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Experimental and theoretical study of core-valence double photoionization of OCS
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2010 (Engelska)Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 82, nr 4, s. 043436-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

O 1s, C 1s, and S 2p core-valence double ionization electron spectra of the OCS molecule have been obtained experimentally by a time-of-flight photoelectron-photoelectron coincidence spectroscopy technique. In order to analyze and assign the spectral features observed, we present a protocol for computing core-valence ionization energies of such systems. The protocol is based on a restricted active space multiconfigurational self-consistent field (MCSCF) methodology with a freeze-relax procedure to guarantee a correct core-valence state root index without variational collapse. Corrections for extended dynamical correlation and core-core correlation, respectively, are made by multiconfigurational perturbation theory and by uncontracted basis set Moller-Plesset theory. Envisioning applications to larger molecules, a spin-restricted open-shell density functional method is also applied for the lowest core-valence energies. Furthermore, cross sections through a scheme for computing multiatom Auger transitions generating core-valence holes are presented. We find that the procedure outlined is capable of deriving the energy onset of core-valence ionization within a fraction of an eV and that assignments can be made of the most salient spectral features.

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2010. Vol. 82, nr 4, s. 043436-
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URN: urn:nbn:se:su:diva-51459DOI: 10.1103/PhysRevA.82.043436ISI: 000283536100011OAI: oai:DiVA.org:su-51459DiVA, id: diva2:385270
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authorCount :12Tillgänglig från: 2011-01-11 Skapad: 2011-01-10 Senast uppdaterad: 2022-02-24Bibliografiskt granskad

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Linusson, Per

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