Thermal entanglement in two-qutrit spin-1 anisotropic Heisenberg model with inhomogeneous magnetic field

The thermal entanglement of a two-qutrit spin-1 anisotropic Heisenberg XXZ chain in an inhomogeneous magnetic field is studied in detail. The effects of the external magnetic field (B), a parameter b which controls the inhomogeneity of B, and the bilinear interaction parameters J_{x=Jy≠Jz on the thermal variation of the negativity are studied in detail. It is found that negativity N decreases when the values of magnetic field, inhomogeneity b and temperature are increasing. In addition, N remains at higher temperatures for higher values of Jz and lower values of B and b.}     

Thermal entanglement in the anisotropic Heisenberg model with Dzyaloshinskii-Moriya interaction in an inhomogeneous magnetic field

The thermal entanglement of a two-qubit anisotropic Heisenberg XXZ chain with Dzyaloshinskii-Moriya (DM) interaction in an inhomogeneous magnetic field was studied in detail. The effects of the DM parameter, external magnetic field (B), a parameter b which controls the inhomogeneity of B and the bilinear interaction parameters J_x = J_y ≠ J_z (the anisotropic case) on the concurrence (C) was formulated and studied in detail. The behaviors of the concurrences for the cases between (J = J_z = 1) and (J = -1,J_z = 1) and, (J = J_z = -1) and (J = 1,J_z = -1) at the ground state and at the thermal equilibrium are exactly the same. It was found that for the antiferromagnetic (AFM) case the entanglements persist to higher temperatures in comparison with the ferromagnetic (FM) case. In addition, the AFM case presents a special point at which the nonzero concurrences are all equal at some special temperatures. The further properties will be given in the text.     

Causal particle detectors and topology

We investigate particle detector responses in some topologically non-trivial spacetimes. We extend a recently proposed regularization of the massless scalar field Wightman function in four-dimensional Minkowski space to arbitrary dimension, to the massive scalar field, to quotients of Minkowski space under discrete isometry groups and to the massless Dirac field. We investigate in detail the transition rate of inertial and uniformly accelerated detectors on the quotient spaces under groups generated by (t, x, y, z) ? (t, x, y, z + 2a), (t, x, y, z) ? (t, −x, y, z), (t, x, y, z) ? (t, −x, −y, z), (t, x, y, z) ? (t, −x, −y, z + a) and some higher dimensional generalizations. For motions in at constant y and z on the latter three spaces the response is time dependent. We also discuss the response of static detectors on the RP³ geon and inertial detectors on RP³ de Sitter space via their associated global embedding Minkowski spaces (GEMS). The response on RP³ de Sitter space, found both directly and in its GEMS, provides support for the validity of applying the GEMS procedure to detector responses and to quotient spaces such as RP³ de Sitter space and the RP³ geon where the embedding spaces are Minkowski spaces with suitable identifications.     

Thiolated cyclodextrin self-assembled monolayer-like characterized with secondary ion mass spectrometry

In the work the focus is on the preparation of self-assembled monolayer-like films consisting of thiolated cyclodextrin on gold substrate and a characterization by using secondary ion mass spectrometry. The short (1 min) and long (1 h) time preparations of self-assembled monolayer-like films, resulting in submonolayer and monolayer regimes, are investigated, respectively. The observed species of thiolated cyclodextrin (M as molecular ion) self-assembled monolayer-like films are assigned to three groups: Au_xH_yS_z clusters, fragments with origin in cyclodextrin molecule associated with Au, and molecular ions. The group of Au_xH_yS_z (x = 2-17, y = 0-2, z = 1-5) clusters have higher intensities than other species in the positive and even more in negative mass spectra. Interestingly, the dependence between the number of Au and S atoms shows that with the increasing size of Au_xH_yS_z clusters up to 11 Au atoms, the number of associated S atoms is also increasing and then decreasing. Molecular species as (M−S+H)Na⁺, (M+H)Na⁺, AuMNa⁺, (M₂−S)Na⁺, and M₂Na⁺ are determined, and also in cationized forms with K⁺. The intensities of thiolated cyclodextrin fragments at the long time preparation are approximately 10 times higher than the intensities of the same fragments observed at the short time. The largest observed ions in thiolated cyclodextrin self-assembled monolayer-like films are AuM₂ and Au₂M. The thiolated cyclodextrin molecular ions are compared with hexadecanethiol molecular ions in the form of Au_xM_w where the values of x and w are smaller for thiolated cyclodextrin than for hexadecanethiol. This result is supported with larger, more compact, and more stabile thiolated cyclodextrin molecule.     

