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Absorption profile and femtosecond intraband relaxation of the intense upper Davydov component in oligothiophenes

机译:寡噻吩中高浓度达维多夫组分的吸收曲线和飞秒带内弛豫

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摘要

The diffuse shape of the high-energy absorption band observed in oligothiophene crystals is interpreted in terms of Fano-type mixing between the discrete upper Davydov component at k?0 and the continuum of phonon-accompanied exciton states at other values of crystal momentum. In temporal domain, this mixing is viewed as a crystal version of radiationless transition, and is followed by subsequent intra-band exciton relaxation due to scattering processes with phonon release. The rates of energy dissipation in these latter processes, mediated by different intramolecular vibrational modes, are estimated from a simple expression based on the Fermi golden rule. Depopulation of long-lived vibronic intermediates, acting as bottlenecks, is attributed to thermally activated processes with absorption of low-frequency phonons. All essential input parameters are obtained from independent nonempirical calculations. The results are in excellent agreement both with the experimentally observed absorption band shapes and with energy-dependent femtosecond dynamics afforded by measurements of sexithiophene (6T) fluorescence and photoinduced absorption.
机译:寡聚噻吩晶体中观察到的高能吸收带的扩散形状是根据k≥0的离散上达维多夫分量与晶体动量其他值处的声子伴随激子态的连续体之间的Fano型混合来解释的。在时域中,这种混合被视为无辐射跃迁的晶体形式,并且由于声子释放的散射过程而导致随后的带内激子弛豫。这些后期过程中的能量耗散率是由不同的分子内振动模式介导的,是根据费米黄金定律从一个简单的表达式估算出来的。长寿命振动电子中间体的减少(作为瓶颈)归因于吸收低频声子的热活化过程。所有必要的输入参数均来自独立的非经验计算。该结果与实验观察到的吸收带形状以及通过测量六噻吩(6T)荧光和光致吸收所提供的能量依赖的飞秒动力学都非常吻合。

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