Zongdeng and Mandler, Daniel and Lei, Wu and Hao, Qingli}
}
@article { WOS:000978454900001,
	title = {Electrochemical Detection of Silica Nanoparticles by Nanoparticle Imprinted Matrices},
	journal = {CHEMELECTROCHEM},
	volume = {10},
	number = {11},
	year = {2023},
	month = {JUN 1},
	issn = {2196-0216},
	doi = {10.1002/celc.202300039},
	author = {Dery, Linoy and Sava, Bogdan and Mandler, Daniel}
}
@article { WOS:000906178600001,
	title = {Elucidation of the Charging Mechanisms and the Coupled Structural-Mechanical Behavior of Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> (MXenes) Electrodes by In Situ Techniques},
	journal = {ADVANCED ENERGY MATERIALS},
	volume = {13},
	number = {8},
	year = {2023},
	month = {FEB},
	issn = {1614-6832},
	doi = {10.1002/aenm.202203154},
	author = {Bergman, Gil and Ballas, Elad and Gao, Qiang and Nimkar, Amey and Gavriel, Bar and Levi, Mikhael D. and Sharon, Daniel and Malchik, Fyodor and Wang, Xuehang and Shpigel, Netanel and Mandler, Daniel and Aurbach, Doron}
}
@article { WOS:000906178600001,
	title = {Elucidation of the Charging Mechanisms and the Coupled Structural-Mechanical Behavior of Ti3C2Tx (MXenes) Electrodes by In Situ Techniques},
	journal = {ADVANCED ENERGY MATERIALS},
	volume = {13},
	number = {8},
	year = {2023},
	month = {FEB},
	issn = {1614-6832},
	doi = {10.1002/aenm.202203154},
	author = {Bergman, Gil and Ballas, Elad and Gao, Qiang and Nimkar, Amey and Gavriel, Bar and Levi, Mikhael D. and Sharon, Daniel and Malchik, Fyodor and Wang, Xuehang and Shpigel, Netanel and Mandler, Daniel and Aurbach, Doron}
}
@article { WOS:001054596800002,
	title = {Essential role of lattice oxygen in methanol electrochemical refinery toward formate},
	journal = {SCIENCE ADVANCES},
	volume = {9},
	number = {34},
	year = {2023},
	month = {AUG},
	pages = {eadh9487},
	issn = {2375-2548},
	doi = {10.1126/sciadv.adh9487},
	author = {Meng, Fanxu and Wu, Qian and Elouarzaki, Kamal and Luo, Songzhu and Sun, Yuanmiao and Dai, Chencheng and Xi, Shibo and Chen, Yubo and Lin, Xinlong and Fang, Mingliang and Wang, Xin and Mandler, Daniel and Xu, Zhichuan J.}
}
@article { WOS:001054596800002,
	title = {Essential role of lattice oxygen in methanol electrochemical refinery toward formate},
	journal = {SCIENCE ADVANCES},
	volume = {9},
	number = {34},
	year = {2023},
	month = {AUG},
	issn = {2375-2548},
	doi = {10.1126/sciadv.adh9487},
	author = {Meng, Fanxu and Wu, Qian and Elouarzaki, Kamal and Luo, Songzhu and Sun, Yuanmiao and Dai, Chencheng and Xi, Shibo and Chen, Yubo and Lin, Xinlong and Fang, Mingliang and Wang, Xin and Mandler, Daniel and Xu, Zhichuan J.}
}
@article { WOS:001015967700001,
	title = {High Recognition of Isomer-Stabilized Gold Nanoparticles through Matrix Imprinting},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {15},
	number = {27},
	year = {2023},
	month = {JUN 26},
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}
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}
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}
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}
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}
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}
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}
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}
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}
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}
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}
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}
@article { WOS:000626133200005,
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}
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}
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}
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@article { WOS:000579121600001,
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	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {24},
	number = {9, SI},
	year = {2020},
	month = {SEP},
	pages = {2133-2135},
	issn = {1432-8488},
	doi = {{10.1007/s10008-020-04764-2, Early Access Date = UL 2020}
}
@article { WOS:000548483100001,
	title = {The future of electrochemical deposition: nanomaterial building blocks},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {24},
	number = {9, SI},
	year = {2020},
	month = {SEP},
	pages = {2133-2135},
	issn = {1432-8488},
	doi = {10.1007/s10008-020-04764-2},
	author = {Mandler, Daniel}
}
@article { WOS:000505224200008,
	title = {Overcoming the barrier of conventional electrochemical deposition of inorganic composites},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {56},
	number = {3},
	year = {2020},
	month = {JAN 11},
	pages = {379-382},
	issn = {1359-7345},
	doi = {10.1039/c9cc07039g},
	author = {Geuli, Ori and Mandler, Daniel}
}
@article { WOS:000529915900001,
	title = {Side by Side Battery Technologies with Lithium-Ion Based Batteries},
	journal = {ADVANCED ENERGY MATERIALS},
	volume = {10},
	number = {24},
	year = {2020},
	month = {JUN},
	issn = {1614-6832},
	doi = {{10.1002/aenm.202000089, Early Access Date = AY 2020}
}
@article { WOS:000529915900001,
	title = {Side by Side Battery Technologies with Lithium-Ion Based Batteries},
	journal = {ADVANCED ENERGY MATERIALS},
	volume = {10},
	number = {24},
	year = {2020},
	month = {JUN},
	issn = {1614-6832},
	doi = {10.1002/aenm.202000089},
	author = {Durmus, Yasin Emre and Zhang, Huang and Baakes, Florian and Desmaizieres, Gauthier and Hayun, Hagay and Yang, Liangtao and Kolek, Martin and Kuepers, Verena and Janek, Juergen and Mandler, Daniel and Passerini, Stefano and Ein-Eli, Yair}
}
@article { WOS:000582677200005,
	title = {Using nanomaterials as building blocks for electrochemical deposition: A mini review},
	journal = {ELECTROCHEMISTRY COMMUNICATIONS},
	volume = {120},
	year = {2020},
	month = {NOV},
	issn = {1388-2481},
	doi = {10.1016/j.elecom.2020.106830},
	author = {Liu, Liang and Mandler, Daniel}
}
@article { WOS:000495760400001,
	title = {Additive-Free Electrophoretic Deposition of Graphene Quantum Dots Thin Films},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {25},
	number = {72},
	year = {2019},
	month = {DEC 20},
	pages = {16573-16581},
	issn = {0947-6539},
	doi = {{10.1002/chem.201903596, Early Access Date = OV 2019}
}
@article { WOS:000454137400013,
	title = {Adsorption and detection of organic pollutants by fixed bed carbon nanotube electrochemical membrane},
	journal = {CHEMICAL ENGINEERING JOURNAL},
	volume = {359},
	year = {2019},
	month = {MAR 1},
	pages = {130-137},
	issn = {1385-8947},
	doi = {10.1016/j.cej.2018.11.069},
	author = {Buffa, Andrea and Mandler, Daniel}
}
@article { ISI:000454137400013,
	title = {Adsorption and detection of organic pollutants by fixed bed carbon nanotube electrochemical membrane},
	journal = {CHEMICAL ENGINEERING JOURNAL},
	volume = {359},
	year = {2019},
	month = {MAR 1},
	pages = {130-137},
	abstract = {An electrically conductive, flow-through, fixed bed adsorption membrane (FCME) made of carbon nanotubes (CNT) installed in an electrochemical flow cell, was applied for the highly efficient adsorption and detection of organic pollutants. Three analytes with different chemical nature, i.e., parathion ethyl, tartrazine and diquat, were chosen as model systems to demonstrate the capabilities of the system. Adsorptive stripping voltammetry (AdSV) performed by the FCME provided directly the amount of analyte adsorbed; in contrast to an adsorption column, that monitors the effluent concentration. The adsorption capacity and kinetic constants were obtained by AdSV and were comparable with those predicted by the Thomas model. The FCME enabled the detection of nanomolar levels of tartrazine and parathion, and submicromolar levels of diquat with a linear range of three orders of magnitude. In addition to being a very sensitive analytical tool, FCME is an adsorption membrane that enables its simple electrochemical regeneration.},
	issn = {1385-8947},
	doi = {10.1016/j.cej.2018.11.069},
	author = {Buffa, Andrea and Mandler, Daniel}
}
@article { WOS:000468628400001,
	title = {Approaches for measuring the surface areas of metal oxide electrocatalysts for determining their intrinsic electrocatalytic activity},
	journal = {CHEMICAL SOCIETY REVIEWS},
	volume = {48},
	number = {9},
	year = {2019},
	month = {MAY 7},
	pages = {2518-2534},
	issn = {0306-0012},
	doi = {10.1039/c8cs00848e},
	author = {Wei, Chao and Sun, Shengnan and Mandler, Daniel and Wang, Xun and Qiao, Shi Zhang and Xu, Zhichuan J.}
}
@article { WOS:000478969600053,
	title = {Arsenic(III) detection in water by flow-through carbon nanotube membrane decorated by gold nanoparticles},
	journal = {ELECTROCHIMICA ACTA},
	volume = {318},
	year = {2019},
	month = {SEP 20},
	pages = {496-503},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2019.06.114},
	author = {Buffa, Andrea and Mandler, Daniel}
}
@article { WOS:000469410000041,
	title = {Composition-Tailoring of ZnO-Hydroxyapatite Nanocomposite as Bioactive and Antibacterial Coating},
	journal = {ACS APPLIED NANO MATERIALS},
	volume = {2},
	number = {5},
	year = {2019},
	month = {MAY},
	pages = {2946-2957},
	issn = {2574-0970},
	doi = {10.1021/acsanm.9b00369},
	author = {Geuli, Ori and Lewinstein, Israel and Mandler, Daniel}
}
@article { WOS:000454705900017,
	title = {Direct Electron Transfer between Glucose Oxidase and Gold Nanoparticles; When Size Matters},
	journal = {CHEMELECTROCHEM},
	volume = {6},
	number = {1, SI},
	year = {2019},
	month = {JAN 2},
	pages = {147-154},
	issn = {2196-0216},
	doi = {10.1002/celc.201801091},
	author = {Malel, Esteban and Mandler, Daniel}
}
@article { ISI:000454705900017,
	title = {Direct Electron Transfer between Glucose Oxidase and Gold Nanoparticles; When Size Matters},
	journal = {CHEMELECTROCHEM},
	volume = {6},
	number = {1, SI},
	year = {2019},
	month = {JAN 2},
	pages = {147-154},
	abstract = {We studied the direct electron transfer (DET) between glucose and electrogenerated AuCl4- catalysed by glucose oxidase (GOx) and gold nanoparticles (AuNPs) by scanning electrochemical microscopy (SECM). Well-defined AuNPs were prepared and attached onto an insulating surface. Studying the current transients of a gold microelectrode held within a few microns from the surface revealed that the AuNPs interacted with the GOx and were crucial for the DET from the glucose. We investigated very carefully the effect of pH and the size of the AuNPs on electron transfer. AuNPs of 16, 40 and 80 nm diameter were applied. The kinetics of electron transfer was analysed by the Michael-Menten kinetic mechanism. Interestingly, we found that the fastest DET was exhibited by the 40 nm AuNPs at pH 3 and 5. At higher pH, electron transfer was better catalysed by the 80 nm AuNPs. This was rationalized by the effect of the pH on the enzymatic structure and the charge of the AuNPs.},
	issn = {2196-0216},
	doi = {10.1002/celc.201801091},
	author = {Malel, Esteban and Mandler, Daniel}
}
@article { WOS:000455549200003,
	title = {Effect of matrix-nanoparticle interactions on recognition of aryldiazonium nanoparticle-imprinted matrices},
	journal = {NANO RESEARCH},
	volume = {12},
	number = {2},
	year = {2019},
	month = {FEB},
	pages = {265-271},
	issn = {1998-0124},
	doi = {10.1007/s12274-018-2129-2},
	author = {Bruchiel-Spanier, Netta and Dery, Linoy and Tal, Noam and Dery, Shahar and Gross, Elad and Mandler, Daniel}
}
@article { ISI:000455549200003,
	title = {Effect of matrix-nanoparticle interactions on recognition of aryldiazonium nanoparticle-imprinted matrices},
	journal = {NANO RESEARCH},
	volume = {12},
	number = {2},
	year = {2019},
	month = {FEB},
	pages = {265-271},
	abstract = {The selective recognition of nanoparticles (NPs) can be achieved by nanoparticle-imprinted matrices (NAIMs), where NPs are imprinted in a matrix followed by their removal to form voids that can reuptake the original NPs. The recognition depends on supramolecular interactions between the matrix and the shell of the NPs, as well as on the geometrical suitability of the imprinted voids to accommodate the NPs. Here, gold NPs stabilized with citrate (AuNPs-cit) were preadsorbed onto a conductive surface followed by electrografting of p-aryldiazonium salts (ADS) with different functional groups. The thickness of the matrix was carefully controlled by altering the scan number. The AuNPs-cit were removed by electrochemical dissolution. The recognition of the NAIMs was determined by the reuptake of the original AuNPs-cit by the imprinted voids. We found that the recognition efficiency is a function of the thickness of the NAIM layer and is sensitive to the chemical structure of the matrix. Specifically, a subtle change of the functional group of the p-aryldiazonium building block, which was varied from an ether to an ester, significantly affected the recognition of the NPs.},
	issn = {1998-0124},
	doi = {10.1007/s12274-018-2129-2},
	author = {Bruchiel-Spanier, Netta and Dery, Linoy and Tal, Noam and Dery, Shahar and Gross, Elad and Mandler, Daniel}
}
@article { WOS:000465160400021,
	title = {Efficient Near Infrared Modulation with High Visible Transparency Using SnO2-WO3 Nanostructure for Advanced Smart Windows},
	journal = {ADVANCED OPTICAL MATERIALS},
	volume = {7},
	number = {8},
	year = {2019},
	month = {APR},
	issn = {2195-1071},
	doi = {10.1002/adom.201801389},
	author = {Tarn Duy Nguyen and Yeo, Loo Pin and Kei, Tan Chiew and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred Ling Yoong}
}
@article { ISI:000465160400021,
	title = {Efficient Near Infrared Modulation with High Visible Transparency Using SnO2-WO3 Nanostructure for Advanced Smart Windows},
	journal = {ADVANCED OPTICAL MATERIALS},
	volume = {7},
	number = {8},
	year = {2019},
	month = {APR},
	abstract = {Renewable energy technology and effective energy management are the most crucial factors to consider in the progress toward worldwide energy sustainability. Smart window technology has a huge potential in energy management as it assists in reducing energy consumption of indoor lighting and air-conditioning in buildings. Electrochromic (EC) materials, which can electrically modulate the transmittance of solar radiation, are one of the most studied smart window materials. In this work, highly transparent SnO2 inverse opal (IO) is used as the framework to electrochemically deposit amorphous WO3 layer to fabricate hybrid SnO2-WO3 core-shell IO structure. The hybrid structure is capable of effective near infrared (NIR) modulation while maintaining high visible light transparency in the colored and bleached states. By varying the initial diameter of the polystyrene (PS) opal template and the WO3 electrodeposition time, optimal results can be obtained with the smallest PS diameter of 392 nm and 180 s WO3 electrodeposition. In its colored state, the 392-SnO2-WO3-180 core-shell IO structure shows approximate to 70\% visible light transparency, 62\% NIR blockage at 1200 nm, and approximate to 15\% drop in NIR blocking stability after 300 cycles. The SnO2-WO3 core-shell IO structure in this study is a promising EC material for advanced smart window technology.},
	issn = {2195-1071},
	doi = {10.1002/adom.201801389},
	author = {Tarn Duy Nguyen and Yeo, Loo Pin and Kei, Tan Chiew and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred Ling Yoong}
}
@article { WOS:000616369200017,
	title = {Electrochemical Triggered Dissolution of Hydroxyapatite/Doxorubicin Nanocarriers},
	journal = {ACS APPLIED BIO MATERIALS},
	volume = {2},
	number = {5},
	year = {2019},
	month = {MAY 20},
	pages = {1956-1966},
	issn = {2576-6422},
	doi = {10.1021/acsabm.9b00011},
	author = {Geuli, Ori and Miller, Maya and Leader, Avia and He, Lijie and Melamed-Book, Naomi and Tshuva, Edit Y. and Reches, Meital and Mandler, Daniel}
}
@article { WOS:000470753700044,
	title = {Electrodeposition of amorphous WO3 on SnO2-TiO2 inverse opal nano-framework for highly transparent, effective and stable electrochromic smart window},
	journal = {RSC ADVANCES},
	volume = {9},
	number = {29},
	year = {2019},
	month = {MAY 28},
	pages = {16730-16737},
	doi = {10.1039/c9ra03084k},
	author = {Nguyen, Tam Duy and Yeo, Loo Pin and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred Iing Yoong}
}
@article { WOS:000485135500008,
	title = {Electrophoretic deposition of reduced graphene oxide thin films for reduction of cross-sectional heat diffusion in glass windows},
	journal = {JOURNAL OF SCIENCE-ADVANCED MATERIALS AND DEVICES},
	volume = {4},
	number = {2},
	year = {2019},
	month = {JUN},
	pages = {252-259},
	issn = {2468-2284},
	doi = {10.1016/j.jsamd.2019.04.002},
	author = {Yeo, Loo Pin and Nguyen, Tam Duy and Ling, Han and Lee, Ying and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred Iing Yoong}
}
@article { WOS:000458682100028,
	title = {Hierarchical electrodes of NiCo2S4 nanosheets-anchored sulfur-doped Co3O4 nanoneedles with advanced performance for battery-supercapacitor hybrid devices},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {7},
	number = {7},
	year = {2019},
	month = {FEB 21},
	pages = {3228-3237},
	issn = {2050-7488},
	doi = {10.1039/c8ta11426a},
	author = {Ouyang, Yu and Ye, Haitao and Xia, Xifeng and Jiao, Xinyan and Li, Guangmin and Mutahir, Sadaf and Wang, Liang and Mandler, Daniel and Lei, Wu and Hao, Qingli}
}
@article { ISI:000458682100028,
	title = {Hierarchical electrodes of NiCo2S4 nanosheets-anchored sulfur-doped Co3O4 nanoneedles with advanced performance for battery-supercapacitor hybrid devices},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {7},
	number = {7},
	year = {2019},
	month = {FEB 21},
	pages = {3228-3237},
	abstract = {Binder-free electrodes with core-shell structures have shown great potential in a variety of important energy storage systems. In order to endow the core-shell hierarchical structure with enhanced electrochemical properties, rationally designed and fabricated hierarchical structures with controllable morphology and great electrical conductivity are highly desired. In this work, a uniform dendritic SCo3O4@NiCo2S4 hierarchical structure grown on Ni foam was successfully designed and synthesized via sulfur-doping of Co3O4 (S-Co3O4) as the inner core with enhanced conductivity. The hierarchical electrode exhibited high areal capacity (10.9 mA h cm(-2) at a current density of 8 mA cm(-2)), a good rate performance (72.5\% retention after increasing the current densities from 8 to 30 mA cm(-2)), and excellent cycling stability (97.3\% retention after 5000 cycles). Moreover, a hybrid energy storage batterysupercapacitor device, constructed from a S-Co3O4@NiCo2S4 positive electrode and an active carbon (AC) negative electrode, showed high energy density and power density. Contributing to short ion diffusion, large electroactive sites and low contact resistance, our work not only demonstrates a promising electrode for energy storage battery-supercapacitor hybrid (BSH) devices, but also provides an attractive strategy for the design of electrode materials.},
	issn = {2050-7488},
	doi = {10.1039/c8ta11426a},
	author = {Ouyang, Yu and Ye, Haitao and Xia, Xifeng and Jiao, Xinyan and Li, Guangmin and Mutahir, Sadaf and Wang, Liang and Mandler, Daniel and Lei, Wu and Hao, Qingli}
}
@article { WOS:000454617200109,
	title = {Manganese doped Co3O4 mesoporous nanoneedle array for long cycle-stable supercapacitors},
	journal = {APPLIED SURFACE SCIENCE},
	volume = {469},
	year = {2019},
	month = {MAR 1},
	pages = {941-950},
	issn = {0169-4332},
	doi = {10.1016/j.apsusc.2018.11.099},
	author = {Li, Guangmin and Chen, Mingzhi and Ouyang, Yu and Yao, Di and Li, Lei and Wang, Liang and Xia, Xifeng and Lei, Wu and Chen, Shen-Ming and Mandler, Daniel and Hao, Qingli}
}
@article { ISI:000454617200109,
	title = {Manganese doped Co3O4 mesoporous nanoneedle array for long cycle-stable supercapacitors},
	journal = {APPLIED SURFACE SCIENCE},
	volume = {469},
	year = {2019},
	month = {MAR 1},
	pages = {941-950},
	abstract = {Long-term cycling stability is an important criterion and big challenge for pseudocapacitive materials. Ultra-stable manganese doped Co3O4 mesoporous nanoneedles were synthesized via one-step hydrothermal reaction followed by annealing grown on nickel foam (noted as MnxCoyO/NF, x + y = 2.25) for supercapacitors. The Mn doping in Co3O4 was confirmed by several techniques. Among various MnxCoyO/NF electrodes, the Mn1.5Co0.75O/NF demonstrated the superior electrochemical performance, with an excellent cycling stability of 104\% capacitance retention after 10 000 charge-discharge cycles at 6 A g(-1), as well as a good capability (668.4 F g(-1) at 1 A g(-1 )compared to that of undoped Co3O4 which is 201.3 F g(-1)). Moreover, the assembled asymmetric supercapacitor based on Mn1.5Co0.75O/NF//graphene performs a high energy density of 25.88 Wh kg(-1) (at 359.5 W kg(-1)) and a high power density of 14.7 kW kg(-1) (at 10.63 Wh kg(-1)). The improved electrochemical properties are mainly owing to the enhanced intrinsic conductivity and electrochemical activity of Co3O4 after doped with appropriate Mn concentration. The three-dimensional nanostructure of mesoporous nanoneedle array grown on NF also provides short ion diffusion path and large active surface areas, contributing to the high rate performance and high energy density. This study may offer a new approach to fabricate the unique 3D nanostructured electrode materials based on doped metal oxides for supercapacitors with long-term cycling stability and high energy density.},
	issn = {0169-4332},
	doi = {10.1016/j.apsusc.2018.11.099},
	author = {Li, Guangmin and Chen, Mingzhi and Ouyang, Yu and Yao, Di and Li, Lei and Wang, Liang and Xia, Xifeng and Lei, Wu and Chen, Shen-Ming and Mandler, Daniel and Hao, Qingli}
}
@article { WOS:000472176900025,
	title = {Novel spinel nanocomposites of NixCo1-xFe2O4 nanoparticles with N-doped graphene for lithium ion batteries},
	journal = {APPLIED SURFACE SCIENCE},
	volume = {481},
	year = {2019},
	month = {JUL 1},
	pages = {200-208},
	issn = {0169-4332},
	doi = {10.1016/j.apsusc.2019.03.063},
	author = {Jiao, Xinyan and Cai, Li and Xia, Xifeng and Lei, Wu and Hao, Qingli and Mandler, Daniel}
}
@article { WOS:000478969600006,
	title = {One-step fabrication of NiOx-decorated carbon nanotubes-NiCo2O4 as an advanced electroactive composite for supercapacitors},
	journal = {ELECTROCHIMICA ACTA},
	volume = {318},
	year = {2019},
	month = {SEP 20},
	pages = {51-60},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2019.06.044},
	author = {Geuli, Ori and Hao, Qingli and Mandler, Daniel}
}
@article { WOS:000477961200005,
	title = {Preparation of Biomass-Based Porous Carbons with High Specific Capacitance for Applications in Supercapacitors},
	journal = {CHEMELECTROCHEM},
	volume = {6},
	number = {14},
	year = {2019},
	month = {JUL 15},
	pages = {3599-3605},
	issn = {2196-0216},
	doi = {10.1002/celc.201900395},
	author = {Shen, Honglong and Xia, Xifeng and Ouyang, Yu and Jiao, Xinyan and Mutahir, Sadaf and Mandler, Daniel and Hao, Qingli}
}
@article { WOS:000489678800032,
	title = {Switch of the Rate-Determining Step of Water Oxidation by Spin-Selected Electron Transfer in Spinel Oxides},
	journal = {CHEMISTRY OF MATERIALS},
	volume = {31},
	number = {19},
	year = {2019},
	month = {OCT 8},
	pages = {8106-8111},
	issn = {0897-4756},
	doi = {10.1021/acs.chemmater.9b02737},
	author = {Sun, Shengnan and Sun, Yuanmiao and Zhou, Ye and Shen, Jingjing and Mandler, Daniel and Neumann, Ronny and Xu, Zhichuan J.}
}
@article { WOS:000494891700031,
	title = {Ultrafine Ni(OH)(2) nanoplatelets grown on 3D graphene hydrogel fabricated by electrochemical exfoliation for high-performance battery-type asymmetric supercapacitor applications},
	journal = {JOURNAL OF POWER SOURCES},
	volume = {439},
	year = {2019},
	month = {NOV 1},
	issn = {0378-7753},
	doi = {10.1016/j.jpowsour.2019.227046},
	author = {Huang, Yang and Buffa, Andrea and Deng, Haiqiang and Sarkar, Sujoy and Ouyang, Yu and Jiao, Xinyan and Hao, Qingli and Mandler, Daniel}
}
@article { WOS:000432096400013,
	title = {Atomically resolved calcium phosphate coating on a gold substrate},
	journal = {NANOSCALE},
	volume = {10},
	number = {18},
	year = {2018},
	month = {MAY 14},
	pages = {8451-8458},
	issn = {2040-3364},
	doi = {10.1039/c8nr00372f},
	author = {Metoki, Noah and Baik, Sung-Il and Isheim, Dieter and Mandler, Daniel and Seidman, David N. and Eliaz, Noam}
}
@article { ISI:000432096400013,
	title = {Atomically resolved calcium phosphate coating on a gold substrate},
	journal = {NANOSCALE},
	volume = {10},
	number = {18},
	year = {2018},
	month = {MAY 14},
	pages = {8451-8458},
	abstract = {Some articles have revealed that the electrodeposition of calcium phosphate (CaP) coatings entails a precursor phase, similarly to biomineralization in vivo. The chemical composition of the initial layer and its thickness are, however, still arguable, to the best of our knowledge. Moreover, while CaP and electrodeposition of metal coatings have been studied utilizing atom-probe tomography (APT), the electrodeposition of CaP ceramics has not been heretofore studied. Herein, we present an investigation of the CaP deposition on a gold substrate. Using APT and transmission electron microscopy (TEM) it is found that a mixture of phases, which could serve as transient precursor phases to hydroxyapatite (HAp), can be detected. The thickness of these phases is tens of nanometers, and they consist of amorphous CaP (ACP), dibasic calcium phosphate dihydrate (DCPD), and octacalcium phosphate (OCP). This demonstrates the value of using atomic-resolved characterization techniques for identifying the precursor phases. It also indicates that the kinetics of their transformation into the more stable HAp is not too fast to enable their observation. The coating gradually displays higher Ca/P atomic ratios, a porous nature, and concomitantly a change in its density.},
	issn = {2040-3364},
	doi = {10.1039/c8nr00372f},
	author = {Metoki, Noah and Baik, Sung-Il and Isheim, Dieter and Mandler, Daniel and Seidman, David N. and Eliaz, Noam}
}
@article { WOS:000433581100010,
	title = {Chiral self-assembled monolayers in electrochemistry},
	journal = {CURRENT OPINION IN ELECTROCHEMISTRY},
	volume = {7},
	year = {2018},
	month = {JAN},
	pages = {42-47},
	issn = {2451-9103},
	doi = {10.1016/j.coelec.2017.09.030},
	author = {Mandler, Daniel}
}
@article { ISI:000433581100010,
	title = {Chiral self-assembled monolayers in electrochemistry},
	journal = {CURRENT OPINION IN ELECTROCHEMISTRY},
	volume = {7},
	year = {2018},
	month = {JAN},
	pages = {42-47},
	abstract = {The activity of chiral self-assembled monolayers (SAMs) in electrochemistry is reviewed. Chiral SAMs have been used as a means of introducing stereoselectivity in electron transfer at the electrode/electrolyte interface. In most cases, a cysteine-based SAM was used on gold electrodes. Different attempts have involved the application of chiral thiolated molecules, e.g., cyclodextrin, imprinting of chiral objects and competitive complexation. More recently, spintronics in which magnetic fields applied next to chiral SAM induced chiral effects, were also reported. Yet, there is much room for additional and innovative ideas in this field of electrochemistry.},
	issn = {2451-9103},
	doi = {10.1016/j.coelec.2017.09.030},
	author = {Mandler, Daniel}
}
@article { ISI:000438007200026,
	title = {Control of Crystal Growth in Local Electroless Gold Deposition by Pyridinium Based Surfactants},
	journal = {CRYSTAL GROWTH \& DESIGN},
	volume = {18},
	number = {7},
	year = {2018},
	month = {JUL},
	pages = {3913-3920},
	abstract = {The formation and local deposition of well-shaped Au nanostructures on a nonconducting surface are described. Specifically, the local electroless deposition of Au in aqueous solutions in the presence of various n-alkylpyridinium surfactants is driven by electrochemically generating a flux of AuCl4- at a gold tip close to a 3-mercaptopropyltrimethoxysilane modified Si oxidized wafer. Two reducing agents, NaBH4 and ascorbic acid, were used for the reduction of the gold ions. We studied the effect of the solution temperature, the potential applied to the gold tip and its distance from the surface, the reductant, and the nature of the alkylpyridinium on the structure of the gold deposit. The chloride salts of methylpyridinium, butylpyridinium, cetylpyridinium, 4-carbamoyl-1-cetylpyridinium, and 4-methyl-l-cetylpyridinium were added separately and showed remarkable effect on the shape of the structures that were formed. We find that short chain n-alkylpyridinium salts do not adsorb preferentially on the gold facets, whereas the longer chain n-alkylpyridinium ions cause the formation of well-faceted Au structures, such as cubes, hexagons, and even multipods. Moreover, comparison between local and bulk deposition revealed a significant difference in Au structures that were formed, presumably due to the different concentration profile of the AuCl4-.},
	issn = {1528-7483},
	doi = {10.1021/acs.cgd.8b00228},
	author = {Fedorov, Roman G. and Mandler, Daniel}
}
@article { WOS:000438007200026,
	title = {Control of Crystal Growth in Local Electroless Gold Deposition by Pyridinium Based Surfactants},
	journal = {CRYSTAL GROWTH \& DESIGN},
	volume = {18},
	number = {7},
	year = {2018},
	month = {JUL},
	pages = {3913-3920},
	issn = {1528-7483},
	doi = {10.1021/acs.cgd.8b00228},
	author = {Fedorov, Roman G. and Mandler, Daniel}
}
@article { WOS:000450934400016,
	title = {Core-shell nanoparticles for gas phase detection based on silver nanospheres coated with a thin molecularly imprinted polymer adsorbed on a chemiresistor},
	journal = {NANOSCALE},
	volume = {10},
	number = {37},
	year = {2018},
	month = {OCT 7},
	pages = {17593-17602},
	issn = {2040-3364},
	doi = {10.1039/c8nr01437j},
	author = {Shahar, Tehila and Feldheim, Gil and Marx, Sharon and Mandler, Daniel}
}
@article { ISI:000450934400016,
	title = {Core-shell nanoparticles for gas phase detection based on silver nanospheres coated with a thin molecularly imprinted polymer adsorbed on a chemiresistor},
	journal = {NANOSCALE},
	volume = {10},
	number = {37},
	year = {2018},
	month = {OCT 7},
	pages = {17593-17602},
	abstract = {We present a novel gas phase detection prototype based on assembling core-shell nanospheres made of a silver core and coated with a molecularly imprinted polymer (MIP) adsorbed onto an interdigitated array (IDA) electrode chemiresistor (CR). The core-shell nanospheres, AgNP@MIPs, were imprinted with linalool, a volatile terpene alcohol, as a model system. The thickness of the MIP layer was tuned to a few nanometers to enable the facile ingress and egress of the linalool, as well as to enhance the electrical transduction through the Ag core. The AgNP@MIPs were spread onto the IDA-CR modified with various positively charged polymers, by drop casting and dip-coating. The AgNP@MIPs were characterized by various techniques such as extra high-resolution scanning and tunnelling electron microscopy and X-ray diffraction. The MIP recognition event was transduced into a measurable increase in the resistance. The response to linalool exposure and removal was fast and the device was fully recovered and could be reused. Finally, the difference in the resistance change between imprinted and non-imprinted nanospheres was substantial.},
	issn = {2040-3364},
	doi = {10.1039/c8nr01437j},
	author = {Shahar, Tehila and Feldheim, Gil and Marx, Sharon and Mandler, Daniel}
}
@article { WOS:000448290800004,
	title = {Electrochemical detection of dopamine by a calixarene-cellulose acetate mixed Langmuir-Blodgett monolayer},
	journal = {ANALYTICA CHIMICA ACTA},
	volume = {1042},
	year = {2018},
	month = {DEC 26},
	pages = {29-36},
	issn = {0003-2670},
	doi = {10.1016/j.aca.2018.08.019},
	author = {Xu, Yujuan and Hao, Qingli and Mandler, Daniel}
}
@article { ISI:000448290800004,
	title = {Electrochemical detection of dopamine by a calixarene-cellulose acetate mixed Langmuir-Blodgett monolayer},
	journal = {ANALYTICA CHIMICA ACTA},
	volume = {1042},
	year = {2018},
	month = {DEC 26},
	pages = {29-36},
	abstract = {The sensing performance of a Langmuir-Blodgett monolayer was significantly improved by controlling the film organization at the air-water interface. Cellulose acetate (CA) and 4-tert-butylcalix [6] arene (calix) were co-spread and formed a Langmuir film, which was efficiently transferred onto a preoxidized gold electrode, Au-ox. The modified gold electrode was applied as a fast, highly sensitive electrochemical sensing platform for the quantitative determination of a model molecule, dopamine (DA). The modified gold electrode, CA-calix/Au-ox, demonstrated better recognition and sensing ability towards dopamine as compared with electrodes modified by a single component. Under the optimized conditions, the reduction peak currents at the CA-calix/Au-ox increased linearly within the concentration range of dopamine from 5 to 100 and 100-7500 nM, and exhibited a very low limit of detection (LOD) of 2.54 nM (S/N = 3). These results suggest a simple, superior and efficient approach for the controllable rearrangement of Langmuir-Blodgett monolayers on a molecular level. The electroanalytical performance was optimized from the perspective of the electrode-electrolyte interface. (C 2018 Elsevier B.V. All rights reserved.},
	issn = {0003-2670},
	doi = {10.1016/j.aca.2018.08.019},
	author = {Xu, Yujuan and Hao, Qingli and Mandler, Daniel}
}
@article { WOS:000427235600033,
	title = {Electrochemical Dynamics of a Single Platinum Nanoparticle Collision Event for the Hydrogen Evolution Reaction},
	journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
	volume = {57},
	number = {13},
	year = {2018},
	month = {MAR 19},
	pages = {3464-3468},
	issn = {1433-7851},
	doi = {10.1002/anie.201712454},
	author = {Xiang, Zhi-peng and Deng, Hai-qiang and Peljo, Pekka and Fu, Zhi-yong and Wang, Su-li and Mandler, Daniel and Sun, Gong-quan and Liang, Zhen-xing}
}
@article { ISI:000427235600033,
	title = {Electrochemical Dynamics of a Single Platinum Nanoparticle Collision Event for the Hydrogen Evolution Reaction},
	journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
	volume = {57},
	number = {13},
	year = {2018},
	month = {MAR 19},
	pages = {3464-3468},
	abstract = {Chronoamperometry was used to study the dynamics of Pt nanoparticle (NP) collision with an inert ultramicroelectrode via electrocatalytic amplification (ECA) in the hydrogen evolution reaction. ECA and dynamic light scattering (DLS) results reveal that the NP colloid remains stable only at low proton concentrations (1.0mm) under a helium (He) atmosphere, ensuring that the collision events occur at genuinely single NP level. Amperometry of single NP collisions under a He atmosphere shows that each discrete current profile of the collision event evolves from spike to staircase at more negative potentials, while a staircase response is observed at all of the applied potentials under hydrogen-containing atmospheres. The particle size distribution estimated from the diffusion-controlled current in He agrees well with electron microscopy and DLS observations. These results shed light on the interfacial dynamics of the single nanoparticle collision electrochemistry.},
	issn = {1433-7851},
	doi = {10.1002/anie.201712454},
	author = {Xiang, Zhi-peng and Deng, Hai-qiang and Peljo, Pekka and Fu, Zhi-yong and Wang, Su-li and Mandler, Daniel and Sun, Gong-quan and Liang, Zhen-xing}
}
@article { ISI:000461401100029,
	title = {Electrochemically Deposited Sol-Gel Based Nanoparticle-Imprinted Matrices for the Size-Selective Detection of Gold Nanoparticles},
	journal = {ACS APPLIED NANO MATERIALS},
	volume = {1},
	number = {10},
	year = {2018},
	month = {OCT},
	pages = {5612-5619},
	abstract = {Nanoparticles imprinted matrices (NAIMs) is a new approach, in which nanoparticles (NPs) are imprinted in a matrix followed by their removal to form highly selective voids that can recognize the original NPs. In this study, the effect of a sol-gel matrix on the imprinting and reuptake of gold nanoparticles (AuNPs) is examined. Specifically, indium tin oxide (ITO) films were modified with a positively charged polymer, on which the negatively charged AuNPs stabilized with citrate (AuNPs-cit) were adsorbed. This was followed by the electrochemical deposition of sol-gel matrices with different thicknesses and functional groups onto the ITO/AuNPs-cit. Electrochemical oxidation dissolved the AuNPs-cit and formed cavities in the sol-gel films, which fit both the size and shape of the AuNPs-cit. Reuptake of these NPs from an aqueous solution was successful using the imprinted films, whereas the non-imprinted films did not re-uptake the AuNPs-cit. Furthermore, the thickness of the sol-gel layers as well as the type of the silanes that were deposited play an important role on the recognition ability of the NAIM. Finally, we found that the NAIMs are selective, and larger AuNPs-cit were not recognized by the imprinted matrix.},
	issn = {2574-0970},
	doi = {10.1021/acsanm.8b01215},
	author = {Bruchiel-Spanier, Netta and Giordano, Gianmarco and Vakahi, Atzmon and Guglielmi, Massimo and Mandler, Daniel}
}
@article { WOS:000461401100029,
	title = {Electrochemically Deposited Sol-Gel Based Nanoparticle-Imprinted Matrices for the Size-Selective Detection of Gold Nanoparticles},
	journal = {ACS APPLIED NANO MATERIALS},
	volume = {1},
	number = {10},
	year = {2018},
	month = {OCT},
	pages = {5612-5619},
	issn = {2574-0970},
	doi = {10.1021/acsanm.8b01215},
	author = {Bruchiel-Spanier, Netta and Giordano, Gianmarco and Vakahi, Atzmon and Guglielmi, Massimo and Mandler, Daniel}
}
@article { WOS:000427005900012,
	title = {Free-Standing Hybrid Graphene Paper Encapsulating Nanostructures for High Cycle-Life Supercapacitors},
	journal = {CHEMSUSCHEM},
	volume = {11},
	number = {5},
	year = {2018},
	month = {MAR 9},
	pages = {907-915},
	issn = {1864-5631},
	doi = {10.1002/cssc.201702283},
	author = {Jiao, Xinyan and Hao, Qingli and Xia, Xifeng and Lei, Wu and Ouyang, Yu and Ye, Haitao and Mandler, Daniel}
}
@article { ISI:000427005900012,
	title = {Free-Standing Hybrid Graphene Paper Encapsulating Nanostructures for High Cycle-Life Supercapacitors},
	journal = {CHEMSUSCHEM},
	volume = {11},
	number = {5},
	year = {2018},
	month = {MAR 9},
	pages = {907-915},
	abstract = {The incorporation of spacers between graphene sheets has been investigated as an effective method to improve the electrochemical performance of graphene papers (GPs) for supercapacitors. Here, we report the design of free-standing GP@NiO and GP@Ni hybrid GPs in which NiO nanoclusters and Ni nanoparticles are encapsulated into graphene sheets through electrostatic assembly and subsequent vacuum filtration. The encapsulated NiO nanoclusters and Ni nanoparticles can mitigate the restacking of graphene sheets, providing sufficient spaces for high-speed ion diffusion and electron transport. In addition, the spacers strongly bind to graphene sheets, which can efficiently improve the electrochemical stability. Therefore, at a current density of 0.5 Ag-1, the GP@NiO and GP@Ni electrodes exhibit higher specific capacitances of 306.9 and 246.1 Fg(-1) than the GP electrode (185.7 Fg(-1)). The GP@NiO and GP@Ni electrodes exhibit capacitance retention of 98.7\% and 95.6\% after 10000 cycles, demonstrating an outstanding cycling stability. Additionally, the GP@NiO vertical bar GP@Ni delivers excellent cycling stability (93.7\% after 10000 cycles) and high energy density. These free-standing encapsulated hybrid GPs have great potential as electrode for high-performance supercapacitors.},
	issn = {1864-5631},
	doi = {10.1002/cssc.201702283},
	author = {Jiao, Xinyan and Hao, Qingli and Xia, Xifeng and Lei, Wu and Ouyang, Yu and Ye, Haitao and Mandler, Daniel}
}
@article { ISI:000423968600109,
	title = {A high-performance electrochemical sensor based on g-C3N4-E-PEDOT for the determination of acetaminophen},
	journal = {ELECTROCHIMICA ACTA},
	volume = {259},
	year = {2018},
	month = {JAN 1},
	pages = {994-1003},
	abstract = {A fast, ultrasensitive electrochemical sensing platform based on graphitic carbon nitride-electrochemically deposited-poly(3,4-ethylenedioxythiophene) (g-C3N4-E-PEDOT) composite was constructed by in-situ electropolymerization and applied for the quantitative determination of acetaminophen (AP). E-PEDOT was introduced as the conducting matrix for developing g-C3N4 composite to complement the poor conductivity disadvantage of g-C3N4. The strong affinity and synergetic effect between g-C3N4 and E-PEDOT, which were analyzed by PM6 computational calculation, highly improved the electron transfer property and remarkably enhanced the electrochemical catalytic activity of the composite. The g-C3N4-E-PEDOT modified glassy carbon electrode (GCE) demonstrated better electrocatalytic activity towards the oxidation of AP than bare, g-C3N4 and E-PEDOT modified ones. Under the optimized conditions, the oxidation peak currents at the g-C3N4-E-PEDOT/GCE increased linearly in the concentration range of AP from 0.01 to 2 mu M and 2-100 mu M, and an ultra-low limit of detection (LOD) of 34.28 nM was obtained (S/N = 3). In addition, the g-C3N4-E-PEDOT/GCE was successfully applied for the AP determination in the clinical human serum, and also exhibited excellent selectivity, reproducibility and stability. Except the novel AP determination approach, moreover, this work provided a new electrochemical application angle of graphitic carbon nitride theoretically as well as experimentally. (C) 2017 Elsevier Ltd. All rights reserved.},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2017.11.034},
	author = {Xu, Yujuan and Lei, Wu and Su, Juan and Hu, Jinjin and Yu, Xiaodan and Zhou, Tong and Yang, Yun and Mandler, Daniel and Hao, Qingli}
}
@article { WOS:000423968600109,
	title = {A high-performance electrochemical sensor based on g-C3N4-E-PEDOT for the determination of acetaminophen},
	journal = {ELECTROCHIMICA ACTA},
	volume = {259},
	year = {2018},
	month = {JAN 1},
	pages = {994-1003},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2017.11.034},
	author = {Xu, Yujuan and Lei, Wu and Su, Juan and Hu, Jinjin and Yu, Xiaodan and Zhou, Tong and Yang, Yun and Mandler, Daniel and Hao, Qingli}
}
@article { WOS:000415930900153,
	title = {Index-tunable anti-reflection coatings: Maximizing solar modulation ability for vanadium dioxide-based smart thermochromic glazing},
	journal = {JOURNAL OF ALLOYS AND COMPOUNDS},
	volume = {731},
	year = {2018},
	month = {JAN 15},
	pages = {1197-1207},
	issn = {0925-8388},
	doi = {10.1016/j.jallcom.2017.10.045},
	author = {Liu, Chang and Wang, Shancheng and Zhou, Yang and Yang, Haibo and Lu, Qi and Mandler, Daniel and Magdassi, Shlomo and Tay, Chor Yong and Long, Yi}
}
@article { ISI:000415930900153,
	title = {Index-tunable anti-reflection coatings: Maximizing solar modulation ability for vanadium dioxide-based smart thermochromic glazing},
	journal = {JOURNAL OF ALLOYS AND COMPOUNDS},
	volume = {731},
	year = {2018},
	month = {JAN 15},
	pages = {1197-1207},
	abstract = {Vanadium dioxide (VO2) nanoparticles with reversible semiconductor-metal phase transition holds the tremendous potential as a thermochromic material for the energy-saving smart glazing. However, the trade-off between improving the luminous transmittance (T-lum) while sacrificing the solar modulation ability (Delta T-sol) hampers its bench-to-market translation. Previous studies of anti-reflection coatings (ARCs) focused primarily on increasing Tlum while neglecting DTsol, which is a key energy-saving determinant. The intrinsically low Delta T-sol (< 16\%) is due to the fact that VO2 has a higher refractive index (RI) from 500 nm to 2200 nm wavelength (lambda) below its critical transition temperature (tau(c)), which causes excessive reflection at a lower temperature. This study aims to investigate ARCs with tunable RI (1.47-1.92 at lambda = 550 nm) to improve the antireflection effect at a lower temperature, thereby maximizing Delta T-sol for various VO2 nanosubstrates, e.g. continuous thin films, nanocomposites, and periodic micro-patterning films. We showed that the best performing coatings could maximize Delta T-sol (from 15.7\% to 18.9\%) and increase T-lum(avg) (from 39\% to 44\%) simultaneously, which surpasses the current benchmark specifications ever reported for ARC-coated VO2 smart glazing. In addition, the cytotoxicity analyses evidence that ARCs are feasible to improve the cyto-compatibility of VO2 nanoparticles-based nanocomposites. The presented RI-tunable ARC, which circumvents the complex materials selection and optical design, not only paves the way for practical applications of VO2-based smart windows but also has extensive applications in the field of solar cells, optical lenses, smart display, etc. (C) 2017 Elsevier B.V. All rights reserved.},
	issn = {0925-8388},
	doi = {10.1016/j.jallcom.2017.10.045},
	author = {Liu, Chang and Wang, Shancheng and Zhou, Yang and Yang, Haibo and Lu, Qi and Mandler, Daniel and Magdassi, Shlomo and Tay, Chor Yong and Long, Yi}
}
@article { WOS:000440931800024,
	title = {Modern Jewish Scholarship in Hungary - the {\textquoteleft}{\textquoteleft}Science of Judaism{\textquoteright}{\textquoteright} Between East and West},
	journal = {HUNGARIAN CULTURAL STUDIES},
	volume = {11},
	year = {2018},
	pages = {196-201},
	issn = {2471-965X},
	doi = {10.5195/ahea.2018.341},
	author = {Mandler, David}
}
@article { ISI:000440931800024,
	title = {Modern Jewish Scholarship in Hungary - the {\textquoteleft}{\textquoteleft}Science of Judaism{\textquoteright}{\textquoteright} Between East and West},
	journal = {HUNGARIAN CULTURAL STUDIES},
	volume = {11},
	year = {2018},
	pages = {196-201},
	issn = {2471-965X},
	doi = {10.5195/ahea.2018.341},
	author = {Mandler, David}
}
@article { WOS:000452484800020,
	title = {The role of hydrophobic, aromatic and electrostatic interactions between amino acid residues and a titanium dioxide surface},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {20},
	number = {47},
	year = {2018},
	month = {DEC 21},
	pages = {29811-29816},
	issn = {1463-9076},
	doi = {10.1039/c8cp05775c},
	author = {Leader, Avia and Mandler, Daniel and Reches, Meital}
}
@article { ISI:000452484800020,
	title = {The role of hydrophobic, aromatic and electrostatic interactions between amino acid residues and a titanium dioxide surface},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {20},
	number = {47},
	year = {2018},
	month = {DEC 21},
	pages = {29811-29816},
	abstract = {Understanding the nature of interactions between inorganic surfaces and biomolecules, such as amino acids and peptides, can enhance the development of new materials. Here, we present single molecule force spectroscopy (SMFS) measurements of the interactions between an atomic force microscopy (AFM) probe, modified with various amino acids, and a titanium dioxide surface. Specifically, we study the affinity of amino acids toward a titanium dioxide surface bearing hydrophobic (Leu), aromatic (Phe) and hydrophilic (Orn) residues. We find that aromatic interactions dominate over aliphatic in their affinity to the titanium dioxide surface. In addition, we show that by combining aromatic and hydrophilic moieties in a single amino acid (NH2-Phe), the adhesion of the latter to the surface increases. Furthermore, the affinity of positively charged amino acids to the titanium dioxide surface is higher than that of uncharged, and can be increased more, with elevating the pH of the buffer above the pK(a) of the basic residues. The kinetic and thermodynamic parameters imply that the dynamics of the surface-amino acid interface are mostly governed by hydrophobic interactions.},
	issn = {1463-9076},
	doi = {10.1039/c8cp05775c},
	author = {Leader, Avia and Mandler, Daniel and Reches, Meital}
}
@article { WOS:000426495100014,
	title = {Selective Binding and Precipitation of Cesium Ions from Aqueous Solutions: A Size-Driven Supramolecular Reaction},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {24},
	number = {13},
	year = {2018},
	month = {MAR 2},
	pages = {3161-3164},
	issn = {0947-6539},
	doi = {10.1002/chem.201706181},
	author = {Bengiat, Ravell and Bogoslaysky, Benny and Mandler, Daniel and Almog, Joseph}
}
@article { ISI:000426495100014,
	title = {Selective Binding and Precipitation of Cesium Ions from Aqueous Solutions: A Size-Driven Supramolecular Reaction},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {24},
	number = {13},
	year = {2018},
	month = {MAR 2},
	pages = {3161-3164},
