Intrinsic pinning properties of FeSe0.5Te0.5

The intrinsic pinning properties of FeSe_0.5Te_0.5, which is a superconductor with a critical temperature T_c of approximately 14 K, were studied through the analysis of magnetization curves obtained using an extended critical state model. For the magnetization measurements carried out with a superconducting quantum interference device (SQUID), external magnetic fields were applied parallel and perpendicular to the c-axis of the sample. The critical current density J_c under the perpendicular magnetic field of 1 T was estimated using the Kimishima model to be equal to approximately 1.6 × 10⁴, 8.8 × 10³, 4.1 × 10³, and 1.5 × 10³ A/cm² at 5, 7, 9, and 11 K, respectively. Furthermore, the temperature dependence of J_c was fitted to the exponential law of J_c(0) × exp(?αT/T_c) up to 9 K and the power law of J_c(0) × (1 ? T/T_c)ⁿ near T_c.     

Effects of Ni and Co doping on the physical properties of tetragonal FeSe0.5Te0.5 superconductor

Isoelectronic Tellurium (Te) substitution for Selenium (Se) in the tetragonal phase of FeSe (β-FeSe) increases the superconducting transition temperature (T_c) by applying a negative pressure on the lattice. However, the normal state resistivity increases and shows semi-metallic behavior for samples with higher Te concentration. With increasing Te concentration, the T_c increases and reaches a maximum for FeSe_0.5Te_0.5 and then decreases with further increase of Te. We have investigated the effect of Cobalt (Co) and Nickel (Ni) doping in FeSe_0.5Te_0.5 in the nominal composition range Fe_1?xTM_xSe_0.5Te_0.5 (TM = Co (x = 0.05, 0.1, 0.15, 0.2) and Ni (x = 0.05, 0.1)). Both Co and Ni doping suppress T_c and drives the system to metal–insulator transition. The in-plane (‘a’) and out-of-plane (‘c’) lattice constants decrease with increasing dopant concentration.     

STM spectroscopy of an organic superconductor

Electron tunneling spectroscopy of the organic superconductor κ-(BEDT-TTF)₂Cu(NCS)₂using low temperature scanning tunneling microscope (STM) is reported. The tunneling differential conductance in the superconducting phase was obtained in theb–cplane of a single crystal, by varying the tip position on the sample surface. The differential conductance is reduced near zero bias voltage and enhanced at the gap edge, associated with the superconducting gap structure below[formula] K. The gap width differs slightly from sample to sample, while the overall functional shape of the conductance is sample-independent. The tunneling conductance is reduced to almost zero near zero bias voltage, while it is finite inside the gap edge. The curve obtained cannot be fit to the BCS density of states withs-wave pairing symmetry, even if the life-time broadening of one-electron levels is taken into account. Finite conductance inside the gap edge suggests anisotropy of the gap. However, the conductance curve obtained is not explained by a simpled-wave symmetry for Δ(k). The reduced conductance near zero bias voltage suggests a finite gap. An anisotropic model with a finite gap, in which Δ(k) varies depending on the direction ink-space, is examined. The tunneling conductance in the low-energy region is almost fit by the model with Δ_min = 2 meV and Δ_max = 6 meV. The finite conductance is explained by introducing a small effect of life time broadening. We conclude that the gap is anisotropic and is finite (at least Δ_min = 2 meV) on the entire Fermi surface.     

Oxygen non-stoichiometry and electrical conductivity of Pr2−xSrxNiO4±δ with x = 0–0.5

Oxygen non-stoichiometry and electrical conductivity of the Pr_2−xSr_xNiO_4±δ series with x = 0.0–0.5 were investigated in Ar/O₂ (pO₂ = 2.5 to 21 000 Pa) within a temperature range of 20–1000 °C. The equilibrium values of oxygen non-stoichiometry and electrical conductivity of these nickelates were determined as functions of temperature and oxygen partial pressure (pO₂). The nickelates with x = 0–0.5 appear to be p-type semiconductors in the investigated temperature and pO₂ ranges. The nickelates with x = 0.3–0.5 show very feebly marked pO₂ dependencies of the conductivity. Pr_1.7Sr_0.3NiO_4±δ shows the anomalies of the conductivity versus oxygen partial pressure which can be related to the orthorhombic–tetragonal crystal structure transformations. The conductivity of the Pr_2−xSr_xNiO_4±δ samples correlates with the average oxidation state of the nickel cations. The samples with x = 0.5 have the highest nickel oxidation state (≈ 2.5+), the highest [Ni³⁺]/[Ni²⁺] ratio close to 1 and show the highest conductivity (≈ 120 S/cm) in the whole pO₂ and temperature ranges investigated.     

