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Optimal Basis Set for Electron Dynamics in Strong Laser Fields: The case of Molecular Ion H(2)(+)
[Image: see text] A clear understanding of the mechanisms that control the electron dynamics in a strong laser field is still a challenge that requires interpretation by advanced theory. Development of accurate theoretical and computational methods, able to provide a precise treatment of the fundame...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255052/ https://www.ncbi.nlm.nih.gov/pubmed/30247900 http://dx.doi.org/10.1021/acs.jctc.8b00656 |
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author | Labeye, Marie Zapata, Felipe Coccia, Emanuele Véniard, Valérie Toulouse, Julien Caillat, Jérémie Taïeb, Richard Luppi, Eleonora |
author_facet | Labeye, Marie Zapata, Felipe Coccia, Emanuele Véniard, Valérie Toulouse, Julien Caillat, Jérémie Taïeb, Richard Luppi, Eleonora |
author_sort | Labeye, Marie |
collection | PubMed |
description | [Image: see text] A clear understanding of the mechanisms that control the electron dynamics in a strong laser field is still a challenge that requires interpretation by advanced theory. Development of accurate theoretical and computational methods, able to provide a precise treatment of the fundamental processes generated in the strong field regime, is therefore crucial. A central aspect is the choice of the basis for the wave function expansion. Accuracy in describing multiphoton processes is strictly related to the intrinsic properties of the basis, such as numerical convergence, computational cost, and representation of the continuum. By explicitly solving the 1D and 3D time-dependent Schrödinger equation for H(2)(+) in the presence of an intense electric field, we explore the numerical performance of using a real-space grid, a B-spline basis, and a Gaussian basis (improved by optimal Gaussian functions for the continuum). We analyze the performance of the three bases for high-harmonic generation and above-threshold ionization for H(2)(+). In particular, for high-harmonic generation, the capability of the basis to reproduce the two-center interference and the hyper-Raman phenomena is investigated. |
format | Online Article Text |
id | pubmed-6255052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62550522018-11-27 Optimal Basis Set for Electron Dynamics in Strong Laser Fields: The case of Molecular Ion H(2)(+) Labeye, Marie Zapata, Felipe Coccia, Emanuele Véniard, Valérie Toulouse, Julien Caillat, Jérémie Taïeb, Richard Luppi, Eleonora J Chem Theory Comput [Image: see text] A clear understanding of the mechanisms that control the electron dynamics in a strong laser field is still a challenge that requires interpretation by advanced theory. Development of accurate theoretical and computational methods, able to provide a precise treatment of the fundamental processes generated in the strong field regime, is therefore crucial. A central aspect is the choice of the basis for the wave function expansion. Accuracy in describing multiphoton processes is strictly related to the intrinsic properties of the basis, such as numerical convergence, computational cost, and representation of the continuum. By explicitly solving the 1D and 3D time-dependent Schrödinger equation for H(2)(+) in the presence of an intense electric field, we explore the numerical performance of using a real-space grid, a B-spline basis, and a Gaussian basis (improved by optimal Gaussian functions for the continuum). We analyze the performance of the three bases for high-harmonic generation and above-threshold ionization for H(2)(+). In particular, for high-harmonic generation, the capability of the basis to reproduce the two-center interference and the hyper-Raman phenomena is investigated. American Chemical Society 2018-09-24 2018-11-13 /pmc/articles/PMC6255052/ /pubmed/30247900 http://dx.doi.org/10.1021/acs.jctc.8b00656 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Labeye, Marie Zapata, Felipe Coccia, Emanuele Véniard, Valérie Toulouse, Julien Caillat, Jérémie Taïeb, Richard Luppi, Eleonora Optimal Basis Set for Electron Dynamics in Strong Laser Fields: The case of Molecular Ion H(2)(+) |
title | Optimal Basis Set for Electron Dynamics in Strong
Laser Fields: The case of Molecular Ion H(2)(+) |
title_full | Optimal Basis Set for Electron Dynamics in Strong
Laser Fields: The case of Molecular Ion H(2)(+) |
title_fullStr | Optimal Basis Set for Electron Dynamics in Strong
Laser Fields: The case of Molecular Ion H(2)(+) |
title_full_unstemmed | Optimal Basis Set for Electron Dynamics in Strong
Laser Fields: The case of Molecular Ion H(2)(+) |
title_short | Optimal Basis Set for Electron Dynamics in Strong
Laser Fields: The case of Molecular Ion H(2)(+) |
title_sort | optimal basis set for electron dynamics in strong
laser fields: the case of molecular ion h(2)(+) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255052/ https://www.ncbi.nlm.nih.gov/pubmed/30247900 http://dx.doi.org/10.1021/acs.jctc.8b00656 |
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