	abstract = {The nuclear disasters of Chernobyl and Fukushima presented an urgent need for finding solutions to treatment of radioactive wastes. Among the by-products of nuclear fission is radioactive Cs-137, which evokes an environmental hazard due to its long half-life (> 30 years) and high solubility in water. In this work, a water-soluble organic ligand, readily obtained from alloxan and 1,3,5-benzenetriol, has been found to selectively bind and precipitate Cs+ ions from aqueous solutions. The special rigid structure of the ligand, which consists of a {\textquoteleft}{\textquoteleft}tripodal{\textquoteright}{\textquoteright} carbonyl base above and below an aromatic plane, contributes to the size-driven selectivity towards the large Cs+ ions and the formation of a giant, insoluble supramolecular complex. In addition to the low costs of the ligand, high yields and effectiveness in precipitating Cs+ ions, the Cs- complex revealed a high endurance to continuous doses of gamma-radiation, increasing its potential to act as a precipitating agent for Cs-137.},
	issn = {0947-6539},
	doi = {10.1002/chem.201706181},
	author = {Bengiat, Ravell and Bogoslaysky, Benny and Mandler, Daniel and Almog, Joseph}
}
@article { WOS:000435619700030,
	title = {SP1 based self-assembled selective molecular nanochannels},
	journal = {JOURNAL OF ELECTROANALYTICAL CHEMISTRY},
	volume = {819},
	number = {SI},
	year = {2018},
	month = {JUN 15},
	pages = {220-225},
	issn = {1572-6657},
	doi = {10.1016/j.jelechem.2017.10.036},
	author = {Gdor, Efrat and Levy, Dorit and Aharon, Linoy and Shoseyov, Oded and Mandler, Daniel}
}
@article { ISI:000435619700030,
	title = {SP1 based self-assembled selective molecular nanochannels},
	journal = {JOURNAL OF ELECTROANALYTICAL CHEMISTRY},
	volume = {819},
	number = {SI},
	year = {2018},
	month = {JUN 15},
	pages = {220-225},
	abstract = {Controlling the permeability and porosity of an inorganic layer using biomolecule building blocks has raised interest for nanotechnological applications. The challenge lies mostly in the fabrication, usually a long, expensive and tedious process, involving many steps. Using biomaterials for this purpose is highly appealing; due to both ease of fabrication and the final output, that contains a bioelement. The biomolecule, specifically, stable protein 1 (SP1), serving as the scaffold for our pattern, is of great stability and durability, and presents size, charge and structural selectivity towards electroactive species. Here, we demonstrate the ability of SP1 to form a rigid template within a sol-gel matrix, allowing selective electron transfer to the gold electrode. Specifically, a thiolated SP1 was first adsorbed on a gold surface followed by filling the non-occupied areas by sol-gel. The latter was electrochemically deposited. The various steps were carefully characterized. Finally, we studied the electrochemistry of numerous redox couple at the Au/SP1/sol-gel interface and found that the nanochannel array shows charge and structural selectivity, which is based on the interactions between the redox species and the functionalities of SP1. The resulted surface shows promise towards electrochemical sensing applications.},
	issn = {1572-6657},
	doi = {10.1016/j.jelechem.2017.10.036},
	author = {Gdor, Efrat and Levy, Dorit and Aharon, Linoy and Shoseyov, Oded and Mandler, Daniel}
}
@article { WOS:000447570500032,
	title = {The synergistic effect of benzotriazole and trimethylsiloxysilicate towards corrosion protection of printed Cu-based electronics},
	journal = {CORROSION SCIENCE},
	volume = {143},
	year = {2018},
	month = {OCT},
	pages = {329-336},
	issn = {0010-938X},
	doi = {10.1016/j.corsci.2018.08.027},
	author = {Geuli, Ori and Mandler, Daniel}
}
@article { ISI:000447570500032,
	title = {The synergistic effect of benzotriazole and trimethylsiloxysilicate towards corrosion protection of printed Cu-based electronics},
	journal = {CORROSION SCIENCE},
	volume = {143},
	year = {2018},
	month = {OCT},
	pages = {329-336},
	abstract = {The development of printed electronics has gained much attention as an alternative for conventional metal-based electronics, mainly due to the ability to print electronic circuits on plastics and by much cheaper means as compared with conventional microelectronics. Here we report on a single stage formation of a highly corrosion resistance coating with hydrophobic properties on printed-Cu nanoparticles. Our method is based on the synergistic effect of benzotriazole (BTA) as corrosion inhibitor and trimethylsiloxysilicate (TMS) as hydrophobic component. Printed-Cu coated with such TMS/BTA layer exhibited excellent corrosion resistance in 3.5\% NaCl solution, reducing the dissolution of Cu into soluble species by one order of magnitude.},
	issn = {0010-938X},
	doi = {10.1016/j.corsci.2018.08.027},
	author = {Geuli, Ori and Mandler, Daniel}
}
@article { WOS:000444823900020,
	title = {TiO2-WO3 core-shell inverse opal structure with enhanced electrochromic performance in NIR region},
	journal = {JOURNAL OF MATERIALS CHEMISTRY C},
	volume = {6},
	number = {31},
	year = {2018},
	month = {AUG 21},
	pages = {8488-8494},
	issn = {2050-7526},
	doi = {10.1039/c8tc01954a},
	author = {Ling, Han and Yeo, Loo Pin and Wang, Zhiwei and Li, Xianglin and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred Iing Yoong}
}
@article { ISI:000444823900020,
	title = {TiO2-WO3 core-shell inverse opal structure with enhanced electrochromic performance in NIR region},
	journal = {JOURNAL OF MATERIALS CHEMISTRY C},
	volume = {6},
	number = {31},
	year = {2018},
	month = {AUG 21},
	pages = {8488-8494},
	abstract = {More than 50\% of solar energy comes from the infrared region (as radiant heat) of the solar spectrum. Electrochromic (EC) materials, which can dynamically modulate the transmittance of infrared (IR) radiation, can be effectively applied in smart windows for thermal management in buildings. In this work, a core-shell TiO2-WO3 inverse opal (IO) structure was fabricated through the electrodeposition of WO3 onto TiO2 IO templates. The TiO2 IO templates were synthesized by introducing TiO2 into the voids of a polystyrene (PS) colloidal crystal template, followed by calcination to remove the PS microspheres. It was found that the TiO2-WO3 IO core-shell structure can modulate NIR transmittance at wavelengths from 700 to 1600 nm in the NIR range when potential is applied in LiClO4/PC electrolyte. When -0.3 V is applied, up to 60\% of NIR radiation in this range can be blocked. The NIR transmittance can be modulated by tuning the applied potential. This study focuses on comparing the novel TiO2-WO3 IO structure with electrodeposited WO3 thin film to fully elucidate the effect of the inverse opal morphology and the TiO2-WO3 hybrid system on the optical properties. Results show that the NIR blockage can be sustained up to 90\% after 1200 reversible cycles for TiO2-WO3 IO structure. The greater surface area of the IO structure increases the number of active sites available for the redox reactions by providing a larger contact area with the electrolyte. The more electroactive area with improved charge transfer enhances the overall NIR transmittance contrast as compared to bulk WO3 thin film. Furthermore, the addition of WO3 to TiO2 to form a composite has been shown to enhance cycling performance and device lifespan.},
	issn = {2050-7526},
	doi = {10.1039/c8tc01954a},
	author = {Ling, Han and Yeo, Loo Pin and Wang, Zhiwei and Li, Xianglin and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred Iing Yoong}
}
@conference { WOS:000464596500012,
	title = {Voltammetry of Electroactive Species at the Interface in Langmuir-Blodgett Trough},
	booktitle = {PROCEEDINGS OF THE INTERNATIONAL CONFERENCE MODERN ELECTROCHEMICAL METHODS XXXVIII},
	year = {2018},
	note = {38th International Conference on Modern Electrochemical Methods, Jetrichovice, CZECH REPUBLIC, MAY 21-25, 2018},
	pages = {54-57},
	publisher = {Czech Acad Sci, J Heyrovsky Inst Phys Chem; Czech Acad Sci, Inst Biophys; Charles Univ, Fac Sci, Dept Analyt Chem, UNESCO Lab Environm Electrochemistry},
	organization = {Czech Acad Sci, J Heyrovsky Inst Phys Chem; Czech Acad Sci, Inst Biophys; Charles Univ, Fac Sci, Dept Analyt Chem, UNESCO Lab Environm Electrochemistry},
	isbn = {978-80-905221-6-9},
	author = {Gajdar, Julius and Sarkar, Sujoy and Mandler, Daniel and Fischer, Jan and Barek, Jiri},
	editor = {Navratil, T and Fojta, M and Schwarzova, K}
}
@article { WOS:000396820900007,
	title = {Discomfort as a means of pre-service teachers{\textquoteright} professional development - an action research as part of the {\textquoteleft}Research Literacy{\textquoteright} course},
	journal = {EUROPEAN JOURNAL OF TEACHER EDUCATION},
	volume = {40},
	number = {2},
	year = {2017},
	pages = {231-245},
	issn = {0261-9768},
	doi = {10.1080/02619768.2017.1284197},
	author = {Amir, Aliza and Mandler, Daphna and Hauptman, Sara and Gorev, Dvora}
}
@article { ISI:000396820900007,
	title = {Discomfort as a means of pre-service teachers{\textquoteright} professional development - an action research as part of the {\textquoteleft}Research Literacy{\textquoteright} course},
	journal = {EUROPEAN JOURNAL OF TEACHER EDUCATION},
	volume = {40},
	number = {2},
	year = {2017},
	pages = {231-245},
	abstract = {This paper focus on defining a research question while conducting action research among third-year students attending a course on Research Literacy at a teacher education college. This paper discusses the process of preparing for and conducting action research among third-year students attending a course on Research Literacy at a teacher education college. The students were asked to conduct an action research on their classroom activities. The aim of this article is to present the process and pinpointing the discomfort of the students in formulating a research question suited to action research thanks to two prerequisite conditions: the {\textquoteleft}safe space{\textquoteright} and the {\textquoteleft}tender spot{\textquoteright}. The research findings illustrate that the students had difficulty defining their {\textquoteleft} tender spot{\textquoteright}. It was necessary to create a {\textquoteleft}safe space{\textquoteright}. Furthermore, the findings show that the {\textquoteleft}tender spot{\textquoteright} issues were associated with disciplinary content far more than with generic lesson management or classroom management issues. The approach discussed here is leading to positive change and it may be that this professional development tool can facilitate the induction of novice teachers everywhere.},
	issn = {0261-9768},
	doi = {10.1080/02619768.2017.1284197},
	author = {Amir, Aliza and Mandler, Daphna and Hauptman, Sara and Gorev, Dvora}
}
@article { ISI:000407540400094,
	title = {Electrochemical Approach for Effective Antifouling and Antimicrobial Surfaces},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {9},
	number = {31},
	year = {2017},
	month = {AUG 9},
	pages = {26503-26509},
	abstract = {Biofouling, the adsorption of organisms to a surface, is a major problem today in many areas of our lives. This includes: (i) health, as biofouling on medical device leads to hospital-acquired infections, (ii) water, since the accumulation of organisms on membranes and pipes in desalination systems harms the function of the system, and (iii) energy, due to the heavy load of the organic layer that accumulates on marine vessels and causes a larger consumption of fuel. This paper presents an effective electrochemical approach for generating antifouling and antimicrobial surfaces. Distinct from previously reported antifouling or antimicrobial electrochemical studies, we demonstrate the formation of a hydrogen gas bubble layer through the application of a low-voltage square waveform pulses to the conductive surface. This electrochemically generated gas bubble layer serves as a separation barrier between the surroundings and the target surface where the adhesion of bacteria can be deterred. Our results indicate that this barrier could effectively reduce the adsorption of bacteria to the surface by 99.5\%. We propose that the antimicrobial mechanism correlates with the fundamental of hydrogen evolution reaction (HER). HER leads to an arid environment that does not allow the existence of live bacteria. In addition, we show that this drought condition kills the preadhered bacteria on the surface due to water stress. This work serves as the basis for the exploration of future self-sustainable antifouling techniques such as incorporating it with photocatalytic and photoelectrochemical reactions.},
	issn = {1944-8244},
	doi = {10.1021/acsami.7b03761},
	author = {Gaw, Sheng Long and Sarkar, Sujoy and Nir, Sivan and Schnell, Yafit and Mandler, Daniel and Xu, Zhichuan J. and Lee, Pooi See and Reches, Meital}
}
@article { WOS:000407540400094,
	title = {Electrochemical Approach for Effective Antifouling and Antimicrobial Surfaces},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {9},
	number = {31},
	year = {2017},
	month = {AUG 9},
	pages = {26503-26509},
	issn = {1944-8244},
	doi = {10.1021/acsami.7b03761},
	author = {Gaw, Sheng Long and Sarkar, Sujoy and Nir, Sivan and Schnell, Yafit and Mandler, Daniel and Xu, Zhichuan J. and Lee, Pooi See and Reches, Meital}
}
@article { WOS:000399727100026,
	title = {Electrochemically stimulated drug release from flexible electrodes coated electrophoretically with doxorubicin loaded reduced graphene oxide},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {53},
	number = {28},
	year = {2017},
	month = {APR 11},
	pages = {4022-4025},
	issn = {1359-7345},
	doi = {10.1039/c7cc00381a},
	author = {He, Lijie and Sarkar, Sujoy and Barras, Alexandre and Boukherroub, Rabah and Szunerits, Sabine and Mandler, Daniel}
}
@article { ISI:000399727100026,
	title = {Electrochemically stimulated drug release from flexible electrodes coated electrophoretically with doxorubicin loaded reduced graphene oxide},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {53},
	number = {28},
	year = {2017},
	month = {APR 11},
	pages = {4022-4025},
	abstract = {The electrochemically triggered release of doxorubicin (DOX) from flexible electrodes modified electrophoretically with reduced graphene oxide (rGO)-DOX is reported. The release is driven by a positive potential pulse that decreases the pH of the rGO-DOX surface locally, which is confirmed by scanning electrochemical microscopy (SECM) in situ. In vitro cell viability tests confirms that the delivery system meets therapeutic needs.},
	issn = {1359-7345},
	doi = {10.1039/c7cc00381a},
	author = {He, Lijie and Sarkar, Sujoy and Barras, Alexandre and Boukherroub, Rabah and Szunerits, Sabine and Mandler, Daniel}
}
@article { ISI:000411394700003,
	title = {Highly Selective Solar Thermal Sprayable Coating Based on Carbon Nanotubes},
	journal = {SOLAR RRL},
	volume = {1},
	number = {9},
	year = {2017},
	month = {SEP},
	abstract = {A key component in solar thermal energy conversion system is the light collector that is coated with an absorbing material. Optimal performance is accomplished by high absorptance and low emittance. The best collectors are fabricated by vacuum deposition processes, which are limited to small size and flat objects. Here, the formation and performance of a new three-layer solar selective coating, which is formed by a simple wet-deposition process is reported. The solar absorbing layer is based on carbon nanotubes, which are considered the most absorbing material. This layer is coated by a second layer of ITO, which functions as an IR reflecting layer, followed by an AlOOH anti-reflective layer. The resulting CNT/ITO/AlOOH coating exhibited the best-reported spectral selectivity by wet deposition process, with high absorptance of 0.941 +/- 0.004 and low emittance of 0.13 +/- 0.02 at room temperature. Furthermore, the multilayer sprayable coating is stable at elevated temperature for a prolong time and therefore, shows promise for application in large scale and on-site solar thermal facilities.},
	issn = {2367-198X},
	doi = {10.1002/solr.201700080},
	author = {Bera, Raj Kumar and Binyamin, Yaniv and Mhaisalkar, Subodh G. and Magdassi, Shlomo and Mandler, Daniel}
}
@article { WOS:000411394700003,
	title = {Highly Selective Solar Thermal Sprayable Coating Based on Carbon Nanotubes},
	journal = {SOLAR RRL},
	volume = {1},
	number = {9},
	year = {2017},
	month = {SEP},
	issn = {2367-198X},
	doi = {10.1002/solr.201700080},
	author = {Bera, Raj Kumar and Binyamin, Yaniv and Mhaisalkar, Subodh G. and Magdassi, Shlomo and Mandler, Daniel}
}
@article { ISI:000394780200001,
	title = {Ionic strength induced electrodeposition: a universal approach for nanomaterial deposition at selective areas},
	journal = {NANOSCALE},
	volume = {9},
	number = {2},
	year = {2017},
	month = {JAN 14},
	pages = {485-490},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {An appealing alternative approach to the conventional electro-chemical deposition is presented, which can be universally utilized to form nanomaterial coatings from their aqueous dispersions without involving their oxidation-reduction. It is based on altering the ionic strength by electrical potential in the vicinity of the electrode surface, which causes the nanomaterials to deposit. The concept has been demonstrated for four different systems.},
	issn = {2040-3364},
	doi = {10.1039/c6nr06614c},
	author = {Liu, Chang and Long, Yi and Magdassi, Shlomo and Mandler, Daniel}
}
@article { WOS:000394780200001,
	title = {Ionic strength induced electrodeposition: a universal approach for nanomaterial deposition at selective areas},
	journal = {NANOSCALE},
	volume = {9},
	number = {2},
	year = {2017},
	month = {JAN 14},
	pages = {485-490},
	issn = {2040-3364},
	doi = {10.1039/c6nr06614c},
	author = {Liu, Chang and Long, Yi and Magdassi, Shlomo and Mandler, Daniel}
}
@article { ISI:000394780200001,
	title = {Ionic strength induced electrodeposition: a universal approach for nanomaterial deposition at selective areas},
	journal = {NANOSCALE},
	volume = {9},
	number = {2},
	year = {2017},
	month = {JAN 14},
	pages = {485-490},
	abstract = {An appealing alternative approach to the conventional electro-chemical deposition is presented, which can be universally utilized to form nanomaterial coatings from their aqueous dispersions without involving their oxidation-reduction. It is based on altering the ionic strength by electrical potential in the vicinity of the electrode surface, which causes the nanomaterials to deposit. The concept has been demonstrated for four different systems.},
	issn = {2040-3364},
	doi = {10.1039/c6nr06614c},
	author = {Liu, Chang and Long, Yi and Magdassi, Shlomo and Mandler, Daniel}
}
@article {13797,
	title = {Ionic strength induced electrodeposition: a universal approach for nanomaterial deposition at selective areas.},
	journal = {NanoscaleNanoscale},
	volume = {9},
	number = {2},
	year = {2017},
	note = {CAPLUS AN 2016:1703416(Journal; Online Computer File)},
	month = {2017///},
	pages = {485 - 490},
	publisher = {Royal Society of Chemistry},
	abstract = {An appealing alternative approach to the conventional electrochem. deposition is presented, which can be universally utilized to form nanomaterial coatings from their aq. dispersions without involving their oxidn.-redn. It is based on altering the ionic strength by elec. potential in the vicinity of the electrode surface, which causes the nanomaterials to deposit. The concept has been demonstrated for four different systems. [on SciFinder(R)]},
	isbn = {2040-3372},
	author = {Liu, Chang and Long, Yi and Magdassi, Shlomo and Mandler, Daniel.}
}
@article { WOS:000415949000006,
	title = {Ionic strength induced electrodeposition of two-dimensional layered MoS2 nanosheets},
	journal = {APPLIED MATERIALS TODAY},
	volume = {8},
	number = {SI},
	year = {2017},
	month = {SEP},
	pages = {44-53},
	issn = {2352-9407},
	doi = {10.1016/j.apmt.2017.04.004},
	author = {Rastogi, Pankaj Kumar and Sarkar, Sujoy and Mandler, Daniel}
}
@article { ISI:000415949000006,
	title = {Ionic strength induced electrodeposition of two-dimensional layered MoS2 nanosheets},
	journal = {APPLIED MATERIALS TODAY},
	volume = {8},
	number = {SI},
	year = {2017},
	month = {SEP},
	pages = {44-53},
	abstract = {A new redox-free electrochemical approach for driving the deposition of two-dimensional (2D) layered MoS2 nanosheets is described. First, poly(acylic acid) (PAA) functionalized layered MoS2 nanosheets (PAA-MoS2) is prepared to form a stable aqueous PAA-MoS2 dispersion, which is subsequently used for the electrochemical deposition. In contrast to previous electrodeposition methods of MoS2, which involve the redox of molecular precursors of Mo and S, herein we introduce an electrochemical approach for the deposition of 2D layered MoS2 nanosheets directly from their nanometric building blocks, namely from their aqueous dispersion. This {\textquoteleft}{\textquoteleft}nano to nano{\textquoteright}{\textquoteright} approach is based on altering the ionic strength at the vicinity of the electrode surface by applying a potential. Specifically, the electrogeneration of Cue-1 ions, cause the PAA-MoS2 nanosheets in the dispersion to aggregate and deposit on the copper electrode. Scanning electron microscopy, X-ray diffraction, Raman and X-ray photoelectron spectroscopy analysis show clearly that the deposited layered MoS2 maintains its original structure. Furthermore, the ;electrodeposited PAA-MoS2 nanosheets on copper show excellent catalytic activity for the hydrogen evolution reaction with low overpotential. Hence, we believe that these findings could lead to a generic approach for the formation of thin films or patterns of 2D nanomaterials. (C) 2017 Elsevier Ltd. All rights reserved.},
	issn = {2352-9407},
	doi = {10.1016/j.apmt.2017.04.004},
	author = {Rastogi, Pankaj Kumar and Sarkar, Sujoy and Mandler, Daniel}
}
@article { ISI:000391077000064,
	title = {Label-free femtomolar cancer biomarker detection in human serum using graphene-coated surface plasmon resonance chips},
	journal = {BIOSENSORS \& BIOELECTRONICS},
	volume = {89},
	number = {1, SI},
	year = {2017},
	month = {MAR 15},
	pages = {606-611},
	abstract = {Sensitive and selective detection of cancer biomarkers is vital for the successful diagnosis of early stage cancer and follow-up treatment. Surface Plasmon Resonance (SPR) in combination with different amplification strategies is one of the analytical approaches allowing the screening of protein biomarkers in serum. Here we describe the development of a point-of-care sensor for the detection of folic acid protein (FAP) using graphene-based SPR chips. The exceptional properties of CVD graphene were exploited to construct a highly sensitive and selective SPR chip for folate biomarker sensing in serum. The specific recognition of FAP is based on the interaction between folic acid receptors integrated through pi-stacking on the graphene coated SPR chip and the FAP analyte in serum. A simple post-adsorption of human serum:bovine serum albumin (HS:BSA) mixtures onto the folic acid modified sensor resulted in a highly anti-fouling interface, while keeping the sensing capabilities for folate biomarkers. This sensor allowed femtomolar (fM) detection of FAP, a detection limit well adapted and promising for quantitative clinical analysis. (C) 2016 Elsevier B.V. All rights reserved.},
	issn = {0956-5663},
	doi = {10.1016/j.bios.2016.01.076},
	author = {He, Lijie and Pagneux, Quentin and Larroulet, Iban and Serrano, Aritz Yanguas and Pesquera, Amaia and Zurutuza, Amaia and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine}
}
@article { WOS:000391077000064,
	title = {Label-free femtomolar cancer biomarker detection in human serum using graphene-coated surface plasmon resonance chips},
	journal = {BIOSENSORS \& BIOELECTRONICS},
	volume = {89},
	number = {1, SI},
	year = {2017},
	month = {MAR 15},
	pages = {606-611},
	issn = {0956-5663},
	doi = {10.1016/j.bios.2016.01.076},
	author = {He, Lijie and Pagneux, Quentin and Larroulet, Iban and Serrano, Aritz Yanguas and Pesquera, Amaia and Zurutuza, Amaia and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine}
}
@article {11234,
	title = {Label-free femtomolar cancer biomarker detection in human serum using graphene-coated surface plasmon resonance chips.},
	journal = {Biosens. Bioelectron.Biosensors \& Bioelectronics},
	volume = {89},
	number = {Part_1},
	year = {2017},
	note = {CAPLUS AN 2016:220193(Journal; Online Computer File)},
	month = {2017///},
	pages = {606 - 611},
	publisher = {Elsevier B.V.},
	abstract = {Sensitive and selective detection of cancer biomarkers is vital for the successful diagnosis of early stage cancer and follow-up treatment. Surface Plasmon Resonance (SPR) in combination with different amplification strategies is one of the anal. approaches allowing the screening of protein biomarkers in serum. Here we describe the development of a point-of-care sensor for the detection of folic acid protein (FAP) using graphene-based SPR chips. The exceptional properties of CVD graphene were exploited to construct a highly sensitive and selective SPR chip for folate biomarker sensing in serum. The specific recognition of FAP is based on the interaction between folic acid receptors integrated through π-stacking on the graphene coated SPR chip and the FAP analyte in serum. A simple post-adsorption of human serum:bovine serum albumin (HS:BSA) mixts. onto the folic acid modified sensor resulted in a highly anti-fouling interface, while keeping the sensing capabilities for folate biomarkers. This sensor allowed femtomolar (fM) detection of FAP, a detection limit well adapted and promising for quant. clin. anal. [on SciFinder(R)]},
	keywords = {serum cancer biomarker femtomolar graphene surface plasmon resonance chip},
	isbn = {0956-5663},
	author = {He, Lijie and Pagneux, Quentin and Larroulet, Iban and Serrano, Aritz Yanguas and Pesquera, Amaia and Zurutuza, Amaia and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine.}
}
@article { WOS:000408178400044,
	title = {Localized Charge Transfer in Two-Dimensional Molybdenum Trioxide},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {9},
	number = {32},
	year = {2017},
	month = {AUG 16},
	pages = {27045-27053},
	issn = {1944-8244},
	doi = {10.1021/acsami.7b09641},
	author = {Kumar, Vipin and Liu, Liang and Viet Cuong Nguyen and Bhavanasi, Venkateswarlu and Parida, Kaushik and Mandler, Daniel and Lee, Pooi See}
}
@article { ISI:000408178400044,
	title = {Localized Charge Transfer in Two-Dimensional Molybdenum Trioxide},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {9},
	number = {32},
	year = {2017},
	month = {AUG 16},
	pages = {27045-27053},
	abstract = {Molybdenum trioxide is an interesting inorganic system in which the empty 4d states have potential to hold extra electrons and therefore can change states from insulating opaque (MoO3) to colored semimetallic (HxMoO3). Here, we characterize the local electrogeneration and charge transfer of the synthetic layered two-dimensional 2D MoO3-II (a polymorph of MoO3 and analogous to alpha-MoO3) in response,to two different redox couples; i.e., [Ru(NH3)(6)](3+) and [Fe(CN)(6)](3-) by scanning electrochemical microscopy (SECM). We identify the reduction of [Ru(NH3)(6)](3+) to [Ru(NH3)(6)](2+) at the microelectrode that leads to the reduction of MoO3-11 to conducting blue-colored molybdenum bronze H MoO3. It is recognized that the dominant conduction of the charges occurred preferentially at the edges active sites of the sheets, as edges of the sheets are found to be more conducting. This yields positive feedback current when approaching the microelectrode toward 2D MoO3-II-coated electrode. In contrast, the [Fe(CN)(6)](4-), which is reduced from [Fe(CN)(6)](3-), is found unfavorable to reduce MoO3-II due to its higher redox potential, thus showing a negative feedback current. The charge transfer on MoO3-II is further studied as a function of applied potential. The results shed light on the charge transfer behavior on the surface of MoO3-II coatings and opens the possibility of locally tuning of their oxidation states.},
	issn = {1944-8244},
	doi = {10.1021/acsami.7b09641},
	author = {Kumar, Vipin and Liu, Liang and Viet Cuong Nguyen and Bhavanasi, Venkateswarlu and Parida, Kaushik and Mandler, Daniel and Lee, Pooi See}
}
@article { ISI:000395447600027,
	title = {Nanosphere molecularly imprinted polymers doped with gold nanoparticles for high selectivity molecular sensors},
	journal = {NANO RESEARCH},
	volume = {10},
	number = {3},
	year = {2017},
	month = {MAR},
	pages = {1056-1063},
	abstract = {We report the first attempt of using molecularly imprinted polymers (MIPs) in the shape of nanoparticles that were doped with gold nanoparticles (AuNPs) for surface enhanced Raman scattering (SERS)-based sensing of molecular species. Specifically, AuNPs doped molecularly imprinted nano-spheres (AuNPs@nanoMIPs) were synthesized by one-pot precipitation polymerization using Sudan IV as the template for the SERS sensing. The AuNPs@nanoMIPs were characterized by various modes of scanning transmission electron microscopy (STEM) that showed the exact location of the AuNPs inside the MIP particles. The effects of Au concentration and solution stirring on the shape and the polydispersity of the particles were studied. Significant enhancement of the Raman signals was observed only when the MIP particles were doped with the AuNPs. The SERS signal improved significantly with increase in the Au concentration inside the AuNPs@nanoMIPs. Selectivity measurements of the Sudan IV imprinted AuNPs@nanoMIPs carried out with different Sudan derivatives showed high selectivity of the AuNPs-doped MIP particles.},
	issn = {1998-0124},
	doi = {10.1007/s12274-016-1366-5},
	author = {Shahar, Tehila and Sicron, Tama and Mandler, Daniel}
}
@article {13799,
	title = {Nanosphere molecularly imprinted polymers doped with gold nanoparticles for high selectivity molecular sensors.},
	journal = {Nano Res.Nano Research},
	year = {2017},
	note = {CAPLUS AN 2017:163429(Journal)},
	month = {2017///},
	pages = {Ahead of Print},
	publisher = {Springer GmbH},
	abstract = {We report the first attempt of using molecularly imprinted polymers (MIPs) in the shape of nanoparticles that were doped with gold nanoparticles (AuNPs) for surface enhanced Raman scattering (SERS)-based sensing of mol. species. Specifically, AuNPs doped molecularly imprinted nano-spheres (AuNPs@nanoMIPs) were synthesized by one-pot pptn. polymn. using Sudan IV as the template for the SERS sensing. The AuNPs@nanoMIPs were characterized by various modes of scanning transmission electron microscopy (STEM) that showed the exact location of the AuNPs inside the MIP particles. The effects of Au concn. and soln. stirring on the shape and the polydispersity of the particles were studied. Significant enhancement of the Raman signals was obsd. only when the MIP particles were doped with the AuNPs. The SERS signal improved significantly with increase in the Au concn. inside the AuNPs@nanoMIPs. Selectivity measurements of the Sudan IV imprinted AuNPs@nanoMIPs carried out with different Sudan derivs. showed high selectivity of the AuNPs-doped MIP particles. [Figure not available: see fulltext.]. [on SciFinder(R)]},
	isbn = {1998-0000},
	author = {Shahar, Tehila and Sicron, Tama and Mandler, Daniel.}
}
@article { WOS:000395447600027,
	title = {Nanosphere molecularly imprinted polymers doped with gold nanoparticles for high selectivity molecular sensors},
	journal = {NANO RESEARCH},
	volume = {10},
	number = {3},
	year = {2017},
	month = {MAR},
	pages = {1056-1063},
	issn = {1998-0124},
	doi = {10.1007/s12274-016-1366-5},
	author = {Shahar, Tehila and Sicron, Tama and Mandler, Daniel}
}
@article { ISI:000395447600027,
	title = {Nanosphere molecularly imprinted polymers doped with gold nanoparticles for high selectivity molecular sensors},
	journal = {NANO RESEARCH},
	volume = {10},
	number = {3},
	year = {2017},
	month = {MAR},
	pages = {1056-1063},
	publisher = {TSINGHUA UNIV PRESS},
	type = {Article},
	address = {TSINGHUA UNIV, RM A703, XUEYAN BLDG, BEIJING, 100084, PEOPLES R CHINA},
	abstract = {We report the first attempt of using molecularly imprinted polymers (MIPs) in the shape of nanoparticles that were doped with gold nanoparticles (AuNPs) for surface enhanced Raman scattering (SERS)-based sensing of molecular species. Specifically, AuNPs doped molecularly imprinted nano-spheres (AuNPs@nanoMIPs) were synthesized by one-pot precipitation polymerization using Sudan IV as the template for the SERS sensing. The AuNPs@nanoMIPs were characterized by various modes of scanning transmission electron microscopy (STEM) that showed the exact location of the AuNPs inside the MIP particles. The effects of Au concentration and solution stirring on the shape and the polydispersity of the particles were studied. Significant enhancement of the Raman signals was observed only when the MIP particles were doped with the AuNPs. The SERS signal improved significantly with increase in the Au concentration inside the AuNPs@nanoMIPs. Selectivity measurements of the Sudan IV imprinted AuNPs@nanoMIPs carried out with different Sudan derivatives showed high selectivity of the AuNPs-doped MIP particles.},
	keywords = {doping, Gold nanoparticles, molecularly imprinted polymers, Sudan TV, surface enhanced Raman scattering (SERS)},
	issn = {1998-0124},
	doi = {10.1007/s12274-016-1366-5},
	author = {Shahar, Tehila and Sicron, Tama and Mandler, Daniel}
}
@article { WOS:000402663300004,
	title = {Quickly Manufactured, Drug Eluting, Calcium Phosphate Composite Coating},
	journal = {CHEMISTRYSELECT},
	volume = {2},
	number = {2},
	year = {2017},
	month = {JAN 13},
	pages = {753-758},
	issn = {2365-6549},
	doi = {10.1002/slct.201601954},
	author = {Ben Thomas, Midhun and Metoki, Noah and Geuli, Ori and Sharabani-Yosef, Orna and Zada, Tal and Reches, Meital and Mandler, Daniel and Eliaz, Noam}
}
@article { ISI:000402663300004,
	title = {Quickly Manufactured, Drug Eluting, Calcium Phosphate Composite Coating},
	journal = {CHEMISTRYSELECT},
	volume = {2},
	number = {2},
	year = {2017},
	month = {JAN 13},
	pages = {753-758},
	publisher = {WILEY-V C H VERLAG GMBH},
	type = {Article},
	address = {POSTFACH 101161, 69451 WEINHEIM, GERMANY},
	abstract = {Calcium phosphate (CaP) ceramics have been prevalently used as coatings for implants because of their excellent osteoconductive and bioactive properties. Yet, bone regeneration procedures might have complications such as bacterial infection, local inflammation, bone destruction, and impaired bone healing. Here, we present a novel in situ electrodeposition of CaP with chitosan nanoparticles containing antibiotics. The deposition was shown to be fast and efficient. The deposited layer of octacalcium phosphate (OCP) and monotite contained a large amount of gentamicin, which was released gradually over a period of 15 days. These phases may be beneficial for bone growth, as OCP has higher solubility than the stoichiometric hydroxyapatite (HAp) and is commonly considered as a precursor to HAp, while monotite has even faster resorbability. In addition, both the cytotoxicity and biomineralization of the coating were studied, and the coating was proven to be noncytotoxic and highly biomimetic.},
	keywords = {Calcium phosphate, cytotoxicity, Drug eluting, gentamicin, In situ deposition},
	issn = {2365-6549},
	doi = {10.1002/slct.201601954},
	author = {Ben Thomas, Midhun and Metoki, Noah and Geuli, Ori and Sharabani-Yosef, Orna and Zada, Tal and Reches, Meital and Mandler, Daniel and Eliaz, Noam}
}
@article { ISI:000402663300004,
	title = {Quickly Manufactured, Drug Eluting, Calcium Phosphate Composite Coating},
	journal = {CHEMISTRYSELECT},
	volume = {2},
	number = {2},
	year = {2017},
	month = {JAN 13},
	pages = {753-758},
	abstract = {Calcium phosphate (CaP) ceramics have been prevalently used as coatings for implants because of their excellent osteoconductive and bioactive properties. Yet, bone regeneration procedures might have complications such as bacterial infection, local inflammation, bone destruction, and impaired bone healing. Here, we present a novel in situ electrodeposition of CaP with chitosan nanoparticles containing antibiotics. The deposition was shown to be fast and efficient. The deposited layer of octacalcium phosphate (OCP) and monotite contained a large amount of gentamicin, which was released gradually over a period of 15 days. These phases may be beneficial for bone growth, as OCP has higher solubility than the stoichiometric hydroxyapatite (HAp) and is commonly considered as a precursor to HAp, while monotite has even faster resorbability. In addition, both the cytotoxicity and biomineralization of the coating were studied, and the coating was proven to be noncytotoxic and highly biomimetic.},
	issn = {2365-6549},
	doi = {10.1002/slct.201601954},
	author = {Ben Thomas, Midhun and Metoki, Noah and Geuli, Ori and Sharabani-Yosef, Orna and Zada, Tal and Reches, Meital and Mandler, Daniel and Eliaz, Noam}
}
@article { WOS:000419105200034,
	title = {Scanning Electrochemical Microscopy versus Scanning Ion Conductance Microscopy for Surface Patterning},
	journal = {CHEMELECTROCHEM},
	volume = {4},
	number = {11},
	year = {2017},
	month = {NOV},
	pages = {2981-2988},
	issn = {2196-0216},
	doi = {10.1002/celc.201700719},
	author = {Sarkar, Sujoy and Mandler, Daniel}
}
@article { ISI:000419105200034,
	title = {Scanning Electrochemical Microscopy versus Scanning Ion Conductance Microscopy for Surface Patterning},
	journal = {CHEMELECTROCHEM},
	volume = {4},
	number = {11},
	year = {2017},
	month = {NOV},
	pages = {2981-2988},
	abstract = {Scanning electrochemical microscopy (SECM) offers an alternative approach for precise local electrodeposition of micro and nanometer structures driven by electrochemistry. The tip generation and substrate collection mode of SECM has been applied to deposit sub-micron palladium structures by using a Pd microelectrode. This was compared with a different approach based on scanning ion conductance microscopy (SICM). The latter was utilized also for the localized electrochemical deposition of Pd patterns using a pulled micropipette as a tip. The micropipette was filled with PdCl42- and biased versus a reference electrode placed in a NaCl solution. The application of a negative potential to the micropipette causes negatively charged ions, PdCl4-, to egress the pipette, which were electrochemically reduced on a conducting surface. The Pd patterns locally deposited by SECM and SICM were used for the local electroless deposition of Cu. Comparison between the two techniques shows that SICM is superior to SECM in terms of resolution and ease of tip preparation.},
	issn = {2196-0216},
	doi = {10.1002/celc.201700719},
	author = {Sarkar, Sujoy and Mandler, Daniel}
}
@article { WOS:000412233000005,
	title = {Synthesis, coating, and drug-release of hydroxyapatite nanoparticles loaded with antibiotics},
	journal = {JOURNAL OF MATERIALS CHEMISTRY B},
	volume = {5},
	number = {38},
	year = {2017},
	month = {OCT 14},
	pages = {7819-7830},
	issn = {2050-750X},
	doi = {10.1039/c7tb02105d},
	author = {Geuli, Ori and Metoki, Noah and Zada, Tal and Reches, Meital and Eliaz, Noam and Mandler, Daniel}
}
@article { ISI:000412233000005,
	title = {Synthesis, coating, and drug-release of hydroxyapatite nanoparticles loaded with antibiotics},
	journal = {JOURNAL OF MATERIALS CHEMISTRY B},
	volume = {5},
	number = {38},
	year = {2017},
	month = {OCT 14},
	pages = {7819-7830},
	abstract = {Post-surgery infections are considered the most challenging complication in the orthopedic and dental field. The local release of antibiotics is evidently highly efficient in delivering the drug to the vicinity of the infected area without the risk of systemic toxicity. Bioactive materials, such as hydroxyapatite (HAp) among other calcium phosphates, are reputed as superior antibiotic vehicles, and combine drug-delivery properties and enhanced osteoconductivity. Here, we report on the single-step electrophoretic deposition (EPD) of drug-loaded HAp nanoparticles (NPs) on titanium implants. This approach provides a purely bioactive coating with drug delivery properties in a simple, economic, and fast process. We synthesized pure HAp NPs with 12.5\% and 12.8\% loading weight percentages of gentamicin sulfate (Gs) and ciprofloxacin (Cip), and electrophoretically deposited them on a titanium substrate. Furthermore, we co-deposited Gs-HAp and Cip-HAp in one-step to yield a drug-loaded system consisting of two types of antibiotics. The drug- loaded NPs as well as the coatings were carefully characterized. The release profiles of the Gs-HAp and Cip-HAp NP coatings showed prolonged release of up to 10 and 25 days, respectively. The bioactivity test revealed superior bioactivity with enhanced precipitation of HAp crystals along with inorganic minerals, such as Mg2+, Na+, and Cl-. The antibacterial in vitro tests of the Cip and Gs-HAp coatings showed efficient inhibition of Pseudomonas aeruginosa bacteria.},
	issn = {2050-750X},
	doi = {10.1039/c7tb02105d},
	author = {Geuli, Ori and Metoki, Noah and Zada, Tal and Reches, Meital and Eliaz, Noam and Mandler, Daniel}
}
@article {11224,
	title = {Carbon Nanotube Based Flow-Through Electrochemical Cell for Electroanalysis.},
	journal = {Anal. Chem. (Washington, DC, U. S.)Analytical Chemistry (Washington, DC, United States)},
	volume = {88},
	number = {22},
	year = {2016},
	note = {CAPLUS AN 2016:1686824(Journal; Online Computer File)},
	month = {2016///},
	pages = {11007 - 11015},
	publisher = {American Chemical Society},
	abstract = {A flow-through electrode made of a C nanotubes (CNT) film deposited on a polytetrafluoroethylene (PTFE) membrane was assembled and employed for the detn. of low concn. of Cu as a model system by linear sweep anodic stripping voltammetry (LSASV). CNT films with areal mass ranging from 0.12 to 0.72 mg cm-2 were characterized by measurement of sheet resistance, H2O permeation flux and capacitance. Also, CNT with two different sizes and PTFE membrane with two different pore diams. (0.45 and 5.0 μm) were evaluated during the optimization of the electrode. Thick layers made of small CNT exhibited the lowest sheet resistance and the greatest anal. response, whereas thin layers of large CNT had the lowest capacitance and the highest permeation flux. Electrodes made of 0.12 mg cm-2 of large CNT deposited on 5.0 μm PTFE enabled sufficiently high mass transfer and collection efficiency for detecting 64 ppt of Cu(II) within 5 min of deposition and 4.0 mL min-1 flow rate. The anal. response was linear over 4 orders of magnitude (10-9 to 10-5 M) of Cu(II). The excellent performance of the flow-through CNT membrane integrated in a flow cell makes it an appealing approach not only for electroanal., but also for the electrochem. treatment of waters, such as the removal of low concns. of heavy metals and orgs. [on SciFinder(R)]},
	keywords = {carbon nanotube electrochem cell electroanalysis},
	isbn = {0003-2700},
	author = {Buffa, Andrea and Erel, Yigal and Mandler, Daniel.}
}
@article { WOS:000388154700035,
	title = {Carbon Nanotube Based Flow-Through Electrochemical Cell for Electroanalysis},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {88},
	number = {22},
	year = {2016},
	month = {NOV 15},
	pages = {11007-11015},
	issn = {0003-2700},
	doi = {10.1021/acs.analchem.6b02827},
	author = {Buffa, Andrea and Erel, Yigal and Mandler, Daniel}
}
@article { WOS:000362862000051,
	title = {Detection of folic acid protein in human serum using reduced graphene oxide electrodes modified by folic-acid},
	journal = {BIOSENSORS \& BIOELECTRONICS},
	volume = {75},
	year = {2016},
	month = {JAN 15},
	pages = {389-395},
	issn = {0956-5663},
	doi = {10.1016/j.bios.2015.08.060},
	author = {He, Lijie and Wang, Qian and Mandler, Daniel and Li, Musen and Boukherroub, Rabah and Szunerits, Sabine}
}
@article {6832,
	title = {Detection of folic acid protein in human serum using reduced graphene oxide electrodes modified by folic-acid.},
	journal = {Biosensors \& Bioelectronics},
	volume = {75},
	year = {2016},
	note = {CAPLUS AN 2015:1463065(Journal; Online Computer File)},
	month = {2016///},
	pages = {389 - 395},
	publisher = {Elsevier B.V.},
	abstract = {The detection of disease markers is considered an important step for early diagnosis of cancer. We design in this work a novel electrochem. sensing platform for the sensitive and selective detection of folic acid protein (FP). The platform is fabricated by electrophoretic deposition (EPD) of reduced graphene oxide (rGO) onto a gold electrode and post-functionalization of rGO with folic acid. Upon FP binding, a significant current decrease can be measured using differential pulse voltammetry (DPV). Using this scheme, a detection limit of 1 pM is achieved. Importantly, the method also allows the detection of FP in serum being thus an appealing approach for the sensitive detection of biomarkers in clin. samples. [on SciFinder(R)]},
	keywords = {folic acid protein serum reduced graphene oxide electrode},
	isbn = {0956-5663},
	author = {He, Lijie and Wang, Qian and Mandler, Daniel and Li, Musen and Boukherroub, Rabah and Szunerits, Sabine.}
}
@article {11231,
	title = {Effect of Decorating Titanium with Different Self-Assembled Monolayers on the Electrodeposition of Calcium Phosphate.},
	journal = {Cryst. Growth Des.Crystal Growth \& Design},
	volume = {16},
	number = {5},
	year = {2016},
	note = {CAPLUS AN 2016:565837(Journal; Online Computer File)},
	month = {2016///},
	pages = {2756 - 2764},
	publisher = {American Chemical Society},
	abstract = {Calcium phosphate (CaP) ceramics are used in orthopedics and dentistry due to their excellent osseointegration and biocompatibility. The electrodeposition of CaP on titanium alloy covered with self-assembled monolayers (SAMs) was studied with respect to the influence of chain length, end-group charge, and anchoring group. SAMs with end-groups similar to the functional groups on the side chains of collagen were selected. This study is divided to three parts: (1) studying the effects of SAMs on the titanium substrate, (2) studying the process of nucleation and growth of the CaP on specific SAMs, and (3) characterizing the CaP coatings using various surface anal. techniques. It was concluded that the nucleation and growth behavior of CaP changed in the presence of the SAMs. Different surface energies and crystallog. phases were assocd. with this change. Although the nucleation remained progressive, the growth changed from three-dimensional on bare surfaces to two-dimensional on SAMs-covered surfaces. Moreover, the deposition kinetics was slower on SAMs-covered surfaces, with phases contg. a higher Ca/P ratio. Examn. of the coating revealed that different SAMs lead to different surface morphologies of the coating while maintaining its degree of crystallinity. Yet, the phase content changes from hydroxyapatite and octacalcium phosphate (HAp + OCP) on the bare electrode to OCP only on the SAMs-covered electrode. These changes may have a substantial effect on the in vivo behavior by changing the coating{\textquoteright}s soly. and surface morphol., thus affecting cell adhesion, proliferation, and differentiation processes. [on SciFinder(R)]},
	keywords = {titanium self assembly monolayer electrodeposition calcium phosphate},
	isbn = {1528-7483},
	author = {Metoki, Noah and Mandler, Daniel and Eliaz, Noam.}
}
@article { WOS:000375520900037,
	title = {Effect of Decorating Titanium with Different Self-Assembled Monolayers on the Electrodeposition of Calcium Phosphate},
	journal = {CRYSTAL GROWTH \& DESIGN},
	volume = {16},
	number = {5},
	year = {2016},
	month = {MAY},
	pages = {2756-2764},
	issn = {1528-7483},
	doi = {10.1021/acs.cgd.6b00057},
	author = {Metoki, Noah and Mandler, Daniel and Eliaz, Noam}
}
@article { WOS:000380735300009,
	title = {Effect of Self-Assembled Monolayers on the Locally Electrodeposited Silver Thin Layers},
	journal = {JOURNAL OF PHYSICAL CHEMISTRY C},
	volume = {120},
	number = {29},
	year = {2016},
	month = {JUL 28},
	pages = {15608-15617},
	issn = {1932-7447},
	doi = {10.1021/acs.jpcc.5b06680},
	author = {Fedorov, Roman G. and Mandler, Daniel}
}
@article {11235,
	title = {Effect of Self-Assembled Monolayers on the Locally Electrodeposited Silver Thin Layers.},
	journal = {J. Phys. Chem. CJournal of Physical Chemistry C},
	volume = {120},
	number = {29},
	year = {2016},
	note = {CAPLUS AN 2016:39246(Journal; Online Computer File)},
	month = {2016///},
	pages = {15608 - 15617},
	publisher = {American Chemical Society},
	abstract = {{The localized electrodeposition of Ag on Au coated with self-assembled monolayers (SAMs) by scanning electrochem. microscopy (SECM) is reported. The SAMs were ω-functionalized alkanethiols X-(CH2)2SH},
	keywords = {self assembled monolayer thiol electrodeposit silver layer},
	isbn = {1932-7447},
	author = {Fedorov, Roman G. and Mandler, Daniel.}
}
@article { WOS:000376535100045,
	title = {Electro-Assisted Deposition of Calcium Phosphate on Self-Assembled Monolayers},
	journal = {ELECTROCHIMICA ACTA},
