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A full-dimensional wave packet dynamics study of the photodetachment spectra of FCH~-_4

机译:FCH〜__4光解谱的全维波包动力学研究

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The low-resolution photodetachment spectrum of FCH?4 is studied in full dimensionality employing the multi-configurational time-dependent Hartree approach and potential energy surfaces recently developed by Bowman and co-workers. The computed spectrum qualitatively agrees with the lowresolution spectrum measured by Neumark and co-workers. It displays two peaks which can be assigned to different vibrational states of methane in the quasi-bound F ·CH4 van der Waals complex.The first intense peak correlates to methane in its vibrational ground state while the second much smaller peak results from methane where one of the bending modes is excited. The present simulations consider only a single potential energy surface for the neutral FCH4 system and thus do not include spectral contributions arising from transitions to excited electronic states correlating to the F(2P)+CH4 asymptote. Considering the quantitative differences between the computed and the experimental spectra, one cannot decide whether beside the vibrational excitation of the methane fragment also electronic excitation of FCH4 contributes to the second peak in the experimental photodetachment spectrum.
机译:FCH?4的低分辨率光解离光谱是采用多构型的时变Hartree方法和Bowman及其同事最近开发的势能面进行的全尺寸研究。计算得出的光谱在质量上与Neumark及其同事测得的低分辨率光谱一致。它显示了两个峰,这些峰可以分配给准结合的F·CH4 Van der Waals络合物中的甲烷不同振动状态。第一个强峰与处于振动基态的甲烷相关,第二个强峰与甲烷相关,而第二个小峰来自甲烷弯曲模式的激发。本模拟仅考虑中性FCH4系统的单个势能面,因此不包括因跃迁到与F(2P)+ CH4渐近线相关的激发电子态而引起的光谱贡献。考虑到计算光谱与实验光谱之间的定量差异,人们无法确定除甲烷碎片的振动激发外,FCH4的电子激发是否也有助于实验光解光谱中的第二个峰。

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