Different from the conventional Rydberg antiblockade (RAB) regime that either requires weak Rydberg-Rydberg interaction (RRI), or compensates Rydberg-Rydberg interaction (RRI)-induced energy shift by introducing dispersive interactions, we show that RAB regime can be achieved by resonantly driving the transitions between ground state and Rydberg state under strong RRI. The Rabi frequencies are of small amplitude and time-dependent harmonic oscillation, which plays a critical role for the presented RAB. The proposed unconventional RAB regime is used to construct high-fidelity controlled-Z (CZ) gate and controlled-not (CNOT) gate in one step. Each atom requires single external driving. And the atomic addressability is not required for the presented unconventional RAB, which would simplify experimental complexity and reduce resource consumption.

Chlorine termination of mixed Ge/Si(100) surfaces substantially enhances the contrast between Ge and Si sites in scanning tunneling microscopy observations. This finding enables a detailed investigation of the spatial distribution of Ge atoms deposited on Si(100) by atomic layer epitaxy. The results are corroborated by photoemission measurements aided by an unusually large chemical shift between Cl adsorbed on Si and Ge. Adsorbate-substrate atomic exchange during growth is shown to be important. The resulting interface is thus graded, but characterized by a very short length scale of about one monolayer.

One scheme is presented to construct the robust multi-qubit arbitrary-phase controlled-phase gate (CPG) with one control and multiple target qubits in Rydberg atoms using the Lewis-Riesenfeld (LR) invariant method. The scheme is not limited by adiabatic condition while preserves the robustness against control parameter variations of adiabatic evolution. Comparing with the adiabatic case, our scheme does not require very strong Rydberg interaction strength. Taking the construction of two-qubit π CPG as an example, our scheme is more robust against control parameter variations than non-adiabatic scheme and faster than adiabatic scheme.

We propose to discriminate chiral molecules by combining one-and two-photon processes in a closed-loop configuration. The one-photon-coupling intrinsic π-phase difference between two enantiomers leads to their different superposition states, which is then followed by a two-photon process through three-mode parallel paths (3MPPs), enabling the discrimination of enantiomers by inducing their entirely-different population distributions. The 3MPPs are constructed by "chosen paths", a method of shortcuts to adiabaticity (STA), exhibiting a fast two-photon process. As an example, we propose to perform the scheme in 1, 2-propanediol molecules, which shows relatively robust and highly-efficient results under considering the experimental issues concerning unwanted transitions, imperfect initial state, pulse shaping, control errors and the effect of energy relaxations. The present work may provide help for laboratory researchers in a robust separation of chiral molecules.

Quantum optical methods have great potential for highly efficient discrimination of chiral molecules. We propose quantum interference-based schemes of enantio-discrimination under microwave regime among molecular rotational states. The quantum interference between field-driven one- and two-photon transitions of two higher states is designed to be constructive for one enantiomer but destructive for the other, since a certain transition dipole moment can be set to change sign with enantiomers. Therefore, two enantiomers can evolve into entirely different states from the same ground state. Through strengthening the constructive interference, the quantum Zeno effect is found in one enantiomer and then its excitation is suppressed, which also enables the enantio-discrimination. We simulate the schemes for differentiating between S and R enantiomers of 1, 2-propanediol (C3H8O2) molecules. With the analysis of the phase sensitivity to microwave fields and the effect of energy relaxations, the highly efficient enantio-discrimination of the 1, 2-propanediol molecules may be achieved.

With a resonant amplitude-modulation field on two Rydberg atoms, we propose a Rydberg antiblockade (RAB) regime, where the Rabi oscillation between collective ground and excited states is induced. A controlled-Z gate can be yielded through a Rabi cycle. Further, several common issues of the RAB gates are solved by modifying the parameter relation. The gate fidelity and the gate robustness against the control error are enhanced with a shaped pulse. The requirement of control precision of the Rydberg-Rydberg interaction strength is relaxed. In addition, the atomic excitation is restrained and therefore the gate robustness against the atomic decay is enhanced.

With a microwave-regime cyclic three-state configuration, an enantiomer-selective state transfer (ESST) is carried out through the two-path interference between a direct one-photon coupling and an effective two-photon coupling. The π-phase difference in the one-photon process between two enantiomers makes the interference constructive for one enantiomer but destructive for the other. Therefore only one enantiomer is excited into a higher rotational state while the other remains in the ground state. The scheme is of flexibility in the pulse waveforms and the time order of two paths. We simulate the scheme in a sample of cyclohexylmethanol (C7H14O) molecules. Simulative results show the robust and high-fidelity ESST can be obtained when experimental concerns are considered. Finally, we propose to employ the finished ESST in implementing enantio-separation and determining enantiomeric excess.

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