	volume = {206},
	year = {2016},
	month = {JUL 10},
	pages = {400-408},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2016.04.143},
	author = {Metoki, Noah and Sadman, Kazi and Shull, Kenneth and Eliaz, Noam and Mandler, Daniel}
}
@article {11230,
	title = {Electro-Assisted Deposition of Calcium Phosphate on Self-Assembled Monolayers.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {206},
	year = {2016},
	note = {CAPLUS AN 2016:773550(Journal; Online Computer File)},
	month = {2016///},
	pages = {400 - 408},
	publisher = {Elsevier Ltd.},
	abstract = {Ca phosphate (CaP) ceramics were used in orthopedics and dentistry due to their excellent biocompatibility and osseointegration. Here, the electro-assisted deposition of CaP on two different self-assembled monolayers (SAMs), 2-mercaptoacetic acid (MAA) and 2-mercaptoethanol (ME), was studied both at short (up to 3 min) and long (2 h) deposition periods on well-defined evapd. Au surfaces. The end group of the monolayer has a major effect on the growth of the CaP coating. The deposition was slower and less elec. efficient on MAA SAM, but surface cracking was essentially eliminated due to redn. of the crystallog. mismatch. The carboxylic acid may facilitate CaP growth by attracting Ca2+ ions to the surface, which could explain the higher amt. of side reactions occurring at the beginning of the deposition. [on SciFinder(R)]},
	keywords = {electro assisted deposition calcium phosphate self assembled monolayer},
	isbn = {0013-4686},
	author = {Metoki, Noah and Sadman, Kazi and Shull, Kenneth and Eliaz, Noam and Mandler, Daniel.}
}
@article { WOS:000388171100007,
	title = {Electrochemically Driven Hydroxyapatite Nanoparticles Coating of Medical Implants},
	journal = {ADVANCED FUNCTIONAL MATERIALS},
	volume = {26},
	number = {44},
	year = {2016},
	month = {NOV 22},
	pages = {8003-8010},
	issn = {1616-301X},
	doi = {10.1002/adfm.201603575},
	author = {Geuli, Ori and Metoki, Noah and Eliaz, Noam and Mandler, Daniel}
}
@article {11225,
	title = {Electrochemically Driven Hydroxyapatite Nanoparticles Coating of Medical Implants.},
	journal = {Adv. Funct. Mater.Advanced Functional Materials},
	year = {2016},
	note = {CAPLUS AN 2016:1534906(Journal)},
	month = {2016///},
	pages = {Ahead of Print},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Calcium phosphates are of great interest for biomedical applications such as bone tissue engineering, bone fillers, drug and gene delivery, and orthopedic and dental implant coating. Here, the first electrochem. driven coating of medical implants using hydroxyapatite (HAp) nanoparticles (NPs) as building blocks is reported. This uncommon combination offers a simple, straightforward, and economic process with well controllable, pure, single-phase HAp. Cryst., pure HAp NPs are formed by pptn. reaction. The HAp NPs are dispersed by either citrate or poly(acrylic acid) to form pH sensitive dispersion. Controllable and homogeneous coating of medical implants is accomplished by altering the pH on the surface upon applying either a const. potential or current. The process involves protonation of the carboxylic acid moieties, which causes the irreversible aggregation of the HAp NPs due to diminishing the repulsive forces between the particles. Deposition is further demonstrated on a com. dental implant. Moreover, the adhesion of the coating satisfies FDA and international std. requirements. A porous interconnected network of bone-like HAp layer is formed during soaking in a simulated body fluid for 30 d and is similar to bone generation, and it therefore holds promise for further in vivo testing. [on SciFinder(R)]},
	keywords = {electrochem deposition hydroxyapatite nanoparticle coating implant},
	isbn = {1616-301X},
	author = {Geuli, Ori and Metoki, Noah and Eliaz, Noam and Mandler, Daniel.}
}
@article { WOS:000379882200012,
	title = {Facile preparation of aqueous suspensions of WO3/sulfonated PEDOT hybrid nanoparticles for electrochromic applications},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {52},
	number = {60},
	year = {2016},
	pages = {9379-9382},
	issn = {1359-7345},
	doi = {10.1039/c6cc03813a},
	author = {Ling, Han and Ding, Guoqiang and Mandler, Daniel and Lee, Pooi See and Xu, Jianwei and Lu, Xuehong}
}
@article {11228,
	title = {Facile preparation of aqueous suspensions of WO3/sulfonated PEDOT hybrid nanoparticles for electrochromic applications.},
	journal = {Chem. Commun. (Cambridge, U. K.)Chemical Communications (Cambridge, United Kingdom)},
	volume = {52},
	number = {60},
	year = {2016},
	note = {CAPLUS AN 2016:1046792(Journal; Online Computer File)},
	month = {2016///},
	pages = {9379 - 9382},
	publisher = {Royal Society of Chemistry},
	abstract = {An aq. suspension of WO3/poly(4-(2,3-dihydrothieno[3,4-b]-[1,4]dioxin-2-yl-methoxy)-1-butanesulfonic acid) (PEDTS) hybrid nanoparticles (NPs) is prepd. by air-assisted oxidative polymn. and simultaneous attachment of PEDTS on WO3-NPs, and used for electrochromic (EC) film fabrication via air-brush spraying. The hybrid EC device exhibits enhanced EC properties compared to the ones based on WO3-NP or PEDTS alone. [on SciFinder(R)]},
	keywords = {tungsten oxide PEDOT hybrid nanoparticle prepn oxidative polymn electrochromic},
	isbn = {1359-7345},
	author = {Ling, Han and Ding, Guoqiang and Mandler, Daniel and Lee, Pooi See and Xu, Jianwei and Lu, Xuehong.}
}
@article {11229,
	title = {Formation and performance of highly absorbing solar thermal coating based on carbon nanotubes and boehmite.},
	journal = {Energy Convers. Manage.Energy Conversion and Management},
	volume = {120},
	year = {2016},
	note = {CAPLUS AN 2016:791558(Journal; Online Computer File)},
	month = {2016///},
	pages = {287 - 293},
	publisher = {Elsevier Ltd.},
	abstract = {A major component of solar thermal systems is the solar absorber, which converts light into heat. We report on achieving high absorptance, excellent adhesion, and high thermal stability of carbon nanotube-based black coatings by applying a layer of Boehmite (AlOOH) on top of the carbon nanotube (CNT) film by soln.-processed spray deposition. The CNT layer made-up by spraying, functions as an absorbing layer and the AlOOH serves as an anti-reflecting and protecting film. The anti-reflecting property of AlOOH layer effectively increases the absorptance of CNT coating by decreasing the reflectance. The effect of the thickness of AlOOH layer on the absorptance, adhesion, and thermal stability of the resulting CNT/AlOOH coating was investigated. The CNT/AlOOH coating with optimized thickness of AlOOH layer shows very high absorptance (α) of 0.975. The adhesion of the coating is in the range of 95-100\% with significant increase of thermal stability. This new approach is expected to open new possibilities for fabricating low-cost, highly efficient and thermally stable solar-thermal devices which are based on simple coating processes. [on SciFinder(R)]},
	isbn = {0196-8904},
	author = {Bera, Raj Kumar and Mhaisalkar, Subodh Gautam and Mandler, Daniel and Magdassi, Shlomo.}
}
@article { WOS:000377726300025,
	title = {Formation and performance of highly absorbing solar thermal coating based on carbon nanotubes and boehmite},
	journal = {ENERGY CONVERSION AND MANAGEMENT},
	volume = {120},
	year = {2016},
	month = {JUL 15},
	pages = {287-293},
	issn = {0196-8904},
	doi = {10.1016/j.enconman.2016.04.081},
	author = {Bera, Raj Kumar and Mhaisalkar, Subodh Gautam and Mandler, Daniel and Magdassi, Shlomo}
}
@article { WOS:000392566200040,
	title = {In Situ Potentiostatic Deposition of Calcium Phosphate with Gentamicin-Loaded Chitosan Nanoparticles on Titanium Alloy Surfaces},
	journal = {ELECTROCHIMICA ACTA},
	volume = {222},
	year = {2016},
	month = {DEC 20},
	pages = {355-360},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2016.10.186},
	author = {Thomas, Midhun B. and Metoki, Noah and Mandler, Daniel and Eliaz, Noam}
}
@article {11178,
	title = {In Situ Potentiostatic Deposition of Calcium Phosphate with Gentamicin-Loaded Chitosan Nanoparticles on Titanium Alloy Surfaces.},
	journal = {Electrochim. ActaElectrochimica Acta},
	year = {2016},
	note = {CAPLUS AN 2016:1823543(Journal)},
	month = {2016///},
	pages = {Ahead of Print},
	publisher = {Elsevier Ltd.},
	abstract = {Bone implants must be biocompatible and are usually built to promote osseointegration, e.g. by application of plasma spray calcium phosphate (CaP) coating. The risk of infection and biofilm formation on implant surfaces is a well-known problem. The combination of electrochem. deposited CaP coating with antibiotics may offer significant benefits. Here, we demonstrate an innovative in situ electrodeposition of gentamicin encapsulated in chitosan nanoparticles along with CaP. The deposition of the coating was obsd. and studied at several temps. A high drug loading into the coating and a controlled release of the drug over two days were demonstrated. [on SciFinder(R)]},
	isbn = {0013-4686},
	author = {Thomas, Midhun B. and Metoki, Noah and Mandler, Daniel and Eliaz, Noam.}
}
@article {11179,
	title = {Ionic strength induced electrodeposition: a universal approach for nanomaterial deposition at selective areas.},
	journal = {NanoscaleNanoscale},
	year = {2016},
	note = {CAPLUS AN 2016:1703416(Journal)},
	month = {2016///},
	pages = {Ahead of Print},
	publisher = {Royal Society of Chemistry},
	abstract = {An appealing alternative approach to the conventional electrochem. deposition is presented, which can be universally utilized to form nanomaterial coatings from their aq. dispersions without involving their oxidn.-redn. It is based on altering the ionic strength by elec. potential in the vicinity of the electrode surface, which causes the nanomaterials to deposit. The concept has been demonstrated for four different systems. [on SciFinder(R)]},
	isbn = {2040-3372},
	author = {Liu, Chang and Long, Yi and Magdassi, Shlomo and Mandler, Daniel.}
}
@article {6827,
	title = {Label-free femtomolar cancer biomarker detection in human serum using graphene-coated surface plasmon resonance chips.},
	journal = {Biosens. Bioelectron.Biosensors \& Bioelectronics},
	year = {2016},
	note = {CAPLUS AN 2016:220193(Journal)},
	month = {2016///},
	pages = {Ahead of Print},
	publisher = {Elsevier B.V.},
	abstract = {Sensitive and selective detection of cancer biomarkers is vital for the successful diagnosis of early stage cancer and follow-up treatment. Surface Plasmon Resonance (SPR) in combination with different amplification strategies is one of the anal. approaches allowing the screening of protein biomarkers in serum. Here we describe the development of a point-of-care sensor for the detection of folic acid protein (FAP) using graphene-based SPR chips. The exceptional properties of CVD graphene were exploited to construct a highly sensitive and selective SPR chip for folate biomarker sensing in serum. The specific recognition of FAP is based on the interaction between folic acid receptors integrated through π-stacking on the graphene coated SPR chip and the FAP analyte in serum. A simple post-adsorption of human serum:bovine serum albumin (HS:BSA) mixts. onto the folic acid modified sensor resulted in a highly anti-fouling interface, while keeping the sensing capabilities for folate biomarkers. This sensor allowed femtomolar (fM) detection of FAP, a detection limit well adapted and promising for quant. clin. anal. [on SciFinder(R)]},
	isbn = {0956-5663},
	author = {He, Lijie and Pagneux, Quentin and Larroulet, Iban and Serrano, Aritz Yanguas and Pesquera, Amaia and Zurutuza, Amaia and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine.}
}
@article {6826,
	title = {Molecularly imprinted polymer particles: Formation, characterization and application.},
	journal = {Colloids Surf., AColloids and Surfaces, A: Physicochemical and Engineering Aspects},
	volume = {495},
	year = {2016},
	note = {CAPLUS AN 2016:222036(Journal; Online Computer File)},
	month = {2016///},
	pages = {11 - 19},
	publisher = {Elsevier B.V.},
	abstract = {Molecularly imprinted polymer (MIP) particles offer many advantages as recognition objects. Therefore, we examd. thoroughly the effect of various exptl. parameters including cross-linker concn., nature of solvent, type of template and its concn., reaction vol. and temp. on the formation of particulate MIPs using pptn. polymn. The particles were characterized by various methods, such as XHR-SEM, HR-TEM and BET. Statistical calcns. were carried out using ImageJ software over population of at least 200 particles in each expt. The reproducibility of MIP synthesis was examd. and the SD was better than 10\%. MIP particles were imprinted with different Sudan dye derivs. (Sudan II, III, IV and Sudan orange G). Raman and FTIR spectroscopies were used to prove the successful imprinting. Reuptake measurements were carefully compared between non-imprinted molecularly polymer (NIP) and MIP particles employing the same quantity and similar diam. and polydispersity of NIP and MIP, as never reported before. The results showed that MIP particles imprinted by Sudan IV showed higher selectivity toward this specific dye as compared with MIPs imprinted by other Sudan dyes and NIPs. [on SciFinder(R)]},
	isbn = {0927-7757},
	author = {Shahar, Tehila and Tal, Noam and Mandler, Daniel.}
}
@article { WOS:000371395500002,
	title = {Molecularly imprinted polymer particles: Formation, characterization and application},
	journal = {COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS},
	volume = {495},
	year = {2016},
	month = {APR 20},
	pages = {11-19},
	issn = {0927-7757},
	doi = {10.1016/j.colsurfa.2016.01.027},
	author = {Shahar, Tehila and Tal, Noam and Mandler, Daniel}
}
@article {11233,
	title = {Molecularly imprinted polymer particles: Formation, characterization and application.},
	journal = {Colloids Surf., AColloids and Surfaces, A: Physicochemical and Engineering Aspects},
	volume = {495},
	year = {2016},
	note = {CAPLUS AN 2016:222036(Journal; Online Computer File)},
	month = {2016///},
	pages = {11 - 19},
	publisher = {Elsevier B.V.},
	abstract = {Molecularly imprinted polymer (MIP) particles offer many advantages as recognition objects. Therefore, we examd. thoroughly the effect of various exptl. parameters including cross-linker concn., nature of solvent, type of template and its concn., reaction vol. and temp. on the formation of particulate MIPs using pptn. polymn. The particles were characterized by various methods, such as XHR-SEM, HR-TEM and BET. Statistical calcns. were carried out using ImageJ software over population of at least 200 particles in each expt. The reproducibility of MIP synthesis was examd. and the SD was better than 10\%. MIP particles were imprinted with different Sudan dye derivs. (Sudan II, III, IV and Sudan orange G). Raman and FTIR spectroscopies were used to prove the successful imprinting. Reuptake measurements were carefully compared between non-imprinted molecularly polymer (NIP) and MIP particles employing the same quantity and similar diam. and polydispersity of NIP and MIP, as never reported before. The results showed that MIP particles imprinted by Sudan IV showed higher selectivity toward this specific dye as compared with MIPs imprinted by other Sudan dyes and NIPs. [on SciFinder(R)]},
	keywords = {polymer particle mol imprinting formation characterization application},
	isbn = {0927-7757},
	author = {Shahar, Tehila and Tal, Noam and Mandler, Daniel.}
}
@article {11226,
	title = {Nanoparticle Imprinted Matrices as Sensing Layers forSize-Selective Recognition of Silver Nanoparticles.},
	journal = {ChemElectroChemChemElectroChem},
	year = {2016},
	note = {CAPLUS AN 2016:1294211(Journal)},
	month = {2016///},
	pages = {Ahead of Print},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {This study extends the concept of nanoparticle imprinted matrixes (NAIMs) to systems, in which template nanoparticles (NPs) are immobilized on a conducting surface and a polymer matrix is built around them before the release of the template NPs. Specifically, citrate-stabilized AuNPs, 40 nm in diam., were bound to a 3-aminopropyltriethoxysilane (APTES)-modified indium tin oxide (ITO) electrode at pH 5. Subsequently, a polymer matrix was generated by electropolymn. of self-inhibiting poly(phenol) (PPh) layer. The template AuNPs were removed either by electrooxidn. of the Au core during linear sweep voltammetry (LSV) in Cl{\textendash}contg. aq. soln. or by chem. oxidn. in aq. KCN soln. After template removal, nanocavities were left behind, which showed size-selective in the competitive reuptake of analyte NPs demonstrated by the preference for citrate-stabilized silver nanoparticles (AgNPs) with 20 nm diam. over AuNPs with 50 nm diam. The remaining nanocavities and their size-recognition ability were examd. by SEM and LSV. Complementing studies by X ray photoelectron spectroscopy and scanning force microscopy corroborated the template embedding, template release and analyte NP uptake. [on SciFinder(R)]},
	isbn = {2196-0216},
	author = {Witt, Julia and Mandler, Daniel and Wittstock, Gunther.}
}
@article { WOS:000390800900025,
	title = {Nanoparticle-Imprinted Matrices as Sensing Layers for Size-Selective Recognition of Silver Nanoparticles},
	journal = {CHEMELECTROCHEM},
	volume = {3},
	number = {12},
	year = {2016},
	month = {DEC},
	pages = {2116-2124},
	issn = {2196-0216},
	doi = {10.1002/celc.201600321},
	author = {Witt, Julia and Mandler, Daniel and Wittstock, Gunther}
}
@article { WOS:000367761900019,
	title = {A novel approach for oxidation analysis of therapeutic proteins},
	journal = {ANALYTICAL BIOCHEMISTRY},
	volume = {494},
	year = {2016},
	month = {FEB 1},
	pages = {108-113},
	issn = {0003-2697},
	doi = {10.1016/j.ab.2015.10.015},
	author = {Turyan, Iva and Khatwani, Nikhil and Sosic, Zoran and Jayawickreme, Shiranthi and Mandler, Daniel}
}
@article {6829,
	title = {A novel approach for oxidation analysis of therapeutic proteins.},
	journal = {Anal. Biochem.Analytical Biochemistry},
	volume = {494},
	year = {2016},
	note = {CAPLUS AN 2015:1916495(Journal; Online Computer File)},
	month = {2016///},
	pages = {108 - 113},
	publisher = {Elsevier B.V.},
	abstract = {Measuring and monitoring of protein oxidn. modifications is important for biopharmaceutical process development and stability assessment during long-term storage. Currently available methods for biomols. oxidn. anal. use time-consuming peptide mapping anal. Therefore, it is desirable to develop high-throughput methods for advanced process control of protein oxidn. Here, we present a novel approach by which oxidative protein modifications are monitored by an indirect potentiometric method. The method is based on adding an electron mediator, which enhances electron transfer (ET) between all redox species and the electrode surface. Specifically, the procedure involves measuring the sharp change in the open circuit potential (OCP) for the mediator system (redox couple) as a result of its interaction with the oxidized protein species in the soln. Application of Pt and Ag/AgCl microelectrodes allowed for a high-sensitivity protein oxidn. anal. We found that the Ru(NH3)2+/3+6 redox couple is suitable for measuring the total oxidn. of a wide range of therapeutic proteins between 1.1 and 13.6\%. Accuracy detd. by comparing with the known percentage oxidn. of the ref. std. showed that percentage oxidn. detd. for each sample was within {\textpm}20\% of the expected percentage oxidn. detd. by mass spectrometry. [on SciFinder(R)]},
	keywords = {therapeutic protein oxidn analysis potentiometry},
	isbn = {0003-2697},
	author = {Turyan, Iva and Khatwani, Nikhil and Sosic, Zoran and Jayawickreme, Shiranthi and Mandler, Daniel.}
}
@article {11227,
	title = {Periodic micro-patterned VO2 thermochromic films by mesh printing.},
	journal = {J. Mater. Chem. CJournal of Materials Chemistry C: Materials for Optical and Electronic Devices},
	volume = {4},
	number = {36},
	year = {2016},
	note = {CAPLUS AN 2016:1185251(Journal; Online Computer File)},
	month = {2016///},
	pages = {8385 - 8391},
	publisher = {Royal Society of Chemistry},
	abstract = {VO2 has garnered much attention in recent years as a promising candidate for thermochromic window applications due to rising awareness about energy conservation. However, the trade-off between improving the luminous transmittance (Tlum) and solar modulation ability (ΔTsol) limits the commercialization of VO2-based smart windows. Four major nanostructuring approaches were implemented to enhance both Tlum and ΔTsol, namely nanocomposites, nanoporous films, biomimetic moth-eye structures and anti-reflection coating (ARC) multilayers. This work demonstrates a novel approach that fabricates periodic, micro-patterned structures of VO2 using a facile screen printing method. The micro-patterned structure is able to favorably transmit visible light without sacrificing high near-IR modulation, and the patterned film shows improved Tlum (67\% vs. 60\%) and ΔTsol (8.8\% vs. 6.9\%) compared with continuous films. By varying the thickness, periodicity and solid concn., this approach can give a ΔTsol of 14.9\% combined with a Tlum of 43.3\%, which is comparable, if not superior to, some of the best reported results found using other approaches. [on SciFinder(R)]},
	keywords = {periodic micro patterned vanadium oxide thermochromic printing screen nanoparticle},
	isbn = {2050-7534},
	author = {Lu, Qi and Liu, Chang and Wang, Ning and Magdassi, Shlomo and Mandler, Daniel and Long, Yi.}
}
@article { WOS:000384554000005,
	title = {Periodic micro-patterned VO2 thermochromic films by mesh printing},
	journal = {JOURNAL OF MATERIALS CHEMISTRY C},
	volume = {4},
	number = {36},
	year = {2016},
	pages = {8385-8391},
	issn = {2050-7526},
	doi = {10.1039/c6tc02694j},
	author = {Lu, Qi and Liu, Chang and Wang, Ning and Magdassi, Shlomo and Mandler, Daniel and Long, Yi}
}
@article {11232,
	title = {Speciation of nanoscale objects by nanoparticle imprinted matrices.},
	journal = {NanoscaleNanoscale},
	volume = {8},
	number = {29},
	year = {2016},
	note = {CAPLUS AN 2016:286369(Journal; Online Computer File)},
	month = {2016///},
	pages = {13934 - 13943},
	publisher = {Royal Society of Chemistry},
	abstract = {The toxicity of nanoparticles is not only a function of the constituting material but depends largely on their size, shape and stabilizing shell. Hence, the speciation of nanoscale objects, namely, their detection and sepn. based on the different species, similarly to heavy metals, is of outmost importance. Here we demonstrate the speciation of gold nanoparticles (AuNPs) and their electrochem. detection using the concept of "nanoparticles imprinted matrixes" (NAIM). Neg. charged AuNPs are adsorbed as templates on a conducting surface previously modified with polyethylenimine (PEI). The selective matrix is formed by the adsorption of either oleic acid (OA) or poly(acrylic acid) (PAA) on the non-occupied areas. The AuNPs are removed by electrooxidn. to form complementary voids. These voids are able to recognize the AuNPs selectively based on their size. Furthermore, the selectivity could be improved by adsorbing an addnl. layer of 1-hexadecylamine, which deepened the voids. Interestingly, silver nanoparticles (AgNPs) were also recognized if their size matched those of the template AuNPs. The steps in assembling the NAIMs and the reuptake of the nanoparticles were characterized carefully. The prospects for the anal. use of NAIMs, which are simple, of small dimension, cost-efficient and portable, are in the sensing and sepn. of nanoobjects. [on SciFinder(R)]},
	keywords = {gold nanoscale nanoparticle imprinted matrice},
	isbn = {2040-3372},
	author = {Hitrik, Maria and Pisman, Yamit and Wittstock, Gunther and Mandler, Daniel.}
}
@article {6825,
	title = {Speciation of nanoscale objects by nanoparticle imprinted matrices.},
	journal = {NanoscaleNanoscale},
	year = {2016},
	note = {CAPLUS AN 2016:286369(Journal)},
	month = {2016///},
	pages = {Ahead of Print},
	publisher = {Royal Society of Chemistry},
	abstract = {The toxicity of nanoparticles is not only a function of the constituting material but depends largely on their size, shape and stabilizing shell. Hence, the speciation of nanoscale objects, namely, their detection and sepn. based on the different species, similarly to heavy metals, is of outmost importance. Here we demonstrate the speciation of gold nanoparticles (AuNPs) and their electrochem. detection using the concept of "nanoparticles imprinted matrixes" (NAIM). Neg. charged AuNPs are adsorbed as templates on a conducting surface previously modified with polyethylenimine (PEI). The selective matrix is formed by the adsorption of either oleic acid (OA) or poly(acrylic acid) (PAA) on the non-occupied areas. The AuNPs are removed by electrooxidn. to form complementary voids. These voids are able to recognize the AuNPs selectively based on their size. Furthermore, the selectivity could be improved by adsorbing an addnl. layer of 1-hexadecylamine, which deepened the voids. Interestingly, silver nanoparticles (AgNPs) were also recognized if their size matched those of the template AuNPs. The steps in assembling the NAIMs and the reuptake of the nanoparticles were characterized carefully. The prospects for the anal. use of NAIMs, which are simple, of small dimension, cost-efficient and portable, are in the sensing and sepn. of nanoobjects. [on SciFinder(R)]},
	isbn = {2040-3372},
	author = {Hitrik, Maria and Pisman, Yamit and Wittstock, Gunther and Mandler, Daniel.}
}
@article { WOS:000381815000013,
	title = {Speciation of nanoscale objects by nanoparticle imprinted matrices},
	journal = {NANOSCALE},
	volume = {8},
	number = {29},
	year = {2016},
	pages = {13934-13943},
	issn = {2040-3364},
	doi = {10.1039/c6nr01106c},
	author = {Hitrik, Maria and Pisman, Yamit and Wittstock, Gunther and Mandler, Daniel}
}
@article {7054,
	title = {Correction to Electrochemical Detection of Low Concentrations of Mercury in Water Using Gold Nanoparticles},
	journal = {Anal ChemAnalytical chemistry},
	volume = {87},
	number = {14},
	year = {2015},
	note = {MEDLINE AN 2015992689(Errata; (PUBLISHED ERRATUM))},
	month = {2015///},
	pages = {7492},
	isbn = {1520-6882},
	author = {Ratner, Noga and Mandler, Daniel}
}
@booklet {6836,
	title = {Electroactive bioadhesive compositions.},
	howpublished = {PCT Int. Appl.},
	number = {WO2015108487A1},
	year = {2015},
	note = {CAPLUS AN 2015:1201680(Patent)},
	month = {2015/07/23/},
	pages = {44pp.},
	publisher = {Nanyang Technological University, Singapore; Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. .},
	abstract = {The present invention relates to electrochem. initiated bioadhesive compns. comprising biocompatible polymers contg. derivs. of diazonium, arylsulfonium, or diaryliodonium in general, and to their use in tissue fixation, in particular. [on SciFinder(R)]},
	keywords = {electrochem initiated polymer bioadhesive diazonium arylsulfonium diaryliodonium compns},
	author = {Steele, Terry W. J. and Mandler, Daniel.}
}
@article { WOS:000348300300025,
	title = {Electrochemical co-deposition of sol-gel/carbon nanotube composite thin films for antireflection and non-linear optics},
	journal = {JOURNAL OF MATERIALS CHEMISTRY C},
	volume = {3},
	number = {5},
	year = {2015},
	pages = {1099-1105},
	issn = {2050-7526},
	doi = {10.1039/c4tc01601g},
	author = {Liu, Liang and Yellinek, Shai and Tal, Noam and Toledano, Reut and Donval, Ariela and Yadlovker, Doron and Mandler, Daniel}
}
@article {6845,
	title = {Electrochemical co-deposition of sol-gel/carbon nanotube composite thin films for antireflection and non-linear optics.},
	journal = {J. Mater. Chem. CJournal of Materials Chemistry C: Materials for Optical and Electronic Devices},
	volume = {3},
	number = {5},
	year = {2015},
	note = {CAPLUS AN 2014:2001508(Journal; Online Computer File)},
	month = {2015///},
	pages = {1099 - 1105},
	publisher = {Royal Society of Chemistry},
	abstract = {Sol-gel/carbon nanotube (CNT) nano-composite films were electrochem. deposited by applying a neg. potential to a conducting substrate, i.e. indium tin oxide (ITO) and an Ag grid printed on polyethylene terephthalate (PET). The deposition is driven by the local pH rise on the cathode that catalyzes the formation of sol-gel films. The latter serve as a binder and trap for CNTs. The deposition can be well manipulated by the deposition potential and time, and the film can be selectively electrodeposited on the conductive parts of Ag grids printed on PET from an optimized dispersion. The thickness, transmittance, morphol. and hydrophilicity of the films are characterized by profilometry, spectrophotometry, SEM (SEM) and water contact angle, resp. It is further revealed that the electrodeposited sol-gel/CNT composite films have non-linear optical properties and exhibit pronounced antireflective performance (specular reflection < 0.5\%) over a visible to long-wave IR range, allowing their potential application as optical materials. [on SciFinder(R)]},
	keywords = {electrodeposition sol gel carbon nanotube composite NLO property},
	isbn = {2050-7534},
	author = {Liu, Liang and Yellinek, Shai and Tal, Noam and Toledano, Reut and Donval, Ariela and Yadlovker, Doron and Mandler, Daniel.}
}
@article { WOS:000358555900069,
	title = {Electrochemical Detection of Low Concentrations of Mercury in Water Using Gold Nanoparticles (vol 87, pg 5148, 2015)},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {87},
	number = {14},
	year = {2015},
	month = {JUL 21},
	pages = {7492},
	issn = {0003-2700},
	doi = {10.1021/acs.analchem.5b02313},
	author = {Ratner, Noga and Mandler, Daniel}
}
@article {6842,
	title = {Electrochemical Detection of Low Concentrations of Mercury in Water Using Gold Nanoparticles.},
	journal = {Anal. Chem. (Washington, DC, U. S.)Analytical Chemistry (Washington, DC, United States)},
	volume = {87},
	number = {10},
	year = {2015},
	note = {CAPLUS AN 2015:667448(Journal; Online Computer File)},
	month = {2015///},
	pages = {5148 - 5155},
	publisher = {American Chemical Society},
	abstract = {The electrochem. detection of Hg in aq. solns. was studied at glassy C (GC) and In-Sn oxide (ITO) electrodes modified by Au nanoparticles (Au NPs). Two methods of modification were used: electrochem. redn. of HAuCl4 and electrostatic adsorption of Au NPs stabilized by citrate. We found that the Au NPs modified surfaces yielded higher sensitivity and sharper and more reproducible stripping peaks of Hg as compared with the bare electrodes. The effect of the modification by Au NPs on the stripping potential was examd. Interestingly, the stripping of Hg on GC and ITO modified by Au NPs occurred at the same potential as on bare GC and ITO, resp. Only the full coverage of ITO by either electrochem. deposited Au for a long time or by vapor deposition, shifted the stripping potential more pos. by \~0.4 V to that obsd. on a bare Au electrode. These and further expts. led us to conclude that the Au NPs served as nucleation sites for the deposition of Hg, whereas the GC or ITO are superior for the stripping of Hg. Hence, a combination of well-defined Au NPs on ITO or GC were found ideal for the electrochem. detection of Hg. We achieved a remarkable detection limit of 1 μm/L of Hg using an ITO surface modified by electrostatically adsorbed Au NPs. [on SciFinder(R)]},
	keywords = {electrochem detection mercury water gold nanoparticle},
	isbn = {0003-2700},
	author = {Ratner, Noga and Mandler, Daniel.}
}
@article { WOS:000355057700021,
	title = {Electrochemical Detection of Low Concentrations of Mercury in Water Using Gold Nanoparticles},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {87},
	number = {10},
	year = {2015},
	month = {MAY 19},
	pages = {5148-5155},
	issn = {0003-2700},
	doi = {10.1021/ac504584f},
	author = {Ratner, Noga and Mandler, Daniel}
}
@article {7055,
	title = {Electrochemical detection of low concentrations of mercury in water using gold nanoparticles},
	journal = {Anal ChemAnalytical chemistry},
	volume = {87},
	number = {10},
	year = {2015},
	note = {MEDLINE AN 2015760977(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2015///},
	pages = {5148 - 55},
	abstract = {The electrochemical detection of mercury in aqueous solutions was studied at glassy carbon (GC) and indium-tin oxide (ITO) electrodes modified by gold nanoparticles (Au NPs). Two methods of modification were used: electrochemical reduction of HAuCl4 and electrostatic adsorption of Au NPs stabilized by citrate. We found that the Au NPs modified surfaces yielded higher sensitivity and sharper and more reproducible stripping peaks of Hg as compared with the bare electrodes. The effect of the modification by Au NPs on the stripping potential was examined. Interestingly, the stripping of Hg on GC and ITO modified by Au NPs occurred at the same potential as on bare GC and ITO, respectively. Only the full coverage of ITO by either electrochemically deposited Au for a long time or by vapor deposition, shifted the stripping potential more positive by ca. 0.4 V to that observed on a bare Au electrode. These and further experiments led us to conclude that the Au NPs served as nucleation sites for the deposition of Hg, whereas the GC or ITO are superior for the stripping of mercury. Hence, a combination of well-defined Au NPs on ITO or GC were found ideal for the electrochemical detection of Hg. Indeed, we achieved a remarkable detection limit of 1 μm{\textperiodcentered}L(-1) of Hg using an ITO surface modified by electrostatically adsorbed Au NPs.[on SciFinder (R)]},
	isbn = {1520-6882},
	author = {Ratner, Noga and Mandler, Daniel}
}
@article {6838,
	title = {Electrochemical Detection of Low Concentrations of Mercury in Water Using Gold Nanoparticles [Erratum to document cited in CA162:582409].},
	journal = {Anal. Chem. (Washington, DC, U. S.)Analytical Chemistry (Washington, DC, United States)},
	volume = {87},
	number = {14},
	year = {2015},
	note = {CAPLUS AN 2015:1119652(Journal; Online Computer File)},
	month = {2015///},
	pages = {7492},
	publisher = {American Chemical Society},
	abstract = {The units of concn. of mercury noted as "μm L-1" should read as "ng L-1.". [on SciFinder(R)]},
	keywords = {erratum electrochem detection mercury water gold nanoparticle},
	isbn = {0003-2700},
	author = {Ratner, Noga and Mandler, Daniel.}
}
@article { WOS:000347590400083,
	title = {Electrochemical Determination of Low Levels of Uranyl by a Vibrating Gold Microelectrode},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {87},
	number = {1, SI},
	year = {2015},
	month = {JAN 6},
	pages = {768-776},
	issn = {0003-2700},
	doi = {10.1021/ac503719r},
	author = {Peled, Y. and Krent, E. and Tal, N. and Tobias, H. and Mandler, D.}
}
@article {7056,
	title = {Electrochemical determination of low levels of uranyl by a vibrating gold microelectrode},
	journal = {Anal ChemAnalytical chemistry},
	volume = {87},
	number = {1},
	year = {2015},
	note = {MEDLINE AN 2015317328(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2015///},
	pages = {768 - 76},
	abstract = {In this work we report the sensitive electroanalytical detection of uranium(VI) in aqueous solutions. Uranium commonly exists in aqueous solutions in the form of its oxo ion, uranyl (U(VI)O2(2+)). The detection of uranyl has been accomplished by us through its deposition upon reduction by two electrons to the insoluble UO2 using a bare disk gold macroelectrode and anodic stripping voltammetry (ASV). This gave an unsatisfactory detection limit of ca. 1 {\texttimes} 10(-5) M uranyl. Moreover, the evolution of hydrogen bubbles blocked the electrode surface as a result of water reduction at negative deposition potential (-0.7 V vs Ag/AgCl). The application of a 25 μm diameter Au microwire electrode on which UO2 precipitated at negative potential (-1.2 V) improved substantially the detection limit. Further improvement was accomplished by vibrating the microwire working electrode, which increased the amounts of UO2 deposition due to decreasing the diffusion layer. The effect of the vibrating amplitude and frequency on the electroanalytical response was studied and optimized. Eventually, a detection limit of ca. 1 {\texttimes} 10(-9) M uranyl was achieved using a 5 min deposition time, -1.2 V deposition potential, and vibrating the electrode at frequency of 250 Hz and amplitude of 6 V.[on SciFinder (R)]},
	isbn = {1520-6882},
	author = {Peled, Y. and Krent, E. and Tal, N. and Tobias, H. and Mandler, D}
}
@article {6844,
	title = {Electrochemical Determination of Low Levels of Uranyl by a Vibrating Gold Microelectrode.},
	journal = {Anal. Chem. (Washington, DC, U. S.)Analytical Chemistry (Washington, DC, United States)},
	volume = {87},
	number = {1},
	year = {2015},
	note = {CAPLUS AN 2014:2011759(Journal; Online Computer File)},
	month = {2015///},
	pages = {768 - 776},
	publisher = {American Chemical Society},
	abstract = {The authors report the sensitive electroanal. detection of uranium(VI) in aq. solns. Uranium commonly exists in aq. solns. as its oxo ion, uranyl (UVIO22+). The detection of uranyl was accomplished by the authors through its deposition upon redn. by two electrons to the insol. UO2 using a bare disk gold macroelectrode and anodic stripping voltammetry (ASV). This gave an unsatisfactory detection limit of \~1 {\texttimes} 10-5 M uranyl. Also, the evolution of hydrogen bubbles blocked the electrode surface as a result of water redn. at neg. deposition potential (-0.7 V vs. Ag/AgCl). The application of a 25 μm diam. Au microwire electrode on which UO2 pptd. at neg. potential (-1.2 V) improved substantially the detection limit. Further improvement was accomplished by vibrating the microwire working electrode, which increased the amts. of UO2 deposition due to decreasing the diffusion layer. The effect of the vibrating amplitude and frequency on the electroanal. response was studied and optimized. Eventually, a detection limit of \~1 {\texttimes} 10-9 M uranyl was achieved using a 5 min deposition time, -1.2 V deposition potential, and vibrating the electrode at frequency of 250 Hz and amplitude of 6 V. [on SciFinder(R)]},
	keywords = {low level uranyl electrochem detn vibrating gold microelectrode},
	isbn = {0003-2700},
	author = {Peled, Y. and Krent, E. and Tal, N. and Tobias, H. and Mandler, D}
}
@article {7052,
	title = {Electrochemically triggered release of human insulin from an insulin-impregnated reduced graphene oxide modified electrode},
	journal = {Chem Commun (Camb)Chemical communications (Cambridge, England)},
	volume = {51},
	number = {75},
	year = {2015},
	note = {MEDLINE AN 2016112087(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2015///},
	pages = {14167 - 70},
	abstract = {An electrochemical insulin-delivery system based on reduced graphene oxide impregnated with insulin is described. Upon application of a potential pulse of -0.8 V for 30 min, up to 70 {\textpm} 4\% of human insulin was released into a physiological medium while preserving its biological activity.[on SciFinder (R)]},
	isbn = {1364-548X},
	author = {Teodorescu, Florina and Rolland, Laure and Ramarao, Viswanatha and Abderrahmani, Amar and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine}
}
@article { WOS:000360792800004,
	title = {Electrochemically triggered release of human insulin from an insulin-impregnated reduced graphene oxide modified electrode},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {51},
	number = {75},
	year = {2015},
	pages = {14167-14170},
	issn = {1359-7345},
	doi = {10.1039/c5cc05539c},
	author = {Teodorescu, Florina and Rolland, Laure and Ramarao, Viswanatha and Abderrahmani, Amar and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine}
}
@article {6834,
	title = {Electrochemically triggered release of human insulin from an insulin-impregnated reduced graphene oxide modified electrode.},
	journal = {Chem. Commun. (Cambridge, U. K.)Chemical Communications (Cambridge, United Kingdom)},
	volume = {51},
	number = {75},
	year = {2015},
	note = {CAPLUS AN 2015:1265474(Journal; Online Computer File)},
	month = {2015///},
	pages = {14167 - 14170},
	publisher = {Royal Society of Chemistry},
	abstract = {An electrochem. insulin-delivery system based on reduced graphene oxide impregnated with insulin is described. Upon application of a potential pulse of -0.8 V for 30 min, up to 70 {\textpm} 4\% of human insulin was released into a physiol. medium while preserving its biol. activity. [on SciFinder(R)]},
	keywords = {gold reduced graphene oxide electrode insulin delivery, human insulin controlled delivery system},
	isbn = {1359-7345},
	author = {Teodorescu, Florina and Rolland, Laure and Ramarao, Viswanatha and Abderrahmani, Amar and Mandler, Daniel and Boukherroub, Rabah and Szunerits, Sabine.}
}
@booklet {6843,
	title = {Electrochromic device.},
	howpublished = {PCT Int. Appl.},
	number = {WO2015038067A1},
	year = {2015},
	note = {CAPLUS AN 2015:461548(Patent)},
	month = {2015/03/19/},
	pages = {60pp.},
	publisher = {Nanyang Technological University, Singapore; Yissum Research Development Company of the Hebrew University of Jerusalem, Ltd. .},
	abstract = {A method of manufg. an electrochromic device is provided. The method includes providing a patterned arrangement of an elec. conductive material; and applying one or more layers of an electrochromic material to the patterned arrangement, wherein at least a portion of the electrochromic material is in elec. contact with the elec. conductive material. An electrochromic device and an electrochromic ink compn. are also provided. [on SciFinder(R)]},
	keywords = {electrochromic device ink transparent conductive material},
	author = {Magdassi, Shlomo and Lee, Pooi See and Kamyshny, Alexander and Mandler, Daniel and Darmawan, Peter and Layani, Michael.}
}
@article {6830,
	title = {Fabrication of Carbon Nanotube/Indium Tin Oxide "Inverse Tandem" Absorbing Coatings with Tunable Spectral Selectivity for Solar-Thermal Applications.},
	journal = {Energy Technol. (Weinheim, Ger.)Energy Technology (Weinheim, Germany)},
	volume = {3},
	number = {10},
	year = {2015},
	note = {CAPLUS AN 2015:1643974(Journal; Online Computer File)},
	month = {2015///},
	pages = {1045 - 1050},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {We report the fabrication of a new selective "inverse tandem" absorbing coating based on carbon nanotube (CNT)/indium-tin oxide (ITO) on aluminum (Al) for mid-temp. solar-thermal application. The CNT layer is formed by spraying and functions as an excellent solar absorber whereas the ITO layer produced on top of the CNTs by sputtering serves as an IR reflector. The effect of the thickness of the ITO on the spectral selectivity of the absorbing coating was investigated. Controlling the thickness of ITO allowed the spectral selectivity of the coating to be tuned. The CNT/ITO solar coatings with optimized thickness of ITO showed excellent spectral selectivity values of absorptance (α) of 0.927 and emittance (ε) of 0.2. The performance of the coatings at high temp. after heating in air in the range of 25-300{\textdegree}C for different durations was also investigated. The performance and structure of the CNT/ITO coating was also compared with the wet deposition method in which the ITO coating was formed by spraying. [on SciFinder(R)]},
	keywords = {carbon nanotube indium tin oxide absorbing coating solar thermal},
	isbn = {2194-4296},
	author = {Bera, Raj Kumar and Azoubel, Suzanna and Mhaisalkar, Subodh Gautam and Magdassi, Shlomo and Mandler, Daniel.}
}
@article { WOS:000362913600007,
	title = {Fabrication of Carbon Nanotube/Indium Tin Oxide {\textquoteleft}{\textquoteleft}Inverse Tandem{\textquoteright}{\textquoteright} Absorbing Coatings with Tunable Spectral Selectivity for Solar-Thermal Applications},
	journal = {ENERGY TECHNOLOGY},
	volume = {3},
	number = {10},
	year = {2015},
	month = {OCT},
	pages = {1045-1050},
	issn = {2194-4288},
	doi = {10.1002/ente.201500128},
	author = {Bera, Raj Kumar and Azoubel, Suzanna and Mhaisalkar, Subodh Gautam and Magdassi, Shlomo and Mandler, Daniel}
}
@article { WOS:000360918000165,
	title = {Important Implications of the Electrochemical Reduction of ITO},
	journal = {ELECTROCHIMICA ACTA},
	volume = {176},
	year = {2015},
	month = {SEP 10},
	pages = {1374-1381},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2015.07.129},
	author = {Liu, Liang and Yellinek, Shai and Valdinger, Ido and Donval, Ariela and Mandler, Daniel}
}
@article {6833,
	title = {Important Implications of the Electrochemical Reduction of ITO.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {176},
	year = {2015},
	note = {CAPLUS AN 2015:1306951(Journal; Online Computer File)},
	month = {2015///},
	pages = {1374 - 1381},
	publisher = {Elsevier Ltd.},
	abstract = {The electrochem. redn. of indium tin oxide (ITO) on glass is systematically studied. The light absorbance and elec. resistance of ITO increases upon redn. SEM images show that the integrate ITO films dissolve and form particles upon applying neg. potentials. The particles consist of metallic In and Sn, as characterized by XRD and XPS. The redn. of ITO strongly depends on the electrolyte conditions, mainly pH and anions. The onset potential is found to shift neg. as the pH of the electrolyte increases. NO-3 ions significantly inhibit the redn. of ITO, shifting the redn. potential neg. by \~500 mV as compared with SO2-4, Cl- and Br-. It can also serve as inhibitor by adding very low concn. to the Cl{\textendash}dominant electrolyte. Also, the electrochem. reduced ITO show excellent nonlinear optical performance, with transmittance tuneable by redn. potential and time. This suggests a promising useful application of the electrochem. redn. of ITO. [on SciFinder(R)]},
	keywords = {electrochem redn indium tin oxide},
	isbn = {0013-4686},
	author = {Liu, Liang and Yellinek, Shai and Valdinger, Ido and Donval, Ariela and Mandler, Daniel.}
}
@article {6839,
	title = {Layer-by-Layer Assembly of PEDOT:PSS and WO3 Nanoparticles: Enhanced Electrochromic Coloration Efficiency and Mechanism Studies by Scanning Electrochemical Microscopy.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {174},
	year = {2015},
	note = {CAPLUS AN 2015:927237(Journal; Online Computer File)},
	month = {2015///},
	pages = {57 - 65},
	publisher = {Elsevier Ltd.},
	abstract = {Layer-by-layer assembly method is employed to fabricate multilayer hybrid films based on poly(styrenesulfonate)-doped poly(3,4-ethylenedioxythiophene) (PEDOT:PSS) and W oxide nanoparticles (WO3 NPs). Polyethylenimine (PEI) is deposited in between to introduce electrostatic force between the components. In the hybrid films, randomly oriented disk-like WO3 NPs are homogeneously distributed in the polymers and form an interdigitated structure. This very rough surface morphol. hinders the formation of a continuous PEI layer between the electrochromic layers. Owing to the efficient charge transfer between the two active components and complementary elec. cond. of the two components in the redox switching process, the coloration efficiency of the hybrid film is significantly improved to 117.7 cm2/C at wavelength of 633 nm. The underlying mechanism for the enhancement is verified by scanning electrochem. microscopic studies through probing the cond. changes of PEDOT:PSS, WO3-NP and hybrid films under various applied potentials. [on SciFinder(R)]},
	keywords = {layer assembly PEDOT PSS tungsten oxide nanoparticle electrochromism SEM},
	isbn = {0013-4686},
	author = {Ling, Han and Liu, Liang and Lee, Pooi See and Mandler, Daniel and Lu, Xuehong.}
}
@article { WOS:000359873400008,
	title = {Layer-by-Layer Assembly of PEDOT:PSS and WO3 Nanoparticles: Enhanced Electrochromic Coloration Efficiency and Mechanism Studies by Scanning Electrochemical Microscopy},
	journal = {ELECTROCHIMICA ACTA},
	volume = {174},
	year = {2015},
	month = {AUG 20},
	pages = {57-65},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2015.05.147},
	author = {Ling, Han and Liu, Liang and Lee, Pooi See and Mandler, Daniel and Lu, Xuehong}
}
@article { WOS:000360027100055,
	title = {Multienzyme Inkjet Printed 2D Arrays},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {7},
	number = {32},
	year = {2015},
	month = {AUG 19},
	pages = {17985-17992},
	issn = {1944-8244},
	doi = {10.1021/acsami.5b04726},
	author = {Gdor, Efrat and Shemesh, Shay and Magdassi, Shlomo and Mandler, Daniel}
}
@article {7053,
	title = {Multienzyme Inkjet Printed 2D Arrays},
	journal = {ACS Appl Mater InterfacesACS applied materials \& interfaces},
	volume = {7},
	number = {32},
	year = {2015},
	note = {MEDLINE AN 2016066885(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2015///},
	pages = {17985 - 92},
