[July 19, 2017] Resonant Femtosecond Stimulated Raman Scattering Spectroscopy: An Nonperturbative Formalism
|초청강사||Dr. Jayachander Borker|
|소속||IBS Center for Molecular Spectroscopy and Dynamics|
|일시||July 19, 2017 (Wednesday, 5:00 - 6:00 pm|
|장소||Seminar Room 116, KU R&D Center|
Femtosecond stimulated Raman Scattering (FSRS) spectroscopy is a set of vibrational spectroscopic techniques designed to probe nuclear dynamics with high temporal and spectral resolution. In a typical application, FSRS is a three-pulse experimental technique. A short actinic pump initiates the process to be studied, which is subsequently probed by a pair of Raman pulses. The latter are picosecond narrowband Raman pump and a femtosecond broad-band Raman probe. The theory of FSRS is based on the perturbative solution of time-dependent Schrödinger equation in terms of system-field interaction. Herein, I describe an alternative method of simulation of FSRS spectra, which is based on the solution of nonperturbative equation of motion. Such a method is quite general and applicable for arbitrary shapes and durations of the Raman pulses, accounts for the excited-state absorption, and describes nonstationary preparation of the system by an actinic pulse. Moreover, the present method is applicable for arbitrary field strengths of the photochemical pump.
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