Petrone Alessio, Williams-Young David B, Lingerfelt David B, Li Xiaosong
Department of Chemistry, University of Washington , Seattle, Washington 98195, United States.
J Phys Chem A. 2017 May 25;121(20):3958-3965. doi: 10.1021/acs.jpca.7b02905. Epub 2017 May 12.
Time-resolved Raman spectroscopy has proven useful for studying the formation of polarons in conjugated polymers, verifying the presence of reactive intermediates in photochemical reactions, investigating nonradiative transitions in the short lifetime of the photoexcited species, and resolving electron-phonon coupling strengths and exciton dissociation in crystalline materials. In this paper, we present an excited state transient Raman analysis protocol combining ab initio direct molecular dynamics, transient excited state Hessian, and excited state nonresonant Raman activities evaluations. Prototypical molecules are used as test cases, showing the evolution of the transient Raman signatures that follow electronic excitation. This protocol provides a direct route to assigning the vibrations implicated in the (photo)dynamics of several (photoactive) systems, complementary to the transient infrared analysis.
