Quantum dynamics of electron transfer in single-molecule systems coupled to polaritons: A macroscopic quantum electrodynamics approach

Controlling electron transfer and related chemical processes through polaritons has emerged as a promising direction in chemical physics. We present a general framework for electron transfer in molecules strongly coupled to polaritons. The theory is formulated within macroscopic quantum electrodynamics, a quantization scheme for electromagnetic fields in non-homogeneous, dispersive, and lossy media. To capture both molecular and dielectric contributions, our formulation incorporates two baths: molecular vibrations and a dielectric-photonic continuum that generates polaritons. This formulation is then transformed into a numerically tractable form that can be naturally combined with methods such as the pseudomode approach or the hierarchical equations of motion. Using a molecule above a plasmonic surface as an example, we show that the framework captures accurate dynamics across light-matter coupling regimes, thereby providing a powerful tool for investigating polariton-mediated electron transfer.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-12-08
DOI
https://doi.org/10.1063/5.0300152
Citations
1
Primary Topic
Strong Light-Matter Interactions
Type
article
Field-Weighted Citation Impact
1.25
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article

Quantum dynamics of electron transfer in single-molecule systems coupled to polaritons: A macroscopic quantum electrodynamics approach

Yi-Ting Chuang, Liang‐Yan Hsu
1 citations
The Journal of Chemical Physics
Strong Light-Matter Interactions
1.25
article

Quantum dynamics of electron transfer in single-molecule systems coupled to polaritons: A macroscopic quantum electrodynamics approach

Yi-Ting Chuang, Liang‐Yan Hsu
article en
1 citations

Abstract

Controlling electron transfer and related chemical processes through polaritons has emerged as a promising direction in chemical physics. We present a general framework for electron transfer in molecules strongly coupled to polaritons. The theory is formulated within macroscopic quantum electrodynamics, a quantization scheme for electromagnetic fields in non-homogeneous, dispersive, and lossy media. To capture both molecular and dielectric contributions, our formulation incorporates two baths: molecular vibrations and a dielectric-photonic continuum that generates polaritons. This formulation is then transformed into a numerically tractable form that can be naturally combined with methods such as the pseudomode approach or the hierarchical equations of motion. Using a molecule above a plasmonic surface as an example, we show that the framework captures accurate dynamics across light-matter coupling regimes, thereby providing a powerful tool for investigating polariton-mediated electron transfer.

The Journal of Chemical PhysicsVol. 163(22)
National Taiwan University (TW), National Center for Theoretical Sciences (TW), Institute of Atomic and Molecular Sciences, Academia Sinica (TW), National Center for Theoretical Sciences, Physics Division, National Taipei University (TW)
Openalex Percentile: Top 15%
Strong Light-Matter Interactions
1.25
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