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Register a new userThe effect of Fe and Ru substitution for Ni on the thermopower in MgCNi_3
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The intermetallic perovskite MgCNi3 is a superconductor with a Tc=7 K. Substitution of Fe and Ru for Ni decreases Tc monotonically as the doping concentration is increased. Here we report thermopower measurements, S(T), on MgCNi3, MgCNi3-xFex and MgCNi3-xRux. For MgCNi3, the thermopower is negative, - 12.5 mikroV/K, at 300 K. The absolute value of S decreases as x increases in MgCNi3-xFex and MgCNi3-xRux. The sign of S changes from negative to positive at low temperatures for values of x > 0.01. These data show that the carriers in MgCNi3 are electrons, and by increasing x and decreasing temperature, the participation of hole carriers clearly increases. The influence of the magnetic moments of the Fe atoms on the thermopower is not visible.
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We report the superconductivity at enhanced temperature of 5.2 K in the polycrystalline sample of ZrTe3 and Ni intercalated ZrTe3. ZrTe3 is a Charge Density Wave (T = 63K) compound, which is known to superconduct only below 2K in single crystalline form. We discuss that the intergrain strains in the polycrystalline samples induces an intrinsic pressure and thus enhances the transition temperature. Fe intercalation of ZrTe3 kills both the charge density wave and superconducting states, gives rise to the magnetic ordering in the compound.
The antiferromagnetic order and structural distortion in the LaFe(As1-xSbx)O system have been investigated by powder neutron diffraction and physical properties measurements. Polycrystalline samples of LaFe(As1-xSbx)O (x<0.5) were prepared using solid state synthesis at ambient and high pressure. We find that the isoelectronic substitution of Sb for As decreases the structural and magnetic transition temperatures but, contrary to the effects of phosphorus substitution, superconductivity is not induced. Instead a slight increase in the Fe magnetic moment is observed.
We report the effect of Ni doping on superconductivity of FeSe0.5Te0.5. The single crystal samples of series Fe1-xNixSe0.5Te0.5 (x=0.0, 0.01, 0.03, 0.05, 0.07, 0.10 and 0.20) are synthesized via vacuum shield solid state reaction route and high temperature heating followed by slow cooling. All the crystals of Fe1-xNixSe0.5Te0.5 series with x up to 0.20, i.e., 20% substitution of Ni at Fe site are crystallized in single phase tetragonal structure with space group P4/nmm. The electrical resistivity measurements revealed that Tc decreases fast with increase of Ni concentration in Fe1-xNixSe0.5Te0.5. Namely the superconducting transition temperature (Tc) being defined as resistivity =0 decrease from 12K to around 4K and 2K for x=0.01 and 0.03 samples respectively. For x=0.05 (5at% Ni at Fe site) though Tconset is observed in resistivity measurements but r{ho}=0 is not seen down to 2K. For x more than 0.07, neither the Tconset nor Tcr{ho}=0 is seen down 2K in R-T measurements. It is demonstrated that Ni doping at Fe site in FeSe0.5Te0.5 superconductor suppresses superconductivity fast. The rate of Tc depression is albeit non monotonic. Summarily, a systematic study on suppression of superconductivity with Fe site Ni doping in flux free gown FeSe0.5Te0.5 single crystals is presented in the current communication.
The Fe K X-ray absorption near edge structure (XANES) of BaFe2-xCoxAs2 superconductors was investigated. No appreciable alteration in shape or energy position of this edge was observed with Co substitution. This result provides experimental support to previous ab initio calculations in which the extra Co electron is concentrated at the substitute site and do not change the electronic occupation of the Fe ions. Superconductivity may emerge due to bonding modifications induced by the substitute atom that weakens the spin-density-wave ground state by reducing the Fe local moments and/or increasing the elastic energy penalty of the accompanying orthorhombic distortion.
The ab-plane resistivity of Ba(Fe1-xRux)2As2 (x = 0.00, 0.09, 0.16, 0.21, and 0.28) was studied under nearly hydrostatic pressures, up to 7.4 GPa, in order to explore the T-P phase diagram and to compare the combined effects of iso-electronic Ru substitution and pressure. The parent compound BaFe2As2 exhibits a structural/magnetic phase transition near 134 K. At ambient pressure, progressively increasing Ru concentration suppresses this phase transition to lower temperatures at the approximate rate of ~5 K/% Ru and is correlated with the emergence of superconductivity. By applying pressure to this system, a similar behavior is seen for each concentration: the structural/magnetic phase transition is further suppressed and superconductivity induced and ultimately, for larger x Ru and P, suppressed. A detailed comparison of the T-P phase diagrams for all Ru concentrations shows that 3 GPa of pressure is roughly equivalent to 10% Ru substitution. Furthermore, due to the sensitivity of Ba(Fe1-xRux)2As2 to pressure conditions, the melting of the liquid media, 4 : 6 light mineral oil : n-pentane and 1 : 1 iso-pentane : n-pentane, used in this study could be readily seen in the resistivity measurements. This feature was used to determine the freezing curves for these media and infer their room temperature, hydrostatic limits: 3.5 and 6.5 GPa, respectively.
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