Attosecond spectroscopy reveals alignment dependent core-hole dynamics in the ICl molecule

The removal of electrons located in the core shells of molecules creates transient states that live between a few femtoseconds to attoseconds. Owing to these short lifetimes, time-resolved studies of these states are challenging and complex molecular dynamics driven solely by electronic correlation...

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Hauptverfasser: Marroux, Hugo J. B. (VerfasserIn) , Fidler, Ashley P. (VerfasserIn) , Ghosh, Aryya (VerfasserIn) , Kobayashi, Yuki (VerfasserIn) , Gokhberg, Kirill (VerfasserIn) , Kuleff, Alexander I. (VerfasserIn) , Leone, Stephen R. (VerfasserIn) , Neumark, Daniel M. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 16 November 2020
In: Nature Communications
Year: 2020, Jahrgang: 11
ISSN:2041-1723
DOI:10.1038/s41467-020-19496-0
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/s41467-020-19496-0
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/s41467-020-19496-0
Volltext
Verfasserangaben:Hugo J.B. Marroux, Ashley P. Fidler, Aryya Ghosh, Yuki Kobayashi, Kirill Gokhberg, Alexander I. Kuleff, Stephen R. Leone & Daniel M. Neumark
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Zusammenfassung:The removal of electrons located in the core shells of molecules creates transient states that live between a few femtoseconds to attoseconds. Owing to these short lifetimes, time-resolved studies of these states are challenging and complex molecular dynamics driven solely by electronic correlation are difficult to observe. Here, we obtain few-femtosecond core-excited state lifetimes of iodine monochloride by using attosecond transient absorption on iodine 4d−16p transitions around 55 eV. Core-level ligand field splitting allows direct access of excited states aligned along and perpendicular to the ICl molecular axis. Lifetimes of 3.5 ± 0.4 fs and 4.3 ± 0.4 fs are obtained for core-hole states parallel to the bond and 6.5 ± 0.6 fs and 6.9 ± 0.6 fs for perpendicular states, while nuclear motion is essentially frozen on this timescale. Theory shows that the dramatic decrease of lifetime for core-vacancies parallel to the covalent bond is a manifestation of non-local interactions with the neighboring Cl atom of ICl.
Beschreibung:Gesehen am 21.01.2021
Beschreibung:Online Resource
ISSN:2041-1723
DOI:10.1038/s41467-020-19496-0