arXiv subjects

Chong Ye

Publications and source records attributed to Chong Ye.

31 records · Page 2Linked to original sources

arXiv2021

Enantio-specific state transfer for symmetric-top chiral molecules

We study the enantio-specific state transfer in a four-level model for symmetric-top chiral molecules. Such a model is formed by coupling the electric-dipole transitions among four appropriate working states with three electromagnetic fields. It includes two cyclic three-level substructures, where the overall phases differ by $π$ with enantiomers and reflect the chirality dependence of the molecule. Based on this four-level model, two dynamic ways are proposed to achieve the approximately perfect enantio-specific state transfer for symmetric-top chiral molecules.

quant-ph↗

arXiv2021

Enantio-conversion of chiral mixtures via optical pumping

Enantio-conversion with the help of electromagnetic fields is an essential issue due to the chirality-dependence of many chemical, biological, and pharmaceutical processes. Here, we propose a method for this issue based on a five-level double-$Δ$ model of chiral molecules. By utilizing the breaking of left-right symmetry in the two $Δ$-type sub-structures, we can establish the chiral-state-selective excitation with one chiral ground state being excited to an achiral excited state and the other one being undisturbed. In the meanwhile, the achiral excited state will relax to the two chiral ground states. The two effects simultaneously acting on the chiral mixtures can convert molecules of different chiralities to the ones of the same chirality, i.e., the enantio-conversion via optical pumping. With typical parameters in gas-phase experiments, we numerically show that highly efficient enantio-conversion can be achieved. Our method works in the appearance of decoherences and without the precise control of pulse-durations (pulse-areas) and/or pulse-shapes. These advantages offer it promising features in promoting the future exploring of enantio-conversion.

quant-ph↗

arXiv2021

Improved laser-distillation method for complete enantio-conversion of chiral mixtures

Laser-assisted enantio-conversion is an ambitious issue related to chiral molecules in the atomic, molecular, and optical physics. The theoretical laser-distillation method had been proposed to realize enantio-conversion based on a four-level double-$Δ$ model of two degenerated chiral ground states and two achiral excited states. Here, we re-investigate and improve the laser-distillation method so that a chiral mixture can be converted to an enantiopure sample of the desired chirality, i.e., complete enantio-conversion, which has not been discussed in the previous theoretical works of the laser-distillation method. Since the undesired chirality may be inefficient or even cause serious side effects in pharmacology, our work plays as an important improvement to the original theoretical works of the laser-assisted enantio-conversion.

physics.chem-ph↗

arXiv2020

Evading thermal population influence in enantiomeric-specific state transfer based on a cyclic three-level system via ro-vibrational transitions

Optical methods of enantiomeric-specific state transfer had been proposed theoretically based on a cyclic three-level system of chiral molecule. According to these theoretical methods, recently the breakthrough progress has been reported in experiments [S. Eibenberger et al., Phys. Rev. Lett. 118, 123002 (2017); C. Pérez et al., Angew. Chem. Int. Ed. 56, 12512 (2017)] for cold gaseous chiral molecules but with low state-specific enantiomeric enrichment. One of the limiting factors is the influence of the thermal population in the selected three purely rotational states in experiment. Here, we theoretically propose an improved optical method of enantiomeric-specific state transfer to effectively evade such an adverse impact of thermal population by introducing ro-vibrational transitions for the cyclic three-level system of chiral molecules. Then, at the typical temperature in experiments approximately only the lowest state in the chosen three-level system is thermally occupied and the optical method of enantiomeric-specific state transfer works well. Comparing with the case of purely rotational transitions where all the three states are thermally occupied, this modification will remarkably increase the obtained state-specific enantiomeric enrichment with enantiomeric excess approximately 100%.

