Charge transfer dynamics of the Ar+(2P3/2) + N2 reaction at very low collision energies

The charge transfer reaction Ar+ + N2 → Ar + N2+ has been studied for collision energies of 40, 90, and 170 meV with product energy and angle-differential crossed-beam velocity map imaging. Resonant multi-photon ionization was employed to create the charged reactant Ar+ in the 2P3/2 spin-orbit ground state with high purity. At the lowest studied collision energy of 40 meV, we could observe the N2+ product in the v = 0 vibrational level with a high amount of rotational excitation. This level is strongly dynamically suppressed at higher collision energies, where excited vibrational levels become accessible. In addition, a higher fraction of backward scattering is observed at this low collision energy compared to higher collision energies. This shows that the reaction dynamics of the charge-transfer reaction undergo a profound change from direct to unusual complex-mediated charge transfer dynamics at very low collision energy.

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Journal
The Journal of Chemical Physics
Published
2026-03-23
DOI
https://doi.org/10.1063/5.0322634
Primary Topic
Atomic and Molecular Physics
Type
article
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article

Charge transfer dynamics of the Ar+(2P3/2) + N2 reaction at very low collision energies

Dasarath Swaraj, Roland Wester, Fábio Zappa, Jerin Judy et al.
The Journal of Chemical Physics
Atomic and Molecular Physics
article

Charge transfer dynamics of the Ar+(2P3/2) + N2 reaction at very low collision energies

Dasarath Swaraj, Roland Wester, Fábio Zappa, Jerin Judy, Viviane C. Schmidt
article en

Abstract

The charge transfer reaction Ar+ + N2 → Ar + N2+ has been studied for collision energies of 40, 90, and 170 meV with product energy and angle-differential crossed-beam velocity map imaging. Resonant multi-photon ionization was employed to create the charged reactant Ar+ in the 2P3/2 spin-orbit ground state with high purity. At the lowest studied collision energy of 40 meV, we could observe the N2+ product in the v = 0 vibrational level with a high amount of rotational excitation. This level is strongly dynamically suppressed at higher collision energies, where excited vibrational levels become accessible. In addition, a higher fraction of backward scattering is observed at this low collision energy compared to higher collision energies. This shows that the reaction dynamics of the charge-transfer reaction undergo a profound change from direct to unusual complex-mediated charge transfer dynamics at very low collision energy.

The Journal of Chemical PhysicsVol. 164(12)
Universität Innsbruck (AT)
Affordable and clean energy
Openalex Percentile: Top 10%
Atomic and Molecular Physics
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Charge transfer dynamics of the Ar+(2P3/2) + N2 reaction at very low collision energies — Dasarath Swaraj, Roland Wester, et al. · The Journal of Chemical Physics (2026) | TGRS Research Map | TGRS