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.
Authors
- Yi-Ting Chuang (ORCID: https://orcid.org/0000-0002-1596-3497)
- Liang‐Yan Hsu (ORCID: https://orcid.org/0000-0001-9165-1033)
Institutions
- 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)
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