4.7 Article

Stochastic Liouville equations for femtosecond stimulated Raman spectroscopy

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 142, Issue 2, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/1.4905139

Keywords

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Funding

  1. National Science Foundation (NSF) [CHE-1361516]
  2. Chemical Sciences, Geo sciences and Bio sciences Division, Office of Basic Energy Sciences, Office of Science, and (U.S.) Department of Energy (DOE)
  3. National Institutes of Health (NIH) [GM-59230]
  4. DOE

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Electron and vibrational dynamics of molecules are commonly studied by subjecting them to two interactions with a fast actinic pulse that prepares them in a nonstationary state and after a variable delay period T, probing them with a Raman process induced by a combination of a broadband and a narrowband pulse. This technique, known as femtosecond stimulated Raman spectroscopy (FSRS), can effectively probe time resolved vibrational resonances. We show how FSRS signals can be modeled and interpreted using the stochastic Liouville equations (SLE), originally developed for NMR lineshapes. The SLE provide a convenient simulation protocol that can describe complex dynamics caused by coupling to collective bath coordinates at much lower cost than a full dynamical simulation. The origin of the dispersive features that appear when there is no separation of time-scales between vibrational variations and the dephasing time is clarified. (C) 2015 AIP Publishing LLC.

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