Single photon transport properties in coupled cavity arrays nonlocally coupled to a two-level atom in the presence of dissipation

We discuss the effects of dissipation on the behavior of single photon transport in a system of coupled cavity arrays, with the two nearest cavities nonlocally coupled to a two-level atom. The single photon transmission amplitude is solved exactly by employing the quasi-boson picture. We investigate two different situations of local and nonlocal couplings, respectively. Comparing the dissipative case with the nondissipative one reveals that the dissipation of the system increases the middle dip and lowers the peak of the single photon transmission amplitudes, broadening the line width of the transport spectrum. It should be noted that the influence of the cavity dissipation to the single photon transport spectrum is asymmet- ric. By comparing the nonlocal coupling with the local one, one can find that the enhancement of the middle dip of single photon transmission amplitudes is mostly caused by the atom dissipation and that the reduced peak is mainly caused by the cavity dissipation, no matter whether it is a nonlocal or local coupling case. Whereas in the nonlocal coupling case, when the coupling strength gets stronger, the cavity dissipation has a greater effect on the single photon transport spectrum and the atom dissipation affection becomes weak, so it can be ignored.

Vacuum induced transparency and slow light phenomena in a two-level atomic ensemble controlled by a cavity

We study the optical properties of a two-level atomic ensemble controlled by a high-finesse cavity. Even though the cavity is initially in the vacuum state in the absence of external driving, the probe response of the atomic ensemble can be dramatically modified. When the collectively enhanced atom–cavity coupling is strong enough and the cavity decay rate is much smaller than the atomic damping rate, an electromagnetically induced transparency-like coherent phenomenon emerges with a dip absorption for the response of the two-level atoms in the cavity without driving, and thus is called vacuum induced transparency. We also show the slow light with very low group velocity in such an atomic ensemble.

Effects of an applied low frequency field on the dynamics of a two-level atom interacting with a single-mode field

The effects of an applied low frequency field on the dynamics of a two-level atom interacting with a single-mode field are investigated. It is shown that the time evolution of the atomic population is mainly controlled by the coupling constants and the frequency of the low frequency field, which leads to a low frequency modulation function for the time evolution of the upper state population. The amplitude of the modulation function becomes larger as the coupling constants increase. The frequency of the modulation function is proportional to the frequency of the low frequency field, and decreases with increasing coupling constant.

The breaking point between fast-and slow-light in a degenerate two-level atomic system

This paper investigates the breaking point between fast- and slow-light in a degenerate two-level atomic system, where fast-light can be converted to slow-light arbitrarily on a single transition line by adjusting the strength of the pumping field. An equivalent incoherent pumping rate is introduced in this simplified theoretical model which exploits the dependence of this feature. The experimental observation is presented as evidence of the breaking point where the injected power is about 0.08 mW.

The entanglement evolution of two coupling two-level atoms interacting with a single-mode vacuum field in multiphoton Tavis-Cummings model

Using multipohton Tavis-Cummings model,the entanglement evolution of two coupling two-level atoms in Bell states interacting with a single-mode vacuum field is investigated by using negativity.The influences of coupling constants between atoms,the atomic initial states and the photon number of transition on the entanglement evolution of two coupling two-level atoms are discussed.The results obtained using the numerical method show that the entanglement of two atoms is related with coupling constants between atoms,the atomic initial states and the photon number of transition.The two-atom entanglement state will forever stay in the maximum entanglement state when the initial state is β11〉.When the initial state of two atoms is β01〉,the entanglement of two atoms displays periodic oscillation behavior.And its oscillation period decreases with increasing of coupling constant between atoms or the photon number of transition.On the other hand,when the initial state is β00〉 or β10〉,the entanglement of two atoms displays quasiperiodic oscillation behavior and its oscillation period decreases with increasing of coupling constant between atoms or the photon number of transition.