	abstract = {The use of printing to produce 2D arrays is well established, and should be relatively facile to adapt for the purpose of printing biomaterials; however, very few studies have been published using enzyme solutions as inks. Among the printing technologies, inkjet printing is highly suitable for printing biomaterials and specifically enzymes, as it offers many advantages. Formulation of the inkjet inks is relatively simple and can be adjusted to a variety of biomaterials, while providing nonharmful environment to the enzymes. Here we demonstrate the applicability of inkjet printing for patterning multiple enzymes in a predefined array in a very straightforward, noncontact method. Specifically, various arrays of the enzymes glucose oxidase (GOx), invertase (INV) and horseradish peroxidase (HP) were printed on aminated glass surfaces, followed by immobilization using glutardialdehyde after printing. Scanning electrochemical microscopy (SECM) was used for imaging the printed patterns and to ascertain the enzyme activity. The successful formation of 2D arrays consisting of enzymes was explored as a means of developing the first surface confined enzyme based logic gates. Principally, XOR and AND gates, each consisting of two enzymes as the Boolean operators, were assembled, and their operation was studied by SECM.[on SciFinder (R)]},
	keywords = {biomolecular logic gates, Enzymes, patterning, printing, scanning electrochemical microscopy},
	isbn = {1944-8252},
	author = {Gdor, Efrat and Shemesh, Shay and Magdassi, Shlomo and Mandler, Daniel}
}
@article {6835,
	title = {Multienzyme Inkjet Printed 2D Arrays.},
	journal = {ACS Appl. Mater. InterfacesACS Applied Materials \& Interfaces},
	volume = {7},
	number = {32},
	year = {2015},
	note = {CAPLUS AN 2015:1226830(Journal; Online Computer File)},
	month = {2015///},
	pages = {17985 - 17992},
	publisher = {American Chemical Society},
	abstract = {The use of printing to produce 2D arrays is well established, and should be relatively facile to adapt for the purpose of printing biomaterials; however, very few studies have been published using enzyme solns. as inks. Among the printing technologies, inkjet printing is highly suitable for printing biomaterials and specifically enzymes, as it offers many advantages. Formulation of the inkjet inks is relatively simple and can be adjusted to a variety of biomaterials, while providing nonharmful environment to the enzymes. Here we demonstrate the applicability of inkjet printing for patterning multiple enzymes in a predefined array in a very straightforward, noncontact method. Specifically, various arrays of the enzymes glucose oxidase (GOx), invertase (INV) and horseradish peroxidase (HP) were printed on aminated glass surfaces, followed by immobilization using glutardialdehyde after printing. Scanning electrochem. microscopy (SECM) was used for imaging the printed patterns and to ascertain the enzyme activity. The successful formation of 2D arrays consisting of enzymes was explored as a means of developing the first surface confined enzyme based logic gates. Principally, XOR and AND gates, each consisting of two enzymes as the Boolean operators, were assembled, and their operation was studied by SECM. [on SciFinder(R)]},
	keywords = {multienzyme inkjet printing array immobilization glucose oxidase invertase peroxidase},
	isbn = {1944-8244},
	author = {Gdor, Efrat and Shemesh, Shay and Magdassi, Shlomo and Mandler, Daniel.}
}
@article {6841,
	title = {Nanoparticle-Imprinted Polymers: Shell-Selective Recognition of Au Nanoparticles by Imprinting Using the Langmuir-Blodgett Method.},
	journal = {ChemElectroChemChemElectroChem},
	volume = {2},
	number = {6},
	year = {2015},
	note = {CAPLUS AN 2015:845050(Journal; Miscellaneous; Online Computer File)},
	month = {2015///},
	pages = {771},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {The front cover artwork is provided by Prof. Mandler{\textquoteright}s group at the Hebrew University (Israel). The image shows the reuptake process in which only the particles with the original shell size are captured by the imprinted cavities, while the others are not recognized. Read the full text of the Article at10.1002/celc.201402407. [on SciFinder(R)]},
	isbn = {2196-0216},
	author = {Bruchiel-Spanier, Netta and Mandler, Daniel.}
}
@article { WOS:000357862100003,
	title = {Nanoparticle-Imprinted Polymers: Shell-Selective Recognition of Au Nanoparticles by Imprinting Using the Langmuir-Blodgett Method},
	journal = {CHEMELECTROCHEM},
	volume = {2},
	number = {6},
	year = {2015},
	month = {JUN 10},
	pages = {795-802},
	issn = {2196-0216},
	doi = {10.1002/celc.201402407},
	author = {Bruchiel-Spanier, Netta and Mandler, Daniel}
}
@article {6840,
	title = {Nanoparticle-imprinted polymers: shell-selective recognition of Au nanoparticles by imprinting using the Langmuir-Blodgett method.},
	journal = {ChemElectroChemChemElectroChem},
	volume = {2},
	number = {6},
	year = {2015},
	note = {CAPLUS AN 2015:922879(Journal; Online Computer File)},
	month = {2015///},
	pages = {795 - 802},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Speciation of nanoparticles, i.e., their differentiation based on size, shape and stabilizing shell is becoming important since their properties depend on these parameters. Nanoparticle-imprinted polymers (NIPs) are a new approach that aims to selectively recognize nanoparticles based on their structural properties. In this study, monolayers of cellulose acetate (CA) accommodating gold nanoparticles stabilized with dodecanethiol (AuNPs/C12) are transferred onto indium tin oxide (ITO) by the Langmuir-Blodgett technique. One to five monolayers are assembled. Electrochem. oxidn. dissolves the AuNPs/C12 to form cavities in the films, which fit the size and shape of the AuNPs/C12. Reuptake of the nanoparticles from a soln. is successful using the imprinted films, whereas the control films contg. only CA layers do not reuptake the AuNPs/C12. The NIPs are highly selective and other gold nanoparticles stabilized by other thiols are not recognized by the imprinted matrix. [on SciFinder(R)]},
	keywords = {gold nanoparticle selective recognition imprinting cellulose acetate film dodecanethiol},
	isbn = {2196-0216},
	author = {Bruchiel-Spanier, Netta and Mandler, Daniel.}
}
@article { WOS:000358653500005,
	title = {Novel felt pseudocapacitor based on carbon nanotube/metal oxides},
	journal = {JOURNAL OF MATERIALS SCIENCE},
	volume = {50},
	number = {20},
	year = {2015},
	month = {OCT},
	pages = {6578-6585},
	issn = {0022-2461},
	doi = {10.1007/s10853-015-9199-2},
	author = {Fam, Derrick W. H. and Azoubel, Sue and Liu, Liang and Huang, Jingfeng and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred I. Y.}
}
@article {6837,
	title = {Novel felt pseudocapacitor based on carbon nanotube/metal oxides.},
	journal = {J. Mater. Sci.Journal of Materials Science},
	volume = {50},
	number = {20},
	year = {2015},
	note = {CAPLUS AN 2015:1122279(Journal; Online Computer File)},
	month = {2015///},
	pages = {6578 - 6585},
	publisher = {Springer},
	abstract = {This work describes a novel supercapacitor electrode based on a glass fiber felt substrate, single-walled carbon nanotube (SWCNT) and metal oxide layers (RuO2 or MnO2). It is fabricated by the repeated and alternate deposition of SWCNTs and metal oxides via dipping and electrodeposition, resp., to achieve three-dimensional layered hierarchical structured supercapacitor electrodes. The results show that the layered structured electrodes fabricated by alternating deposition of SWCNTs and metal oxides have higher capacitance as compared with the bulk deposited samples, which are fabricated by deposition of SWCNTs followed by metal oxides. The best configuration studied in this work shows specific capacitance of 72 and 98 F/g for the SWCNT-MnO2 and SWCNT-RuO2, resp., whereas the corresponding areal capacitances are 0.07 and 0.09 F/cm2. This three-dimensional porous electrode structure design combines the high mech. stability of the felt substrate with the high cond. and sp. surface area of SWCNTs, and the high capacitance of metal oxides. This will add immensely to the research and development of wearable lightwt. electronics in harsh environments. [on SciFinder(R)]},
	keywords = {felt pseudocapacitor carbon nanotube metal oxide electrode},
	isbn = {0022-2461},
	author = {Fam, Derrick W. H. and Azoubel, Sue and Liu, Liang and Huang, Jingfeng and Mandler, Daniel and Magdassi, Shlomo and Tok, Alfred I. Y.}
}
@booklet {6831,
	title = {Spectrally selective solar thermal coating combining a light-absorbing coating and an infrared reflecting layer positioned on top of the absorber coating.},
	howpublished = {PCT Int. Appl.},
	number = {WO2015136531A2},
	year = {2015},
	note = {CAPLUS AN 2015:1505573(Patent)},
	month = {2015/09/17/},
	pages = {76pp.},
	publisher = {Yissum Research Development Company of the Hebrew University of Jerusalem Ltd, Israel; Nanyang Technological University .},
	abstract = {The invention relates to a light-absorbing element coated on at least a region of its surface with a film of at least one light-absorbing material, the light-absorbing material being assocd. with at least one binder material, the film being 1 - 20 μm thick and having light absorption of at least 90\%. The invention also relates to a device comprising a light-absorbing element. The invention also claims a thermosolar device comprising a light-absorbing element. The invention also relates to a method of fabricating a light-absorbing film on a surface region of a substrate, the method comprising: (a) forming on a surface region at least one absorbing layer comprising: (I) a light-absorbing material; and (II) a polymerizable binder resin; (b) heating the at least one absorbing layer to induce polymn. of the binder resin; and (c) optionally forming at least one IR radiation reflecting layer on the polymd. binder. [on SciFinder(R)]},
	keywords = {light absorbing IR reflective coating solar absorber polysiloxane ceramic},
	author = {Magdassi, Shlomo and Zwicker, Camille and Mhaisalkar, Subodh Gautam and Mandler, Daniel and Levi, Lihi and Azoubel, Suzanna.}
}
@article { WOS:000332604200015,
	title = {Amplified detection of femtomolar DNA based on a one-to-few recognition reaction between DNA-Au conjugate and target DNA},
	journal = {NANOSCALE},
	volume = {6},
	number = {6},
	year = {2014},
	pages = {3110-3115},
	issn = {2040-3364},
	doi = {10.1039/c3nr05625b},
	author = {Wang, Zhijuan and Zhang, Juan and Zhu, Changfeng and Wu, Shixin and Mandler, Daniel and Marks, Robert S. and Zhang, Hua}
}
@article {7060,
	title = {Amplified detection of femtomolar DNA based on a one-to-few recognition reaction between DNA-Au conjugate and target DNA},
	journal = {NanoscaleNanoscale},
	volume = {6},
	number = {6},
	year = {2014},
	note = {MEDLINE AN 2014411439(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2014///},
	pages = {3110 - 5},
	abstract = {A sensitive electrochemical DNA biosensor based on the amplification of Au nanoparticles (AuNPs) has been developed. The AuNPs were modified with two types of signaling reporter DNAs, i.e. a methylene blue probe (MB-probe 2-SH) and T10 with a methylene blue signaling molecule (MB-T10-SH), forming DNA-AuNP conjugates. The MB-probe 2-SH is complementary to the target DNA, while MB-T10-SH is not. The presence of MB-T10-SH reduces the cross-reaction between target DNA and MB-probe 2-SH on the AuNPs, resulting in increased sensitivity of the biosensor. In our assay, the DNA sensor is fabricated by immobilizing a capture probe on the surface of the Au electrode, which then hybridizes with the corresponding target DNA, and further hybridizes with a DNA-Au conjugate. The signal of MB is measured by differential pulse voltammetry, while the DNA-Au conjugate enables the detection of target DNA in the linear range of 10(-13) to 10(-8) M with the detection limit as low as 50 fM.[on SciFinder (R)]},
	isbn = {2040-3372},
	author = {Wang, Zhijuan and Zhang, Juan and Zhu, Changfeng and Wu, Shixin and Mandler, Daniel and Marks, Robert S. and Zhang, Hua}
}
@article {6855,
	title = {Amplified detection of femtomolar DNA based on a one-to-few recognition reaction between DNA-Au conjugate and target DNA.},
	journal = {NanoscaleNanoscale},
	volume = {6},
	number = {6},
	year = {2014},
	note = {CAPLUS AN 2014:328635(Journal; Online Computer File)},
	month = {2014///},
	pages = {3110 - 3115},
	publisher = {Royal Society of Chemistry},
	abstract = {A sensitive electrochem. DNA biosensor based on the amplification of Au nanoparticles (AuNPs) has been developed. The AuNPs were modified with two types of signaling reporter DNAs, i.e. a methylene blue probe (MB-probe 2-SH) and T10 with a methylene blue signaling mol. (MB-T10-SH), forming DNA-AuNP conjugates. The MB-probe 2-SH is complementary to the target DNA, while MB-T10-SH is not. The presence of MB-T10-SH reduces the cross-reaction between target DNA and MB-probe 2-SH on the AuNPs, resulting in increased sensitivity of the biosensor. In our assay, the DNA sensor is fabricated by immobilizing a capture probe on the surface of the Au electrode, which then hybridizes with the corresponding target DNA, and further hybridizes with a DNA-Au conjugate. The signal of MB is measured by differential pulse voltammetry, while the DNA-Au conjugate enables the detection of target DNA in the linear range of 10-13 to 10-8 M with the detection limit as low as 50 fM. [on SciFinder(R)]},
	keywords = {DNA gold conjugate electrochem biosensor differential pulse voltammetry},
	isbn = {2040-3372},
	author = {Wang, Zhijuan and Zhang, Juan and Zhu, Changfeng and Wu, Shixin and Mandler, Daniel and Marks, Robert S. and Zhang, Hua.}
}
@article { WOS:000334555500005,
	title = {Developing and Implementing Inquiry-Based, Water Quality Laboratory Experiments for High School Students To Explore Real Environmental Issues Using Analytical Chemistry},
	journal = {JOURNAL OF CHEMICAL EDUCATION},
	volume = {91},
	number = {4},
	year = {2014},
	month = {APR},
	pages = {492-496},
	issn = {0021-9584},
	doi = {10.1021/ed200586r},
	author = {Mandler, Daphna and Blonder, Ron and Yayon, Malka and Mamlok-Naaman, Rachel and Hofstein, Avi}
}
@article {7064,
	title = {Electrochemically "writing" graphene from graphene oxide},
	journal = {SmallSmall (Weinheim an der Bergstrasse, Germany)},
	volume = {10},
	number = {17},
	year = {2014},
	note = {MEDLINE AN 2013873913(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2014///},
	pages = {3555 - 9},
	abstract = {A novel approach of patterning graphene on conductive surfaces based on local electrochemical reduction of graphene oxide is reported. Graphene is "written" from typical graphene oxide dispersion by applying negative potential on conductive surfaces vs. a micrometer-sized counter electrode "pen" with scanning electrochemical microscopy (SECM). Micrometer scaled patterns are successfully generated on gold and stainless steel surfaces.[on SciFinder (R)]},
	keywords = {direct mode, electrodeposition, graphene, graphene oxide, scanning electrochemical microscopy (secm)},
	isbn = {1613-6829},
	author = {Liu, Liang and Tan, Chaoliang and Chai, Jianwei and Wu, Shixin and Radko, Anna and Zhang, Hua and Mandler, Daniel}
}
@article {6863,
	title = {Electrochemically "writing" graphene from graphene oxide.},
	journal = {SmallSmall},
	volume = {10},
	number = {17},
	year = {2014},
	note = {CAPLUS AN 2013:1219102(Journal)},
	month = {2014///},
	pages = {3555 - 3559},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Graphene has been successfully patterned on stainless steel and gold at micrometer-scale resoln. The concept is based on the electrochem. redn. of graphene oxide on conductive surfaces localized by a microelectrode that is positioned close to the surface. [on SciFinder(R)]},
	keywords = {graphene Electrochem synthesis graphene oxide},
	isbn = {1613-6810},
	author = {Liu, Liang and Tan, Chaoliang and Chai, Jianwei and Wu, Shixin and Radko, Anna and Zhang, Hua and Mandler, Daniel.}
}
@article { WOS:000341713500011,
	title = {Electrochemically {\textquoteleft}{\textquoteleft}Writing{\textquoteright}{\textquoteright} Graphene from Graphene Oxide},
	journal = {SMALL},
	volume = {10},
	number = {17, SI},
	year = {2014},
	month = {SEP 10},
	pages = {3555-3559},
	issn = {1613-6810},
	doi = {10.1002/smll.201301953},
	author = {Liu, Liang and Tan, Chaoliang and Chai, Jianwei and Wu, Shixin and Radko, Anna and Zhang, Hua and Mandler, Daniel}
}
@article { WOS:000332038300019,
	title = {Europium Doped Vanadium Dioxide Material: Reduced Phase Transition Temperature, Enhanced Luminous Transmittance and Solar Modulation},
	journal = {SCIENCE OF ADVANCED MATERIALS},
	volume = {6},
	number = {3},
	year = {2014},
	month = {MAR},
	pages = {558-561},
	issn = {1947-2935},
	doi = {10.1166/sam.2014.1777},
	author = {Cao, X. and Wang, N. and S.Magdassi and Mandler, D. and Long, Y.}
}
@article {6853,
	title = {Europium doped vanadium dioxide material: reduced phase transition temperature, enhanced luminous transmittance and solar modulation.},
	journal = {Sci. Adv. Mater.Science of Advanced Materials},
	volume = {6},
	number = {3},
	year = {2014},
	note = {CAPLUS AN 2014:606902(Journal)},
	month = {2014///},
	pages = {558 - 561},
	publisher = {American Scientific Publishers},
	abstract = {Vanadium dioxide is a well-known near room temp. phase transition material with a transition temp. (τC) at 68 {\textdegree}C. In this paper, Eu3+ dopant with different doping levels was introduced into the crystal lattice of VO2. The thermochromic properties, including the integrated visible transmittance (Tlum) and the solar modulating ability (ΔTsol) were favorably affected by the Eu-doping. It is of great interest that the substitution of V4+ by Eu3+ in the VO2 crystal structure reduced the τC from 68 {\textdegree}C to 47.5 {\textdegree}C with an approx. decreasing rate of 6.5 {\textdegree}C/at\% up to 4 at\%. More importantly, the Eu dopant helped in improving the properties of luminous transmittance and solar modulating ability, which were difficult to be achieved by other dopants. [on SciFinder(R)]},
	keywords = {europium vanadium oxide phase transition temp transmittance solar modulation},
	isbn = {1947-2935},
	author = {Cao, X. and Wang, N and Magdassi, S. and Mandler, D and Long, Y.}
}
@booklet {6846,
	title = {High absorptivity, heat resistant coatings and related apparatus and methods.},
	howpublished = {U.S. Pat. Appl. Publ.},
	number = {US20140326236A1},
	year = {2014},
	note = {CAPLUS AN 2014:1872025(Patent)},
	month = {2014/11/06/},
	pages = {20pp.},
	publisher = {Brightsource Industries Israel Ltd., Israel; Yissum Research Development Company of the Hebrew University of Jerusalem .},
	abstract = {A paint formulation can include an inorg. oxide-based pigment and an org. binder. The org. binder can be irreversibly converted to an inorg. binder upon curing of the paint formulation at a temp. greater than 200{\textdegree} C. The oxide-based pigment and/or the paint formulation itself can have an absorptivity of at least 80\% with respect to the AM 1.5 spectrum. The paint formulation can also include at least one org. solvent, an inorg. filler, and/or at least one additive. Such paint formulations may be stable at high temps. (e.g., 750{\textdegree} C.) and can be used as solar-radiation-absorbing heat-resistant coatings for components of a solar tower system. [on SciFinder(R)]},
	keywords = {high absorptivity heat resistant coating app method},
	author = {Magdassi, Shlomo and Mandler, Daniel and Baidossi, Mubeen and Larush, Liraz and Zwicker, Camille and Nirenberg, Anna and Binyamin, Yaniv.}
}
@article {6849,
	title = {In situ electrodeposition of an asymmetric sol-gel membrane based on an octadecyltrimethoxysilane langmuir film.},
	journal = {Chem. - Eur. J.Chemistry - A European Journal},
	volume = {20},
	number = {38},
	year = {2014},
	note = {CAPLUS AN 2014:1330891(Journal)},
	month = {2014///},
	pages = {12104 - 12113},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {The unique properties of Langmuir film formation were utilized in assembling a thin skin of an asym. membrane. An octadecyltrimethoxysilane (ODTMS) Langmuir monolayer was formed at the air-water interface and served as the substrate for growing a bulky sol-gel polymer in situ. The latter was based on the electrochem. deposition of tetramethoxysilane dissolved in the water subphase by means of horizontal touch electrochem. The resultant asym. layer that consisted of a thin hydrophobic ODTMS Langmuir film connected to a bulk hydrophilic sol-gel network was studied in situ and ex situ by using various techniques, such as cyclic voltammetry, electrochem. impedance spectroscopy (EIS), SEM, transmission electron microscopy (TEM), and goniometry. We found that a porous hydrophilic film grew on top of a hydrophobic layer as was evident from TEM, contact angle, and EIS analyses. The film thickness and film permeability could be controlled by changing the deposition conditions such as the potential window applied and its duration. Hence, this method offers an alternative approach for assembling asym. films for various applications. [on SciFinder(R)]},
	keywords = {octadecyltrimethoxysilane langmuir film asym sol gel membrane electrodeposition},
	isbn = {0947-6539},
	author = {Hitrik, Maria and Lev, Ovadia and Mandler, Daniel.}
}
@article { WOS:000341831600020,
	title = {In Situ Electrodeposition of an Asymmetric Sol-Gel Membrane Based on an Octadecyltrimethoxysilane Langmuir Film},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {20},
	number = {38},
	year = {2014},
	month = {SEP 15},
	pages = {12104-12113},
	issn = {0947-6539},
	doi = {10.1002/chem.201403289},
	author = {Hitrik, Maria and Lev, Ovadia and Mandler, Daniel}
}
@article {7057,
	title = {In situ electrodeposition of an asymmetric sol-gel membrane based on an octadecyltrimethoxysilane Langmuir film},
	journal = {ChemistryChemistry (Weinheim an der Bergstrasse, Germany)},
	volume = {20},
	number = {38},
	year = {2014},
	note = {MEDLINE AN 2015004784(Journal; Article; (JOURNAL ARTICLE))},
	month = {2014///},
	pages = {12104 - 13},
	abstract = {The unique properties of Langmuir film formation were utilized in assembling a thin skin of an asymmetric membrane. An octadecyltrimethoxysilane (ODTMS) Langmuir monolayer was formed at the air-water interface and served as the substrate for growing a bulky sol-gel polymer in situ. The latter was based on the electrochemical deposition of tetramethoxysilane dissolved in the water subphase by means of horizontal touch electrochemistry. The resultant asymmetric layer that consisted of a thin hydrophobic ODTMS Langmuir film connected to a bulk hydrophilic sol-gel network was studied in situ and ex situ by using various techniques, such as cyclic voltammetry, electrochemical impedance spectroscopy (EIS), scanning electron microscopy, transmission electron microscopy (TEM), and goniometry. We found that a porous hydrophilic film grew on top of a hydrophobic layer as was evident from TEM, contact angle, and EIS analyses. The film thickness and film permeability could be controlled by changing the deposition conditions such as the potential window applied and its duration. Hence, this method offers an alternative approach for assembling asymmetric films for various applications.[on SciFinder (R)]},
	keywords = {Electrochemistry, langmuir-blodgett films, membranes, silanes, sol-gel processes},
	isbn = {1521-3765},
	author = {Hitrik, Maria and Lev, Ovadia and Mandler, Daniel}
}
@article { WOS:000342079200068,
	title = {{\textquoteleft}{\textquoteleft}Nano to nano{\textquoteright}{\textquoteright} electrodeposition of WO3 crystalline nanoparticles for electrochromic coatings},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {2},
	number = {38},
	year = {2014},
	pages = {16224-16229},
	issn = {2050-7488},
	doi = {10.1039/c4ta03431g},
	author = {Liu, Liang and Layani, Michael and Yellinek, Shai and Kamyshny, Alexander and Ling, Han and Lee, Pooi See and Magdassi, Shlomo and Mandler, Daniel}
}
@article {6850,
	title = {"Nano to nano" electrodeposition of WO3 crystalline nanoparticles for electrochromic coatings.},
	journal = {J. Mater. Chem. AJournal of Materials Chemistry A: Materials for Energy and Sustainability},
	volume = {2},
	number = {38},
	year = {2014},
	note = {CAPLUS AN 2014:1247190(Journal; Online Computer File)},
	month = {2014///},
	pages = {16224 - 16229},
	publisher = {Royal Society of Chemistry},
	abstract = {A nano to nano electrodeposition approach for prepg. nano-structured thin films from the dispersion of nano-objects is reported. A typical WO3 system is demonstrated, where nanocryst. films are electrodeposited onto transparent conductive electrodes such as ITO and Ag grid printed PET (Ag grid/PET) from the H2O dispersion of WO3 nanoparticles without applying high potential, adding surfactants or polymers. The process is based on the redn. of WO3, which eliminates the electrostatic repulsion between the nanoparticles causing film deposition on the cathode. The reduced WO3 (HWO3) is conductive, thus it allows further film growth towards higher thickness and coverage. The electrodeposited films consist of stacked cryst. nanoparticles, which provide a highly active surface area, facilitate the penetration of electrolyte and the intercalation/deintercalation of Li+ in the nanocrystals and therefore result in outstanding electrochromic performance and stability (92\% contrast, 9 s coloring and 15 s bleaching, retaining 76\% contrast after 1000 coloring-bleaching cycles). The thickness, electrochromic performance and surface coverage of the films are well tuned by potential and time. This novel nano to nano electrodeposition approach based on the electrochem. redox of nano-objects can be extended to various transition metal oxide nano-objects with different sizes and shapes. [on SciFinder(R)]},
	keywords = {nano electrodeposition tungsten oxide cryst nanoparticle electrochromic coating},
	isbn = {2050-7496},
	author = {Liu, Liang and Layani, Michael and Yellinek, Shai and Kamyshny, Alexander and Ling, Han and Lee, Pooi See and Magdassi, Shlomo and Mandler, Daniel.}
}
@article {7061,
	title = {Nanoparticle-imprinted polymers for size-selective recognition of nanoparticles},
	journal = {Angew Chem Int Ed EnglAngewandte Chemie (International ed. in English)},
	volume = {53},
	number = {1},
	year = {2014},
	note = {MEDLINE AN 2014304303(Journal; Article; (JOURNAL ARTICLE))},
	month = {2014///},
	pages = {294 - 8},
	abstract = {Citrate-stabilized gold nanoparticles 15 nm and 33 nm in diameter were transferred concomitantly with a monolayer of positively charged polyaniline by Langmuir-Blodgett transfer at pH 5 onto a conducting indium-doped tin oxide (ITO) support. Films consisting of one to three layers of polyaniline with thicknesses of 1-3 nm were prepared and characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy. After electro-oxidation of the Au nanoparticles in 0.1 M KCl, cavities were left behind in the film that could be analyzed by SEM. These cavities were able to recapture analyte nanoparticles from a solution of pH 10 and showed size-exclusion properties. The amount of nanoparticles taken up by the cavities was conveniently analyzed by measuring the charge associated with the electro-oxidation of these particles in 0.1 M KCl after the film had been rinsed with water. The size-exclusion properties improved with the number of Langmuir-Blodgett layers transferred.[on SciFinder (R)]},
	keywords = {analytical methods, Imprinting, Nanoparticles, size-selective recognition, thin films},
	isbn = {1521-3773},
	author = {Kraus-Ophir, Shlomit and Witt, Julia and Wittstock, Gunther and Mandler, Daniel}
}
@article { WOS:000328714900046,
	title = {Nanoparticle-Imprinted Polymers for Size-Selective Recognition of Nanoparticles},
	journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
	volume = {53},
	number = {1},
	year = {2014},
	month = {JAN 3},
	pages = {294-298},
	issn = {1433-7851},
	doi = {10.1002/anie.201305962},
	author = {Kraus-Ophir, Shlomit and Witt, Julia and Wittstock, Gunther and Mandler, Daniel}
}
@article {6858,
	title = {Nanoparticle-Imprinted Polymers for Size-Selective Recognition of Nanoparticles.},
	journal = {Angew. Chem., Int. Ed.Angewandte Chemie, International Edition},
	volume = {53},
	number = {1},
	year = {2014},
	note = {CAPLUS AN 2013:1715404(Journal)},
	month = {2014///},
	pages = {294 - 298},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Citrate-stabilized gold nanoparticles 15 nm and 33 nm in diam. were transferred concomitantly with a monolayer of pos. charged polyaniline by Langmuir-Blodgett transfer at pH 5 onto a conducting indium-doped tin oxide (ITO) support. Films consisting of one to three layers of polyaniline with thicknesses of 1-3 nm were prepd. and characterized by SEM, at. force microscopy (AFM), and XPS. After electrooxidn. of the Au nanoparticles in 0.1 M KCl, cavities were left behind in the film that could be analyzed by SEM. These cavities were able to recapture analyte nanoparticles from a soln. of pH 10 and showed size-exclusion properties. The amt. of nanoparticles taken up by the cavities was conveniently analyzed by measuring the charge assocd. with the electrooxidn. of these particles in 0.1 M KCl after the film had been rinsed with water. The size-exclusion properties improved with the no. of Langmuir-Blodgett layers transferred. [on SciFinder(R)]},
	keywords = {nanoparticle imprinted polymer size selective recognition},
	isbn = {1433-7851},
	author = {Kraus-Ophir, Shlomit and Witt, Julia and Wittstock, Gunther and Mandler, Daniel.}
}
@article { WOS:000334855500022,
	title = {Nanostructured electrochromic films by inkjet printing on large area and flexible transparent silver electrodes},
	journal = {NANOSCALE},
	volume = {6},
	number = {9},
	year = {2014},
	pages = {4572-4576},
	issn = {2040-3364},
	doi = {10.1039/c3nr06890k},
	author = {Layani, Michael and Darmawan, Peter and Foo, Wan Ling and Liu, Liang and Kamyshny, Alexander and Mandler, Daniel and Magdassi, Schlomo and Lee, Pooi See}
}
@article {6854,
	title = {Nanostructured electrochromic films by inkjet printing on large area and flexible transparent silver electrodes.},
	journal = {NanoscaleNanoscale},
	volume = {6},
	number = {9},
	year = {2014},
	note = {CAPLUS AN 2014:601543(Journal; Online Computer File)},
	month = {2014///},
	pages = {4572 - 4576},
	publisher = {Royal Society of Chemistry},
	abstract = {Printed electrochromic flexible films were obtained by combining transparent silver grid electrodes formed by self-assembly and inkjet printed WO3 nanoparticles. Concd. dispersions of WO3 nanoparticles were inkjet printed on transparent plastic silver grid electrodes with a high transparency of 83\% in the spectral range of 400-800 nm, and a low sheet resistance in the range of 1-5 Ω sq-1. These electrodes were used for electrochromic applications for the first time. The resultant patterned nanostructured electrochromic films maintained their coloring and bleaching performance after bending of the flexible films. [on SciFinder(R)]},
	keywords = {nanostructured electrochromic film inkjet printing flexible transparent silver electrode},
	isbn = {2040-3372},
	author = {Layani, Michael and Darmawan, Peter and Foo, Wan Ling and Liu, Liang and Kamyshny, Alexander and Mandler, Daniel and Magdassi, Schlomo and Lee, Pooi See.}
}
@article {7059,
	title = {Nanostructured electrochromic films by inkjet printing on large area and flexible transparent silver electrodes},
	journal = {NanoscaleNanoscale},
	volume = {6},
	number = {9},
	year = {2014},
	note = {MEDLINE AN 2014580443(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2014///},
	pages = {4572 - 6},
	abstract = {Printed electrochromic flexible films were obtained by combining transparent silver grid electrodes formed by self-assembly and inkjet printed WO3 nanoparticles. Concentrated dispersions of WO3 nanoparticles were inkjet printed on transparent plastic silver grid electrodes with a high transparency of 83\% in the spectral range of 400-800 nm, and a low sheet resistance in the range of 1-5 Ω sq(-1). These electrodes were used for electrochromic applications for the first time. The resultant patterned nanostructured electrochromic films maintained their coloring and bleaching performance after bending of the flexible films.[on SciFinder (R)]},
	isbn = {2040-3372},
	author = {Layani, Michael and Darmawan, Peter and Foo, Wan Ling and Liu, Liang and Kamyshny, Alexander and Mandler, Daniel and Magdassi, Schlomo and Lee, Pooi See}
}
@article {6860,
	title = {A novel non-selective coating material for solar thermal potential application formed by reaction between sol-gel titania and copper manganese spinel.},
	journal = {Sol. Energy Mater. Sol. CellsSolar Energy Materials \& Solar Cells},
	volume = {120},
	number = {PA},
	year = {2014},
	note = {CAPLUS AN 2013:1477218(Journal; Online Computer File)},
	month = {2014///},
	pages = {23 - 29},
	publisher = {Elsevier B.V.},
	abstract = {A method for prepg. a novel bixbyite non-selective coating for solar thermal conversion is described. The coating is formed by a thermal reaction between a titania sol-gel precursor with a copper manganese spinel to form a new material, Cu0.44Ti0.44Mn0.84Fe0.28O3, with a bixbyite structure. The effect of temp. and ratio between the two components on the formation of the bixbyite layer (deposited on Inconel by spray-coating) was studied. The absorptance of the films (AM 1.5; 335-2500 nm) with a thickness of 10{\textpm}2 μm after annealing at 2 h at 650 {\textdegree}C and 750 {\textdegree}C was 97.4\% and 94.7\%, resp. This synthesis represents a novel approach in which the final solar thermal coating is formed as a continuous and uniform layer which combines both the absorber and the ceramic binder. The developed material shows promising results for future applications as absorber in solar thermal energy conversion. [on SciFinder(R)]},
	keywords = {titania copper manganese ceramic composite solar thermal energy conversion},
	isbn = {0927-0248},
	author = {Tulchinsky, Dani and Uvarov, Vladimir and Popov, Inna and Mandler, Daniel and Magdassi, Shlomo.}
}
@article { WOS:000329595400004,
	title = {A novel non-selective coating material for solar thermal potential application formed by reaction between sol-gel titania and copper manganese spinel},
	journal = {SOLAR ENERGY MATERIALS AND SOLAR CELLS},
	volume = {120},
	number = {A, SI},
	year = {2014},
	month = {JAN},
	pages = {23-29},
	issn = {0927-0248},
	doi = {10.1016/j.solmat.2013.08.004},
	author = {Tulchinsky, Dani and Uvarov, Vladimir and Popov, Inna and Mandler, Daniel and Magdassi, Shlomo}
}
@article { WOS:000331247500035,
	title = {One-pot sequential electrochemical deposition of multilayer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic acid)/tungsten trioxide hybrid films and their enhanced electrochromic properties},
	journal = {JOURNAL OF MATERIALS CHEMISTRY A},
	volume = {2},
	number = {8},
	year = {2014},
	pages = {2708-2717},
	issn = {2050-7488},
	doi = {10.1039/c3ta14781a},
	author = {Ling, Han and Lu, Jinlin and Phua, Silei and Liu, Hai and Liu, Liang and Huang, Yizhong and Mandler, Daniel and Lee, Pooi See and Lu, Xuehong}
}
@article {6856,
	title = {One-pot sequential electrochemical deposition of multilayer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic acid)/tungsten trioxide hybrid films and their enhanced electrochromic properties.},
	journal = {J. Mater. Chem. AJournal of Materials Chemistry A: Materials for Energy and Sustainability},
	volume = {2},
	number = {8},
	year = {2014},
	note = {CAPLUS AN 2014:152400(Journal; Online Computer File)},
	month = {2014///},
	pages = {2708 - 2717},
	publisher = {Royal Society of Chemistry},
	abstract = {Hybrid thin films composed of multilayer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonic acid) (PEDOT:PSS) and W trioxide (WO3) were electrochem. deposited on In Sn oxide (ITO) from a 1-pot soln. using a square-wave galvanostatic method. The morphol. of the hybrid thin films could be easily manipulated to optimize their electrochromic properties by adjusting deposition conditions. In the hybrids, both components can be simultaneously switched to colored or bleached states. The hybrid film obtained with very short deposition times of PEDOT:PSS and WO3 in each cycle exhibits significantly enhanced electrochromic properties. The optical contrast of the hybrid film is higher than that of PEDOT:PSS or WO3 films of the same thickness. Also, the stability of the hybrid film is also drastically enhanced. The enhancement may be attributed to the favorable interactions between the two components, i.e., PEDOT:PSS may enter the defect sites in electrodeposited WO3, preventing surface-defect-induced anodic dissoln. during cycling, while the surface functional groups of WO3 may act as dopants to inhibit over-oxidn. of PEDOT, as well as the large interfacial area created using this unique 1-pot multilayer deposition method. [on SciFinder(R)]},
	keywords = {one pot sequential electrochem deposition multilayer, polyethylenedioxythiophene polystyrenesulfonic acid tungsten trioxide hybrid film electrochromic property},
	isbn = {2050-7496},
	author = {Ling, Han and Lu, Jinlin and Phua, Silei and Liu, Hai and Liu, Liang and Huang, Yizhong and Mandler, Daniel and Lee, Pooi See and Lu, Xuehong.}
}
@article { WOS:000345208000015,
	title = {Patterning carbon nanotubes with silane by scanning electrochemical microscopy},
	journal = {ELECTROCHEMISTRY COMMUNICATIONS},
	volume = {48},
	year = {2014},
	month = {NOV},
	pages = {56-60},
	issn = {1388-2481},
	doi = {10.1016/j.elecom.2014.08.015},
	author = {Liu, Liang and Mandler, Daniel}
}
@article {6848,
	title = {Patterning carbon nanotubes with silane by scanning electrochemical microscopy.},
	journal = {Electrochem. Commun.Electrochemistry Communications},
	volume = {48},
	year = {2014},
	note = {CAPLUS AN 2014:1440934(Journal; Online Computer File)},
	month = {2014///},
	pages = {56 - 60},
	publisher = {Elsevier B.V.},
	abstract = {This work reports a novel approach of patterning carbon nanotubes (CNTs) with scanning electrochem. microscopy (SECM). The concept is based on the localized cathodic current flux, which induces the pH increase on the conductive surface confined under the microelectrode. The latter facilitates the local deposition of silane sol-gel films, which embed the CNTs from the dispersion. The patterns can be tuned by deposition potential, time and scan rate of the microelectrode, as characterized by optical microscopy, SEM (SEM), energy-dispersive X-ray anal. (EDX) and profilometry. [on SciFinder(R)]},
	keywords = {carbon nanotube silane patterning scanning electrochem microscopy},
	isbn = {1388-2481},
	author = {Liu, Liang and Mandler, Daniel.}
}
@article { WOS:000348281700012,
	title = {Perpendicular Orientation of Anisotropic Au-Tipped CdS Nanorods at the Air/Water Interface},
	journal = {ADVANCED MATERIALS INTERFACES},
	volume = {1},
	number = {1},
	year = {2014},
	month = {FEB 13},
	issn = {2196-7350},
	doi = {10.1002/admi.201300030},
	author = {Kraus-Ophir, Shlomit and Ben-Shahar, Yuval and Banin, Uri and Mandler, Daniel}
}
@article {6847,
	title = {Perpendicular orientation of anisotropic Au-tipped CdS nanorods at the air/water interface.},
	journal = {Adv. Mater. InterfacesAdvanced Materials Interfaces},
	volume = {1},
	number = {1},
	year = {2014},
	note = {CAPLUS AN 2014:1701150(Journal; Online Computer File)},
	month = {2014///},
	pages = {1300030/1 - 1300030/9},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Anisotropic CdS nanorods tipped by Au nanoparticles on one edge (Au-CdSNRs) are perpendicularly oriented at the air/water interface, whereby all the Au tips are located in the subphase, using the Langmuir-Blodgett technique. Since these nano-objects reveal light-induced charge sepn. at the semiconductor/metal interface, it is of high interest to control their organization. The orientation of these assemblies was studied in situ while compressing the Langmuir-Blodgett trough using the π-A isotherm, Brewster angle microscopy, and horizontal touch voltammetry. All these analyses clearly confirm the induced organization of the amphiphilic Au-CdS-NRs by compression of the Langmuir layer. The compressed layers are successfully transferred by the Langmuir-Schaefer method onto transmission electron microscopy grids while maintaining the preferential orientation as analyzed by TEM, SEM, STEM, and XPS. As far as can be detd., the Langmuir-Blodgett technique was not used so far for perpendicularly orienting anisotropic nano-objects. Moreover, these findings clearly demonstrate that anisotropic amphiphilic nano-objects can be treated with some similarity to the traditional amphiphilic mol. building blocks. [on SciFinder(R)]},
	keywords = {perpendicular orientation gold tipped cadmium sulfide nanorod water surface},
	isbn = {2196-7350},
	author = {Kraus-Ophir, Shlomit and Ben-Shahar, Yuval and Banin, Uri and Mandler, Daniel.}
}
@article {7058,
	title = {Preparation and characterization of alkylphosphonic acid self-assembled monolayers on titanium alloy by chemisorption and electrochemical deposition},
	journal = {LangmuirLangmuir : the ACS journal of surfaces and colloids},
	volume = {30},
	number = {23},
	year = {2014},
	note = {MEDLINE AN 2014726186(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2014///},
	pages = {6791 - 9},
	abstract = {Ti-6Al-4V alloy is the most commonly used alloy for dental and orthopedic implants. In order to improve osseointegration, different surface modification methods are usually employed, including self-assembled monolayers (SAMs). This study presents an investigation of both active (electroassisted) and passive (adsorption) approaches for the modification of Ti-6Al-4V using alkylphosphonic acid. The monolayers were characterized by cyclic voltammetry, double-layer capacitance, contact angle measurements, X-ray photoelectron spectroscopy, polarization modulation infrared reflection adsorption spectroscopy, electrochemical impedance spectroscopy, and corrosion potentiodynamic polarization measurements. It is shown that the electrochemically assisted monolayers, which are assembled faster, exhibit better control over surface properties, a superior degree of order, and a somewhat higher packing density. The electrosorbed SAMs also exhibit better blockage of electron transfer across the interface and thus have better corrosion resistance.[on SciFinder (R)]},
	isbn = {1520-5827},
	author = {Metoki, Noah and Liu, Liang and Beilis, Edith and Eliaz, Noam and Mandler, Daniel}
}
@article { WOS:000337644200019,
	title = {Preparation and Characterization of Alkylphosphonic Acid Self-Assembled Mono layers on Titanium Alloy by Chemisorption and Electrochemical Deposition},
	journal = {LANGMUIR},
	volume = {30},
	number = {23},
	year = {2014},
	month = {JUN 17},
	pages = {6791-6799},
	issn = {0743-7463},
	doi = {10.1021/la404829b},
	author = {Metoki, Noah and Liu, Liang and Beilis, Edith and Eliaz, Noam and Mandler, Daniel}
}
@article {6852,
	title = {Preparation and characterization of alkylphosphonic acid self-assembled monolayers on titanium alloy by chemisorption and electrochemical deposition.},
	journal = {LangmuirLangmuir},
	volume = {30},
	number = {23},
	year = {2014},
	note = {CAPLUS AN 2014:789252(Journal; Online Computer File)},
	month = {2014///},
	pages = {6791 - 6799},
	publisher = {American Chemical Society},
	abstract = {Ti-6Al-4V alloy is the most commonly used alloy for dental and orthopedic implants. In order to improve osseointegration, different surface modification methods are usually employed, including self-assembled monolayers (SAMs). This study presents an investigation of both active (electroassisted) and passive (adsorption) approaches for the modification of Ti-6Al-4V using alkylphosphonic acid. The monolayers were characterized by cyclic voltammetry, double-layer capacitance, contact angle measurements, XPS, polarization modulation IR reflection adsorption spectroscopy, electrochem. impedance spectroscopy, and corrosion potentiodynamic polarization measurements. It is shown that the electrochem. assisted monolayers, which are assembled faster, exhibit better control over surface properties, a superior degree of order, and a somewhat higher packing d. The electrosorbed SAMs also exhibit better blockage of electron transfer across the interface and thus have better corrosion resistance. [on SciFinder(R)]},
	keywords = {alkylphosphonic acid selfassembled monolayers titanium alloy chemisorption electrodeposition},
	isbn = {0743-7463},
	author = {Metoki, Noah and Liu, Liang and Beilis, Edith and Eliaz, Noam and Mandler, Daniel.}
}
@inbook { WOS:000357718500025,
	title = {Remote Sensing},
	booktitle = {ENVIRONMENTAL ANALYSIS BY ELECTROCHEMICAL SENSORS AND BIOSENSORS: FUNDAMENTALS, VOL 1},
	series = {Nanostructure Science and Technology},
	year = {2014},
	pages = {667-690},
	isbn = {978-1-4939-0676-5; 978-1-4939-0675-8},
	doi = {10.1007/978-1-4939-0676-5_23},
	author = {Noyhouzer, Tomer and Mandler, Daniel},
	editor = {Moretto, LM and Kalcher, K}
}
@booklet {6851,
	title = {Solar-radiation-absorbing formulations, application of paint, painted metal article and related apparatus.},
	howpublished = {U.S. Pat. Appl. Publ.},
	number = {US20140141236A1},
	year = {2014},
	note = {CAPLUS AN 2014:830676(Patent)},
	month = {2014/05/22/},
	pages = {19pp.},
	publisher = {BrightSource Industries Ltd., Israel .},
	abstract = {Paint formulations having a high absorptivity with respect to solar radiation are described. The paint formulations are also thermally and mech. durable, enabling the paint formulations to be used on components in solar thermal applications where exposure to high temps. and environmental conditions may be an issue. The paint formulation can include an oxide-based pigment, an org. binder, >=1 additives, an inorg. filler, and/or an org. solvent. The pigment can have a relatively high absorptivity with respect to light having a wavelength in the range 250-3000 nm. Curing of the paint formulation can irreversibly convert the org. binder into an inorg. binder. [on SciFinder(R)]},
	keywords = {ceramic oxide pigment paint solar radiation absorbing},
	author = {Magdassi, Shlomo and Mandler, Daniel and Baidossi, Mubeen and Assa, Rachel and Chernin, Ophir and Binyamin, Yaniv.}
}
@article {6865,
	title = {Allen J. Bard, Gyoergy Inzelt, Fritz Scholz (Eds.): Electrochemical dictionary, 2nd ed.},
	journal = {Anal. Bioanal. Chem.Analytical and Bioanalytical Chemistry},
	volume = {405},
	number = {21},
	year = {2013},
	note = {CAPLUS AN 2013:985597(Journal; Online Computer File)},
	month = {2013///},
	pages = {6607 - 6608},
	publisher = {Springer},
	isbn = {1618-2642},
	author = {Mandler, Daniel.}
}
@article { WOS:000328920600014,
	title = {Biomolecular AND Logic Gate Based on Immobilized Enzymes with Precise Spatial Separation Controlled by Scanning Electrochemical Microscopy},
	journal = {JOURNAL OF PHYSICAL CHEMISTRY B},
	volume = {117},
	number = {50},
	year = {2013},
	month = {DEC 19},
	pages = {16058-16065},
	issn = {1520-6106},
	doi = {10.1021/jp4095672},
	author = {Gdor, Efrat and Katz, Evgeny and Mandler, Daniel}
}
@article {7062,
	title = {Biomolecular AND logic gate based on immobilized enzymes with precise spatial separation controlled by scanning electrochemical microscopy},
	journal = {J Phys Chem BThe journal of physical chemistry. B},
	volume = {117},
	number = {50},
	year = {2013},
	note = {MEDLINE AN 2014189675(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T); (RESEARCH SUPPORT, U.S. GOV{\textquoteright}T, NON-P.H.S.))},
	month = {2013///},
	pages = {16058 - 65},
	abstract = {A surface-localized enzymatic AND gate based on scanning electrochemical microscopy was designed and studied. The gate is composed of an insulating glass surface modified with the enzyme glucose oxidase (GOx) and another surface opposing it made of a microelectrode. The latter was modified with a second enzyme, invertase (INV). The distance separating the modified microelectrode and surface controlled the output of the AND gate produced upon the biocatalytic reaction of the confined enzymes. Specifically, as the GOx-modified glass substrate entered the diffusion layer of the microelectrode, it catalyzed the regeneration of an electron-transfer mediator, ferroceniummethanol, generated electrochemically at the tip by oxidizing glucose, also generated at the tip, by catalytic cleaving of sucrose by INV. To enhance the activity of the GOx, mutarotase was added to convert α- to β-glucose to be further consumed by GOx. Hence, an increase of the current at the microelectrode was obtained by approaching the glass surface only in the presence of all the components. This is the first micrometer-sized biomolecular logic gate, of which we are aware, that is surface-confined and shows the promise held by the localization of biomolecular information-processing species.[on SciFinder (R)]},
