Ion momentum imaging study of the ion-molecule reaction Ar + O → Ar + O

Charge exchange reactions between Ar + ( 2 P) and O 2 (X 3 Σ − g ) are investigated in the collision energy range of 3.40-9.24 eV within the center-of-mass coordinate, by using the ion momentum imaging technique. The internal energy of the product O 2 + is enhanced gradually with the increase of col...

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Published inPhysical chemistry chemical physics : PCCP Vol. 22; no. 8; pp. 464 - 4646
Main Authors Wu, Chun-Xiao, Hu, Jie, He, Miao-Miao, Zhi, Yaya, Tian, Shan Xi
Format Journal Article
Published 26.02.2020
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Summary:Charge exchange reactions between Ar + ( 2 P) and O 2 (X 3 Σ − g ) are investigated in the collision energy range of 3.40-9.24 eV within the center-of-mass coordinate, by using the ion momentum imaging technique. The internal energy of the product O 2 + is enhanced gradually with the increase of collision energy, and the forward-scattered O 2 + ions are distributed in the broader range of scattering angle at higher collision energies. At the low collision energy of 3.40 eV, the resonant charge transfer, similar to a photon ionization process, leads to the Franck-Condon-like vibrational state population of O 2 + at the a 4 Π u state. At the higher collision energies, besides a 4 Π u and the high-lying states that are visible in the photoionization process, the O 2 + products could be populated at some electronically bound states in the non-Franck-Condon region. The present observations indicate again the strong collision-energy dependences of the charge exchange reactions, but distinctly different from our previous findings for Ar + + NO → Ar + NO + . O 2 + products of the charge exchange reactions between Ar + and O 2 are distributed in the wider range of scattering angle at higher collision energy.
ISSN:1463-9076
1463-9084
DOI:10.1039/c9cp06289k