Resonant Cavity Modification of Ground State Chemical Kinetics
Lachlan P. Lindoy, Arkajit Mandal, David R. Reichman

TL;DR
This paper develops an analytical rate theory showing how optical cavity coupling can either enhance or suppress ground state chemical reaction rates depending on solvent friction, with resonance effects near vibrational frequencies.
Contribution
It introduces a comprehensive analytical model for cavity-modified ground state kinetics covering all solvent friction regimes, explaining resonance effects and rate modifications.
Findings
Reaction rate can be enhanced or suppressed depending on bath friction.
Maximum rate modification occurs near the reactant well or barrier frequency depending on friction.
Rate changes are sharper and more significant in weak friction regimes.
Abstract
Recent experiments have suggested that ground state chemical kinetics can be suppressed or enhanced by coupling the vibrational degrees of freedom of a molecular system with a radiation mode inside an optical cavity. Experiments show that the chemical rate is strongly modified when the photon frequency is close to characteristic vibrational frequencies. The origin of this remarkable effect remains unknown. In this work, we develop an analytical rate theory for cavity-modified ground state chemical kinetics based on the Pollak-Grabert-H\"anggi rate theory. Unlike previous work, our theory covers the complete range of solvent friction values, from the energy-diffusion limited to the spatial-diffusion limited regimes. We show that the chemical reaction rate can either be enhanced or suppressed depending on the bath friction; when bath friction is weak chemical kinetics is enhanced as…
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