Exploration of layered-type pseudo four-component Li-Ni-Co-Ti oxides

A series of layered-type pseudo four-component Li-Ni-Co-Ti oxides were prepared to explore optimal cathode materials for a lithium-ion secondary battery. The new layered-type compounds were prepared using a combinatorial material-preparation system based on electrostatic spray deposition (the “M-ist Combi” system), and combinatorial powder X-ray diffraction. The composition region of the new compounds (Li_α(Ni_xCo_yTi_z)O₂ (α∼1, 0 ≤ x ≤ 1, 0 ≤ y ≤ 1, z∼0.2, x + y + z = 1.0)) was found to be wider than the composition region previously reported (LiNi_0.8−yCo_0.2Ti_yO₂ (0 ≤ y ≤ 0.1)).     

Evaluation of magnetic force distribution on a pair of superconducting bulk magnets

We study the construction of superconducting permanent magnets by RE123 bulk materials and the investigation of these industrial applications such as a magnetic separation. A bulk magnet can generate strong magnetic fields exceeding 2 T, which is the limit of ordinary iron-cored electromagnets, in a compact device with a low running cost. A magnetic field distribution of the bulk magnet is a cone shape, and it contributes to an increase of magnetic force which is proportional to the product of a magnetic field and its gradient. It is important to evaluate magnetic force when the application of the bulk magnet is discussed. In this paper, two Gd123 bulk materials of 65 mm in diameter were magnetized using a pair of superconducting bulk magnet system and three-axis components of magnetic flux density (B_x,⋅B_y, and B_z) in an open space between the magnetic poles were scanned with pitch of 2 mm in each direction. From these measured data, the axial and radial components of magnetic force factor, B_z⋅dB_z/dz and B_r⋅dB_r/dr, were calculated. At 10 mm gap, the B_z⋅dB_z/dz value reached 180.6 T²/m for a field of 2.33 T, which is comparable to B_z = 6.76 T for a common 10 T–100 mm∅ superconducting magnet.     

Electrical conductivity and dynamics of quasi-solidified lithium-ion conducting ionic liquid at oxide particle surfaces

Lithium ion conducting solid-state composites consisting of lithium ion conducting ionic liquid, lithium bis(trifluoromethanesulfonyl)amide (Li-TFSA) dissolved 1-ethyl-3-methyl imidazolium bis(trifluoromethylsulfonyl)amide (EMI-TFSA), denoted by [yMLi⁺][EMI⁺][TFSA⁻] in this study, and various oxide particles such as SiO₂, Al₂O₃, TiO₂ (anatase and rutile) and 3YSZ are synthesized via a liquid route for the molar concentration of lithium, y, to be 1. The composite consists of SiO₂ and the ionic liquid with y = 0.2 was also prepared. The ionic liquid are quasi-solidified at the above oxide particle surfaces when x is below 40 for y = 1 and x is below 30 for y = 0.2, corresponding to the confinable thickness of the ionic liquid at the oxides' surfaces to be approximately 5-10 nm regardless of the oxide compositions. The electrical conductivities of x vol.%[yMLi⁺][EMI⁺][TFSA^-]-SiO₂, Al₂O₃, TiO₂s or 3YSZ composites are evaluated by ac impedance measurements. The quasi-solid-state composites exhibited liquid-like high apparent conductivity, e.g. 10^− 3.3-10^− 2.0 S cm^− 1 in the temperature range of 323-538 K for SiO₂-ionic liquid composites with y = 1. The self-diffusion coefficients of the constituent species of x vol.% [yMLi⁺][EMI⁺][TFSA⁻] (x is below 40, y = 0.2 and 1) − SiO₂ are evaluated by the Pulse Gradient Spin Echo (PGSE)-NMR technique in the temperature range of 298-348 K. By the quasi-solidification of the ionic liquid at SiO₂ particle surfaces, the absolute values of the diffusion coefficients of all constituent species decreased. The SiO₂ surfaces work to promote ionization of ion pair, [EMI⁺][TFSA⁻], while significant influence on the solvation coordination, [Li(TFSA)_n + 1]ⁿ⁻, was not observed. The apparent transport numbers of Li-containing species both in the bulk and the quasi-solidified ionic liquid showed similar values with each other, which was evaluated to be in the range of 0.010-0.017 for y = 0.2 and 0.051-0.093 for y = 1 in the abovementioned temperature range.     

