Chemical reactivity under collective vibrational strong coupling

Author:

Wang Derek S.1ORCID,Flick Johannes234ORCID,Yelin Susanne F.5ORCID

Affiliation:

1. Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, USA

2. Center for Computational Quantum Physics, Flatiron Institute, New York, New York 10010, USA

3. Department of Physics, City College of New York, New York, New York 10031, USA

4. Department of Physics, The Graduate Center, City University of New York, New York, New York 10016, USA

5. Department of Physics, Harvard University, Cambridge, Massachusetts 02138, USA

Abstract

Recent experiments of chemical reactions in optical cavities have shown great promise to alter and steer chemical reactions, but still remain poorly understood theoretically. In particular, the origin of resonant effects between the cavity and certain vibrational modes in the collective limit is still subject to active research. In this paper, we study the unimolecular dissociation reactions of many molecules, collectively interacting with an infrared cavity mode, through their vibrational dipole moment. We find that the reaction rate can slow down by increasing the number of aligned molecules, if the cavity mode is resonant with a vibrational mode of the molecules. We also discover a simple scaling relation that scales with the collective Rabi splitting, to estimate the onset of reaction rate modification by collective vibrational strong coupling and numerically demonstrate these effects for up to 104molecules.

Funder

National Science Foundation Graduate Research Fellowship

Publisher

AIP Publishing

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

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