Fabrication of Cu2+ substituted nanocrystalline Ni–Zn ferrite by solution combustion route: Investigations on structure, cation occupancy and magnetic behavior

► Synthesis of ferrite by solution combustion route. ► Characterization techniques XRD, SEM, magnetization. ► Structural properties. ► Cation distribution. ► Magnetic properties. The reactivity of Cu2+ ion concentration in Ni–Zn spinel matrix fabricated using solution combustion route has been inves...

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Bibliographic Details
Published inJournal of alloys and compounds Vol. 553; pp. 157 - 162
Main Authors Awati, V.V., Rathod, S.M., Shirsath, Sagar E., Mane, Maheshkumar L.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 15.03.2013
Elsevier
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Summary:► Synthesis of ferrite by solution combustion route. ► Characterization techniques XRD, SEM, magnetization. ► Structural properties. ► Cation distribution. ► Magnetic properties. The reactivity of Cu2+ ion concentration in Ni–Zn spinel matrix fabricated using solution combustion route has been investigated. The specimens of nanocrystalline Ni0.8−xCuxZn0.2Fe2O4 (x=0.0⩽0.6 with steps of 0.2) exhibits single phase cubic structure. The detailed studies regarding the physico-chemical stability, crystal structural stability, surface morphology and magnetic properties as a function of Cu2+ ion concentration were performed. The annealing treatment does not alter the crystal structure but increases the crystallinity of the samples. The cation occupancies of the prepared materials were estimated by using X-ray diffraction (XRD) data analysis. The morphological investigations of the samples were studied by using field emission scanning electron microscopy (FE-SEM) technique. The crystallographic analyses of all the compositions were systematically investigated by Fourier transform infrared spectroscopy (FTIR). The saturation magnetization (M–H plots) at room temperature with field 10kOe exhibits strong influence of Cu2+ ion content and annealing temperature.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2012.11.045