Electronic bandstructures on 5d-transition metal pyrochlore: Cd2Re2O7 and Cd2Os2O7

The electronic bandstructure calculations for Cd₂Re₂O₇ and Cd₂Os₂O₇ are performed by using an FLAPW method based on the local density approximation, where the spin–orbit interactions are taken into account. It is found that the spin–orbit interaction changes significantly Re/Os-5d (t_2g) band dispersion situated near the Fermi level. Cd₂Re₂O₇ is a semi-metal, the Fermi level is located just in the valley, the specific heat coefficient is calculated as 2.7 mJ/K² mol Re and the carrier number is 0.039/cell in each hole and electron. The Re/Os-5d bands hybridize well with the O-p bands so that the Re/Os-5d component significantly appears even in the bottom of the wide O-p bands. Therefore, it is important to consider Re-5d O-p hybridization to investigate the physical properties of these compounds.     

On the superconductivity and structural properties of YBa2Cu3 − xCdxO7 − y

A series of superconducting cuprates with the nominal composition YBa₂Cu_3 − xCd_xO_7 − yand the effect of Cd substitution on Cu sites in this compound is presented. X-ray powder diffraction patterns for these cadmium cuprates with reduced diamagnetism indicate an orthorhombic unit cell like-perovskite structure for (0 ≤ x ≤ 0.15), while for higher Cd concentration, i.e.x = 1.0 the material is polyphasic. The observed superconducting transition temperature of the samples is nearly the same ([formula] K), except for (x = 1.0) whereT_cdrops to 72 K and a transition from metallic to semiconducting behavior of the normal state of the resistivity is observed. Such a decrease inT_cfor higher Cd concentration could be attributed to the presence of the green phase in this composition.     

Deposition of Gd2Zr2O7 single buffer layers with different thickness for YBa2Cu3O7−δ coated conductors on metallic substrates

A series of Gd₂Zr₂O₇ (GZO) single buffer layers with different thicknesses were epitaxially grown on highly textured Ni–5 at.% W tapes using pulsed laser deposition. These allow the subsequent growth of high-quality superconducting YBa₂Cu₃O_7?δ layers. The superconducting transition temperature T_c reaches a maximum value of 92.4 K as well as a narrow transition width of 0.8 K for the optimized GZO layer thickness. The inductive measurements show the critical current density as high as 1.2 MA/cm² at 77 K in self-field, indicating that a GZO single buffer layer is a suitable alternative for simplifying the second generation high T_c superconducting coated conductors architecture.     

Synthesis and electrical transport properties of Lu2+xTi2−xO7−x/2 oxide-ion conductors

The Lu_2+xTi_2−xO_7−x/2 (x = 0; 0.052; 0.096; 0.286; 0.44; 0.63; 33.3–49 mol% Lu₂O₃) nanoceramics with partly disordered pyrochlore-type structure are prepared by sintering freeze-dried powders obtained by a co-precipitation technique with 1600 °C annealing. Similar to pyrochlore-like compositions in the zirconate system, some of the new titanates are good oxide-ion conductors in air. The new solid-state electrolytes have oxide-ion conductivity in the interval of 1.0 × 10^− 3 – 2.5 × 10^− 3 S/cm at 740 °C in air. This value of conductivity is comparable with that of ZrO₂/Y₂O₃ ceramics. The conductivity of Lu_2+xTi_2−xO_7−x/2 depends on the chemical composition. The highest ionic conductivity is exhibited by nearly stoichiometric Lu_2+xTi_2−xO_7−x/2 (x = 0.096; 35.5 mol% Lu₂O₃) material containing ∼ 4.8 at.% Lu_Ti anti-site defects.     

Coexistence of superconductivity and ferromagnetism in hybrid rutheno-cuprate superconductors RuSr2RCu2O8

I consider the extended two-band s–f model with additional terms, describing inter-site Cooper pairs interaction between two-subsystems s and f, respectively. Following Green’s function technique and equation of motion method self-consistent equations for superconducting order parameter (Δ) and magnetic order parameter (m_f) are derived. The expressions for specific heat, density of states, and free energy are also derived. The theory has been applied to explain the coexistence of superconductivity and ferromagnetism in hybrid rutheno-cuprate superconductors RuSr₂RECu₂O₈ (RE = Gd, Eu). The theory shows that it is possible to become superconducting via a second order phase transition if the system is already ferromagnetic. The agreement between theory and experimental observations is quite satisfactory.     

