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Title: Magnetic dilution of the iron sublattice in CoFe{sub 2-x}Sc{sub x}O{sub 4} (0{<=}x{<=}1)

Journal Article · · Journal of Solid State Chemistry
 [1]; ;  [1];  [2];  [1]
  1. Institut de Physique et Chimie des Materiaux de Strasbourg, UMR 7504 (CNRS-Universite de Strasbourg), 23 rue du Loess, BP 43, 67034 Strasbourg (France)
  2. Laboratoire de Physique de l'Etat Condense, UMR 6087 (CNRS-Universite du Maine), Avenue Olivier Messiaen, 72085 Le Mans (France)

Substitution of Fe for Sc in CoFe{sub 2}O{sub 4} spinel structure is presented. All CoFe{sub 2-x}Sc{sub x}O{sub 4} compounds crystallize in the spinel type structure (space group Fd3-bar m). By using X-ray diffraction studies, magnetic measurements and in-field {sup 57}Fe Moessbauer spectrometry, the limit of substitution has been determined to be equal to x=0.56. An increase in the cell parameter and the strains and a decrease in the apparent crystallites size are observed. For x>0.3, a partial oxidation of cobalt is evidenced and Co{sup 3+} is stabilized in the structure. A ferromagnetic behavior has been observed for all investigated compounds. As x increases, the Curie temperature and the hyperfine fields decrease. Following the Stephenson model, the diminution of T{sub C} is ascribed to a decrease of the main J{sub AB} interaction. -- Graphical abstract: Evolution of the cell parameters, the magnetic properties and the Moessbauer spectra in CoFe{sub 2-r}Sc{sub r}O{sub 4} (0{<=}r{<=}1). Display Omitted

OSTI ID:
21494116
Journal Information:
Journal of Solid State Chemistry, Vol. 183, Issue 11; Other Information: DOI: 10.1016/j.jssc.2010.09.004; PII: S0022-4596(10)00387-7; Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0022-4596
Country of Publication:
United States
Language:
English

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