Breakdown of Polarons in Conducting Polymers at Device Field Strengths

被引:11
|
作者
Mahani, M. R. [1 ]
Mirsakiyeva, A. [1 ]
Delin, Anna [1 ,2 ,3 ]
机构
[1] KTH Royal Inst Technol, Dept Appl Phys, Sch Engn Sci, Electrum 229, SE-16440 Kista, Sweden
[2] Uppsala Univ, Dept Phys & Astron, Mat Theory Div, Box 516, SE-75120 Uppsala, Sweden
[3] KTH Royal Inst Technol, Swedish E Sci Res Ctr SeRC, SE-10044 Stockholm, Sweden
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2017年 / 121卷 / 19期
关键词
ELECTRIC-FIELD; CHARGE-TRANSPORT; CONJUGATED POLYMERS; DYNAMICS; SOLITONS; MOTION; ELECTROLUMINESCENCE; SEMICONDUCTORS; POLYACETYLENE; TEMPERATURE;
D O I
10.1021/acs.jpcc.7b02368
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
Conducting polymers have become standard engineering materials used in many electronic devices. Despite this, there is a lack of understanding of the microscopic origin of the conducting properties, especially at realistic device field strengths. We present simulations of doped poly(p-phenylene) (PPP) using a Su-Schrieffer-Heeger (SSH) tight-binding model, with the electric field included in the Hamiltonian through a time-dependent vector potential via Peierls substitution of the phase factor. We find that polarons typically break down within less than a picosecond after the field has been switched on, already for electric fields as low as around 1.6 mV/angstrom. This is a field strength common in many flexible organic electronic devices. Our results challenge the relevance of the polaron as charge carrier in conducting polymers for a wide range of applications.
引用
收藏
页码:10317 / 10324
页数:8
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