Conductivity of SnP2O7 and In-doped SnP2O7 prepared by an aqueous solution method

SnP₂O₇ and In-doped SnP₂O₇ have been prepared by an aqueous solution method using (NH₄)₂HPO₄ as phosphorous source. It was found that the solid solution limit in Sn_1 ? xIn_x(P₂O₇)_1 ? δ was at least x = 0.12. All pyrophosphates in the Sn_1 ? xIn_x(P₂O₇)_1 ? δ (x ≤ 0.12) series exhibit 3 × 3 × 3 superlattice structures. The conductivities of Sn_0.92In_0.08(P₂O₇)_1 ? δ in air are 6.5 × 10^? 6 and 8.0 × 10^? 9 S/cm at 900 and 400 °C, respectively, when prepared by an aqueous solution method and annealed at 1000 °C. The conductivity of undoped SnP₂O₇ is slightly lower. However, it was also found that the low-temperature conductivities of pyrophosphates annealed only at 650 °C are several orders of magnitude higher than those annealed at 1000 °C, which could be related to a trace amount of an amorphous secondary phase. The peak conductivity was in this case observed at around 250 °C, which is the same temperature as previously observed in In-doped SnP₂O₇ although the conductivity is still three orders of magnitude lower in the present study. These differences can be related to large differences in particle size and morphology, and all in all, the conductivities of SnP₂O₇-based materials are very sensitive to the synthetic history.     

Superconductivity in Nb2InC

In this work the Nb₂InC phase is investigated by X-ray diffraction, heat capacity, magnetic and resistivity measurements. Polycrystalline samples with Nb₂InC nominal compositions were prepared by solid state reaction. X-ray powder patterns suggest that all peaks can be indexed with the hexagonal phase of Cr₂AlC prototype. The electrical resistance as a function of temperature for Nb₂InC shows superconducting behavior below 7.5 K. The M(H) data show typical type-II superconductivity with H_C1 ～ 90 Oe at 1.8 K. The specific heat data are consistent with bulk superconductivity. The Sommerfeld constant is estimated as γ ～ 12.6 mJ mol^?1 K^?1.     

Flux pinning and superconducting properties of melt-textured NEG-123 superconductor with TiO2 addition

We studied the effect of TiO₂ doping on flux pinning and superconducting properties of a melt-grown (Nd_0.33Eu_0.33Gd_0.33) Ba₂Cu₃O_y + 35 mol% Gd₂BaCuO₅ (70 nm in size) composite (NEG-123) processed in Ar–1% O₂ atmosphere. As indicated by similar, sharp superconducting transitions, the small quantities of TiO₂ used in our experiments did not deteriorate superconducting properties of the NEG material. Transmission electron microscopy (TEM) analysis found 20–50 nm Ti-based particles in the NEG-123 matrix. However, we have not observed the clouds of <10 nm sized particles in the NEG-123 matrix, as in the case of recently reported NEG-123 composites doped by Mo and Nb nanoparticles. Nevertheless, quite a good J_c–B performance in the 0.1 mol% Ti-doped sample, namely 550 kA/cm² at the self-field and at the secondary peak field (4.5 T) was achieved at 65 K, while 320 kA/cm² was obtained at zero-field at 77 K, and 50 kA/cm² at 90.2 K. The pinning effectiveness decreased with increasing Ti content above 0.2 mol%. The analysis of the pinning force showed that higher concentration of Ti (>0.2 mol%) increased the amount of normal pins (δl pinning), indicated by the Fp(h) peak shift from h = 0.42–0.36. The maximum pinning effect in a broad field range could be achieved by optimizing Ti content and adding sub-micron Gd-211 particles.     

AC response of YBa2Cu3O7 thin film superconductor

Low-field ac measurements of magnetic susceptibility of YBa₂Cu₃O₇ high-temperature superconducting thin film were carried out over a wide range of temperatures and ac magnetic field amplitudes. A strong field dependence of the real χ′ and imaginary χ″ components was observed. The field dependence of the imaginary component is used to extract the temperature dependence of the critical current density in the sample using the critical state model. The exponent β of the power law relation J_c ～ (1 ? T/T_c)^β was determined from ac-susceptibility data and different values were found. Experimental results are compared with predictions of some existing theoretical models describing the ac response of superconducting thin film in perpendicular ac field.     

