Charge carrier transport in thin conjugated polymer films: influence of morphology and polymer/substrate interactions

被引:6
|
作者
Dong, Ban Xuan [1 ]
Wenderott, J. K. [1 ]
Green, Peter F. [1 ,2 ]
机构
[1] Univ Michigan, Biointerfaces Inst, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[2] Natl Renewable Energy Lab, 15013 Denver W Pkwy, Golden, CO 80401 USA
关键词
Conjugated polymers; Charge transport; Thickness dependence; Band bending; Polymer; substrate interactions; PULSED-LASER EVAPORATION; INDIUM-TIN-OXIDE; SELF-ASSEMBLED MONOLAYERS; FIELD-EFFECT MOBILITY; DENSITY-OF-STATES; MOLECULAR-WEIGHT; SEMICONDUCTING POLYMERS; MACROSCOPIC ALIGNMENT; GLASSY POLYARYLATE; GAS-PERMEABILITY;
D O I
10.1007/s00396-020-04725-1
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 performance of conjugated polymer (CP)-based electronic devices relies on optimal charge carrier mobilities, which are determined by monomeric architecture, degree of polymerization, chain conformation, and the nano- and mesoscale morphologies. With regard to the latter, we discuss two effects that have received limited attention in the literature, yet important for device performance optimization: (1) the role of morphological disorder and of CP/substrate interactions on the in-plane and out-of-plane carrier transport in CPs; (2) the impact of morphological disorder on charge transfer at the CP/substrate interface. The emergence of film thickness-dependent carrier mobilities, varying over two orders of magnitude within a length scale of 200 nm, and band-bending phenomena, extending tens of nanometers within the CP, are associated with these effects. These findings suggest areas for further research in order to enable widespread applications of next-generation CP-based devices.
引用
收藏
页码:439 / 456
页数:18
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