Superconducting properties of the pyrochlore oxide Cd2Re2O7

We report the superconducting properties of the pyrochlore oxide Cd₂Re₂O₇. The bulk superconducting transition temperature T_c is about 1.0 K, and the upper critical field H_c2 determined by the measurement of specific heat under magnetic fields is 0.29 T. The superconducting coherence length is estimated to be 34 nm. Specific heat data measured on single crystals suggest that the superconducting gap of Cd₂Re₂O₇ is nodeless.     

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.     

Inelastic neutron scattering on iron-based superconductor BaFe2(As,P)2

Inelastic neutron scattering has been performed on powder sample of an iron-based superconductor BaFe₂(As_0.65P_0.35)₂ with superconducting transition temperature (T_c) = 30 K, whose superconducting (SC) order parameter is expected to have line node. In the normal state, constant-E scan of dynamical structure factor, S(Q, E), exhibits a peak structure centered at momentum transfer Q ～ 1.20 Å^?1, corresponding to antiferromagnetic wave vector. Below T_c, the redistribution of the magnetic spectral weight takes place, resulting in the formation of a peak at E ～ 12 meV and a gap below 6 meV. The enhanced magnetic peak structure is ascribed to the spin resonance mode, evidencing sign change in the SC order parameter similar to other iron-based high-T_c superconductors. It suggests that fully-gapped s_± symmetry dominates in this superconductor, which gives rise to high-T_c (=30 K) despite the nodal symmetry.     

Comparison of the local structures of Ca0.82La0.18FeAs2 and Ba0.64K0.36Fe2As2 pnictide superconductors using atomic pair distribution function analysis

A comparative local structure study of pnictide superconductors Ca_0.82La_0.18FeAs₂ (112-type, T_c∼ 40 K) and Ba_0.64K_0.36Fe₂As₂ (122-type, T_c∼ 37 K), using room temperature x-ray total scattering measurements is reported. The Fe–As superconducting active layer is found to be globally similar in both the systems consisting of edge-sharing FeAs_4/4 tetrahedra as in all the iron-pnictide superconductors discovered so far. Although optimally superconducting, the active layer in these compounds is found to sustain a large local inhomogeneity. These results thus imply that a nanoscopic manipulation of the Fe–As active layer, rather than its isotropic structural tuning, is the key parameter to control the superconducting properties of the iron-based systems.     

Yttrium doped La1−xYxO0.9F0.1FeAs superconductors: Hall and thermopower studies

The effect of yttrium substitution at the lanthanum site on the superconducting properties of La_1?xY_xO_0.9F_0.1FeAs (‘x’ = 0, 0.10, 0.20, 0.30, 0.50 and 0.60) oxypnictides has been studied. Powder X-ray diffraction studies confirm single phases till x = 0.1 beyond which minor amount of Y₂O₃ is observed. The temperature dependence of resistivity measurements confirm the superconducting transition temperature (T_c) of 34.8 (±0.05) K and corresponding Meissner transition at 34.3 K in the ‘x’ = 0.3 composition which is higher than that reported for the parent phase (LaO_0.9F_0.1FeAs (T_c = 28 K)). Further increase in the concentration of yttrium leads to broadening and suppression of the superconducting transition. The value of H_c2 at zero temperature is estimated to be about 60.5 T. The Seebeck coefficient (S) shows a negative sign indicating that the major contribution to the conductivity is by electrons. The Hall coefficient (R_H) also remains negative throughout the temperature range supporting the thermopower results. The lattice parameters (a and c) decreases and the charge-carrier density increases with yttrium doping.     

Electronic structure and fundamental absorption edges of KPb2Br5, K0.5Rb0.5Pb2Br5, and RbPb2Br5 single crystals

X-ray photoelectron core-level and valence-band spectra for pristine and Ar⁺-ion irradiated (001) surfaces of KPb₂Br₅, K_0.5Rb_0.5Pb₂Br₅, and RbPb₂Br₅ single crystals grown by the Bridgman method have been measured and fundamental absorption edges of the ternary bromides have been recorded in the polarized light at 300 K and 80 K. The present X-ray photoelectron spectroscopy (XPS) results reveal high chemical stability of (001) surfaces of K_xRb_1?xPb₂Br₅ (x=0, 0.5, and 1.0) single crystals. Substitution of potassium for rubidium in K_xRb_1?xPb₂Br₅ does not cause any changes of binding energy values and shapes of the XPS constituent element core-level spectra. Measurements of the fundamental absorption edges indicate that band gap energy, E_g, increases by about 0.14 and 0.19 eV when temperature decreases from 300 K to 80 K in KPb₂Br₅ and RbPb₂Br₅, respectively. Furthermore, there is no dependence of the E_g value for KPb₂Br₅ upon the light polarization, whilst the band gap energy value for RbPb₂Br₅ is bigger by 0.03–0.05 eV in the case of E6c compared to those in the cases of E6a and E6b.     

