Low temperature specific heat and magnetic properties of V/FE and V/FE/H alloys

Low temperature specific heats of V_1?xFe_x (0?x?0.34) and V_1?xFe_xH_n (x = 0.02; 0.05; 0.1; 0.15 a 0 ? n ? 0.98) were investigated between 1.5 and 16 K.In V/Fe alloys temperature independent band paramagnetism was observed at iron concentrations below 20at%; at higher iron contents local magnetic moments occur and contribute magnetic terms to the low temperature specific heat. According to Schröder [14] these contributions can be explained by thermal agitation of superparamagnetic clusters of the Fe atoms with local moments. In the temperature range of the specific heat measurements the magnetic terms are dependent on temperature (contrary to Schröder) and can be described by Planck-Einstein functions. A separation of the magnetic contributions from the lattice and electronic term of heat capacity could be obtained in a satisfying way by least squares fitting with three Planck-Einstein functions.In “nonmagnetic” V/Fe alloys with less than 20at% Fe absorption of hydrogen generates local magnetic moments and superparamagnetic contributions. These are, therefore, connected primarily more with the band electron concentration n_e, than with the iron content X_Fe At the highest n_e, values, n_e >0, large negative deviations from the regular course of the heat capacity plot are observed; these can be related to mictomagnetic behavior (freezing temperature of spin-glass state above the range of measurements, T_F > 16 K).After correction for the superparamagnetic contributions there remains in the Fe containing alloys an appreciable enhancement of the electronic heat coefficient γ, up to a factor of about 2 when compared with the iron-free V/H samples. This effect is interpreted as resulting from mass enhancements of the itinerant electrons by electron-magnon (and-paramagnon) interactions.     

Analysis of nuclear spin-lattice relaxation rates in transition metal dihydrides,TMH2 (TM = Sc,Ti, V and Nb) based on LAPW electronic band calculations

The spin-lattice relaxation rates (T _1e T)^?1 of transition metal nuclei ⁴⁵Sc, ⁴⁹Ti, ⁵¹V and ⁹³Nb in cubic dihydrides ScH₂, TiH₂, VH₂ and NbH₂ are calculated on the basis of scalar-relativistic self-consistent LAPW band structure calculations. It is found that the s and p electron contributions to the relaxation rates are negligibly small for all the hydrides studied here due to their very low partial densities of electron states at the Fermi level. The d- orbital contributions are dominant and the core polarization and d-dipolar contributions play a minor role. The theoretical relaxation rates reproduce the experiments very well for ScH₂ and TiH₂ but less satisfactory for VH₂ and NbH₂. The experimental data were taken from our earlier studies and the results of additional measurements on ⁹³Nb in NbH₂ are reported. These have been made in the 30–292K temperature range and at a magnetic field of 7 T.     

Characteristics of the thermodynamic and kinetic properties of NbH0.83 in the phase transition region

Measurements were made of the specific heat (in the temperature range 80–400 K), electrical resistivity (4.2–300 K), thermo-emf (4.2–300 K), thermal conductivity (7–300 K), magnetic susceptibility (4.2–400 K), and lattice parameters (30–300 K) of the alloy NbH_0.83. The λ′→λβ phase transitions were studied. It was established that the structure of the niobium matrix of the hydride remains unchanged as a result of these transitions. It is shown that the β→λ phase transition (one-dimensional hydrogen ordering) is a three-stage one and is accompanied by a substantial change in the shear modulus of the hydride. The λ′ phase existing at T<110 K was determined. The electron thermal conductivity κ_el calculated for the λ′ phase in the range T<23 K is 25% higher than the measured thermal conductivity. In order to explain this fact and also the discontinuity in the concentration dependence of the coefficient of thermal expansion of NbHx for x?0.83–0.84 and the approximately 1.5% compression of the NbH_0.84 volume it is assumed that in the region of x _c in the λ′ phase the topology of the Fermi surface of the NbH_x interstitial alloy changes substantially.     

