Phase State as a Limiting Case of SU（1,1） Coherent State

We show that the Susskind-Glogower phase state is a limiting case of a kind of SU（1,1） coherent states. By analogy, based on the bipartite entangled state representation （ESR） we demonstrate that an appropriate SU（1,1） coherent state composed of the two-mode unitary phase operator e^i also leads to a new phase state in two-mode Fock space, e^i is diagonalized in the ESR.     

Statistical Properties of the nonlinear SU（1,1） Coherent States

Using non-Hermitian realizations of SU(1,1) Lie algebra in terms of an f-oscillator,we generalize the notion of nonlinear coherent states to the single-mode and two-mode nonlinear SU(1,1) coherent states.Taking the nonlinearity function f(k)=Lk^1(η^2)[(k 1)Lk^0(η^2)]^-1,their statistical properties are studied.     

Energy Distribution in the SU（1,1）Coherent State of Hydrogen

We Construct and SU(1,1)coherent state for hydrogen,we discuss its properties,and we give the energy distribution law of the atom.The coherent state may be used to describe the atomic states of the discrete spectrum.     

Fidelity Susceptibility in the SU（2） and SU（1,1） Algebraic Structure Models

We mainly explore the fidelity susceptibility based on the Lie algebraic method. On physical grounds, the exact expressions of fidelity susceptibilities can be respectively obtained in SU（2） and SU（1,1） algebraic structure models, which are applied to one-body system and many-body systems, such as the single spin model, the single-mode squeeze harmonic oscillator model and the BCS model. In terms of the double-time Green-function method, our general conclusions are illustrated with two models which exhibit the fidelity susceptibilities at the finite temperature and T = O.     

Generation of SU（2） Coherent States for a Cavity Mode and a Collective Atomic Mode

We propose a scheme for generation of SU（2） coherent states for an atomic ensemble and a cavity mode. In the scheme a collection of two-level atoms resonantly interact with a single-mode quantized field. Under certain conditions, the system can evolve from a Fock state to a highly entangled SU（2） coherent state. The operation speed increases as the number of atoms increases, which is important in view of deeoherence.     

Nonlinear Interaction and Entanglement Transfer from SU（1,1） Coherent State to Mixed Atoms

For nonlinear interactions with different forms of intensity-dependent coupling, entanglement transfer from the correlated two-mode SU（1,1） coherent states （SCS） to the initially separable and mixed atoms is investigated. It is found that suitable intensity-dependent coupling can enhance the entanglement transfer and make the atomic entanglement evolve periodically especially for the initially mixed atomic states. For SCS, the entanglement between the two modes is strengthened with the increase of the photon number difference （PND） between the two modes of the fields. When PND is odd, the entanglement between the atoms is less than that when PND is even.     

Chiral SU（3） Quark Model Study of Tetraquark States： cnn^-s^-/css^-s^-

The new members of the charm-strange family Dsj^＊（2317）, Dsj（2460）, and Ds（2632）, which have the surprising properties, are challenging the present models. Many theoretical interpretations have been devoted to this issue. Most authors suggest that they are not the conventional cs^- quark model states, but possibly are four-quark states, molecule states, or mixtures of a P-wave cs^- and a four-quark state. In this work, we follow the four-quark-state picture, and study the masses of cnn^-s^-/css^-s^- states （n is u or d quark） in the chiral SU（3） quark model. The numerical results show that the mass of the mixed four-quark state （cnn^-s^-/css^-s^-） with spin parity j^P ： 0^＋ might not be Ds （2632）. At the same time, we also conclude that Dsj^＊（2317） and Dsj（2460） cannot be explained as the pure four-quark state.     

EPR Entangled States for Bipartite Kinematics and New Bosonic Representation of SU（2） Algebra

We find that the Einstein-Podolsky-Rosen (EPR) entangled state representation descr/bing bipartite kinematics is closely related to a new Bose operator realization of SU(2) Lie algebra. By virtue of the new realization some ttamiltonian eigenfunction equation can be directly converted to the generalized confluent equation in the EPR entangled state representation and its solution is obtainable. This thus provides a new approach for studying dynamics of angular momentum systems.     

Luminescence Kinetic Model for Long-Afterglow Phosphor （Sr0.5 Ca1.5 ） MgSi2O7 ：Eu^2＋ ,Dy^3＋

A luminescence kinetic model for the green-emission long-afterglow phosphor (Sr0.5 Ca1.5)MgSi2O7:Eu^2 ,Dy^3 is proposed based on the studies of the thermoluminescence and isothermal decay curves at different temperatures.The isothermal decay curves at different temperatures meet the hyperbolic law and show to be dependent on temperature. Combined with the decay curves and the thermoluminescence curves, it can be concluded that the long afterglow of this material originates from the traps with energy distribution rather than a single level trap.Upon illumination with ultra-violet or visible light, the trap filling can proceed via excitation of 4f electrons to the 5d level of Eu^2 ions. After excitation, 5d electrons can be transferred to the trap related to Dy3 ions, and Eu^3 is left behind. Upon subsequent heating, the electron is released from this trap and recombines with Eu^3 to produce Eu^2 emission.     

Dissociative Chemisorption of an H2（v,j） Molecule on Rigid Ni （100） Surface： Dependence on Surface Topologies and Initial Rovibrational States of the Molecules

The H2(v,j) Ni(100) collision system has been studied to understand the effects of the surface sites and initial rovibrational states of the molecule on molecule-surface interactions, by a quasiclassical molecular dynamic simulation method. Dissociative adsorption of an H2 molecule on the rigid Ni(100) surface is investigated at topologically different three sites of the surface. Interaction between the molecule and Ni surface was described by a London-Eyring-Polani-Sato (LEPS) potential. Dissociative chemisorption probabilities of the H2(v, j) molecule on various sites of the surface are presented as a function of the translation energies between 0.001-1.0eV. The probabilities obtained at each collision site have unique behaviour. At lower collision energies, indirect processes enhance the reactivity, effects of the rotational excitations and impact sites on the reactivity are more pronounced. The results are compared with the available studies. The physical mechanisms underlying the results and quantum effects are discussed.