Magnetic and transport properties of Mn3+xGa1?xN compounds

Mn_3+x Ga_1−x N compounds with x = 0.0 and 0.1 were prepared by re-sintering Mn₂N_0.86, Ga bulk and Mn powders. These compounds are deduced to be the N-deficiency ones. In Mn₃GaN, a step-like magnetic transition, from frustrated antiferromagnetism to paramagnetism with increasing temperature, occurs at 370 K, while the same magnetic transition of Mn_3.1Ga_0.9N is far above 380 K. The enhanced magnetization of Mn₃GaN at low temperatures is ascribed to the fast lowering of antiferromagnetism. The electrical resistivity of Mn₃GaN exhibits a typically metallic conducting behavior with a positive magnetoresistance of 4–7%.     

Magnetic and dielectric properties of Mg1+x Mnx, Fe2?2x, O4 ferrite system

Ferrites with the general formula Mg_1+xMn_xFe_2–2xO₄(where x = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8 and 0.9) were prepared by the standard ceramic technique and studied by means of X-ray diffraction, magnetization, a.c. susceptibility and dielectric constant measurements. The X-ray analysis confirmed the single-phase formation of the samples. The lattice parameter is found to increase up to x = 0.3 and thereafter it decreases as x increases. The cation distribution has been studied by X-ray analysis and magnetization. Magnetization results exhibit collinear ferrimagnetic structure for x 0.3 and thereafter structure changes into non-collinear for x > 0.3. Curie temperature (T_C) obtained from a.c. susceptibility data decreases with increasing x. The dielectric constant (), loss tangent (tan ) show strong frequency dependence.     

Magnetic order and evolution of the electronic state aroundx=0.12 in La2?xBaxCuO4 and La2?xSrxCuO4

Muon spin rotation ( ⁺SR) measurement provides clear evidence of the antiferromagnetic order of Cu moments below 35 K for La_2–x Ba _x CuO₄ and below 15 K for La_2–x Sr _x CuO₄ in the narrow range ofx where the high-T _c superconductivity (SC) is suppressed remarkably. The results suggest that the change of the electronic state coupled with the lattice instability is relevant to the local suppression of SC and freezing of spin fluctuations of the Cu moment.     

Structural and dielectric properties of Na1?xBaxNb1?x(Sn0.5Ti0.5)xO3 ceramics

Lead-free (1 − x)NaNbO₃/xBa(Ti_0.5Sn_0.5)O₃ (x = 0.1, 0.125, 0.15, 0.175, 0.2, and 0.3) ceramics were elaborated by the conventional ceramic technique. Sintering has been made at 1523 K for 2 h. The crystal structure was investigated by X-ray diffraction with CuKα radiation at room temperature. As a function of composition, these compounds crystallize with tetragonal or cubic symmetry. Dielectric measurements show that the materials have a classical ferroelectric behavior for compositions in the range 0.10 ≤ x ≤ 0.15 and relaxor one for compositions in the range 0.15 < x ≤ 0.30. Temperatures T _C or T _m decrease as x content increases. The ferroelectric behavior has been confirmed by hysteresis characterization. For x = 0.1, a piezoelectric coefficient d ₃₁ of 42.146 pC N⁻¹ was obtained at room temperature. The evolution of the Raman spectra was studied as a function of temperature for x = 0.1.     

Room-temperature oxidation of La2?xSrxCuO4

A series of oxidized La_2–x Sr _x CuO_4+y compounds has been prepared by treating the starting materials with a solution of Br₂ in NaOH at room temperature. The structural modifications due to the oxidation of the materials have been studied by X-ray diffraction. Some of the observed changes are: (i) a large increase in the long parameter of the unit cell for samples with Sr content and (ii) a slight decrease in a along the whole range ofx. Interesting features have been observed regarding the critical temperatures of these materials: transition temperatures are higher for those containing lower Sr amounts (some of them were even nonsuperconducting before the oxidation treatment) in contrast to materials with x0.15, whoseT _c's do not change very much. The influence of both oxygen and strontium contents on the structural modifications and the superconducting properties of the oxidized materials will be discussed.     