Quantum Fisher Information of Two-Level Atomic System under the Influence of Thermal Field, Intrinsic Decoherence, Stark Effect and Kerr-Like Medium

In this paper, we have proposed the numerical calculations to study the quantum entanglement (QE) of moving two-level atom interacting with a coherent and the thermal field influenced by intrinsic decoherence (ID), Kerr medium (non-linear) and the Stark effect. The wave function of the complete system interacting with a coherent and the thermal field is calculated numerically affected by ID, Kerr (non-linear) and Stark effects. It has been seen that the Stark, Kerr, ID and the thermal environment have a significant effect during the time evolution of the quantum system. Quantum Fisher information (QFI) and QE decrease as the value of the ID parameter is increased in the thermal field without the atomic movement. It is seen that QFI and von Neumann entropy (VNE) show an opposite and periodic response in the presence of atomic motion. The non-linear Kerr medium has a more prominent and significant effect on the QE as the value of the Kerr parameter is decreased. At smaller values of the non-linear Kerr parameter, the VNE increases, however, QFI decreases, so QFI and VNE have a monotonic connection with one another. As the value of the Kerr parameter is increased, the effect of non-linear Kerr doesn’t stay critical on both QFI and QE. However, a periodic response of QE is seen because of the atomic movement which becomes modest under natural impacts. Moreover, it has been seen that QFI and QE rot soon at the smaller values of the Stark parameter. However, as the value of the Stark parameter is increased, the QFI and QE show periodic response even when the atomic movement is absent.

Selective reflection combined with Fabry-Perot effects from two-level atoms confined between two dielectric walls

The coefficient of selective reflection at oblique incidence from two-level atoms confined between two dielectric walls is calculated in this paper. It is found to be related to the transient behaviour of atoms after colliding with the wall and the distribution of the field inside the vapour corresponds to L/λ, with L the thickness of the film and λ the incident wavelength. We find that the sub-Doppler structure is manifest both for normal incidence and small angle oblique incidence, It is feasible to detect the real part of selective reflection in several cases that have not been achieved before.

Preparation and control of atomic optimal entropy squeezing states for a moving two-level atom under control of the two-mode squeezing vacuum fields

From the viewpoint of quantum information, this paper studies preparation and control of atomic optimal entropy squeezing states （AOESS） for a moving two-level atom under control of the two-mode squeezing vacuum fields. Necessary conditions of preparation of the AOESS are analysed, and numerical verification of the AOESS is finished. It shows that the AOESS can be prepared by controlling the time of the atom interaction with the field, cutting the entanglement between the atom and field, and adjusting squeezing factor of the field. An atomic optimal entropy squeezing sudden generation in different components can alternately be realized by controlling the field-mode structure parameter.

Entanglement Quantifier Based on Atomic Wehrl Entropy for Non-Linear Interaction between a Single Two-Level Atom and SU(1,1) Quantum System

In this paper, we study the dynamics of the atomic inversion, scaled atomic Wehrl entropy and marginal atomic Wehrl density for a single two-level atom interacting with SU(1,1) quantum system. We obtain the expectation values of the atomic variables using specific initial conditions. We examine the effects of different parameters on the scaled atomic Wehrl entropy and marginal atomic Wehrl density. We observe an interesting monotonic relation between the different physical quantities for different values of the initial atomic position and detuning parameter.

Entanglement of two-level atoms' quantum states in a strong thermal radiation field

The two-level atom is described by Pauli sign and environment is described by infinite harmonic particle thermal reservoir.We have studied the entanglement of two-level atoms which are put in the strongly thermal radiation field.The two-level atoms' reducible density rectangular array is obtained.We discuss the properties of entanglement by virtue of concurrence.It is shown that the two two-level atoms initially situated in different coherent superposition states,entanglement of atoms have obvious dissimilarity.

Analytical solutions for a doubly driven two-level atom

We have deduced analytical solutions of an energy level diagram of the doubly driven/dressed atom for a two-level atom exposed to a strong near-resonant bichromatic laser field in a special case, i.e., the bichromatic field with frequencies ω1 and ω2, and Rabi frequencies ？1 and ？2, in which the first coupling field of ？1 acts on the bare atomic levels, and then the resulting singly dressed states are driven by the second coupling field of ？2, thus resulting in the doubly dressed atom.We have measured the probe absorption spectra of a doubly driven two-level atom. The system consists of 52S1/2, F= 2 and 5~2P_（3/2）, F＇= 3 states of ^（87）Rb atoms in a magneto-optical trap（MOT） as well as the cooling/trapping beams and an additional coupling field. As for the spectroscopic properties of the doubly driven two-level atom, theoretical analytical solutions are in general agreement with the experimental spectrum as a whole.

