Verwey transition in mixed-valence TbBaFe2O5: Two attempts to order charges

Pavel Karen, Patrick M. Woodward, Johan Lindén, Tom Vogt, Andrew Studer, and Peter Fischer
Phys. Rev. B 64, 214405 – Published 1 November 2001
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Abstract

Electronic, magnetic, and structural phase transitions in nearly stoichiometric TbBaFe2O5+w(0.00<w<0.05) have been investigated. At high temperatures this compound is a paramagnetic, mixed-valence (Fe2.5+) conductor with identical square-pyramidal coordinations at all iron atoms. Upon cooling below TN=450K, an antiferromagnetic (AFM) spin order appears, accompanied by a magnetostrictive orthorhombic distortion. At lower temperatures the increasing distortion sets the frame for a first attempt to order charges. Mössbauer spectroscopy shows that one squeezed and one expanded square pyramid appear with different orientations of their magnetic and electric field tensors, each centered by its own mixed-valence iron state, one Fe2.5+ε, the other Fe2.5ε. The lattice retains its distortion, but a small, structurally homogeneous, and continuous increase in volume is experienced. At somewhat lower temperature (TV) a discontinuous increase of the orthorhombic distortion occurs, marking the second attempt to order charges, now with the classical symptoms of the Verwey transition: a large change in volume, entropy, and electrical conductivity. Below TV, a normal Fe3+ high-spin state in a symmetrical square-pyramidal coordination appears, whereas Fe2+ is distorted. The long-range order of this arrangement is solved from high-resolution powder neutron diffraction data. Rietveld refinements show that the charge-ordered spins have AFM interactions in all three directions (G type) whereas in the mixed-valence state a ferromagnetic (FM) interaction appears between the iron atoms facing each other across the Tb layer. This FM interaction is suggested to be essential for the appearance of the mixed-valence state via the double-exchange sharing of the Fe2+-originated electron. This also allows for the total ordered spin moment being unchanged at the Verwey transition, following one single Brillouin curve. Analogous cases are pointed out where the Verwey transition proceeds in a similar manner, also at the molecular level.

  • Received 24 June 2001

DOI:https://doi.org/10.1103/PhysRevB.64.214405

©2001 American Physical Society

Authors & Affiliations

Pavel Karen

  • Department of Chemistry, University of Oslo, Blindern, N-0315 Oslo, Norway

Patrick M. Woodward

  • Department of Chemistry, Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210-1185

Johan Lindén

  • Department of Physics, Åbo Akademi, FIN-20500 Turku, Finland

Tom Vogt

  • Physics Department, Brookhaven National Laboratory, Upton, New York 11973-5000

Andrew Studer

  • Australian Nuclear Science & Technology Organization, Private Mail Bag 1, Menai, NSW 2234, Australia

Peter Fischer

  • Laboratory for Neutron Scattering, ETH Zurich & Paul Scherrer Institute, WHGA/133, CH-5232 Villigen, Switzerland

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Vol. 64, Iss. 21 — 1 December 2001

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