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Reactions of C+ + Cl-, Br-, and I--A comparison of theory and experiment
Stockholm University, Faculty of Science, Department of Physics.
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Number of Authors: 82019 (English)In: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 151, no 24, article id 244301Article in journal (Refereed) Published
Abstract [en]

Rate constants for the reactions of C+ + Cl-, Br-, and I- were measured at 300 K using the variable electron and neutral density electron attachment mass spectrometry technique in a flowing afterglow Langmuir probe apparatus. Upper bounds of <10(-8) cm(3) s(-1) were found for the reaction of C+ with Br- and I-, and a rate constant of 4.2 +/- 1.1 x 10(-9) cm(3) s(-1) was measured for the reaction with Cl-. The C+ + Cl- mutual neutralization reaction was studied theoretically from first principles, and a rate constant of 3.9 x 10(-10) cm(3) s(-1), an order of magnitude smaller than experiment, was obtained with spin-orbit interactions included using a semiempirical model. The discrepancy between the measured and calculated rate constants could be explained by the fact that in the experiment, the total loss of C+ ions was measured, while the theoretical treatment did not include the associative ionization channel. The charge transfer was found to take place at small internuclear distances, and the spin-orbit interaction was found to have a minor effect on the rate constant.

Place, publisher, year, edition, pages
2019. Vol. 151, no 24, article id 244301
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:su:diva-180659DOI: 10.1063/1.5126689ISI: 000513160200034PubMedID: 31893916Scopus ID: 2-s2.0-85077324570OAI: oai:DiVA.org:su-180659DiVA, id: diva2:1424125
Available from: 2020-04-16 Created: 2020-04-16 Last updated: 2023-10-05Bibliographically approved
In thesis
1. Coupling mechanisms in scattering reactions involving small molecular systems
Open this publication in new window or tab >>Coupling mechanisms in scattering reactions involving small molecular systems
2023 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

In this thesis, theoretical ab initio treatments of two-body molecular collision reactions are studied, having in common that the interaction region including all coupling mechanisms driving the reaction amounts to a molecular description. The main goal is to gain an understanding in the underlying coupling mechanisms involved in these reactions.The thesis is divided into three projects. In project one, mutual neutralization in collisions of Na+ + I, C+ + Cl and H++H are studied, with an emphasis on the inclusion of spin-orbit and/or rotational couplings which are most often neglected for in mutual neutralization. Scattering quantities are computed ab initio and compared to approximative models and experimental results. In project two, the problem of asymptotic non-adiabatic couplings is studied. Specifically, the inclusion of higher order terms in the reprojection method is shown to give a much faster convergence of the relevant scattering cross section. The method is here applied to mutual neutralization in H++Hcollisions and inelastic scattering in Li+Na and H+H collisions. In project three, a generalized pseudo Jahn-Teller model is introduced an applied to electronic resonant states of H3. Model parameters are extracted using electron scattering calculations resultingin a non-Hermitian Hamiltonian describing the system. The topology of the resulting complex adiabatic potential energy surfaces, including complex conical intersections and non-Hermitian degeneracies, are furthermore studied and classified.

Place, publisher, year, edition, pages
Stockholm: Department of Physics, Stockholm University, 2023. p. 138
National Category
Physical Sciences
Research subject
Theoretical Physics
Identifiers
urn:nbn:se:su:diva-221876 (URN)978-91-8014-520-6 (ISBN)978-91-8014-521-3 (ISBN)
Public defence
2023-11-20, sal FA32, AlbaNova universitetscentrum, Roslagstullsbacken 21, Stockholm, 13:00 (English)
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Supervisors
Available from: 2023-10-26 Created: 2023-10-05 Last updated: 2023-10-20Bibliographically approved

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Hedvall, PatrikLarson, Åsa

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