Skip to main navigation Skip to search Skip to main content

Core-valence double photoionization of the CS2 molecule

  • E. Andersson*
  • , J. Niskanen
  • , L. Hedin
  • , J. H.D. Eland
  • , P. Linusson
  • , L. Karlsson
  • , J. E. Rubensson
  • , V. Carravetta
  • , H. Ågren
  • , R. Feifel
  • *Corresponding author for this work
  • Uppsala University
  • University of Oulu
  • KTH Royal Institute of Technology
  • University of Oxford
  • Stockholm University
  • National Research Council of Italy

Research output: Contribution to journalArticlepeer-review

Abstract

Double photoionization spectra of the CS2 molecule have been recorded using the TOF-PEPECO technique in combination with synchrotron radiation at the photon energies h=220, 230, 240, 243, and 362.7 eV. The spectra were recorded in the S 2p and C 1s inner-shell ionization regions and reflect dicationic states formed out of one inner-shell vacancy and one vacancy in the valence region. MCSCF calculations were performed to model the energies of the dicationic states. The spectra associated with a S 2p vacancy are well structured and have been interpreted in some detail by comparison to conventional S 2p and valence photoelectron spectra. The lowest inner-shell-valence dicationic state is observed at the vertical double ionization energy 188.45 eV and is associated with a (2 p3/2)-1 (2 π g)-1 double vacancy. The spectrum connected to the C 1s vacancy shows a distinct line at 310.8 eV, accompanied by additional broad features at higher double ionization energies. This line is associated with a (C 1s)-1 (2 π g)-1 double vacancy.

Original languageEnglish
Article number094305
JournalJournal of Chemical Physics
Volume133
Issue number9
DOIs
StatePublished - 7 Sep 2010
Externally publishedYes

Fingerprint

Dive into the research topics of 'Core-valence double photoionization of the CS2 molecule'. Together they form a unique fingerprint.

Cite this