Emissivity and Optical Properties of Thermochromic Material La0.7Ca0.3?xSrxMnO3?(0 ≤ x ≤ 0.3)

La_0.7Ca_0.3−x Sr _x MnO₃ (0 ≤ x ≤ 0.3) (LCSMO) is a thermochromic material. The material can show a phase transition from ferromagnetic-metal to paramagnetic-insulator under the appropriate doping level (x). In this paper, LCSMO compounds were synthesized by a conventional solid-state reaction method. The normal emissivity and the spectral reflectance of LCSMO with different doping levels (x) are experimentally investigated. Based on the spectral reflectance data, the optical constants (refractive index n and extinction coefficient k) are calculated by using Kramers–Kronig (K–K) relations. Then, the emissivity changing mechanism is discussed. The experimental results show that the emissivity of LCSMO increases with increasing temperature. For the samples with x = 0.1 and 0.15, their emissivity has a sudden change in the vicinity of the phase transition temperature T _p.     

Electronic Properties and Superconductivity of Electron-Doped La1?x/2Pr1?x/2CexCuO4

La_1−x/2Pr_1−x/2Ce _x CuO _y (LPCCO) samples with doping level up to 20% have been synthesized and their electronic and superconductive properties are studied. X-ray diffraction revealed that the LPCCO system is a pure phase system with a T’214 structure. Magnetic and resistive measurements show that the system is superconducting at 0.08≤x<0.20 with T _cmax=25 K at x=0.12. An anti-ferromagnetism transition was also observed in under-doped PLCCO (x=0.05) with the window width of the anti-ferromagnetism phase being significantly narrower than that NCCO and PCCO systems. The behavior of the Ce doping is compared with Sr doping in this system, and the mechanism is discussed.     

Structural, spectroscopic and microwave characterizations of (Sm0.5Y0.5)Ti(Nb1?xTax)O6 ceramics

Microwave dielectric ceramics of the type (Sm_0.5Y_0.5)Ti(Nb_1−x Ta _x )O₆ were prepared for x = 0, 0.2, 0.4, 0.6, 0.8 and 1 through the conventional solid state ceramic route. The ball-milled compositions were calcined at 1,250 °C. The cylindrical pellets were sintered at temperatures between 1,385 and 1,450 °C. The densities were determined by Archimedes method. The structure was analyzed using X-ray diffraction method. The microwave dielectric properties of the polished pellets were measured using cavity resonator method. The morphological studies were done using Scanning Electron Microscopy and Transmission Electron Microscopy. The Raman spectra were recorded and analyzed to confirm the structural change. The photoluminescence spectra were also taken and the emission lines were identified. A correlation study was done among the measured properties and parameters. Most of the samples have high dielectric constant, high quality factor and low temperature coefficient of resonant frequency and hence suitable for microwave applications.     

Superconducting Properties of Carbon and Zn Double-doped Mg1?xZnx(B1?xCx)2

A series of polycrystalline samples of Mg_1−x Zn _x (B_1−x C _x )₂ (x=0.00, 0.02, 0.04, 0.06, 0.08, and 0.10) were synthesized by a conventional solid-state reaction method under a background pressure about 10⁻³ Pa. Phase identification, crystal structure and superconducting transition temperature (T _c) were studied by means of X-ray diffraction (XRD) and resistivity measurements. The results indicated that the lattice parameters a and c show no clear trend in their changes with increasing doping level, and it turned out that the dopants had a marked effect on the crystal-lattice parameters and changed the crystal structure of the samples. The T _c for Mg_1−x Zn _x (B_1−x C _x )₂ decreased with C and Zn doping, but the rate of decrease was slower than single C-doped. We propose that the suppression of T _c by doping originates largely from the structural change.     

