Superconducting Properties of Zn-Doped Cu0.5Tl0.5Ba2Ca2Cu3?yZnyO10?δ Superconductors

A reproducible synthesis and characterization of Zn-doped Cu_0.5Tl_0.5Ba₂Ca₂Cu_3−y Zn _y O_12−δ (y=0, 0.5, 1.0, 1.5) superconductors at a relatively lower synthesis temperature of 840°C are studied by using X-ray diffraction, resistivity, ac-susceptibility and FTIR absorption measurements. The X-ray diffraction (XRD) studies of these samples have shown a tetragonal structure in which the c-axis length has been found to decrease with increased Zn doping. The critical temperature and magnitude of diamagnetism have not been significantly affected with the doping of Zn at this synthesis temperature. The magnitude of diamagnetism in the as-prepared undoped samples is decreased, whereas it remains stable (unchanged) in oxygen post-annealed samples. The apical oxygen phonon’s modes of type Tl–O_A–M(2) and Cu(1)–O_A–M(2) {where M=Cu/Zn} and the planar oxygen phonon modes of type M(2)–O_P–M(2) are also softened with the increase of Zn doping. We interpreted the softening of these oxygen related phonon modes linked with the decreased c-axis length, reduced John–Teller distortions and increased mass of Zn (65.38 amu) as compared to that of Cu (63.54 amu) (Kaplan et al., Phys. Rev. B 65, 214509, 2002).     

Suppression of Superconductivity Due to Enhanced Co Doping in?Cu0.5Tl0.5Ba2Ca2Cu3?yCoyO10?δ Superconductors

Fluctuation Induced Conductivity (FIC) of Co-doped Cu_0.5Tl_0.5Ba₂Ca₂Cu_3−y Co _y O_10−δ (y=0, 0.05, 0.1, 0.5) Superconductors have been studied as to find the possible cause of T _c suppression in these compounds. We used Aslamazov–Larkin (AL) and Lawrence–Donaich (LD) equations to analyze the FIC of our samples. In this regard, it is observed that the data seems to fit well with 3D (three-dimensional) AL equations. In addition, crossover temperature from 2D to 3D has been found. The width of the temperature window for 3D conductivity is continuously decreasing with enhanced Co concentration. The shrinking of 3D temperature region with increased Co doping can be correlated with the suppression of superconductivity. It is observed that the coherence length and th interplanar coupling strength have also been decreased with increased Co doping, consistent with the magnetic pair-breaking effect.     

Cd-Doped Cu0.5Tl0.5Ba2Ca2Cu3?yCdyO10?δ (y=0,0.5,1.0,1.5,2.0) Superconductors

Superconducting properties of cadmium doped Cu_0.5Tl_0.5Ba₂Ca₂Cu_3−y Cd _y O_10−δ (y=0,0.5,1.0,1.5,2.0) samples have been studied using X-ray diffraction, resistivity, ac-susceptibility and FTIR absorption measurements. In X-ray diffraction studies these samples have shown to have tetragonal structure. The zero resistivity critical temperature and magnitude of diamagnetism are suppressed with the increased incorporation of Cd in the final compound. A change in the shape of FTIR absorption spectra, after doping, has shown the incorporation of Cd in the unit cell. A systematic hardening of the apical oxygen modes and softening of the CuO₂ planar modes of vibration with increased Cd doping have shown that it is incorporated in the unit cell of Cu_0.5Tl_0.5Ba₂Ca₂Cu_3−y Cd _y O_10−δ (y=0,0.5,1.0,1.5,2.0) superconductors. The FTIR absorption measurements of these samples have shown that hardening of the apical oxygen modes of types Cu(1)–O(2)–Tl and Cu(1)–O(2)–Cu(2)/Cd _y (y=0,0.5,1.0,1.5,2.0) increases with the increase of Cd doping in the samples. A softening of the CuO₂ planar oxygen mode Cu(2)–O–Cu(2) is also observed with the increased Cd doping in the final compound. It is most likely that hardening of the apical oxygen modes and the softening of the planar modes of vibration are associated damped harmonic oscillations produced by heavier Cd atoms in the CuO₂ planes, which suppress the phonon population from a desired level, reducing the magnitude of superconductivity in the final compound.     