Entanglement of Moving and Non-Moving Two-Level Atoms

In this paper we study the dynamics of the atomic inversion, von Neumann entropy and entropy squeezing for moving and non-moving two-level atoms interacting with a Perelomov coherent state. The final state of the system using specific initial conditions is obtained. The effects of Perelomov and detuning parameters are examined in the absence and presence of the atomic motion. Important phenomena such as the collapse and revival are shown to be very sensitive to the variation of the Perelomov parameter in the presence of detuning parameter. The results show that the Perelomov parameter is very useful in generating a high amount of entanglement due to variation of the detuning parameter.

Some studies of the interaction between two two-level atoms and SU(1,1) quantum systems

Herein, we present an approach to look for the best phenomenon to measure quantum correlation. The system of two isolated qubits each interacting with a single-mode cavity was theoretically created to study the quantum correlation. Some of the phenomena, such as the quantum discord and concurrence, were generated through such a system. The influences of initial state purity, qubit motion, and detuning parameters were discussed for the phenomena. These parameters for a specific value show that the behavior of phenomena are analogous. It is interesting to mention that some values of detuning undergo a sudden death of phenomena, and the quantum discord still captures the qubits quantum correlation. We predict that the quantum discord may be a better measure of quantum correlation than concurrence.

Observation of Superluminal in Doppler Broadened Two-Level Atomic Systems in Magnetic Field

A novel method to control the group velocity of light propagation in a two-level atomic system without additional optical field is proposed. Numerical result and experimental data shows that by changing the magnetic field intensity and vapor temperature, the group velocity of probe light can be controlled in an appropriate region.

Nonreciprocal photon blockade in a spinning resonator coupled to two two-level atoms

We propose a scheme to simultaneously achieve nonreciprocal conventional photon blockade(NCPB) and unconventional photon blockade(NUPB) in a spinning resonator coupled to two two-level atoms. We show that, with the unequal frequency detuning of cavity and atoms from the driving laser, the quantum efect of the nonreciprocal photon blockade can be realized based on two regimes under diferent driving strengths. We confirm that, the NUPB results from the quantum destructive interference between distinct pathways when the driving laser is loaded from one side, whereas the destructive interference is broken when the system is driven from the other side. Moreover, the NCPB originates from whether the single excitation resonance condition is satisfied, corresponding to the opposite driving direction in contrast to the former. Besides, we obtain the optimal nonreciprocal results by appropriately choosing the system parameters. Interestingly, the UPB exhibits stronger robustness to thermal noises,and the nonreciprocity still exists up to a high thermal excitation. This work provides an alternative way to achieve nonreciprocal quantum devices based on the nonreciprocal photon blockade, which may help to develop information network processing.

Metal-organic framework-based single-atom electro-/ photocatalysts: Synthesis, energy applications, and opportunities

Single-atom catalysts(SACs)have gained substantial attention because of their exceptional catalytic properties.However,the high surface energy limits their synthesis,thus creating significant challenges for further development.In the last few years,metal–organic frameworks(MOFs)have received significant consideration as ideal candidates for synthesizing SACs due to their tailorable chemistry,tunable morphologies,high porosity,and chemical/thermal stability.From this perspective,this review thoroughly summarizes the previously reported methods and possible future approaches for constructing MOF-based(MOF-derived-supported and MOF-supported)SACs.Then,MOF-based SAC's identification techniques are briefly assessed to understand their coordination environments,local electronic structures,spatial distributions,and catalytic/electrochemical reaction mechanisms.This review systematically highlights several photocatalytic and electrocatalytic applications of MOF-based SACs for energy conversion and storage,including hydrogen evolution reactions,oxygen evolution reactions,O_(2)/CO_(2)/N_(2) reduction reactions,fuel cells,and rechargeable batteries.Some light is also shed on the future development of this highly exciting field by highlighting the advantages and limitations of MOF-based SACs.