	isbn = {1520-5207},
	author = {Gdor, Efrat and Katz, Evgeny and Mandler, Daniel}
}
@article {6857,
	title = {Biomolecular AND Logic Gate Based on Immobilized Enzymes with Precise Spatial Separation Controlled by Scanning Electrochemical Microscopy.},
	journal = {J. Phys. Chem. BJournal of Physical Chemistry B},
	volume = {117},
	number = {50},
	year = {2013},
	note = {CAPLUS AN 2013:1815066(Journal; Online Computer File)},
	month = {2013///},
	pages = {16058 - 16065},
	publisher = {American Chemical Society},
	abstract = {A surface-localized enzymic AND gate based on scanning electrochem. microscopy was designed and studied. The gate is composed of an insulating glass surface modified with the enzyme glucose oxidase (GOx) and another surface opposing it made of a microelectrode. The latter was modified with a second enzyme, invertase (INV). The distance sepg. the modified microelectrode and surface controlled the output of the AND gate produced upon the biocatalytic reaction of the confined enzymes. Specifically, as the GOx-modified glass substrate entered the diffusion layer of the microelectrode, it catalyzed the regeneration of an electron-transfer mediator, ferroceniummethanol, generated electrochem. at the tip by oxidizing glucose, also generated at the tip, by catalytic cleaving of sucrose by INV. To enhance the activity of the GOx, mutarotase was added to convert α- to β-glucose to be further consumed by GOx. Hence, an increase of the current at the microelectrode was obtained by approaching the glass surface only in the presence of all the components. This is the first micrometer-sized biomol. logic gate, of which the authors are aware, that is surface-confined and shows the promise held by the localization of biomol. information-processing species. [on SciFinder(R)]},
	keywords = {logic gate immobilized enzyme scanning electrochem microscopy},
	isbn = {1520-5207},
	author = {Gdor, Efrat and Katz, Evgeny and Mandler, Daniel.}
}
@article {7068,
	title = {Characterization of thin films and membranes},
	journal = {Anal Bioanal ChemAnalytical and bioanalytical chemistry},
	volume = {405},
	number = {5},
	year = {2013},
	note = {MEDLINE AN 2013242500(Editorial)},
	month = {2013///},
	pages = {1433 - 4},
	isbn = {1618-2650},
	author = {Vadgama, Pankaj and Mandler, Daniel}
}
@article {6875,
	title = {Characterization of thin films and membranes.},
	journal = {Anal. Bioanal. Chem.Analytical and Bioanalytical Chemistry},
	volume = {405},
	number = {5},
	year = {2013},
	note = {CAPLUS AN 2012:1889042(Journal; Online Computer File)},
	month = {2013///},
	pages = {1433 - 1434},
	publisher = {Springer},
	isbn = {1618-2642},
	author = {Vadgama, Pankaj and Mandler, Daniel.}
}
@article { WOS:000313960000001,
	title = {Characterization of thin films and membranes},
	journal = {ANALYTICAL AND BIOANALYTICAL CHEMISTRY},
	volume = {405},
	number = {5},
	year = {2013},
	month = {FEB},
	pages = {1433-1434},
	issn = {1618-2642},
	doi = {10.1007/s00216-012-6629-8},
	author = {Vadgama, Pankaj and Mandler, Daniel}
}
@article {6869,
	title = {Electro-assist deposition of binary sol-gel films with graded structure.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {102},
	year = {2013},
	note = {CAPLUS AN 2013:857284(Journal; Online Computer File)},
	month = {2013///},
	pages = {212 - 218},
	publisher = {Elsevier Ltd.},
	abstract = {Graded SiO2-TiO2 binary composite films were prepd. by a unique electro-assist deposition approach from a mixt. of sol-gel precursors contg. tetramethoxysilane (TMOS) and Ti tetraisopropoxide (TTIP). A neg. potential applied to either stainless steel or ITO substrates causes the redn. of the solvent, thus increasing the concn. of hydroxyl ions, which enhances the precursor condensation and film deposition. The Ti:Si ratio in the films depends on the deposition potential, time and compn. of the precursor soln. This ratio decreases as the films grow thicker due to the more facile kinetics of SiO2 deposition. Nevertheless, the Ti:Si ratio in the films is always lower than in the corresponding precursor soln. As the Ti:Si ratio in the deposition soln. increases, the thickness of the electro-assist deposited films at the same conditions gradually decreases. SIMS and cross-section EDX anal. show that the Ti:Si ratio in the films increases from the surface to the substrate, suggesting electro-assist deposition as a potential method for 1-step prepn. of graded sol-gel films. [on SciFinder(R)]},
	keywords = {electro assist deposition binary sol gel film graded structure},
	isbn = {0013-4686},
	author = {Liu, Liang and Mandler, Daniel.}
}
@article { WOS:000321481300026,
	title = {Electro-assist deposition of binary sol-gel films with graded structure},
	journal = {ELECTROCHIMICA ACTA},
	volume = {102},
	year = {2013},
	month = {JUL 15},
	pages = {212-218},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2013.03.188},
	author = {Liu, Liang and Mandler, Daniel}
}
@article {7065,
	title = {Electrochemical co-deposition of conductive polymer-silica hybrid thin films},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {15},
	number = {26},
	year = {2013},
	note = {MEDLINE AN 2013660588(Journal; Article; (JOURNAL ARTICLE))},
	month = {2013///},
	pages = {10876 - 84},
	abstract = {Conductive polymers, such as polypyrrole (ppy), have been the subject of numerous studies due to their promising applications in organic solar cells, flexible electronics, electrochromic devices, super capacitors, etc. Yet, their application is still limited as a result of poor processability. Silica has been reported to improve the mechanical strength and adhesion of conductive polymer films. In this work, we propose a controllable electrochemical approach for preparing ppy-silica hybrid thin films from a solution containing both pyrrole and silane monomers. It is known that pyrrole can be electropolymerised using anodic potentials, while silica can be electrodeposited under cathodic potentials. Thus, we studied the formation of ppy-silica hybrid thin films on a stainless steel surface by applying alternating potentials, i.e. cathodic followed by anodic pulses (denoted C + A) or anodic followed by cathodic pulses (denoted A + C). We show that by controlling the deposition potential and time for the cathodic and anodic pulses, the film thickness and composition can be manipulated well as analysed using profilometry and EDX. The element depth profile of the films was characterized using secondary ion mass spectroscopy (SIMS). In essence, for the C + A process, pyrrole diffuses through the cathodically electrodeposited wet silica gel layer and undergoes anodic polymerisation on the substrate, while for the A + C process, silane can be electrodeposited both on top of the anodically electrodeposited conductive ppy films as well as on the stainless steel through the pinholes in the ppy film. This offers a simple approach for tuning the structure of conductive polymer-sol-gel composite films.[on SciFinder (R)]},
	isbn = {1463-9084},
	author = {Raveh, Moran and Liu, Liang and Mandler, Daniel}
}
@article {6868,
	title = {Electrochemical co-deposition of conductive polymer-silica hybrid thin films.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {15},
	number = {26},
	year = {2013},
	note = {CAPLUS AN 2013:914464(Journal; Online Computer File)},
	month = {2013///},
	pages = {10876 - 10884},
	publisher = {Royal Society of Chemistry},
	abstract = {Conductive polymers, such as polypyrrole (ppy), were the subject of numerous studies due to their promising applications in org. solar cells, flexible electronics, electrochromic devices, super capacitors, etc. Yet, their application is still limited as a result of poor processability. SiO2 is reported to improve the mech. strength and adhesion of conductive polymer films. The authors propose a controllable electrochem. approach for prepg. ppy-SiO2 hybrid thin films from a soln. contg. both pyrrole and silane monomers. Pyrrole can be electropolymd. using anodic potentials, while SiO2 can be electrodeposited under cathodic potentials. Thus, the authors studied the formation of ppy-SiO2 hybrid thin films on a stainless steel surface by applying alternating potentials, i.e. cathodic followed by anodic pulses (denoted C + A) or anodic followed by cathodic pulses (denoted A + C). By controlling the deposition potential and time for the cathodic and anodic pulses, the film thickness and compn. can be manipulated well as analyzed using profilometry and EDX. The element depth profile of the films was characterized using secondary ion mass spectroscopy (SIMS). In essence, for the C + A process, pyrrole diffuses through the cathodically electrodeposited wet silica gel layer and undergoes anodic polymn. on the substrate, while for the A + C process, silane can be electrodeposited both on top of the anodically electrodeposited conductive ppy films as well as on the stainless steel through the pinholes in the ppy film. This offers a simple approach for tuning the structure of conductive polymer-sol-gel composite films. [on SciFinder(R)]},
	keywords = {electrochem co deposition conductive polymer silica hybrid thin film},
	isbn = {1463-9076},
	author = {Raveh, Moran and Liu, Liang and Mandler, Daniel.}
}
@article { WOS:000320321600035,
	title = {Electrochemical co-deposition of conductive polymer-silica hybrid thin films},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {15},
	number = {26},
	year = {2013},
	pages = {10876-10884},
	issn = {1463-9076},
	doi = {10.1039/c3cp50457c},
	author = {Raveh, Moran and Liu, Liang and Mandler, Daniel}
}
@article {7063,
	title = {Enhanced potentiometry by metallic nanoparticles},
	journal = {Anal ChemAnalytical chemistry},
	volume = {85},
	number = {17},
	year = {2013},
	note = {MEDLINE AN 2013903956(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2013///},
	pages = {8347 - 53},
	abstract = {Measuring the oxidation-reduction potential (Eh) requires an interface that is not selective toward specific species but exchanges electrons with all redox couples in the solution. Sluggish electron transfer (ET) kinetics with the species will not reflect the "true" Eh of the solution. Here, we present a novel approach by which adsorbed metal nanoparticles (NPs) are used for enhancing ET exchange rates between redox species and electrode surface and therefore affect significantly the measurement of the open circuit potential (OCP) and cyclic voltammetry (CV). The OCP and CV of various organic and inorganic species such as l-dopa, dopac, iron(II), and iodide are measured by bare stainless steel and by stainless steel modified by either Pt or Au NPs. We study the effect of the surface coverage of the stainless steel surface by NPs on the electrochemical response. Moreover, the stainless steel electrode was modified simultaneously by Au and Pt nanoparticles. This improved concurrently the stainless steel response (CV and potentiometry) toward two different species; l-dopa, which shows fast electron transfer on Pt, and catechol, which exhibits fast electron transfer on Au. We believe that this approach could be a first step toward developing a superior electrode for measuring the "true" Eh of complex aquatic systems.[on SciFinder (R)]},
	isbn = {1520-6882},
	author = {Noyhouzer, T. and Valdinger, I. and Mandler, D}
}
@article {6864,
	title = {Enhanced Potentiometry by Metallic Nanoparticles.},
	journal = {Anal. Chem. (Washington, DC, U. S.)Analytical Chemistry (Washington, DC, United States)},
	volume = {85},
	number = {17},
	year = {2013},
	note = {CAPLUS AN 2013:1139195(Journal; Online Computer File)},
	month = {2013///},
	pages = {8347 - 8353},
	publisher = {American Chemical Society},
	abstract = {Measuring the oxidn.-redn. potential (Eh) requires an interface that is not selective toward specific species but exchanges electrons with all redox couples in the soln. Sluggish electron transfer (ET) kinetics with the species will not reflect the true Eh of the soln. Here, the authors present a novel approach by which adsorbed metal nanoparticles (NPs) were used for enhancing ET exchange rates between redox species and electrode surface and therefore affect significantly the measurement of the open circuit potential (OCP) and cyclic voltammetry (CV). The OCP and CV of various org. and inorg. species such as l-dopa, dopac, Fe(II), and iodide are measured by bare stainless steel and by stainless steel modified by either Pt or Au NPs. The authors study the effect of the surface coverage of the stainless steel surface by NPs on the electrochem. response. Also, the stainless steel electrode was modified simultaneously by Au and Pt nanoparticles. This improved concurrently the stainless steel response (CV and potentiometry) toward two different species; l-dopa, which shows fast electron transfer on Pt, and catechol, which exhibits fast electron transfer on Au. Probably this approach is a 1st step toward developing a superior electrode for measuring the true Eh of complex aquatic systems. [on SciFinder(R)]},
	keywords = {enhanced potentiometry metal nanoparticle},
	isbn = {0003-2700},
	author = {Noyhouzer, T. and Valdinger, I. and Mandler, D}
}
@article { WOS:000330017300047,
	title = {Enhanced Potentiometry by Metallic Nanoparticles},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {85},
	number = {17},
	year = {2013},
	month = {SEP 3},
	pages = {8347-8353},
	issn = {0003-2700},
	doi = {10.1021/ac401744w},
	author = {Noyhouzer, T. and Valdinger, I. and Mandler, D.}
}
@article {6871,
	title = {Formation of VO2 zero-dimensional/nanoporous layers with large supercooling effects and enhanced thermochromic properties.},
	journal = {RSC Adv.RSC Advances},
	volume = {3},
	number = {19},
	year = {2013},
	note = {CAPLUS AN 2013:632082(Journal; Online Computer File)},
	month = {2013///},
	pages = {7124 - 7128},
	publisher = {Royal Society of Chemistry},
	abstract = {Vanadium dioxide is an intriguing candidate for use in intelligent devices such as sensors, magnetic refrigeration and particularly as solar modulating smart window materials. A facile sol-gel route is developed to produce pure VO2 with different nanostructures in a CO2 atmosphere. It was found that the nanoporous structures demonstrated a 16\% increase in the luminous transmittance (Tlum) (from 20\% to 36\%) compared with the vacuum results, while large supercooling effects of up to 30 {\textdegree}C have been obsd. in zero-dimensional structures. [on SciFinder(R)]},
	keywords = {vanadium oxide nanoporous dimensional layer supercooling thermochromic property},
	isbn = {2046-2069},
	author = {Wang, Ning and Huang, Yizhong and Magdassi, S. and Mandler, D and Liu Hai and Yi, Long.}
}
@article { WOS:000317929800060,
	title = {Formation of VO2 zero-dimensional/nanoporous layers with large supercooling effects and enhanced thermochromic properties},
	journal = {RSC ADVANCES},
	volume = {3},
	number = {19},
	year = {2013},
	pages = {7124-7128},
	issn = {2046-2069},
	doi = {10.1039/c3ra40370j},
	author = {Wang Ning and Huang Yizhong and S.Magdassi and Mandler, D. and Liu Hai and Long Yi}
}
@article { WOS:000326245600013,
	title = {High switching speed and coloration efficiency of titanium-doped vanadium oxide thin film electrochromic devices},
	journal = {JOURNAL OF MATERIALS CHEMISTRY C},
	volume = {1},
	number = {44},
	year = {2013},
	pages = {7380-7386},
	issn = {2050-7526},
	doi = {10.1039/c3tc31508h},
	author = {Lu, Yingxi and Liu, Liang and Mandler, Daniel and Lee, Pooi See}
}
@article {6859,
	title = {High switching speed and coloration efficiency of titanium-doped vanadium oxide thin film electrochromic devices.},
	journal = {J. Mater. Chem. CJournal of Materials Chemistry C: Materials for Optical and Electronic Devices},
	volume = {1},
	number = {44},
	year = {2013},
	note = {CAPLUS AN 2013:1667841(Journal; Online Computer File)},
	month = {2013///},
	pages = {7380 - 7386},
	publisher = {Royal Society of Chemistry},
	abstract = {Ti-doped V oxide thin films were fabricated by electrochem. deposition on linear polyethylenimine (LPEI)-modified In Sn oxide-coated glass from mixed V oxide and Ti oxide solns. with different Ti concns. The as-prepd. films were studied by XRD, at. force microscopy (AFM), and XPS. The electrochem. behavior of the films was studied using cyclic voltammetry (CV) in 1.0 M LiClO4/propylene carbonate soln. Electrochromism of the oxide films upon Li-ion intercalation/deintercalation was studied by transmittance measurements during the CV process. The charge transfer resistance of the Ti-doped V oxide film was systematically analyzed with electrochem. impedance spectroscopy (EIS). The amorphous Ti-doped V oxide film contg. 4 mol\% Ti exhibited the highest transmittance contrast (Δ\%T = Tmax - Tmin) of \~51.1\%T, and coloration efficiency of 95.7 cm2 C-1 at 415 nm. By increasing the Ti content to 10 mol\%, the Ti-doped V oxide film exhibited high switching speed and good cycling reversibility reaching 80\% of coloring and bleaching time of 5 and 6 s, resp. Also, the transmittance contrast drops by only 10\% after 600 cycles in a two-electrode system. [on SciFinder(R)]},
	keywords = {switching speed coloration efficiency titanium vanadium oxide electrochromic device},
	isbn = {2050-7534},
	author = {Lu, Yingxi and Liu, Liang and Mandler, Daniel and Lee, Pooi See.}
}
@article {7067,
	title = {Local deposition of anisotropic nanoparticles using scanning electrochemical microscopy (SECM)},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {15},
	number = {8},
	year = {2013},
	note = {MEDLINE AN 2013313956(Journal; Article; (JOURNAL ARTICLE))},
	month = {2013///},
	pages = {2725 - 32},
	abstract = {We demonstrate localized electrodeposition of anisotropic metal nanoobjects, namely Au nanorods (GNR), on indium tin oxide (ITO) using scanning electrochemical microscopy (SECM). A gold microelectrode was the source of the gold ions whereby double pulse chronoamperometry was employed to generate initially Au seeds which were further grown under controlled conditions. The distance between the microelectrode and the ITO surface as well as the different experimental parameters (electrodeposition regime, solution composition and temperature) were optimized to produce faceted gold seeds with the required characteristics (size and distribution). Colloidal chemical synthesis was successfully exploited for better understanding the role of the surfactant and different additives in breaking the crystallographic symmetry and anisotropic growth of GNR. Experiments performed in a conventional three-electrode cell revealed the most appropriate electrochemical conditions allowing high yield synthesis of nanorods with well-defined shape as well as nanocubes and bipyramids.[on SciFinder (R)]},
	isbn = {1463-9084},
	author = {Fedorov, Roman G. and Mandler, Daniel}
}
@article {6874,
	title = {Local deposition of anisotropic nanoparticles using scanning electrochemical microscopy (SECM).},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {15},
	number = {8},
	year = {2013},
	note = {CAPLUS AN 2013:184310(Journal; Online Computer File)},
	month = {2013///},
	pages = {2725 - 2732},
	publisher = {Royal Society of Chemistry},
	abstract = {We demonstrate localized electrodeposition of anisotropic metal nanoobjects, namely Au nanorods (GNR), on indium tin oxide (ITO) using scanning electrochem. microscopy (SECM). A gold microelectrode was the source of the gold ions whereby double pulse chronoamperometry was employed to generate initially Au seeds which were further grown under controlled conditions. The distance between the microelectrode and the ITO surface as well as the different exptl. parameters (electrodeposition regime, soln. compn. and temp.) were optimized to produce faceted gold seeds with the required characteristics (size and distribution). Colloidal chem. synthesis was successfully exploited for better understanding the role of the surfactant and different additives in breaking the crystallog. symmetry and anisotropic growth of GNR. Expts. performed in a conventional three-electrode cell revealed the most appropriate electrochem. conditions allowing high yield synthesis of nanorods with well-defined shape as well as nanocubes and bipyramids. [on SciFinder(R)]},
	keywords = {local deposition anisotropic nanoparticle scanning electrochem microscopy SECM},
	isbn = {1463-9076},
	author = {Fedorov, Roman G. and Mandler, Daniel.}
}
@article { WOS:000314365800013,
	title = {Local deposition of anisotropic nanoparticles using scanning electrochemical microscopy (SECM)},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {15},
	number = {8},
	year = {2013},
	pages = {2725-2732},
	issn = {1463-9076},
	doi = {10.1039/c2cp42823g},
	author = {Fedorov, Roman G. and Mandler, Daniel}
}
@article { WOS:000327077000004,
	title = {Local surface patterning by chitosan-stabilized gold nanoparticles using the direct mode of scanning electrochemical microscopy (SECM)},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {17},
	number = {12, SI},
	year = {2013},
	month = {DEC},
	pages = {2989-2997},
	issn = {1432-8488},
	doi = {10.1007/s10008-013-2194-0},
	author = {Danieli, Tamar and Mandler, Daniel}
}
@article {6861,
	title = {Local surface patterning by chitosan-stabilized gold nanoparticles using the direct mode of scanning electrochemical microscopy (SECM).},
	journal = {J. Solid State Electrochem.Journal of Solid State Electrochemistry},
	volume = {17},
	number = {12},
	year = {2013},
	note = {CAPLUS AN 2013:1335253(Journal; Online Computer File)},
	month = {2013///},
	pages = {2989 - 2997},
	publisher = {Springer},
	abstract = {An approach for patterning surfaces with prepd. nanoparticles is described. Chitosan-stabilized gold nanoparticles (Au/chitosan NPs) were locally deposited on stainless steel (StSt), indium tin oxide (ITO), and highly-ordered pyrolytic graphite (HOPG). Deposition was driven by local pH gradient formed between a surface and a scanning electrochem. microscopy tip set in the direct mode. The pH at the substrate was increased upon biasing the surface by neg. potentials, which caused the redn. of water. As the pH on the surface exceeded that of pKchitosanH+\~6.3 deprotonation of the amino groups of chitosan caused the irreversible deposition of the chitosan/AuNPs. The effect of different parameters, such as tip-surface distance and time, on deposition was studied. While the potential duration showed no clear influence, smaller tip-substrate distance and more neg. potentials applied to the surface caused larger deposits. The overpotential needed for the deposition of nanoparticles on HOPG was the highest while that for StSt was the lowest. On the former, the sluggish kinetics caused the deposition of ring-shaped structures while disk-shaped deposits were formed on the other surfaces. [on SciFinder(R)]},
	keywords = {surface patterning chitosan stabilized gold nanoparticle scanning electrochem microscopy},
	isbn = {1432-8488},
	author = {Danieli, Tamar and Mandler, Daniel.}
}
@conference {6862,
	title = {Micro- and nanopatterning using scanning electrochemical microscopy.},
	booktitle = {Scanning Electrochem. Microsc. (2nd Ed.)},
	year = {2013},
	note = {CAPLUS AN 2013:1282783(Conference; General Review)},
	month = {2013///},
	pages = {489 - 524},
	publisher = {CRC Press},
	organization = {CRC Press},
	abstract = {A review. The following topics are discussed: Patterning by the Direct and Feedback modes of the SECM (Semiconductor, metal, and inorg. material etching and deposition; deposition of conducting polymers; self-assembled monolayers, polymers, and biomol. patterning); Speed of patterning, resoln., and scope of materials and approaches. [on SciFinder(R)]},
	keywords = {review micropatterning nanopatterning scanning electrochem microscopy},
	author = {Mandler, Daniel.}
}
@article {6878,
	title = {A New Electrochemical Flow Cell for the Remote Sensing of Heavy Metals.},
	journal = {ElectroanalysisElectroanalysis},
	volume = {25},
	number = {1},
	year = {2013},
	note = {CAPLUS AN 2012:1524365(Journal)},
	month = {2013///},
	pages = {109 - 115},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Remote sensing is a fast developing field. The ability to detect various elements in secluded or inaccessible areas holds great opportunities. We present a new electrochem. flow cell which was developed as part of an autonomous flow system for measuring heavy metals in aquatic environments. The system was designed for remote sensing. Our system can utilize different com. available electrodes and apply a range of electrochem. methods. The system was studied through both electrochem. expts. and simulation. The potential of the platform was demonstrated by analyzing seawater spiked with Cd. Good agreement was found between our results and those obtained by ICP-MS anal. [on SciFinder(R)]},
	keywords = {electrochem flow cell remote sensing heavy metal detn water},
	isbn = {1040-0397},
	author = {Noyhouzer, Tomer and Mandler, Daniel.}
}
@article { WOS:000313807600014,
	title = {A New Electrochemical Flow Cell for the Remote Sensing of Heavy Metals},
	journal = {ELECTROANALYSIS},
	volume = {25},
	number = {1, SI},
	year = {2013},
	note = {14th International Conference on Electroanalysis (ESEAC), Portoroz, SLOVENIA, JUN 03-07, 2012},
	month = {JAN},
	pages = {109-115},
	issn = {1040-0397},
	doi = {10.1002/elan.201200369},
	author = {Noyhouzer, Tomer and Mandler, Daniel}
}
@article {7066,
	title = {A novel approach to fingerprint visualization on paper using nanotechnology: reversing the appearance by tailoring the gold nanoparticles{\textquoteright} capping ligands},
	journal = {Chem Commun (Camb)Chemical communications (Cambridge, England)},
	volume = {49},
	number = {35},
	year = {2013},
	note = {MEDLINE AN 2013502517(Journal; Article; (JOURNAL ARTICLE))},
	month = {2013///},
	pages = {3688 - 90},
	abstract = {Gold nanoparticles, AuNPs, capped with mercaptocarboxylic acids followed by silver precipitation develop latent fingermarks on paper as high quality "negative" impressions. This effect stems from hydrogen bonding between the carboxylic group and the paper cellulose and may improve the yield of latent fingermarks since the results are less dependent on sweat composition.[on SciFinder (R)]},
	isbn = {1364-548X},
	author = {Shenawi, Sanaa and Jaber, Nimer and Almog, Joseph and Mandler, Daniel}
}
@article {6872,
	title = {A novel approach to fingerprint visualization on paper using nanotechnology: reversing the appearance by tailoring the gold nanoparticles{\textquoteright} capping ligands.},
	journal = {Chem. Commun. (Cambridge, U. K.)Chemical Communications (Cambridge, United Kingdom)},
	volume = {49},
	number = {35},
	year = {2013},
	note = {CAPLUS AN 2013:539631(Journal; Online Computer File)},
	month = {2013///},
	pages = {3688 - 3690},
	publisher = {Royal Society of Chemistry},
	abstract = {Gold nanoparticles, AuNPs, capped with mercaptocarboxylic acids followed by silver pptn. develop latent fingermarks on paper as high quality "neg." impressions. This effect stems from hydrogen bonding between the carboxylic group and the paper cellulose and may improve the yield of latent fingermarks since the results are less dependent on sweat compn. [on SciFinder(R)]},
	keywords = {forensic analysis fingerprint paper gold nanoparticles},
	isbn = {1359-7345},
	author = {Shenawi, Sanaa and Jaber, Nimer and Almog, Joseph and Mandler, Daniel.}
}
@article { WOS:000317052800022,
	title = {A novel approach to fingerprint visualization on paper using nanotechnology: reversing the appearance by tailoring the gold nanoparticles{\textquoteright} capping ligands},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {49},
	number = {35},
	year = {2013},
	pages = {3688-3690},
	issn = {1359-7345},
	doi = {10.1039/c3cc41610k},
	author = {Shenawi, Sanaa and Jaber, Nimer and Almog, Joseph and Mandler, Daniel}
}
@article { WOS:000319360700003,
	title = {Self-assembled polymer layers of linear polyethylenimine for enhancing electrochromic cycling stability},
	journal = {JOURNAL OF MATERIALS CHEMISTRY C},
	volume = {1},
	number = {23},
	year = {2013},
	pages = {3651-3654},
	issn = {2050-7526},
	doi = {10.1039/c3tc30447g},
	author = {Lu, Yingxi and Liu, Liang and Foo, Wan Ling and Magdassi, Shlomo and Mandler, Daniel and Lee, Pooi See}
}
@article {6870,
	title = {Self-assembled polymer layers of linear polyethylenimine for enhancing electrochromic cycling stability.},
	journal = {J. Mater. Chem. CJournal of Materials Chemistry C: Materials for Optical and Electronic Devices},
	volume = {1},
	number = {23},
	year = {2013},
	note = {CAPLUS AN 2013:809645(Journal; Online Computer File)},
	month = {2013///},
	pages = {3651 - 3654},
	publisher = {Royal Society of Chemistry},
	abstract = {A self-assembled polymer of linear polyethylenimine (LPEI) on indium tin oxide (ITO) is found to stabilize the titanium-doped vanadium oxide film. After modification by LPEI, the oxide film shows good cycling stability, and sustains over 1500 cycles in a three-electrode system, a remarkable improvement compared to that without LPEI modification. [on SciFinder(R)]},
	keywords = {self assembled polymer layer linear polyethylenimine enhancing electrochromic cycling},
	isbn = {2050-7534},
	author = {Lu, Yingxi and Liu, Liang and Foo, Wan Ling and Magdassi, Shlomo and Mandler, Daniel and Lee, Pooi See.}
}
@article {6873,
	title = {Simple sol-gel process and one-step annealing of vanadium dioxide thin films: Synthesis and thermochromic properties.},
	journal = {Thin Solid FilmsThin Solid Films},
	volume = {534},
	year = {2013},
	note = {CAPLUS AN 2013:339160(Journal; Online Computer File)},
	month = {2013///},
	pages = {594 - 598},
	publisher = {Elsevier B.V.},
	abstract = {A simple and cost effective sol-gel process for producing vanadium dioxide thin films was developed via thermolysis of V2O5{\textperiodcentered}nH2O (n ≈ 2) VV precursors prepd. by dissolving vanadium powder or V2O5 powder in 30\% hydrogen peroxide solns. After spin-coating on fused silica substrates and annealing at 750{\textdegree} in vacuum, without any intermediate gas reducing step, the major phase VO2(M, monoclinic phase) was found in both of the films based on V-H2O2 and V2O5-H2O2 precursor, exhibiting large transmittance changes (> 40\%) in the IR region (> 2000 nm) and small hysteresis loop width (< 5{\textdegree}) which were comparable to reported epitaxial VO2 films. The two films have similar metal-to-insulator transition temp. τC = 62.5{\textdegree}, lower than the classical value of 68{\textdegree} for VO2 thin films. In addn., the method enables simple doping, as found for 0.56 at.\% W-doped VO2 films. This intrinsically simple soln. process followed by one-step annealing makes it potentially useful in smart window applications. [on SciFinder(R)]},
	keywords = {sol gel spin coating annealing vanadium dioxide film prepn, vanadium pentoxide prepn thermolysis sol gel spin coating},
	isbn = {0040-6090},
	author = {Wang, N and Magdassi, S. and Mandler, D and Long, Y.}
}
@article { WOS:000317736700099,
	title = {Simple sol-gel process and one-step annealing of vanadium dioxide thin films: Synthesis and thermochromic properties},
	journal = {THIN SOLID FILMS},
	volume = {534},
	year = {2013},
	month = {MAY 1},
	pages = {594-598},
	issn = {0040-6090},
	doi = {10.1016/j.tsf.2013.01.074},
	author = {Wang, N. and S.Magdassi and Mandler, D. and Long, Y.}
}
@article { WOS:000320380700001,
	title = {Special issue dedicated to Anna Brainina},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {17},
	number = {6, SI},
	year = {2013},
	month = {JUN},
	pages = {1491-1492},
	issn = {1432-8488},
	doi = {10.1007/s10008-013-2124-1},
	author = {Mandler, Daniel}
}
@article {6867,
	title = {Special issue dedicated to Anna Brainina.},
	journal = {J. Solid State Electrochem.Journal of Solid State Electrochemistry},
	volume = {17},
	number = {6},
	year = {2013},
	note = {CAPLUS AN 2013:956328(Journal; Miscellaneous; Online Computer File)},
	month = {2013///},
	pages = {1491 - 1492},
	publisher = {Springer},
	isbn = {1432-8488},
	author = {Mandler, Daniel.}
}
@article {6866,
	title = {The synthesis and characterization of thiol-based aryl diazonium modified glassy carbon electrode for the voltammetric determination of low levels of Hg(II).},
	journal = {J. Solid State Electrochem.Journal of Solid State Electrochemistry},
	volume = {17},
	number = {6},
	year = {2013},
	note = {CAPLUS AN 2013:956331(Journal; Online Computer File)},
	month = {2013///},
	pages = {1543 - 1552},
	publisher = {Springer},
	abstract = {Electrochem. detn. of Hg(II) in aquatic solns. on bare and modified glassy carbon electrode (GCE) is reported. Optimizing the parameters used for a bare GCE, such as the electrolyte soln., the potential and time of deposition, resulted in linear response over a large range of Hg(II) concns. (4-160 ppb) using linear sweep anodic stripping voltammetry. Modification of the electrode with 4,4{\textquoteright}-disulfanediyldibenzenediazonium (DSBD) yielded a lowest detection limit of 1 ppb. Two procedures for DSBD synthesis are described for the 1st time, and the product was characterized by microanal., FTIR and 1H-NMR. The electrochem. attachment of DSBD to the electrode was studied and compared with the electrochem. behavior of DSBD analogous mols., i.e. 4-aminophenyl disulfide, p-aminothiophenol and Ph disulfide. [on SciFinder(R)]},
	keywords = {thiol aryl diazonium glassy carbon electrode voltammetry detn mercury},
	isbn = {1432-8488},
	author = {Shahar, Tehila and Tal, Noam and Mandler, Daniel.}
}
@article { WOS:000320380700008,
	title = {The synthesis and characterization of thiol-based aryl diazonium modified glassy carbon electrode for the voltammetric determination of low levels of Hg(II)},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {17},
	number = {6, SI},
	year = {2013},
	month = {JUN},
	pages = {1543-1552},
	issn = {1432-8488},
	doi = {10.1007/s10008-013-2009-3},
	author = {Shahar, Tehila and Tal, Noam and Mandler, Daniel}
}
@conference { WOS:000326700300009,
	title = {Wet-chemistry based selective coatings for concentrating solar power},
	booktitle = {NONIMAGING OPTICS: EFFICIENT DESIGN FOR ILLUMINATION AND SOLAR CONCENTRATION X},
	series = {Proceedings of SPIE},
	volume = {8834},
	year = {2013},
	note = {Conference on Nonimaging Optics - Efficient Design for Illumination and Solar Concentration X, San Diego, CA, AUG 25-26, 2013},
	publisher = {SPIE},
	organization = {SPIE},
	isbn = {978-0-8194-9684-3},
	issn = {0277-786X},
	doi = {10.1117/12.2025579},
	author = {Maimon, Eran and Kribus, Abraham and Flitsanov, Yuri and Shkolnik, Oleg and Feuermann, Daniel and Zwicker, Camille and Larush, Liraz and Mandler, Daniel and Magdassi, Shlomo},
	editor = {Winston, R and Gordon, J}
}
@article { WOS:000299409500071,
	title = {Electrochemically Controlled Drug-Mimicking Protein Release from Iron-Alginate Thin-Films Associated with an Electrode},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {4},
	number = {1},
	year = {2012},
	month = {JAN},
	pages = {466-475},
	issn = {1944-8244},
	doi = {10.1021/am201578m},
	author = {Jin, Zhiyuan and Gueven, Guray and Bocharova, Vera and Halamek, Jan and Tokarev, Ihor and Minko, Sergiy and Melman, Artem and Mandler, Daniel and Katz, Evgeny}
}
@article {7072,
	title = {Electrochemically controlled drug-mimicking protein release from iron-alginate thin-films associated with an electrode},
	journal = {ACS Appl Mater InterfacesACS applied materials \& interfaces},
	volume = {4},
	number = {1},
	year = {2012},
	note = {MEDLINE AN 2012178185(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T); (RESEARCH SUPPORT, U.S. GOV{\textquoteright}T, NON-P.H.S.))},
	month = {2012///},
	pages = {466 - 75},
	abstract = {Novel biocompatible hybrid-material composed of iron-ion-cross-linked alginate with embedded protein molecules has been designed for the signal-triggered drug release. Electrochemically controlled oxidation of Fe(2+) ions in the presence of soluble natural alginate polymer and drug-mimicking protein (bovine serum albumin, BSA) results in the formation of an alginate-based thin-film cross-linked by Fe(3+) ions at the electrode interface with the entrapped protein. The electrochemically generated composite thin-film was characterized by electrochemistry and atomic force microscopy (AFM). Preliminary experiments demonstrated that the electrochemically controlled deposition of the protein-containing thin-film can be performed at microscale using scanning electrochemical microscopy (SECM) as the deposition tool producing polymer-patterned spots potentially containing various entrapped drugs. Application of reductive potentials on the modified electrode produced Fe(2+) cations which do not keep complexation with alginate, thus resulting in the electrochemically triggered thin-film dissolution and the protein release. Different experimental parameters, such as the film-deposition time, concentrations of compounds and applied potentials, were varied in order to demonstrate that the electrodepositon and electrodissolution of the alginate composite film can be tuned to the optimum performance. A statistical modeling technique was applied to find optimal conditions for the formation of the composite thin-film for the maximal encapsulation and release of the drug-mimicking protein at the lowest possible potential.[on SciFinder (R)]},
	isbn = {1944-8252},
	author = {Jin, Zhiyuan and Guven, Guray and Bocharova, Vera and Halamek, Jan and Tokarev, Ihor and Minko, Sergiy and Melman, Artem and Mandler, Daniel and Katz, Evgeny}
}
@article {6880,
	title = {Electrochemically Controlled Drug-Mimicking Protein Release from Iron-Alginate Thin-Films Associated with an Electrode.},
	journal = {ACS Appl. Mater. InterfacesACS Applied Materials \& Interfaces},
	volume = {4},
	number = {1},
	year = {2012},
	note = {CAPLUS AN 2011:1670894(Journal; Online Computer File)},
	month = {2012///},
	pages = {466 - 475},
	publisher = {American Chemical Society},
	abstract = {Novel biocompatible hybrid-material composed of iron-ion-crosslinked alginate with embedded protein mols. has been designed for the signal-triggered drug release. Electrochem. controlled oxidn. of Fe2+ ions in the presence of sol. natural alginate polymer and drug-mimicking protein (bovine serum albumin, BSA) results in the formation of an alginate-based thin-film crosslinked by Fe3+ ions at the electrode interface with the entrapped protein. The electrochem. generated composite thin-film was characterized by electrochem. and at. force microscopy (AFM). Preliminary expts. demonstrated that the electrochem. controlled deposition of the protein-contg. thin-film can be performed at microscale using scanning electrochem. microscopy (SECM) as the deposition tool producing polymer-patterned spots potentially contg. various entrapped drugs. Application of reductive potentials on the modified electrode produced Fe2+ cations which do not keep complexation with alginate, thus resulting in the electrochem. triggered thin-film dissoln. and the protein release. Different exptl. parameters, such as the film-deposition time, concns. of compds. and applied potentials, were varied in order to demonstrate that the electrodeposition and electrodissoln. of the alginate composite film can be tuned to the optimum performance. A statistical modeling technique was applied to find optimal conditions for the formation of the composite thin-film for the maximal encapsulation and release of the drug-mimicking protein at the lowest possible potential. [on SciFinder(R)]},
	keywords = {electrochem controlled drug release iron alginate thin film electrode},
	isbn = {1944-8244},
	author = {Jin, Zhiyuan and Guven, Guray and Bocharova, Vera and Halamek, Jan and Tokarev, Ihor and Minko, Sergiy and Melman, Artem and Mandler, Daniel and Katz, Evgeny.}
}
@article {6879,
	title = {Fabrication of nanoelectrode ensembles by electrodeposition of Au nanoparticles on single-layer graphene oxide sheets.},
	journal = {NanoscaleNanoscale},
	volume = {4},
	number = {8},
	year = {2012},
	note = {CAPLUS AN 2012:467656(Journal; Online Computer File)},
	month = {2012///},
	pages = {2728 - 2733},
	publisher = {Royal Society of Chemistry},
	abstract = {Nanoelectrode ensembles (NEEs) have been fabricated by the electrodeposition of Au nanoparticles (AuNPs) on single-layer graphene oxide (GO) sheets coated on a glassy carbon electrode (GCE). The fabricated NEEs show a typical sigmoidal shaped voltammetric profile, arising from the low coverage d. of AuNPs on GCE and large distance among them, which can be easily controlled by varying the electrodeposition time. As a proof of concept, after the probe HS-DNA is immobilized on the NEEs through the Au-S bonding, the target DNA was detected with the methylene blue intercalator. The authors{\textquoteright} results show that the target DNA can be detected as low as 100 fM, i.e. 0.5 amol DNA in 5 μL soln. [on SciFinder(R)]},
	keywords = {nanoelectrode electrodeposition gold nanoparticle graphene oxide DNA detn},
	isbn = {2040-3372},
	author = {Wang, Zhijuan and Zhang, Juan and Yin, Zongyou and Wu, Shixin and Mandler, Daniel and Zhang, Hua.}
}
@article { WOS:000302063600026,
	title = {Fabrication of nanoelectrode ensembles by electrodepositon of Au nanoparticles on single-layer graphene oxide sheets},
	journal = {NANOSCALE},
	volume = {4},
	number = {8},
	year = {2012},
	pages = {2728-2733},
	issn = {2040-3364},
	doi = {10.1039/c2nr30142c},
	author = {Wang, Zhijuan and Zhang, Juan and Yin, Zongyou and Wu, Shixin and Mandler, Daniel and Zhang, Hua}
}
@article {7070,
	title = {Fabrication of nanoelectrode ensembles by electrodepositon of Au nanoparticles on single-layer graphene oxide sheets},
	journal = {NanoscaleNanoscale},
	volume = {4},
	number = {8},
	year = {2012},
	note = {MEDLINE AN 2012481497(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2012///},
	pages = {2728 - 33},
	abstract = {Nanoelectrode ensembles (NEEs) have been fabricated by the electrodeposition of Au nanoparticles (AuNPs) on single-layer graphene oxide (GO) sheets coated on a glassy carbon electrode (GCE). The fabricated NEEs show a typical sigmoidal shaped voltammetric profile, arising from the low coverage density of AuNPs on GCE and large distance among them, which can be easily controlled by varying the electrodeposition time. As a proof of concept, after the probe HS-DNA is immobilized on the NEEs through the Au-S bonding, the target DNA is detected with the methylene blue intercalator. Our results show that the target DNA can be detected as low as 100 fM, i.e. 0.5 amol DNA in 5 μL solution.[on SciFinder (R)]},
	isbn = {2040-3372},
	author = {Wang, Zhijuan and Zhang, Juan and Yin, Zongyou and Wu, Shixin and Mandler, Daniel and Zhang, Hua}
}
@article { WOS:000302807900004,
	title = {High-school chemistry teaching through environmentally oriented curricula},
	journal = {CHEMISTRY EDUCATION RESEARCH AND PRACTICE},
	volume = {13},
	number = {2},
	year = {2012},
	pages = {80-92},
	issn = {1109-4028},
	doi = {10.1039/c1rp90071d},
	author = {Mandler, Daphna and Mamlok-Naaman, Rachel and Blonder, Ron and Yayon, Malka and Hofstein, Avi}
}
@article {7069,
	title = {Visualization of latent fingermarks by nanotechnology: reversed development on paper{\textendash}a remedy to the variation in sweat composition},
	journal = {Angew Chem Int Ed EnglAngewandte Chemie (International ed. in English)},
	volume = {51},
	number = {49},
	year = {2012},
	note = {MEDLINE AN 2013107744(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, U.S. GOV{\textquoteright}T, NON-P.H.S.))},
	month = {2012///},
	pages = {12224 - 7},
	isbn = {1521-3773},
	author = {Jaber, Nimer and Lesniewski, Adam and Gabizon, Hadar and Shenawi, Sanaa and Mandler, Daniel and Almog, Joseph}
}
@article { WOS:000311706500012,
	title = {Visualization of Latent Fingermarks by Nanotechnology: Reversed Development on PaperA Remedy to the Variation in Sweat Composition},
	journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
	volume = {51},
	number = {49},
	year = {2012},
	pages = {12224-12227},
	issn = {1433-7851},
	doi = {10.1002/anie.201205259},
	author = {Jaber, Nimer and Lesniewski, Adam and Gabizon, Hadar and Shenawi, Sanaa and Mandler, Daniel and Almog, Joseph}
}
@article {6877,
	title = {Visualization of Latent Fingermarks by Nanotechnology: Reversed Development on Paper-A Remedy to the Variation in Sweat Composition.},
	journal = {Angew. Chem., Int. Ed.Angewandte Chemie, International Edition},
	volume = {51},
	number = {49},
	year = {2012},
	note = {CAPLUS AN 2012:1623037(Journal)},
	month = {2012///},
	pages = {12224 - 12227},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {In this work, "neg." fingermarks have been developed on paper, even after soaking in water, by the application of a new bifunctional reagent attached to gold nanoparticles, and then a silver phys. developer. The bifunctional reagent is composed of an active head, i.e., a polar group with high affinity to cellulose, attached by a long chain to an active tail contg. a sulfur group, which can stabilize gold nanoparticles. Through the active head, the gold nanoparticles, which are stabilized by the active tail, adhere preferentially to the paper cellulose rather than to the fingerprint material, to which they conventionally bind. Consequently, silver developer, which normally develops sebaceous fingermarks by pptg. dark silver on the sebaceous material, ppt. preferentially on the gold-coated areas giving rise to the appearance of uncolored ridge detail on a dark background. In this competing process, the paper itself serves as the substrate, whereas the fingermarks serve as a mask. This process may increase the overall yield of developed fingermarks as it bypasses the issue of the remarkable differences in sweat compn. between individual persons. [on SciFinder(R)]},
	keywords = {forensic analysis latent fingerprint paper sweat gold nanoparticle silver},
	isbn = {1433-7851},
	author = {Jaber, Nimer and Lesniewski, Adam and Gabizon, Hadar and Shenawi, Sanaa and Mandler, Daniel and Almog, Joseph.}
}
@article { WOS:000296871500040,
	title = {Deposition of Au and Ag nanoparticles on PEDOT},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {13},
	number = {45},
	year = {2011},
	pages = {20345-20353},
	issn = {1463-9076},
	doi = {10.1039/c1cp22093d},
	author = {Danieli, Tamar and Colleran, John and Mandler, Daniel}
}
@article {6882,
	title = {Deposition of Au and Ag nanoparticles on PEDOT.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {13},
	number = {45},
	year = {2011},
	note = {CAPLUS AN 2011:1443862(Journal; Online Computer File)},
	month = {2011///},
	pages = {20345 - 20353},
	publisher = {Royal Society of Chemistry},
	abstract = {The deposition of Au and Ag, locally and from bulk soln., on poly(3,4-ethylenedioxythiophene) (PEDOT) was studied. Specifically, PEDOT was electrochem. polymd. onto a glassy carbon (GC) electrode and used for bulk deposition of Au and Ag from their resp. ions dissolved in the soln. as well as for the local deposition of these metals using scanning electrochem. microscopy (SECM). These two sets of expts. were utilized to investigate the difference between Au and Ag electrochem. deposition on PEDOT. In particular, SECM expts., which were conducted by the controlled anodic dissoln. of Au and Ag microelectrodes close to GC/PEDOT, probed the effect of different PEDOT oxidn. states on local deposition. The current-time transients recorded during the deposition, combined with SEM and energy-dispersive x-ray anal. provided insight into the redn. processes. AuCl4- and Ag+ ions were electrochem. reduced at a potential equal to and more neg. than the ions redox potentials (0.4 and 0.2 V, resp.) and more pos. than -0.7 V, where the PEDOT starts transforming into the reduced, i.e. insulating, state. We found that the electroredn. of Ag+ ions was diffusion-controlled and the PEDOT film served as a simple conductor. The redn. of AuCl4- ions was enhanced on GC/PEDOT as compared with bare GC, indicating that PEDOT catalyzes the redn. of AuCl4- to Au. [on SciFinder(R)]},
	keywords = {electrodeposition gold silver nanoparticle PEDOT},
	isbn = {1463-9076},
	author = {Danieli, Tamar and Colleran, John and Mandler, Daniel.}
}
@article {7073,
	title = {Deposition of Au and Ag nanoparticles on PEDOT},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {13},
	number = {45},
	year = {2011},
	note = {MEDLINE AN 2011988380(Journal; Article; (JOURNAL ARTICLE))},
	month = {2011///},
	pages = {20345 - 53},
