Influence of Velocity Shell Correlations on Anomalous Scaling Exponents of Passive Scalars in Shell Models

We propose a new approach to the old-standing problem of the anomaly of the scaling exponents of passive scalars of turbulence. Different to the original problem, the distribution function of the prescribed random velocity field is multi-dimensional normal and delta-correlated in time. Here, our random velocity field is spatially correlative. For comparison, we also give the result obtained by the Gaussian random velocity field without spatial correlation. The anomalous scaling exponents H(p) of passive scalar advected by two kinds of random velocity above are determined for structure function up to p=15 by numerical simulations of the random shell model with Runge-Kutta methods to solve the stochastic differential equations. We observed that the H(p)'s obtained by the multi-dimensional normal distribution random velocity are more anomalous than those obtained by the independent Gaussian random velocity.     

Influence of velocity spatiotemporal correlations on the anomalous scaling exponents of passive scalars

In this paper, we consider spatial-temporal correlation functions of the turbulent velocities. With numerical simulations on the Gledzer--Ohkitani--Yamada (GOY) shell model, we show that the correlation function decays exponentially. The advecting velocity field is regarded as a colored noise field, which is spatially and temporally correlative. For comparison, we are also given the scaling exponents of passive scalars obtained by the Gaussian random velocity field, the multi-dimensional normal velocity field and the She--Leveque velocity field, introduced by She, et al. We observe that extended self-similarity scaling exponents H(p)/ H(2) of passive scalar obtained by the colored noise field are more anomalous than those obtained by the other three velocity fields.     

Anomalous scaling in helical turbulent environment

The influence of helicity on the anomalous scaling of the single-time structure functions of a passive scalar advected by a non-Gaussian velocity field driven by the stochastic Navier-Stokes equation is investigated by the field theoretic renormalization group and the operator-product expansion within the second order of the perturbation theory (two-loop approximation). The set of compositeoperators with the minimal critical dimensions is identified and their dependence on the helicity parameter is found. It is shown that the contribution to the critical dimensions of the structure functions of a passive scalar is given only by parts of the composite operators which are independent of the helicity parameter. Therefore, it is shown that the spatial parity violation has no impact on the anomalous scaling behavior of the passively advected scalar quantity in the turbulent environment.     

Active and passive scalar intermittent statistics in turbulent atmospheric convection

We study the small-scale statistics of active and passive scalar fields, obtained from 3D large-eddy simulations of the atmospheric boundary layer turbulence. The velocity field is anisotropic and inhomogeneous, due to the action of both buoyancy and shear. We focus on scalar field rare fluctuations dominated by the so-called fronts. Temperature, coupled to the velocity field by the Boussinesq equations, exhibits anomalous scaling and saturation of the scaling exponents to a constant value, due to the presence of thermal fronts. Although qualitatively similar, the small-scale statistics of a passive tracer advected by the convective flow shows quantitative differences: the large fluctuations of the tracer concentration field distribute differently and appear to be less intermittent than the temperature ones. To better understand these results, the role of boundaries in this problem is discussed.     

Temperature-frequency dependence and mechanism of dielectric properties for γ-Y2Si2O7

This paper reports that single-phase γ-Y2Si2O7 is prepared via a sufficient blending and cold-pressed sintering technique from Y2O3 powder and SiO2 nanopowder. It studies the dielectric properties of γ-Y2Si2O7 as a function of the temperature and frequency. The γ-Y2Si2O7 exhibits low dielectric loss and non-Debye relaxation behaviour from 25 to 1400℃ in the range of 7.3-18 GHz. The mechanism for polarization relaxation of the as-prepared γ-Y2Si2O7 differing from that of SiO 2 is explained. Such particular dielectric properties could potentially make specific attraction for extensive practical applications.     

