Full quantum state control of chiral molecules

Fuente: arXiv
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Autori principali: Lee, JuHyeon, Abdiha, Elahe, Sartakov, Boris G., Meijer, Gerard, Eibenberger-Arias, Sandra
Natura: Preprint
Pubblicazione: 2024
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author Lee, JuHyeon
Abdiha, Elahe
Sartakov, Boris G.
Meijer, Gerard
Eibenberger-Arias, Sandra
author_facet Lee, JuHyeon
Abdiha, Elahe
Sartakov, Boris G.
Meijer, Gerard
Eibenberger-Arias, Sandra
contents Controlling the internal quantum states of chiral molecules for a selected enantiomer has a wide range of fundamental applications. Using tailored microwave fields, a chosen rotational state can be enriched for a selected enantiomer, even starting from a racemic mixture. This enables rapid switching between samples of different enantiomers in a given state, holding great promise, for instance, for measuring parity violation in chiral molecules. Achieving full enantiomer-specific state transfer is a key requirement for this and many other applications. Although theoretically feasible, achieving the required experimental conditions seemed unrealistic. Here, we realize near-ideal conditions, overcoming both the limitations of thermal population and spatial degeneracy in rotational states. Our results show that 96% state-specific enantiomeric purity can be obtained from a racemic mixture, in an approach that is universally applicable to all chiral molecules of C1 symmetry.
format Preprint
id arxiv_https___arxiv_org_abs_2402_17308
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Full quantum state control of chiral molecules
Lee, JuHyeon
Abdiha, Elahe
Sartakov, Boris G.
Meijer, Gerard
Eibenberger-Arias, Sandra
Chemical Physics
Quantum Physics
Controlling the internal quantum states of chiral molecules for a selected enantiomer has a wide range of fundamental applications. Using tailored microwave fields, a chosen rotational state can be enriched for a selected enantiomer, even starting from a racemic mixture. This enables rapid switching between samples of different enantiomers in a given state, holding great promise, for instance, for measuring parity violation in chiral molecules. Achieving full enantiomer-specific state transfer is a key requirement for this and many other applications. Although theoretically feasible, achieving the required experimental conditions seemed unrealistic. Here, we realize near-ideal conditions, overcoming both the limitations of thermal population and spatial degeneracy in rotational states. Our results show that 96% state-specific enantiomeric purity can be obtained from a racemic mixture, in an approach that is universally applicable to all chiral molecules of C1 symmetry.
title Full quantum state control of chiral molecules
topic Chemical Physics
Quantum Physics
url https://arxiv.org/abs/2402.17308