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Spin reorientation and disordered rare earth magnetism in Ho2FeCoO6

We report the experimental observation of spin reorientation in the double perovskite Ho2FeCoO6. The magnetic phase transitions in this compound are characterized and studied through magnetization and specific heat, and the magnetic structures are elucidated through neutron powder diffraction. Two m...

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Bibliographic Details
Published in:Journal of physics. Condensed matter 2017-11, Vol.29 (47), p.475804-475804
Main Authors: Haripriya, G R, Nair, Harikrishnan S, Pradheesh, R, Rayaprol, S, Siruguri, V, Singh, Durgesh, Venkatesh, R, Ganesan, V, Sethupathi, K, Sankaranarayanan, V
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Language:English
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Summary:We report the experimental observation of spin reorientation in the double perovskite Ho2FeCoO6. The magnetic phase transitions in this compound are characterized and studied through magnetization and specific heat, and the magnetic structures are elucidated through neutron powder diffraction. Two magnetic phase transitions are observed in this compound-one at TN1≈250 K, from paramagnetic to antiferromagnetic, and the other at TN2≈45 K, from a phase with mixed magnetic structures to a single phase through a spin reorientation process. The magnetic structure in the temperature range 200-45 K is a mixed phase of the irreducible representations Γ1 and Γ3, both of which are antiferromagnetic. The phase with mixed magnetic structures that exists in Ho2FeCoO6 gives rise to a large thermal hysteresis in magnetization that extends from 200 K down to the spin reorientation temperature. At TN2, the magnetic structure transforms to Γ1. Though long-range magnetic order is established in the transition metal lattice, it is seen that only short-range magnetic order prevails in the Ho3+ lattice. Our results should motivate further detailed studies on single crystals in order to explore the spin reorientation process, spin switching and the possibility of anisotropic magnetic interactions giving rise to electric polarization in Ho2FeCoO6.
ISSN:0953-8984
1361-648X
DOI:10.1088/1361-648X/aa919e