Abstract

Polycrystalline samples, FeSe1-xTex (x = 0.1, 0.4, 0.5, 0.6, 0.9), have been synthesized by the solid state reaction method and studied by means of X-ray diffraction, magnetization measurements and Seebeck measurements. As Te concentration increases, crystal structures change from FeSe-type to FeTe-type tetragonal structures. The optimal superconducting transition temperature (Tc) has been observed in the x = 0.5 and 0.6 samples. All the compounds exhibit an antiferromagnetic transition near ∼125 K. Compound with x = 0.5 shows the maximum value (absolute) in Seebeck coefficient as compared to others. Fermi temperature of all the compounds varies with Te substitution and found to be the lowest for the sample with the highest Tc. The ratio of Tc/TF indicates strong electronics correlations for the samples with optimal superconducting transitions pointing towards unconventional superconductivity.Polycrystalline samples, FeSe1-xTex (x = 0.1, 0.4, 0.5, 0.6, 0.9), have been synthesized by the solid state reaction method and studied by means of X-ray diffraction, magnetization measurements and Seebeck measurements. As Te concentration increases, crystal structures change from FeSe-type to FeTe-type tetragonal structures. The optimal superconducting transition temperature (Tc) has been observed in the x = 0.5 and 0.6 samples. All the compounds exhibit an antiferromagnetic transition near ∼125 K. Compound with x = 0.5 shows the maximum value (absolute) in Seebeck coefficient as compared to others. Fermi temperature of all the compounds varies with Te substitution and found to be the lowest for the sample with the highest Tc. The ratio of Tc/TF indicates strong electronics correlations for the samples with optimal superconducting transitions pointing towards unconventional superconductivity.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.