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Interpretation of Coupled-Cluster Many-Electron Dynamics in Terms of Stationary States
[Image: see text] We demonstrate theoretically and numerically that laser-driven many-electron dynamics, as described by bivariational time-dependent coupled-cluster (CC) theory, may be analyzed in terms of stationary-state populations. Projectors heuristically defined from linear response theory an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808707/ https://www.ncbi.nlm.nih.gov/pubmed/33337895 http://dx.doi.org/10.1021/acs.jctc.0c00977 |
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author | Pedersen, Thomas Bondo Kristiansen, Håkon Emil Bodenstein, Tilmann Kvaal, Simen Schøyen, Øyvind Sigmundson |
author_facet | Pedersen, Thomas Bondo Kristiansen, Håkon Emil Bodenstein, Tilmann Kvaal, Simen Schøyen, Øyvind Sigmundson |
author_sort | Pedersen, Thomas Bondo |
collection | PubMed |
description | [Image: see text] We demonstrate theoretically and numerically that laser-driven many-electron dynamics, as described by bivariational time-dependent coupled-cluster (CC) theory, may be analyzed in terms of stationary-state populations. Projectors heuristically defined from linear response theory and equation-of-motion CC theory are proposed for the calculation of stationary-state populations during interaction with laser pulses or other external forces, and conservation laws of the populations are discussed. Numerical tests of the proposed projectors, involving both linear and nonlinear optical processes for He and Be atoms and for LiH, CH(+), and LiF molecules show that the laser-driven evolution of the stationary-state populations at the coupled-cluster singles-and-doubles (CCSD) level is very close to that obtained by full configuration interaction (FCI) theory, provided that all stationary states actively participating in the dynamics are sufficiently well approximated. When double-excited states are important for the dynamics, the quality of the CCSD results deteriorates. Observing that populations computed from the linear response projector may show spurious small-amplitude, high-frequency oscillations, the equation-of-motion projector emerges as the most promising approach to stationary-state populations. |
format | Online Article Text |
id | pubmed-7808707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78087072021-01-15 Interpretation of Coupled-Cluster Many-Electron Dynamics in Terms of Stationary States Pedersen, Thomas Bondo Kristiansen, Håkon Emil Bodenstein, Tilmann Kvaal, Simen Schøyen, Øyvind Sigmundson J Chem Theory Comput [Image: see text] We demonstrate theoretically and numerically that laser-driven many-electron dynamics, as described by bivariational time-dependent coupled-cluster (CC) theory, may be analyzed in terms of stationary-state populations. Projectors heuristically defined from linear response theory and equation-of-motion CC theory are proposed for the calculation of stationary-state populations during interaction with laser pulses or other external forces, and conservation laws of the populations are discussed. Numerical tests of the proposed projectors, involving both linear and nonlinear optical processes for He and Be atoms and for LiH, CH(+), and LiF molecules show that the laser-driven evolution of the stationary-state populations at the coupled-cluster singles-and-doubles (CCSD) level is very close to that obtained by full configuration interaction (FCI) theory, provided that all stationary states actively participating in the dynamics are sufficiently well approximated. When double-excited states are important for the dynamics, the quality of the CCSD results deteriorates. Observing that populations computed from the linear response projector may show spurious small-amplitude, high-frequency oscillations, the equation-of-motion projector emerges as the most promising approach to stationary-state populations. American Chemical Society 2020-12-18 2021-01-12 /pmc/articles/PMC7808707/ /pubmed/33337895 http://dx.doi.org/10.1021/acs.jctc.0c00977 Text en © 2020 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Pedersen, Thomas Bondo Kristiansen, Håkon Emil Bodenstein, Tilmann Kvaal, Simen Schøyen, Øyvind Sigmundson Interpretation of Coupled-Cluster Many-Electron Dynamics in Terms of Stationary States |
title | Interpretation of Coupled-Cluster Many-Electron Dynamics
in Terms of Stationary States |
title_full | Interpretation of Coupled-Cluster Many-Electron Dynamics
in Terms of Stationary States |
title_fullStr | Interpretation of Coupled-Cluster Many-Electron Dynamics
in Terms of Stationary States |
title_full_unstemmed | Interpretation of Coupled-Cluster Many-Electron Dynamics
in Terms of Stationary States |
title_short | Interpretation of Coupled-Cluster Many-Electron Dynamics
in Terms of Stationary States |
title_sort | interpretation of coupled-cluster many-electron dynamics
in terms of stationary states |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808707/ https://www.ncbi.nlm.nih.gov/pubmed/33337895 http://dx.doi.org/10.1021/acs.jctc.0c00977 |
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