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Shining light on the microscopic resonant mechanism responsible for cavity-mediated chemical reactivity

MPS-Authors
/persons/resource/persons180973

Schäfer,  C.
Theory Group, Theory Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
Center for Free-Electron Laser Science;
The Hamburg Center for Ultrafast Imaging;
Department of Physics, Chalmers University of Technology;
Department of Microtechnology and Nanoscience, MC2, Chalmers University of Technology;

/persons/resource/persons22028

Rubio,  A.
Theory Group, Theory Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
Center for Free-Electron Laser Science;
The Hamburg Center for Ultrafast Imaging;
Center for Computational Quantum Physics, Flatiron Institute, New York;

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フルテキスト (公開)

s41467-022-35363-6.pdf
(出版社版), 3MB

付随資料 (公開)

suppl.zip
(付録資料), 8MB

引用

Schäfer, C., Flick, J., Ronca, E., Narang, P., & Rubio, A. (2022). Shining light on the microscopic resonant mechanism responsible for cavity-mediated chemical reactivity. Nature Communications, 13(1):. doi:10.1038/s41467-022-35363-6.


引用: https://hdl.handle.net/21.11116/0000-0008-6D97-4
要旨
Strong light–matter interaction in cavity environments is emerging as a promising approach to control chemical reactions in a non-intrusive and efficient manner. The underlying mechanism that distinguishes between steering, accelerating, or decelerating a chemical reaction has, however, remained unclear, hampering progress in this frontier area of research. We leverage quantum-electrodynamical density-functional theory to unveil the microscopic mechanism behind the experimentally observed reduced reaction rate under cavity induced resonant vibrational strong light-matter coupling. We observe multiple resonances and obtain the thus far theoretically elusive but experimentally critical resonant feature for a single strongly coupled molecule undergoing the reaction. While we describe only a single mode and do not explicitly account for collective coupling or intermolecular interactions, the qualitative agreement with experimental measurements suggests that our conclusions can be largely abstracted towards the experimental realization. Specifically, we find that the cavity mode acts as mediator between different vibrational modes. In effect, vibrational energy localized in single bonds that are critical for the reaction is redistributed differently which ultimately inhibits the reaction.