Determination of superconducting gap of SmFeAsFxO1−x superconductors by Andreev reflection spectroscopy

The superconducting gap in FeAs-based superconductor SmFeAs(O_1?xF_x) (x = 0.15 and 0.30) and the temperature dependence of the sample with x = 0.15 have been measured by Andreev reflection spectroscopy. The intrinsic superconducting gap is independent of contacts while many other “gap-like” features vary appreciably for different contacts. The determined gap value of 2Δ = 13.34 ± 0.47 meV for SmFeAs(O_0.85F_0.15) gives 2Δ/k_BT_C = 3.68, close to the BCS prediction of 3.53. The superconducting gap decreases with temperature and vanishes at T_C, in a manner similar to the BCS behavior but dramatically different from that of the nodal pseudogap behavior in cuprate superconductors.     

Fluctuation induced magneto-conductivity studies in YBa2Cu3O7−δ + xBaZrO3 composite high-Tc superconductors

Fluctuations on the electrical conductivity of polycrystalline YBa₂Cu₃O_7?δ + xBaZrO₃ (x = 1.0, 2.5, 5.0 and 10.0 wt.%) superconductors were investigated from the resistivity vs. temperature data for zero field and 8 T (Tesla) external magnetic fields. Attempts have been made to identify the optimum inclusion of BaZrO₃ (BZO) in YBa₂Cu₃O_7?δ (YBCO) superconductors. The phase formation, texture and grain alignments were analyzed by XRD and SEM techniques. Then the effects of superconducting fluctuations on the electrical conductivity of granular composite superconductors were studied for zero field and 8 T external magnetic fields. Though inclusions of BZO sub-micron particles are not expected to influence superconducting order-parameter fluctuation (SCOPF) much, the transition from 2D to 3D of the order parameter in the mean-field region depends on the BZO content in the composites. It has been observed that BZO residing at the grain boundary of YBCO matrix influences the tailing region without having significant change in the mean-field critical temperature. In the present work, attention has been focused mostly in the experimental domain relatively above the T_c. It reveals that, 1 wt.% composite exhibits a better superconducting property in comparison with pure YBCO.     

Effects of doping with nanoscale Co3O4 particles on the superconducting properties of powder-in-tube processed MgB2 tapes

Nanoscale Co₃O₄ particles were doped into MgB₂ tapes with the aim of developing superconducting wires with high-current-carrying capacity. Fe-sheathed MgB₂ tapes with a mono-core were prepared using the in situ powder-in-tube (PIT) process with the addition of 0.2–1.0 mol% Co₃O₄. The critical temperature decreased monotonically with an increasing amount of doped Co₃O₄ particles for all heat-treatment temperatures from 600 to 900 °C. However, the transport critical current density (J_c) at 4.2 K varied with the heat-treatment temperatures. The J_c values in magnetic fields ranging from 7 to 12 T decreased monotonically with increasing Co₃O₄ doping level for a heat-treatment temperature of 600 °C. In contrast, some improvements on the J_c values of the Co₃O₄ doped tapes were observed in the magnetic fields below 10 T for 700 and 800 °C. Furthermore, J_c values in all the fields measured increased as the Co₃O₄ doping level increase from 0 to 1 mol% for 900 °C. This heat-treatment temperature dependence of the J_c values could be explained in terms of the heat-treatment temperature dependence of the irreversibility field with Co₃O₄ doping.     

Chemical diffusion of water in the double perovskites Ba4Ca2Nb2O11 and Sr6Ta2O11

The mechanism and kinetics of water incorporation in the double perovskites Ва₄Ca₂Nb₂O₁₁ and Sr₆Ta₂O₁₁ has been investigated (T = 300÷500 °C and aH₂O = 1 · 10^− 3÷2.2 · 10^− 2). The formation of hydration products Ba₄Ca₂Nb₂O₁₁·xH₂O and Sr₆Ta₂O₁₁·xH₂O (0.2 < x < 0.50) was limited by the diffusion of H₂O. It has been found that the concentration dependences of D˜_H2O are the same for both samples: small increasing of D˜_H2O with increasing x. The temperature dependences of the chemical diffusion coefficients of water for compositions of Ba₄Ca₂Nb₂O₁₁·0.35H₂O and Sr₆Ta₂O₁₁·0.35H₂O could be described with close activation energies of E_a = 0.38 ± 0.03 eV and E_a = 0.49 ± 0.03 eV, respectively. The chemical diffusion coefficients of water are nearly one order of magnitude smaller for tantalate Sr₆Ta₂O₁₁. This result correlates with lower oxygen and proton conductivities in Sr₆Ta₂O₁₁ as the consequence of lower mobilities.     