	abstract = {The deposition of Au and Ag, locally and from bulk solution, on poly(3,4-ethylenedioxythiophene) (PEDOT) was studied. Specifically, PEDOT was electrochemically polymerized onto a glassy carbon (GC) electrode and used for bulk deposition of Au and Ag from their respective ions dissolved in the solution as well as for the local deposition of these metals using scanning electrochemical microscopy (SECM). These two sets of experiments were utilized to investigate the difference between Au and Ag electrochemical deposition on PEDOT. In particular, SECM experiments, which were conducted by the controlled anodic dissolution of Au and Ag microelectrodes close to GC/PEDOT, probed the effect of different PEDOT oxidation states on local deposition. The current-time transients recorded during the deposition, combined with scanning electron microscopy and EDX analysis provided insight into the reduction processes. AuCl(4)(-) and Ag(+) ions were electrochemically reduced at a potential equal to and more negative than the ions redox potentials (0.4 and 0.2 V, respectively) and more positive than -0.7 V, where the PEDOT starts transforming into the reduced, i.e. insulating, state. We found that the electroreduction of Ag(+) ions was diffusion-controlled and the PEDOT film served as a simple conductor. On the other hand, the reduction of AuCl(4)(-) ions was enhanced on GC/PEDOT as compared with bare GC, indicating that PEDOT catalyzes the reduction of AuCl(4)(-) to Au.[on SciFinder (R)]},
	isbn = {1463-9084},
	author = {Danieli, Tamar and Colleran, John and Mandler, Daniel}
}
@article { WOS:000286848400001,
	title = {Determination of low levels of cadmium ions by the under potential deposition on a self-assembled monolayer on gold electrode},
	journal = {ANALYTICA CHIMICA ACTA},
	volume = {684},
	number = {1-2},
	year = {2011},
	month = {JAN 17},
	pages = {1-7},
	issn = {0003-2670},
	doi = {10.1016/j.aca.2010.10.021},
	author = {Noyhouzer, Tomer and Mandler, Daniel}
}
@article {7077,
	title = {Determination of low levels of cadmium ions by the under potential deposition on a self-assembled monolayer on gold electrode},
	journal = {Anal Chim ActaAnalytica chimica acta},
	volume = {684},
	number = {1-2},
	year = {2011},
	note = {MEDLINE AN 2011052602(Journal; Article; (JOURNAL ARTICLE))},
	month = {2011///},
	pages = {1 - 7},
	abstract = {The electrochemical determination of low levels of Cd using a self-assembled monolayer (SAM) modified Au electrode is reported. Determination was based on the stripping of Cd, which was deposited by under potential deposition (UPD). A series of short alkanethiol SAMs bearing different end groups, i.e., sulfonate, carboxylate and ammonium, were examined. Lowest level of detection (ca. 50 ngL(-1)) was achieved with a 3-mercaptopropionic acid (MPA) monolayer using subtractive anodic square wave voltammetry (SASV). Additional surface methods, namely, reductive desorption and X-ray photoelectron spectroscopy, were applied to determine the interfacial structure of the electrodeposited Cd on the modified electrodes. We conclude that the deposited Cd forms a monoatomic layer, which bridges between the gold surface and the alkanethiol monolayer associating with both the gold and the sulfur atoms.[on SciFinder (R)]},
	isbn = {1873-4324},
	author = {Noyhouzer, Tomer and Mandler, Daniel}
}
@article {6889,
	title = {Determination of low levels of cadmium ions by the under potential deposition on a self-assembled monolayer on gold electrode.},
	journal = {Anal. Chim. ActaAnalytica Chimica Acta},
	volume = {684},
	number = {1-2},
	year = {2011},
	note = {CAPLUS AN 2010:1595370(Journal)},
	month = {2011///},
	pages = {1 - 7},
	publisher = {Elsevier B.V.},
	abstract = {The electrochem. detn. of low levels of Cd using a self-assembled monolayer (SAM) modified Au electrode is reported. Detn. was based on the stripping of Cd, which was deposited by under potential deposition (UPD). Short alkanethiol SAMs bearing different end groups, i.e., sulfonate, carboxylate and ammonium, were examd. Lowest level of detection (\~50 ng/L-1) was achieved with a 3-mercaptopropionic acid (MPA) monolayer using subtractive anodic square wave voltammetry (SASV). Addnl. surface methods, namely, reductive desorption and XPS, were applied to det. the interfacial structure of the electrodeposited Cd on the modified electrodes. The deposited Cd forms a monoat. layer, which bridges between the gold surface and the alkanethiol monolayer assocg. with both the gold and the sulfur atoms. [on SciFinder(R)]},
	keywords = {cadmium ion detn potential deposition self assembled gold electrode},
	isbn = {0003-2670},
	author = {Noyhouzer, Tomer and Mandler, Daniel.}
}
@inbook { WOS:000301514400004,
	title = {Electrochemical Coating of Medical Implants},
	booktitle = {APPLICATIONS OF ELECTROCHEMISTRY AND NANOTECHNOLOGY IN BIOLOGY AND MEDICINE I},
	series = {Modern Aspects of Electrochemistry},
	number = {52},
	year = {2011},
	pages = {291-340},
	isbn = {978-1-4614-0347-0; 978-1-4614-0346-3},
	issn = {0076-9924},
	doi = {10.1007/978-1-4614-0347-0_4},
	author = {Guslitzer-Okner, Regina and Mandler, Daniel},
	editor = {Eliaz, N}
}
@article {6876,
	title = {Electrochemical coating of medical implants.},
	journal = {Mod. Aspects Electrochem.Modern Aspects of Electrochemistry},
	volume = {52},
	number = {Applications of Electrochemistry and Nanotechnology in Biology and Medicine I},
	year = {2011},
	note = {CAPLUS AN 2012:1863053(Journal; General Review)},
	month = {2011///},
	pages = {291 - 342},
	publisher = {Springer},
	abstract = {A review on the various studies of electroplating of medical devices, such as implants, including the different methods of electrochem. deposition and the various substrates electrochem. coated. [on SciFinder(R)]},
	keywords = {review electrochem deposition coating medical implant},
	isbn = {0076-9924},
	author = {Guslitzer-Okner, Regina and Mandler, Daniel.}
}
@article {6886,
	title = {Electrochemically assisted deposition of biodegradable polymer nanoparticles/sol-gel thin films.},
	journal = {J. Mater. Chem.Journal of Materials Chemistry},
	volume = {21},
	number = {32},
	year = {2011},
	note = {CAPLUS AN 2011:970092(Journal; Online Computer File)},
	month = {2011///},
	pages = {12145 - 12150},
	publisher = {Royal Society of Chemistry},
	abstract = {Biodegradable nanoparticles represent a promising platform for controlled release and other applications in medicine. To alter the interface of the medical device with the living tissue successfully, a thin coating needs to be applied onto the surface. The traits and functionality of the coating depends on its components, which in the presented work are sol-gel and biodegradable nanoparticles (NPs) deposited onto the substrate using the electrochem. sol-gel method. Aspects affecting the deposition process were investigated such as the applied potential and its duration. The properties of the deposits with emphasis on the biodegradable NPs within the deposited films were characterized and studied. Another element examd. was the loading ability of the NPs. A fluorescent org. mol. was incorporated in the biodegradable NPs as a drug model, to demonstrate loading capability. [on SciFinder(R)]},
	keywords = {electrochem deposition biodegradable polymer nanoparticle sol thin film},
	isbn = {0959-9428},
	author = {Gdor, Efrat and Mandler, Daniel.}
}
@article { WOS:000293504500066,
	title = {Electrochemically assisted deposition of biodegradable polymer nanoparticles/sol-gel thin films},
	journal = {JOURNAL OF MATERIALS CHEMISTRY},
	volume = {21},
	number = {32},
	year = {2011},
	pages = {12145-12150},
	issn = {0959-9428},
	doi = {10.1039/c1jm11262g},
	author = {Gdor, Efrat and Mandler, Daniel}
}
@article { WOS:000291395800042,
	title = {Electrochemically patterning sol-gel structures on conducting and insulating surfaces},
	journal = {CHEMICAL COMMUNICATIONS},
	volume = {47},
	number = {24},
	year = {2011},
	pages = {6909-6911},
	issn = {1359-7345},
	doi = {10.1039/c1cc00007a},
	author = {Liu, Liang and Toledano, Reut and Danieli, Tamar and Zhang, Jian-Qing and Hu, Ji-Ming and Mandler, Daniel}
}
@article {7075,
	title = {Electrochemically patterning sol-gel structures on conducting and insulating surfaces},
	journal = {Chem Commun (Camb)Chemical communications (Cambridge, England)},
	volume = {47},
	number = {24},
	year = {2011},
	note = {MEDLINE AN 2011612385(Journal; Article; (JOURNAL ARTICLE))},
	month = {2011///},
	pages = {6909 - 11},
	abstract = {A new approach for the local deposition of sol-gel films on conducting and insulating surfaces using scanning electrochemical microscopy (SECM) via the feedback and direct modes is presented. Patterning is based on enhancing sol-gel condensation by altering the local pH due to water electrolysis as a result of applying negative potentials.[on SciFinder (R)]},
	isbn = {1364-548X},
	author = {Liu, Liang and Toledano, Reut and Danieli, Tamar and Zhang, Jian-Qing and Hu, Ji-Ming and Mandler, Daniel}
}
@article {6888,
	title = {Electrochemically patterning sol-gel structures on conducting and insulating surfaces.},
	journal = {Chem. Commun. (Cambridge, U. K.)Chemical Communications (Cambridge, United Kingdom)},
	volume = {47},
	number = {24},
	year = {2011},
	note = {CAPLUS AN 2011:766911(Journal; Online Computer File)},
	month = {2011///},
	pages = {6909 - 6911},
	publisher = {Royal Society of Chemistry},
	abstract = {A new approach for the local deposition of sol-gel films on conducting and insulating surfaces using scanning electrochem. microscopy (SECM) via the feedback and direct modes is presented. Patterning is based on enhancing sol-gel condensation by altering the local pH due to H2O electrolysis as a result of applying neg. potentials. [on SciFinder(R)]},
	keywords = {electrochem patterning sol gel structure conducting insulating surface},
	isbn = {1359-7345},
	author = {Liu, Liang and Toledano, Reut and Danieli, Tamar and Zhang, Jian-Qing and Hu, Ji-Ming and Mandler, Daniel.}
}
@article {6881,
	title = {Improving the adhesion of polymethacrylate thin films onto indium tin oxide electrodes using a silane-based "Molecular Adhesive".},
	journal = {J. Solid State Electrochem.Journal of Solid State Electrochemistry},
	volume = {15},
	number = {11-12},
	year = {2011},
	note = {CAPLUS AN 2011:1459334(Journal; Online Computer File)},
	month = {2011///},
	pages = {2401 - 2407},
	publisher = {Springer},
	abstract = {Indium tin oxide (ITO) is the most commonly used transparent conducting substance. It has been used in numerous applications such as light-emitting diodes. In most applications and studies, the ITO surface is further coated with addnl. layers. The interface between the ITO and the coating is of utmost importance since it affects the phys. and chem. properties of the final device. Improving the adhesion between ITO and a coating layer can be achieved by applying a "mol. adhesive" as an inter-phasing mol. layer. In this study, we used 3-(trimethoxysilyl)propyl methacrylate as a "mol. adhesive" for better connection between ITO and a polymethacrylate layer. The samples were studied by electrochem., contact angle goniometry, at. force microscopy, and nano scratch microscopy. These studies clearly show that a simple silanization process formed a thin mol. adhesive layer, which did not influence the phys. and chem. properties of the final coated electrode and at the same time increased significantly the adhesion between the ITO and the polymethacrylate coating. [on SciFinder(R)]},
	keywords = {adhesion polymethacrylate silane modified ITO},
	isbn = {1432-8488},
	author = {Ginzburg-Turgeman, Roni and Guion, Jean-Baptiste and Mandler, Daniel.}
}
@article { WOS:000297135800015,
	title = {Improving the adhesion of polymethacrylate thin films onto indium tin oxide electrodes using a silane-based {\textquoteleft}{\textquoteleft}Molecular Adhesive{\textquoteright}{\textquoteright}},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {15},
	number = {11-12},
	year = {2011},
	month = {DEC},
	pages = {2401-2407},
	issn = {1432-8488},
	doi = {10.1007/s10008-011-1454-0},
	author = {Ginzburg-Turgeman, Roni and Guion, Jean-Baptiste and Mandler, Daniel}
}
@article { WOS:000295187300023,
	title = {Preparation and Characterization of Mono- and Multilayer Films of Polymerizable 1,2-Polybutadiene Using the Langmuir-Blodgett Technique},
	journal = {LANGMUIR},
	volume = {27},
	number = {19},
	year = {2011},
	month = {OCT 4},
	pages = {11889-11898},
	issn = {0743-7463},
	doi = {10.1021/la201534e},
	author = {Hitrik, Maria and Gutkin, Vitaly and Lev, Ovadia and Mandler, Daniel}
}
@article {7074,
	title = {Preparation and characterization of mono- and multilayer films of polymerizable 1,2-polybutadiene using the Langmuir-Blodgett technique},
	journal = {LangmuirLangmuir : the ACS journal of surfaces and colloids},
	volume = {27},
	number = {19},
	year = {2011},
	note = {MEDLINE AN 2011862264(Journal; Article; (JOURNAL ARTICLE))},
	month = {2011///},
	pages = {11889 - 98},
	abstract = {The essence of this study is to apply the Langmuir-Blodgett (LB) technique for assembling asymmetric membranes. Accordingly, Langmuir films of a (further) polymerizable polymer, 1,2-polybutadiene (1,2-pbd), were studied and transferred onto different solid supports, such as gold, indium tin oxide (ITO), and silicon. The layers were characterized both at the air/water interface as well as on different substrates using numerous methods including cyclic voltammetry, impedance spectroscopy, spectroscopic ellipsometry, atomic force microscopy, X-ray photoelectron spectroscopy, and reflection-absorption Fourier transform infrared spectroscopy. The Langmuir films were stable at the air-water interface as long as they were not exposed to UV irradiation. The LB films formed disorganized layers, which gradually blocked the permeation of different species with increasing the number of deposited layers. The thickness was ca. 4-7 {\r A} per layer. Irradiating the Langmuir films caused their cross-linking at the air-water interface. Furthermore, we took advantage of the reactivity of the double bond of the LB films on the solid supports and graft polymerized acrylic acid on top of the 1,2-pbd layers. This approach is the basis of the formation of an asymmetric membrane that requires different porosity on both of its sides.[on SciFinder (R)]},
	isbn = {1520-5827},
	author = {Hitrik, Maria and Gutkin, Vitaly and Lev, Ovadia and Mandler, Daniel}
}
@article {6884,
	title = {Preparation and Characterization of Mono- and Multilayer Films of Polymerizable 1,2-Polybutadiene Using the Langmuir-Blodgett Technique.},
	journal = {LangmuirLangmuir},
	volume = {27},
	number = {19},
	year = {2011},
	note = {CAPLUS AN 2011:1145784(Journal; Online Computer File)},
	month = {2011///},
	pages = {11889 - 11898},
	publisher = {American Chemical Society},
	abstract = {The essence of this study is to apply the Langmuir-Blodgett (LB) technique for assembling asym. membranes. Accordingly, Langmuir films of a (further) polymerizable polymer, 1,2-polybutadiene (1,2-pbd), were studied and transferred onto different solid supports, such as Au, In Sn oxide (ITO), and Si. The layers were characterized both at the air/H2O interface as well as on different substrates using numerous methods including cyclic voltammetry, impedance spectroscopy, spectroscopic ellipsometry, at. force microscopy, XPS, and reflection-absorption FTIR spectroscopy. The Langmuir films were stable at the air-H2O interface as long as they were not exposed to UV irradn. The LB films formed disorganized layers, which gradually blocked the permeation of different species with increasing the no. of deposited layers. The thickness was \~4-7 {\r A} per layer. Irradiating the Langmuir films caused their crosslinking at the air-H2O interface. Also, the authors took advantage of the reactivity of the double bond of the LB films on the solid supports and graft polymd. acrylic acid on top of the 1,2-pbd layers. This approach is the basis of the formation of an asym. membrane that requires different porosity on both of its sides. [on SciFinder(R)]},
	keywords = {Langmuir Blodgett film polymerizable polybutadiene asym membrane},
	isbn = {0743-7463},
	author = {Hitrik, Maria and Gutkin, Vitaly and Lev, Ovadia and Mandler, Daniel.}
}
@article {6887,
	title = {Self-assembled monolayers (SAMs) for electrochemical sensing.},
	journal = {J. Solid State Electrochem.Journal of Solid State Electrochemistry},
	volume = {15},
	number = {7-8},
	year = {2011},
	note = {CAPLUS AN 2011:947142(Journal; General Review; Online Computer File)},
	month = {2011///},
	pages = {1535 - 1558},
	publisher = {Springer},
	abstract = {A review. The past, present, and future of the application of self-assembled monolayers (SAMs) in electroanal. chem. is reviewed. SAMs for electroanal. applications were introduced in the early 1990s and since then were exploited for the detection of different species ranging from metal ions to biomols. and microorganisms. This review describes the different types of monolayers, surfaces on which they were assembled, the various analytes, which were detd., and the various electrochem. techniques employed. The prospective and perspectives of this topic are discussed. [on SciFinder(R)]},
	keywords = {review self assembled monolayer application electrochem sensor electroanalysis},
	isbn = {1432-8488},
	author = {Mandler, Daniel and Kraus-Ophir, Shlomit.}
}
@article { WOS:000294226100021,
	title = {Self-assembled monolayers (SAMs) for electrochemical sensing},
	journal = {JOURNAL OF SOLID STATE ELECTROCHEMISTRY},
	volume = {15},
	number = {7-8},
	year = {2011},
	month = {JUL},
	pages = {1535-1558},
	issn = {1432-8488},
	doi = {10.1007/s10008-011-1493-6},
	author = {Mandler, Daniel and Kraus-Ophir, Shlomit}
}
@article { WOS:000294881400011,
	title = {Studying the localized deposition of Ag nanoparticles on self-assembled monolayers by scanning electrochemical microscopy (SECM)},
	journal = {ELECTROCHIMICA ACTA},
	volume = {56},
	number = {20},
	year = {2011},
	month = {AUG 1},
	pages = {6954-6961},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2011.06.017},
	author = {Malel, Esteban and Colleran, John and Mandler, Daniel}
}
@article {6885,
	title = {Studying the localized deposition of Ag nanoparticles on self-assembled monolayers by scanning electrochemical microscopy (SECM).},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {56},
	number = {20},
	year = {2011},
	note = {CAPLUS AN 2011:987528(Journal; Online Computer File)},
	month = {2011///},
	pages = {6954 - 6961},
	publisher = {Elsevier Ltd.},
	abstract = {The local deposition of Ag nanoparticles (NPs) on ω-mercaptoalkanoic acid, HS(CH2)nCO2H, (n = 2, 10) self-assembled monolayers (SAMs) by scanning electrochem. microscopy (SECM) is reported. We found that the presence of a SAM had a pronounced effect on Ag deposition. Expts. were conducted by applying different potentials to an Au(1 1 1) substrate either in the presence of a const. concn. of Ag+ ions in soln. (bulk deposition) or by generating a flux of Ag+ from an Ag microelectrode that was positioned close to the Au(1 1 1) substrate (SECM deposition). SECM was used for generating a controlled flux of silver ions by anodic dissoln. of an Ag microelectrode close to the SAMs modified Au(1 1 1). We found that the shape of the NPs was affected by the length of the carbon-chain of the SAM. Tetrahedral NPs were obtained on bare Au(1 1 1) surfaces while rod like and cubic Ag NPs were deposited onto 3-mercaptopropanoic acid (MPA) and 11-mercaptoundecanoic acid (MUA) SAMs, resp. The size and shape of the deposited NPs were influenced by the deposition potential. We conclude that the shape and distribution of locally deposited Ag NPs on Au(1 1 1) can be controlled by modification of the substrate with a SAM and through controlling the Ag+ flux generated by SECM. [on SciFinder(R)]},
	keywords = {localized deposition silver nanoparticle selfassembled monolayer mercaptoalkanoic acid},
	isbn = {0013-4686},
	author = {Malel, Esteban and Colleran, John and Mandler, Daniel.}
}
@article {6883,
	title = {Symmetrical thiol functionalized polyhedral oligomeric silsesquioxanes as building blocks for LB films.},
	journal = {Soft MatterSoft Matter},
	volume = {7},
	number = {19},
	year = {2011},
	note = {CAPLUS AN 2011:1190092(Journal; Online Computer File)},
	month = {2011///},
	pages = {8862 - 8869},
	publisher = {Royal Society of Chemistry},
	abstract = {The Langmuir-Blodgett (LB) method was used for depositing cubic polyhedral oligomeric silsesquioxanes (T8POSS) onto Au, indium tin oxide (ITO) and mica supports. Three different T8POSS were examd.; two were amphiphilic and aggregated upon transfer to a solid support, while the highly sym. POSS (termed MP8) gave stable and reproducible Langmuir films as studied by surface pressure and transfer ratio measurements. This was attributed to the eight identical alkanethiol groups located on each of the eight corners of the cubic like skeleton. The LB films were studied by RA-FTIR, XPS, contact angle and cyclic voltammetry. These techniques revealed the formation of a permeable, yet, stable layer. The sym. MP8 was utilized as a bridging building block between the support and Au nanoparticles (Au-NPs). This assembly was examd. by means of AFM, SEM and anodic oxidn. of the nanoparticles. An av. d. of 1.45 {\texttimes} 109 nanoparticles cm-2 was obtained for the deposited Au-NPs on the MP8 layer. Furthermore, anodic stripping voltammetry was used for studying the extn. of Hg2+ by the MP8 LB film. [on SciFinder(R)]},
	keywords = {sym thiol functionalized polyhedral oligomeric silsesquioxane Langmuir Blodgett film},
	isbn = {1744-683X},
	author = {Kraus-Ophir, Shlomit and Jerman, Ivan and Orel, Boris and Mandler, Daniel.}
}
@article { WOS:000295085700025,
	title = {Symmetrical thiol functionalized polyhedral oligomeric silsesquioxanes as building blocks for LB films},
	journal = {SOFT MATTER},
	volume = {7},
	number = {19},
	year = {2011},
	pages = {8862-8869},
	issn = {1744-683X},
	doi = {10.1039/c1sm05443k},
	author = {Kraus-Ophir, Shlomit and Jerman, Ivan and Orel, Boris and Mandler, Daniel}
}
@inbook { WOS:000294006100004,
	title = {Vambery, Victorian Culture, and Stoker{\textquoteright}s Dracula},
	booktitle = {COMPARATIVE HUNGARIAN CULTURAL STUDIES},
	series = {Comparative Cultural Studies},
	year = {2011},
	pages = {47-58},
	isbn = {978-1-55753-593-1},
	issn = {1556-2905},
	author = {Mandler, David},
	editor = {DeZepetnek, ST and Vasvari, LO}
}
@article {6899,
	title = {Electroanalytical methods: Guide to experiments and applications, 2nd ed: Edited by Fritz Scholz.},
	journal = {Anal. Bioanal. Chem.Analytical and Bioanalytical Chemistry},
	volume = {398},
	number = {7-8},
	year = {2010},
	note = {CAPLUS AN 2010:1172522(Journal; Book Review; Online Computer File)},
	month = {2010///},
	pages = {2771 - 2772},
	publisher = {Springer},
	isbn = {1618-2642},
	author = {Mandler, Daniel.}
}
@booklet {6898,
	title = {Electrochemical coating of conductive surfaces by organic nanoparticles.},
	howpublished = {PCT Int. Appl.},
	number = {WO2010119443A1},
	year = {2010},
	note = {CAPLUS AN 2010:1311125(Patent)},
	month = {2010/10/21/},
	pages = {25pp.},
	publisher = {Yissum Research Development Company of the Hebrew University of Jerusalem, Ltd., Israel .},
	abstract = {An electrodeposition process is provided for depositing a film of org. nanoparticles from liq. dispersion on conductive surfaces. A special feature of the nanoparticles is their ability to aggregate as a response to pH change. The diffusing phase was formed by polylactic acid (43.9 mg) dissoln. in acetone (7.5 mL) and this phase was added dropwise to the dispersing phase of water (TDW, 20 mL) contg. Na oleate (22.2 mg) and NaOH (0.3 mg) while applying continuous moderate stirring to give a dispersion of polylactic acid nanoparticles (av. diam. 153 nm). [on SciFinder(R)]},
	keywords = {polymeric nanoparticle electrodeposition conductive substrate},
	author = {Magdassi, Shlomo and Mandler, Daniel and Levy, Ido.}
}
@article {7078,
	title = {Electrochemical codeposition of sol-gel films on stainless steel: controlling the chemical and physical coating properties of biomedical implants},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {12},
	number = {46},
	year = {2010},
	note = {MEDLINE AN 2010975088(Journal; Article; (JOURNAL ARTICLE))},
	month = {2010///},
	pages = {15265 - 73},
	abstract = {The electrochemically assisted codeposition of sol-gel thin films on stainless steel is described. Specifically, electrodeposition of films based on aminopropyltriethoxysilane (APTS), and its codeposition with propyltrimethoxysilane (PrTMOS) and phenyltrimethoxysilane (PhTMOS) has been accomplished by applying negative potentials. The latter increases the concentration of hydroxyl ions on the stainless steel surface and thus catalyzes the condensation and deposition of the sol-gel films. The films were characterized by profilometry, electrochemical impedance spectroscopy (EIS), alternating current voltammetry (ACV), goniometry, atomic force microscopy (AFM) and scanning electron microscopy (SEM). AFM and SEM analysis of codeposited APTS:PrTMOS films disclosed the structural changes induced by altering the deposition solution composition and the applied potential. Codeposited APTS:PhTMOS did not show any structural differences from their electrodeposited homopolymers, while Nano Scratch Test clearly revealed the changes in the elastic and adhesion properties, suggesting the formation of an APTS:PhTMOS composite. EIS of the films showed good resistance towards penetration of hydrophilic species, such as hexacyanoferrate. ACV measurements of the homo and codeposits showed the decrease of the interfacial capacity as a result of the electrochemical deposition. In essence, controllable sol-gel films with tunable chemical and physical properties based on controlling the combination of the precursors, pH and electrochemical properties can be electrodeposited on conducting surfaces. The application of this approach has been demonstrated by coating a stainless steel coronary stent.[on SciFinder (R)]},
	isbn = {1463-9084},
	author = {Okner, Regina and Favaro, Gregory and Radko, Anna and Domb, Abraham Jacob and Mandler, Daniel}
}
@article { WOS:000284313600016,
	title = {Electrochemical codeposition of sol-gel films on stainless steel: controlling the chemical and physical coating properties of biomedical implants},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {12},
	number = {46},
	year = {2010},
	month = {DEC},
	pages = {15265-15273},
	issn = {1463-9076},
	doi = {10.1039/c0cp00601g},
	author = {Okner, Regina and Favaro, Gregory and Radko, Anna and Domb, Abraham Jacob and Mandler, Daniel}
}
@article {6891,
	title = {Electrochemical codeposition of sol-gel films on stainless steel: controlling the chemical and physical coating properties of biomedical implants.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {12},
	number = {46},
	year = {2010},
	note = {CAPLUS AN 2010:1430390(Journal)},
	month = {2010///},
	pages = {15265 - 15273},
	publisher = {Royal Society of Chemistry},
	abstract = {The electrochem. assisted codeposition of sol-gel thin films on stainless steel is described. Specifically, electrodeposition of films based on aminopropyltriethoxysilane (APTS), and its codeposition with propyltrimethoxysilane (PrTMOS) and phenyltrimethoxysilane (PhTMOS) has been accomplished by applying neg. potentials. The latter increases the concn. of hydroxyl ions on the stainless steel surface and thus catalyzes the condensation and deposition of the sol-gel films. The films were characterized by profilometry, electrochem. impedance spectroscopy (EIS), a.c. voltammetry (ACV), goniometry, at. force microscopy (AFM) and SEM. AFM and SEM anal. of codeposited APTS:PrTMOS films disclosed the structural changes induced by altering the deposition soln. compn. and the applied potential. Codeposited APTS:PhTMOS did not show any structural differences from their electrodeposited homopolymers, while Nano Scratch Test clearly revealed the changes in the elastic and adhesion properties, suggesting the formation of an APTS:PhTMOS composite. EIS of the films showed good resistance towards penetration of hydrophilic species, such as hexacyanoferrate. ACV measurements of the homo and codeposits showed the decrease of the interfacial capacity as a result of the electrochem. deposition. In essence, controllable sol-gel films with tunable chem. and phys. properties based on controlling the combination of the precursors, pH and electrochem. properties can be electrodeposited on conducting surfaces. The application of this approach has been demonstrated by coating a stainless steel coronary stent. [on SciFinder(R)]},
	keywords = {electrochem codeposition sol gel film stainless steel coating implant},
	isbn = {1463-9076},
	author = {Okner, Regina and Favaro, Gregory and Radko, Anna and Domb, Abraham Jacob and Mandler, Daniel.}
}
@article { WOS:000279389200017,
	title = {Electrochemical Codeposition of Thin Gold Nanoparticles/Sol-Gel Nanocomposite Films},
	journal = {CHEMISTRY OF MATERIALS},
	volume = {22},
	number = {13},
	year = {2010},
	month = {JUL 13},
	pages = {3943-3951},
	issn = {0897-4756},
	doi = {10.1021/cm1005295},
	author = {Toledano, Reut and Mandler, Daniel}
}
@article {6902,
	title = {Electrochemical Codeposition of Thin Gold Nanoparticles/Sol-Gel Nanocomposite Films.},
	journal = {Chem. Mater.Chemistry of Materials},
	volume = {22},
	number = {13},
	year = {2010},
	note = {CAPLUS AN 2010:755184(Journal)},
	month = {2010///},
	pages = {3943 - 3951},
	publisher = {American Chemical Society},
	abstract = {The authors present a new method for deposition of thin nanocomposite films made of sol-gel-based Au nanoparticles using a single electrochem. step. Applying a neg. potential to an electrode (indium Sn oxide or stainless steel) immersed in a soln. of Au nanoparticles stabilized with N-[3-(trimethoxysilyl)propyl]ethylenediamine (EDAS) caused the redn. of the protic solvent, which altered the pH and therefore catalyzed the deposition. The nanocomposite thin films were characterized by various techniques: the morphol. and structure of the layers were examd. by high-resoln. SEM and at. force microscopy; their thickness was detd. by profilometry; and the permeability of the films was studied by electrochem. Homogeneous defect-free layers could be deposited only upon adding tetramethoxysilane (TMOS) to the deposition soln. Also, the applied potential, the ratio between the TMOS and the Au nanoparticles, and the type of the substrate significantly affected the aggregation and d. of the Au nanoparticles in the nanocomposite. Finally, by applying a pos. potential to the nanocomposite films the authors succeeded to electrochem. dissolve the embedded Au nanoparticles, forming holes and channels. The oxidn. treatment had a remarkable effect on the permeability of the film and exposed the electrode to faradic activity. This method seems to be of general applicability in templating of nanometer-sized objects in thin films. [on SciFinder(R)]},
	keywords = {electrochem codeposition thin gold nanoparticle sol gel nanocomposite film, electrooxidn embedded gold nanoparticle sol gel nanocomposite hole channel},
	isbn = {0897-4756},
	author = {Toledano, Reut and Mandler, Daniel.}
}
@article {6894,
	title = {Exciting New Directions in Electrochemistry: Honoring 2008 Wolf Prize Recipient Allen J. Bard.},
	journal = {Isr. J. Chem.Israel Journal of Chemistry},
	volume = {50},
	number = {3},
	year = {2010},
	note = {CAPLUS AN 2010:1327309(Journal)},
	month = {2010///},
	pages = {249 - 251},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	isbn = {0021-2148},
	author = {Lev, Ovadia and Mandler, Daniel.}
}
@article { WOS:000284079100001,
	title = {Exciting New Directions in Electrochemistry: Honoring 2008 Wolf Prize Recipient Allen J. Bard},
	journal = {ISRAEL JOURNAL OF CHEMISTRY},
	volume = {50},
	number = {3},
	year = {2010},
	month = {OCT},
	pages = {249-251},
	issn = {0021-2148},
	doi = {10.1002/ijch.201000048},
	author = {Lev, Ovadia and Mandler, Daniel}
}
@book {6890,
	title = {Exciting New Directions in Electrochemistry. [In: Isr. J. Chem., 2010; 50(3)].},
	year = {2010},
	note = {CAPLUS AN 2010:1519207(Book)},
	month = {2010///},
	pages = {136 pp.},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	organization = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	keywords = {book electrochem},
	author = {Lev, Ovadia and Mandler, Daniel and Editors.}
}
@article { WOS:000284079100007,
	title = {Formation, Characterization, and Applications of Organic and Inorganic Nanometric Films},
	journal = {ISRAEL JOURNAL OF CHEMISTRY},
	volume = {50},
	number = {3},
	year = {2010},
	month = {OCT},
	pages = {306-311},
	issn = {0021-2148},
	doi = {10.1002/ijch.201000028},
	author = {Mandler, Daniel}
}
@article {6895,
	title = {Formation, Characterization, and Applications of Organic and Inorganic Nanometric Films.},
	journal = {Isr. J. Chem.Israel Journal of Chemistry},
	volume = {50},
	number = {3},
	year = {2010},
	note = {CAPLUS AN 2010:1327304(Journal; General Review)},
	month = {2010///},
	pages = {306 - 311},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {A review. The formation of thin coatings based on either self-assembled monolayers or polymeric films is discussed. These coatings are used to structure surfaces and control their phys. and chem. properties. Different examples are given from our work emphasizing the advantages of monolayers and polymeric films. Finally, different approaches, which benefit from both monolayers and polymeric films, are presented. [on SciFinder(R)]},
	keywords = {org inorg nanometric film characterization review},
	isbn = {0021-2148},
	author = {Mandler, Daniel.}
}
@article { WOS:000284079100003,
	title = {ISRANALYTICA 2010, Tel Aviv, Israel, January 19-20, 2010},
	journal = {ISRAEL JOURNAL OF CHEMISTRY},
	volume = {50},
	number = {3},
	year = {2010},
	month = {OCT},
	pages = {262-264},
	issn = {0021-2148},
	doi = {10.1002/ijch.201000042},
	author = {Mandler, Daniel}
}
@article {6896,
	title = {ISRANALYTICA 2010, Tel Aviv, Israel, January 19-20, 2010.},
	journal = {Isr. J. Chem.Israel Journal of Chemistry},
	volume = {50},
	number = {3},
	year = {2010},
	note = {CAPLUS AN 2010:1327301(Journal)},
	month = {2010///},
	pages = {262 - 264},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	isbn = {0021-2148},
	author = {Mandler, Daniel.}
}
@article { WOS:000283634900026,
	title = {Localized Deposition of Au Nanoparticles by Direct Electron Transfer through Cellobiose Dehydrogenase},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {16},
	number = {38},
	year = {2010},
	pages = {11697-11706},
	issn = {0947-6539},
	doi = {10.1002/chem.201000453},
	author = {Malel, Esteban and Ludwig, Roland and Gorton, Lo and Mandler, Daniel}
}
@article {6892,
	title = {Localized deposition of Au nanoparticles by direct electron transfer through cellobiose dehydrogenase.},
	journal = {Chem. - Eur. J.Chemistry - A European Journal},
	volume = {16},
	number = {38},
	year = {2010},
	note = {CAPLUS AN 2010:1408460(Journal)},
	month = {2010///},
	pages = {11697 - 11706},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {Cellobiose dehydrogenase (CDH) is a fascinating extracellular fungal enzyme that consists of two domains, one carrying a FAD and the other a cytochrome-type heme b group as cofactors. The two domains are interconnected by a linker, and electrons can shuttle from the FAD to the heme group by intramol. electron transfer. Electron transfer between CDH and an electrode can occur by direct electron transfer (DET) and by mediated electron transfer (MET). This characteristic makes CDH an interesting candidate for integration in systems such as biosensors and biofuel cells. Moreover, it makes CDH an alternative for the redn. of metal ions through DET and MET. In this work we have explored the localized deposition of gold on Pd substrates by CDH through DET and MET. For this purpose we exploited the advantage of scanning electrochem. microscopy (SECM) as a patterning tool. We first demonstrated that gold nanoparticles can be formed in homogeneous soln. Then we showed that Au nanoparticles can also be locally formed and deposited on surfaces through DET at low pH and by MET at neutral pH using benzoquinone/hydroquinone as mediator. [on SciFinder(R)]},
	keywords = {localized deposition gold nanoparticle electron transfer cellobiose dehydrogenase},
	isbn = {0947-6539},
	author = {Malel, Esteban and Ludwig, Roland and Gorton, Lo and Mandler, Daniel.}
}
@article {7071,
	title = {Localized deposition of Au nanoparticles by direct electron transfer through cellobiose dehydrogenase},
	journal = {ChemistryChemistry (Weinheim an der Bergstrasse, Germany)},
	volume = {16},
	number = {38},
	year = {2010},
	note = {MEDLINE AN 2012328094(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2010///},
	pages = {11697 - 706},
	abstract = {Cellobiose dehydrogenase (CDH) is a fascinating extracellular fungal enzyme that consists of two domains, one carrying a flavin adenine dinucleotide (FAD) and the other a cytochrome-type heme b group as cofactors. The two domains are interconnected by a linker and electrons can shuttle from the FAD to the heme group by intramolecular electron transfer. Electron transfer between CDH and an electrode can occur by direct electron transfer (DET) and by mediated electron transfer (MET). This characteristic makes CDH an interesting candidate for integration in systems such as biosensors and biofuel cells. Moreover, it makes CDH an alternative for the reduction of metal ions through DET and MET. In this work we have explored the localized deposition of gold on Pd substrates by CDH through DET and MET. For this purpose we exploited the advantage of scanning electrochemical microscopy (SECM) as a patterning tool. We first demonstrated that gold nanoparticles can be formed in homogenous solution. Then we showed that Au nanoparticles can also be locally formed and deposited on surfaces through DET at low pH and by MET at neutral pH using benzoquinone/hydroquinone as mediator.[on SciFinder (R)]},
	isbn = {1521-3765},
	author = {Malel, Esteban and Ludwig, Roland and Gorton, Lo and Mandler, Daniel}
}
@article {6900,
	title = {Nanometric thin polymeric films based on molecularly imprinted technology: towards electrochemical sensing applications.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {12},
	number = {36},
	year = {2010},
	note = {CAPLUS AN 2010:1119774(Journal)},
	month = {2010///},
	pages = {11041 - 11050},
	publisher = {Royal Society of Chemistry},
	abstract = {A new approach for assembling selective electrodes based on molecularly imprinted polymers (MIPs) is presented. The approach is based on the radical polymn. of a mixt. of methacrylic acid (MAA) and ethyleneglycol dimethacrylate (EGDMA) in the presence of an initiator, benzoyl peroxide (BPO) and an activator, N,N{\textquoteright}-dimethyl-p-toluidine (DMpT) at room temp. and atm. pressure. To form nanometric thin polymeric films the polymn. soln. was spin-coated in the course of polymn. The different phys. and chem. parameters that affected the properties of the films, such as the spinning rate and the EGDMA:MAA ratio, were studied and optimized. A variety of techniques, e.g., rheoscopy, SEM, AFM, profilometry and electrochem., were used to characterize the films and the polymn. process. By optimizing the conditions very thin and reproducible films could be prepd. and imprinted. The electrochem. behavior of the films showed that they were permeable to water-sol. electroactive species providing that either polyethylene glycol or template species were added to the polymn. mixt. Finally, we demonstrated that films imprinted with ferrocenylmethyl alc. (Fc-MeOH) successfully extd. the imprinted species after their removal from MIPs. [on SciFinder(R)]},
	keywords = {nanometric thin polymeric film molecularly imprinted technol electrochem sensor},
	isbn = {1463-9076},
	author = {Ginzburg-Turgeman, Roni and Mandler, Daniel.}
}
@article { WOS:000281613300051,
	title = {Nanometric thin polymeric films based on molecularly imprinted technology: towards electrochemical sensing applications},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {12},
	number = {36},
	year = {2010},
	pages = {11041-11050},
	issn = {1463-9076},
	doi = {10.1039/b927478b},
	author = {Ginzburg-Turgeman, Roni and Mandler, Daniel}
}
@article {7079,
	title = {Nanometric thin polymeric films based on molecularly imprinted technology: towards electrochemical sensing applications},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {12},
	number = {36},
	year = {2010},
	note = {MEDLINE AN 2010796310(Journal; Article; (JOURNAL ARTICLE))},
	month = {2010///},
	pages = {11041 - 50},
	abstract = {A new approach for assembling selective electrodes based on molecularly imprinted polymers (MIPs) is presented. The approach is based on the radical polymerization of a mixture of methacrylic acid (MAA) and ethyleneglycol dimethacrylate (EGDMA) in the presence of an initiator, benzoyl peroxide (BPO) and an activator, N,N{\textquoteright}-dimethyl-p-toluidine (DMpT) at room temperature and atmospheric pressure. To form nanometric thin polymeric films the polymerization solution was spin-coated in the course of polymerization. The different physical and chemical parameters that affected the properties of the films, such as the spinning rate and the EGDMA:MAA ratio, were studied and optimized. A variety of techniques, e.g., rheoscopy, SEM, AFM, profilometry and electrochemistry, were used to characterize the films and the polymerization process. By optimizing the conditions very thin and reproducible films could be prepared and imprinted. The electrochemical behavior of the films showed that they were permeable to water-soluble electroactive species providing that either polyethylene glycol or template species were added to the polymerization mixture. Finally, we demonstrated that films imprinted with ferrocenylmethyl alcohol (Fc-MeOH) successfully extracted the imprinted species after their removal from MIPs.[on SciFinder (R)]},
	isbn = {1463-9084},
	author = {Ginzburg-Turgeman, Roni and Mandler, Daniel}
}
@article { WOS:000276751100020,
	title = {Pattern recognition in oxides thin-film electrodeposition: Printed circuits},
	journal = {COMPTES RENDUS CHIMIE},
	volume = {13},
	number = {1-2, SI},
	year = {2010},
	month = {JAN-FEB},
	pages = {237-241},
	issn = {1631-0748},
	doi = {10.1016/j.crci.2009.05.007},
	author = {Shacham, Ronen and Mandler, Daniel and Avnir, David}
}
@article {6904,
	title = {Pattern recognition in oxides thin-film electrodeposition: Printed circuits.},
	journal = {C. R. Chim.Comptes Rendus Chimie},
	volume = {13},
	number = {1-2},
	year = {2010},
	note = {CAPLUS AN 2010:300550(Journal)},
	month = {2010///},
	pages = {237 - 241},
	publisher = {Elsevier Masson SAS},
	abstract = {A novel method for a low-voltage electrodeposition of insulating oxide sol-gel thin films on complex conducting patterns is described. By this method gold meshes and printed chips were selectively coated with titania and zirconia thin films. This method solves a classical problem in the thin-films world: dip-coating, spin-coating, spraying without masks-all cannot be used for selective coating of a complex conductive pattern, because these methods do not differentiate between conducting vs non-conducting areas. The newly developed method provides an electrochem. pattern recognition, which solves this problem. [on SciFinder(R)]},
	keywords = {printed circuit oxide film electrodeposition pattern recognition},
	isbn = {1631-0748},
	author = {Shacham, Ronen and Mandler, Daniel and Avnir, David.}
}
@article {6897,
	title = {Potential induced pH change: Towards electrochemical coating of medical implants by organic nanoparticles.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {55},
	number = {28},
	year = {2010},
	note = {CAPLUS AN 2010:1321814(Journal)},
	month = {2010///},
	pages = {8590 - 8594},
	publisher = {Elsevier B.V.},
	abstract = {The electrochem. deposition of org. nanoparticles on conducting surface, such as a coronary stents, in the absence of a polymeric matrix is demonstrated. A novel approach, whereby pH-responsive org. nanoparticles coagulate on a conducting surface as a result of applying pos. potential, has been studied. Specifically, latex nanoparticles stabilized by sodium oleate in aq. solns. were deposited by applying a pos. potential that oxidized the water and caused the decrease of pH on various conducting surfaces. It was found that the applied potential, its duration and the concn. of the dispersed nanoparticles govern the deposition characteristics of the coating. This generic approach allows coating objects with complex geometries with thickness ranging from nanometers to microns and therefore can be utilized for coating medical and other devices as well as for controlling drug release. [on SciFinder(R)]},
	keywords = {pH electrochem coating implant latex nanoparticle},
	isbn = {0013-4686},
	author = {Levy, Ido and Magdassi, Shlomo and Mandler, Daniel.}
}
@article { WOS:000284443400033,
	title = {Potential induced pH change Towards electrochemical coating of medical implants by organic nanoparticles},
	journal = {ELECTROCHIMICA ACTA},
	volume = {55},
	number = {28},
	year = {2010},
	month = {DEC 1},
	pages = {8590-8594},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2010.07.067},
	author = {Levy, Ido and Magdassi, Shlomo and Mandler, Daniel}
}
@article { WOS:000277956800027,
	title = {Preparation and comparison between different thiol-protected Au nanoparticles},
	journal = {JOURNAL OF NANOPARTICLE RESEARCH},
	volume = {12},
	number = {5},
	year = {2010},
	month = {JUN},
	pages = {1807-1811},
	issn = {1388-0764},
	doi = {10.1007/s11051-009-9738-3},
	author = {Gofberg, Itamar and Mandler, Daniel}
}
@article {6903,
	title = {Preparation and comparison between different thiol-protected Au nanoparticles.},
	journal = {J. Nanopart. Res.Journal of Nanoparticle Research},
	volume = {12},
	number = {5},
	year = {2010},
	note = {CAPLUS AN 2010:657903(Journal)},
	month = {2010///},
	pages = {1807 - 1811},
	publisher = {Springer},
	abstract = {We report on the synthesis of monolayer-protected gold cluster (MPCs) in aquatic phase under different conditions. Three thiols, i.e., 2-mercaptoethanesulfonic acid (MPS), 3-mercaptopropionic acid (MPA), and cystamine (CYS) have been used as the protecting monolayer. Furthermore, we studied the effect of varying the ratio between the concns. of the protecting layer, the gold ions, and the reducing agent in the prepn. soln. Comparison was based on measuring the av. diam., stability, and size distribution of the MPCs. Best results were obtained for MPS-based MPCs and that the optimum molar concn. ratio between the protecting layer, the gold ions, and the reducing agent was 1:1:2. [on SciFinder(R)]},
	keywords = {thiol gold nanoparticle cluster stability},
	isbn = {1388-0764},
	author = {Gofberg, Itamar and Mandler, Daniel.}
}
@article { WOS:000280237200044,
	title = {Selective complexation between a novel bowl-shaped molecule and Fe3+ or PdCl42- ions},
	journal = {INORGANICA CHIMICA ACTA},
	volume = {363},
	number = {11},
	year = {2010},
	month = {AUG 10},
	pages = {2677-2681},
	issn = {0020-1693},
	doi = {10.1016/j.ica.2010.04.032},
	author = {Kraus, Shlomit and Almog, Joseph and Mandler, Daniel}
}
@article {6901,
	title = {Selective complexation between a novel bowl-shaped molecule and Fe3+ or PdCl42- ions.},
	journal = {Inorg. Chim. ActaInorganica Chimica Acta},
	volume = {363},
	number = {11},
	year = {2010},
	note = {CAPLUS AN 2010:922606(Journal)},
	month = {2010///},
	pages = {2677 - 2681},
	publisher = {Elsevier B.V.},
	abstract = {We report the selective assocn. of a novel bipolarofacial, bowl-shaped mol. (I) with Fe3+ and PdCl42- ions. UV-vis titrn. expts. and Langmuir isotherm measurements revealed stronger assocn. with the palladate over the iron ions, both in homogeneous org. medium as well as at the air-water interface. Interestingly, we found that the complexation is solvent-dependent, suggesting that I undergoes isomerization prior to assocn. with the metal ions. [on SciFinder(R)]},
	keywords = {complexation bowl mol iron palladium chloride},
	isbn = {0020-1693},
	author = {Kraus, Shlomit and Almog, Joseph and Mandler, Daniel.}
}
@article { WOS:000284750200022,
	title = {Thin functionalized films on cylindrical microelectrodes for electrochemical determination of Hg(II)},
	journal = {JOURNAL OF ELECTROANALYTICAL CHEMISTRY},
	volume = {649},
	number = {1-2, SI},
	year = {2010},
	month = {NOV 15},
	pages = {153-158},
	issn = {1572-6657},
	doi = {10.1016/j.jelechem.2010.02.026},
	author = {Fink, Lea and Mandler, Daniel}
}
@article {6893,
	title = {Thin functionalized films on cylindrical microelectrodes for electrochemical determination of Hg(II).},
	journal = {J. Electroanal. Chem.Journal of Electroanalytical Chemistry},
	volume = {649},
	number = {1-2},
	year = {2010},