Single crystal EPR and optical absorption study of Cr doped l-histidine hydrochloride monohydrate

EPR study of the Cr³⁺ ion doped l-histidine hydrochloride monohydrate single crystal is done at room temperature. Two magnetically inequivalent interstitial sites are observed. The hyperfine structure for Cr⁵³ isotope is also obtained. The zero field and spin Hamiltonian parameters are evaluated from the resonance lines obtained at different angular rotations and the parameters are: D=(300±2)×10⁻⁴ cm⁻¹, E=(96±2)×10⁻⁴ cm⁻¹, g_x=1.9108±0.0002, g_y=1.9791±0.0002, g_z=2.0389±0.0002, A_x=(252±2)×10⁻⁴ cm⁻¹, A_y=(254±2)×10⁻⁴ cm⁻¹, A_z=(304±2)×10⁻⁴ cm⁻¹ for site I and D=(300±2)×10⁻⁴ cm⁻¹, E=(96±2)×10⁻⁴ cm⁻¹, g_x=1.8543±0.0002, g_y=1.9897±0.0002, g_z=2.0793±0.0002, A_x=(251±2)×10⁻⁴ cm⁻¹, A_y=(257±2)×10⁻⁴ cm⁻¹, A_z=(309±2)×10⁻⁴ cm⁻¹ for site II, respectively. The optical absorption studies of single crystals are also carried out at room temperature in the wavelength range 195-925 nm. Using EPR and optical data, different bonding parameters are calculated and the nature of bonding in the crystal is discussed. The values of Racah parameters (B and C), crystal field parameter (Dq) and nephelauxetic parameters (h and k) are: B=636, C=3123, Dq=2039 cm⁻¹, h=1.46 and k=0.21, respectively.     

Magnetic properties, phase evolution, and microstructure of melt spun Sm(Co1−zZrz)xCy (x=5-9; y=0-0.15; z=0.03 and 0.06) ribbons

Magnetic properties, phase evolution, and microstructure of melt spun Zr-substituted Sm(Co_1−zZr_z)_xC_y (x=5-9; y=0-0.15; z=0.03 and 0.06) ribbons quenched at the wheel speed of 40 m/s have been studied. The x-ray diffraction analysis showed that the main phases, found in Sm(Co_0.97Zr_0.03)_x ribbons, were 1:5 phase for x=5-5.5; 1:5 and 1:7 phases for x=6; 1:7 phase for x=6.5-7.5; 1:7 and 2:17 phases for x=8; and only 2:17 phase for x=8.5-9, respectively. For Sm(Co_0.97Zr_0.03)_x ribbons, the attractive magnetic properties of remanent magnetization (B_r) of 5.5 kG, intrinsic coercivity (_iH_c) of 9.5 kOe, and energy product ((BH)_max) of 7.0 MGOe were obtained for Sm(Co_0.97Zr_0.03)_6.5 ribbons. Furthermore, a slight amount of C addition in Sm(Co_0.97Zr_0.03)_x ribbons could not only effectively refine the grain size from 200 to 500 nm for C-free ribbon to 10-70 nm for C-added ribbons, but also bring extremely fine fcc-Co grains (2-10 nm), leading to the strengthened exchange coupling effect between the magnetic grains. As a result, magnetic properties were further improved. In this study, the optimal magnetic properties of B_r=6.3 kG, _iH_c=10.5 kOe, and (BH)_max=9.0 MGOe were achieved for Sm(Co_0.97Zr_0.03)₇C_0.1 nanocomposites.     