Relating Lagrangian passive scalar scaling exponents to Eulerian scaling exponents in turbulence

Intermittency is a basic feature of fully developed turbulence, for both velocity and passive scalars. Intermittency is classically characterized by Eulerian scaling exponent of structure functions. The same approach can be used in a Lagrangian framework to characterize the temporal intermittency of the velocity and passive scalar concentration of a an element of fluid advected by a turbulent intermittent field. Here we focus on Lagrangian passive scalar scaling exponents, and discuss their possible links with Eulerian passive scalar and mixed velocity-passive scalar structure functions. We provide different transformations between these scaling exponents, associated to different transformations linking space and time scales. We obtain four new explicit relations. Experimental data are needed to test these predictions for Lagrangian passive scalar scaling exponents.     

Thermoluminescence and optically stimulated luminescence disadvantages of α-Al2O3:C crystal grown by the temperature gradient technique

Recently, α-Al₂O₃:C crystal with highly sensitive thermoluminescence (TL) and optically stimulated luminescence (OSL) has been successfully grown by the temperature gradient technique. This paper investigates the heating rate dependence of TL sensitivity, light-induced fading of TL signals and thermal stability of OSL of α-Al₂O₃:C crystals. As the heating rate increases, the integral TL response decreases and the dosimetric glow peak shifts to higher temperatures in α-Al₂O₃:C crystals. Light-induced fading of TL increases with the irradiation dose, and TL response decreases as the exposure time increases, especially in the first 15 minutes. With the increasing intensity of the exposure light, the TL fading of α-Al₂O₃:C crystal increases sharply. The OSL response of as-grown α-Al₂O₃:C crystal is quite stable below 373 K and decreases sharply for higher temperatures.     

Dy2 AlFe13 Mn3 化合物的本征磁致伸缩

通过X-射线衍射及磁测量手段研究了Dy2AlFe13Mn3化合物的结构及磁性质。研究结果表明Dy2AlFe13Mn3化合物具有六角相的Th2Ni17型结构。通过X-射线热膨胀测定法发现Dy2AlFe13Mn3化合物在245到344K的温度范围内存在负热膨胀现象，其平均热膨胀系数为α＝-1.1×10-4K-1K-1。在105到360K的温度范围内，通过比较磁性状态下的晶胞参数和由高温顺磁状态外延得到的低温顺磁状态下的晶胞参数间的差别计算了Dy2AlFe13Mn3化合物的本征磁致伸缩。结果表明Dy2AlFe13Mn3化合物的本征体磁致伸缩ωS在105到245K的温度范围内随着温度的升高而增大，由105K时的7.0×10-3 增加到245K时的9.1×10-3。随着温度的进一步升高，ωS反而减小。沿c轴方向的本征线磁致伸缩λc随着温度的升高而减小。基面内的本征线磁致伸缩λa在105到270K的温度范围内随着温度的升高而增大，从105K时的0.8×10-3增大到270K时的3.4×10-3，然后随着温度的进一步升高而减小。     

Topology of a parity-time symmetric non-Hermitian rhombic lattice

We investigate the topological properties of a trimerized parity–time(PT)symmetric non-Hermitian rhombic lattice.Although the system is PT-symmetric,the topology is not inherited from the Hermitian lattice;in contrast,the topology can be altered by the non-Hermiticity and depends on the couplings between the sublattices.The bulk–boundary correspondence is valid and the Bloch bulk captures the band topology.Topological edge states present in the two band gaps and are predicted from the global Zak phase obtained through the Wilson loop approach.In addition,the anomalous edge states compactly localize within two diamond plaquettes at the boundaries when all bands are flat at the exceptional point of the lattice.Our findings reveal the topological properties of the??PT-symmetric non-Hermitian rhombic lattice and shed light on the investigation of multi-band non-Hermitian topological phases.     