	note = {CAPLUS AN 2010:1383056(Journal)},
	month = {2010///},
	pages = {153 - 158},
	publisher = {Elsevier B.V.},
	abstract = {Cylindrical carbon fiber microelectrodes (CFMEs) were used for the detn. of Hg(II) in aquatic solns. using anodic stripping voltammetry (ASV). Optimizing the parameters, such as the potential and time of deposition, resulted in linear response of the fiber over a large range of Hg(II) concns. (5 {\texttimes} 10-8 - 1 {\texttimes} 10-5 M). Furthermore, three methods of modification of glassy carbon and CFMEs with thiol or other Hg(II)-complexing groups, have also been examd. Electrodes were modified by electrochem. reducing 4,4{\textquoteright}-disulfanediyldibenzenediazonium, followed by redn. of the disulfide bond, by electrodepositing sol-gel based on 3-mercaptopropyltrimethoxysilane and by spin-coating or adsorbing cellulose acetate thin films in which 4,13-didecyl-1,7,10,16-tetraoxa-4,13-diazacyclooctadecane (Kryptofix 22DD) was incorporated. We found that all modified glassy carbon electrodes extd. Hg(II) under open-circuit potential, however, only the cylindrical microelectrode modified via the electrochem. redn. of the diazonium was capable of extg. mercuric ions. The interference of Pb(II), Cd(II), and Cu(II) with the detn. of Hg(II) with 4,4{\textquoteright}-disulfanediyldibenzenediazonium modified CFME was also studied. [on SciFinder(R)]},
	keywords = {carbon fiber microelectrode electrochem detn mercury, thin functionalized film cylindrical microelectrode electrochem detn mercury},
	isbn = {1572-6657},
	author = {Fink, Lea and Mandler, Daniel.}
}
@article { WOS:000275226700070,
	title = {Thin Nanocomposite Films of Polyaniline/Au Nanoparticles by the Langmuir-Blodgett Technique},
	journal = {LANGMUIR},
	volume = {26},
	number = {6},
	year = {2010},
	month = {MAR 16},
	pages = {4239-4245},
	issn = {0743-7463},
	doi = {10.1021/la903284g},
	author = {Tanami, Golan and Gutkin, Vitaly and Mandler, Daniel}
}
@article {7082,
	title = {Thin nanocomposite films of polyaniline/Au nanoparticles by the Langmuir-Blodgett technique},
	journal = {LangmuirLangmuir : the ACS journal of surfaces and colloids},
	volume = {26},
	number = {6},
	year = {2010},
	note = {MEDLINE AN 2010168582(Journal; Article; (JOURNAL ARTICLE))},
	month = {2010///},
	pages = {4239 - 45},
	abstract = {The Langmuir-Blodgett (LB) method was used to deposit multilayers of polyaniline (PANI)- and mercaptoethanesulfonate (MES)-stabilized Au nanoparticles. The electrostatic interaction between the negatively charged nanoparticles in the subphase and the positively charged PANI at the air-water interface assisted the deposition of the nanocomposite film onto a solid support. These PANI/Au-NPs films were characterized using cyclic voltammetry, copper under potential deposition, scanning electron microscopy, atomic force microscopy, and X-ray photoelectron spectroscopy. We found that the nanocomposite layers were uniform and reproducible. The density of Au-NPs in the monolayer depended on the acidity of the subphase as well as on the nanoparticles concentration. Moreover, the Au-NPs extrude above the PANI and therefore could be used as nanoelectrodes for the underpotential deposition (UPD) of copper.[on SciFinder (R)]},
	isbn = {1520-5827},
	author = {Tanami, Golan and Gutkin, Vitaly and Mandler, Daniel}
}
@article {6905,
	title = {Thin Nanocomposite Films of Polyaniline/Au Nanoparticles by the Langmuir-Blodgett Technique.},
	journal = {LangmuirLangmuir},
	volume = {26},
	number = {6},
	year = {2010},
	note = {CAPLUS AN 2009:1616524(Journal)},
	month = {2010///},
	pages = {4239 - 4245},
	publisher = {American Chemical Society},
	abstract = {The Langmuir-Blodgett (LB) method was used to deposit multilayers of polyaniline (PANI)- and mercaptoethanesulfonate (MES)-stabilized Au nanoparticles. The electrostatic interaction between the neg. charged nanoparticles in the subphase and the pos. charged PANI at the air-H2O interface assisted the deposition of the nanocomposite film onto a solid support. These PANI/Au-NPs films were characterized using cyclic voltammetry, Cu underpotential deposition, SEM, at. force microscopy, and XPS. The nanocomposite layers were uniform and reproducible. The d. of Au-NPs in the monolayer depended on the acidity of the subphase as well as on the nanoparticles concn. Also, the Au-NPs extrude above the PANI and therefore could be used as nanoelectrodes for the underpotential deposition (UPD) of Cu. [on SciFinder(R)]},
	keywords = {multilayer polyaniline mercaptoethanesulfonate stabilized gold nanoparticle ITO, nanocomposite film polyaniline gold nanoparticle Langmuir Blodgett technique},
	isbn = {0743-7463},
	author = {Tanami, Golan and Gutkin, Vitaly and Mandler, Daniel.}
}
@article {6915,
	title = {Control of locally deposited gold nanoparticle on polyaniline films.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {54},
	number = {11},
	year = {2009},
	note = {CAPLUS AN 2009:312759(Journal)},
	month = {2009///},
	pages = {2951 - 2956},
	publisher = {Elsevier B.V.},
	abstract = {Local and bulk deposition of Au particles was accomplished by the spontaneous reaction between chem. reduced polyaniline (PAN) thin films and AuCl4- ions. PAN layers were electrodeposited on glassy C (GC). Characterization of the PAN films was carried out by microscopy and electrochem. Local deposition of Au particles was performed by scanning electrochem. microscopy, where a Au microelectrode was used to produce a flux of Au ions in close vicinity to an unbiased PAN film. The nature of the Au particles was greatly affected by the potential applied at the microelectrode as well as the oxidn. state of the PAN films. [on SciFinder(R)]},
	keywords = {control locally deposited gold nanoparticle polyaniline film},
	isbn = {0013-4686},
	author = {Sheffer, Marisa and Mandler, Daniel.}
}
@article { WOS:000265342100001,
	title = {Control of locally deposited gold nanoparticle on polyaniline films},
	journal = {ELECTROCHIMICA ACTA},
	volume = {54},
	number = {11},
	year = {2009},
	month = {APR 15},
	pages = {2951-2956},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2008.12.027},
	author = {Sheffer, Marisa and Mandler, Daniel}
}
@article { WOS:000270868600039,
	title = {Drug-Eluting Stent With Improved Durability and Controllability Properties, Obtained Via Electrocoated Adhesive Promotion Layer},
	journal = {JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS},
	volume = {91B},
	number = {2},
	year = {2009},
	month = {NOV},
	pages = {819-830},
	issn = {1552-4973},
	doi = {10.1002/jbm.b.31461},
	author = {Levy, Yair and Tal, Noam and Tzemach, Gilad and Weinberger, Judah and Domb, Abraham J. and Mandler, Daniel}
}
@article {7084,
	title = {Drug-eluting stent with improved durability and controllability properties, obtained via electrocoated adhesive promotion layer},
	journal = {J Biomed Mater Res B Appl BiomaterJournal of biomedical materials research. Part B, Applied biomaterials},
	volume = {91},
	number = {2},
	year = {2009},
	note = {MEDLINE AN 2009671827(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2009///},
	pages = {819 - 30},
	abstract = {Drug-eluting stents (DES) have become an accepted technology in intravascular intervention. Manufacturing methodologies of DES are based mainly on mechanical processes, which tend to generate coatings that have poor stability properties; these were recently related as a potential hazard. A novel approach for significantly increasing the adhesion of polymer coatings onto DES is presented. The method is based on the electrochemistry of diazonium salts. These substances are organic compounds with the characteristic structure of R-N(2) (+) X(-), where R is an organic residue and X(-) is an anion. The objective of this article is to study the properties of a selected diazonium salt 4-(1-dodecyloxy)-phenyldiazonium tetrafluoroborate, referred as C(12)-phenyldiazonium. This material was found to be a superior adhesive promoter for polymeric coatings applied onto metallic stents. C(12)-phenyldiazonium was synthesized and electrocoated on metallic stents and plates. The multilayer films of C(12)-phenyldiazonium were further characterized through electrochemical (cyclic voltammetry, impedance spectroscopy), physical (light and scanning electron microscopy, X-ray photoelectron spectroscopy, peeling tests), and chemical methodology (high pressure liquid chromatography). Further biocompatibility properties of the electrocoated basecoat were evaluated using in vitro and in vivo models. Synthesized C(12)-phenyldiazonium was successfully electrocoated onto metallic surfaces. Electrochemical tests demonstrated its efficient and controllable electrocoating. C(12)-phenyldiazonium was found to increase polymeric coating stability as was reflected by a standard adhesion test. Electrocoated metallic stents spray-coated with a second polymeric film showed improved durability following incubation in physiological buffer. Furthermore, this improvement in durability exhibits stabilized drug release. In addition, biocompatibility evaluations have demonstrated basecoat{\textquoteright}s inert properties.[on SciFinder (R)]},
	isbn = {1552-4981},
	author = {Levy, Yair and Tal, Noam and Tzemach, Gilad and Weinberger, Judah and Domb, Abraham J. and Mandler, Daniel}
}
@article {6908,
	title = {Drug-eluting stent with improved durability and controllability properties, obtained via electrocoated adhesive promotion layer.},
	journal = {J. Biomed. Mater. Res., Part BJournal of Biomedical Materials Research, Part B: Applied Biomaterials},
	volume = {91B},
	number = {2},
	year = {2009},
	note = {CAPLUS AN 2009:1223301(Journal)},
	month = {2009///},
	pages = {819 - 830},
	publisher = {John Wiley \& Sons, Inc.},
	abstract = {Drug-eluting stents (DES) have become an accepted technol. in intravascular intervention. Manufg. methodologies of DES are based mainly on mech. processes, which tend to generate coatings that have poor stability properties; these were recently related as a potential hazard. A novel approach for significantly increasing the adhesion of polymer coatings onto DES is presented. The method is based on the electrochem. of diazonium salts. These substances are org. compds. with the characteristic structure of R-N X-, where R is an org. residue and X- is an anion. The objective of this article is to study the properties of a selected diazonium salt 4-(1-dodecyloxy)-phenyldiazonium tetrafluoroborate, referred as C12-phenyldiazonium. This material was found to be a superior adhesive promoter for polymeric coatings applied onto metallic stents. C12-phenyldiazonium was synthesized and electrocoated on metallic stents and plates. The multilayer films of C12-phenyldiazonium were further characterized through electrochem. (cyclic voltammetry, impedance spectroscopy), phys. (light and SEM, XPS, peeling tests), and chem. methodol. (high pressure liq. chromatog.). Further biocompatibility properties of the electrocoated basecoat were evaluated using in vitro and in vivo models. Synthesized C12-phenyldiazonium was successfully electrocoated onto metallic surfaces. Electrochem. tests demonstrated its efficient and controllable electrocoating. C12-phenyldiazonium was found to increase polymeric coating stability as was reflected by a std. adhesion test. Electrocoated metallic stents spray-coated with a second polymeric film showed improved durability following incubation in physiol. buffer. Furthermore, this improvement in durability exhibits stabilized drug release. In addn., biocompatibility evaluations have demonstrated basecoat{\textquoteright}s inert properties. {\textcopyright} 2009 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2009. [on SciFinder(R)]},
	keywords = {drug eluting stent adhesive promoter diazonium salt coating},
	isbn = {1552-4973},
	author = {Levy, Yair and Tal, Noam and Tzemach, Gilad and Weinberger, Judah and Domb, Abraham J. and Mandler, Daniel.}
}
@article { WOS:000270670600049,
	title = {Electrochemical Determination of Uranyl Ions Using a Self-Assembled Monolayer},
	journal = {ANALYTICAL CHEMISTRY},
	volume = {81},
	number = {20},
	year = {2009},
	month = {OCT 15},
	pages = {8627-8631},
	issn = {0003-2700},
	doi = {10.1021/ac901092t},
	author = {Becker, Amit and Tobias, Haim and Mandler, Daniel}
}
@article {7083,
	title = {Electrochemical determination of uranyl ions using a self-assembled monolayer},
	journal = {Anal ChemAnalytical chemistry},
	volume = {81},
	number = {20},
	year = {2009},
	note = {MEDLINE AN 2009687703(Journal; Article; (JOURNAL ARTICLE))},
	month = {2009///},
	pages = {8627 - 31},
	abstract = {Uranyl, UO(2)(2+), was electrochemically determined by a phosphate based self-assembled monolayer. A pretreated gold electrode with 2-mercatpoethanol was chemically modified by POCl(3) or POBr(3) to obtain the surface phosphate active sites. The different stages were characterized by reflection-absorption Fourier transform-infrared (FT-IR) spectroscopy, capacity, and X-ray photoelectron spectroscopy (XPS). The electrochemical determination of UO(2)(2+) was accomplished, after preconcentration under open circuit potential, by square wave voltammetry.[on SciFinder (R)]},
	isbn = {1520-6882},
	author = {Becker, Amit and Tobias, Haim and Mandler, Daniel}
}
@article {6909,
	title = {Electrochemical Determination of Uranyl Ions Using a Self-Assembled Monolayer.},
	journal = {Anal. Chem. (Washington, DC, U. S.)Analytical Chemistry (Washington, DC, United States)},
	volume = {81},
	number = {20},
	year = {2009},
	note = {CAPLUS AN 2009:1156118(Journal)},
	month = {2009///},
	pages = {8627 - 8631},
	publisher = {American Chemical Society},
	abstract = {Uranyl, UO22+, was electrochem. detd. by a phosphate based self-assembled monolayer. A pretreated Au electrode with 2-mercatpoethanol was chem. modified by POCl3 or POBr3 to obtain the surface phosphate active sites. The different stages were characterized by reflection-absorption FTIR spectroscopy, capacity, and XPS. The electrochem. detn. of UO22+ was accomplished, after preconcn. under open circuit potential, by square wave voltammetry. [on SciFinder(R)]},
	keywords = {electrochem detn uranyl ion self assembled monolayer},
	isbn = {0003-2700},
	author = {Becker, Amit and Tobias, Haim and Mandler, Daniel.}
}
@article {6912,
	title = {Electrochemically deposited poly(ethylene glycol)-based sol-gel thin films on stainless steel stents.},
	journal = {New J. Chem.New Journal of Chemistry},
	volume = {33},
	number = {7},
	year = {2009},
	note = {CAPLUS AN 2009:814312(Journal)},
	month = {2009///},
	pages = {1596 - 1604},
	publisher = {Royal Society of Chemistry},
	abstract = {Poly(ethylene glycol) (PEG) was modified with 3-isocyanatopropyltriethoxysilane (IPTS) to obtain PEG-disilane. This monomer was electrochem. polymd. and deposited onto a stainless steel surface to form a thin PEGylated sol-gel film. The monomer was characterized by 1H-NMR and FTIR spectroscopy. The sol-gel film was characterized by absorption-reflection IR spectroscopy (AR-FTIR), energy dispersive X-ray anal. (EDX), cyclic voltammetry (CV), profilometry, SEM and potentiodynamic polarization. AR-FTIR confirmed the formation of a polymer, while the stability of the polymeric film on stainless steel in buffer phosphate was studied by SEM. The polymer was successfully electrodeposited onto 316L coronary stents. Its flexibility was examd. by dilating the coated stents and inspecting it by SEM. The hydrophilic, smooth PEGylated sol-gel coating significantly reduced the activation and adhesion of platelets as compared with the bare stainless steel surface. This coating, which can be applied to complex geometries, such as stents, is likely to serve as an excellent biomaterial. [on SciFinder(R)]},
	keywords = {electrochem deposition polyethylene glycol film stainless steel stent},
	isbn = {1144-0546},
	author = {Okner, Regina and Domb, Abraham Jacob and Mandler, Daniel.}
}
@article { WOS:000267728200023,
	title = {Electrochemically deposited poly(ethylene glycol)-based sol-gel thin films on stainless steel stents},
	journal = {NEW JOURNAL OF CHEMISTRY},
	volume = {33},
	number = {7},
	year = {2009},
	pages = {1596-1604},
	issn = {1144-0546},
	doi = {10.1039/b901864f},
	author = {Okner, Regina and Domb, Abraham Jacob and Mandler, Daniel}
}
@article {7087,
	title = {Electrocoating of stainless steel coronary stents for extended release of paclitaxel},
	journal = {J Biomed Mater Res AJournal of biomedical materials research. Part A},
	volume = {88},
	number = {2},
	year = {2009},
	note = {MEDLINE AN 2009013931((EVALUATION STUDIES); Journal; Article; (JOURNAL ARTICLE))},
	month = {2009///},
	pages = {427 - 36},
	abstract = {Nonbiodegradable polymer coating based on N-(2-carboxyethyl)pyrrole (PPA) and butyl ester of PPA (BuOPy) were successfully electrodeposited on a stainless steel stent surface using cyclic voltammetry. Chemical composition of the coating was examined by X-ray photoelectron spectroscopy. Polymer stability was examined by immersing the coated stent into 1:1 solution of fetal calf serum:seline solution up to 1 year and implantation subcutaneously in mouse for 1 week. Morphology changes were then recorded by scanning electron microscopy. Paclitaxel loading was carried out by immersion into drug solution and its release was detected by HPLC. The results show that thin (single micrometers), uniform coating with various morphology and hydrophobicity can be created by electrochemical deposition. The polymer did not show significant histopathological or morphological changes in vitro and in vivo. The surface properties allow loading appropriate amounts of paclitaxel and release it slowly up to a month.[on SciFinder (R)]},
	isbn = {1552-4965},
	author = {Okner, R. and M. Oron and Tal, N. and Nyska, A. and Kumar, N. and Mandler, D and Domb, A. J.}
}
@article { WOS:000262228300017,
	title = {Electrocoating of stainless steel coronary stents for extended release of paclitaxel},
	journal = {JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A},
	volume = {88A},
	number = {2},
	year = {2009},
	month = {FEB},
	pages = {427-436},
	issn = {1549-3296},
	doi = {10.1002/jbm.a.31896},
	author = {Okner, R. and Oron, M. and Tal, N. and Nyska, A. and Kumar, N. and Mandler, D. and Domb, A. J.}
}
@article { WOS:000267536100004,
	title = {Electropolymerized Tricopolymer Based on N-Pyrrole Derivatives as a Primer Coating for Improving the Performance of a Drug-Eluting Stent},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {1},
	number = {4},
	year = {2009},
	month = {APR},
	pages = {758-767},
	issn = {1944-8244},
	doi = {10.1021/am800139s},
	author = {Okner, Regina and Shaulov, Yulia and Tal, Noam and Favaro, Gregory and Domb, Abraham J. and Mandler, Daniel}
}
@article {7081,
	title = {Electropolymerized tricopolymer based on N-pyrrole derivatives as a primer coating for improving the performance of a drug-eluting stent},
	journal = {ACS Appl Mater InterfacesACS applied materials \& interfaces},
	volume = {1},
	number = {4},
	year = {2009},
	note = {MEDLINE AN 2010227866(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2009///},
	pages = {758 - 67},
	abstract = {The coating of medical implants by polymeric films aims at increasing their biocompatibility as well as providing a durable matrix for the controlled release of a drug. In many cases, the coating is divided into a primer layer, which bridges between the medical implant and the drug-eluting matrix. The primer coating must be very carefully designed in order to provide optimal interactions with the surface of the medical implant and the outer layer. Here we present a simple and versatile approach for designing the primer layer based on electropolymerization of a carefully chosen blend of three different pyrrole derivatives: N-methylpyrrole (N-me), N-(2-carboxyethyl)pyrrole (PPA), and the butyl ester of N-(2-carboxyethyl)pyrrole (BuOPy). The composition and physical properties of the primer layer were studied in detail by atomic force microscopy (AFM) and a nano scratch tester. The latter provides the in-depth analysis of the adhesion and viscoelasticity of the coating. AFM phase imaging reveals a uniform distribution of the three monomers forming rough morphology. This primer layer significantly improved the morphology, stability, and paclitaxel release profile of a paclitaxel-eluting matrix based on methyl and lauryl methacrylates.[on SciFinder (R)]},
	isbn = {1944-8244},
	author = {Okner, Regina and Shaulov, Yulia and Tal, Noam and Favaro, Gregory and Domb, Abraham J. and Mandler, Daniel}
}
@article {6916,
	title = {Electropolymerized Tricopolymer Based on N-Pyrrole Derivatives as a Primer Coating for Improving the Performance of a Drug-Eluting Stent.},
	journal = {ACS Appl. Mater. InterfacesACS Applied Materials \& Interfaces},
	volume = {1},
	number = {4},
	year = {2009},
	note = {CAPLUS AN 2009:300164(Journal)},
	month = {2009///},
	pages = {758 - 767},
	publisher = {American Chemical Society},
	abstract = {The coating of medical implants by polymeric films aims at increasing their biocompatibility as well as providing a durable matrix for the controlled release of a drug. In many cases, the coating is divided into a primer layer, which bridges between the medical implant and the drug-eluting matrix. The primer coating must be very carefully designed in order to provide optimal interactions with the surface of the medical implant and the outer layer. Here we present a simple and versatile approach for designing the primer layer based on electropolymn. of a carefully chosen blend of three different pyrrole derivs.: N-methylpyrrole (N-me), N-(2-carboxyethyl)pyrrole (PPA), and the Bu ester of N-(2-carboxyethyl)pyrrole (BuOPy). The compn. and phys. properties of the primer layer were studied in detail by at. force microscopy (AFM) and a nano scratch tester. The latter provides the in-depth anal. of the adhesion and viscoelasticity of the coating. AFM phase imaging reveals a uniform distribution of the three monomers forming rough morphol. This primer layer significantly improved the morphol., stability, and paclitaxel release profile of a paclitaxel-eluting matrix based on Me and lauryl methacrylates. [on SciFinder(R)]},
	keywords = {electropolymn tricopolymer pyrrole primer coating controlled release stent},
	isbn = {1944-8244},
	author = {Okner, Regina and Shaulov, Yulia and Tal, Noam and Favaro, Gregory and Domb, Abraham J. and Mandler, Daniel.}
}
@article { WOS:000269897100051,
	title = {Evaluation of Drug-Eluting Stents{\textquoteright} Coating Durability-Clinical and Regulatory Implications},
	journal = {JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS},
	volume = {91B},
	number = {1},
	year = {2009},
	month = {OCT},
	pages = {441-451},
	issn = {1552-4973},
	doi = {10.1002/jbm.b.31420},
	author = {Levy, Yair and Mandler, Daniel and Weinberger, Judah and Domb, Abraham J.}
}
@article {6910,
	title = {Evaluation of drug-eluting stents{\textquoteright} coating durability-Clinical and regulatory implications.},
	journal = {J. Biomed. Mater. Res., Part BJournal of Biomedical Materials Research, Part B: Applied Biomaterials},
	volume = {91B},
	number = {1},
	year = {2009},
	note = {CAPLUS AN 2009:1097371(Journal)},
	month = {2009///},
	pages = {441 - 451},
	publisher = {John Wiley \& Sons, Inc.},
	abstract = {Drug-eluting stents (DES) revolutionized cardiovascular treatment by virtually eliminating in-stent restenosis. However, in the past 3 years the U.S. Food and Drug Administration and published studies have raised several safety issues regarding DES such as late state thrombosis and increased mortality. Recent publications have described DES coating delaminating, cracking, and peeling in com. available stents. It has been suggested that these properties are responsible for the deleterious effects. The goal of this work is to describe a quant. in vitro durability tests for DES, referred to as Quantified Defects (QD). The technique was implemented on various stent polymer-coated models to det. its ability to differentiate between coating properties. Stents{\textquoteright} coating defects were tested using light microscopy, SEM, and a micro-balance. High-performance liq. chromatog. was used for measuring drug release. Stents were incubated at either 37{\textdegree} or 60{\textdegree} and sampled at 0, 3, and 30 days. Stent coating durability was tested using stainless steel control stents vs. stents having increased surface adhesion, both of which were then coated with conventional spray-coating methods. Drug-coated stents tested for defects demonstrated a deteriorating durability profile as reflected by QD indexes. Different coating models showed unique QD indexes that reflected their superior or inferior coating durability. These results indicated that the methodol. was able to differentiate between different models. In conclusion, this simple low-cost testing methodol. can be easily used during DES development, with either durable or biodegradable polymers. {\textcopyright} 2009 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2009. [on SciFinder(R)]},
	keywords = {controlled release stent spray coating durability testing safety},
	isbn = {1552-4973},
	author = {Levy, Yair and Mandler, Daniel and Weinberger, Judah and Domb, Abraham J.}
}
@article {7085,
	title = {Evaluation of drug-eluting stents{\textquoteright} coating durability{\textendash}clinical and regulatory implications},
	journal = {J Biomed Mater Res B Appl BiomaterJournal of biomedical materials research. Part B, Applied biomaterials},
	volume = {91},
	number = {1},
	year = {2009},
	note = {MEDLINE AN 2009627604((EVALUATION STUDIES); Journal; Article; (JOURNAL ARTICLE))},
	month = {2009///},
	pages = {441 - 51},
	abstract = {Drug-eluting stents (DES) revolutionized cardiovascular treatment by virtually eliminating in-stent restanosis. However, in the past 3 years the U.S. Food and Drug Administration and published studies have raised several safety issues regarding DES such as late state thrombosis and increased mortality. Recent publications have described DES coating delaminating, cracking, and peeling in commercially available stents. It has been suggested that these properties are responsible for the deleterious effects. The goal of this work is to describe a quantitative in vitro durability tests for DES, referred to as Quantified Defects (QD). The technique was implemented on various stent polymer-coated models to determine its ability to differentiate between coating properties. Stents{\textquoteright} coating defects were tested using light microscopy, scanning electron microscopy, and a micro-balance. High-performance liquid chromatography was used for measuring drug release. Stents were incubated at either 37 or 60 degrees C and sampled at 0, 3, and 30 days. Stent coating durability was tested using stainless steel control stents versus stents having increased surface adhesion, both of which were then coated with conventional spray-coating methods. Drug-coated stents tested for defects demonstrated a deteriorating durability profile as reflected by QD indices. Different coating models showed unique QD indices that reflected their superior or inferior coating durability. These results indicated that the methodology was able to differentiate between different models. In conclusion, this simple low-cost testing methodology can be easily used during DES development, with either durable or biodegradable polymers.[on SciFinder (R)]},
	isbn = {1552-4981},
	author = {Levy, Yair and Mandler, Daniel and Weinberger, Judah and Domb, Abraham J.}
}
@article { WOS:000264063500019,
	title = {Monitoring Heavy Metals in Seawater by Their Electrochemically Induced Deposition as Hydroxides},
	journal = {ELECTROANALYSIS},
	volume = {21},
	number = {3-5},
	year = {2009},
	note = {12th International Conference on Electroanalysis, Prague, CZECH REPUBLIC, JUN 16-19, 2008},
	month = {FEB},
	pages = {368-378},
	publisher = {European Soc Electroanal Chem; Int Soc Electrochem; Czech Chem Soc; Charles Univ, Fac Sci},
	issn = {1040-0397},
	doi = {10.1002/elan.200804454},
	author = {Eldan, Michael and Shoham, Tamar and Erel, Yigal and Mandler, Daniel}
}
@article {6914,
	title = {Monitoring heavy metals in seawater by their electrochemically induced deposition as hydroxides.},
	journal = {ElectroanalysisElectroanalysis},
	volume = {21},
	number = {3-5},
	year = {2009},
	note = {CAPLUS AN 2009:339513(Journal)},
	month = {2009///},
	pages = {368 - 378},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {A novel method for monitoring heavy metals in seawater is presented. The method is based on the electrochem. codeposition of metal hydroxides driven by the change of pH at the surface of a gold electrode. Altering the pH is achieved by applying a neg. potential or current that reduces the water and thereby increases the concn. of hydroxyl ions. This, in turn, causes metals to coppt. with Mg(OH)2. The continuous deposition enriches the ppt. with the metals (as compared with their concn. in the aq. phase) and allows their detn. by ICP-MS upon dissolving the deposit. A set of expts. in which seawater was spiked with 1-10 ppm of Cu, Cr, Co, Zn and Pb, was conducted. It was obsd. that metals were accumulated in the ppt. as a function of time and their concn. in seawater. The ppts. were analyzed by SEM, EDS and XPS indicating that the metal hydroxides formed a sep. phase from Mg(OH)2 and even water electroreducible metals, e.g., Cu2+, preferentially pptd. as hydroxides. Distribution consts. correlating the concns. of the metals in the deposited salts to their concns. in seawater were calcd. These calcns. imply that the mechanism governing the pptn. of the metal hydroxides by the electrochem. induced process is likely to be kinetically and mass-transport driven rather than thermodynamically controlled. [on SciFinder(R)]},
	keywords = {heavy metal electrodeposition hydroxide seawater pollution monitoring},
	isbn = {1040-0397},
	author = {Eldan, Michael and Shoham, Tamar and Erel, Yigal and Mandler, Daniel.}
}
@article { WOS:000275164700002,
	title = {A new approach for measuring the redox state and redox capacity in milk},
	journal = {ANALYTICAL METHODS},
	volume = {1},
	number = {2},
	year = {2009},
	month = {NOV},
	pages = {93-99},
	issn = {1759-9660},
	doi = {10.1039/b9ay00078j},
	author = {Noyhouzer, Tomer and Ron Kohen and Mandler, Daniel}
}
@article {6906,
	title = {A new approach for measuring the redox state and redox capacity in milk.},
	journal = {Anal. MethodsAnalytical Methods},
	volume = {1},
	number = {2},
	year = {2009},
	note = {CAPLUS AN 2009:1555853(Journal; Online Computer File)},
	month = {2009///},
	pages = {93 - 99},
	publisher = {Royal Society of Chemistry},
	abstract = {Milk is one of the most fundamental ingredients in our diet. It is a complex biol. fluid, which contains numerous substances, ranging from metal ions to enzymes. There is a const. search for an improved way of monitoring its quality and freshness. These are highly affected by the redox state of milk, which is governed by different species. In this study, we investigated the redox state and capacity of milk. Specifically, milk was potentiometrically titrated using different redox mediators, which enabled facilitation of electron transfer between different oxidizable species and the electrode. We found that the iodine/iodide redox couple was superior for measuring the redox capacity of milk. These measurements revealed that milk is not a well-poised system due to the presence of at least two different oxidizable species, one of which is hydrophobic while the other is hydrophilic and therefore could be sepd. by phase sepn. of milk. [on SciFinder(R)]},
	keywords = {potentiometry redox state capacity milk},
	isbn = {1759-9679},
	url = {http://chemistry.rsc.org/ej/AY/2009/b9ay00078j.pdf},
	author = {Noyhouzer, Tomer and Ron Kohen and Mandler, Daniel.}
}
@article {6913,
	title = {Polyaniline Langmuir-Blodgett films: formation and properties.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {11},
	number = {18},
	year = {2009},
	note = {CAPLUS AN 2009:485466(Journal)},
	month = {2009///},
	pages = {3490 - 3496},
	publisher = {Royal Society of Chemistry},
	abstract = {The deposition and characterization of Langmuir-Blodgett (LB) layers of polyaniline (PAN) on solid supports is described. Langmuir films were spread as a mixt. of PAN and dodecylbenzenesulfonic acid (DBSA) at the water/air interface and deposited on either glass or indium tin oxide (ITO). Mono- and multi-layer films of PAN/DBSA were characterized by XPS, at. force microscopy (AFM), absorption spectroscopy and cyclic voltammetry (CV). The ultrathin films produced are highly uniform and very stable. Further characterization of the films was accomplished by scanning electrochem. microscopy (SECM) in the feedback mode. The cond. depended strongly on the pH of the soln. and the no. of layers deposited. Values for the pH-dependent lateral cond. of PAN LB films are reported. [on SciFinder(R)]},
	keywords = {polyaniline Langmuir Blodgett film},
	isbn = {1463-9076},
	author = {Zhang, Jie and Burt, David P. and Whitworth, Anna L. and Mandler, Daniel and Unwin, Patrick R.}
}
@article { WOS:000265413300017,
	title = {Polyaniline Langmuir-Blodgett films: formation and properties},
	journal = {PHYSICAL CHEMISTRY CHEMICAL PHYSICS},
	volume = {11},
	number = {18},
	year = {2009},
	pages = {3490-3496},
	issn = {1463-9076},
	doi = {10.1039/b819809h},
	author = {Zhang, Jie and Burt, David P. and Whitworth, Anna L. and Mandler, Daniel and Unwin, Patrick R.}
}
@article {7086,
	title = {Polyaniline Langmuir-Blodgett films: formation and properties},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {11},
	number = {18},
	year = {2009},
	note = {MEDLINE AN 2009327260(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2009///},
	pages = {3490 - 6},
	abstract = {The deposition and characterisation of Langmuir-Blodgett (LB) layers of polyaniline (PAN) on solid supports is described. Langmuir films were spread as a mixture of PAN and dodecylbenzenesulfonic acid (DBSA) at the water/air interface and deposited on either glass or indium tin oxide (ITO). Mono- and multi-layer films of PAN/DBSA were characterized by X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), absorption spectroscopy and cyclic voltammetry (CV). The ultrathin films produced were found to be highly uniform and very stable. Further characterisation of the films was accomplished by scanning electrochemical microscopy (SECM) in the feedback mode. It was found that the conductivity depended strongly on the pH of the solution and the number of layers deposited. Values for the pH-dependent lateral conductivity of PAN LB films are reported.[on SciFinder (R)]},
	isbn = {1463-9076},
	author = {Zhang, Jie and Burt, David P. and Whitworth, Anna L. and Mandler, Daniel and Unwin, Patrick R.}
}
@article { WOS:000272039700015,
	title = {Poly(methyl methacrylate) Grafting onto Stainless Steel Surfaces: Application to Drug-Eluting Stents},
	journal = {ACS APPLIED MATERIALS \& INTERFACES},
	volume = {1},
	number = {11},
	year = {2009},
	month = {NOV},
	pages = {2519-2528},
	issn = {1944-8244},
	doi = {10.1021/am900465t},
	author = {Shaulov, Yulia and Okner, Regina and Levi, Yair and Tal, Noam and Gutkin, Vitaly and Mandler, Daniel and Domb, Abraham J.}
}
@article {7080,
	title = {Poly(methyl methacrylate) grafting onto stainless steel surfaces: application to drug-eluting stents},
	journal = {ACS Appl Mater InterfacesACS applied materials \& interfaces},
	volume = {1},
	number = {11},
	year = {2009},
	note = {MEDLINE AN 2010227904(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2009///},
	pages = {2519 - 28},
	abstract = {Drug-eluting stents (DESs) have been associated with adverse clinical effects. Moreover, recent publications have shown that the coating of DESs suffers from defects. The purpose of this contribution is to examine a three-step process for surface modification as a means of improving the durability of DESs. In the first step, 4-(2-bromoethyl)benzenediazonium tetrafluoroborate was electrografted onto a stainless steel (SS) stent. X-ray photoelectron spectroscopy (XPS) of the modified stent confirmed the formation of the organic layer. In the second step, methyl methacrylate was polymerized onto the grafted surface by atom-transfer radical polymerization. XPS, electrochemical impedance spectroscopy, and contact-angle measurements were used to characterize the polymer brushes. The last step involved spray-coating of the stent with a drug-in-polymer matrix [poly(n-butyl methacrylate)/poly(ethylene-co-vinyl acetate) + paclitaxel]. Scanning electron microscopy confirmed the considerably improved durability of the drug-in-polymer matrix. Bare controls showed greater cracking and delamination of the coating than did the two-step modified stents after incubation under physiological (37 degrees C) and accelerated (60 degrees C) conditions. Finally, paclitaxel controlled release from the modified SS DESs was moderate compared with that of nontreated samples. In conclusion, the proposed method significantly improves the durability of drug-in-polymer matrixes on a SS DESs.[on SciFinder (R)]},
	isbn = {1944-8244},
	author = {Shaulov, Yulia and Okner, Regina and Levi, Yair and Tal, Noam and Gutkin, Vitaly and Mandler, Daniel and Domb, Abraham J.}
}
@article {6907,
	title = {Poly(methyl methacrylate) Grafting onto Stainless Steel Surfaces: Application to Drug-Eluting Stents.},
	journal = {ACS Appl. Mater. InterfacesACS Applied Materials \& Interfaces},
	volume = {1},
	number = {11},
	year = {2009},
	note = {CAPLUS AN 2009:1271694(Journal)},
	month = {2009///},
	pages = {2519 - 2528},
	publisher = {American Chemical Society},
	abstract = {Drug-eluting stents (DESs) have been assocd. with adverse clin. effects. Moreover, recent publications have shown that the coating of DESs suffers from defects. The purpose of this contribution is to examine a three-step process for surface modification as a means of improving the durability of DESs. In the first step, 4-(2-bromoethyl)benzenediazonium tetrafluoroborate was electrografted onto a stainless steel (SS) stent. XPS of the modified stent confirmed the formation of the org. layer. In the second step, Me methacrylate was polymd. onto the grafted surface by atom-transfer radical polymn. XPS, electrochem. impedance spectroscopy, and contact-angle measurements were used to characterize the polymer brushes. The last step involved spray-coating of the stent with a drug-in-polymer matrix [poly(Bu methacrylate)/poly(ethylene-co-vinyl acetate) + paclitaxel]. SEM confirmed the considerably improved durability of the drug-in-polymer matrix. Bare controls showed greater cracking and delamination of the coating than did the two-step modified stents after incubation under physiol. (37{\textdegree}) and accelerated (60{\textdegree}) conditions. Finally, paclitaxel controlled release from the modified SS DESs was moderate compared with that of nontreated samples. In conclusion, the proposed method significantly improves the durability of drug-in-polymer matrixes on a SS DESs. [on SciFinder(R)]},
	keywords = {polymethyl methacrylate stainless steel surface treatment drug eluting stent},
	isbn = {1944-8244},
	author = {Shaulov, Yulia and Okner, Regina and Levi, Yair and Tal, Noam and Gutkin, Vitaly and Mandler, Daniel and Domb, Abraham J.}
}
@article { WOS:000256177800007,
	title = {Corrosion inhibition of magnesium by combined zirconia silica sol-gel films},
	journal = {ELECTROCHIMICA ACTA},
	volume = {53},
	number = {16},
	year = {2008},
	month = {JUN 30},
	pages = {5118-5127},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2008.02.029},
	author = {Tamar, Yair and Mandler, Daniel}
}
@article {6925,
	title = {Corrosion inhibition of magnesium by combined zirconia silica sol-gel films.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {53},
	number = {16},
	year = {2008},
	note = {CAPLUS AN 2008:550288(Journal)},
	month = {2008///},
	pages = {5118 - 5127},
	publisher = {Elsevier B.V.},
	abstract = {The inhibition of Mg (AZ91D) corrosion by thin sol-gel films was studied. The sol-gel films were prepd. by the traditional acid or base-catalyzed hydrolysis and condensation, and finally deposited by dip coating. Two different sol-gel monomers were used: phenyltrimethoxysilane (PTMOS) and Zr(IV) tetra-1-propoxide (ZrTPO). Films were made of each of the individual monomers and by depositing 1st a PTMOS film followed by ZrTPO-based film. The corrosion inhibition of the films and their characterization were examd. by different methods including potentiodynamic polarization, contact angle measurement, adhesion test, XPS, SEM and electrochem. impedance spectroscopy (EIS). While the ZrTPO-based film did not show a significant corrosion inhibition, the PTMOS-based film provided moderate protection. The combined film exhibited superior corrosion inhibition as compared with the other films. [on SciFinder(R)]},
	keywords = {corrosion inhibition magnesium zirconia silica sol gel film, phenyl modified silica zirconia sol gel coating zirconium},
	isbn = {0013-4686},
	author = {Tamar, Yair and Mandler, Daniel.}
}
@article {6911,
	title = {Deposition of gold nanoparticles on thin polyaniline films.},
	journal = {Isr. J. Chem.Israel Journal of Chemistry},
	volume = {48},
	number = {3-4},
	year = {2008},
	note = {CAPLUS AN 2009:954669(Journal)},
	month = {2008///},
	pages = {349 - 357},
	publisher = {Science from Israel},
	abstract = {Local and bulk deposition of gold particles was accomplished by the spontaneous reaction between chem. reduced polyaniline (PAN) thin films and AuCl4-. PAN layers were deposited on glass, ITO, and glassy C (GC) by the Langmuir-Blodgett method and spin-coating. Characterization of the PAN films was carried out by microscopy, UV-vis spectroscopy, and electrochem. The nature of the Au deposit was greatly affected by the thickness of the PAN. Scanning electrochem. microscopy was used as a means of locally depositing Au nanoparticles on an unbiased PAN film by anodically dissolving a Au microelectrode. This represents a generic approach whereby a variety of metal micro- and nanoparticles can be locally deposited on insulating supports. [on SciFinder(R)]},
	keywords = {gold nanoparticle deposition polyaniline surface structure},
	isbn = {0021-2148},
	author = {Sheffer, Marisa and Martina, Virginia and Seeber, Renato and Mandler, Daniel.}
}
@article { WOS:000259874100011,
	title = {Detection of uranium(VI) in aqueous solution by a calix[6]arene modified electrode},
	journal = {JOURNAL OF ELECTROANALYTICAL CHEMISTRY},
	volume = {621},
	number = {2},
	year = {2008},
	month = {SEP 15},
	pages = {214-221},
	issn = {1572-6657},
	doi = {10.1016/j.jelechem.2007.11.009},
	author = {Becker, Amit and Tobias, Haim and Porat, Ze{\textquoteright}ev and Mandler, Daniel}
}
@article {6919,
	title = {Detection of uranium(VI) in aqueous solution by a calix[6]arene modified electrode.},
	journal = {J. Electroanal. Chem.Journal of Electroanalytical Chemistry},
	volume = {621},
	number = {2},
	year = {2008},
	note = {CAPLUS AN 2008:1079401(Journal)},
	month = {2008///},
	pages = {214 - 221},
	publisher = {Elsevier B.V.},
	abstract = {This work describes attempts to develop a new type of modified electrode with high selectivity for uranyl ions, UO22+. The goal was addressed by binding derivs. of calix[6]arene, a macrocyclic mol. composed of 6 phenol units known as a super uranophile, to the electrode surface. Selective extn. of UO22+ onto the electrode surface, followed by a voltammetric measurement provides a quant. uranyl anal. The initial approach to binding calix[6]arene mols. onto electrodes involved an ionic deriv., 4-sulfonic-calix[6]arene, electrostatically attached to a pos.-charged, self-assembled monolayer of cysteamine (2-aminoethanethiol) on a Au electrode. Attachment of the 4-sulfonic-calix[6]arene to the cysteamine monolayer was verified by XPS, IR spectroscopy, and capacitance measurements. Voltammetric expts. showed UO22+ can be pre-concd. and measured using these modified electrodes. [on SciFinder(R)]},
	keywords = {cysteamine self assembled monolayer gold electrode calix arene binding, sulfonic calix arene bound gold electrode uranyl ion detn, uranium ion uranyl ion detn water cyclic voltammetry},
	author = {Becker, Amit and Tobias, Haim and Porat, Ze{\textquoteright}ev and Mandler, Daniel.}
}
@booklet {6927,
	title = {Electrochemical co-deposition of sol-gel films.},
	howpublished = {PCT Int. Appl.},
	number = {WO2008038293A2},
	year = {2008},
	note = {CAPLUS AN 2008:411194(Patent)},
	month = {2008/04/03/},
	pages = {39pp.},
	publisher = {Yissum Research Development Company of the Hebrew University of Jerusalem, Israel .},
	abstract = {The invention provides a new method for the electrochem. co-deposition of sol-gel and one or more additives selected amongst a great variety of agents such as monomers, oligomers, polymers, metals and others. The method affords continuous films of high stability and precision. [on SciFinder(R)]},
	keywords = {electrodeposition composite sol gel film copper titanium dioxide polymer},
	author = {Mandler, Daniel and Avnir, David and Shacham, Ronen.}
}
@article { WOS:000257279200019,
	title = {Electrochemical co-deposition of sol-gel/metal thin nanocomposite films},
	journal = {CHEMISTRY OF MATERIALS},
	volume = {20},
	number = {13},
	year = {2008},
	month = {JUL 8},
	pages = {4276-4283},
	issn = {0897-4756},
	doi = {10.1021/cm800002z},
	author = {Toledano, Rent and Shacham, Ronen and Avnir, David and Mandler, Daniel}
}
@article {6923,
	title = {Electrochemical Co-deposition of Sol-Gel/Metal Thin Nanocomposite Films.},
	journal = {Chem. Mater.Chemistry of Materials},
	volume = {20},
	number = {13},
	year = {2008},
	note = {CAPLUS AN 2008:721058(Journal)},
	month = {2008///},
	pages = {4276 - 4283},
	publisher = {American Chemical Society},
	abstract = {A single-step method for the prepn. of thin sol-gel/Cu mixed films is described, which is based on a novel electrochem. sol-gel methodol., resulting in nanocomposite coating. The method combines electrochem. with the acceleration of sol-gel hydrolysis and condensation processes. While sol-gel is deposited of increasing the pH in the vicinity of the electrode surface, Cu ions are electrochem. reduced. Characterization of the deposited films was accomplished by SEM, XPS, tunneling at. force microscopy, and other surface techniques. The different parameters that affect the structure and compn. of the deposited films were examd. The morphol. and grain size of the films are strongly affected by the ratio between the sol-gel monomer and Cu ions. Also, the potential of deposition affects also the compn. of the films as it controls the kinetics of sol-gel and Cu deposition. [on SciFinder(R)]},
	keywords = {electrochem codeposition sol gel metal thin nanocomposite film, silica copper film electrodeposition sol gel methodol, titania copper film electrodeposition sol gel methodol},
	isbn = {0897-4756},
	author = {Toledano, Reut and Shacham, Ronen and Avnir, David and Mandler, Daniel.}
}
@article { WOS:000258975400011,
	title = {Electrochemical detection of Cd2+ ions by a self-assembled monolayer of 1,9-nonanedithiol on gold},
	journal = {ELECTROCHIMICA ACTA},
	volume = {53},
	number = {23, SI},
	year = {2008},
	note = {58th Annual Meeting of the International-Society-of-Electrochemisty, Banff, CANADA, SEP 10-14, 2007},
	month = {OCT 1},
	pages = {6753-6758},
	publisher = {Int Soc Electrochem},
	issn = {0013-4686},
	doi = {10.1016/j.electacta.2008.02.033},
	author = {Malel, Esteban and Sinha, Jatin K. and Zawisza, Izabella and Wittstock, Gunther and Mandler, Daniel}
}
@article {6922,
	title = {Electrochemical detection of Cd2+ ions by a self-assembled monolayer of 1,9-nonanedithiol on gold.},
	journal = {Electrochim. ActaElectrochimica Acta},
	volume = {53},
	number = {23},
	year = {2008},
	note = {CAPLUS AN 2008:869535(Journal)},
	month = {2008///},
	pages = {6753 - 6758},
	publisher = {Elsevier B.V.},
	abstract = {The application of 1,9-nonanedithiol (NDT) self-assembled monolayer (SAM) on gold for the electrochem. detn. of Cd2+ was studied. A NDT SAM strongly affects the stripping wave of Cd, resulting in a sharp peak that was used for electroanal. detn. of Cd2+ in aq. solns. The different parameters, such as potential and time of deposition of Cd, were examd. Also, polarization-modulated IR reflection absorption spectroscopy (PM IRRAS) and XPS were used for exploring the interaction between the deposited Cd and the thiol groups on Au. FTIR measurements clearly indicate that NDT is assembled in a disordered liq. type monolayer interacting with the Au electrode via both thiol moieties. XPS reveals that Cd is stripped at two different potentials and that the signal of sulfur is almost unchanged by deposition and desorption of Cd. All these finding allude to the interesting conclusion that Cd is deposited on Au lifting to some extent the thiol groups. [on SciFinder(R)]},
