Effective pinning barriers of NdFeAsO0.88F0.12 superconductor

Resistivities of polycrystalline iron-based NdFeAsO_0.88F_0.12 superconductors prepared via solid-state reaction in ambient pressure (AP) and high pressure (HP) were measured in various magnetic fields ranging from 0 to 9 T. Different resistivity broadening behaviors of the AP and HP samples, which may originate from the anisotropic superconductivity, the vortex motion, or the connectivity, were investigated in detail. The effective pinning barriers of both the AP and HP samples were obtained from the Arrhenius plot of the resistivity data by two analytic methods of which one assuming the prefactor 2ρ_cU/T of the thermally activated ?ux ?ow (TAFF) resistivity ρ=(2ρ_cU/T)exp(−U/T) is a constant, while the other assuming the prefactor is temperature dependent. The results determined from the two methods were compared and analysed, and the true effective pinning barriers were obtained. The origin of different pinning barriers of the AP and HP samples is discussed.     

Comparative study of type-II superconducting properties in polycrystalline NdFeAsO0.88F0.12 prepared by different methods

Polycrystalline NdFeAsO_0.88F_0.12 superconductors prepared by high pressure (HP) and ambient pressure (AP) methods were comparatively studied by magnetization and transport measurements. Upper critical field H_c2, irreversibility field H_irr and the anisotropy parameter Γ were estimated from resistance transition curves. The broadening of transition width was observed, and was ascribed to both H_c2 anisotropy and superconductivity inhomogeneity of samples. Magnetic hysteresis loops (MHLs) in low fields were measured to detect the trace of weak-link behavior. The reclosed hysteresis loops in low fields indicate that there are weak links in both samples. Magnetization critical current density J_cm were derived from MHLs. Sample HP shows higher J_cm than sample AP. Direct transport I–V measurements show that the transport critical current density J_ct are very low but persist up to 9 T, suggesting intrinsic strong-link existing in both samples.     

Temperature dependence of luminescence from ZnS0.11Se0.89 random and ordered alloys

Temperature dependence of the luminescence spectra was investigated for a ZnS_0.11Se_0.89 random alloy and a (ZnSe)₁/(ZnS_0.22Se_0.78)₁ ordered alloy with equivalent mean sulfur compositions. The luminescence peak for the random alloy as a function of temperature shows anomalous behavior, while that for the ordered alloy exhibits normal behavior. From the temperature dependence of luminescence intensity for the random alloy, the quenching process can be understood with additional thermal activation energy besides exciton dissociation energy. Through the analysis of the temperature variation of the luminescence line width, the exciton-optical phonon coupling constant is found to be reduced in the random alloy. The results of this study demonstrate that exciton is localized by the potential fluctuation in the random alloy and that the potential fluctuation is significantly constrained in the ordered alloy.     

Influence of magnetic impurities on superconducting property of polycrystalline iron-based NdFeAsO0.88F0.12

Polycrystalline iron-based superconducting NdFeAsO_0.88F_0.12 was prepared via solid-state reaction in ambient pressure. Small amounts of ferromagnetic impurities were detected by Scanning Electron Microscopy (SEM) analysis. To study the influence of magnetism on superconducting properties of the sample, magnetization M(T, H) measurements were performed in fields up to 1.5 T and in the temperature range of 5-60 K. The abnormal behavior was observed in the χ(T) curves, and the magnetization hysteresis loops (MHLs) can be described by a sum of the contributions of superconductive hysteresis, ferromagnetic hysteresis of the impurities and the paramagnetic background of the isolated Nd³⁺ ions. The influence of the ferromagnetic impurities and the paramagnetic background were investigated and discussed. After the corrections of the magnetism contributions, the intrinsic superconductive MHLs as well as the critical current density were obtained.     