First principles studies of elastic and thermodynamic properties of fcc-VH2 with pressure and temperature

In this work, we study elastic and thermodynamic properties of VH₂ at different pressures and temperatures. Elastic constants and bulk modulus of VH₂ decrease with increase in temperature, and hence increase with pressure. Thermal expansion of the crystal lattice will be suppressed by high pressure. When the temperature is 1500 K, 15.99 GPa of pressure can completely restrain the volume expansion caused by temperature. At a given pressure, the lower the temperature, the easier the cell compression. At low temperatures, C_v is proportional to T³, and C_v tends to the Dulong-Petit limit at higher temperatures. The Debye temperature increases with pressure, but decreases with temperature. At low temperature and low pressure, thermal expansion coefficient increases sharply with temperature. At high temperature and high pressure, the increasing trend slows down.     

Low temperature elastic constants and Debye temperature of NbO2

The transit times of ultrasonic waves have been measured in single crystal NbO₂ from 295 K down to 1.5 K for quasilongitudinal and shear waves propagating in the [100] direction and down to 160 K for eight other waves. Values are obtained for the C₄₄ elastic constant and for an elastic constant combination which is approximately equal to C₁₁ for temperatures down to 1.5 K and for C₁₁, C₁₂, C₁₃, C₁₆, C₃₃, and C₆₆ down to 160 K. These results are used to deduce 0 K values for the elastic constants and an elastic Debye temperature of 596 ± 7 K at 1.5 K. The acoustic mode heat capacity calculated from the latter is significantly smaller than the heat capacity measured by Wenger and Keesom at low temperatures. Following Wenger and Keesom, the difference is attributed to phasons (excitations involving the phase modulation of charge density waves). An average velocity is deduced for the phasons.     

Calculation of the Compton profiles of vanadium,niobium and their dihydrides

We have calculated the Compton profiles of V, Nb, VH₂ and NbH₂ using the self-consistent augmented plane wave (APW) method within the local-density approximation of Hedin-Lundqvist. The results are compared with other theoretical works and available experiments. In going from the pure metals to the metal dihydrides we observe significant changes in the directional Compton profiles due to their different band structures.     

Electronic conductivity and thermopower of Ca2NaMg2V3O12−x garnet

Results are reported from conductivity and thermoelectric power measurements on partially reduced Ca₂NaMg₂V₃O_12?x, with x < 5.10^?2, at temperatures of 300–1100 K. The conductivity is thermally activated with activation energies 0.26 ? E_a ? 1.28 eV for differently reduced samples. The thermopower is temperature independent in the 300–800 K region. These results are shown to be consistent with the adiabatic hopping of small polarons localised on the vanadium sublattice, where defect interactions result in the formation of multiple conduction pathways.     

Proton spin-lattice relaxation time in ordering VHx alloys

Proton spin-lattice relaxation time is determined in VH_0.68 and VH_0.73 alloys in the temperature range of β₁, β₂ and δ ordered phases (400-100 K). Experimental results are described in terms of dipole-dipole interaction mechanism. On comparing calculated and experimental data in the complete temperature range the values of temperature dependent activation energy E_a and time constant τ₀ are estimated.     

Heavy fermion state and pressure-induced resistive behaviour in CeRu2Si2

Pressure-induced variation in the resistive behaviour of CeRu₂Si₂, a Kondo-lattice system, has been studied in the temperature interval 1.5K – 300K. At low temperatures, resistivity exhibits (i) a linear temperature dependence at low applied pressures (P ?2.26 kbar) and (ii) a quadratic temperature dependence

(T) ～ AT² at higher pressures (6.5 kbar ? P ? 16.8 kbar). The coefficient A decrease, which in turn implies that the spin fluctuation temperature T_sf increases, with increasing applied pressure. The temperature coefficient γ of specific heat C = γ T at low temperature (0.3K ? T ? 1.6K) is quite large (385 mJ/mole-K²) confirming the heavy fermi liquid nature of the material.     

