Abstract
We report fully differential photoelectron spectra from an ab initio coupled-channels treatment of CO2. Photoionization by laser pulses centered atwavelengths of 400 and 800 nm is considered, with arbitrary molecular alignment and polarization (linear and elliptic). Calculations reveal significant excited-state channel contributions that are, at certain molecular orientations, an order of magnitude larger than the ground-state channel in the rescattering plateau. A partial washout of the multiphoton structure in the above threshold ionization spectra and of the nodal features in angle-resolved spectra is observed due to ionization to excited-state channels. The qualitative nature of the spectra is determined by ionization thresholds, orbital symmetries, and interchannel coupling, in order of precedence.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Physik |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 530 Physik |
ISSN: | 2469-9926 |
Sprache: | Englisch |
Dokumenten ID: | 53997 |
Datum der Veröffentlichung auf Open Access LMU: | 14. Jun. 2018, 09:54 |
Letzte Änderungen: | 04. Nov. 2020, 13:33 |