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Published on: July 19, 2019
Hybrid equilibrium-nonequilibrium molecular dynamics approach for two-dimensional solute-pump/solvent-probe
1Division of Arts and Sciences, NYU Shanghai, 1555 Century Avenue, Shanghai 200122, China; Department of Chemistry, New York University, New York, New York 10003, USA; NYU-ECNU Center for Computational Chemistry at NYU Shanghai, 3663 Zhongshan Road North, Shanghai 200062, China; and State Key Laboratory of Precision Spectroscopy, East China Normal University, Shanghai 200062, China.
Abstract:
There has been a tremendous effort in accessing liquid-phase solvation dynamics using ultrafast spectroscopies for decades. It is recently demonstrated that one can go beyond tracking the relaxation of the solute-solvent interaction energy as reported in traditional time-dependent fluorescence spectroscopy. Combining a resonant solute pump with a subsequent nonresonant 4-wave-mixing light-scattering solvent probe gives rise to two-dimensional solute-pump/solvent probe (SPSP) spectroscopy, which displays the nonequilibrium relaxation of the intermolecular vibrations after the solute gets electronically excited. However, the response function of the SPSP spectra has been challenging to calculate, even on the classical-mechanical level, due to the difficulty of evaluating the surviving Poisson bracket. In this work, a hybrid equilibrium-nonequilibrium molecular dynamics simulation approach is proposed where the Poisson bracket can be estimated using nonequilibrium molecular dynamics. Applying the resulting numerically exact formalism and the previously proposed hybrid instantaneous-normal-mode/molecular-dynamics approach to a preferential solvation model system reveals that the SPSP spectroscopy provides an alternative measure for solvation dynamics, which is more sensitive to the local solvent structures than the traditional energetic dynamics measured in the time-dependent fluorescence spectroscopy.
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