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时间分辨荧光光谱中相干波包激发态的振动光谱与黄-里斯因子

Vibrational Spectrum of an Excited State and Huang-Rhys Factors by Coherent Wave Packets in Time-Resolved Fluorescence Spectroscopy.

作者信息

Lee Gyeongjin, Kim Junwoo, Kim So Young, Kim Dong Eon, Joo Taiha

机构信息

Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, South Korea.

Physics Department, Center for Attosecond Science and Technology, and Max Planck Center for Attosecond Science, Pohang University of Science and Technology (POSTECH), Pohang, 37673, South Korea.

出版信息

Chemphyschem. 2017 Mar 17;18(6):670-676. doi: 10.1002/cphc.201601295. Epub 2017 Feb 2.

Abstract

Coherent nuclear wave packet motions in an electronic excited state of a molecule are measured directly by time-resolved spontaneous fluorescence spectroscopy with an unprecedented time resolution by using two-photon absorption excitation and fluorescence upconversion by noncollinear sum frequency generation. With an estimated time resolution of approximately 25 fs, wave packet motions of vibrational modes up to 1600 cm are recorded for coumarin 153 in ethanol. Two-color transient absorption at 13 fs time resolution are measured to confirm the result. Vibrational displacements between the ground and excited states and Huang-Rhys factors (HRFs) are calculated by quantum mechanical methods and are compared with the experimental results. HRFs calculated by density functional theory (DFT) and time-dependent DFT reproduce the experiment adequately. This fluorescence-based method provides a unique and direct way to obtain the vibrational spectrum of a molecule in an electronic excited state and the HRFs, as well as the dynamics of excited states, and it might provide information on the structure of an excited state through the HRFs.

摘要

通过使用双光子吸收激发和非共线和频产生的荧光上转换技术,以前所未有的时间分辨率,利用时间分辨自发荧光光谱法直接测量了分子电子激发态中的相干核波包运动。在乙醇中的香豆素153中,以约25 fs的估计时间分辨率记录了高达1600 cm的振动模式的波包运动。测量了13 fs时间分辨率的双色瞬态吸收以证实该结果。通过量子力学方法计算了基态和激发态之间的振动位移以及黄昆-里斯因子(HRFs),并与实验结果进行了比较。通过密度泛函理论(DFT)和含时DFT计算的HRFs充分再现了实验结果。这种基于荧光的方法提供了一种独特而直接的方式来获得分子电子激发态的振动光谱和HRFs,以及激发态的动力学,并且它可能通过HRFs提供有关激发态结构的信息。

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