quant-ph↗

arXiv2020

Enantio-discrimination via light deflection effect

We propose a theoretical method for enantio-discrimination based on the light deflection effect in four-level models of chiral molecules. This four-level model consists of a cyclic three-level subsystem coupled by three strong driving fields and an auxiliary level connected to the cyclic three-level subsystem by a weak probe field. It is shown that the induced refractive index for the weak probe field is chirality-dependent. Thus it will lead to chirality-dependent light deflection when the intensities of two of the three strong driving fields are spatially inhomogeneous. As a result, the deflection angle of the weak probe light can be utilized to detect the chirality of pure enantiomers and enantiomeric excess of chiral mixture. Therefore, our method may act as a tool for enantio-discrimination.

physics.optics↗

arXiv2020

Fast enantioconversion of chiral mixtures based on a four-level double-$Δ$ model

Based on the four-level double-$Δ$ model composed of two degenerated (left- and right-handed) chiral ground states and two achiral excited states, we propose a purely optical method for enantio-conversion of chiral mixture. By choosing appropriate parameters, the original four-level model will be simplified to two effective two-level sub-systems with each of them involving one chiral ground state. Then, with the help of well-designed optical operations, the initial unwanted and wanted chiral ground states are converted, respectively, to the wanted chiral ground state and an auxiliary chiral excited state with the wanted chirality, i.e., achieving the enantioconversion of the chiral mixture. Comparing with the original work of enantioconversion based on the four-level double-$Δ$ model with the requirement of the time-consuming relaxation step and repeated operations, our method can be three orders of magnitude faster since we use only purely optical operations. Thus, it offers a promising candidate for fast enantioconversion when the total operation time is limited due to the racemization and/or experimental conditions.

physics.optics↗

arXiv2019

Enantiomeric excess determination based on nonreciprocal transition induced spectral line elimination

The spontaneous emission spectrum of a multi-level atom or molecule with nonreciprocal transition is investigated. It is shown that the nonreciprocal transition can lead to the elimination of a spectral line in the spontaneous emission spectrum. As an application, we show that nonreciprocal transition arises from the phase-related driving fields in chiral molecules with cyclic three-level transitions, and the elimination of a spectral line induced by nonreciprocal transition provides us a method to determine the enantiomeric excess for the chiral molecules without requiring the enantio-pure samples.

quant-ph↗

arXiv2019

On the boundary condition and related instability in the Smoothed Particle Hydrodynamics

In this work, we explore various relevant aspects of the Smoothed Particle Hydrodynamics regarding Burger's equation. The stability, precision, and efficiency of the algorithm are investigated in terms of different implementations. In particular, we argue that the boundary condition plays an essential role in the stability of numerical implementation. Besides, the issue is shown to be closely associated with the initial particle distribution and the interpolation scheme. Among others, we introduce an interpolation scheme termed symmetrized finite particle method. The main advantage of the scheme is that its implementation does not involve any derivative of the kernel function. Concerning the equation of motion, the calculations are carried out using two distinct scenarios where the particles are chosen to be either stationary or dynamically evolved. The obtained results are compared with those obtained by using the standard finite difference method for spatial derivatives. Our numerical results indicate subtle differences between different schemes regarding the choice of boundary condition. In particular, a novel type of instability is observed where the regular distribution is compromised as the particles start to traverse each other. Implications and further discussions of the present study are also addressed.

physics.comp-ph↗

arXiv2019

Effective two-level models for highly efficient inner-state enantio-separation based on cyclic three-level systems of chiral molecules

Based on cyclic three-level systems of chiral molecules, we propose two methods to realize highly efficient inner-state enantio-separations of a chiral mixture with the two enantiomers initially prepared in their ground states. Our methods work in the region where the evolutions of the two enantiomers can be described by their corresponding effective two-level models, simultaneously. The approximately $100\%$-efficiency inner-state enantio-separations can be realized when the probability occupying the ground state of one enantiomer becomes $0$ by experiencing half-integer periods of its corresponding on-resonance Rabi oscillation and in the meanwhile the other one still stays approximately in the ground state, under the conditions that the two enantiomers are governed by the effective on-resonance and large-detuning two-level models, respectively. Alternatively, the exactly $100\%$-efficiency inner-state enantio-separation can be obtained when the probabilities occupying the ground states of the two enantiomers simultaneously experience half-integer and integer periods of their corresponding on-resonance and detuned (instead of largely-detuned) Rabi oscillations with final $0$ and $1$ probabilities occupying the ground state, respectively.

