Strong-Field Molecular Ionization Beyond The Single Active Electron
Approximation
- URL: http://arxiv.org/abs/2209.07174v1
- Date: Thu, 15 Sep 2022 09:49:14 GMT
- Title: Strong-Field Molecular Ionization Beyond The Single Active Electron
Approximation
- Authors: Jean-Nicolas Vigneau (ISMO), Tung Nguyen-Dang, Eric Charron (ISMO),
Osman Atabek (ISMO)
- Abstract summary: We study signals of the single ionization of $H$ under a strong near-infrared (NIR) four-cycle, linearly-polarized laser pulse of varying intensity.
We give an interpretation of this in terms of a Resonance-Enhanced-Multiphoton Ionization (REMPI) mechanism with interfering resonances resulting from excited electronic states.
- Score: 0.0
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: The present work explores quantitative limits to the Single-Active Electron
(SAE) approximation, often used to deal with strong-field ionization and
subsequent attosecond dynamics. Using a time-dependent multi\-configuration
approach, specifically a Time-Dependent Configuration Interaction (TDCI)
method, we solve the time-dependent Schr{\"o}dinger equation (TDSE) for the
two-electron dihydrogen molecule, with the possibility of tuning at will the
electron-electron interaction by an adiabatic switch-on/switch-off function. We
focus on signals of the single ionization of $H_2$ under a strong near-infrared
(NIR) four-cycle, linearly-polarized laser pulse of varying intensity, and
within a vibrationally frozen molecule model. The observables we address are
post-pulse total ionization probability profiles as a function of the laser
peak intensity. Three values of the internuclear distance R taken as a
parameter are considered, R = R$_{eq}$ = 1.4 a.u, the equilibrium geometry of
the molecule, R = 5.0 a.u for an elongated molecule and R = 10.2 a.u for a
dissociating molecule. The most striking observation is the non-monotonous
behavior of the ionization probability profiles at intermediate elongation
distances with an instance of enhanced ionization and one of partial ionization
quenching. We give an interpretation of this in terms of a
Resonance-Enhanced-Multiphoton Ionization (REMPI) mechanism with interfering
overlapping resonances resulting from excited electronic states.
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