Theoretical description of mixed-field orientation of asymmetric top molecules: a time-dependent study
arXiv:1610.01284 · doi:10.1103/PhysRevA.94.063408
Abstract
We present a theoretical study of the mixed-field-orientation of asymmetric top molecules in tilted static electric field and non-resonant linearly polarized laser pulse by solving the time-dependent Schrödinger equation. Within this framework, we compute the mixed-field orientation of a state selected molecular beam of benzonitrile (CHN) and compare with the experimental observations [J. L. Hansen et al., Phys. Rev. A 83, 023406 (2011)], and with our previous time-independent descriptions [J. J. Omiste et al., Phys. Chem. Chem. Phys. 13, 18815 (2011)]. For an excited rotational state, we investigate the field-dressed dynamics for several field configurations as those used in the mixed-field experiments. The non-adiabatic phenomena and their consequences on the rotational dynamics are analyzed in detail.
arXiv comment10 figures, 8 figures
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Cited by in corpus (7)
- Quantum control of molecular rotation
- Time-dependent analysis of the mixed-field orientation of molecules without rotational symmetry
- Shaping of the time-evolution of field-free molecular orientation by THz laser pulses
- Theoretical study of asymmetric superrotors: alignment and orientation
- Long-Lasting Orientation of Symmetric-top Molecules Excited by Two-Color Femtosecond Pulses
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