physics.optics↗

arXiv2019

Static non-linear Schrödinger equations for the achiral-chiral transitions of polar chiral molecules

In the mean-field theory, the stabilization of polar chiral molecules is understood as a quantum phase transition where the mean-field ground state of molecules changes from the achiral eigenstate of the molecular Hamiltonian to one of the degenerated chiral states as the increase of the intermolecular interaction. Starting from the many-body Hamiltonian of the molecular gases with electric dipole-dipole interactions, we give the static non-linear Schrödinger equations without free parameters to explore the achiral-chiral transitions of polar chiral molecules. We find that the polar chiral molecules of different species can be classified into two categories: At the critical point for the achiral-chiral transition, the mean-field ground state changes continuously in one category, and changes discontinuously in the other category. We further give the mean-field phase diagram of the achiral-chiral transitions for both two categories.

physics.chem-ph↗

arXiv2019

Determination of enantiomeric excess with chirality-dependent AC Stark effects in cyclic three-level models

Determination of enantiomeric excess is important and remains challenges. We theoretically propose a new spectroscopic method for this issue based on the chirality-dependent AC Stark effects in cyclic three-level models under the three-photon resonance condition. The enantiomeric excess of the chiral mixture is determined by comparing the amplitudes of the two chosen AC Stark peaks in the Fourier transform spectrum of the induced polarizations, which are (approximately) proportional to the molecule numbers of the two enantiomers, respectively. Comparing with current spectroscopic methods based on the interference between the electric- and (usually weak) magnetic-dipole transition moments and/or with the need for enantio-pure samples, our method only involves electric-dipole transitions and does not require the enantio-pure samples. Therefore, it will give strong chiral signals and can be applied to the determinations of enantiomeric excess for chiral molecules whose enantio-pure samples are still challenging to achieve.

physics.optics↗

arXiv2018

Real single-loop cyclic three-level configuration of chiral molecules

Single-loop cyclic three-level ($Δ$-type) configuration of chiral molecules was used for enantio-separation in many theoretical works. Considering the effect of molecular rotation, this simple single-loop configuration is generally replaced by a complicated multiple-loop configuration containing multiple degenerate magnetic sub-levels and the ability of the enantio-separation methods is suppressed. For chiral asymmetric top molecules, we propose a scheme to construct a real single-loop $Δ$-type configuration with no connections to other states by applying three microwave fields with appropriate polarization vectors and frequencies. With our scheme, the previous theoretical proposals for enantio-separation based on single-loop $Δ$-type configurations can be experimentally realized when the molecular rotation is considered.

quant-ph↗

arXiv2018

The Role of Interaction in the Pairing of Two Spin-orbit Coupled Fermions

We investigate the role of a repulsive s-wave interaction in the two-body problem in the presence of spin orbit couplings, motivated by current interests in exploring exotic superfluid phases in spin-orbit coupled Fermi gases. For weak spin orbit coupling where the density of states is not significantly altered, we analytically show that the high-energy states become more important in determining the binding energy when the interaction strength decreases. Consequently, tuning the interaction gives rise to a rich ground state behavior, including a zigzag of the ground state momentum or inducing transitions among the meta-stable states. By exactly solving the two-body problem for a spin-orbit coupled Fermi mixture, we demonstrate that our analysis can also apply to the case when the density of states is significantly modified by the spin-orbit coupling. Our findings pave the way for understanding and controlling the paring of fermions in the presence of spin orbit couplings.

cond-mat.quant-gas↗