Ground state for CH2 and symmetry for methane decomposition

Using the different level of methods B3P86, BLYP, B3PW91, HF, QCISD、 CASSCF （4,4） and MP2 with the various basis functions 6-311G^＊＊, D95, cc-pVTZ and DGDZVP, the calculations of this paper confirm that the ground state is X^-3B1 with C2v group for CH2. Furthermore, the three kinds of theoretical methods, i.e. B3P86、 CCSD（T, MP4） and G2 with the same basis set cc-pVTZ only are used to recalculate the zero-point energy revision which are modified by scaling factor 0.989 for the high level based on the virial theorem, and also with the correction for basis set superposition error. These results are also contrary to X^-3∑^-g for the ground state of CH2 in reference. Based on the atomic and molecular reaction statics, this paper proves that the decomposition type （1） i.e. CH4 →CH2＋H2, is forbidden and the decomposition type （2） i.e. CH4→CHa＋H is allowed for CH4. This is similar to the decomposition of SiH4.     

Novel material for nonvolatile ovonic unified memory (OUM)－Ag11In12Te26Sb51 phase change semiconductor

In this paper, Ag_{11}In_{12}Te_{26}Sb_{51} phase change semiconductor films have been prepared by dc sputtering. The crystallization behaviour of amorphous Ag_{11}In_{12}Te_{26}Sb_{51} thin films was investigated by using differential scanning calorimetry and x-ray diffraction. It was found that the crystallization temperature is about 483K and the melting temperature is 754.8K and the activation energy for crystallization, E_a, is 2.07eV. The crystalline Ag_{11}In_{12}Te_{26}Sb_{51} films were obtained using initializer. The initialization conditions have a great effect on the sheet resistance of Ag_{11}In_{12}Te_{26}Sb_{51} films. We found that the effect of the initialization condition on the sheet resistance can be ascribed to the crystallinity of Ag_{11}In_{12}Te_{26}Sb_{51} films. The sheet resistance of the amorphous (R_{amo}) film is found to be larger than 1×10^6Ω and that of the crystalline (R_{cry}) film lies in the range from about 10^3 to 10^4Ω. So we have the ratio R_{amo}/R_{cry}=10^2～10^3, which is sufficiently large for application in memory devices.     

${ \mathcal P }{ \mathcal T }$-symmetry berry phases,topology and ${ \mathcal P }{ \mathcal T }$-symmetry breaking

We study the complex Berry phases in non-Hermitian systems with parity- and time-reversal $\left({ \mathcal P }{ \mathcal T }\right)$ symmetry. We investigate a kind of two-level system with ${ \mathcal P }{ \mathcal T }$ symmetry. We find that the real part of the the complex Berry phases have two quantized values and they are equal to either 0 or π, which originates from the topology of the Hermitian eigenstates. We also find that if we change the relative parameters of the Hamiltonian from the unbroken-${ \mathcal P }{ \mathcal T }$-symmetry phase to the broken-${ \mathcal P }{ \mathcal T }$-symmetry phase, the imaginary part of the complex Berry phases are divergent at the exceptional points. We exhibit two concrete examples in this work, one is a two-level toys model, which has nontrivial Berry phases; the other is the generalized Su–Schrieffer–Heeger (SSH) model that has physical loss and gain in every sublattice. Our results explicitly demonstrate the relation between complex Berry phases, topology and ${ \mathcal P }{ \mathcal T }$-symmetry breaking and enrich the field of the non-Hermitian physics.     

Correspondence between classical dynamics and recurrence spectra of Rydberg hydrogen atom near a metal surface

The chaotic behaviours of the Rydberg hydrogen atom near a metal surface are presented. A numerical comparison of Poincare surfaces of section with recurrence spectra for a few selected scaled energies indicates the correspondence between classical motion and quantum properties of an excited electron. Both results demonstrate that the scaled energy dominates sensitively the dynamical properties of system. There exists a critical scaled energy εc, for ε 〈 εc, the system is near-integrable, and as the decrease of ε the spectrum is gradually rendered regular and finally turns into a pure Coulomb field situation. On the contrary, if ε 〉 εc, with the increase of ε, the system tends to be non-integrable, the ergodic motion in phase space presages that chaotic motion appears, and more and more electrons are adsorbed on the metal surface, thus the spectrum becomes gradually simple.     

