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Updated: Sep 19, 2025

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Polariton mediated electron transfer under the collective molecule-cavity coupling regime
Eric R Koessler1, Arkajit Mandal2, Andrew J Musser3
1Department of Chemistry, University of Rochester 120 Trustee Road Rochester NY 14627 USA ekoessle@ur.rochester.edu.
None:
We investigate polariton-mediated electron transfer (PMET) under the collective molecule-cavity coupling regime, with the presence of dark state transfer, cavity loss, and continuous-wave (CW) laser driving using quantum dynamics simulations and analytic rate constant theories. We demonstrate how the PMET rate constant can be enhanced by the collective coupling effect, where the light-matter coupling strength is small, yet there are many molecules collectively coupled to the cavity. We first show how reactions initialized in the collective upper polariton (UP) state can significantly enhance the PMET rate constant by decreasing the reaction driving force of an otherwise uphill ET reaction with collective strong coupling and positive detuning. We further show how the PMET rate constant is affected by dark states and cavity loss, which are often regarded as obstacles, and how to overcome them to provide a significant cavity-induced rate constant enhancement under the collective coupling regime. In particular, we show that by driving the UP state with a CW laser in a positively detuned cavity, the effective PMET rate constant can be several orders of magnitude larger than outside the cavity, even with significant molecular disorder and cavity loss. These results reveal a promising approach to realize photochemical rate enhancement with collective strong coupling in disordered and lossy polariton systems, as well as enabling otherwise impractical uphill ET reactions.
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