Attosecond laser control of photoelectron angular distributions in XUV-induced ionization of H2
We investigate how attosecond XUV pump/IR probe schemes can be used to exert control on the ionization dynamics of the hydrogen molecule. The aim is to play with all available experimental parameters in the problem, namely the XUV pump–IR probe delay, the energy and emission direction of the produce...
| Autores: | , , |
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| Formato: | artículo |
| Fecha de publicación: | 2020 |
| País: | España |
| Recursos: | Universidad Autónoma de Madrid |
| Repositorio: | Biblos-e Archivo. Repositorio Institucional de la UAM |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.uam.es:10486/730180 |
| Acesso em linha: | https://hdl.handle.net/10486/730180 https://dx.doi.org/10.1039/d0fd00114g |
| Access Level: | acceso abierto |
| Palavra-chave: | Angular distribution electron emission kinetic energy molecules photoelectrons Química |
| Resumo: | We investigate how attosecond XUV pump/IR probe schemes can be used to exert control on the ionization dynamics of the hydrogen molecule. The aim is to play with all available experimental parameters in the problem, namely the XUV pump–IR probe delay, the energy and emission direction of the produced photo-ions, as well as combinations of them, to uncover control strategies that can lead to preferential electron ejection directions. We do so by accurately solving the time-dependent Schrodinger equation, with inclusion of both electronic and nuclear motions, as well as the coupling between them. We show that both the IR pulse and the nuclear motion can be used to break the molecular inversion symmetry, thus leading to asymmetric molecular-frame photoelectron angular distributions. The preferential electron emission direction can thus be tuned by varying the pump–probe delay, by choosing specific ranges of proton kinetic energies, or both. We expect that similar control strategies could be used in more complex molecules containing light nuclei |
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