Electric-quadrupole interaction at 181Ta in f.c.t. ZrHi1.97

Time-differential perturbed γ-ray angular correlation experiments have been carried out on ¹⁸¹Ta impurities in ?-phase zirconium hydride over the temperature range from 20 to 588 K. A static, slightly asymmetric electric quadripole interaction is found at all temperatures. The static nature of the pattern indicates the absence of significant hydrogen diffusion at these temperatures on the time scale of the experiment (0.1 μsec). The temperature dependence of the static quadrupole frequency is given by the relation v_q(t) = 130[1 ? (1.9 × 10^?5)T^1.5] MHz.     

Hydrostatic pressure study of the structural phase transitions and superconductivity in single crystals of (Ba1−xKx)Fe2As2 (x=0 and 0.45) and CaFe2As2

We studied the effect of hydrostatic pressure (P) on the structural phase transitions and superconductivity in the ternary and pseudo-ternary iron arsenides CaFe₂As₂, BaFe₂As₂, and (Ba_0.55K_0.45)Fe₂As₂, by means of measurements of electrical resistivity (ρ) in the 1.8-300 K temperature (T) range, pressures up to 20 kbar, and magnetic fields up to 9 T. CaFe₂As₂ and BaFe₂As₂ (lightly doped with Sn) display structural phase transitions near 170 and 85 K, respectively, and do not exhibit superconductivity in ambient pressure, while K-doped (Ba_0.55K_0.45)Fe₂As₂ is superconducting for T<30 K. The effect of pressure on BaFe₂As₂ is to shift the onset of the crystallographic transformation down in temperature at the rate of ~−1.04 K/kbar, while shifting the whole ρ(T) curves downward, whereas its effect on superconducting (Ba_0.55K_0.45)Fe₂As₂ is to shift the onset of superconductivity to lower temperatures at the rate of ~−0.21 K/kbar. The effect of pressure on CaFe₂As₂ is first to suppress the crystallographic transformation and induce superconductivity with onset near 12 K very rapidly, i.e., for P<5 kbar. However, higher pressures bring about another phase transformation characterized by reduced-resistivity, and the suppression of superconductivity, confining superconductivity to a narrow pressure dome centered near 5 kbar. Upper critical field (H_c2) data in (Ba_0.55K_0.45)Fe₂As₂ and CaFe₂As₂ are discussed.     

An accurate determination of the excess low temperature heat capacity of a superconducting metallic glass

The specific heat of an amorphous superconductor Zr₃Rh (T_{c = 4.3 K}) has been measured in the temperature range from 0.35 K to 10 K and with an applied magnetic field of 75 kG. The high field suppresses superconductivity and allows accurate determination of the phonon (βT³) term for the lowest temperatures studied. A careful subtraction of the normal electronic specific heat (γT) and phonon terms reveals a well defined excess linear heat capacity γ'T at low temperature. This excess term is attributed to localized lattice excitations using the two-level tunneling defect model of Phillips.     

Electron scattering in CdxHg1−xTe

Experimental studies of the electron mobility in Cdinx,Hgin1?xTe/0x/0.33, 10¹⁵ cm^?3n10¹⁸ cm^?3, 4.2 K ?T ?300 K/and of the thermoelectric power of intrinsic HgTe from 300 K down to 5 K are reported. These results are interpreted in terms of calculations based on the variational solution of the Boltzmann equation. Analysis shows that in pure samples at low temperatures, the electron mobility is limited by ionized donors, heavy holes, and, in some cases, unresolved defect scattering. In the doped samples with x0&#x0306;.1, disorder scattering also becomes significant. Polar-optical phonon scattering is dominant at high temperatures. The sharp decrease of mobility in the region 20–40 K, which occurs for pure samples with x0&#x030C;.14, is explained by interband optical phonon scattering. The thermoelectric power of intrinsic HgTe is strongly affected by phonon-drag of holes at low temperatures and by electron-electron scattering at high temperatures.     

