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Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction

The charge transfer reaction of Ar+ with H2 and D2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are h...

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Published in:The Journal of chemical physics 2017-07, Vol.147 (1), p.013940-013940
Main Authors: Michaelsen, Tim, Bastian, Björn, Carrascosa, Eduardo, Meyer, Jennifer, Parker, David H., Wester, Roland
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cited_by cdi_FETCH-LOGICAL-c2755-89434c1e3783c12e14f64ab7962c8a5cebf9555c0d19faa71fce92e4107efd53
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container_title The Journal of chemical physics
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creator Michaelsen, Tim
Bastian, Björn
Carrascosa, Eduardo
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Wester, Roland
description The charge transfer reaction of Ar+ with H2 and D2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are highly internally excited. In the reaction with H2, the spin-orbit excited Ar+ state’s coupling to the “resonant” vibrationally excited product H 2 + ( υ = 2) dominates for both investigated energies, in line with previous investigations. The observed angular distributions, however, show significantly less back-scattering than was found previously. Furthermore, we discovered that the product ions are highly rotationally excited. In the case of Ar+ reacting with D2, the energetically closest lying vibrational levels are not strictly preferred and higher-lying vibrational levels are also populated. For both species, the backward-scattered products show higher internal excitation.
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source American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list); AIP - American Institute of Physics
subjects Charge transfer
Investigations
Scattering
title Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction
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