Inner-valence states of N2+ and the dissociation dynamics studied by threshold photoelectron spectroscopy and configuration interaction calculation

The N2(+) states lying in the ionization region of 26-45 eV and the dissociation dynamics are investigated by high-resolution threshold photoelectron spectroscopy and threshold photoelectron-photoion coincidence spectroscopy. The threshold photoelectron spectrum exhibits several broad bands as well...

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Veröffentlicht in:The Journal of chemical physics 2006-06, Vol.124 (23), p.234306-234306
Hauptverfasser: Aoto, Tomohiro, Ito, Kenji, Hikosaka, Yasumasa, Shibasaki, Akihiro, Hirayama, Ryo, Yamamono, Norifumi, Miyoshi, Eisaku
Format: Artikel
Sprache:eng
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Zusammenfassung:The N2(+) states lying in the ionization region of 26-45 eV and the dissociation dynamics are investigated by high-resolution threshold photoelectron spectroscopy and threshold photoelectron-photoion coincidence spectroscopy. The threshold photoelectron spectrum exhibits several broad bands as well as sharp peaks. The band features are assigned to the N2(+) states associated with the removal of an inner-valence electron, by a comparison with a configuration interaction calculation. In contrast, most of the sharp peaks on the threshold photoelectron spectrum are allocated to ionic Rydberg states converging to N2(2+). Dissociation products formed from the inner-valence N2(+) states are determined by threshold photoelectron-photoion coincidence spectroscopy. The dissociation dynamics of the inner-valence ionic states is discussed with reference to the potential energy curves calculated.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.2206586