Photogeneration in an acceptor-type poly(phenylenevinylene)

被引:7
作者
Hertel, D
Bässler, H
Möller, S
Tillmann, H
Hörhold, HH
机构
[1] Univ Marburg, Inst Phys Nucl & Macromol Chem, D-35032 Marburg, Germany
[2] Univ Marburg, Ctr Mat Sci, D-35032 Marburg, Germany
[3] Univ Marburg, Dept Phys, D-35037 Marburg, Germany
[4] Univ Jena, Inst Organ & Macromol Chem, D-07743 Jena, Germany
来源
MOLECULAR CRYSTALS AND LIQUID CRYSTALS | 2001年 / 355卷
关键词
photoconductivity; poly(phenylene-vinylene) derivatives;
D O I
10.1080/10587250108023660
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stationary photoconduction in thin films of a cyano-phenylamine-substituted poly-phenylenevinylene, in both sandwich and gap arrangement, has been studied. In order to separate electrode from bulk effects a thin layer of SiOx could be inserted between the indium-tinoxide (ITO) electrode and the film. Photocurrents were measured as a function of electric field, temperature (100 to 300K), photon energy (2.5 to 5 eV) and polarity of the applied bias. The results indicate that for h upsilon P < 3.2 eV the photocurrent is a superposition of bulk ionization involving relaxed singlet excitons and, depending on the direction of the electric field, exciton induced injection of predominantly electrons from the ITO. For h<upsilon> > 3.2 eV intrinsic photogeneration from hot singlet excitons takes over.
引用
收藏
页码:175 / 190
页数:16
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