Induced effects of Zn+2 on the transport and complex impedance properties of Gadolinium substituted nickel-zinc nano ferrites

•Gd substituted Ni-Zn nanoferrites were synthesized via Low-temperature citrate precursor method.•Rietveld refinement suggests the formation of a good nanocrystalline phase in the samples.•Maximum dielectric constant with a minimum dielectric loss obtained for x = 0.4 and y = 0.1.•With the increase...

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Veröffentlicht in:Journal of magnetism and magnetic materials 2019-05, Vol.478, p.12-19
Hauptverfasser: Santhosh Kumar, M.V., Shankarmurthy, G.J., Melagiriyappa, E., Nagaraja, K.K., Jayanna, H.S., Telenkov, M.P.
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Sprache:eng
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Zusammenfassung:•Gd substituted Ni-Zn nanoferrites were synthesized via Low-temperature citrate precursor method.•Rietveld refinement suggests the formation of a good nanocrystalline phase in the samples.•Maximum dielectric constant with a minimum dielectric loss obtained for x = 0.4 and y = 0.1.•With the increase in the Zn+2 concentration, a reduction in the Curie temperature is observed. We report on the preparation and transport properties of Gadolinium substituted Ni(1-x)ZnxGdyFe(2-y)O4 (0⩽x⩽1,y=0.1) nano particles using low temperature citrate precursor combustion method. The Rietveld refinement of PXRD data suggests the crystal structure of sample belongs to Fd-3m space group with an octahedral occupation of Gd+3 ions. FESEM micrographs show the existence of porosity in the samples. The dielectric studies reveal the good dielectric behaviour with high dielectric constant in Zn+2 substituted sample (x = 0.4). An increase in a.c conductivity observed in the Zn+2 substituted sample due to the hopping mechanism. The impedance spectroscopy of the samples shows the existence of high grain boundary resistance and an alternate switching of dielectric relaxation from non-Debye to Debye type. The activation energies and Curie temperature estimated using D. C. conductivity measurements drop linearly with an increase in Zn+2 concentration. We attribute the observed transport properties mainly to the hopping of Fe+2 ↔ Fe+3 ions.
ISSN:0304-8853
1873-4766
DOI:10.1016/j.jmmm.2019.01.058