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arXiv · 2302.03880

Thermodynamic coupling of reactions via few-molecule vibrational polaritons

Arghadip Koner·Matthew Du·Sindhana Pannir-Sivajothi·Randall H. Goldsmith·Joel Yuen-Zhou
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Abstract

Interaction between light and molecular vibrations leads to hybrid light-matter states called vibrational polaritons. Even though many intriguing phenomena have been predicted for single-molecule vibrational strong coupling (VSC), several studies suggest that these effects tend to be diminished in the many-molecule regime due to the presence of dark states. Achieving single or few-molecule vibrational polaritons has been constrained by the need for fabricating extremely small mode volume infrared cavities. In this work, we propose an alternative strategy to achieve single-molecule VSC in a cavity-enhanced Raman spectroscopy (CERS) setup, based on the physics of cavity optomechanics. We then present a scheme harnessing few-molecule VSC to thermodynamically couple two reactions, such that a spontaneous electron transfer can now fuel a thermodynamically uphill reaction that was non-spontaneous outside the cavity.

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Arghadip Koner, Matthew Du, Sindhana Pannir-Sivajothi, Randall H. Goldsmith, Joel Yuen-Zhou. 2023-02-08. Thermodynamic coupling of reactions via few-molecule vibrational polaritons. https://arxiv.org/abs/2302.03880

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