Abstract
We propose a streamlined method of fast enantiomer-specific state transfer (ESST) of chiral molecules in cyclic three-level systems. Such three-level enantiomers are chirality-dependent systems driven by one of the three Rabi frequencies differing with a sign for the left- and right-handed chiral molecules. When the Hamiltonian of the three-level chiral molecules possesses the specific SU(2) algebraic structure, the populations transferred to the two excited states are shown to be exchanged between the left- and right-handed chiral molecules if they are initially prepared in their ground states. By employing unitary SU(2) transformation and inversely engineering time-dependent Hamiltonians with designed Rabi frequencies, we can make the left- and right-handed chiral molecules evolve respectively to different excited states from their initial ground states simultaneously. Thus a fast ESST is achieved.
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