Single-atom Pt on carbon nanotubes for selective electrocatalysis

Utilizing supported single atoms as catalysts presents an opportunity to reduce the usage of critical raw materials such as platinum,which are essential for electrochemical reactions such as hydrogen oxidation reaction(HOR).Herein,we describe the synthesis of a Pt single electrocatalyst inside single-walled carbon nanotubes(SWCNTs)via a redox reaction.Characterizations via electron microscopy,X-ray photoelectron microscopy,and X-ray absorption spectroscopy show the single-atom nature of the Pt.The electrochemical behavior of the sample to hydrogen and oxygen was investigated using the advanced floating electrode technique,which minimizes mass transport limitations and gives a thorough insight into the activity of the electrocatalyst.The single-atom samples showed higher HOR activity than state-of-the-art 30%Pt/C while almost no oxygen reduction reaction activity in the proton exchange membrane fuel cell operating range.The selective activity toward HOR arose as the main fingerprint of the catalyst confinement in the SWCNTs.

Strong synergy between physical and chemical properties:Insight into optimization of atomically dispersed oxygen reduction catalysts

Atomically dispersed catalysts exhibit significant influence on facilitating the sluggish oxygen reduction reaction(ORR)kinetics with high atom economy,owing to remarkable attributes including nearly 100%atomic utilization and exceptional catalytic functionality.Furthermore,accurately controlling atomic physical properties including spin,charge,orbital,and lattice degrees of atomically dispersed catalysts can realize the optimized chemical properties including maximum atom utilization efficiency,homogenous active centers,and satisfactory catalytic performance,but remains elusive.Here,through physical and chemical insight,we review and systematically summarize the strategies to optimize atomically dispersed ORR catalysts including adjusting the atomic coordination environment,adjacent electronic orbital and site density,and the choice of dual-atom sites.Then the emphasis is on the fundamental understanding of the correlation between the physical property and the catalytic behavior for atomically dispersed catalysts.Finally,an overview of the existing challenges and prospects to illustrate the current obstacles and potential opportunities for the advancement of atomically dispersed catalysts in the realm of electrocatalytic reactions is offered.

Atom substitution of the solid-state electrolyte Li_(10)GeP_(2)S_(12)for stabilized all-solid-state lithium metal batteries

Solid-state electrolyte Li_(10)GeP_(2)S_(12)(LGPS)has a high lithium ion conductivity of 12 mS cm^(-1)at room temperature,but its inferior chemical stability against lithium metal anode impedes its practical application.Among all solutions,Ge atom substitution of the solid-state electrolyte LGPS stands out as the most promising solution to this interface problem.A systematic screening framework for Ge atom substitution including ionic conductivity,thermodynamic stability,electronic and mechanical properties is utilized to solve it.For fast screening,an enhanced model Dop Net FC using chemical formulas for the dataset is adopted to predict ionic conductivity.Finally,Li_(10)SrP_(2)S_(12)(LSrPS)is screened out,which has high lithium ion conductivity(12.58 mS cm^(-1)).In addition,an enhanced migration of lithium ion across the LSr PS/Li interface is found.Meanwhile,compared to the LGPS/Li interface,LSrPS/Li interface exhibits a larger Schottky barrier(0.134 eV),smaller electron transfer region(3.103?),and enhanced ability to block additional electrons,all of which contribute to the stabilized interface.The applied theoretical atom substitution screening framework with the aid of machine learning can be extended to rapid determination of modified specific material schemes.

Optimizing high-coordination shell of Co-based single-atom catalysts for efficient ORR and zinc-air batteries

Atom-level modulation of the coordination environment for single-atom catalysts(SACs)is considered as an effective strategy for elevating the catalytic performance.For the MNxsite,breaking the symmetrical geometry and charge distribution by introducing relatively weak electronegative atoms into the first/second shell is an efficient way,but it remains challenging for elucidating the underlying mechanism of interaction.Herein,a practical strategy was reported to rationally design single cobalt atoms coordinated with both phosphorus and nitrogen atoms in a hierarchically porous carbon derived from metal-organic frameworks.X-ray absorption spectrum reveals that atomically dispersed Co sites are coordinated with four N atoms in the first shell and varying numbers of P atoms in the second shell(denoted as Co-N/P-C).The prepared catalyst exhibits excellent oxygen reduction reaction(ORR)activity as well as zinc-air battery performance.The introduction of P atoms in the Co-SACs weakens the interaction between Co and N,significantly promoting the adsorption process of ^(*)OOH,resulting in the acceleration of reaction kinetics and reduction of thermodynamic barrier,responsible for the increased intrinsic activity.Our discovery provides insights into an ultimate design of single-atom catalysts with adjustable electrocatalytic activities for efficient electrochemical energy conversion.