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Excitonic intraband relaxation and polarization anisotropies in PTCDA on femtosecond and picosecond timescales

机译:飞秒和皮秒时间尺度上PTCDA中的激子带内弛豫和极化各向异性

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We report on investigations of optical excitations in polycrystalline organic molecular crystals with quasi-1D-stacked crystal structure and negative exciton dispersion. As model system, we choose thin films of the perylene derivative 3,4,9, 10-perylenetetracarboxylic dianhydride (PTCDA). Using pump-probe spectroscopy, we show how the relaxation from the absorbing state towards the border of the Brillouin zone occurs on a 120 fs timescale. Time-resolved luminescence anisotropy gives evidence that as a result of the coherent coupling between adjacent stacks, populations of the Davydovsplit states that are prepared during photo-excitation relax into the emitting states in less than 5 ps. The behavior of the luminescence anisotropy can be explained by the orientation of the two PTCDA molecules in the unit cell. However, a full understanding of the ultrafast pump-probe anisotropy requires novel explanations beyond current models. (c) 2004 Elsevier B.V. All rights reserved.
机译:我们报告了对具有准1D堆叠晶体结构和负激子色散的多晶有机分子晶体中光激发的研究。作为模型系统,我们选择the衍生物3,4,9,10-per四羧酸二酐(PTCDA)的薄膜。使用泵浦探针光谱,我们显示了在120 fs的时间尺度上从吸收态到布里渊区边界的弛豫是如何发生的。时间分辨的发光各向异性证明,由于相邻堆叠之间的相干耦合,在光激发过程中制备的Davydovsplit态的种群在不到5 ps的时间内弛豫到了发射态。发光各向异性的行为可以通过两个PTCDA分子在晶胞中的取向来解释。但是,要全面了解超快泵浦探针各向异性,还需要超越当前模型的新颖解释。 (c)2004 Elsevier B.V.保留所有权利。

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