Abstract

This paper theoretically treats the spontaneous resonant inelastic scattering of Laguerre-Gauss (LG) beams from the totally symmetric vibrations of complex polyatomic molecules within the semi-classical framework. We develop an interaction Hamiltonian that accounts for the position of the molecule within the excitation beam to derive the effective differential scattering cross-section of a classical LG beam from a molecule using the frequency domain third order nonlinear optical response function. To gain physical insight into this scattering process, we utilize a model vibronic molecule to study the changes to this scattering process. For specific molecular parameters including vibrational frequency and relative displacement of the involved electronic states, this investigation shows that an incident LG beam asymmetrically enhances one of two participating excitation transitions causing modulation of the interference present in the scattering process. This modulation allows a pathway to coherent control of resonant inelastic scattering from complex, poly-atomic molecules. We discuss the possible application of this control to the resonant x-ray inelastic scattering (RIXS) of small poly-atomic molecules central to applications ranging from single molecule electronics to solar energy science.

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