Single-shot Non-destructive Quantum Sensing for Gaseous Samples with Hundreds of Chiral Molecules

Abstract

Chiral discrimination that is efficient to tiny amounts of chiral substances, especially at the single-molecule level, is highly demanded. Here, we propose a single-shot nondestructive quantum sensing method addressing such an issue. Our scheme consists of two steps. In the first step, the two enantiomers are prepared in different rotational states via microwave enantio-specific state transfer. Then, the chiral discrimination is transferred to quantum hypothesis testing. In the second step, we for the first time introduce a non-destructive quantum-state detection technique assisted with a microwave resonator to chiral discrimination, through which the molecular chirality is determined by the sign of the output signals. Using a typical chiral molecule, 1,2-propanediol, and an experimentally feasible model based on spherical Fabry-Pérot cavity, we show that the molecular chirality of slowly moving enantiopure gaseous samples with $10^2-10^3$ molecules can be highly credibly distinguished in a single-shot detection. By further trapping chiral molecules, it is promising to achieve chiral discrimination at the single molecule level by using our approach.

References in corpus (8)

• Enantiomer-Specific State Transfer of Chiral Molecules
• Generalized Stern-Gerlach Effect for Chiral Molecules
• Cavity-based single atom preparation and high-fidelity hyperfine state readout
• Field locked to Fock state by quantum feedback with single photon corrections
• Optically-Induced Highly-Efficient Detection and Separation of Chiral Molecules through Shortcuts to Adiabaticity
• Entanglement-Assisted Quantum Chiral Spectroscopy
• High-resolution 'magic'-field spectroscopy on trapped polyatomic molecules
• Nondestructive dispersive imaging of rotationally excited ultracold molecules