AC-field Frequency Response of?Cu0.5Tl0.5Ba2(Ca2?qMgq)Cu3O10?δ Bulk Superconductor

The dielectric properties of Cu_0.5Tl_0.5Ba₂Ca_2−q Mg _q Cu₃O_10−δ (q=0, 0.5, 1.0 1.5) superconductor samples were studied at two temperatures of 80 and 290 K by capacitance (C) and conductance (G) measurements with the test frequency (f) in the range of 10 KHz to 10 MHz. We have presented the measurements of the dielectric constants (ε′ and ε″), dielectric loss factor (tan δ) and ac-conductivity (σ _ac) as a function of frequency and temperature. A negative capacitance (NC) experience has been observed, which is most likely due to different contact electrodes and superconductor samples’ Fermi levels. Since metals have their Fermi levels higher than ceramics, there is a flow of the carriers from the ceramic samples towards the metal electrodes. The dielectric polarization phenomenon is observed, which is due to dislodgment of mobile charges from their equilibrium position relative to fixed charges of the reservoir layer. The improved inter plane coupling promoted by Mg substitution at Ca site would change the dielectric response of Cu_0.5Tl_0.5Ba₂Ca_2−q Mg _q Cu₃O_10−δ superconductors. To observe such effects in Mg doped Cu_0.5Tl_0.5Ba₂Ca_2−q Mg _q Cu₃O_10−δ superconductors, di- electric measurements were carried out both at room temperature (290 K) and in the superconducting state closer to the boiling point of liquid nitrogen (80 K). The excess conductivity arising due to superconducting state of material has been determined, and its role in the mechanism of superconductivity is suggested. The negative dielectric constant (ε′) and dielectric loss factor (tan δ) show strong dispersion at low frequencies. The lower thermal agitation at 80 K may enhance the polarizability and hence the dielectric constants (ε′ and ε″).     

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.     

Synthesis of New Pb-Based 1232 Cuprate Containing Boron in?the?(Pb0.5B0.5) Sr2(Er3?x?yCexSry)Cu2Oz System

New Pb-based layered cuprates containing boron with the 1232 structure have been synthesized in the (Pb_0.5B_0.5)Sr₂(Er_3−x−y Ce _x Sr _y )Cu₂O _z system. Nearly the single 1232 phase samples are obtained for the nominal composition of 1.6≤x≤1.9 and y=0.2. A sample with the composition of (Pb_0.5B_0.5)Sr₂(Er_1.2Ce_1.6Sr_0.2)Cu₂O _z shows resistivity-dropping phenomenon below 10 K and it shows a diamagnetic signal at about 9.0 K, though the superconducting volume fraction is very small. From these results, the sample may well be a new Pb-based superconductor with the 1232 structure.     

Improvement of Superconductivity with the Modification of Charge Reservoir Layer in (Cu0.5Tl0.5?xMx)Ba2Ca2Cu3O10?δ

The relatively higher electronegative elements (M = Pd, Nb, Bi, Hg) have been partially doped at Tl sites in Cu_0.5Tl_0.5−x M _x Ba₂O_4−δ (x=0,0.25) charge reservoir layer of Cu_0.5Tl_0.5−x M _x Ba₂Ca₂Cu₃O_10−δ superconductor. These elements may retain more oxygen in the charge reservoir layer due to their higher electronegativity as compared to Tl, and the higher population of oxygen in the charge reservoir layer can optimize the charge carriers’ density in the conducting CuO₂ planes. The optimum density of mobile charge carriers in the conducting CuO₂ increases Fermi wave-vector K _F and Fermi velocity v _F of the carriers, which results in the improvement of superconducting properties of the material.     

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.     

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.     

Role of Mobile Charge Carriers and Fluctuation Induced Conductivity in (Cu0.5Tl0.5?xKx)Ba2Ca3Cu1Zn3O12?δ Superconductor

The main role played by mobile carriers and fluctuation induced conductivity (FIC) in (Cu_0.5Tl_0.5−x K _x )Ba₂Ca₃Cu₁Zn₃O_12−δ (x=0, 0.25) superconductor samples are analyzed in the light of the Aslamazov–Larken (AL) theory. The enhancement of three-dimensional (3D) conductivity and grain size is achieved with K-doping at Tl sites in the (Cu_0.5Tl_0.5−x K _x )Ba₂O_4−δ charge reservoir layer, which are further improved by post-annealing the samples in oxygen. The improvement of these factors causes the increase in cross-over temperature (T _o), zero resistivity critical temperature {T _c(R=0)} and T _c(onset) of diamagnetism to their higher values. We have also evaluated the exponents (λ _2D and λ _3D), zero temperature coherence lengths ξ _c(0), and interlayer coupling (J) for these samples and tried to correlate them to the superconductivity order parameters.     

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.     

Stabilization of the anatase phase of Ti1?xSnxO2 (x < 0.5) nanofibers

We experimentally investigate the stabilization of the anatase phase of Ti_1−x Sn _x O₂ (x < 0.5) nanofibers when synthesized by an electrospinning method. The as-spun nanofibers became nano-grained, polycrystalline nanofibers after calcination and the diameters of the nanofibers depend on Sn content. Stabilization of the anatase phase in Ti-rich compositions and incorporation of Sn ions were confirmed by X-ray diffraction, Raman, X-ray absorption near-edge structure, and photoluminescence (PL) spectroscopies. Results from the PL study also demonstrated the tunable nature of the optical properties, with the emission maximum shifting towards higher wavelength with increasing Sn concentration.      

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.     

