Bulletin of the American Physical Society
53rd Annual Meeting of the APS Division of Atomic, Molecular and Optical Physics
Volume 67, Number 7
Monday–Friday, May 30–June 3 2022; Orlando, Florida
Session Q04: Electron-Atom/Molecule Collisions
8:00 AM–9:36 AM,
Thursday, June 2, 2022
Room: Salon 3/4
Chair: Mark Zammit, LANL
Abstract: Q04.00006 : An investigation of the radiative electron attachment of C3N through dipole-bound states*
9:00 AM–9:12 AM
Presenter:
Joshua B Forer
(University of Central Florida)
Authors:
Joshua B Forer
(University of Central Florida)
Thierry Stoecklin
(Institute of Molecular Sciences, CNRS UMR 5255, University of Bordeaux)
Viatcheslav Kokoouline
(University of Central Florida)
Although their formation may not yet be well understood, several formation mechanisms have been proposed.
One such pathway is radiative electron attachment (REA), the process by which an electron encounters a neutral molecule and forms a stable anion through photon emission.
Previous calculations have shown that REA rates are too low to explain the observed abundance of CN-, C3N-, and C5N-.
REA through weakly bound dipole states, or dipole-bound states (DBSs), has recently been proposed to enhance REA rates and explain the observed abundance of anions in the case of a neutral counterpart with a supercritical dipole moment, such as C3N.
Although the effects of the rotation and vibration of polar molecules on DBSs have been studied in the past, no prior fully quantum treatment has considered rotation and short-range electron-molecule interactions.
Doing so in the case of C3N/C3N- is the purpose of this study.
The rotationally selected DBSs of C3N are computed using Close Coupling calculations and an ab initio local model of the interaction potential.
The results are compared to those theoretical results obtained by the simple point-charge-dipole potential and to experimental data.
The rotationally selected REA cross-section through C3N- DBSs are then calculated by a quantum approach and are found to still be too small to explain the abundance of this anion in the ISM.
*This work acknowledges the support of the National Science Foundation grant No. PHY-1806915 and the University of Bordeaux through the Franco-American Fulbright Commission.
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