Published September 3, 2010 | Version v1
Journal article

Impact of Pr-Ni substitution on the electrical and magnetic properties of chemically derived nanosized strontium-barium hexaferrites

  • 1. Surface and Solid State Chemistry Laboratory, Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan)

Description

This work is part of our comprehensive study on the synthesis and characterization of Sr0.5Ba0.5-xPrxFe12-yNiyO19 (0.00 ≤ x ≥ 0.10, 0.00 ≤ y ≥ 1.00) hexaferrite nanomaterials and, to the best of our knowledge, is the first of its kind in this area of research. The results of the study reveal that this material may have potential applications in the area of magnetic and high-frequency devices, particularly those requiring high electrical resistivity to reduce eddy current losses. Solid state studies using X-ray diffraction show characteristic peaks of the magnetoplumbite structure for these compounds. Electrical and magnetic properties of the co-precipitated ferrites were investigated using state-of-the-art techniques. Values of saturation magnetization and remanence are found to increase in the ranges of 66-78 and 43-48 emu/g, respectively, whereas coercivity is inversely related to Pr-Ni content. AC-magnetic susceptibility investigations show a sharp ferri- to paramagnetic transition in the temperature range of 500-672 K. DC-electrical resistivity shows a maxima for the nominal composition: Sr0.5Ba0.44Pr0.06Fe11.4Ni0.6O19. The electrical properties of the synthesized materials are discussed in terms of charge-transport via electron-hopping mechanism between Fe3+/Fe2+ ions at the octahedral site.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2010.06.073

Additional details

Identifiers

DOI
10.1016/j.jallcom.2010.06.073;
PII
S0925-8388(10)01526-4;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
505
Journal Issue
2
Journal Page Range
p. 560-567
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.