Superconductivity and Electron–Phonon Interaction in?Cu0.5Tl0.5Ba2Ca2Cu3?yMyO10?δ (M=0, Si, Ge, Sn, and?y=0,?1)

Superconducting properties of Cu_0.5Tl_0.5Ba₂Ca₂Cu_3−y M _y O_10−δ (M=0, Si, Ge, Sn and y=0, 1) samples have been studied by using x-ray diffraction (XRD), resistivity, ac-susceptibility and Fourier Transform Infrared (FTIR) absorption measurements. We have tried to explore the role of the electron-phonon interaction in bringing about superconductivity in the Cu_0.5Tl_0.5Ba₂Ca₂Cu_3−y M _y O_10−δ material. A change in the cell parameters from XRD and the change in the shape of FTIR absorption spectra have shown the incorporation of doped elements (M=Si, Ge, Sn) in the unit cell of the final compound. It is most likely that the change in oxygen phonon modes is associated with the oscillations of heavier and lighter atoms in MO₂/CuO₂ planes. These oscillations of heavier and lighter atoms suppress the density of the phonon population from the desired level for optimum superconductivity in the final compound.     

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.     

Extraordinary behaviour of the Y1?xPrxBa2Cu3O7?δ system

Investigations of Y_1–x M _x Ba₂Cu₃O_7– (M=Ce, Th)c-axis oriented thin film specimens show that the rate of depression ofT _c withx is larger for M=Th, than for M=Ce and Pr, and suggest that Ce, like Th, is tetravalent in this compound. Hall effect measurements on Y_1–x Pr _x Ba₂Cu₃O_7– single crystals reveal aT ² dependence of the cotangent of the Hall angle in the normal state and a negative Hall anomaly belowT _c in the superconducting state, in agreement with recent reports. Our research shows that the depth, , of the negative Hall signal scales withT/T _c and that the maximum value of decreases linearly withx and vanishes atx0.24. Magnetoresistance measurements on Y_1–x Pr _x Ba₂Cu₃O_7– single crystals indicate that the irreversibility lineH(T ^*) obeys a universal scaling relation characterized by anm=3/2 power law nearT _c, with a crossover to a more rapid temperature dependence of belowT/T _c 0.6, similar to that observed for polycrystalline specimens.     

Superconductivity of YBa2?xNdxCu3Oy Solid Solution

The solubility of Nd at the Ba sites and the superconductivity of YBa_2–x Nd _x Cu₃O _y were investigated by X-ray powder diffraction and measurements of the electrical resistance and ac susceptibility. The single Re123 phase was obtained for x0.30. The onset transition temperature is insensitive to the Nd content x in the region of x0.40. All are higher than 95 K. The zero resistance transition temperatures , however, exhibits two-step variation with the increase of x. For x0.25, are all above 92 K. The highest of 94 K was obtained for x=0.25. For x0.3 drops sharply to about 84 K. Finally falls to 30 K and is below 10 K for x=0.5. The two-step variation of T _c might be an indication of the existence of two trap levels for holes.     

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.     

Preparation and Magnetic Properties of?(La1?xSr1+x)(Mn0.5Co0.5)O4

A series of single phase (La_1−x Sr_1+x ) (Mn_0.5Co_0.5)O₄ (0≤x≤0.40) materials with a tetragonal K₂NiF₄ structure was prepared by a solid state reaction method at 1400 or 1450 °C with a short period of heating time. Powder X-ray diffraction (XRD) and the Rietveld refinement method were employed for the structural analysis. Unit cell a- and c-axes decrease with increasing amount of Sr substitution. A discrepancy between the zero-field-cooled and the field-cooled magnetization is observed in all samples investigated below a characteristic temperature, T ^*, which likely arises from the canted nature of spins or the random freezing of spins. It appears that T ^* decreases with increasing amount of Sr substitution, which is possibly due to the enhancement of chemical pressure induced by Sr and a corresponding increases of the valence of Mn and/or Co.     

Normal-state Conduction Mechanisms in GdBa2Cu3?xRuxO7?δ Superconducting Phase

Bulk superconducting samples of type GdBa₂Cu_3−x Ru _x O_7−δ , Gd-123, with x=0.0–0.3 were prepared by the conventional solid-state reaction technique. X-ray powder diffraction (XRD), scanning electron microscope (SEM), electron dispersive X-ray (EDX) and electrical-resistivity measurements were performed in order to investigate the effect of Ru⁴⁺ ions substitution on Gd-123 phase. Enhancement of both phase formation and the superconducting transition temperature T _c for GdBa₂Cu_3−x Ru _x O_7−δ phase up to x=0.05 was observed from XRD and electrical-resistivity measurement, respectively. This enhancement was confirmed with the calculated relative volume fraction. For x>0.05, suppression of both phase formation and T _c was obtained and the superconductivity was completely destroyed around x=0.3. The normal-state electrical resistivity was analyzed by the two- and three-dimensional variable range hopping (2D-VRH and 3D-VRH) and Coulomb gap CG. The results showed that the dominant mechanism was CG for x≤0.075, while was 3D-VRH for x≥0.15.