Superconductivity of hydrides Ti3SbHx

The effect of interstitially dissolved hydrogen on the transition temperature T_c of superconductivity has been investigated in cubic A-15 type (Cr₃Si type) hydrides Ti₃SbH_x, 0 ? x ? 2. The transition temperature T_c decreases with increasing hydrogen content x from 5.6 K in Ti₃Sb to 1.0 K in Ti₃SbH_1.0.     

Superconductivity in the Th-doped Y NiC2 compounds

We have observed superconductivity in the two-phase samples with nominal compositions (Y _1−xTh_x)NiC₂ (x=0.1,0.2,0.3,0.4,0.5). As determined by magnetic, electrical and heat capacity measurements, the superconductivity phase transition temperature T_c increases with Th concentration to . Powder X-ray diffraction data provide the evidence for bulk superconductivity in an orthorhombic CeNiC₂-type majority fraction of the sample volume while the minor impurity phase ThC₂ has no effect on the superconductivity. The variation of room temperature lattice parameters, a, b, c and v of these substitutional intermetallic samples indicates the systematic substitution of Y ³⁺ ions by Th⁴⁺ ions irrespective of the existence of the 2nd impurity phase.     

Die optischen Konstanten des Rubidiums im Wellenlängenbereich von 0,3 bis 2,4 μ und ihre Abhängigkeit von Temperatur und Aggregatzustand

The optical constants of the alkali metal rubidium have been measured in the wavelength region from 0,3 to 2,4 μ in the solid and liquid state at temperatures between 195 and 313 °K, by analysing intensity and polarisation of the monochromatic radiations reflected by the surface of the metal. These mirrorlike surfaces, free of any contamination and not distorted by any treatment, were prepared and measured in ultrahigh vacuum. The purity of the metal was checked by measuring the residual resistance at liquid helium temperatures. The values thus obtained forn,k, ?₁=n ²?k ² and ?₂=2nk, listed in tables, and their temperature dependence permit the determination of 1. the frequency of the volume-plasmaoscillation, 2. the core polarizability, 3. the optical mass, 4. the optical conductivity resp. relaxation time, 5. and to separate the temperature dependent “Drude”-absorption from other temperature independent absorption mechanisms, particularely the interband absorption. Values of the reflectivity for perpendicular incidence and of the penetration depth are determined and given.     

Spin effects on oscillatory magnetoresistances in n-Pb1−xSnxTe

Shubnikov-de Haas oscillations in n-Pb_1?xSn_xTe have been measured in the magnetic field parallel to the [100] crystal direction at 1.5 K. In the longitudinal magnetoresistances, the one-side peaks of spin-splitting pair series are completely missing. This anomaly is well explained by the selection rules, theoretically derived in the study on a similar effect in Hg_1?xCd_xTe. Landau sublevel-crossings are also discussed.     

吸气溅射Mo1-xSix薄膜的超导性能

对于四个Mo_1-xSi_x薄膜样品进行了超导转变温度、临界温度附近的临界磁场以及在4.2K下的临界电流的测试,并且测量了室温(300K)及低温(8K)下的电阻率,结果显示四个样品具有非晶的特征,其中Mo₇₈Si₂₂薄膜样品有较好的非晶特性。 关键词：     

The heat capacities of arsenic,phosphorous and GexSe1−x glasses below 1 K

The heat capacities of amorphous arsenic and phosphorous have been measured down to 0.1 K. Both glasses have heat capacities larger than the values calculated from the sound velocities, but in a-As the magnitude of the excess is significantly less than in vitreous silica. Ge_xSe_1?x glasses also show an excess heat capacity below 1 K, but in contrast to the behavior at higher temperatures the results do not vary systematically with composition.