Redox Reaction Mechanisms with Non-triiodide Mediators in Dye-Sensitized Solar Cells by Redox Potential Calculations

被引:18
|
作者
Jono, Ryota [1 ]
Sumita, Masato [2 ,3 ]
Tateyama, Yoshitaka [2 ,3 ,4 ]
Yamashita, Koichi [1 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, Tsukuba, Ibaraki 3050044, Japan
[3] Japan Sci & Technol Agcy JST, CREST, Kawaguchi, Saitama 3330012, Japan
[4] Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3330012, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2012年 / 3卷 / 23期
关键词
DENSITY-FUNCTIONAL THEORY; ORGANIC-DYES; REGENERATION; OXIDATION; DESIGN; LIGHT; CONVERSION; COMPLEXES; SHUTTLE; IODIDE;
D O I
10.1021/jz301589a
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 investigate reaction mechanisms of the redox mediators in dye-sensitized solar cells through systematic calculations of redox potentials of possible cobalt complexes and iodides in acetonitrile solution by use of the thermodynamic cycle method with continuum solvent model. The calculated redox potentials were in good agreement with the experimental values, although the experimentalists used different reference electrodes. The maximum open circuit voltage (V-OC) of the mediators calculated in this work indicate that the I-2(center dot-)/2I(-) and I-2/I-2(center dot-) as well as the net I-2/2I(-) redox reactions can dominate at both photoanode and counter-electrode.
引用
收藏
页码:3581 / 3584
页数:4
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