Local dynamic deformation of the superconducting CuO2 plane in the Nd2 − x Ce x CuO4 + δ compound

The local structure of the electron-doped high-temperature superconductor Nd_{2 ? x} Ce _x CuO_{4 + δ} has been investigated by EXAFS spectroscopy using synchrotron radiation in the temperature range 5–300 K. The radii, coordination numbers, and Debye-Waller factors of the nearest coordination spheres of the copper, neodymium, and cerium local environment have been obtained. The Einstein temperatures, characterizing the strength of Cu-O, Nd-O, and Ce-O interatomic bonds have been determined. The dynamic local deformation of the superconducting CuO₂ plane in the form of vibrations of some part of oxygen ions in a double-well potential due to the difference in the electronic filling of neighboring CuO₄ complexes has been established.     

Thermoelectric properties of the Nd2−x Ce x CuO4−y system

The temperature dependence of the Seebeck coefficient (in region 300–900 K) and the lattice constants of Nd_2–x Ce_xCuO_4–y (x=0, 0.05, 0.10, 0.15) with different oxygen content were measured. The value of S is always negative and it decreases with both Ce content and oxygen non-stoichiometry. At a certain concentration of Ce and oxygen in the material, the Seebeck coefficient becomes temperature-independent.The authors would like to thank Professor J. Horák of University of Chemical Technology, Pardubice for helpful discussions.     

Thermal conductivity of single crystals of the Ca1 − x Y x F2 + x solid solution

The thermal conductivity of single crystals of the solid solution of yttrium fluoride in calcium fluoride Ca_{1 ? x} Y _x F_{2 + x} with the fluorite structure (x ≤ 0.20) and the Ca_0.27Y_0.73F_2.73 phase with the tisonite structure has been studied by the absolute steady-state longitudinal heat flow method in the temperature range 50–300 K. It has been established that the thermal conductivity drops sharply with increasing yttrium trifluoride concentration, especially in the low-temperature region.     

Pressure Effects in the Raman Spectra of La 2−x Sr x CuO 4

Micro-Raman measurements under hydrostatic pressures up to 6 GPa have been carried out on high-quality La 2 m x Sr x CuO 4 polycrystalline compounds with Sr concentration up to x =0.45. The zz scattering polarization has been investigated, where two strong modes due to La/Sr and the apex oxygen, and (in the low Sr concentrations) the soft mode at ～100 cm m 1 are observed. The frequency of the strong modes increases almost linearly with pressure for the Sr concentrations studied. Modifications in the increment rate d y /d p and the phonon width have been detected depending on the amount of doping. For x =0.45 a considerable increase in the width of both strong phonons with pressure was found, which must reflect a separation into phases, since this concentration is close to the solubility limit. The relative intensity of the strong phonons was investigated in connection with its correlation to the transition temperature.     

Valence change of europium in the Eu(Ir1−x Pd x )2Si2 silicides

Eu(Ir_1–x Pd _x )₂Si₂ solid solutions which exist only for 0x0.125 and 0.75x1 crystallize in the tetragonal ThCr₂Si₂-type structure. X-ray diffraction data, magnetic susceptibility and¹⁵¹Eu Mössbauer measurements suggest that these compounds can be characterized as homogeneous mixed valence systems. At room temperature and for 0x0.125, the europium valence decreases asx increases. For 0.75x1, a sharp continuous valence transition from Eu²⁺ to Eu³⁺ occurs near 48 K, 54 K and 78 K forx=0.75, 0.81 and 0.94 respectively. These valence changes are discussed in relation with the Eu–(Ir, Pd) interatomic distance.     

Correlation between the magnetic and electrical properties of the (VS)x(Fe2O3)2−x oxysulfide system

The correlation between the magnetic and electrical properties of the (VS)_x(Fe₂O₃)_2?x (0.9<x<1.25) oxysulfide solid solutions has been studied. The crossover of conductivity from the semimetallic to semiconducting type is accompanied by changes in the magnetic susceptibility, which are characteristic of the transition from delocalized to localized electrons. For x=1.25, a region of the ferromagnetic ordering has been established in the temperature range 90–120 K.     

