Published January 15, 2017 | Version v1
Journal article

Structural and magnetic investigations of CaBaCo4−xFexO7 solid solutions

  • 1. Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, Ekaterinburg GSP-145, 620990 (Russian Federation)
  • 2. Institute of Metal Physics, Ural Branch of the Russian Academy of Sciences, 620041 Ekaterinburg GSP-145, 620999 (Russian Federation)

Description

Solid solutions of CaBaCo4−xFexO7 (x=0, 0.05, 0.2, 1, 2) were synthesized by glycine-nitrate combustion process. Their structural and magnetic properties were characterized by means of x-ray diffraction and magnetization measurements. In the examined range of the solid solutions, their crystal lattice symmetry changes from orthorhombic with space group Pbn21 (03mc (x>0.5). The magnetic measurements revealed that even small doping (x=0.05) of the transition metal sublattice noticeably suppresses ferrimagnetism of the parent compound and induces an AF transition at 88 K. An increase in the doping concentration lowers the frustration parameter |θCW|/TC from 17.2 (for x=0.05) to 13.7 (for x=2) and strengthens the antiferromagnetic interactions, which manifests itself in the Curie–Weiss temperature (θCW) growth. The samples with x=0.05 and x=0.2 also show an additional magnetic transition at temperatures Tg (55 and 70 K respectively). The temperature irreversibility between the ZFC and FC magnetization curves may suggest the formation of a spin-glass state below that temperature. - Highlights: • CaBaCo4−xFexO7 solid solutions were synthesized by glycine-nitrate process. • At x=1 symmetry became hexagonal instead orthorhombic. • Fe-doping abruptly suppresses ferrimagnetism of CaBaCo4O7. • Increase of x is followed by enhancing of antiferromagnetic interactions.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jmmm.2016.08.062

Additional details

Identifiers

DOI
10.1016/j.jmmm.2016.08.062;
PII
S0304-8853(16)31891-1;

Publishing Information

Journal Title
Journal of Magnetism and Magnetic Materials
Journal Volume
422
Journal Page Range
p. 66-72
ISSN
0304-8853
CODEN
JMMMDC

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.