Anomalous Charge Transport in Conjugated Polymers Reveals Underlying Mechanisms of Trapping and Percolation

被引:32
|
作者
Mollinger, Sonya A. [1 ]
Salleo, Alberto [1 ]
Spakowitz, Andrew J. [1 ,2 ,3 ,4 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[4] Stanford Univ, Biophys Program, Stanford, CA 94305 USA
关键词
ELECTRIC-FIELD DEPENDENCE; SEMICONDUCTING POLYMERS; MOLECULAR-WEIGHT; HOPPING CONDUCTION; HIGH-EFFICIENCY; HOLE TRANSPORT; DRIFT MOBILITY; SOLAR-CELLS; DISORDER; PERFORMANCE;
D O I
10.1021/acscentsci.6b00251
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While transport in conjugated polymers has many similarities to that in crystalline inorganic materials, several key differences reveal the unique relationship between the morphology of polymer films and the charge mobility. We develop a model that directly incorporates the molecular properties of the polymer film and correctly predicts these unique transport features. At low degree of polymerization, the increase of the mobility with the polymer chain length reveals trapping at chain ends, and saturation of the mobility at high degree of polymerization results from conformational traps within the chains. Similarly, the inverse field dependence of the mobility reveals that transport on single polymer chains is characterized by the ability of the charge to navigate around kinks and loops in the chain. These insights emphasize the connection between the polymer conformations and the transport and thereby offer a route to designing improved device morphologies through molecular design and materials processing.
引用
收藏
页码:910 / 915
页数:6
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