Anomalous Hall effect of facing-target sputtered ferrimagnetic Mn4N epitaxial films with perpendicular magnetic anisotropy

Epitaxial Mn$_{4}$N films with different thicknesses were fabricated by facing-target reactive sputtering and their anomalous Hall effect (AHE) is investigated systematically. The Hall resistivity shows a reversed magnetic hysteresis loop with the magnetic field. The magnitude of the anomalous Hall resistivity sharply decreases with decreasing temperature from 300 K to 150 K. The AHE scaling law in Mn$_{4}$N films is influenced by the temperature-dependent magnetization, carrier concentration and interfacial scattering. Different scaling laws are used to distinguish the various contributions of AHE mechanisms. The scaling exponent $\gamma > 2$ for the conventional scaling in Mn$_{4}$N films could be attributed to the residual resistivity $\rho_{xx0}$. The longitudinal conductivity $\sigma_{xx}$ falls into the dirty regime. The scaling of $\rho_{\rm AH}=\alpha \rho_{xx0} +b\rho_{xx}^{n}$ is used to separate out the temperature-independent $\rho_{xx0}$ from extrinsic contribution. Moreover, the relationship between $\rho_{\rm AH}$ and $\rho_{xx}$ is fitted by the proper scaling to clarify the contributions from extrinsic and intrinsic mechanisms of AHE, which demonstrates that the dominant mechanism of AHE in the Mn$_{4}$N films can be ascribed to the competition between skew scattering, side jump and the intrinsic mechanisms.     

Lyapunov Exponents for Particles Advected in Compressible Random Velocity Fields at Small and Large Kubo Numbers

We calculate the Lyapunov exponents describing spatial clustering of particles advected in one- and two-dimensional random velocity fields at finite Kubo numbers $\operatorname {Ku}$ (a dimensionless parameter characterising the correlation time of the velocity field). In one dimension we obtain accurate results up to $\operatorname {Ku}\sim 1$ by resummation of a perturbation expansion in $\operatorname {Ku}$ . At large Kubo numbers we compute the Lyapunov exponent by taking into account the fact that the particles follow the minima of the potential function corresponding to the velocity field. The Lyapunov exponent is always negative. In two spatial dimensions the sign of the maximal Lyapunov exponent λ ₁ may change, depending upon the degree of compressibility of the flow and the Kubo number. For small Kubo numbers we compute the first four non-vanishing terms in the small- $\operatorname {Ku}$ expansion of the Lyapunov exponents. By resumming these expansions we obtain a precise estimate of the location of the path-coalescence transition (where λ ₁ changes sign) for Kubo numbers up to approximately $\operatorname{Ku} = 0.5$ . For large Kubo numbers we estimate the Lyapunov exponents for a partially compressible velocity field by assuming that the particles sample those stagnation points of the velocity field that have a negative real part of the maximal eigenvalue of the matrix of flow-velocity gradients.     

Growth and transport features of electron-doped superconductor Pr1-xLaCexCuO4-δ thin films

<正>T’-phase electron-doped superconductor Pr_1-xLaCe_xCuO_4-δ（PLCCO） thin films are successfully prepared on SrTiO₃（100） substrates by using the dc magnetron sputtering method.It is found that the films each have a highly oriented structure along the c-axis.For optimally doped films with x≈0.10,the superconducting transition temperature T_c is 23.5 K,which is similar to that of a single crystal.The quadratic temperature dependence of the resistivity is observed when T > T_c,which can be attributed to the two-dimensional Fermi liquid behaviour.Besides,the optimal conditions for preparing the T’-phase PLCCO thin films are also discussed in detail.     

