Coexisting magnetic structures and spin-reorientation in Er0.5Dy0.5FeO3: Bulk magnetization, neutron scattering, specific heat, and Ab-initio studies
Abstract
The complex magnetic structures, spin-reorientation and associated exchange interactions have been investigate in Er0.5Dy0.5FeO3 using bulk magnetization, neutron diffraction, specific heat measurements and density functional theory calculations. The Fe3+ spins order as G-type antiferromagnet structure depicted by 4(Gx,Ay,Fz) irreducible representation below 700K, similar to its end compounds. The bulk magnetization data indicate occurrence of the spin-reorientation and rare-earth magnetic ordering below 75 K and 10 K, respectively. The neutron diffraction studies confirm an "incomplete" 4→ 2(Fx,Cy,Gz) spin-reorientation initiated ≤75 K. Although, the relative volume fraction of the two magnetic structures varies with decreasing temperature, both co-exist even at 1.5 K. At 8 K, Er3+/Dy3+ moments order as cyR arrangement develop, which gradually increases in intensity with decreasing temperature. At 2 K, magnetic structure associated with czR arrangement of Er3+/Dy3+ moments also appears. At 1.5 K the magnetic structure of Fe3+ spins is represented by a combination of 2+4+1, while the rare earth moments coexists as cyR and czR corresponding to 2 and 1 representation, respectively. The observed Schottky anomaly at 2.5 K suggests that the "rare-earth ordering" is induced by polarization due to Fe3+ spins. The Er3+-Fe3+ and Er3+-Dy3+ exchange interactions, obtained from first principle calculations, primarily cause the complicated spin-reorientation and cyR rare-earth ordering, respectively, while the dipolar interactions between rare-earth moments, result in the czR type rare-earth ordering at 2 K.
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