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Electronic control of initial nuclear dynamics adjacent to a conical intersection

Authors :
Michael J. Bearpark
Jan Meisner
Morgane Vacher
David Mendive-Tapia
Michael A. Robb
Imperial College London
Source :
Journal of Physical Chemistry A, Journal of Physical Chemistry A, American Chemical Society, 2015, 119 (21), pp.5165-72. ⟨10.1021/jp509774t⟩
Publication Year :
2015
Publisher :
HAL CCSD, 2015.

Abstract

International audience; Photoionization can create a nonstationary electronic state and therefore initiates coupled electron-nuclear dynamics in molecules. Using a CASSCF implementation of the Ehrenfest method, we study the nuclear dynamics following vertical ionization of toluene, starting close to the conical intersection between ground and first excited states of its cation. The results show how the initial nuclear dynamics is controlled by the nonstationary electronic state character. In particular, ionization of this system leading to an equal superposition of the two lowest energy states can initiate nuclear dynamics in an orthogonal direction in the branching space to dynamics on the ground or first excited state potential energy surfaces alone.

Details

Language :
English
ISSN :
10895639 and 15205215
Database :
OpenAIRE
Journal :
Journal of Physical Chemistry A, Journal of Physical Chemistry A, American Chemical Society, 2015, 119 (21), pp.5165-72. ⟨10.1021/jp509774t⟩
Accession number :
edsair.doi.dedup.....7ea570f90589ce0ae4938f734a16fda7
Full Text :
https://doi.org/10.1021/jp509774t⟩