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Understanding the Energy Gap Law under Vibrational Strong Coupling

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arxiv 2210.04986 v2 pith:M45G6JHP submitted 2022-10-10 physics.chem-ph quant-ph

classification physics.chem-phquant-ph
keywords energypolaritoncouplinglargeratestrongundervibrational
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The rate of non-radiative decay between two molecular electronic states is succinctly described by the energy gap law, which suggests an approximately-exponential dependence of the rate on the electronic energy gap. Here, we inquire whether this rate is modified under vibrational strong coupling, a regime whereby the molecular vibrations are strongly coupled to an infrared cavity. We show that, under most conditions, the collective light-matter coupling strength is not large enough to counter the entropic penalty involved with using the polariton modes, so the energy gap law remains unchanged. This effect (or the lack thereof) may be reversed with deep strong light-matter couplings or large detunings, both of which increase the upper polariton frequency. Finally, we demonstrate how vibrational polariton condensates mitigate the entropy problem by providing large occupation numbers in the polariton modes.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. FDTD with Auxiliary Bath Fields for Condensed-Phase Polaritonics: Fundamentals and Implementation

    physics.optics 2025-05 conditional novelty 6.0 of 10

    FDTD simulations can now include dark-mode molecular degrees of freedom through a new Lorentz-Bath susceptibility, implemented in MEEP and demonstrated in model Fabry-Perot cavities.

  2. Selective Excitation of IR-Inactive Modes via Vibrational Polaritons: Insights from Atomistic Simulations

    physics.chem-ph 2025-01 conditional novelty 6.0 of 10

    Pumping the upper polariton of liquid methane can transiently excite the IR-inactive symmetric bending mode, and the effect is strongest when the polariton is two-thirds photonic in character.

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