Dissociative electron attachment and electron-impact resonant dissociation of vibrationally excited O2 molecules
arXiv:1501.01771 · doi:10.1103/PhysRevA.91.012701
Abstract
State-by-state cross sections for dissociative electron attachment and electron-impact dissociation for molecular oxygen are computed using ab initio resonance curves calculated with the R-matrix method. When O2 is in its vibrational ground state, the main contribution for both processes comes from the resonance state of but with a significant contribution from the resonant state. Vibrational excitation leads to an increased contribution from the low-lying resonance, greatly increased cross sections for both processes, and the threshold moving to lower energies. These results provide important input for models of O2-containing plasmas in nonequilibrium conditions.
arXiv comment5 figures
References in corpus (2)
Cited by in corpus (10)
- Uncertainty Estimates for Theoretical Atomic and Molecular Data
- QDB: a new database of plasma chemistries and reactions
- Study of vibrational kinetics of CO2 and CO in CO2-O2 plasmas under non-equilibrium conditions
- Zero-dimensional and pseudo-one-dimensional models of atmospheric-pressure plasma jet in binary and ternary mixtures of oxygen and nitrogen with helium background
- Calculated low-energy electron-impact vibrational excitation cross sections for CO2 molecule
- Vibrational excitation and dissociation of deuterium molecule by electron impact
- Dissociative electron attachment cross sections for ro-vibrationally excited NO molecule and N- anion formation
- Vibrationally resolved NO dissociative excitation cross sections by electron impact
- Electron-impact cross sections for dissociation processes of vibrationally excited CH radical
- Resonant electron attachment to mixed hydrogen/oxygen and deuterium/oxygen clusters