Enantio-specific state transfer of chiral molecules through enantio-selective shortcut-to-adiabaticity paths
arXiv:2301.03341 · doi:10.1063/5.0144743
Abstract
An interesting method of fast enantio-specific state transfer is proposed for cyclic three-level systems of chiral molecules. We show that the fast population transfer via shortcut to adiabaticity can be accomplished for the cyclic three-level system of a general (chiral) molecule with invariant-based inverse engineering of the coupling strengths. By choosing appropriate parameters, the two enantiomers, which are initially prepared in their ground states in the three-level systems, will evolve respectively along their enantio-selective shortcut-to-adiabaticity paths to different-energy final states simultaneously, namely achieving the fast enantio-specific state transfer.
8 pages, 4 figures
References in corpus (12)
- Shortcut to adiabatic passage in two and three level atoms
- Lewis-Riesenfeld invariants and transitionless tracking algorithm
- Fast population transfer engineering of three-level systems
- Enantiomer-Specific State Transfer of Chiral Molecules
- Generalized Stern-Gerlach Effect for Chiral Molecules
- Optically-Induced Highly-Efficient Detection and Separation of Chiral Molecules through Shortcuts to Adiabaticity
- Principles of enantio-selective excitation in three-wave mixing spectroscopy of chiral molecules
- Dynamic method to distinguish between left- and right-handed chiral molecules
- Robust and highly-efficient discrimination of chiral molecules through three-mode parallel paths
- Effect of molecular rotation on enantioseparation
- State-specific Enrichment of Chiral Conformers with Microwave Spectroscopy
- Entanglement-Assisted Quantum Chiral Spectroscopy