Universality in passively advected hydrodynamic fields: the case of a passive vector with pressure

Universality of statistical properties of passive quantities advected by turbulent velocity fields at changing the passive forcing mechanism is discussed. In particular, we concentrate on the statistical properties of an hydrodynamic system with pressure. We present theoretical arguments and preliminary numerical results which show that the fluxes of passive vector field and of the velocity field have the same scaling behavior. By exploiting such a property, we propose a way to compute the anomalous exponents of three dimensional turbulent velocity fields. Our findings are in agreement within 5% with experimental values of the anomalous exponents. Received 4 July 2001     

Role of the Λ(1600) in the ${K}^{-}p \rightarrow {\rm{\Lambda }}{\pi }^{0}{\pi }^{0}$ reaction

Role of the Λ(1600) is studied in the ${K}^{-}p\to {\rm{\Lambda }}{\pi }^{0}{\pi }^{0}$ reaction by using the effective Lagrangian approach near the threshold. We perform a calculation for the total and differential cross sections by considering the contributions from the Λ(1600) and Λ(1670) intermediate resonances decaying into ${\pi }^{0}{{\rm{\Sigma }}}^{* 0}(1385)$ with ${{\rm{\Sigma }}}^{* 0}(1385)$ decaying into ${\pi }^{0}{\rm{\Lambda }}$. Additionally, the non-resonance process from u-channel nucleon pole is also taken into account. With our model parameters, the current experimental data on the total cross sections of the ${K}^{-}p\to {\rm{\Lambda }}{\pi }^{0}{\pi }^{0}$ reaction can be well reproduced. It is shown that we really need the contribution from the Λ(1600) with spin-parity ${J}^{P}=1/{2}^{+}$, and that these measurements can be used to determine some of the properties of the Λ(1600) resonance. Furthermore, we also plot the π⁰Λ invariant mass distributions which could be tested by the future experimental measurements.     

Spin polarization effect for Cr2 molecule

Density functional theory （DFT） （B3P86） of Gaussian 03 has been used to optimize the structure of the Cr2 molecule, a transition metal element molecule. The result shows that the ground state for the Cr2 molecule is a 13- multiple state, indicating that there exists a spin polarization effect in the Cr2 molecule. Meanwhile, we have not found any spin pollution because the wave function of the ground state does not mingle with wave functions of higher-energy states. So the ground state for Cr2 molecule being a 13-multiple state is indicative of spin polarization effect of the Cr2 molecule among transition metal elements, that is, there are 12 parallel spin electrons in the Cr2 molecule. The number of non-conjugated electrons is greatest. These electrons occupy different spatial orbitals so that the energy of the Cr2 molecule is minimized. It can be concluded that the effect of parallel spin in the Cr2 molecule is larger than the effect of the conjugated molecule, which is obviously related to the effect of electron d delocalization. In addition, the Murrell Sorbie potential functions with the parameters for the ground state and other states of the Cr2 molecule are derived. The dissociation energy De for the ground state of the Cr2 molecule is 0.1034eV, equilibrium bond length Re is 0.3396 nm, and vibration frequency we is 73.81cm^-1. Its force constants f2, f3 and f4 are 0.0835, -0.2831 and 0.3535 aJ. nm^-4 respectively. The other spectroscopic data for the ground state of the Cr2 molecule ωeχe, Be and αe are 1.2105, 0.0562 and 7.2938 x 10^-4cm^-1 respectively.     

Investigation of isotope effects of dynamic properties for H(D) +OF reactions by the quasi-classical trajectory method

Quasi-classical trajectory (QCT) calculations are employed to study the dynamic properties for \mbox{H(D)} + \mbox{OF} reactions on the adiabatic potential energy surface (PES) of the \mbox{1}{ }^{3}\mbox{A}' triplet state. Obvious differences between the reaction probabilities for J = 0, integral cross sections for J \ne 0, branch ratios of the product and internuclear distances as well as product rotational alignments between the title reactions are found. These differences are attributed mainly to the different reduced masses of the reactants and the different zero-point energies (ZPEs) of the transition state.