Abstract
We explore the question of whether mean-field or “Ehrenfest” mixed quantum-classical dynamics is capable of capturing the quantized vibrational features in photoabsorption spectra that result from infrared and Raman-active vibrational transitions. We show that vibrational and electronic absorption spectra can indeed be obtained together within a single Ehrenfest simulation. Furthermore, the electronic transitions show new sidebands that are absent in electronic dynamics simulations with fixed nuclei. Inspection of the electronic sidebands reveals that the spacing corresponds to vibrational frequencies of totally symmetric vibrational modes of the ground electronic state. A simple derivation of the time-evolving dipole in the presence of external fields and vibrational motion shows the origin of these features, demonstrating that mixed quantum-classical Ehrenfest dynamics is capable of producing infrared, Raman, and electronic absorption spectra from a single simulation.
Original language | English |
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Pages (from-to) | 5193-5197 |
Number of pages | 5 |
Journal | Journal of Physical Chemistry Letters |
Volume | 7 |
Issue number | 24 |
DOIs | |
State | Published - Dec 15 2016 |
Externally published | Yes |
Funding
The development of real-time time-dependent electronic structure theory is supported by the Department of Energy under the contract no. DE-SC0006863. The investigation of vibrational spectroscopy is supported by the National Science Foundation (grant no. CHE-1565520). The University of Washington Student Technology Fund is gratefully acknowledged. This work is further supported by the U.S. National Science Foundation Graduate Research Fellowship No. DGE-1256082 to J.J.G.
Funders | Funder number |
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University of Washington Student Technology Fund | DGE-1256082 |
National Science Foundation | CHE-1565520 |
U.S. Department of Energy | DE-SC0006863 |