Optical properties of glasses activated by the compounds CuInSe2 and CuInTe2 and by the solid solutions CuInSe2x Te(1−x)

The spectral properties of amorphous media synthesized on the basis of glasses of the system SiO₂-CaO-R₂O (R=Na, K, Li), the ternary compounds CuInSe₂, and CuInTe₂, and solid solutions based on them have been investigated. It is shown that the absorption limit of the media investigated lies within 1.4–1.6 μm. It is noted that the three alkali ions constituting the system exert a favorable influence on the state and optical properties of the amorphous media activated with the compound CuInTe₂ and with the solid solutions CuInSe_2xTe_(1−x), where x≤0.5. The influence of the concentration of the solid solution CuInSeTe (x=0.5) on the optical properties of the amorphous media is investigated. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 67, No. 1, pp. 132–134, January–February, 2000.     

Raman spectroscopic study of the uranyl titanate mineral holfertite Ca x U2−x Ti(O8−x OH4x )·3H2O and the lack of metamictization

Raman spectra of the uranyl titanate mineral holfertite Ca _x U_2?x Ti(O_8?x OH_4x )·3H₂O were analyzed and related to the mineral structure. Observed bands are attributed to the TiO and (UO₂)²⁺ stretching and bending vibrations, U–OH bending vibrations, and H₂O stretching and bending. The mineral holfertite is metamict, as is evidenced by the order/disorder of the mineral. Unexpectedly, the Raman spectrum of holfertite does not show any metamictization. The intensities of the UO stretching and bending modes show normal intensity and the bands are sharp.     

Influence of Covalence on the Metal-Insulator Temperature in the CuIr 2 (S 1− x Se x ) 4 Spinels

Influence of the covalence on the metal-insulator (M-I) temperature in the CuIr 2 (S 1 m x Se x ) 4 spinel series is considered. For this purpose a vacancy model and the effective number of valence electrons per molecule are used. Calculations of the vacancy model parameters, i.e., the ion packing coefficients, the filling coefficient of the unit cell, the difference of the Pauling electronegativities and the vacancy parameter suggest that the covalence increases with increasing selenium concentration x , leading to a decrease of the metal-insulator temperature. It was observed that the metal-insulator temperature is related to the effective number of valence electrons per molecule, suggesting that with increasing covalence, less and less valence electrons take part in the metal-insulator transition. These effects are explained within the framework of the mixed valence of the iridium ions including structural defects.     

Properties of certain matrices related to the equilibrium configuration of the one-dimensional many-body problems with the pair potentialsV 1(x)=−log ∣sinx∣ andV 2(x)=1/sin2 x

It is shown that at equilibrium certain matrices associated to the one-dimensional many-body problems with the pair potentialsV ₁(x)=–logsinx andV ₂(x)=1/sin² x have a very simple structure. These matrices are those that characterize the small oscillations of these systems around their equilibrium configurations, and, for the second system, the Lax matrices that demonstrate its integrability.     

Calculation of the electronic structure and hyperfine fields for Fe1 − x Co x B and (Fe1 − x Co x )2B compounds by the Korringa-Kohn-Rostoker method

The magnetic properties of Fe_{1 ? x} Co _x B and (Fe_{1 ? x} Co _x )₂B disordered compounds were investigated using first-principles calculations of the electronic structure in the framework of the density functional theory with the Korringa-Kohn-Rostoker method. The concentration dependences of the magnetic moments and the electron density were calculated for the Fe_{1 ? x} Co _x B solid solutions. The results obtained were used to analyze in detail and to interpret the transition from a magnetic phase to a nonmagnetic phase, which was previously revealed from the experiments in the compounds under investigation. The performed analysis of the calculated hyperfine fields induced by the electronic shells at the iron and cobalt atoms in the (Fe_{1 ? x} Co _x )₂B borides made it possible to explain the experimentally observed magnetic anisotropy.     

On the magnetic susceptibility of Pd1−x Ag x in the range 0.5≦x≦1

The weak variation of the magnetic bulk susceptibility of Pd_1–x Ag _x with temperature T and silver mole fractionx within 0.5x1 has been investigated in the range 5KT400K. Experimental evidence can be given for an intersection point of the susceptibility isotherms (T=const,x) atx=0.55. The observed dependence of on T andx is interpreted by means of a semiphenomenological alloy susceptibility function (T,x).     

