4.7 Article

Ultrafast energy relaxation and anisotropy decay of the librational motion in liquid water: A molecular dynamics study

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JOURNAL OF CHEMICAL PHYSICS
卷 131, 期 16, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.3254518

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资金

  1. Grant-in-Aid for Scientific Research on Priority Areas [18066018]
  2. Grant-in Aid for Scientific Research [19350009]
  3. Molecular-Based New Computational Science Program, NINS
  4. Next Generation Super Computing Project, Nanoscience program
  5. Grants-in-Aid for Scientific Research [19350009, 18066018] Funding Source: KAKEN

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We theoretically investigate intermolecular motions in liquid water in terms of third-order infrared (IR) spectroscopy. We calculate two-dimensional (2D) IR spectra, pump-probe signals, and three-pulse stimulated photon echo signals from the combination of equilibrium and nonequilibrium molecular dynamics simulations. The 2D IR spectra and the three-pulse photon echo peak shift exhibit that the frequency correlation of the librational motion decays with a time scale of 100 fs. The two-color 2D IR spectra and the pump-probe signals reveal that the energy transfer from the librational motion at 700 cm(-1) to the low frequency motion below 300 cm(-1) occurs with a time scale of 60 fs and the subsequent relaxation to the hot ground state takes place on a 500 fs time scale. The time scale of the anisotropy decay of the librational motion is found to be similar to 115 fs. The energy dissipation processes are investigated in detail by using the nonequilibrium molecular dynamics simulation, in which an electric field pulse is applied. We show that the fast energy transfer from the librational motion to the low frequency motion is mainly due to the librational-librational energy transfer. We also show that the fast anisotropy decay mainly arises from the rapid intermolecular energy transfer. (C) 2009 American Institute of Physics. [doi:10.1063/1.3254518]

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