High-pressure X-ray diffraction study of 1T-TaS2

We present a room temperature high-pressure X-ray diffraction study of the layered compound 1T-TaS₂ up to 20 GPa. This material is known to exhibit a variety of structural phase transitions that are ascribed to the stabilization of charge density wave states. It has been recently shown that at pressures larger than 3 GPa and up to 25 GPa, 1T-TaS₂ becomes superconductor below about 5 K. It was suggested that this superconductivity coexists with different CDW states, an hypothesis that can be tested by X-ray diffraction. Our first results at room temperature show that at around 1.9 GPa, the nearly-commensurate (NCCDW) phase transforms into a phase similar to the high temperature incommensurate phase (ICCDW). Above 9 GPa, we show the existence of another IC phase, still discernable up to 20 GPa despite the pressure-induced crystal damage above 13 GPa. These results are consistent with resistivity measurements, but call for a complete exploration of the P–T phase diagram of 1T-TaS₂.     

High pressure X-ray diffraction study of ReS2

The high-pressure behavior of rhenium disulfide (ReS₂) has been investigated to 51.0 GPa by in situ synchrotron X-ray diffraction in a diamond anvil cell at room temperature. The results demonstrate that the ReS₂ triclinic phase is stable up to 11.3 GPa, at which pressure the ReS₂ transforms to a new high-pressure phase, which is tentatively identified with a hexagonal lattice in space group P6?m2. The high-pressure phase is stable up to the highest pressure in this study (51.0 GPa) and not quenchable upon decompression to ambient pressure. The compressibility of the triclinic phase exhibits anisotropy, meaning that it is more compressive along interlayer directions than intralayer directions, which demonstrates the properties of the weak interlayer van der Waals interactions and the strong intralayer covalent bonds. The largest change in the unit cell angles with increasing pressures is the increase of β, which indicates a rotation of the sulfur atoms around the rhenium atoms during the compression. Fitting the experimental data of the triclinic phase to the third-order Birch-Murnaghan EOS yields a bulk modulus of K_OT=23±4 GPa with its pressure derivative K_OT′= 29±8, and the second-order yields K_OT=49±3 GPa.     

稀磁半导体Hg0.89Mn0.11Te磁化强度及磁化率的研究

利用MPMS-7(magnetic property measurement system)型超导量子磁强计对垂直布里奇曼法生长的Hg_0.89Mn_0.11Te晶片磁化强度变化规律进行了测量.试验采用了两种不同的外场和冷却条件.首先在5 K恒温下，-5200到5200 kA/m范围内改变磁场强度进行了测定.然后维持800 kA/m恒定磁场，分别在有场冷却和无场冷却条件下，从5到300 K范围内改变温度，研究了变温条件下的磁化特性.并采用分子场近似模型，用类布里渊函数，最小二乘法对磁化强度随磁场强度变化的实验结果进行拟合和分析，结果表明，Mn²⁺离子之间存在反铁磁相互作用.磁化率和温度关系分析表明：在测试范围内Hg_0.89Mn_0.11Te是单一的顺磁相，在高温区磁化率和温度服从居里-万斯定律，呈线性关系，低于40 K时，磁化率和温度的关系偏离居里-万斯定律，表现出顺磁增强现象. 关键词： 0.89Mn_0.11Te')" href="#">Hg_0.89Mn_0.11Te 磁化强度 磁化率 类布里渊函数     

Neutron diffraction study of the magnetic order in the ternary superconductor GdMo6S8

The coexistence of antiferromagnetism and superconductivity has been demonstrated in GdMo₆S₈ by neutron diffraction experiments. Although the magnetic unit cell (2a,a,a) is determined by the RKKY interactions, the direction of magnetic moments is determined by the anisotropic dipolar interactions i.e. in the (100) cubic plane.     