Thermal entanglement and teleportation in a two-qubit Heisenberg XXZ chain with different Dzyaloshinskii-Moriya interactions

We study the thermal output entanglement and teleportation in a two qubit Heisenberg XXZ chain with different Dzyaloshinskii-Moriya (DM) interactions. The analytical expressions of the output entanglement and the average fidelity are obtained for this model. We find the entanglement of replica states will be induced by some large value of D_z and the output entanglement exists for the case of J_z < − 1. The influences of the different DM interactions on the fidelity of teleportation are studied. We show that by introducing the x-component DM interaction, the average fidelity F_A can reach its maximum value 1.     

Line-mixing between rotational Stark components of CH3F self-perturbed and perturbed by helium: Experimental results and IOS analysis

Self- and He-broadening coefficients of microwave transitions of CH₃F have been measured with and without the presence of an external electric field. This provides values for the J, K → J + 1, K (K = 0 − J) transitions for J = 1 and J = 3 as well as for the various J, K, M → J + 1, K, M′ (|M| = 0 − K, |M - M′| = 0, 1) Stark components. The results and those of a previous experimental study for pure CH₃F, which show significant line-mixing effects, are analyzed with a model based on the Infinite Order Sudden approximation. It is shown that the latter leads to very satisfactory modeling of observed values even though no parameter was adjusted since previously and independently determined basic cross-sections are used. The quality of the present predictions is comparable with that obtained previously with a semi-classical approach. Furthermore, it is shown that the previously stated inaccuracy of the IOS model was due to an oversimplified use of this approach.     

Influence of primary ion species on the secondary cluster ion emission process from SAMs of hexadecanethiol on gold

In order to investigate the secondary cluster ion emission process of organo-metallic compounds under keV ion bombardment, self-assembled monolayers (SAMs) of alkanethiols on gold are ideal model systems. In this experimental study, we focussed on the influence of the primary ion species on the emission processes of gold-alkanethiolate cluster ions from a hexadecanethiol SAM on gold. For this purpose, we carried out time-of-flight secondary ion mass spectrometry (TOF-SIMS) measurements using the following primary ion species and acceleration voltages: Ar⁺, Xe⁺, SF₅⁺ (10 kV), Bi⁺, Bi₃⁺(25 kV), Bi₃²⁺, Bi₅²⁺, Bi₇²⁺ (25 kV).It is well known that molecular ions M⁻ and gold-alkanethiolate cluster ions Au_xM_y⁻ with M = S-(CH₂)₁₅-CH₃, x − 3 ≤ y ≤ x + 1, x, y > 0, show intense peaks in negative mass spectra. We derived yields Y_SI exemplarily for the molecular ions M⁻ and the gold-hexadecanethiolate cluster ions Au_y+1M_y⁻ up to y = 8 and found an exponentially decreasing behaviour for increasing y-values for the cluster ions.In contrast to the well-known increase in secondary ion yield for molecular secondary ions when moving from lighter to heavier (e.g. Ar⁺ to Xe⁺) or from monoatomic to polyatomic (e.g. Xe⁺ to SF₅⁺) primary ions, we find a distinctly different behaviour for the secondary cluster ions. For polyatomic primary ions, there is a decrease in secondary ion yield for the gold-hexadecanethiolate clusters whereas the relative decrease of the secondary ion yield ξ_Y with increasing y remains almost constant for all investigated primary ions.     