	keywords = {cadmium ion electrochem analysis self assembled nonanedithiol gold},
	isbn = {0013-4686},
	author = {Malel, Esteban and Sinha, Jatin K. and Zawisza, Izabella and Wittstock, Gunther and Mandler, Daniel.}
}
@article {6917,
	title = {Electrocoating of stainless steel coronary stents for extended release of paclitaxel.},
	journal = {J. Biomed. Mater. Res., Part AJournal of Biomedical Materials Research, Part A},
	volume = {88A},
	number = {2},
	year = {2008},
	note = {CAPLUS AN 2009:76576(Journal)},
	month = {2008///},
	pages = {427 - 436},
	publisher = {John Wiley \& Sons, Inc.},
	abstract = {Nonbiodegradable polymer coating based on N-(2-carboxyethyl)pyrrole (PPA) and Bu ester of PPA (BuOPy) were successfully electrodeposited on a stainless steel stent surface using cyclic voltammetry. Chem. compn. of the coating was examd. by XPS. Polymer stability was examd. by immersing the coated stent into 1:1 soln. of fetal calf serum:seline soln. up to 1 yr and implantation s.c. in mouse for 1 wk. Morphol. changes were then recorded by SEM. Paclitaxel loading was carried out by immersion into drug soln. and its release was detected by HPLC. The results show that thin (single micrometers), uniform coating with various morphol. and hydrophobicity can be created by electrochem. deposition. The polymer did not show significant histopathol. or morphol. changes in vitro and in vivo. The surface properties allow loading appropriate amts. of paclitaxel and release it slowly up to a month. [on SciFinder(R)]},
	keywords = {electrocoating stainless steel heart stent paclitaxel controlled release},
	isbn = {1549-3296},
	author = {Okner, R. and M. Oron and Tal, N. and Nyska, A. and Kumar, N. and Mandler, D and Domb, A. J.}
}
@article { WOS:000255524100035,
	title = {Localized electroless deposition of gold nanoparticles using scanning electrochemical microscopy},
	journal = {JOURNAL OF THE ELECTROCHEMICAL SOCIETY},
	volume = {155},
	number = {6},
	year = {2008},
	pages = {D459-D467},
	issn = {0013-4651},
	doi = {10.1149/1.2902331},
	author = {Malel, E. and Mandler, D.}
}
@article {6926,
	title = {Localized Electroless Deposition of Gold Nanoparticles Using Scanning Electrochemical Microscopy.},
	journal = {J. Electrochem. Soc.Journal of the Electrochemical Society},
	volume = {155},
	number = {6},
	year = {2008},
	note = {CAPLUS AN 2008:546181(Journal)},
	month = {2008///},
	pages = {D459-D467},
	publisher = {Electrochemical Society},
	abstract = {The aim of this study is to locally deposit nanoparticles on an unbiased surface by electroless deposition (ED) using scanning electrochem. microscopy (SECM). We have developed an ED process that is based on the redn. of gold ions by hydroquinone (H2Q) and catalyzed by a metallic surface, such as palladium. One of the advantages of this system is the ability to drive the ED at pH 1-7. The metal ions were electrogenerated in a soln. consisting of H2Q and KCl by anodic dissoln. of a gold microelectrode. AuCl4- reacted with H2Q at the electrolyte/metallic interface to form benzoquinone and gold deposit. The ED was studied initially in bulk soln. contg. KCl, H2Q, and HAuCl4, and then by SECM. We found that the pH had a significant effect on the nature of the deposited gold and could be correlated with the kinetics of gold ions redn. by H2Q. Hence, either nanoparticles or much larger crystals could be formed, depending on the pH of the deposition soln. Time of deposition and H2Q concn. also affected the shape and d. of the deposition. [on SciFinder(R)]},
	keywords = {gold nanoparticle hydroquinone redn electroless deposition scanning electrochem microscopy},
	isbn = {0013-4651},
	author = {Malel, E. and Mandler, D}
}
@booklet {6921,
	title = {Medical devices having a matrix adhered thereof.},
	howpublished = {PCT Int. Appl.},
	number = {WO2008090555A2},
	year = {2008},
	note = {CAPLUS AN 2008:915787(Patent)},
	month = {2008/07/31/},
	pages = {117pp.},
	publisher = {Elutex Ltd., Israel .},
	abstract = {This invention relates to medical devices having a matrix comprising a pharmaceutically active agent, the matrix being adhered to a surface of the medical device via an adherence to modulate a release of the pharmaceutically active agent. [on SciFinder(R)]},
	keywords = {polymer electrocoating stent},
	author = {Domb, Abraham Jackob and Shaulov, Yulia and Levi, Yair and Mandler, Daniel and Tal, Noam.}
}
@booklet {6920,
	title = {Modified conductive surfaces prepared by electrografting of diazonium salts for medical devices.},
	howpublished = {PCT Int. Appl.},
	number = {WO2008090554A2},
	year = {2008},
	note = {CAPLUS AN 2008:916671(Patent)},
	month = {2008/07/31/},
	pages = {138pp.},
	publisher = {Elutex Ltd., Israel .},
	abstract = {Articles-of-manuf. (for medical devices) comprising 1 aryl moiety electrochem. attached to the surface thereof are disclosed. Further disclosed herein are novel compds. comprising an aryl moiety and substituted by at least 2 diazonium moieties, which may optionally be used to the articles-of-manuf. Stents were electro-coated with tetrakis[(4-diazophenoxy)methyl]methane tetrafluoroborate. [on SciFinder(R)]},
	keywords = {stent medical conductive electrocoating diazophenoxy tetrafluoroborate prepn},
	author = {Domb, Abraham Jackob and Shaulov, Yulia and Levi, Yair and Mandler, Daniel and Tal, Noam.}
}
@article {6928,
	title = {Scanning electrochemical imprinting microscopy: a tool for surface patterning.},
	journal = {J. Electrochem. Soc.Journal of the Electrochemical Society},
	volume = {155},
	number = {3},
	year = {2008},
	note = {CAPLUS AN 2008:257135(Journal)},
	month = {2008///},
	pages = {D203-D208},
	publisher = {Electrochemical Society},
	abstract = {An approach for patterning surface with different structures in a single step is demonstrated. The approach is based on the construction of nondisk shape microelectrodes combined with the feedback mode of scanning electrochem. microscopy (SECM) for generating an anisotropic flux of electroactive species. The latter attains the shape of the microelectrode and imprints its shape upon reaction with the surface. The authors have demonstrated this approach in two model systems. The etching of GaAs using electrogenerated bromine resulted in the formation of etching structures imprinting the shape of the Pt microelectrode on the GaAs. The second system comprised the electrogeneration of silver ions from a silver microelectrode, which reacted with a copper surface causing the deposition of silver patterns matching the shape of the silver microelectrode. SECM tips with different shapes were constructed by different methods, including electron-beam lithog. [on SciFinder(R)]},
	keywords = {scanning electrochem microscopy surface patterning},
	isbn = {0013-4651},
	author = {Sheffer, Marisa and Mandler, Daniel.}
}
@article { WOS:000256738900024,
	title = {Studying the reactions of CdTe nanostructures and thin CdTe films with Ag+ and AuCl4(-)},
	journal = {JOURNAL OF PHYSICAL CHEMISTRY C},
	volume = {112},
	number = {24},
	year = {2008},
	month = {JUN 19},
	pages = {8881-8889},
	issn = {1932-7447},
	doi = {10.1021/jp800877a},
	author = {Danieli, Tamar and Gaponik, Nikolai and Eychmueller, Alexander and Mandler, Daniel}
}
@article {6924,
	title = {Studying the Reactions of CdTe Nanostructures and Thin CdTe Films with Ag+ and AuCl4-.},
	journal = {J. Phys. Chem. CJournal of Physical Chemistry C},
	volume = {112},
	number = {24},
	year = {2008},
	note = {CAPLUS AN 2008:628442(Journal)},
	month = {2008///},
	pages = {8881 - 8889},
	publisher = {American Chemical Society},
	abstract = {The reactions between Ag+ and AuCl4- ions with 3 different CdTe systems, i.e., thermally evapd. thin CdTe films, CdTe nanoparticles (NPs) stabilized by thioglycolic acid (TGA), and 20 layers of these CdTe NPs embedded in poly(diallyldimethylammonium) chloride (CdTe-20lbl), were studied. AuCl4- oxidized the CdTe, in all studied systems, to form metallic Au. However, the kinetics of the reaction was substantially sluggish for the thin CdTe films than with the CdTe NPs systems. However, the reaction with Ag+ was rather complex, and the findings alluded to different reaction for each system. Although it is possible that a Ag-SR bond was formed between Ag+ and the thiol group of the TGA-stabilized NPs, cation exchange between Ag+ and Cd2+ is evidenced when these CdTe NPs were embedded in a polymer (CdTe-20lbl). Also, Ag+ reacted with thin CdTe films to form a ppt. consisting of Ag. The authors studied the reactions between locally generated Ag+ and AuCl4- and CdTe surfaces using scanning electrochem. microscopy (SECM). A flux of Ag and Au chloride ions was electrochem. generated from their resp. microelectrodes upon applying a pos. potential close to thin CdTe films and CdTe-20lbl. The flux of AuCl4- resulted in the local formation of Au NPs on the CdTe surface, whereas local quenching of CdTe-20lbl was achieved by the flux of Ag+ ions. Finally, the current transients recorded during the SECM expts. provided invaluable information regarding the reactions at the CdTe surface below the microelectrodes. [on SciFinder(R)]},
	keywords = {cadmium telluride nanostructure film reaction tetrachloroaurate silver ion SECM},
	isbn = {1932-7447},
	author = {Danieli, Tamar and Gaponik, Nikolai and Eychm{\"u}ller, Alexander and Mandler, Daniel.}
}
@article { WOS:000260235200017,
	title = {Why is copper locally etched by scanning electrochemical microscopy?},
	journal = {JOURNAL OF ELECTROANALYTICAL CHEMISTRY},
	volume = {622},
	number = {1},
	year = {2008},
	month = {OCT 1},
	pages = {115-120},
	issn = {1572-6657},
	doi = {10.1016/j.jelechem.2008.05.005},
	author = {Sheffer, Marisa and Mandler, Daniel}
}
@article {6918,
	title = {Why is copper locally etched by scanning electrochemical microscopy?.},
	journal = {J. Electroanal. Chem.Journal of Electroanalytical Chemistry},
	volume = {622},
	number = {1},
	year = {2008},
	note = {CAPLUS AN 2008:1109078(Journal)},
	month = {2008///},
	pages = {115 - 120},
	publisher = {Elsevier B.V.},
	abstract = {The etching of thin Cu films by scanning electrochem. microscopy (SECM) was studied. It is not trivial that locally injected charge by an oxidized mediator will lead to dissoln. of Cu as the charge can easily be dissipated by lateral charge propagation. The authors studied the effect of different parameters, such as thickness of the Cu film and concn. of the mediator, on the efficiency of etching. The feedback current is the sum of 3 charge transfer contributions: diffusion of mediator species, chem. reaction on the surface and lateral charge propagation across the Cu film. The authors have introduced an approach for isolating the lateral contribution and studied the parameters affecting the fate of the locally injected charge. Etching becomes effective once the lateral contribution cannot dissipate the locally injected charge. This occurs as the concn. of the etchant increases or the film thickness decreases. Measuring the steady-state current above Cu films with different thickness, allowed estg. the p.d. across the Cu area underneath the tip. Driving local processes, such as etching, depends on creating a mechanism which maintains the injected charge focused. [on SciFinder(R)]},
	keywords = {copper etching scanning electrochem microscopy feedback current},
	author = {Sheffer, Marisa and Mandler, Daniel.}
}
@article {6935,
	title = {Application of nanoparticles for the enhancement of latent fingerprints.},
	journal = {Chem. Commun. (Cambridge, U. K.)Chemical Communications (Cambridge, United Kingdom)},
	number = {11},
	year = {2007},
	note = {CAPLUS AN 2007:258552(Journal)},
	month = {2007///},
	pages = {1142 - 1144},
	publisher = {Royal Society of Chemistry},
	abstract = {Two different types of nanoparticles dissolved in org. soln., Au stabilized by n-alkanethiols and CdSe/ZnS stabilized by n-alkaneamine, adhere preferentially to the ridges of latent fingerprints,. The gold deposits catalyze silver electroless deposition from "Silver Phys. Developer" (Ag-PD), an aq. soln. contg. silver colloids stabilized by cationic surfactants, to form dark impressions of the ridge details. The hydrophobic capped gold nanoparticles significantly improve the intensity and clarity of the developed prints compared with Ag-PD alone. Fingermarks treated with CdSe/ZnS nanoparticles can be viewed directly, due to their fluorescence under UV illumination. [on SciFinder(R)]},
	keywords = {cadmium selenide zinc sulfide nanoparticle alkanethiol alkaneamine fingerprint forensic, gold nanoparticle alkanethiol alkaneamine fingerprint forensic},
	isbn = {1359-7345},
	author = {Sametband, Matias and Shweky, Itzhak and Banin, Uri and Mandler, Daniel and Almog, Joseph.}
}
@article {7091,
	title = {Application of nanoparticles for the enhancement of latent fingerprints},
	journal = {Chem Commun (Camb)Chemical communications (Cambridge, England)},
	number = {11},
	year = {2007},
	note = {MEDLINE AN 2007147255(Journal; Article; (JOURNAL ARTICLE))},
	month = {2007///},
	pages = {1142 - 4},
	abstract = {Two different types of nanoparticles dissolved in organic solution, gold stabilized by n-alkanethiols and CdSe/ZnS stabilized by n-alkane-amine, adhere preferentially to the ridges of latent fingerprints; the gold deposits catalyze silver electroless deposition from "Silver Physical Developer" (Ag-PD), an aqueous solution containing silver colloids stabilized by cationic surfactants, to form dark impressions of the ridge details; the hydrophobic capped gold nanoparticles significantly improve the intensity and clarity of the developed prints compared with Ag-PD alone; finger marks treated with CdSe/ZnS nanoparticles can be viewed directly, due to their fluorescence under UV illumination.[on SciFinder (R)]},
	isbn = {1359-7345},
	author = {Sametband, Matias and Shweky, Itzhak and Banin, Uri and Mandler, Daniel and Almog, Joseph}
}
@article {6932,
	title = {Electrochemical Formation and Characterization of Copolymers Based on N-Pyrrole Derivatives.},
	journal = {BiomacromoleculesBiomacromolecules},
	volume = {8},
	number = {9},
	year = {2007},
	note = {CAPLUS AN 2007:860736(Journal)},
	month = {2007///},
	pages = {2928 - 2935},
	publisher = {American Chemical Society},
	abstract = {Org. coatings based on N-(2-carboxyethyl)pyrrole (PPA) and a Bu ester of PPA (BuOPy) were deposited via electrochem. oxidn. The homo- and copolymers were electropolymd. on glassy C and stainless steel in MeCN using Bu4NBF4B as the electrolyte. The mechanism of deposition on stainless steel was studied by chronoamperometry and by the tapping and phase angle imaging modes of at. force microscopy. The electrochem. properties and growth of the films were studied by cyclic voltammetry. The compn. of the copolymers was detd. by reflection-absorption FTIR spectroscopy. While the hydrophilic monomer PPA undergoes progressive nucleation followed by instantaneous growth the hydrophobic BuOPy nucleates instantaneously. The rate of BuOPy electropolymn. was higher than that of PPA, and the resulting film was thicker yet fluffier. Copolymer films were enriched by BuOPy as compared with the electropolymn. soln., which is attributed to the faster rate of electropolymn. of BuOPy than PPA. [on SciFinder(R)]},
	keywords = {electrochem copolymn oxidative carboxyethylpyrrole butyl ester},
	isbn = {1525-7797},
	author = {Okner, Regina and Domb, Abraham J. and Mandler, Daniel.}
}
@article {7089,
	title = {Electrochemical formation and characterization of copolymers based on N-pyrrole derivatives},
	journal = {BiomacromoleculesBiomacromolecules},
	volume = {8},
	number = {9},
	year = {2007},
	note = {MEDLINE AN 2007588910(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2007///},
	pages = {2928 - 35},
	abstract = {Organic coatings based on N-(2-carboxyethyl)pyrrole (PPA) and a butyl ester of PPA (BuOPy) were deposited via electrochemical oxidation. The homo- and copolymers were electropolymerized on glassy carbon and stainless steel in acetonitrile using tetrabutylammonium tetrafluoraborate (Bu4NF4B) as the electrolyte. The mechanism of deposition on stainless steel was studied by chronoamperometry and by the tapping and phase angle imaging modes of atomic force microscopy. The electrochemical properties and growth of the films were investigated by cyclic voltammetry. The composition of the copolymers was determined by reflection-absorption Fourier transform infrared spectroscopy. We found that while the hydrophilic monomer PPA undergoes progressive nucleation followed by instantaneous growth the hydrophobic BuOPy nucleates instantaneously. The rate of BuOPy electropolymerization was higher than that of PPA, and the resulting film was thicker yet fluffier. Copolymer films were enriched by BuOPy as compared with the electropolymerization solution, which is attributed to the faster rate of electropolymerization of BuOPy than PPA.[on SciFinder (R)]},
	isbn = {1525-7797},
	author = {Okner, Regina and Domb, Abraham J. and Mandler, Daniel}
}
@article {6936,
	title = {Electrocoating of stainless steel coronary stents for extended release of Paclitaxel.},
	journal = {Mater. Sci. Eng., CMaterials Science \& Engineering, C: Biomimetic and Supramolecular Systems},
	volume = {27},
	number = {3},
	year = {2007},
	note = {CAPLUS AN 2007:229013(Journal)},
	month = {2007///},
	pages = {510 - 513},
	publisher = {Elsevier B.V.},
	abstract = {The purpose of this study was to examine chem., mech. and Paclitaxel release properties of the new coating onto the stainless steel coronary stents. Stainless steel coronary stents were coated with elec. polymerizable pyrrole deriv., applying cyclic voltammetry technique in a simple 3 electrode cell, while stent represented a working electrode. Resulted polymer coating were examd. by cyclic voltammetry (elec. parameters), SEM (morphol. images), goniometer (hydrophobisity of the surface), profilometer ( thickness of the polymer coating). Polymer stability was examd. by placing the coated stent into 1:1 soln. of fetal calf serum:seline soln. up to 1 yr and under the mouse skin for 1 wk. Paclitaxel loading were carried out by immersion into drug soln. and its release was detected by HPLC. Reproducible one step method for coating different pyrrole derivs. on stainless steel coronary stents provided thin (single micrometers), uniform coating with various morphol. and hydrophobisity. These surface properties allow to load appropriate amt. of Paclitaxel and to release it slowly up to a month. [on SciFinder(R)]},
	keywords = {stainless steel coronary stent electrocoating pyrrole paclitaxel dissoln},
	isbn = {0928-4931},
	author = {Okner, R. and M. Oron and Tal, N. and Mandler, D and Domb, A. J.}
}
@article {7090,
	title = {Electrostatic attachment of gold and poly(lactic acid) nanoparticles onto omega-aminoalkanoic acid self-assembled monolayers on 316L stainless steel},
	journal = {ChemistryChemistry (Weinheim an der Bergstrasse, Germany)},
	volume = {13},
	number = {22},
	year = {2007},
	note = {MEDLINE AN 2007491351(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2007///},
	pages = {6402 - 7},
	abstract = {The assembly of poly(lactic acid) (PLA) nanoparticles on a 12-aminodecanoic acid (ADA) self-assembled monolayer (SAM) is described. Assembly is accomplished through electrostatic interactions between the positively charged SAM and the negatively charged PLA nanoparticles. The strategy used involves two steps in which a preliminary electrochemical coating of the ADA SAM is followed by a second step that involves immersing the SAM in a solution containing gold or PLA nanoparticles. The SAM was characterized by using cyclic voltammetry (CV), X-ray photoelectron spectroscopy (XPS), FTIR spectroscopy, and contact angle measurements, whereas scanning electron microscopy (SEM) was used to image the nanoparticles after electrostatic attachment was achieved. We found that the surface coverage of the nanoparticles could be controlled by modulating the electrostatic interactions between the negatively charged particles and the positively charged SAM surface by varying the pH of the nanoparticle solution, the immersion time, and the number of cyclic voltammetry scans under which the SAM was formed.[on SciFinder (R)]},
	isbn = {0947-6539},
	author = {Shustak, Galit and Shaulov, Yulia and Domb, Abraham J. and Mandler, Daniel}
}
@article {6931,
	title = {Electrostatic attachment of gold and poly(lactic acid) nanoparticles onto ω-aminoalkanoic acid self-assembled monolayers on 316L stainless steel.},
	journal = {Chem. - Eur. J.Chemistry - A European Journal},
	volume = {13},
	number = {22},
	year = {2007},
	note = {CAPLUS AN 2007:901786(Journal)},
	month = {2007///},
	pages = {6402 - 6407},
	publisher = {Wiley-VCH Verlag GmbH \& Co. KGaA},
	abstract = {The assembly of poly(lactic acid) (PLA) nanoparticles on a 12-aminodecanoic acid (ADA) self-assembled monolayer (SAM) is described. Assembly is accomplished through electrostatic interactions between the pos. charged SAM and the neg. charged PLA nanoparticles. The strategy used involves 2 steps in which a preliminary electrochem. coating of the ADA SAM is followed by a second step that involves immersing the SAM in a soln. contg. gold or PLA nanoparticles. The SAM was characterized by cyclic voltammetry (CV), XPS, FTIR spectroscopy, and contact angle measurements, whereas SEM was used to image the nanoparticles after electrostatic attachment was achieved. The authors found that the surface coverage of the nanoparticles could be controlled by modulating the electrostatic interactions between the neg. charged particles and the pos. charged SAM surface by varying the pH of the nanoparticle soln., the immersion time, and the no. of cyclic voltammetry scans under which the SAM was formed. [on SciFinder(R)]},
	keywords = {stainless steel implant aminododecanoic acid gold polylactic acid electrodeposition},
	isbn = {0947-6539},
	author = {Shustak, Galit and Shaulov, Yulia and Domb, Abraham J. and Mandler, Daniel.}
}
@article {6930,
	title = {Formation of a molecular glue based on the electrochemical reduction of 4-hydroxyphenyldiazonium for the attachment of thin sol-gel film on glassy carbon.},
	journal = {Z. Phys. Chem. (Muenchen, Ger.)Zeitschrift fuer Physikalische Chemie (Muenchen, Germany)},
	volume = {221},
	number = {9-10},
	year = {2007},
	note = {CAPLUS AN 2007:1328553(Journal)},
	month = {2007///},
	pages = {1237 - 1243},
	publisher = {Oldenbourg Wissenschaftsverlag GmbH},
	abstract = {The covalent attachment of a sol-gel thin film onto a glassy carbon electrode was accomplished through the electrochem. redn. of 4-hydroxyphenyldiazonium. The latter forms a very thin layer on the glassy carbon with hydroxyl groups, through which the sol-gel is attached. This mol. glue improves the adhesion of thin layers of sol-gel to a carbonaceous surface. [on SciFinder(R)]},
	keywords = {hydroxyphenyldiazonium electrochem redn glue sol gel film glassy carbon},
	isbn = {0942-9352},
	author = {Shapiro, Leora and Mandler, Daniel.}
}
@article {6938,
	title = {A novel electrochemically synthesized biodegradable thin film of polypyrrole-polyethylene glycol-polylactic acid nanoparticles.},
	journal = {New J. Chem.New Journal of Chemistry},
	volume = {31},
	number = {1},
	year = {2007},
	note = {CAPLUS AN 2007:15899(Journal)},
	month = {2007///},
	pages = {163 - 168},
	publisher = {Royal Society of Chemistry},
	abstract = {Nanoparticles having reactive pyrrole residues were prepd. from poly(1-ethoxyethyl glycidyl ether)-block-poly(L,L-lactide) block copolymer. The nanoparticles were electropolymd. in aq. media through the oxidn. of the pyrrole residue and in the presence of pyrrole to form a nanocomposite thin film. The novel synthesis of these pyrrole-functionalized nanoparticles is described and the electrochem. deposition of the corresponding coating is characterized using electrochem., SEM and EDX. [on SciFinder(R)]},
	keywords = {pyrrole substituted ethoxyethyl glycidyl ether lactide block copolymer electropolymn},
	isbn = {1144-0546},
	author = {Shustak, Galit and Gadzinowski, Mariusz and Slomkowski, Stanislaw and Domb, Abraham J. and Mandler, Daniel.}
}
@article {6937,
	title = {Preparation and characterization of ultra-thin sol-gel films.},
	journal = {Thin Solid FilmsThin Solid Films},
	volume = {515},
	number = {11},
	year = {2007},
	note = {CAPLUS AN 2007:213616(Journal)},
	month = {2007///},
	pages = {4624 - 4628},
	publisher = {Elsevier B.V.},
	abstract = {The formation and characterization of nanometer thick sol-gel films are reported. The films were prepd. by spin-coating of a dild. soln. of a silane precursor on a no. of different substrates. The effect of diln., rotation speed and nature of substrate on the thickness and homogeneity of the films was examd. Characterization of the films was carried out by profilometry, reflectance spectroscopy, at. force microscopy, adhesion test and electrochem. We find that the diln. factor has a pronounced effect on the film thickness. Moreover, the time of diln., namely, whether diln. was carried out before or after a period of hydrolysis, has a noticeable effect on the thickness as well as on the permeability of embedded species. [on SciFinder(R)]},
	keywords = {silica film thickness homogeneity sol gel process substrate},
	isbn = {0040-6090},
	author = {Shapiro, Leora and Marx, Sharon and Mandler, Daniel.}
}
@article {6933,
	title = {Preparation, characterization and applications of ultrathin cellulose acetate Langmuir-Blodgett films.},
	journal = {Soft MatterSoft Matter},
	volume = {3},
	number = {8},
	year = {2007},
	note = {CAPLUS AN 2007:775775(Journal)},
	month = {2007///},
	pages = {1053 - 1063},
	publisher = {Royal Society of Chemistry},
	abstract = {The prepn. and characterization of mono- and multilayers of cellulose acetate (CA) Langmuir-Blodgett films on indium tin oxide and gold surfaces were studied in detail for the first time. These layers were characterized by their thickness, wettability, morphol. and structure using various surface techniques. The thickness of a monolayer of CA based on XPS measurement was one nanometer. Multilayers of CA Langmuir films were homogeneously transferred onto solid surfaces. The permeation of different mols. across these films was studied using electrochem. in various redox solns. Our findings suggest that a membrane like structure is formed, which is less permeable as the no. of layers increases. Finally, potential applications of these ultrathin films as supports for accommodating biomols. or metal nanoparticles are presented. [on SciFinder(R)]},
	keywords = {cellulose acetate monolayer Langmuir film permeation nanoparticle support},
	isbn = {1744-683X},
	author = {Cohen-Atiya, Meirav and Vadgama, Pankaj and Mandler, Daniel.}
}
@article {6929,
	title = {Self-assembled monolayers on Au microelectrodes.},
	journal = {Electrochem. Commun.Electrochemistry Communications},
	volume = {9},
	number = {12},
	year = {2007},
	note = {CAPLUS AN 2007:1346478(Journal)},
	month = {2007///},
	pages = {2827 - 2832},
	publisher = {Elsevier B.V.},
	abstract = {Long chain alkanethiols self-assembled monolayers (SAMs) formed on Au microelectrodes showed higher sensitivity towards defects than the same monolayers on macroelectrodes. The anal. of cyclic voltammetry and electrochem. impedance spectroscopy (EIS) expts. performed on covered microelectrodes were consistent with the formation of pinholes of about 10 nm in diam. Moreover, the EIS data exhibited a specific behavior that was interpreted invoking the short circuiting of the pinholes impedance by the surrounding surface of the microelectrode in the high frequency domain, whereas in the low frequencies, the surface covered by the SAM was assume to act as an insulator. [on SciFinder(R)]},
	keywords = {self assembled monolayers gold microelectrode alkanethiols},
	isbn = {1388-2481},
	author = {Sheffer, Marisa and Vivier, Vincent and Mandler, Daniel.}
}
@article {6934,
	title = {Structural insight on organosilica electrodes for waste-free alcohol oxidations.},
	journal = {Catal. Lett.Catalysis Letters},
	volume = {114},
	number = {1-2},
	year = {2007},
	note = {CAPLUS AN 2007:465029(Journal)},
	month = {2007///},
	pages = {55 - 58},
	publisher = {Springer},
	abstract = {Org. modification of sol-gel catalytic glassy electrodes made of a thin layer of organosilica doped with nitroxyl radical TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) crucially enhances stability in the waste-free oxidn. of alcs. to carbonyls in H2O. Structural comparison between analogous films made of organosilica and unmodified SiO2 shows that the origin of the pronounced stable activity of the ORMOSIL film lies in high hydrophobic and also in the pronounced low degree of hydrophilicity. [on SciFinder(R)]},
	keywords = {organosilica electrode wastefree alc oxidn, TEMPO organosilica electrode wastefree alc oxidn},
	isbn = {1011-372X},
	author = {Palmisano, Giovanni and Mandler, Daniel and Ciriminna, Rosaria and Pagliaro, Mario.}
}
@article {6941,
	title = {Characterization of n-alkanethiol self-assembled monolayers on mercury by impedance spectroscopy and potentiometric measurements.},
	journal = {J. Electroanal. Chem.Journal of Electroanalytical Chemistry},
	volume = {593},
	number = {1-2},
	year = {2006},
	note = {CAPLUS AN 2006:696886(Journal)},
	month = {2006///},
	pages = {227 - 240},
	publisher = {Elsevier B.V.},
	abstract = {Long chain n-alkanethiol self-assembled monolayers (SAMs) on a hanging Hg drop electrode were studied in detail for the 1st time by impedance spectroscopy (IS) and potentiometry. IS reveals the detailed behavior of the monolayers in the absence and presence of 2 1-electron redox couple: hexaammineruthenium(III) (Ru(NH3)63+) and tris(2,2{\textquoteright}-bipyridine)cobalt(III) (Co(bpy)33+). The pinholes-free layers behave as almost ideal capacitors and are permeable to some extent to redox species, depending on their hydrophobicity. Co(bpy)33+ that exhibits sluggish kinetics on a bare Hg electrode reveals a more facile kinetics than Ru(NH3)63+ on an n-octadecanethiol/Hg interface. Potentiometric measurements recorded upon immersing the bare and SAM modified Hg electrode into a soln. contg. a mixt. of the oxidized and reduced forms of the redox couples provide invaluable information on the charge transfer across the monolayer and its ohmic resistance. While Ru(NH3)63+ cannot freely penetrate into the monolayer and therefore establishes a p.d. across the monolayer; penetration of Co(bpy)32+ into the film causes the Fermi level of the Hg surface to attain the Nernst potential of the soln. Finally, increasing the length of the alkane chain of the thiols increases linearly the ohmic resistance of the layer. [on SciFinder(R)]},
	keywords = {alkanethiol self assembled monolayer mercury impedance spectroscopy, cobalt bipyridine complex electrochem redox reaction alkanethiol SAM mercury, ruthenium ammine complex electrochem redox reaction alkanethiol SAM mercury},
	author = {Cohen-Atiya, Meirav and Nelson, Andrew and Mandler, Daniel.}
}
@article {7093,
	title = {Complexation of ferrous and cupric ions by phenanthroline and terpyridine langmuir films},
	journal = {LangmuirLangmuir : the ACS journal of surfaces and colloids},
	volume = {22},
	number = {18},
	year = {2006},
	note = {MEDLINE AN 2006499707(Journal; Article; (JOURNAL ARTICLE))},
	month = {2006///},
	pages = {7462 - 4},
	abstract = {The complexation of Fe(II) and Cu(II) ions by phenanthroline and terpyridine-based Langmuir films was studied by the effect the added ions in the subphase on the isotherms. We found that Cu(II) had a pronounced effect on the isotherm consisting of phenanthroline moieties forming a square-planar 1:2 (Cu(II)/phenanthroline) complex. However, Fe(II) affected the isotherm made of 1:1 phenanthroline/terpyridine amphiphiles as a result of forming a pentacoordinate complex.[on SciFinder (R)]},
	isbn = {0743-7463},
	author = {Kraus, Shlomit and Mandler, Daniel}
}
@article {6940,
	title = {Complexation of Ferrous and Cupric Ions by Phenanthroline and Terpyridine Langmuir Films.},
	journal = {LangmuirLangmuir},
	volume = {22},
	number = {18},
	year = {2006},
	note = {CAPLUS AN 2006:753623(Journal)},
	month = {2006///},
	pages = {7462 - 7464},
	publisher = {American Chemical Society},
	abstract = {The complexation of FeII and CuII ions by phenanthroline and terpyridine-based Langmuir films was studied by the effect the added ions in the subphase on the isotherms. We found that CuII had a pronounced effect on the isotherm consisting of phenanthroline moieties forming a square-planar 1:2 (CuII/phenanthroline) complex. However, FeII affected the isotherm made of 1:1 phenanthroline/terpyridine amphiphiles as a result of forming a pentacoordinate complex. [on SciFinder(R)]},
	keywords = {complexation ferrous cupric ion phenanthroline terpyridine based Langmuir monolayer},
	isbn = {0743-7463},
	author = {Kraus, Shlomit and Mandler, Daniel.}
}
@article {7095,
	title = {The effect of surface attachment on ligand binding: studying the association of Mg2+, Ca2+ and Sr2+ by 1-thioglycerol and 1,4-dithiothreitol monolayers},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {8},
	number = {1},
	year = {2006},
	note = {MEDLINE AN 2006095325(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2006///},
	pages = {158 - 64},
	abstract = {The difference in the heterogeneous binding of Mg(2+), Ca(2+) and Sr(2+) ions by 1-thioglycerol (TG) and 1,4-dithiothreitol (DTT) spontaneously adsorbed monolayers on Au has been studied following the changes in the double layer capacity. A mathematical treatment, based on calculating the electrochemical potential difference at the monolayer-electrolyte interface, has followed our recent work which dealt with the acid-base equilibrium at the interface as a means of calculating the pK of ionizable SAMs and their binding with Cd(2+). Experimentally, spontaneously adsorbed monolayers of TG and DTT were assembled on Au surfaces and studied by impedance spectroscopy and alternating current voltammetry (ACV). The capacity was measured for each of the modified surfaces at increasing concentrations of the divalent metal ions separately. The goal of this study has been to examine the effect of metal ion binding by similar ligands that are differently attached onto the surface. TG and DTT monolayers differ in their flexibility, which is a result of their attachment to the surface through one and two arms, respectively. The general trend of the apparent heterogeneous association constants of the divalent metal ions, which were calculated from the capacity measurements, was substantially different from the classical Irving-Williams series that is applicable to homogeneous systems. This difference could be nicely explained by the reduction of the degree of freedom and flexibility of the attached ligands.[on SciFinder (R)]},
	isbn = {1463-9076},
	author = {Burshtain, Doron and Mandler, Daniel}
}
@article {6944,
	title = {The effect of surface attachment on ligand binding: studying the association of Mg2+, Ca2+ and Sr2+ by 1-thioglycerol and 1,4-dithiothreitol monolayers.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {8},
	number = {1},
	year = {2006},
	note = {CAPLUS AN 2005:1317465(Journal)},
	month = {2006///},
	pages = {158 - 164},
	publisher = {Royal Society of Chemistry},
	abstract = {The difference in the heterogeneous binding of Mg2+, Ca2+ and Sr2+ ions by 1-thioglycerol (TG) and 1,4-dithiothreitol (DTT) spontaneously adsorbed monolayers on Au has been studied following the changes in the double layer capacity. A math. treatment, based on calcg. the electrochem. p.d. at the monolayer-electrolyte interface, has followed our recent work1 which dealt with the acid-base equil. at the interface as a means of calcg. the pK of ionizable SAMs and their binding with Cd2+. Exptl., spontaneously adsorbed monolayers of TG and DTT were assembled on Au surfaces and studied by impedance spectroscopy and a.c. voltammetry (ACV). The capacity was measured for each of the modified surfaces at increasing concns. of the divalent metal ions sep. The goal of this study has been to examine the effect of metal ion binding by similar ligands that are differently attached onto the surface. TG and DTT monolayers differ in their flexibility, which is a result of their attachment to the surface through one and two arms, resp. The general trend of the apparent heterogeneous assocn. consts. of the divalent metal ions, which were calcd. from the capacity measurements, was substantially different from the classical Irving-Williams series2-4 that is applicable to homogeneous systems. This difference could be nicely explained by the redn. of the degree of freedom and flexibility of the attached ligands. [on SciFinder(R)]},
	keywords = {adsorption alk earth metal ion thioglycerol dithiothreitol SAM gold},
	isbn = {1463-9076},
	author = {Burshtain, Doron and Mandler, Daniel.}
}
@booklet {6943,
	title = {Modified conductive surfaces having active substances attached thereto and uses thereof.},
	howpublished = {PCT Int. Appl.},
	number = {WO2006008739A2},
	year = {2006},
	note = {CAPLUS AN 2006:79895(Patent)},
	month = {2006/01/26/},
	pages = {120 pp.},
	publisher = {Elutex Ltd., Israel .},
	abstract = {Novel processes for coating metal surfaces and/or for attaching active substances to metal surfaces, objects having coated metal surfaces and/or active substances attached thereto and uses thereof in the prepn. of implantable devices are disclosed. Thus, cyclic voltammetry of a stainless steel electrode in an acetonitrile soln. contg. 0.1 mM decanoic acid was performed to give a self-assembled monolayer on the electrode, showing advancing contact angle 59{\textdegree} and receding contact angle 45{\textdegree}. [on SciFinder(R)]},
	keywords = {decanoic acid selfassembled monolayer coating stainless steel cyclic voltammetry, modified conductive surface having active substance attached use},
	author = {Domb, Abraham J. and Mandler, Daniel and Danziger, Ishaiahu and Orom, Miriam and Okner, Regina and Shustak, Galit and Swed, Avi and Tal, Noam.}
}
@article {7094,
	title = {n-Alkanoic acid monolayers on 316L stainless steel promote the adhesion of electropolymerized polypyrrole films},
	journal = {LangmuirLangmuir : the ACS journal of surfaces and colloids},
	volume = {22},
	number = {12},
	year = {2006},
	note = {MEDLINE AN 2006305864(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2006///},
	pages = {5237 - 40},
	abstract = {The formation of a self-assembled monolayer significantly promotes the adhesion of electrodeposited polypyrrole on stainless steel. The monolayer affects the nucleation and growth mechanism of polypyrrole as a result of its hydrophobic nature. This was confirmed by analyzing current-time transients of the initial stages of electropolymerization and was in agreement with AFM images.[on SciFinder (R)]},
	isbn = {0743-7463},
	author = {Shustak, Galit and Domb, Abraham J. and Mandler, Daniel}
}
@article {6942,
	title = {n-Alkanoic Acid Monolayers on 316L Stainless Steel Promote the Adhesion of Electropolymerized Polypyrrole Films.},
	journal = {LangmuirLangmuir},
	volume = {22},
	number = {12},
	year = {2006},
	note = {CAPLUS AN 2006:447734(Journal)},
	month = {2006///},
	pages = {5237 - 5240},
	publisher = {American Chemical Society},
	abstract = {The formation of a self-assembled monolayer significantly promotes the adhesion of electrodeposited polypyrrole on stainless steel. The monolayer affects the nucleation and growth mechanism of polypyrrole of its hydrophobic nature. This was confirmed by analyzing current-time transients of the initial stages of electropolymn. and was in agreement with AFM images. [on SciFinder(R)]},
	keywords = {alkanoic acid monolayer stainless steel adhesion electropolymerized polypyrrole film, pyrrole electrochem polymn decanoic acid SAM stainless steel},
	isbn = {0743-7463},
	author = {Shustak, Galit and Domb, Abraham J. and Mandler, Daniel.}
}
@article {7092,
	title = {Studying electron transfer through alkanethiol self-assembled monolayers on a hanging mercury drop electrode using potentiometric measurements},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {8},
	number = {38},
	year = {2006},
	note = {MEDLINE AN 2006572179(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2006///},
	pages = {4405 - 9},
	abstract = {A new approach based on measuring the change of the open-circuit potential (OCP) of a hanging mercury drop electrode (HMDE), modified with alkanethiols of different chain length conducted in a solution containing a mixture of Ru(NH3)6(2+) and Ru(NH3)6(3+) is used for studying electron transfer across the monolayer. Following the time dependence of the OCP allowed the extraction of the kinetic parameters, such as the charge transfer resistance (R(ct)) and the electron transfer rate constant (k(et)), for different alkanethiol monolayers. An electron tunneling coefficient, beta, of 0.9 A(-1) was calculated for the monolayers on Hg.[on SciFinder (R)]},
	isbn = {1463-9076},
	author = {Cohen-Atiya, Meirav and Mandler, Daniel}
}
@article {6939,
	title = {Studying electron transfer through alkanethiol self-assembled monolayers on a hanging mercury drop electrode using potentiometric measurements.},
	journal = {Phys. Chem. Chem. Phys.Physical Chemistry Chemical Physics},
	volume = {8},
	number = {38},
	year = {2006},
	note = {CAPLUS AN 2006:990202(Journal)},
	month = {2006///},
	pages = {4405 - 4409},
	publisher = {Royal Society of Chemistry},
	abstract = {A new approach based on measuring the change of the open-circuit potential (OCP) of a hanging Hg drop electrode (HMDE), modified with alkanethiols of different chain length conducted in a soln. contg. a mixt. of Ru(NH3)62+ and Ru(NH3)63+ is used for studying electron transfer across the monolayer. Following the time dependence of the OCP allowed the extn. of the kinetic parameters, such as the charge transfer resistance (Rct) and the electron transfer rate const. (ket), for different alkanethiol monolayers. An electron tunneling coeff., β, of 0.9 {\r A}-1 was calcd. for the monolayers on Hg. [on SciFinder(R)]},
	keywords = {electron transfer alkanethiol SAM hanging mercury drop electrode potentiometry, kinetics electron transfer alkanethiol SAM hanging mercury drop electrode, open circuit potential mercury electrode modified alkanethiol},
	isbn = {1463-9076},
	author = {Cohen-Atiya, Meirav and Mandler, Daniel.}
}
@article {7097,
	title = {Chiral electrochemical recognition by very thin molecularly imprinted sol-gel films},
	journal = {LangmuirLangmuir : the ACS journal of surfaces and colloids},
	volume = {21},
	number = {17},
	year = {2005},
	note = {MEDLINE AN 2005424800(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2005///},
	pages = {7842 - 7},
	abstract = {Thin films with enantioselective properties for electrochemically active chiral probes were developed. Enantioselectivity was accomplished via molecular imprinting. The films were fabricated through the sol-gel technique and were spin-coated on ITO electrodes. The chiral selectivity recognition was detected using two enantiomer pairs: D- and L-3,4-dihydroxyphenylalanine (D- and L-dopa) and (R)- and (S)-N,N{\textquoteright}-dimethylferrocenylethylamine [(R)-Fc and (S)-Fc]. A defined chiral cavity was obtained by selection of functional monomers that interact with the template molecule, followed by its removal. Chiral selection properties were measured by cyclic voltammetry and square wave voltammetry. For both template molecules, very good chiral recognition was revealed by electrochemical measurement. The nonspecific adsorption measured for reference nonimprinted films was negligible (less than 5\%). Dopa imprinted films revealed both high sensitivity, by the detection of 1 nM (0.2 ppb) concentration, and excellent selectivity, when challenged with a series of catechol derivatives. Fc-imprinted films were able to detect ca. 2 ppm of the target molecule, with very good enantioselectivity and low nonspecific adsorption. To our knowledge, this is the first report of successful molecular imprinting of a ferrocene derivative.[on SciFinder (R)]},
	isbn = {0743-7463},
	author = {Fireman-Shoresh, Sharon and Turyan, Iva and Mandler, Daniel and Avnir, David and Marx, Sharon}
}
@article {7099,
	title = {Daniel Mandler, Hebrew University of Jerusalem},
	journal = {AnalystThe Analyst},
	volume = {130},
	number = {2},
	year = {2005},
	note = {MEDLINE AN 2005099412(Biography; Historical; (INTERVIEW); (PORTRAITS))},
	month = {2005///},
	pages = {131 - 3},
	isbn = {0003-2654},
	author = {Mandler, Daniel}
}
@article {7088,
	title = {Identification of firearms handling by the [Fe(PDT)(3)](2+) complex: Chemical and time-dependent factors},
	journal = {TalantaTalanta},
	volume = {67},
	number = {2},
	year = {2005},
	note = {MEDLINE AN 2008705149(Journal; Article; (JOURNAL ARTICLE))},
	month = {2005///},
	pages = {328 - 33},
	abstract = {Handling of a gun results in the formation of invisible impressions, caused by transfer of iron traces to the skin surface. Visualization of these impressions is possible by spraying the palms with a solution of 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine (PDT), which forms a magenta complex with iron(II) residues. Hence, mark intensity is directly related to the amounts of iron transferred to the palm. Palmar sweat plays a major role in iron transfer from the firearm to the hand. More factors, however, are involved in this process. Three time-dependent factors have been studied with relation to their effect on the developed mark: the gripping duration of the weapon; the time elapsed from the contact; and the rate of iron dissolution in aqueous solutions containing sweat components in physiological concentrations. We found that the amounts of iron transferred to the palm depend on both, the gripping period and the levels of palmar moisture. Thus, only a few seconds of gripping were required for developing good marks (corresponding to 80ngcm(-2) of iron) on highly-moistured hands, much longer gripping periods were necessary for developing marks of similar intensity on relatively dry hands. Experiments that aimed at studying the effect of sweat components on metallic iron dissolution were carried out in aqueous solutions. It was found that chloride ions in physiological concentrations remarkably enhanced the dissolution, while l-serine, the major amino acid in palmar sweat, had a detrimental effect on this process. Urea, another sweat component, had only a minor effect on the dissolution rate.[on SciFinder (R)]},
	isbn = {1873-3573},
	author = {Avissar, Yaniv Y. and Sagiv, Assaf E. and Mandler, Daniel and Almog, Joseph}
}
@article {7096,
	title = {Scanning electrochemical microscopy as a probe of Ag+ binding kinetics at Langmuir phospholipid monolayers},
	journal = {Phys Chem Chem PhysPhysical chemistry chemical physics : PCCP},
	volume = {7},
	number = {15},
	year = {2005},
	note = {MEDLINE AN 2005516447(Journal; Article; (JOURNAL ARTICLE); (RESEARCH SUPPORT, NON-U.S. GOV{\textquoteright}T))},
	month = {2005///},
	pages = {2955 - 64},
	abstract = {A new method has been developed for measuring local adsorption rates of metal ions at interfaces based on scanning electrochemical microscopy (SECM). The technique is illustrated with the example of Ag+ binding at Langmuir phospholipid monolayers formed at the water/air interface. Specifically, an inverted 25 microm diameter silver disc ultramicroelectrode (UME) was positioned in the subphase of a Langmuir trough, close to a dipalmitoyl phosphatidic acid (DPPA) monolayer, and used to generate Ag+ via Ag electro-oxidation. The method involved measuring the transient current-time response at the UME when the electrode was switched to a potential to electrogenerate Ag+. Since the Ag+/Ag couple is reversible, the response is highly sensitive to local mass transfer of Ag+ away from the electrode, which, in turn, is governed by the interaction of Ag+ with the monolayer. The methodology has been used to determine the influence of surface pressure on the adsorption of Ag+ ions at a phospholipid (dipalmitoyl phosphatidic acid) Langmuir monolayer. It is shown that the capacity for metal ion adsorption at the monolayer increased as the density of surface adsorption sites increased (by increasing the surface pressure). A model for mass transport and adsorption in this geometry has been developed to explain and characterise the adsorption process.[on SciFinder (R)]},
	isbn = {1463-9076},
	author = {Burt, David P. and Cervera, Javier and Mandler, Daniel and Macpherson, Julie V. and Manzanares, Jose A. and Unwin, Patrick R.}
}