Griffiths Phase and Disorder in Perovskite Manganite Oxides La1?xCaxMnO3 and La0.7Sr0.3MnO3

Polycrystalline samples La_1−x Ca _x MnO₃ (x=0.17, 0.15, 0.10) and La_0.7Sr_0.3MnO₃ were prepared in order to investigate the Griffiths-like features induced by disorder compared with their counterpart single crystals. The magnetization data exhibit the traditional transition from ferromagnetic phase to paramagnetic phase. From the temperature dependence of inverse susceptibility, it can be testified that the Griffiths-like features still exist in as-prepared Ca doped samples, while non-Griffiths-like features exist in La_0.7Sr_0.3MnO₃. All these samples, however, exhibit the large effective spins resulting from formation of the short-order ferromagnetic clusters. The O K-edge X-ray absorption spectra indicate the Jahn–Teller (J-T) distortions are definitely present due to the J-T ion Mn³⁺, which indicate that static J-T distortion is not a sufficient condition for the existence of Griffiths phase in Sr-doped system. And, the size of J-T distortion is a little larger in polycrystalline La_0.7Sr_0.3MnO₃ than that in polycrystalline samples La_1−x Ca _x MnO₃ (x=0.17, 0.15, 0.10), revealed by X-ray diffraction parameters and extended X-ray fine structure absorption data of Mn K-edge. It also testifies that the disorder in La_0.7Sr_0.3MnO₃ caused by both chemical doping and J-T distortions is lower than that in polycrystalline samples La_1−x Ca _x MnO₃, which may be the reason of non-Griffiths-like phase existing in La_0.7Sr_0.3MnO₃ samples.     

Proton conduction and chemical stability of (La0.5Sr0.5)(Mg0.5+yNb0.5−y)O3−δ

Electrical conduction properties of complex perovskite-type oxides in the (La_0.5Sr_0.5)(Mg_0.5+yNb_0.5−y)O_3−δ (y = 0.02-0.06) series at intermediate-high temperatures were investigated; introduction of protons by hydration of oxide-ion vacancies was expected by increasing the Mg/Nb ratio from unity. The conductivity depended on y and a maximum conductivity was obtained at y = 0.04: σ = 4.9 × 10⁻⁶ S cm⁻¹ at 400 °C in wet H₂ atmospheres. From electromotive force measurements of hydrogen and water vapor concentration cells, electrical conduction in wet H₂ atmospheres can be attributed to ionic conduction, and proton conduction is dominant below 700 °C. Unlike other perovskite-type proton conductors, (La_0.5Sr_0.5)(Mg_0.54Nb_0.46)O_3−δ was stable in CO₂ atmospheres even in the low-intermediate temperature region due to dilution of reactive strontium by lanthanum.     

Preparation, characterization and conductivity studies of Li3?2xAl2?xSbx(PO4)3

New NASICON type materials of composition, Li_3−2x Al_2−x Sb _x (PO₄)₃ (x = 0·6 to 1·4), have been prepared and characterized by powder XRD and IR. D.C. conductivities were measured in the temperature range 300–573 K by a two-probe method. Impedance studies were carried out in the frequency region 10²−10⁶ Hz as a function of temperature (300–573 K). An Arrhenius behaviour is observed for all compositions by d.c. conductivity and the Cole-Cole plots obtained from impedance data do not show any spikes on the lower frequency side indicating negligible electrode effects. A maximum conductivity of 4·5 × 10⁻⁶ S cm⁻¹ at 573 K was obtained for x = 0·8 of the Li_3−2x Al_2−x Sb _x (PO₄)₃ system.     

Effect of Pb Doping on the Superconducting Properties of?(Cu0.5?xPbxTl0.5)Ba2Ca2Cu3O10?δ