硅中空穴与核的超精细作用及p型硅的核磁弛豫

本文把半导体中载流子和它的原子核的超精细作用(包括非接触项)表达为作用在有效质量波函数上的“准接触作用”。具体对硅中Si²⁹核和价带空穴的这个作用可表达为{S₁(J_xμ_nx+J_yμ_ny+J_zμ_nz)+S₂(J_x³μ_nx+J_y³μ_ny+J_z³μ_nz)}δ(r-r_n),参量S₁、S₂是联系着价带顶的波函数的一些积分;一般地S₂≈0。用它来处理了p型硅中Si²⁹核的核自旋弛豫,得到弛豫时间的表达式;从弛豫时间的实验值估计了S₁的值;还从价带自旋轨道分裂值估计了同一参量。     

Dielectric, ferroelectric and pyroelectric properties of Pb[(Ni1/3Sb2/3)xTiyZrz]O3 ceramics

In the present study, various Pb[(Ni_1/3Sb_2/3)_xTi_yZr_z]O₃ where x+y+z=1, x=0.08 and y=0.44-0.49, ceramics in the morphotropic phase boundary (MPB) range were studied by dielectric and pyroelectric methods. The results of the investigations revealed an MPB composition range of y≅0.46. The study of the dielectric properties of these compounds as a function of temperature suggests that with increase in y the permittivity maximum increases and transition temperature shifts towards higher temperature. Well-saturated polarization versus electric field (P-E) hysteresis loops were obtained and values of P_r were calculated. The samples revealed good pyroelectric properties for y=0.44 and y=0.45 at room temperature with large figures of merit F_v=0.019 m²/C and F_D=1.34×10^-5Pa^1/2.     

I–V characteristics and critical currents in superconducting/ferromagnetic bilayers

Current–voltage (I–V) characteristics and critical current density, J_c, for the onset of vortex motion were measured at different magnetic fields, H, and temperatures, T, in a superconducting (S)/ferromagnetic (F) bilayer and in a single Nb film. We choose Nb as a superconductor and a weak ferromagnetic alloy, Pd_1−xNi_x with x = 16, as F. We found that J_c was smaller for the S/F bilayer with respect to the single Nb film. The result was related to the reduced value of the superconducting order parameter in the bilayer.     

Magnetocaloric effect and multifunctional properties of Ni–Mn-based Heusler alloys

The studies of magnetocaloric properties, phase transitions, and phenomena related to magnetic heterogeneity in the vicinity of the martensitic transition (MT) in Ni–Mn–In and Ni–Mn–Ga off-stoichiometric Heusler alloys are summarized. The crystal structure, magnetocaloric effect (MCE), and magnetotransport properties were studied for the following alloys: Ni₅₀Mn_50−xIn_x, Ni_50−xCo_xMn₃₅In₁₅, Ni₅₀Mn_35−xCo_xIn₁₅, Ni₅₀Mn₃₅In₁₄Z (Z=Al, Ge), Ni₅₀Mn₃₅In_15−xSi_x, Ni_50−xCo_xMn_25+yGa_25−y, and Ni_50–xCo_xMn_32−yFeyGa₁₈. It was found that the magnetic entropy change, ΔS, associated with the inverse MCE in the vicinity of the temperature of the magneto-structural transition, TM, persists in a range of (125-5) J/(kg K) for a magnetic field change ΔH=5 T. The corresponding temperature varies with composition from 143 to 400 K. The MT in Ni₅₀Mn_50−xIn_x (x=13.5) results in a transition between two paramagnetic states. Associated with the paramagnetic austenite-paramagnetic martensite transition ΔS=24 J/(kg K) was detected for ΔH=5 T at T=350 K. The variation in composition of Ni₂MnGa can drastically change the magnetic state of the martensitic phase below and in the vicinity of TM. The presence of the martensitic phase with magnetic moment much smaller than that in the austenitic phase above TM leads to the large inverse MCE in the Ni₄₂Co₈Mn_32−yFeyGa₁₈ system. The adiabatic change of temperature (ΔT_ad) in the vicinity of TC and TM of Ni₅₀Mn₃₅In₁₅ and Ni₅₀Mn₃₅In₁₄Z (Z=Al, Ge) was found to be ΔT_ad=−2 K and 2 K for ΔH=1.8 T, respectively. It was observed that |ΔT_ad|≈1 K for ΔH=1 T for both types of transitions. The results on resistivity, magnetoresistance, Hall resistivity in some In-based alloys are discussed.     