Adsorption-desorption studies using ESD of CCl2F2, C2H2F2 and C2F6 on tungsten

The behavior of the desorbing F⁺ ion current from electron bombarded CCl₂F₂, C₂H₂F₂ and C₂F₆ adsorbed on tungsten has been used to investigate the processes of adsorption and desorption of these gases. For tungsten near room temperature, measurements of the F⁺ ion current as a function of electron bombardment time indicated very similar or even identical F⁺-yielding adsorbed species resulting from adsorption of either CCl₂F₂ or C₂H₂F₂ and widely different species from C₂F₆. Cl⁺ ions were also observed to desorb from CCl₂F₂ ad-layers. The behavior of the Cl⁺ ion current with time during electron bombardment indicated electronic conversion between adsorbed binding modes. Complementary investigations on the interaction of CCl₂F₂, C₂H₂F₂ and C₂F₆ with tungsten were carried out by thermal desorption experiments in which the F⁺ ion signal was used to observe the coverage decrease of the F⁺-yielding species. The experiments were performed at tungsten temperatures in the 1200–1600 K range. It was concluded that the F⁺-yielding adsorbed species from CCl₂F₂ and C₂H₂F₂ were strongly bound to the tungsten surface. The F⁺-yielding species from C₂F₆ were found to be weakly bound. From a comparison of the ESD and thermal desorption results, the possibility of dissociative adsorption as well as the nature of the adsorbed species is discussed.     

Paramagnetic properties of cubic RbSm3F10 and KHo3F10

The title compounds crystallize in the cubic KY₃F₁₀ structure, with the rare earth ion occupying a site of tetragonal symmetry. Paramagnetic susceptibilities are compared with predictions based on experimental crystal field parameters, down to temperatures of ∼10 mK.     

Magnetic anisotropy in Co73Mo2Si15B10 and (Co0.89Fe0.11) 72Mo3Si15B10 metallic glasses,induced by stress-annealing

Annealing temperature dependence of the stress-induced magnetic anisotropy in Co₇₃Mo₂Si₁₅B₁₀ (λ_s < 0) and (Co_0.89Fe_0.11) ₇₂Mo₃Si₁₅B₁₀ (λ > 0) metallic glass ribbons has been studied experimentally. The room temperature values of the induced anisotropy constants K depend strongly on the annealing conditions, and reveal a change of sign at annealing temperatures well below T_cryst. It is concluded that transient creep and steady-state creep at the elevated temperature give rise to compressive and tensile stresses, respectively, in the expression for the magnetoelastic coupling energy at room temperature.     

A study of thermal parameters of Ag50Pd50 alloy using X-ray diffraction

Thermal parameters of Ag₅₀Pd₅₀ alloy were studied using the in-situ X-ray diffraction (XRD) technique. Diffraction experiments in the temperature range 308-1178 K showed that the alloy forms a face centered cubic (fcc; A1-type) structure. Temperature dependence of the lattice parameter was investigated using the Bragg line displacement method. Results show that the lattice parameter for the alloy increases with increase in temperature. The temperature dependent XRD data was utilized to determine the mean linear thermal expansion (MLTE (%)) and coefficient of thermal expansion (CTE) ‘α’ in the mentioned temperature range. It was observed that the values of CTE vary between 9.3 and 14.6 [K⁻¹][10⁻⁶]. The same data was also utilized to determine the Debye temperatures Θ_D and mean square amplitude of vibration (MSAV) (u²(T)) for this alloy. Values of thermal parameters as determined in this investigation are in good agreement with the estimated values as well as with those for other alloys of noble metals.     

A high-pressure Raman and X-ray diffraction study of the perovskite SrCeO3

A high-pressure structural study of SrCeO₃ has been performed at room temperature by Raman spectroscopy and X-ray diffraction up to 32 and 45 GPa, respectively. A first-order reversible phase transition is observed at about 12 GPa in both techniques. A second weak structural change, taking place between 18 and 25 GPa, can be suspected from Raman data. The increase in the number of Raman bands and diffraction lines is an indication that the symmetry is lowered and the compound does not evolve towards the ideal cubic perovskite structure. A Rietveld analysis of X-ray data was performed for the low-pressure phase and the atomic positions and the cell lattice parameters variations are reported in this paper. The volume compressibility derived from Raman modes (5.6×10⁻¹² Pa⁻¹), involving mainly bond-stretching for each type of polyhedron, is found to be close to the one obtained from volume cell variations measured by X-ray diffraction (7.9×10⁻¹² Pa⁻¹).     

