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

Title: Electron-doping through La{sup III}-for-Sr{sup II} substitution in (Sr{sub 1-} {sub x} La {sub x} ){sub 2}FeTaO{sub 6}: Effects on the valences and ordering of the B-site cations, Fe and Ta

Journal Article · · Journal of Solid State Chemistry
 [1];  [2];  [2];  [3];  [1];  [1]
  1. Materials and Structures Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8503 (Japan)
  2. Department of Chemistry and Center for Nano Storage Research, National Taiwan University, Taipei, (China)
  3. National Synchrotron Radiation Research Center, Hsinchu, (China)

We have employed aliovalent A-site cation substitution, La{sup III}-for-Sr{sup II}, to dope the Sr(Fe{sub 0.5}Ta{sub 0.5})O{sub 3} perovskite oxide with electrons. Essentially single-phase samples of (Sr{sub 1-} {sub x} La {sub x} )(Fe{sub 0.5}Ta{sub 0.5})O{sub 3} were successfully synthesized up to x{approx}0.3 in a vacuum furnace at 1400 deg. C. The samples were found to crystallize (rather than with orthorhombic symmetry) in monoclinic space group P2{sub 1}/n that accounts for the partial ordering of the B-site cations, Fe and Ta. With increasing La-substitution level, x, the degree of Fe/Ta order was found to increase such that the La-richest compositions are best described by the B-site ordered double-perovskite formula (Sr,La){sub 2}FeTaO{sub 6}. From Fe L {sub 3} and Ta L {sub 3} XANES spectra it was revealed that upon electron doping the two B-site cations, Fe{sup III} and Ta{sup V}, are both prone to reduction. Magnetic susceptibility measurements showed spin-glass type behaviour for all the samples with a transition temperature slightly increasing with increasing x. -- Graphical abstract: Valence states of Fe and Ta are controlled in the partially ordered perovskite oxide (Sr,La){sub 2}FeTaO{sub 6}, through aliovalent La{sup III}-for-Sr{sup II} substitu0010ti.

OSTI ID:
20784838
Journal Information:
Journal of Solid State Chemistry, Vol. 179, Issue 1; Other Information: DOI: 10.1016/j.jssc.2005.10.004; PII: S0022-4596(05)00464-0; Copyright (c) 2005 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