N-Methyl-N-Allylpyrrolidinium Based Ionic Liquids for Solvent-Free Dye-Sensitized Solar Cells

被引:42
作者
Cai, Ning [1 ,2 ]
Zhang, Jing [1 ]
Zhou, Difei [1 ,2 ]
Yi, Zhihui [1 ]
Guo, Jin [1 ]
Wang, Peng [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
美国国家科学基金会;
关键词
INTENSITY-MODULATED PHOTOVOLTAGE; PLASTIC CRYSTAL ELECTROLYTE; TEMPERATURE MOLTEN-SALTS; BAND-EDGE MOVEMENT; CHARGE-TRANSPORT; CONVERSION EFFICIENCY; PYRROLIDINIUM CATIONS; BACK-REACTION; LIX MIXTURES; VISCOSITY;
D O I
10.1021/jp810973q
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We prepared four new ionic liquids consisting of N-methyl-N-allylpyrrolidinium cation in conjunction with anions including iodide, nitrate, thiocyanate, and dicyanamide, respectively, and measured their physical properties of density, viscosity, and conductivity. Owing to the relatively lower melting point of electroactive N-methyl-N-allylpyrrolidinium iodide, in combination with three other nonelectroactive ionic liquids, we could construct solvent-free electrolytes possessing high iodide concentrations for dye-sensitized solar cells. We correlated temperature-dependent electrolyte viscosity with molar conductivity and triiodide mobility through applying an empirical Walden's rule and a modified Stokes-Einstein equation, respectively. We have further found that these anions (nitrate, thiocyanate, and dicyanamide) have different influences on surface states and electron transport in the mesoporous titania film, resulting in different photovoltages and photocurrents of dye-sensitized solar cells.
引用
收藏
页码:4215 / 4221
页数:7
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