Crystal structure, phase transition, and magnetic ordering in perovskitelike Pb2xBaxFe2O5 solid solutions

Ivan V. Nikolaev, Hans D’Hondt, Artem M. Abakumov, Joke Hadermann, Anatoly M. Balagurov, Ivan A. Bobrikov, Denis V. Sheptyakov, Vladimir Yu. Pomjakushin, Konstantin V. Pokholok, Dmitry S. Filimonov, Gustaaf Van Tendeloo, and Evgeny V. Antipov
Phys. Rev. B 78, 024426 – Published 23 July 2008

Abstract

The crystal and magnetic structures of the x1 member of the Pb2xBaxFe2O5 solid solution series have been studied using x-ray and neutron powder diffraction, electron diffraction, high-resolution electron microscopy, and Mössbauer spectroscopy. Pb1.08Ba0.92Fe2O5 has two polymorphic forms with the orthorhombic unit cell with a2ap, bap, and c42ap (ap—the parameter of the perovskite subcell) with the Pnma space group of the low-temperature (LT) phase and the Imma space group of the high-temperature (HT) phase, which are related by a phase transition at Tc540K. The crystal structures of both polymorphs were refined from neutron powder-diffraction data at T=14K and T=700K. The structure consists of parallel perovskite blocks with the thickness of two FeO6 octahedra linked together by infinite chains of edge-sharing distorted FeO5 trigonal bipyramids with two columns of the Pb cations in between characterized by the asymmetric coordination environment due to localized 6s2 lone electron pair. Two mirror-related configurations of the trigonal bipyramidal chains are ordered in the LT structure; their arrangement becomes disordered in the HT structure. Below TN=625K, Pb1.08Ba0.92Fe2O5 transforms into an antiferromagnetically ordered state. The antiferromagnetic (AFM) structure with a propagation vector k=[0,12,12] is characterized by an antiparallel spin alignment for all nearest-neighbor Fe atoms in the perovskite blocks, which stack on to each other at the trigonal bipyramidal chains, resulting in alternating antiparallel and parallel arrangement of spins on going along the common edge of the FeO5 trigonal bipyramids. An unusual spin flipping dynamic behavior was revealed by Mössbauer spectroscopy and related to a specific character of superexchange interactions inside the chains of the FeO5 trigonal bipyramids.

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  • Received 4 April 2008

DOI:https://doi.org/10.1103/PhysRevB.78.024426

©2008 American Physical Society

Authors & Affiliations

Ivan V. Nikolaev1, Hans D’Hondt2, Artem M. Abakumov1,*, Joke Hadermann2, Anatoly M. Balagurov3, Ivan A. Bobrikov3, Denis V. Sheptyakov4, Vladimir Yu. Pomjakushin4, Konstantin V. Pokholok1, Dmitry S. Filimonov1, Gustaaf Van Tendeloo2, and Evgeny V. Antipov1

  • 1Department of Chemistry, Moscow State University, 119991 Moscow, Russia
  • 2EMAT, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium
  • 3Frank Laboratory of Neutron Physics, Joint Institute for Nuclear Research, 141980 Dubna, Russia
  • 4Laboratory for Neutron Scattering, ETH Zurich and Paul Scherrer Institut (PSI), CH-5232 Villigen, Switzerland

  • *Corresponding author.

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Vol. 78, Iss. 2 — 1 July 2008

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