Photoionization of aligned excited states in neon by attosecond laser pulses
arXiv:2011.05659 · doi:10.1088/1361-6455/abd610
Abstract
We describe numerically the ionization process induced by linearly and circularly polarized XUV attosecond laser pulses on an aligned atomic target, specifically, the excited state Ne. We compute the excited atomic state by applying the time-dependent restricted-active-space self-consistent field (TD-RASSCF) method to fully account for the electronic correlation. We find that correlation-assisted ionization channels can dominate over channels accessible without correlation. We also observe that the rotation of the photoelectron momentum distribution by circularly polarized laser pulses compared to the case of linear polarization can be explained in terms of differences in accessible ionization channels. This study shows that it is essential to include electron correlation effects to obtain an accurate description of the photoelectron emission dynamics from aligned excited states.
10 figures, 11 pages (minor changes with respect to previous version)
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Cited by in corpus (3)
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- Time-dependent Hole States in Multiconfigurational Time-Dependent Hartree-Fock Approaches: A Time-Domain Generalization of Extended Koopmans' Theorem
- Carrier-envelope phase effects in one- and two-photon directional photoionization of non-isotropic atomic states