Published February 1, 2017 | Version v1
Journal article

Effect of sintering temperature on the structural, dielectric and magnetic properties of Ni0.4Zn0.2Mn0.4Fe2O4 potential for radar absorbing

  • 1. Department of Physics, National Taiwan Normal University, Taipei 11677, Taiwan (China)
  • 2. Department of Physics, Osmania University, Saifabad, Hyderabad 500004 (India)
  • 3. Department of Physics, Presidency University, Dibbur, Itgalpur, Bangalore 560089 (India)
  • 4. Department of Physics, Bangalore University, Bangalore 560056 (India)

Description

Ni0.4Zn0.2Mn0.4Fe2O4 nanopowders were prepared by sol-gel auto-combustion method, densified at different temperatures 400–700 °C/4 h using conventional sintering method. The grain sizes of all the samples vary between 18 nm and 30 nm. The hysteresis loops show high saturation magnetization and low coercivity, indicating magnetically soft behaviour of the material. The real and imaginary parts of permittivity is almost constant upto 1 GHz and increases with further increase of frequency. The permeability is ruled by Snoek's law, the values of μ′ increases with increase of temperature and the resonance frequency increases with an increase of temperature. The reflection coefficient is however increasing with sintering temperature and the maximum loss is observed in the range of 100 MHz–1 GHz. Sample sintered at 700 °C has shown maximum reflection loss and this loss occurs due to absorption, destructive interference and multiple internal reflections in the sample. Quality factor is constant upto 380 MHz and increases with frequency for all the samples sintered at different temperatures. The TC for all the samples is above ~230 °C. The room temperature EPR spectra confirm the oxidation state of Fe3+. The g-factor is in the range of ~2. - Highlights: • The highest reflection loss of –46 dB is achieved by 700 °C sample. • Quality factor is constant upto 380 MHz for all the samples. • The Curie temperature (TC) for all the samples is above ~230 °C. • The room temperature EPR spectra confirm the oxidation state of Fe3+.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jmmm.2016.09.129

Additional details

Identifiers

DOI
10.1016/j.jmmm.2016.09.129;
PII
S0304-8853(16)31631-6;

Publishing Information

Journal Title
Journal of Magnetism and Magnetic Materials
Journal Volume
423
Journal Page Range
p. 343-352
ISSN
0304-8853
CODEN
JMMMDC

Optional Information

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