Collision-Energy Dependence of the Ion-Molecule Charge-Exchange Reaction Ar + CO → Ar + CO.

J Phys Chem A

Hefei National Laboratory for Physical Sciences at the Microscale, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Department of Chemical Physics, University of Science and Technology of China, Hefei 230026, China.

Published: April 2020

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.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.jpca.0c02047DOI Listing

Publication Analysis

Top Keywords

ion-molecule charge-exchange
8
collision-energy range
8
charge transfer
8
intimate collision
8
collision-energy dependence
4
dependence ion-molecule
4
charge-exchange reaction
4
reaction →
4
→ ion-molecule
4
charge-exchange reactions
4

Similar Publications

Inverse Isotope Kinetic Effect of the Charge Transfer Reactions of Ar with HO and DO.

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 PDF

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 PDF
Article Synopsis
  • Ortho-substituted isomers of tricresyl phosphates (TCPs) can lead to neurotoxic effects in humans and are detected using gas chromatography in an ionization source.
  • The study uncovers a proposed reaction mechanism involving the transformation of molecular ions into a distonic isomer, followed by oxidation and decomposition into a neurotoxic metabolite, CBDP.
  • Experimental and computational analyses provide evidence for the existence of hydrogen shift isomers of CBDP, allowing for the identification of potentially harmful TCPs in complex industrial mixtures.
View Article and Find Full Text PDF

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 PDF

Ion-Molecule Charge Exchange Reactions between Ar and -/-Dichloroethylene.

J 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.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!