Enhanced Critical parameters of nano-Carbon doped MgB2 Superconductor

The high field magnetization and magneto transport measurements are carried out to determine the critical superconducting parameters of MgB2-xCx system. The synthesized samples are pure phase and the lattice parameters evaluation is carried out using the Rietveld refinement. The R-T(H) measurements are done up to a field of 140 kOe. The upper critical field values, Hc2 are obtained from this data based upon the criterion of 90% of normal resistivity i.e. Hc2=H at which Rho=90%Rho; where RhoN is the normal resistivity i.e., resistivity at about 40 K in our case. The Werthamer-Helfand-Hohenberg (WHH) prediction of Hc(0) underestimates the critical field value even below than the field up to which measurement is carried out. After this the model, the Ginzburg Landau theory (GL equation) is applied to the R-T(H) data which not only calculates the Hc2(0) value but also determines the dependence of Hc2 on temperature in the low temperature high field region. The estimated Hc(0)=157.2 kOe for pure MgB2 is profoundly enhanced to 297.5 kOe for the x=0.15 sample in MgB2-xCx series. Magnetization measurements are done up to 120 kOe at different temperatures and the other parameters like irreversibility field, Hirr and critical current density Jc(H) are also calculated. The nano carbon doping results in substantial enhancement of critical parameters like Hc2, Hirr and Jc(H) in comparison to the pure MgB2 sample.Comment: 25 pages with 9 Figs: comments/suggestions([email protected]

Superconductivity of non- stoichiometric intermetallic compound NbB2

We report the synthesis, magnetic susceptibility and crystal structure analysis for NbB2+x (x = 0.0 to 1.0) samples. The study facilitates in finding a correlation among the lattice parameters, chemical composition and the superconducting transition temperature Tc. Rietveld analysis is done on the X- ray diffraction patterns of all synthesized samples to determine the lattice parameters. The a parameter decreases slightly and has a random variation with increasing x, while c parameter increases from 3.26 for pure NbB2 to 3.32 for x=0.4 i.e. NbB2.4. With higher Boron content (x>0.4) the c parameter decreases slightly. The stretching of lattice in c direction induces superconductivity in the non- stoichiometric niobium boride. Pure NbB2 is non-superconductor while the other NbB2+x (x>0.0) samples show diamagnetic signal in the temperature range 8.9-11K. Magnetization measurements (M-H) at a fixed temperature of 5K are also carried out in both increasing and decreasing directions of field. The estimated lower and upper critical fields (Hc1 & Hc2) as viewed from M-H plots are around 590 and 2000Oe respectively for NbB2.6 samples. In our case, superconductivity is achieved in NbB2 by varying the Nb/B ratios, rather than changing the processing conditions as reported by others.Comment: 14 pages TEXT+Figs; comments/suggestions ([email protected]). ACCEPTED: Solid State Communications (2008

Superconductivity of various borides: The role of stretched c-parameter

The superconductivity of MgB2, AlB2, NbB2+x, and TaB2+x is intercompared. The stretched c-lattice parameter (c = 3.52 Å) of MgB2 in comparison to NbB2.4 (c = 3.32 Å) and AlB2 (c = 3.25 Å) decides empirically the population of their π and σ bands and as a result their transition temperature Tc values, respectively, at 39 and 9.5 K for the first two and no superconductivity for the later. The nonstoichiometry induces an increase in c parameter with Boron excess both in NbB2+x and TaB2+x. Magnetization (M-T) and resistivity measurements (ρ-T) in case of niobium boride samples show the absence of superconductivity in stoichiometric NbB2 sample (c = 3.26 Å) while a clear diamagnetic signal and a ρ = 0 transition for boron excess NbB2+x samples. On the other hand, superconductivity is not achieved in TaB2+x case. The probable reason behind is the comparatively lesser or insufficient stretching of c parameter

