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- W3137484990 abstract "We show how linear vibronic spectra in molecular systems can be simulated efficiently using first-principles approaches without relying on the explicit use of multiple Born–Oppenheimer potential energy surfaces. We demonstrate and analyze the performance of mean-field and beyond-mean-field dynamics techniques for the H2 molecule in one dimension, in the later case capturing the vibronic structure quite accurately, including quantum Franck–Condon effects. In a practical application of this methodology we simulate the absorption spectrum of benzene in full dimensionality using time-dependent density functional theory at the multitrajectory Ehrenfest level, finding good qualitative agreement with experiment and significant spectral reweighting compared to commonly used single-trajectory Ehrenfest dynamics. These results form the foundation for nonlinear spectral calculations and show promise for future application in capturing phenomena associated with vibronic coupling in more complex molecular and potentially condensed phase systems." @default.
- W3137484990 created "2021-03-29" @default.
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- W3137484990 date "2021-03-22" @default.
- W3137484990 modified "2023-10-14" @default.
- W3137484990 title "Simulating Vibronic Spectra without Born–Oppenheimer Surfaces" @default.
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- W3137484990 doi "https://doi.org/10.1021/acs.jpclett.1c00073" @default.
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