Polariton mediated electron transfer under the collective molecule–cavity coupling regime

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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Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc01911g
Citations
8
Primary Topic
Strong Light-Matter Interactions
Type
article
Field-Weighted Citation Impact
9.97

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article

Polariton mediated electron transfer under the collective molecule–cavity coupling regime

Eric R. Koessler, Arkajit Mandal, Pengfei Huo, Andrew J. Musser et al.
8 citations
Chemical Science
Strong Light-Matter Interactions
9.97
article

Polariton mediated electron transfer under the collective molecule–cavity coupling regime

Eric R. Koessler, Arkajit Mandal, Pengfei Huo, Andrew J. Musser, Todd D. Krauss
article en
8 citations

Abstract

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.

Chemical ScienceVol. 16(25)
Cornell University (US), University of Rochester (US), Texas A&M University (US)
National Science Foundation, U.S. Department of Energy, Research Corporation for Science Advancement, University of Rochester, Centre International de Recherche sur le Cancer, Division of Chemistry
Openalex Percentile: Top 2%
Strong Light-Matter Interactions
9.97
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