Evolution of complex magnetic phases and metal-insulator transition through Nb substitution in La0.5Sr0.5Co1-xNbxO3

Abstract

We report the evolution of structural, magnetic, transport, and electronic properties of bulk polycrystalline La0.5Sr0.5Co1-xNbxO3 (x = 0.025--0.25) samples. The Rietveld refinement of the x-ray diffraction patterns with R3c space group reveals that the lattice parameters and rhombohedral distortion monotonously increase with the Nb5+(4d0) substitution (x). The magnetic susceptibility exhibits a decrease in the magnetic ordering temperature and net magnetization with x, which manifests that the Nb substitution dilutes the ferromagnetic (FM) double exchange interaction and enhances the antiferromagnetic (AFM) super-exchange interaction. Interestingly, for the x> 0.1 samples the FM order is completely suppressed and the emergence of a glassy state is clearly evident. Moreover, the decrease in the coercivity (HC) and remanence (Mr) with x in the magnetic isotherms measured at 5~K further confirms the dominance of AFM interactions and reduction of FM volume fraction for the x> 0.1 samples. More interestingly, we observe resistivity minima for the x= 0.025 and 0.05 samples, which are analyzed using the quantum corrections in the conductivity, and found that the weak localization effect dominates over the renormalized electron-electron interactions in the 3D limit. Further, a semiconducting resistivity behavior is obtained for x> 0.05, which follows the Arrhenius law at high temperatures (160--320~K), and the 3D-variable range hopping prevails in the low-temperature region (<160~K). The core-level photoemission spectra confirm the valence state of constituent elements and the absence of Co2+ is discernible.

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