Photoconduction in organic donor-acceptor systems

被引:17
|
作者
Im, C
Tian, W
Bässler, H
Fechtenkötter, A
Watson, MD
Müllen, K
机构
[1] Univ Marburg, Inst Phys Macromol & Nucl Chem, D-35032 Marburg, Germany
[2] Univ Marburg, Ctr Mat Sci, D-35032 Marburg, Germany
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2003年 / 119卷 / 07期
关键词
D O I
10.1063/1.1590954
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
Stationary photoconduction in either a phenyl-substituted poly-phenylenevinylene copolymer (PhPPV) or an alkylated hexa-peri-hexabenzocoronene (HBC) doped by perylenediimide (PdI) at a broad range of dopant concentrations has been measured and compared to previous results on PhPPV doped by trinitrofluorenone (TNF). At moderate concentration, the yield of the photogeneration is virtually invariant regardless of the system and blend ratio because practically every primary excitation dissociates at a donor-acceptor site and the subsequent escape from the coulombic potential is virtually system-independent. At dopant concentrations >10% the yield of that escape process increases by two to three orders of magnitude. (C) 2003 American Institute of Physics.
引用
收藏
页码:3952 / 3957
页数:6
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