skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Influence of iron addition on the oxygen-deficient Sr{sub 0.85}Bi{sub 0.15}Co{sub 1-x}Fe{sub x}O{sub 3-{delta}} (0.0{<=}x{<=}1.0) perovskites

Journal Article · · Journal of Solid State Chemistry
 [1]; ;  [2];  [3];  [4];  [1]
  1. Department of Environmental Inorganic Chemistry, Chalmers University of Technology, SE-412 96 Goeteborg (Sweden)
  2. Department of Structural Chemistry, Stockholm University, SE-106 91 Stockholm (Sweden)
  3. Department of Engineering sciences, Uppsala University, Box 534, SE-751 21 Uppsala (Sweden)
  4. Institut Laue-Langevin, BP 156, 38042 Grenoble Cedex 9 (France)

A series of oxygen-deficient Sr{sub 0.85}Bi{sub 0.15}Co{sub 1-x}Fe{sub x}O{sub 3-{delta}} (0.0{<=}x{<=}1.0) perovskite phases were prepared using solid-state reaction. Results of neutron powder diffraction analyses show that the introduction of Fe onto the B-site severely effects the long range coherence of the oxygen vacancy ordered, I4/mmm supercell, observed for the x=0.0 sample. For x=0.1 a smaller, a=b{approx}a{sub p}, c{approx}2a{sub p}, P4/mmm supercell gives the best agreement to the diffraction data, whilst phases in the range 0.2{<=}x{<=}0.6 adopt disordered cubic perovskite structures. Pseudo-cubic, a=b{approx}a{sub p}, c{approx}a{sub p}, structures are found for x{>=}0.8. Evidence of weak superstructures, reflecting local oxygen ordering, is also obtained from electron diffraction. For all oxygen-annealed phases the average structure reverts to cubic Pm3-bar m. The as-prepared samples show G-type antiferromagnetic order at room temperature. The oxygen annealed x=0.10, 0.25 and 1.0 samples display low-temperature spin-glass transitions. - Graphical abstract: Evolving crystal structures of the as-prepared Sr{sub 0.85}Bi{sub 0.15}Co{sub 1-x}Fe{sub x}O{sub 3-{delta}} perovskites as a function of iron content for the compositional range 0.1{<=}x{<=}1.0.

OSTI ID:
21128407
Journal Information:
Journal of Solid State Chemistry, Vol. 181, Issue 8; Other Information: DOI: 10.1016/j.jssc.2008.04.037; PII: S0022-4596(08)00221-1; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0022-4596
Country of Publication:
United States
Language:
English