Anomalous thermoelectric power of Mg1-xAlxB2 system with x = 0.0 to 1.0

Thermoelectric power, S(T) of the Mg1-xAlxB2 system has been measured for x = 0.0, 0.1, 0.2, 0.4, 0.6, 0.8 and 1.0. XRD, resistivity and magnetization measurements are also presented. It has been found that the thermoelectric power is positive for x = 0.4 and is negative for x = 0.6 over the entire temperature range studied up to 300 K. The thermoelectric power of x = 0.4 samples vanishes discontinuously below a certain temperature, implying existence of superconductivity. In general, the magnitude of the thermoelectric power increases with temperature up to a certain temperature, and then it starts to decrease towards zero base line. In order to explain the observed behavior of the thermoelectric power, we have used a model in which both diffusion and phonon drag processes are combined by using a phenomenological interpolation between the low and high temperature behaviors of the thermoelectric power. The considered model provides an excellent fit to the observed data. It is further found that Al doping enhances the Debye temperature.Comment: 19 pages Text + Figs. suggestions/comments([email protected]

Superconductivity in SmFe1-xCoxAsO (x = 0.0 to 0.30)

We report synthesis, structural details and magnetization of SmFe1-xCoxAsO with x ranging from 0.0 to 0.30. It is found that Co substitutes fully at Fe site in SmFeAsO in an iso-structural lattice with slightly compressed cell. The parent compound exhibited known spin density wave (SDW) character below at around 140 K. Successive doping of Co at Fe site suppressed the SDW transition for x = 0.05 and later induced superconductivity for x = 0.10, 0.15 and 0.20 respectively at 14, 15.5 and 9K. The lower critical field as seen from magnetization measurements is below 200Oe. The appearance of bulk superconductivity is established by wide open isothermal magnetization M(H) loops. Superconductivity is not observed for higher content of Co i.e. x = 0.30. Clearly the Co substitution at Fe site in SmFe1-xCoxAsO diminishes the Fe SDW character, introduces bulk superconductivity for x between 0.10 and 0.20 and finally becomes non-superconducting for x above 0.20. The Fe2+ site Co3+ substitution injects mobile electrons to the system and superconductivity appears, however direct substitution introduces simultaneous disorder in superconducting FeAs layer and thus superconductivity disappears for higher content of Co.Comment: 14 Pages Text + Figs comments ([email protected]

Synthesis and Physical Properties of FeSe1/2Te1/2 Superconductor

One of the most important properties of very recently reported FeSe based superconductors is the robustness of their superconductivity under applied magnetic field. The synthesis and control of superconductivity in FeSe based compounds is rather a difficult task. Synthesis and physical property characterization for optimized superconductivity of FeSe1/2Te1/2 at 13 K is reported here. The compound crystallized in a tetragonal structure with lattice parameters a = 3.8008(10) and c = 6.0187 (15) A. Magnetization measurements indicated bulk superconductivity with lower critical field (Hc1) of around 180 Oe. By applying Ginzburg Landau (GL) theory, the Hc2(0) value is estimated to be = 1840 kOe for the 90% of resistive transition. A heat capacity measurement revealed bulk superconductivity by a hump at Tc near 13 K, and an expected decrease was observed under an applied magnetic field.Comment: 13 pages text + Figs: commenta ([email protected]

Role of Carbon in Enhancing the Performance of MgB2 superconductor

The enhancement of the critical current density (Jc(H)) of carbon and nano-SiC doped MgB2 is presented and compared. The upper critical field (Hc2) being determined from resistivity under magnetic field experiments is though improved for both C substitution and nano-SiC addition the same is more pronounced for the former. In MgB2-xCx carbon is substituted for boron that induces disorder in the boron network and acts as internal pinning centres. The optimal Jc(H) values are obtained for x = 0.1 sample . In case of nano-SiC doped in MgB2, the Jc(H) improves more profoundly and two simultaneous mechanisms seems responsible to this enhancement. Highly reactive nano-SiC releases free carbon atom, which gets easily incorporated into the MgB2 lattice to act as intrinsic pinning centres. Further enhancement is observed for higher nano-SiC concentrations, where the un-reacted components serve as additional extrinsic pinning centres.Comment: 17 Pages text + Fig