dc.contributor.author
Goldsztejn, G.
dc.contributor.author
Guillemin, R.
dc.contributor.author
Marchenko, T.
dc.contributor.author
Travnikova, O.
dc.contributor.author
Ceolin, D.
dc.contributor.author
Journel, L.
dc.contributor.author
Simon, M.
dc.contributor.author
Piancastelli, M. N.
dc.contributor.author
Püttner, Ralph
dc.date.accessioned
2022-04-08T12:10:40Z
dc.date.available
2022-04-08T12:10:40Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/34659
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-34377
dc.description.abstract
Auger decay after photoexcitation or photoemission of an electron from a deep inner shell in the hard X-ray regime can be rather complex, implying a multitude of phenomena such as multiple-step cascades, post-collision interaction (PCI), and electronic state-lifetime interference. Furthermore, in a molecule nuclear motion can also be triggered. Here we discuss a comprehensive theoretical method which allows us to analyze in great detail Auger spectra measured around an inner-shell ionization threshold. HCl photoexcited or photoionized around the deep Cl 1s threshold is chosen as a showcase. Our method allows calculating Auger cross sections considering the nature of the ground, intermediate and final states (bound or dissociative), and the evolution of the relaxation process, including both electron and nuclear dynamics. In particular, we show that we can understand and reproduce a so-called experimental 2D-map, consisting of a series of resonant Auger spectra measured at different photon energies, therefore obtaining a detailed picture of all above-mentioned dynamical phenomena at once.
en
dc.format.extent
15 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Auger decay dynamics
en
dc.subject
hard X-ray regime
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik::530 Physik
dc.title
Simulation of Auger decay dynamics in the hard X-ray regime: HCl as a showcase
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1039/D1CP05662J
dcterms.bibliographicCitation.journaltitle
Physical Chemistry Chemical Physics
dcterms.bibliographicCitation.number
11
dcterms.bibliographicCitation.pagestart
6590
dcterms.bibliographicCitation.pageend
6604
dcterms.bibliographicCitation.volume
24
dcterms.bibliographicCitation.url
https://doi.org/10.1039/D1CP05662J
refubium.affiliation
Physik
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1463-9084
refubium.resourceType.provider
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