Side chain effects on photoinduced absorption and photovoltaic performance of low bandgap thienylene vinylene and phenylene vinylene copolymers

被引:5
作者
Nguyen, L. H. [1 ]
Guenes, S.
Neugebauer, H.
Sariciftci, N. S.
Colladet, K.
Fourier, S.
Cleij, T. J.
Lutsen, L.
Gelan, J.
Vanderzande, D.
机构
[1] Johannes Kepler Univ Linz, Linz Inst Organ Solar Cells, Altenbergerstr 69, A-4040 Linz, Austria
[2] Hasselt Univ, Inst Mat Res, IMO, B-3590 Diepenbeek, Belgium
[3] IMEC, Div IMOMEC, B-3590 Diepenbeek, Belgium
关键词
D O I
10.1051/epjap:2006142
中图分类号
O59 [应用物理学];
学科分类号
摘要
In this work low bandgap thienylenevinylene and phenylene vinylene copolymers, which possess either 3,4-ethylenedioxylthiophene (EDOT) groups (Polymer 1) or long alkyl side chains (Polymer 2) were investigated and compared in photoinduced electron transfer properties and photovoltaic performance. The results show that the interaction of the photoexcited polymers with an electron acceptor ([6,6]-phenyl C61 - butyric acid methyl ester (PCBM)) leads to charge generation and transfer for both polymers. We found that the long alkyl side chain in Polymer 2 instead of the EDOT group in Polymer 1 enhances the open circuit voltage (VOC) but lowers the short circuit current (ISC). On the other hand the long alkyl side chain in Polymer 2 significantly improves the solubility and enhances processability for solar cells fabrication. Optimization of the chemical structure of these low bandgap polymers could lead to a spectral improvement of photocurrent generation in organic solar cells.
引用
收藏
页码:219 / 223
页数:5
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