The effect of Pb doping on the superconducting properties of (Cu_0.5−x Pb _x Tl_0.5)Ba₂Ca₂Cu₃O_10−δ (x=0.0, 0.15, 0.25, 0.35) samples has been investigated. Lead is doped in Cu_0.5Tl_0.5Ba₂O_4−δ charge reservoir layer and at the CuO₂ planar sites. A multiphase material is achieved with the doping of Pb at the CuO₂ planar sites; however, a predominant single-phase (Cu_0.5−x Pb _x Tl_0.5)Ba₂Ca₂Cu₃O_10−δ (x=0.0, 0.15, 0.25, 0.35) material is synthesized with the doping of Pb at the charge reservoir layers. Formation of multiphase material with the doping of lead at the planar sites showed that its substitution at the planar site is not possible and the formation of PbO₂ planes is less likely. In the samples doped at the charge reservoir layer, the zero critical temperature [T _c (R=0)] is systematically depressed with the increased concentration of lead. The T _c (R=0) and magnitude of the diamagnetism are enhanced after post-annealing the samples in oxygen atmosphere. An apical oxygen mode is observed around 438 cm⁻¹ in undoped samples, which is shifted to 457–461 cm⁻¹ in the Pb-doped samples. This shift in the peak position is most likely associated with the connectivity of apical oxygen atoms with Pb atoms of (Cu_0.5−x Pb _x Tl_0.5)Ba₂O_4−δ (x=0.0, 0.15, 0.25, 0.35) charge reservoir layers. The presence of Pb in the charge reservoir layer and its increased concentration, somehow, stops the flow of mobile carriers to the conducting CuO₂ planes. The decreased density of mobile carriers diminishes the critical temperature and magnitude of diamagnetism in the final compound. The increased oxygen diffusion in the unit cell achieved by post-annealing in oxygen replenishes the concentration of carriers in conducting CuO₂ planes, which increases the T _c (R=0) and the magnitude of diamagnetism. These experiments have shown that the density of mobile carriers plays a vital role in the mechanism of superconductivity and their depressed density suppresses the superconductivity parameters.     

Effect of Mg substitution on microstructure and electrical properties of Mn1.25Ni0.75Co1.0?xMgxO4(0?≤?x?≤?1) NTC ceramics

The NTC thermistors based on spinel-type semiconducting electroceramics with compositions Mn_1.25Ni_0.75Co_1.0−x Mg _x O₄ (0 ≤ x ≤ 1) were synthesized by solid-state method. The influences of Mg content on the Mn_1.25Ni_0.75Co_1.0−x Mg _x O₄ materials were investigated by laser particle size analyzer, XRD, SEM, EDS and electrical measurements, respectively. The experiment results show that the substituted Mg suppresses the separation of NiO phase. Both the grain size and density decrease as the amount of Mg content in Mn_1.25Ni_0.75Co_1.0−x Mg _x O₄ samples increases. In particular, the substituted Mg leads to a decrease in the resistance drift of the Mn_1.25Ni_0.75Co_1.0−x Mg _x O₄ NTC ceramics after aging test. This indicates that the Mg substituted Mn_1.25Ni_0.75Co_1.0−x Mg _x O₄ NTC ceramics display high electrical stability in comparison with the Mg-free Mn_1.25Ni_0.75Co_1.0O₄ ceramics.     

A Study of the Magnetic Properties of?Bi1.64?xPb0.36CdxSr2Ca2Cu3Oy Superconductor

The flux pinning energy and magnetic properties of Bi_1.64−x Pb_0.36Cd _x Sr₂Ca₂Cu₃O _y (BPCSCCO) with x=0.0, 0.02, 0.04 and 0.06 were studied. A series of Bi-2223 superconductor samples with a nominal composition of BPCSCCO was synthesized and the effect of Cd substitution for Bi was investigated. As a result, Cd addition has been found to improve the superconducting properties of the Bi-Pb-Sr-Ca-Cu-O system. The effects of the annealing time and the amount of Cd doping on the structure, AC magnetic susceptibility, ρ–T curves and flux pinning energy were investigated. Also, for all samples the relation between the current and voltage in the mixed state was found to follow the model relationship V=α I ^β . The maximum value of β is 22.30, which is obtained for the sample with an annealing time of 270 h and a Cd content of 0.04.     

Production and dielectric properties of lead-free ceramics with the formula [(Na0.5K0.5)1 ? xLix](Nb1 ? y ? zTaySbz)O3

The influence of past history on the possibility of obtaining high-density ferroelectric ceramics of solid solutions [(Na_0.5K_0.5)_{1 − x} Li _x ](Nb_{1 − y − z} Ta _y Sb _z )O at x = 0–0.14, y = 0, 0.1, 0.2, and z = 0–0.1 is identified. The dynamics of behavior of materials under a field in the process of polarization is evaluated. The relative dielectric permeability of samples in a wide range of temperatures (20–700°C) and frequencies (25 Hz-1 MHz) of a variable electric field is studied. On the basis of study of dielectric, piezoelectric, and elastic properties of solid solutions, prospective objects for further technological elaboration and modification of chemical composition with the goal of improving the electrophysical parameters are selected. Original Russian Text ? I.A. Verbenko, O.N. Razumovskaya, L.A. Shilkina, L.A. Reznichenko, K.P. Andryushin, 2009, published in Neorganicheskie Materialy, 2009, Vol. 45, No. 6, pp. 762–768.     