Properties of amorphous ternary alloy films a-SixCyGez:H prepared by magnetron co-sputtering

Amorphous Si_xC_yGe_z:H (x+y+z=1; z∼0.1) have been deposited by reactive sputtering of Si–Ge composite target in argon–methane gas mixtures. The effects of the addition of Ge and the methane partial pressure P on the film properties were investigated. At high P, the addition of Ge could improve the reduction of the photoconductivity with increasing P observed in a-Si_xC_y:H (z=0).     

Magnetic properties of (Nd,Pr)–Fe–B nanocomposite over quenched and annealed ribbons

The base alloys of nominal composition (Nd_0.75Pr_0.25)_yFe_balanceB_x (y=10−9.2 and x=6−19.2) were chosen to study the influence of RE/B ratio, smaller than stochiometric composition on magnetic properties of over quenched and annealed ribbons. From X-ray diffraction analysis of these ribbons, the α-Fe and Fe₃B phases were observed along with (Nd,Pr)₂Fe₁₄B major phase. The average grain size was calculated using these patterns as: 35 nm for α-Fe, 45 nm for (Nd,Pr)₂Fe₁₄B and 22 nm for Fe₃B particles. TEM analysis also supported the nano distribution of the above phases. These X-ray graphs support the idea of exchange coupling between hard and soft phases responsible for the observed magnetic properties. In these ribbons the saturation magnetization J_s and remnant magnetization J_r increases from 1.19 T to 1.66 T and from 0.65 T to 0.91 T, respectively as RE/B ratio increases. The increase in J_s and J_r may be attributed to the presence of exchange coupling between these phases. The corresponding coercivity _jH_c decreases from 673.33 to 271.33 k Am⁻¹. The maximum energy product (BH)_max initially increases from 72.42 kJ m⁻³to 109.85 kJ m⁻³ up to RE/B≈1 and then decreases to 58.5 kJ m⁻³, depending on the shape of second quadrant B–H loop. The coercivity mechanism observed from initial hysteresis curve was considered to be nucleation of domain wall.     

Effect of microstructure on the conductivity of a NASICON-type lithium ion conductor

Sintering temperature is used to control the microstructure of Li_{1 + x + y}Al_xTi_2 − xSi_yP_3 − yO₁₂ (x = 0.3, y = 0.2), a NASICON-type glass-ceramic. Scanning Electron Microscope imaging, X-Ray Diffraction, and Electrochemical Impedance Spectroscopy are employed to show that increase in sintering temperature increases conductivity while generating secondary crystalline phases. Total conductivity is as high as 3.81 × 10⁻⁴ S cm⁻¹ for sintering temperatures above 1000 °C. Crystallization of dielectric phases places the optimal sintering temperature in the 900 °C to 1000 °C range. Thermal analysis of the glass precursor reveals the glass transition, and crystallization temperatures.     

Magnetic properties of stuffed copper chromium tellurides Cu1+xCr2+yTe4 (x=0-1, y<0.3)

We present a detail study of the effect of excess metal atoms on the magnetic properties of Cu_1+xCr_2+yTe₄ at 2-400 K. With the increase in x=0-1 and y<0.3, these compounds retain metallic behavior, while ferromagnetic ordering temperature reduces from 325 to 160 K. Our low field susceptibility χ_ac measurements reveal a second transition on cooling below the ferromagnetic ordering; the transition at around 160-180 K intensifies with the excess amount of copper and chromium atoms. The value of spontaneous magnetization at 2 K remains between 2.6 and 2.9μ_B across all the compositions and it reduces with temperature as M(T)∼A₀T^3/2+A₁T^5/2, as expected for the excitation of Bloch's spin waves in a model of the Heisenberg ferromagnet. Our terminal composition Cu_1.9Cr_2.25Te₄ showed only second transition at 160 K with short range magnetic order much above the transition temperature and in the absence of the specific heat jump at this temperature. The magnetic properties are explained as a result of random magnetic anisotropy in the excess-metal compositions induced by the interstitial atomic defects in their parent spinel structure. The large stuffing of cations has been made possible in the telluride compounds because of the large size of tellurium and also by the covalent bonding that stabilizes the defect structure.