Abstract

$\mathrm{Gd}({\mathrm{Ba}}_{2\ensuremath{-}x}{\mathrm{Pr}}_{x}){\mathrm{Cu}}_{3}{\mathrm{O}}_{7+\ensuremath{\delta}}$ single phase polycrystalline samples with $0.0<~x<~1.0$ were investigated for their structural and electronic properties. Due to the solubility limit, the 123 structure forms in the $0.0<~x<~0.50$ range; for $x>~0.6,$ a decomposition of the perovskite-type phases occurs. For $x=0.2,$ there is an orthorhombic-tetragonal phase transition, concurrent with a metal-insulator transition, which is evident in the normal state resistivity. For ${x}_{c}=0.35,$ the superconductor-insulator transition occurs. An unusual hump has been observed on the resistivity vs temperature curve of the samples for particular values of Pr doping. Based on the Rietveld refinement of the x-ray diffraction patterns, and bond valence sum calculations, we have found that the Ba atom substitution at the rare earth site could lead to superconductivity in some parts of the grains at ${T}_{m}\ensuremath{\sim}80--90\mathrm{K},$ which appears as a hump on the $\ensuremath{\rho}(T)$ curve. Our result is in line with the previously proposed possibility of the existence of superconductivity in Pr-123 due to the Ba atom substituted at the Pr site. We have also concluded that with increasing Pr doping, O(4) atoms migrate from their sites, and the O(5) occupation increases. So, perovskite substructures with Pr at the rare earth or Ba site, become identical. Hence, Pr at the Ba or rare earth site suppresses the superconductivity by the same mechanism(s).

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.