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Interchain effects in the ultrafast photophysics of a semiconducting polymer: THz time-domain spectroscopy of thin films and isolated chains in solution

机译:半导体聚合物超快光物理中的链间效应:溶液中薄膜和分离链的太赫兹时域光谱

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摘要

We compare the generation and decay dynamics of charges and excitons in a model polymer semiconductor (MEH-PPV) in solution and drop-cast thin films, by recording the sub-ps transient complex conductivity using THz time-domain spectroscopy. The results show that the quantum efficiency of charge generation is two orders of magnitude smaller in solution (~10–5) than in the solid film (~10–3). The proximity of neighboring chains in the films apparently facilitates (hot) exciton dissociation, presumably by allowing the electron and hole to separate on different polymer strands. For both samples, photoexcitation leads to the predominant formation of bound charge pairs (excitons) that can be detected through their polarizability. Surprisingly, the polarizability per absorbed photon is a factor of 3 larger in solution than in the film, suggesting that interchain interactions in the film do not result in a substantial delocalization of the exciton wave function.
机译:通过使用THz时域光谱法记录亚ps瞬态复电导率,我们比较了溶液和滴铸薄膜中的模型聚合物半导体(MEH-PPV)中电荷和激子的产生和衰减动力学。结果表明,电荷产生的量子效率在溶液(〜10-5)中比在固态膜(〜10-3)中小两个数量级。薄膜中相邻链的接近显然促进了(热)激子离解,大概是通过让电子和空穴在不同的聚合物链上分离而实现的。对于两种样品,光激发都会导致结合电荷对(激子)的主要形成,可以通过其极化率来检测。出人意料的是,溶液中每个吸收光子的极化率是溶液中薄膜的3倍,这表明薄膜中的链间相互作用不会导致激子波函数发生明显的离域。

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