Abstract

X-ray and neutron diffraction studies as well as magnetization and electrical resistivity measurementsof Er1−xYxCo3 compounds were performed. In the Er-rich compounds, , a temperature-induced metamagnetic transition takes place between weak and strongCo magnetic states. In the intermediate concentration region, , below 40 K a spin reorientation was observed. The magnetic structure below the spin-reorientationtransition is non-collinear. The Er moments on the ‘cubic’ sites (6c) are tilted from thec-axis by anangle of about 55°, while those on the uniaxial 3a positions compose a smaller angle, of about15°.The spin-reorientation transition is accompanied by a large orthorhombic distortion of the hexagonalPuNi3-type crystal structure, which is accounted for by a large anisotropic magnetostriction ofthe Er sublattice. The distortion parameter varies linearly with x. Itsextrapolated value for ErCo3 is about 2 × 10−3. The concentration dependence of both types of magnetic instabilitiesis depicted in a magnetic phase diagram of the pseudobinaryEr1−xYxCo3 system for the low-temperature region.

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