Many-electron dynamics in laser-driven molecules: wavefunction theory density functional theory.

Phys Chem Chem Phys

Universität Potsdam, Institut für Chemie, Karl-Liebknecht-Str. 24-25, D-14476 Potsdam-Golm, Germany.

Published: June 2021

AI Article Synopsis

  • Recent advances in laser-driven electron dynamics in polyatomic molecules highlight the need for effective theoretical modeling methods, especially Time-Dependent Configuration Interaction Singles (TD-CIS) and Real-Time Time-Dependent Density Functional Theory (RT-TD-DFT).
  • A comparison between these methods shows that TD-CIS is better at predicting population inversion during state-to-state transitions, while both methods yield similar results for dipole moments and lower harmonics in High Harmonic Generation (HHG) spectra, although discrepancies grow with higher harmonics and lower laser intensities.
  • Overall, TD-CIS/AO is found to be significantly more computationally efficient than RT-TD-DFT/Grid, making it a favorable option for modeling these complex electron dynamics.

Article Abstract

With recent experimental advances in laser-driven electron dynamics in polyatomic molecules, the need arises for their reliable theoretical modelling. Among efficient, yet fairly accurate methods for many-electron dynamics are Time-Dependent Configuration Interaction Singles (TD-CIS) (a Wave Function Theory (WFT) method), and Real-Time Time-Dependent Density Functional Theory (RT-TD-DFT), respectively. Here we compare TD-CIS combined with extended Atomic Orbital (AO) bases, TD-CIS/AO, with RT-TD-DFT in a grid representation of the Kohn-Sham orbitals, RT-TD-DFT/Grid. Possible ionization losses are treated by complex absorbing potentials in energy space (for TD-CIS/AO) or real space (for RT-TD-DFT), respectively. The comparison is made for two test cases: (i) state-to-state transitions using resonant lasers (π-pulses), i.e., bound electron motion, and (ii) large-amplitude electron motion leading to High Harmonic Generation (HHG). Test systems are a H2 molecule and cis- and trans-1,2-dichlorethene, C2H2Cl2, (DCE). From time-dependent electronic energies, dipole moments and from HHG spectra, the following observations are made: first, for bound state-to-state transitions enforced by π-pulses, TD-CIS nicely accounts for the expected population inversion in contrast to RT-TD-DFT, in agreement with earlier findings. Secondly, when using laser pulses under non-resonant conditions, dipole moments and lower harmonics in HHG spectra are obtained by TD-CIS/AO which are in good agreement with those obtained with RT-TD-DFT/Grid. Deviations become larger for higher harmonics and at low laser intensities, i.e., for low-intensity HHG signals. We also carefully test effects of basis sets for TD-CIS/AO and grid size for RT-TD-DFT/Grid, different exchange-correlation functionals in RT-TD-DFT, and absorbing boundaries. Finally, for the present examples, TD-CIS/AO is observed to be at least an order of magnitude more computationally efficient than RT-TD-DFT/Grid.

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http://dx.doi.org/10.1039/d1cp01100fDOI Listing

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