On the rate constants of OH + HO2 and HO2 + HO2: A comprehensive study of H2O2 thermal decomposition using multi-species laser absorption

Hydrogen peroxide (H₂O₂) and hydroperoxy (HO₂) reactions present in the H₂O₂ thermal decomposition system are important in combustion kinetics. H₂O₂ thermal decomposition has been studied behind reflected shock waves using H₂O and OH diagnostics in previous studies (Hong et al. (2009) [9] and Hong et al. (2010) [6,8]) to determine the rate constants of two major reactions: H₂O₂ + M → 2OH + M (k₁) and OH + H₂O₂ → H₂O + HO₂ (k₂). With the addition of a third diagnostic for HO₂ at 227 nm, the H₂O₂ thermal decomposition system can be comprehensively characterized for the first time. Specifically, the rate constants of two remaining major reactions in the system, OH + HO₂ → H₂O + O₂ (k₃) and HO₂ + HO₂ → H₂O₂ + O₂ (k₄) can be determined with high-fidelity.No strong temperature dependency was found between 1072 and 1283 K for the rate constant of OH + HO₂ → H₂O + O₂, which can be expressed by the combination of two Arrhenius forms: k₃ = 7.0 × 10¹² exp(550/T) + 4.5 × 10¹⁴ exp(?5500/T) [cm³ mol^?1 s^?1]. The rate constants of reaction HO₂ + HO₂ → H₂O₂ + O₂ determined agree very well with those reported by Kappel et al. (2002) [5]; the recommendation therefore remains unchanged: k₄ = 1.0 × 10¹⁴ exp(?5556/T) + 1.9 × 10¹¹⁺exp(709/T) [cm³ mol^?1 s^?1]. All the tests were performed near 1.7 atm.     

Optical and Raman spectroscopy studies on Fe-based superconductors

A brief review of optical and Raman studies on the Fe-based superconductors is given, with special emphasis on the competing phenomenon in this system. Optical investigations on ReFeAsO (Re = rare-earth element) and AFe₂As₂ (A = alkaline-earth metal) families provide clear evidence for the gap formation in the broken symmetry states, including the partial gaps in the spin-density wave states of parent compounds, and the pairing gaps in the superconducting states for doped compounds. Especially, the superconducting gap has an s-wave pairing lineshape in hole-doped BaFe₂As₂. Optical phonons at zone center detected by Raman and infrared techniques are classified for several Fe-based compounds. Related issues, such as the electron–phonon coupling and the effect of spin-density wave and superconducting transitions on phonons, are also discussed. Meanwhile, open questions including the T-dependent mid-infrared peak at 0.6–0.7 eV, electronic correlation, and the similarities/differences between high-T_c cuprates and Fe-based superconductors are also briefly discussed. Important results from other experimental probes are compared with optical data to better understand the spin-density wave properties, the superconductivity, and the multi-band character in Fe-based compounds.     

Effects of growth rate and buffer-layer on Bi2Sr2CaCu2Oy thin film fabrication

The effect of the growth rate on the Bi₂Sr₂CaCu₂O_y (Bi2212) thin film quality on MgO substrate is investigated at several growth rates from 0.175 to 3 nm/min. The maximal step height on the film surface is improved from about 100 to 6 nm by the reduction of growth rate to 0.5 nm/min and simultaneously the superconducting critical temperature attaining to a zero resistance T_c(R=0), is also improved from 50 to 63 K. The surface morphologies of the upmost Bi-superconducting thin films with the intermediate layers on MgO substrate is also studied in contrast to that deposited directly on the MgO substrate.     