Characterisation of Ba2In2 − x Sn x O5 + x/2 oxide ion conductors

The Ba₂In_2 − x Sn _x O_5 + x/2 solid solution was confirmed up to x = 1 by solid-state reaction. X-ray diffraction at room and at elevated temperatures, Raman scattering and impedance spectroscopy were used to characterise the samples. The structure refinement of the composition x = 0.1 from neutron diffraction data reveals that tin is preferentially located in the tetrahedral layers of the brownmillerite. Paper presented at the 11th EuroConference on the Science and Technology of Ionics, Batz-sur-Mer, Sept. 9–15, 2007     

The influence of the local surrounding on the hyperfine interactions in Zr(Fe1−x Ni x )2 compounds

Mössbauer spectroscopy and the TDPAC method have been used to study Zr(Fe_1–x Ni _x )₂ compounds forx0.30. The hyperfine magnetic field at the Fe sites and the quadrupole splitting as functions of nickel concentration were analysed by use of⁵⁷Fe Mössbauer spectroscopy. Values of the internal magnetic field on¹⁸¹Ta nuclei have been found by means of the TDPAC method.     

The parton distribution functions of the photon and the structure functionF 2 γ (x,Q 2)

We present new parametrisations of the parton distribution functions of the photon including the first parametrisation in next-to-leading order QCD. We take into account some recent theoretical considerations pertaining to the gluon content of the photon,g ^γ. We argue that if an evolution is started at very lowQ ² and a fit to allF ₂ ^γ data performed with no constraints on the gluon distribution, then physically unreasonable gluon distributions may result. Our results support recent indications thatQ ₀ ² ≤1 GeV² is too low a value from which to start a perturbative evolution. Starting our evolution atQ ₀ ² =5.3 GeV², we evolve up inQ ² using a modified version of Rossi's Ansatz. The limited lever arm inQ ² leads to limited sensitivity to the QCD scale parameter Λ, though there is a preference for low values in the 0.1–0.2 GeV range. We also present new parametrisations of the singular asymptotic quark and gluon distribution functions of the photon which we believe are more accurate than those in current use.     

Introduction of bismuth into the highT c superconductor La2−x Sr x CuO4−y

Novel high-T _c superconductors La_2–x Bi _x Sr _x–x CuO_4–y have been isolated and studied. The influence of the experimental conditions of synthesis on the superconductivity has been especially studied for the composition La_1.7Bi_0.1Sr_0.2CuO_4–y ; it is shown thatT _c decreases as oxygen is introduced into the matrix, likely due to the partial oxidation of Bi(III) to Bi(V). The highT _c value observed for one sample (T _c 42 K), as compared withT _c 38 K of La_1.8Sr_0.2CuO_4–y suggests that bismuth is also a potential candidate for improving the superconducting properties in these oxides.     

The influence of praseodymium concentration on the luminescence properties of Ca1 ? x Pr x F2 + x (0.002 ≤ x ≤0.35)

The possibility of implementing photon cascade emission in CaF₂-PrF₃ crystals by increasing the PrF₃ concentration in the CaF₂ matrix is studied. It is shown that an increase in the Pr³⁺ content leads to redistribution of radiative transitions in favor of the ¹ S ₀-luminescence. The decrease in the efficiency of the second step of photon cascade emission at high PrF₃ concentrations is caused by quenching of the ³ P ₀ ?? 4f ² transitions as a result of cross relaxation.     

Features of the Jahn-Teller transition in Ni1 − x Co x Cr2O4 solid solutions

The structure of Ni_{1 ? x} Co _x Cr₂O₄ solid solutions has been investigated by synchrotron X-ray powder diffraction in the temperature range of 90–350 K for compositions x = 0, 0.005, 0.01, 0.015, 0.02, 0.1, 0.5, and 0.8, and their structures have been refined using the Rietveld analysis. The T-x phase diagram for solid solutions in the studied range of temperatures and concentrations has been constructed based on the obtained data. The revealed structural phase transitions have been explained from the viewpoint of the crystal field theory and the Jahn-Teller cooperative effect. Distortions of polyhedra, which are the cause of the structural phase transition, have been evaluated. The applicability of the Landau phenomenological theory and the possibility of using the magnitude of spontaneous strains as the order parameter have been discussed.     

Fermi surface evolution in the ensemble of spin-polarized quasiparticles in La2 − x Sr x CuO4

For the spin-fermion model, it has been shown that the concept of spin polarons makes it possible to reproduce fine details of the Fermi surface evolution in the nodal direction of La_{2 ? x} Sr _x CuO₄ occurring with changes in the doping level x. The physics here is determined by the spin-correlated hopping of charge carriers and by the doping dependence of the inverse magnetic correlation length.