Abstract

Bulk samples of Co1−xNixFe2O4 (x = 0.0, 0.2, 0.4, 0.6, 0.8 1.0) were shaped by a spark plasma sintering (SPS) process. The initial ferrite nano-powders which were prepared using a co-precipitation method were characterized by high-resolution transmission electron microscopy (HRTEM) and Mössbauer spectroscopy. The HRTEM showed nanoparticles with almost 5–35 nm average size. Mössbauer spectrometer is employed to study the magnetic properties of ferrite nano-powders at room temperature. X-ray diffractometer (XRD), field emission scanning electron microscopy (FESEM) coupled with EDS detector for the chemical composition analysis and vibration sample magnetometer (VSM) equipped with FORC software were used to characterize the bulk samples. Without any structural changes to powder samples, a single-phase spinel structure was obtained. In the FE-SEM micrograph, the porosity decrease and consequently the density increase are clearly visible and the EDS study confirms the presence of Fe, Co, Ni and O ions in the fabricated samples by SPS process. The magnetic parameters such as saturation magnetization and the coercivity showed a decreasing behavior with an increase in Ni concentration from 67 emu/g and 787 Oe to 42.77 emu/g and 151 Oe, respectively. FORC analysis implies the coercivity reduction of bulk samples comparing with powders state in cobalt-rich ferrites is due to the multi-domain formation. The coercivity unavoidable in nickel-rich ferrites is due to the occurrence of the multi-domain state along with the disappearance of the superparamagnetic phase.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.