Published August 15, 2011 | Version v1
Journal article

Synthesis and characterization of Bi2Fe4O9 powders

  • 1. Institute of Optoelectronic Science and Engineering, Huazhong University of Science and Technology, Luoyu Road 1037, Wuhan, Hubei 430074 (China)
  • 2. Department of Physics, Wuhan University, Wuhan, Hubei, 430072 (China)

Description

Highlights: → Ethylenediaminetetraacetic (EDTA) acid route was used for the synthesis of Bi2Fe4O9. → The single-phase Bi2Fe4O9 was synthesized successfully at 700 deg. C for 2 h. → Bi2Fe4O9 powders show weak ferromagnetism at room temperature. → Bi2Fe4O9 ceramics show lower leakage current. - Abstract: Bi2Fe4O9 have been successfully prepared using ethylenediaminetetraacetic (EDTA) acid as a chelating agent and ethylene glycol as an esterification agent. Heating of a mixed solution of EDTA, ethylene glycol, and nitrates of iron and bismuth at 140 deg. C produced a transparent polymeric resin without any precipitation, which after pyrolysis at 250 deg. C was converted to a powder precursor for Bi2Fe4O9. The precursors were heated at 400-800 deg. C in air to obtain Bi2Fe4O9 powder and differential scanning calorimetry (DSC), thermogravimetric (TG), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) techniques were used to characterize the precursors and the derived oxide powders. XRD analysis showed that well-crystallized and single-phase Bi2Fe4O9 with orthorhombic symmetry was obtained at 700 deg. C for 2 h and BiFeO3 and Fe2O3/FeCO3 were intermediate phases before the formation of Bi2Fe4O9. Bi2Fe4O9 powders show weak ferromagnetism at room temperature.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2011.03.011

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2011.03.011;
PII
S0254-0584(11)00188-X;

Publishing Information

Journal Title
Materials Chemistry and Physics
Journal Volume
128
Journal Issue
3
Journal Page Range
p. 388-391
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.