Variable-Band-Gap Poly(arylene ethynylene) Conjugated Polyelectrolytes Adsorbed on Nanocrystalline TiO2: Photocurrent Efficiency as a Function of the Band Gap

被引:30
作者
Jiang, Hui [1 ]
Zhao, Xiaoyong [1 ]
Shelton, Abigail H. [1 ]
Lee, Seoung Ho [1 ]
Reynolds, John R. [1 ]
Schanze, Kirk S. [1 ]
机构
[1] Univ Florida, Ctr Macromol Sci & Engn, Dept Chem, Gainesville, FL 32611 USA
基金
美国能源部;
关键词
conjugated polyelectrolyte; band gap; charge transfer; dye sensitized solar cell; photocurrent generation; power conversion; SENSITIZED SOLAR-CELLS; PHOTOVOLTAIC CELLS; ENERGY-TRANSFER; POLYMER; LIGHT; ELECTRON; POLYTHIOPHENE; CONVERSION; COPOLYMERS; DEPENDENCE;
D O I
10.1021/am800089n
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A series of poly(arylene ethynylene) conjugated (CPEs) substituted with carboxylic acid side groups have been synthesized and characterized. The polymers feature a backbone consisting of a carboxylated dialkoxyphenylene 1, 4 ethynlene unit alternating with a second arylene ethynylene moiety of variable electron demand. The HOMO-LUMO gap is varied across the series giving rise to a set of four polymers that have absorption maxima ranging from 404 to 495 nm. The CPEs adsorb effectively from solution onto nanostructured TiO2 films giving rise to TiO2/CPe films that absorp similar to 90% of the incident light at the absorption band maximum. The photocurrent generation efficiency of the TiO2/CPE films was examined in a solar cell configuration using an propyoene carbonate electrolyte and a Pt/fluorine doped tin oxide counter electrode. Most of the films exhibit good photocurrent generation efficiency with a peak quantum efficiency of similar to 50% at wavelengths corresponding to the polymers absorption band maximum. Interestingly the photocurrent generation efficiency for the lowest band gap polymer is substantially lower compared to the other three systems. This effect is attributed to efficient nonradiative decay of excitons at trap sites arising from interchain contacts distel from the TiO2/CPE interface.
引用
收藏
页码:381 / 387
页数:7
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