• Open Access

Strong Coupling in Chiral Cavities: Nonperturbative Framework for Enantiomer Discrimination

Rosario R. Riso, Laura Grazioli, Enrico Ronca, Tommaso Giovannini, and Henrik Koch
Phys. Rev. X 13, 031002 – Published 7 July 2023

Abstract

The development of efficient techniques to distinguish mirror images of chiral molecules (enantiomers) is very important in both chemistry and physics. Enantiomers share most molecular properties except, for instance, the absorption of circularly polarized light. Enantiomer purification is therefore a challenging task that requires specialized equipment. Strong coupling between quantized fields and matter (e.g., in optical cavities) is a promising technique to modify molecular processes in a noninvasive way. The modulation of molecular properties is achieved by changing the field characteristics. In this work, we investigate whether strong coupling to circularly polarized electromagnetic fields is a viable way to discriminate chiral molecules. To this end, we develop a nonperturbative framework to calculate the behavior of molecules in chiral cavities. We show that in this setting the enantiomers have different energies—that is, one is more stable than the other. The field-induced energy differences are also shown to give rise to enantiospecific signatures in rotational spectra.

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  • Received 5 September 2022
  • Revised 3 February 2023
  • Accepted 30 May 2023

DOI:https://doi.org/10.1103/PhysRevX.13.031002

Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.

Published by the American Physical Society

Physics Subject Headings (PhySH)

Atomic, Molecular & Optical

Authors & Affiliations

Rosario R. Riso1, Laura Grazioli2, Enrico Ronca3, Tommaso Giovannini4, and Henrik Koch1,4,*

  • 1Department of Chemistry, Norwegian University of Science and Technology, 7491 Trondheim, Norway
  • 2Institut für Physikalische Chemie, Universität Mainz, D-55099 Mainz, Germany
  • 3Dipartimento di Chimica, Biologia e Biotecnologie, Università degli Studi di Perugia, Via Elce di Sotto, 8,06123, Perugia, Italy
  • 4Scuola Normale Superiore, Piazza dei Cavalieri 7, 56126 Pisa, Italy

  • *henrik.koch@sns.it henrik.koch@ntnu.no

Popular Summary

Chiral molecules are ubiquitous in chemistry and biology. These are molecules whose mirror images cannot be superimposed on each other. All amino acids in our bodies, for example, are chiral, as are most medical drugs. In the case of drugs, only one of the two chiral forms has a healing effect; the other could be inactive or even toxic. The ability to distinguish between pairs of chiral molecules—known as enantiomers—is therefore important but difficult, given that the two forms share nearly all physical properties. Here, we theoretically investigate whether strong coupling to circularly polarized electromagnetic fields is a viable way to differentiate between two enantiomers.

We develop a nonperturbative framework to calculate the behavior of molecules in chiral optical cavities. We show that in this setting the enantiomers have different energies—that is, one is more stable than the other. The field-induced energy differences are also shown to give rise to enantiospecific signatures in rotational spectra.

This work represents the first evidence of field-induced energy differences of the enantiomer ground states through strong coupling.

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Vol. 13, Iss. 3 — July - September 2023

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