Charge-transport model for conducting polymers

被引:0
|
作者
Kang, Stephen Dongmin [1 ,2 ]
Snyder, G. Jeffrey [1 ,2 ]
机构
[1] CALTECH, Dept Appl Phys & Mat Sci, Pasadena, CA 91125 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
关键词
MOBILITY; DISORDER; SEMICONDUCTORS; THERMOPOWER; COEFFICIENT; PERCOLATION;
D O I
10.1038/NMAT4784
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
The growing technological importance of conducting polymers makes the fundamental understanding of their charge transport extremely important for materials and process design. Various hopping and mobility edge transport mechanisms have been proposed, but their experimental verification is limited to poor conductors. Now that advanced organic and polymer semiconductors have shown high conductivity approaching that of metals, the transport mechanism should be discernible by modelling the transport like a semiconductor with a transport edge and a transport parameters. Here we analyse the electrical conductivity and Seebeck coefficient together and determine that most polymers (except possibly PEDOT:tosylate) haves = 3 and thermally activated conductivity, whereas s = 1 and itinerant conductivity is typically found in crystalline semiconductors and metals. The different transport in polymers may result from the percolation of charge carriers from conducting ordered regions through poorly conducting disordered regions, consistent with what has been expected from structural studies.
引用
收藏
页码:252 / 257
页数:6
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