Effect of the composition on the superconducting properties of IBAD-MgO SmBCO coated conductors with superconducting film directly deposited on epi-MgO layer

Sm_1+xBa_2?xCu_3+yO_7?δ (SmBCO) films were directly deposited on the epi-MgO/IBAD-MgO/Y₂O₃/Al₂O₃/Hastelloy template by co-evaporation using the evaporation using drum in dual chambers (EDDC) system without the buffer layer in order to investigate the effect of the composition ratios on superconducting property, microstructure and texture of SmBCO film. The films with gradient composition ratios of Sm:Ba:Cu were deposited using a shield with an opening which was placed between the substrate and the boats. The highest I_c of 52 A (corresponding to J_c = 1.6 MA/cm² and a thickness of 800 nm) was observed at 77 K in self field at a composition x = 0.01–0.05 and y = ?0.23 to ?0.46. When the composition ratio is outside this range, the I_c value rapidly decreased. The superconducting critical current was highly dependent on the composition ratio. As the composition ratio is farther away from that of the highest I_c, the SmBCO (1 0 3) peak intensity increased and the amount of a-axis oriented parts increased. A dense microstructure with round-shape grains was observed in the region showing the highest I_c. The optimum composition ratio can be found by analyzing films deposited with variable deposition rates of each depositing element.     

Electrical conductivity and thermal expansion of the oxy-cuspidine Gd4Al2O9 substituted with Ca and Sr

The series of Gd_4 ? xM_xAl₂O_9 ? x/2 (M = Ca, Sr) with x = 0, 0.01, 0.05, 0.10 and 0.25 was prepared by the citrate complexation method. Both Gd_4 ? xCa_xAl₂O_9 ? x/2 and Gd_4 ? xSr_xAl₂O_9 ? x/2 show the monoclinic cuspidine structure with space group of P2₁/c up to 0.05–0.1 and 0.01–0.05 mol for Ca and Sr, respectively. Beyond the substitution limit of Gd₄Al₂O₉, GdAlO₃ and SrGd₂Al₂O₇ appear as additional phases. The highest electrical conductivity obtained at 900 °C yielded σ = 1.49 × 10^? 4 S/cm for Gd_3.95Ca_0.05Al₂O_8.98. In comparison, the conductivity of pure Gd₄Al₂O₉ was σ = 1.73 × 10^? 5 S/cm. The conductivities determined are in a similar range as those of other cuspidine materials investigated previously. The thermal expansion coefficient of Gd₄Al₂O₉ at 1000 °C was 7.4 × 10^? 6 K^? 1. The phase transition between 1100 and 1200 °C reported earlier changes with increasing substitution of Ca and Sr.     

Excess currents larger than the point contact limit in normal-metal/superconducting junctions

In a point contact NS junction, perfect Andreev reflection occurs over a range of voltages equal to the superconducting energy gap, producing an excess current of I_exc =  (4 / 3)(2 eΔ / h). If the superconductor has a finite width, rather than the infinite width of the point contact, one cannot neglect superfluid flow inside the superconducting contact. The energy range available for perfect Andreev reflections then becomes larger than the superconducting gap, since superfluid flow alters the dispersion relation inside the finite width superconductor. We find a maximum excess current of approximately (7 / 3)(2 eΔ / h) when the width of the superconductor is approximately 7 / 3 times the width of the normal metal.     

Antiferromagnetic phase transition in garnet-type AgCa2Mn2V3O12 and NaPb2Mn2V3O12

Ferrimagnetism has been extensively studied in garnets, whereas it is rare to find the antiferromagnet. Present work will demonstrate antiferromagnetism in the two Mn–V-garnets. Antiferromagnetic phase transition in AgCa₂Mn₂V₃O₁₂ and NaPb₂Mn₂V₃O₁₂ has been found, where the magnetic Mn²⁺ ions locate only on octahedral A site. The heat capacity shows sharp peak due to antiferromagnetic order with the Néel temperature T_N=23.8 K for AgCa₂Mn₂V₃O₁₂ and T_N=14.2 K for NaPb₂Mn₂V₃O₁₂. The magnetic entropy change over a temperature range 0–50 K is 13.9 J K^?1 mol-Mn²⁺-ions^?1 for AgCa₂Mn₂V₃O₁₂ and 13.6 J K^?1 mol-Mn²⁺-ions^?1 for NaPb₂Mn₂V₃O₁₂, which are in good agreement with calculated value of Mn²⁺ ion with spin S=5/2. The magnetic susceptibility shows the Curie–Weiss behavior over the range 29–350 K. The effective magnetic moment μ_eff and the Weiss constant θ are μ_eff=6.20 μ_B Mn²⁺-ion^?1 and θ=?34.1 K (antiferromagnetic sign) for AgCa₂Mn₂V₃O₁₂ and μ_eff=6.02 μ_B Mn²⁺-ion^?1 and θ=?20.8 K for NaPb₂Mn₂V₃O₁₂.