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Updated: Aug 12, 2026

Direct Imaging of Laser-driven Ultrafast Molecular Rotation
Published on: February 4, 2017
Extended rotational diffusion and orientational relaxation of symmetric top molecules in a strong dc electric field:
S V Titov1, P M Dejardin, Yu P Kalmykov
1Institute of Radio Engineering and Electronics of the Russian Academy of Sciences, Vvedenskii Square 1, Fryazino, Moscow Region 141190, Russian Federation.
Abstract:
Second-rank orientational correlation functions (pertaining to Kerr effect relaxation and Raman scattering) are obtained using the extended rotational diffusion (J-diffusion) model of symmetric top polar molecules in a strong constant external field. It is shown that the shape of the molecule noticeably affects all second-rank correlation functions and relaxation times in the rare collision limit. In the opposite limit of frequent collisions, the quantities of interest are shown to be shape independent as a consequence of vanishingly small inertial effects. An interpolation formula for the orientation relaxation times in the intermediate regime between the rare and frequent collision limits is also given.
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