Abstract
A photochemistry study on nitrous oxide making use of site-selective excitation of terminal nitrogen, central nitrogen, and oxygen 1s-->3pi excitations is presented. The resonant Auger decay which takes place following excitation can lead to dissociation of the N(2)O(+) ion. To elucidate the nuclear dynamics, energy-resolved Auger electrons were detected in coincidence with the ionic dissociation products, and a strong dependence of the fragmentation pathways on the core-hole site was observed in the binding energy region of the first satellite states. A description based on the molecular orbitals as well as the correlation between the thermodynamical thresholds of ion formation and the first electronic states of N(2)O(+) has been used to qualitatively explain the observed fragmentation patterns.
Original language | English |
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Pages (from-to) | 024306-9 pp |
Journal | Journal of Chemical Physics |
Volume | 128 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2008 |
Subject classification (UKÄ)
- Atom and Molecular Physics and Optics