Ultrafast conductivity in a low-band-gap polyphenylene and fullerene blend studied by terahertz spectroscopy

被引:24
作者
Nemec, Hynek [1 ,2 ]
Nienhuys, Han-Kwang [3 ]
Perzon, Erik [4 ]
Zhang, Fengling [5 ]
Inganas, Olle [5 ]
Kuzel, Petr [2 ]
Sundstrom, Villy [1 ]
机构
[1] Lund Univ, Dept Chem Phys, S-22241 Lund, Sweden
[2] Acad Sci Czech Republic, Inst Phys, Prague 18221, Czech Republic
[3] FOM, Inst Atom & Mol Phys, NL-1098 SJ Amsterdam, Netherlands
[4] Chalmers, Dept Chem & Biol Engn, S-41296 Gothenburg, Sweden
[5] Linkoping Univ, IFM, S-58153 Linkoping, Sweden
关键词
energy gap; fullerenes; hole mobility; Monte Carlo methods; photoconductivity; polymer blends; terahertz wave spectra; time resolved spectra; CHARGE-CARRIER MOBILITY; CONJUGATED POLYMERS; BULK HETEROJUNCTION; DYNAMICS; TIME; PHOTOGENERATION; POLYTHIOPHENE; TRANSPORT; DISORDER; CHAINS;
D O I
10.1103/PhysRevB.79.245326
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Time-resolved terahertz spectroscopy and Monte Carlo simulations of charge-carrier motion are used to investigate photoinduced transient conductivity in a blend of a low-band-gap polyphenylene copolymer and fullerene derivative. The optical excitation pulse generates free holes delocalized on polymer chains. We show that these holes exhibit a very high initial mobility as their initial excess energy facilitates their transport over defects (potential barriers) on polymer chains. The conductivity then drops down rapidly within 1 ps, and we demonstrate that this decrease occurs essentially by two mechanisms. First, the carriers loose their excess energy and they thus become progressively localized between the on-chain potential barriers-this results in a mobility decay with a rate of (180 fs)(-1). Second, carriers are trapped at defects (potential wells) with a capture rate of (860 fs)(-1). At longer time scales, populations of mobile and trapped holes reach a quasiequilibrium state and further conductivity decrease becomes very slow.
引用
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页数:8
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