Photosensitization of ITO and nanocrystalline TiO2 electrode with a hemicyanine derivative

被引:65
作者
Wang, ZS
Huang, YY
Huang, CH [1 ]
Zheng, J
Cheng, HM
Tian, SJ
机构
[1] Peking Univ & UHK Joint Lab, Rare Earth, State Key Lab Rare Earth Math Chem & Applicat, Beijing 100871, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
photoelectric conversion; hemicyanine; sensitization; nanoparticle; TiO2;
D O I
10.1016/S0379-6779(00)00261-7
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The monochromophore (E)-N-Hexadecyl-4-(2-(4-diethylamino)phenyl)ethenyl) pyridinium stearate was synthesized. The LB film of the dye-modified ITO gives rise to cathodic photocurrent, while the dye-sensitized nanocrystalline TiO2 film generates anodic photocurrent. Having investigated some factors such as electron donor and acceptor, and bias voltage that may affect the magnitude of photocurrent and the direction of current flow, we proposed a mechanismic model for photocurrent generation. The quantum yield is about 0.2% for monolayer LB film-modified ITO electrode and 1.0% for the dye-sensitized nanocrystalline TiO2 film under irradiation of 469-nm light in 0.1 M KCl aqueous solution without applied potential. Under 100 mW/cm(2) illumination of simulated solar light, the dye-sensitized nanocrystalline TiO2 film generated greater than 1 mA/cm(2) of current density, which is comparatively high among the organic dyes. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:201 / 207
页数:7
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