Ion-molecule charge-exchange reactions Ar + CO → Ar + CO at the center-of-mass collision energies of 4.40, 6.40, and 8.39 eV are investigated using ion velocity map imaging technique. Although multiple electronically excited states of CO are accessed, the population of CO at the AΠ state is predominant in the present collision-energy range. In contrast to our previous study for NO, but similar to the case of O, the forward-scattered CO yields show a broader angular distribution at the higher collision energy. Typically, the Franck-Condon-region charge transfer, energy resonant charge transfer, and intimate collision are three different mechanisms in which the intimate collision experiences an intermediate complex, and this mechanism usually plays an essential role in the thermal-energy reactions. However, the present observations indicate that this mechanism, concerning the intermediate (Ar-CO), is still of utmost importance in a relatively high collision-energy range.
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http://dx.doi.org/10.1021/acs.jpca.0c02047 | DOI Listing |
Chemphyschem
November 2024
Department of Chemical Physics, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), University of Science and Technology of China, Hefei, 230026, China.
Hydrogen isotopic effect, as the key to revealing the origin of Earth's water, arises from the H/D mass difference and quantum dynamics at the transition state of reaction. The ion-molecule charge-exchange reaction between water (HO/DO) and argon ion (Ar) proceeds spontaneously and promptly, where there is no transition-state or intermediate complex. In this energetically resonant process, we find an inverse kinetic isotope effect (KIE) leading to the higher charge transfer rate for DO, by the velocity map imaging measurements of HO/DO products.
View Article and Find Full Text PDFJ Phys Chem A
May 2024
Department of Chemical Physics, University of Science and Technology of China, Hefei 230026, China.
The reactive collision between He and CO plays an important role in substance evolutions of the planetary CO-rich atmosphere. Using a three-dimensional ion velocity map imaging technique, we investigate the low-energy ion-molecule reactions He + CO → He + CO/He + CO + O/He + CO + O. The velocity images of the products CO and O of dissociative charge-exchange reactions are distinctly different from those of charge-exchange product CO.
View Article and Find Full Text PDFJ Am Soc Mass Spectrom
April 2023
Department of Chemistry, Memorial University of Newfoundland and Labrador, St. John's, NL, Canada A1C5S7.
Rev Sci Instrum
November 2022
Indian Institute of Science Education and Research Pune, Homi Bhabha Road, Pune 411008, India.
We have designed an electrostatic charge state analyzer for ion beams having energies in the range of 5-20 keV/q. It is primarily built to investigate the different ionization processes involved in the slow (v < 1 a.u.
View Article and Find Full Text PDFJ Phys Chem A
April 2021
Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemical Physics, University of Science and Technology of China, Hefei 230026, China.
We report an ion velocity imaging study of the charge exchange reactions between Ar ion and /-dichloroethylene in the collision energy range of 2.1-9.5 eV, and we find that the energy-resonant charge transfer plays a dominant role in the large impact-parameter reaction.
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