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Title: Structure and magnetic properties of Ca{sub 2}Fe{sub 1-x}Mn{sub x}AlO{sub 5+{delta}}

Journal Article · · Journal of Solid State Chemistry
 [1]; ;  [2];  [3];  [4]
  1. CFMC-UL, Faculdade de Ciencias, Universidade de Lisboa, 1749-016 Lisboa (Portugal)
  2. Dep. Quimica, ITN/CFMC-UL, Estrada Nacional 10, P-2686-953 Sacavem (Portugal)
  3. Dep. de Engenharia Ceramica e do Vidro, CICECO, Universidade de Aveiro, 3810-193 Aveiro (Portugal)
  4. CFMC-UL/Dep. Fisica, Faculdade de Ciencias, Universidade de Lisboa, 1749-016 Lisboa (Portugal)

Ca{sub 2}Fe{sub 1-x}Mn{sub x}AlO{sub 5} (0{<=}x{<=}1) compounds were prepared by a self-combustion method under air (x=0, 0.1, 0.2 and 0.3) and nitrogen (x=0.5, 0.7 and 1.0). The samples prepared under nitrogen were successfully oxidized after short annealing under air. Both X-ray powder diffraction (XRD) Rietveld analysis and electron diffraction revealed that all compounds adopt the brownmillerite-type structure. All samples present an overall antiferromagnetic behaviour and data from magnetic measurements and Moessbauer spectroscopy allowed to conclude that the transition temperature decreases as Mn content increases for x{<=}0.3 and increases in the case of the x{>=}0.5 compounds. Except for x=1, chemical disorder due to the occupancy of both octahedral and tetrahedral sites by different metals as well as the competition between different moments' orientation induce a complex magnetic behaviour characterized by magnetic frustration and canted antiferromagnetism. Moessbauer spectroscopy and chemical titrations also allowed to conclude about the preferential oxidation of Mn{sup 3+} over Fe{sup 3+}, obtained by thermal treatment under air of the x=0.5 and 0.7 compositions. - Graphical abstract: Structure of the Ca{sub 2}Fe{sub 1-x}Mn{sub x}AlO{sub 5} compound and electron diffraction pattern obtained along the [1-bar 01] zone axis (x=0.2), showing a brownmillerite structure.

OSTI ID:
21128480
Journal Information:
Journal of Solid State Chemistry, Vol. 181, Issue 9; Other Information: DOI: 10.1016/j.jssc.2008.06.008; PII: S0022-4596(08)00308-3; 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