Manifestation of multiband optical properties of MgB2

The optical conductivity of MgB₂ has been determined on a dense polycrystalline sample in the spectral range 6 meV–4.6 eV using a combination of ellipsometric and normal incidence reflectivity measurements. σ₁(ω) features a narrow Drude peak with anomalously small plasma frequency (1.4 eV) and a very broad ‘dome’ structure, which comprises the bulk of the low-energy spectral weight. This fact can be reconciled with the results of band structure calculations by assuming that charge carriers from the 2D σ-bands and the 3D π-bands have principally different impurity scattering rates and negligible interband scattering. This also explains a surprisingly small correlation between the defect concentration and T_c, expected for a two-gap superconductor. The large 3D carrier scattering rate suggests their proximity to the localization limit.     

Electrical conductivity of (Ba0.3Sr0.2La0.5)(In1−xFex)O3−δ

We have synthesized the perovskite oxides of the (Ba_0.3Sr_0.2La_0.5)(In_1−xFe_x)O_3−δ system and measured the total electrical conductivity as a function of temperature and oxygen partial pressure. It was found that the single-phase composition region extended from x = 0.0 to x = 1.0, and that the Fe valence increased from 3.06 to 3.50 in that region. The electrical conductivity was semiconducting from x = 0.0 to x = 0.40 and metallic from x = 0.50 to x = 1.0. The total electrical conductivity at 800 °C also increased with the Fe content and achieved a maximum value of 140 (S/cm) at x = 1.0. From the dependence of the electrical conductivity on the oxygen partial pressure, we conclude that above x = 0.50, the majority carriers are holes. The estimated hole conductivity increased exponentially with the amount of Fe⁴⁺ cation present. The oxide ion conductivity was dependent on the oxygen vacancy content.     

Annealing effects on the crystal structure and physical properties of FeSe1−xTex (0.6 ≦ x ≦ 1) single crystals

Annealing effects of FeSe_1?xTe_x (0.6 ≦ x ≦ 1) single crystals have been investigated from measurements of the powder X-ray diffraction and specific heat. Through the annealing, several peaks of powder X-ray diffraction have become sharp and a clean jump of the specific-heat at the superconducting (SC) transition temperature, T_c, has been observed for x = 0.6–0.9, indicating bulk superconductivity. For annealed single-crystals of x = 0.6–0.8, the SC condensation energy, U₀, and the SC gap, Δ₀, at 0 K have been estimated as ～1.8 J/mol and 2.3–2.5 meV, respectively. The value of 2Δ₀/k_BT_c is 3.9–4.5, indicating a little strong-coupling superconductivity. Both the electronic specific-heat coefficient in the normal state, γ_n, and the residual electronic specific-heat coefficient in the SC state, γ₀, have been found to show significant x dependence. The values of γ_n are much larger than those estimated from the band calculation.     

Inelastic neutron scattering studies of the spin and lattice dynamics in iron arsenide compounds

Although neutrons do not couple directly to the superconducting order parameter, they have nevertheless played an important role in advancing our understanding of the pairing mechanism and the symmetry of the superconducting energy gap in the iron arsenide compounds. Measurements of the spin and lattice dynamics have been performed on non-superconducting ‘parent’ compounds based on the LaFeAsO (‘1111’) and BaFe₂As₂ (‘122’) crystal structures, and on electron and hole-doped superconducting compounds, using both polycrystalline and single crystal samples. Neutron measurements of the phonon density-of-state, subsequently supported by single crystal inelastic X-ray scattering, are in good agreement with ab initio calculations, provided the magnetism of the iron atoms is taken into account. However, when combined with estimates of the electron–phonon coupling, the predicted superconducting transition temperatures are less than 1 K, making a conventional phononic mechanism for superconductivity highly unlikely. Measurements of the spin dynamics within the spin density wave phase of the parent compounds show evidence of strongly dispersive spin waves with exchange interactions consistent with the observed magnetic order and a large anisotropy gap. Antiferromagnetic fluctuations persist in the normal phase of the superconducting compounds, but they are more diffuse. Below T_c, there is evidence in three ‘122’ compounds that these fluctuations condense into a resonant spin excitation at the antiferromagnetic wavevector with an energy that scales with T_c. Such resonances have been observed in the high-T_c copper oxides and a number of heavy fermion superconductors, where they are considered to be evidence of d-wave symmetry. In the iron arsenides, they also provide evidence of unconventional superconductivity, but a comparison with ARPES and other measurements, which indicate that the gaps are isotropic, suggests that the symmetry is more likely to be extended-s_± wave in character.     