Normal state and superconductivity of ErBa2(Cu1?xCrx)O7?δ(x=0–0.1)

The effects of Cr in ErBa₂(Cu_1–x Cr _x )O_7– (x=0–0.1) superconductor have been investigated. The critical temperature, which was determined by DC electrical resistance measurements, showed no suppression of the onset temperature (T _{c onset}) within the substitution range. The transition width (T _c ) broadened as the Cr content is increased. The normal state changes from the metal-like to semimetal/semiconductor-like for x0.03. Micrographs from the scanning electron microscope, X-ray diffraction pattern, and energy dispersive X-ray analysis results are used to describe the superconducting properties of these materials. The orthorhombic structure was preserved throughout the substitution range. Some possible roles of Cr in the system are discussed.     

Experimental determination of the spatial distribution of electron defects in La2 ? xSrxCuO4 and Nd2 ? xCexCuO4 crystal lattices

The data of M?ssbauer emission spectroscopy on ⁶⁷Cu(⁶⁷Zn) and ⁶⁷Ga(⁶⁷Zn) isotopes show that holes appearing as a result of the Sr²⁺ substitution for La³⁺ in the La_{2 − x} Sr _x CuO₄ crystal lattice are localized predominantly at oxygen atoms occurring in the same atomic plane as the copper atoms. In contrast, electrons appearing as a result of the Ce⁴⁺ substitution for Nd³⁺ in the Nd_{2 − x} Ce _x CuO₄ crystal lattice are localized in the copper sublattice. These results are consistent with the model assuming that a mechanism responsible for the high-temperature superconductivity in La_{2 − x} Sr _x CuO₄ and Nd_{2 − x} Ce _x CuO₄ crystal lattices is based on the interaction of electrons with two-site two-electron centers possessing negative correlation energies (negative-U centers).     

Structure of Sr1 ? xPbxFeO3 ? δ (0 < x < 0.5) perovskite-like materials

We have synthesized Sr_{1 − x} Pb _x FeO_{3 − δ} (x = 0, 0.05, 0.1, 0.15, 0.2, 0.3, 0.5) perovskite-like materials and studied their structure by X-ray diffraction, M?ssbauer spectroscopy, and electron microscopy. According to the X-ray diffraction data, the Pb solubility limit in the perovskite structure is x ≈ 0.15. The materials with x = 0.05 and 0.1 contained Pb_1.33Sr_0.67Fe₂O₅ inclusions 10–30 nm in size. Using chronopotentiometry and temperature-programmed desorption, we have estimated oxygen mobility in the materials with x = 0.05 and 0.1. The results demonstrate that Pb doping increases oxygen mobility in the strontium-ferrite-based materials.     

Preparation of Y0.5[Yb1?xNdx]0.5Ba2Cu3Oz Superconductors Using Nitrate Routes

The chemical solution nitrate route was used to prepare Y_0.5[Yb_1−x Nd _x ]_0.5Ba₂Cu₃O _z superconducting phase with x=0.1, 0.2 and 0.3. Different calcination temperatures from 870 to 900 °C were used. Both XRD and DSC techniques were utilized in monitoring the Y_0.5[Yb_1−x Nd _x ]_0.5Ba₂Cu₃O _z superconducting phase and the non-superconducting impurity phases such as BaCuO₅, CuO and RE₂BaCuO₅. These two techniques were used to study the effect of impurity phases on the decomposition temperature of Y_0.5[Yb_1−x Nd _x ]_0.5Ba₂Cu₃O _z superconducting phase. The value of x, the Nd amount, and the calcination temperature both influenced the type and number of impurity phases, which resulted in changing the eutectic and peritectic reaction temperatures.