Critical behaviour of Mn1.11Al0.89 alloys

The diffraction maxima (001) and (100) of the Mn_1.11Al_0.89 alloy have been measured by the neutron powder diffraction method in the temperature range from 23 to 427 C. The Curie temperature is found to be (404 ±2)°C. Temperature dependence of the magnetic structure factor gave the critical exponent β = 0.31±0.02.The disorder parameter has been found to decrease with the temperature. A convenient expression describing this behaviour has been proposed and discussed.     

A study on the GVFF of CHF3, CH2F2, and CH3F

The complete GVFF of CHF₃, CH₂F₂, and CH₃F has been calculated from self-consistent-field ab initio energies, using a 4–31 G basis set. The larger part of the interaction force constants is close to those of the best available force fields from experimental data. Only one interaction term in CH₃F and the interaction force constants of the A₁ species in CH₂F₂ differ appreciably from the experimental ones. Using constraints from the ab initio studies we have improved the GVFF of CH₃F and CH₂F₂. It is shown that all comparable stretch-stretch interaction terms are of the same order of magnitude in the three molecules. The sign of all stretch/bend force constants are in accordance with those predicted by the hybrid orbital force field.     

Phase transition and analysis of AC conductivity data of the (Cs)0.26(Rb)0.74H(SO4)0.89(SeO4)0.11 compound

The X-ray diffraction, vibrational and impedance spectroscopy studies of (Cs)_0.26(Rb)_0.74H(SO₄)_0.89(SeO₄)_0.11 (CsRbHSSe) new solid solution are presented. The title compound undergo a superionic phase transition (SPT) at This transition was confirmed by an abrupt increase of conductivity. The bulk impedance parameters of CsRbHSSe, RbH(SO₄)_0.81(SeO₄)_0.19 (RbHSSe) and CsH(SO₄)_0.76(SeO₄)_0.24 (CsHSSe) were determined from an analysis of AC conductivity data measured in a wide temperature range. The charge carriers concentration in the samples investigated has been evaluated using the Almond-West formalism and shown to be independent of temperature.     

10－5000 伏下电子被多原子分子CF4, CF3H, C2F4, C2F6, 及 C2H3F3散射总结面的计算

利用可加性规则和光学势方法计算了能量在10-5000 eV范围内电子被多原子分子CF4, CF3H, C2F4, C2F6, 及 C2H3F3的总结面，并与已有的实验结果和理论计算进行了比较，与这些结果符合得很好。对于CF4, CF3H, C2F4, C2F6, 及 C2H3F3在1000eV以上没有实验数据，本文对实验研究提供了对比和预测的数据。     

Intermediate-temperature polymorphic phase transition in KH2PO4: A synchrotron X-ray diffraction study

We have used synchrotron X-ray diffraction to investigate the structural and chemical changes undergone by polycrystalline KH₂PO₄ (KDP) upon heating within the 30-250 °C temperature interval. Our data show evidence of a polymorphic transition at T∼190 °C from the room-temperature tetragonal KDP phase to a new intermediate-temperature monoclinic KDP modification (spacegroup P2₁/m and lattice parameters a=7.590, b=6.209, c=4.530 Å, and β=107.36°). The monoclinic RDP polymorph remains stable upon further heating to 235 °C, and is isomorphic to its RbH₂PO₄ and CsH₂PO₄ counterparts.     

新超导体MgCNi3的虚晶掺杂研究

用全势线性缀加平面波方法,考虑局域自旋密度近似研究虚晶掺杂MgCNi₃的超导电性和磁性.计算了自旋极化能带结构、体弹性模量和它对压力的导数、原子磁矩m及其变化率.计算结果表明，对于电子掺杂的Mg_1-xAl_xCNi₃(0≤x≤0.5)，超导电性和磁涨落随掺杂量的增加逐渐减小.空穴掺杂的Mg_1-xNa_xCNi₃,在x＝0.12处出现铁磁相变，超导电性消失.在MgCNi₃少量空穴掺杂区域(0≤x<0.12)，表现为超导与磁涨落共存的不稳定状态. 关键词： 超导电性 能带结构 态密度 磁性