Proton tunneling in a two-dimensional potential energy surface with a non-linear system-bath interaction: Thermal suppression of reaction rate.


Journal

The Journal of chemical physics
ISSN: 1089-7690
Titre abrégé: J Chem Phys
Pays: United States
ID NLM: 0375360

Informations de publication

Date de publication:
07 Jun 2020
Historique:
entrez: 8 6 2020
pubmed: 9 6 2020
medline: 9 6 2020
Statut: ppublish

Résumé

We consider a proton transfer (PT) system described by a proton transfer reaction (PTR) coordinate and a rate promoting vibrational (RPV) coordinate interacting with a non-Markovian heat bath. While dynamics of PT processes has been widely discussed using two-dimensional potential energy surfaces, the role of the heat bath, in particular, in a realistic form of the system-bath interaction has not been well explored. Previous studies are largely based on a one-dimensional model and linear-linear system-bath interaction. In the present study, we introduce an exponential-linear (EL) system-bath interaction, which is derived from the analysis of a PTR-RPV system in a realistic situation. This interaction mainly causes vibrational dephasing in the PTR mode and population relaxation in the RPV mode. Numerical simulations were carried out using the hierarchical equations of motion approach. We analyze the role of the heat bath interaction in the chemical reaction rate as a function of the system-bath coupling strength at different temperatures and for different values of the bath correlation time. A prominent feature of the present result is that while the reaction rate predicted from classical and quantum Kramers theory increases as the temperature increases, the present EL interaction model exhibits opposite temperature dependence. The Kramers turn-over profile of the reaction rate as a function of the system-bath coupling is also suppressed in the present EL model, turning into a plateau-like curve for larger system-bath interaction strength. Such features arise from the interplay of the vibrational dephasing process in the PTR mode and the population relaxation process in the RPV mode.

Identifiants

pubmed: 32505152
doi: 10.1063/5.0010580
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

214114

Auteurs

Jiaji Zhang (J)

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

Raffaele Borrelli (R)

DISAFA, University of Torino, Largo Paolo Braccini 2, I-10095 Grugliasco, Italy.

Yoshitaka Tanimura (Y)

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

Classifications MeSH