Quasi solid state dye sensitized solar cells employing a polymer electrolyte and xanthene dyes

被引:53
作者
Sharma, G. D. [1 ]
Balraju, P. [1 ]
Kumar, Manish [1 ]
Roy, M. S. [2 ]
机构
[1] Jai Narain Vyas Univ, Dept Phys, Mol Elect & Optoelect Device Lab, Jadhpur 342005, Rajasthan, India
[2] Def Lab, Jodhpur 342011, Rajasthan, India
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2009年 / 162卷 / 01期
关键词
Quasi solid state solar cell; Photovoltaic effect; Ionic conductivity; Polymer electrolyte; ORGANIC-DYE; HIGHLY EFFICIENT; TETRAHYDROQUINOLINE DYES; IONIC LIQUID; CONVERSION; NANOPARTICLES; INCREASE; NETWORK; BEHAVIOR; LIGHT;
D O I
10.1016/j.mseb.2009.01.033
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series of organic dyes in the xanthene class namely Rose Bengal (RB), Eosin Y(EY) and Fluorescein sodium (FLU) were used as photo-sensitizer for nano-crystal line TiO2, for the application of quasi solid state dye sensitized solar cells. These dyes have same backbone with different number of electron acceptor groups. The dye with the highest number of electron acceptor group, i.e. 8 namely RB shows highest power conversion efficiency due the lower band gap and higher light harvesting efficiency (LHE). The ionic conductivity of polymer electrolyte used in quasi solid state DSSC was examined in terms of polymer content and redox couple concentration. The dependence of photovoltaic performance of the solar cell on the polymer content in the electrolyte used in DSSC, was studied by current-voltage characteristics under illumination and electrochemical impedance spectroscopy (EIS). The result indicates the charge transfer behavior occurred at nano-crystalline TiO2/electrolyte and PEDOT: PSS/electrolyte interface plays an important role in influencing the photovoltaic performance of the device. The quasi solid state dye sensitized solar cell posseses a good long-term stability and power conversion efficiency is almost equal to that of DSSCs with liquid electrolyte. (C) 2009 Elsevier BIN. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
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