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Register a new userAnnealing, acid, and alcoholic beverage effects on Fe1+yTe0.6Se0.4
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We have systematically investigated and compared different methods to induce superconductivity in iron chalcogenide Fe1+yTe0.6Se0.4 including annealing in vacuum, N2, O2, I2 atmosphere, and immersing samples into acid and alcoholic beverages. Vacuum and N2 annealing are proved to be ineffective to induce superconductivity in Fe1+yTe0.6Se0.4 single crystal. O2 and I2 annealing, acid and alcoholic beverages can induce superconductivity by oxidizing the excess Fe in the sample. Superconductivity in O2 annealed sample is in bulk nature, while I2, acid and alcoholic beverages can only induce superconductivity near the surface. By comparing different effects of O2, I2, acid and alcoholic beverages, we propose a scenario to explain how the superconductivity is induced in the non-superconducting as-grown Fe1+yTe0.6Se0.4.
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Effects of iodine annealing to induce bulk superconductivity in Fe1+yTe0.6Se0.4 have been systematically studied by changing the molar ratio of iodine to the sample and annealing temperature. The optimal condition to induce bulk superconductivity with Tc ~14.5 K and self-field Jc(2 K) ~ 5x10^5 A/cm2 is found to be a molar ratio of iodine of 5-7 % at the annealing temperature of 400 C. Furthermore, the fact that no compounds containing iodine are detected in the crystal and a significant amount of FeTe2 is produced after the iodine annealing strongly indicate that the excess iron is consumed to form FeTe2 and iodine works as a catalyst in this process.
Superconductivity in anti-PbO-type iron chalcogenides Fe1-xTe1-ySey (x = 0, 0.1, y = 0.1 0.4) depends on the amount (x) of interstitial iron atoms located between the FeTe1-ySey layers. Non-superconducting samples of nominal Fe1.1Te1-ySey convert to superconductors with critical temperatures up to 14 K after annealing at 300{deg}C in an oxygen atmosphere. The process is irreversible upon subsequent hydrogen annealing. Magnetic measurements are consistent with the formation of iron oxides suggesting that oxygen annealing preferably extracts interstitial iron from Fe1-xTe1-ySey which interfere with superconductivity.
Experimental evidences from transport, magnetic, and magneto-optical (MO) image measurements confirmed that arsenic (As) vapor annealing was another effective way to induce bulk superconductivity with isotropic, large, and homogenous superconducting critical current density (Jc) in Fe1+yTe0.6Se0.4 single crystal. Since As is an exotic and easily detectable heavy element to Fe1+yTe0.6Se0.4 single crystal, As vapor annealing is very advantageous for the study of annealing mechanism. Detailed micro-structural and elemental analyses exclude the possibility that intercalating or doping effect may happen in the other post-annealing methods, proving that Fe reacts with As on the surface of the crystal and the reaction itself acts as a driving force to drag excess Fe out. The removal of excess Fe results in the good superconductivity performance.
We have investigated uniaxial and hydrostatic pressure effects on superconductivity in Fe1.07Te0.88S0.12 through magnetic-susceptibility measurements down to 1.8 K. The superconducting transition temperature Tc is enhanced by out-of-plane pressure (uniaxial pressure along the c-axis); the onset temperature of the superconductivity reaches 11.8 K at 0.4 GPa. In contrast, Tc is reduced by in-plane pressure (uniaxial pressure along the ab-plane) and hydrostatic pressure. Taking into account these results, it is inferred that the superconductivity of Fe1+yTe1-xSx is enhanced when the lattice constant c considerably shrinks. This implies that the relationship between Tc and the anion height for Fe1+yTe1-xSx is similar to that applicable to most iron-based superconductors. We consider the reduction of Tc by hydrostatic pressure due to suppression of spin fluctuations because the system moves away from antiferromagnetic ordering, and the enhancement of Tc by out-of-plane pressure due to the anion height effect on Tc.
We report the temperature dependence of the resistivity and thermoelectric power under hydrostatic pressure of the itinerant antiferromagnet BaFe2As2 and the electron-doped superconductor Ba(Fe0.9Co0.1)2As2. We observe a hole-like contribution to the thermopower below the structural-magnetic transition in the parent compound that is suppressed in magnitude and temperature with pressure. Pressure increases the contribution of electrons to transport in both the doped and undoped compound. In the 10% Co-doped sample, we used a two-band model for thermopower to estimate the carrier concentrations and determine the effect of pressure on the band structure.
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