What determines the mobility of charge carriers in conjugated polymers?

被引:69
作者
Laquai, Frederic
Wegner, Gerhard
Baessler, Heinz
机构
[1] Univ Marburg, Fachbereich Chem, D-35032 Marburg, Germany
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2007年 / 365卷 / 1855期
关键词
time-resolved photoconductivity; hopping transport; conjugated polymers;
D O I
10.1098/rsta.2007.2027
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In a conjugated polymer, the mobility of charge carriers is not a well-defined coefficient of a particular material as it is in an inorganic crystalline semiconductor but depends on the time domain of detection. On a time-scale of typically 100 fs, the on-chain mobility is ultra-high and controlled by the electronic band width of the polymer chain. When a carrier hits a chain imperfection, subsequent mesoscopic on-chain motion is retarded and controlled by intrachain disorder to which the chain environment contributes. Macroscopic transport commences after a time when interchain carrier jumps become rate limiting. It is routinely probed by time-of-flight experiments and can be rationalized in terms of random walk within a rough energy landscape. Experimental signatures of the various modes of transport are discussed.
引用
收藏
页码:1473 / 1487
页数:15
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