Double ionization of the hydrogen sulfide molecule by electron impact: Influence of the target orientation on multiple differential cross sections

•The double ionization of the H2S molecule is here theoretically studied.•The orientation dependence of the differential cross sections is scrutinized.•The specific double ionizing mechanisms are clearly identified. Multiple differential cross sections of double ionization of hydrogen sulfide molecu...

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Veröffentlicht in:J.Electron Spectrosc.Rel.Phenom 2016-07, Vol.210, p.36-48
Hauptverfasser: Imadouchene, N., Aouchiche, H., Champion, C.
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Sprache:eng
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Zusammenfassung:•The double ionization of the H2S molecule is here theoretically studied.•The orientation dependence of the differential cross sections is scrutinized.•The specific double ionizing mechanisms are clearly identified. Multiple differential cross sections of double ionization of hydrogen sulfide molecule impacted by electrons are here investigated within the first Born approximation. In the initial state, the incident electron is represented by a plane wave function whereas the target is described by means of a single-center molecular wave function. In the final state, the two ejected electrons are described by Coulomb wave functions coupled by the Gamow factor, whereas the scattered electron is described by a plane wave. In this work, we analyze the role played by the molecular target orientation in the double ionization of the four outermost orbitals, namely 2b1, 5a1, 2b2 and 4a1 in considering the particular case of two electrons ejected from the same orbital. The contribution of each final state to the double ionization process is studied in terms of shape and magnitude for specific molecular orientations and for each molecular orbital we identified the mechanisms involved in the double ionization process, namely, the Shake-Off and the Two-Step 1.
ISSN:0368-2048
1873-2526
DOI:10.1016/j.elspec.2016.04.003