Oxygen stoichiometry in BaRE(Cu0.5Fe0.5)(2)O5+delta compounds with perovskite or double perovskite structure

Citation
K. Peitola et al., Oxygen stoichiometry in BaRE(Cu0.5Fe0.5)(2)O5+delta compounds with perovskite or double perovskite structure, J L TEMP PH, 117(3-4), 1999, pp. 861-865
Citations number
8
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
JOURNAL OF LOW TEMPERATURE PHYSICS
ISSN journal
00222291 → ACNP
Volume
117
Issue
3-4
Year of publication
1999
Pages
861 - 865
Database
ISI
SICI code
0022-2291(199911)117:3-4<861:OSIBCW>2.0.ZU;2-B
Abstract
The oxygen stoichiometry variation in the BaRE(Cu0.5Fe0.5)(2)O5+delta serie s is established with rare earth elements having ionic radii (CN = 8) in th e range of 0.977-1.160 Angstrom (Lu-La). The double-perovskite structure is stable with RE = Lu-Pr, while La prefers the simple-perovskite structure. In the double-perovskite structures with RE = Lu-Sm the oxygen content was found to be constant (delta approximate to 0) against normal-pressure oxida tive and reductive heat treatments, whereas a larger rare earth ion, i.e. N d or Pr, allows continuous oxygen content tuning within about 0.23 and 0.32 oxygen atoms, respectively. In the La perovskite the oxygen content could be varied from delta approximate to 0 to 0.45. The Fe-57 Mossbauer spectros copy measurements revealed that the transition temperature of magnetic orde ring decreased with an increase in the oxygen content for both the double- and simple-perovskite structures.