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arXiv · 2507.13897

Harnessing multi-mode optical structure for chemical reactivity

Abstract

The prospect of controlling chemical reactivity using frequency-tunable optical microcavities has materialized over the past decade, evolving into a fascinating yet challenging new field of polaritonic chemistry, a multidisciplinary domain at the intersection of quantum optics, chemical dynamics, and non-equilibrium many-body physics. While most theoretical efforts to date have focused on single-mode cavities, practical implementations in polaritonic chemistry typically involve planar optical cavities that support a series of equally spaced photon modes, determined by the cavity geometry. In this work, we present a numerically exact, fully quantum-mechanical study of chemical reactions in few-mode cavities, revealing two key scenarios by which multi-mode effects can enhance cavity-modified reactivity. The first scenario emerges when the free spectral range is comparable to the single-mode Rabi splitting. In such cases, hybridization between a rate-decisive molecular vibration and a central resonant cavity mode reshapes the resonance landscape, enabling additional reaction pathways mediated by adjacent cavity modes. The second scenario exploits the intrinsic anharmonicity of molecular vibrations, which gives rise to multiple dipole-allowed transitions with distinct energies. Under multi-mode strong coupling, where different cavity modes individually resonate with these distinct transitions, multi-photon processes involving sequential absorption across multiple modes become accessible. This leads to a nontrivial and non-additive rate enhancement via cascade-like vibrational ladder climbing. Together, these findings offer new strategies for tailoring chemical reactivity by harnessing the structural richness of multi-mode structure, offering valuable insights for optimal experimental designs in polaritonic catalysis.

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BibTeXRIS

Yaling Ke, Jakob Assan. 2025-10-06. Harnessing multi-mode optical structure for chemical reactivity. https://arxiv.org/abs/2507.13897

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