Scanning tunneling spectroscopy on Bi2SrCaCuO6+δ

Scanning tunneling microscopy and scanning tunneling spectroscopy (STS) measurements were performed on Bi₂SrCaCuO₆ whose superconducting transition temperature T_c is about 80 K. The superconducting gap obtained by the STS measurements was found to be about 40 meV. This value is close to that of optimally doped Bi₂Sr₂CaCu₂O₈ which has similar T_c. The observed spatial inhomogeneity of the gap value was much smaller than that of Bi₂Sr₂CuO₆.     

Structure and electrochemical properties of Sm0.5Sr0.5Co1 − xFexO3 − δ cathodes for solid oxide fuel cells

Crystal structure, thermal expansion coefficient, electrical conductivity and cathodic polarization of compositions in the system Sm_0.5Sr_0.5Co_1 − xFe_xO_3 − δ with 0 ≤ x ≤ 0.9 were studied as function of Co / Fe ratio and temperature, in air. Two phases, including an Orthorhombic symmetry for 0 ≤ x ≤ 0.4 and a cubic symmetry for 0.5 ≤ x ≤ 0.9, were observed in samples of Sm_0.5Sr_0.5Co_1 − xFe_xO_3 − δ at room temperature. The adjustment of thermal expansion coefficient (TEC) to electrolyte, which is one of the main problems of SSC, could be achieved to lower TEC values with more Fe substitution. High electrical conductivity above 100 S/cm at 800 °C was obtained for all specimens, so they could be good conductors as cathodes of IT-SOFC. The polarization behavior of SSCF as a function of Fe content was evaluated by means of AC impedance using LSGM electrolyte. It was discovered that the Area Specific Resistance (ASR) of SSCF increased as the amount of substitution of Fe for Co increased. When the amount of Fe reached to 0.4, the highest ASR was obtained and then the resistance started decreasing above that. The electrode with a composition of Sm_0.5Sr_0.5Co_0.2Fe_0.8O_3 − δ showed high catalytic activity for oxygen reduction operating at temperature ranging from 700 to 800 °C.     

Near-infrared photoluminescence and thermally stimulated current in Cu3Ga5Se9 layered crystals: A comparative study

Near-infrared photoluminescence (PL) and thermally stimulated current (TSC) spectra of Cu₃Ga₅Se₉ layered crystals grown by Bridgman method have been studied in the photon energy region of 1.35–1.46 eV and the temperature range of 15–115 K (PL) and 10–170 K (TSC). An infrared PL band centered at 1.42 eV was revealed at T = 15 K. Radiative transitions from shallow donor level placed at 20 meV to moderately deep acceptor level at 310 meV were suggested to be the reason of the observed PL band. TSC curve of Cu₃Ga₅Se₉ crystal exhibited one broad peak at nearly 88 K. The thermal activation energy of traps was found to be 22 meV. An energy level diagram demonstrating the transitions in the crystal band gap was plotted taking account of results of PL and TSC experiments conducted below room temperature.     

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.     

Point contact Andreev reflection spectroscopy of superconducting energy gaps in 122-type family of iron pnictides

A brief overview of the superconducting energy gap studies on 122-type family of iron pnictides is given. It seems that the situation in the hole doped Ba_1?xK_xFe₂As₂ is well resolved. Most of the measurements including the presented here point contact Andreev reflection spectra agree on existence of multiple nodeless gaps in the excitation spectrum of this multiband system. The gaps have basically two sizes – the small one with a strength up to the BCS weak coupling limit and the large one with a very strong coupling with 2Δ_L/kT_c > 6–8. In the electron doped Ba(Fe_1?xCo_x)₂As₂ the most of the experiments including our point contact measurements reveal in quite broadened spectra only a single gap with a strong coupling strength. The high precision ARPES measurements on this system identified two gaps but very close to each other, both showing a strong coupling with 2Δ/kT_c ～ 5 and 6, respectively.     

Structural,ferroelectric, optical properties of A-site-modified Bi0.5(Na0.78K0.22)0.5Ti0.97Zr0.03O3 lead-free piezoceramics

We reported the role of A-site modification on the structural, ferroelectric, optical and electrical field-induced strain properties of Bi_0.5(Na_0.78K_0.22)_0.5Ti_0.97Zr_0.03O₃ lead-free piezoceramics. The Li⁺ ions with concentration from 0 to 5 mol% were used to substitute at A-site. There was no phase transition when Li⁺ ions was added up to 5 mol%. The electric field-induced strain (S_max/E_max) values increased from 600 to 643 pm/V for 2 mol% Li⁺-added which results from distortion both rhombohedral and tetragonal phase structures. The band gap reduced from 2.88 to 2.68 eV and the saturation polarization decreased from 46.2 to 26.1 μC/cm² when Li⁺ ions concentration increased from 0 to 5 mol% respectively. We expect that this work could be helpful for further understanding the role of A-site dopants in comparison with B-site modification in lead-free Bi_0.5(Na,K)_0.5TiO₃-based ceramics.