Exciton transfer integrals between polymer chains

被引:73
作者
Barford, William [1 ]
机构
[1] Univ Oxford, Phys Theoret Chem Lab, Oxford OX1 3QZ, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1063/1.2714516
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 line-dipole approximation for the evaluation of the exciton transfer integral J between conjugated polymer chains is rigorously justified. Using this approximation, as well as the plane-wave approximation for the exciton center-of-mass wave function, it is shown analytically that J similar to L when the chain lengths are smaller than the separation between them, or J similar to L-1 when the chain lengths are larger than their separation, where L is the chain length. Scaling relations are also obtained numerically for the more realistic standing wave approximation for the exciton center-of-mass wave function, where it is found that for chain lengths larger than their separation J similar to L-1.8 or J similar to L-2, for parallel or collinear chains, respectively. These results have important implications for the photophysics of conjugated polymers and self-assembled molecular systems, as the Davydov splitting in aggregates and the Forster transfer rate for exciton migration decrease with chain lengths larger than their separation. This latter result has obvious deleterious consequences for the performance of polymer photovoltaic devices. (c) 2007 American Institute of Physics.
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页数:6
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