Coordinative interactions in a dye-sensitized solar cell

被引:44
作者
Agrell, HG
Lindgren, J
Hagfeldt, A
机构
[1] Univ Uppsala, Dept Phys Chem, SE-75123 Uppsala, Sweden
[2] Univ Uppsala, Angstrom Lab, Dept Chem Mat, SE-75121 Uppsala, Sweden
关键词
dye-sensitized solar cell; Raman scattering; ligand exchange; mesoporous; nanostructured;
D O I
10.1016/j.jphotochem.2003.12.015
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
Resonance Raman scattering studies of a complete dye-sensitized solar cell (DSC) including iodine and lithium iodide in the electrolyte indicate that triiodide (I-3(-)) exchange the SCN- ligand of the dye bis(tetrabutylammonium) cis-bis(thiocyanato)bis(2,2'-bipyridine-4carboxylic acid, 4'-carboxylate)ruthenium(II). The choice of cation in the iodide salt influenced the ligand stability of the dye. It was proposed that an ion pair Li+ ... I-3(-) formation occurred which by a reduced electrostatic repulsion between I-3(-) and SCN- facilitated the exchange of these anions at Ru(II) of the dye. The additive 1-methylbenzimidazole (MBI) suppressed the SCN-/I-3(-) ligand exchange by forming a complex with Li+. The concentrations of Li+ and MBI have to be carefully balanced due to the SCN- ligand exchange with MBI in deficiency of Li+. In order to observe and understand the prevailing coordinative interactions between the components in a DSC, the use of characterization methods with which complete devices can be studied is necessary. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 27
页数:5
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