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Lattice Vibrations and Time-Dependent Evolution of Local Phonon Modes during Exciton Formation in Conjugated Polymeric Molecules

机译:在共轭聚合物分子中激子形成过程中局部声子模式的晶格振动和时间依赖性演化

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摘要

Based on nonadiabatic molecular dynamics that integrate electronic transitions with the time-dependent phonon spectrum, this article provides a panoramic landscape of the dynamical process during the formation of photoinduced excitons in conjugated polymers. When external optical beam/pulses with intensities of 10 µJ/cm2 and 20 µJ/cm2 are utilized to excite a conjugated polymer, it is found that the electronic transition firstly triggers local lattice vibrations, which not only locally distort alternating bonds but change the phonon spectrum as well. Within the first 60 fs, the occurrence of local distortion of alternating bonds accompanies the localization of the excited-state’s electron. Up to 100 fs, both alternating bonds and the excited electronic state are well localized in the middle of the polymer chain. In the first ~200 fs, the strong lattice vibration makes a local phonon mode at 1097.7 cm−1 appear in the phonon spectrum. The change of electron states then induces the self-trapping effect to act on the following photoexcitation process of 1.2 ps. During the following relaxation of 1.0 ps, new local infrared phonon modes begin to occur. All of this, incorporated with the occurrence of local infrared phonon modes and localized electronic states at the end of the relaxation, results in completed exciton formation.
机译:基于将电子转换与时间依赖性声谱谱集成的非气化分子动力学,本文提供了在共轭聚合物中形成光致谐波期间动态过程的全景景观。当利用具有10μJ/ cm2和20μJ/ cm2的强度的外部光束/脉冲来激发共轭聚合物时,发现电子转变首先触发局部晶格振动,这不仅局部扭曲交替键,而是改变声子光谱也是如此。在前60 fs内,交替键的局部变形的发生伴随着激发状态的电子的定位。最多100 fs,交替键和激发的电子状态良好地定位在聚合物链的中间。在第一个〜200 fs中,强的格子振动在1097.7cm-1中出现在1097.7cm-1的局部声子模式。然后,电子状态的变化诱导自捕集效果,以对1.2 ps的以下光透视过程起作用。在以下放宽1.0 ps期间,新的本地红外声子模式开始发生。所有这些都包含在放松结束时局部红外声子模式和局部电子状态的发生,导致完成的激子形成。

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