Microstructural, thermal, electrical and magnetic analysis of Mg2+ substituted Cobalt ferrite
Magnetic nanoparticles of Co 1– x Mg x Fe 2 O 4 ( x = 0, 0.08, 0.16, and 0.24) were prepared using sol–gel technique with auto-combustion. Citric acid was used as a chelating agent. The X-ray diffraction (XRD) studies showed that the lattice constant of cobalt ferrite decreases with the rise of mag...
Saved in:
Published in: | Applied physics. A, Materials science & processing Vol. 126; no. 11 |
---|---|
Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Berlin/Heidelberg
Springer Berlin Heidelberg
2020
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Magnetic nanoparticles of Co
1–
x
Mg
x
Fe
2
O
4
(
x
= 0, 0.08, 0.16, and 0.24) were prepared using sol–gel technique with auto-combustion. Citric acid was used as a chelating agent. The X-ray diffraction (XRD) studies showed that the lattice constant of cobalt ferrite decreases with the rise of magnesium proportion. Field-effect Scanning Electron Microscopy (FESEM) was used for the morphological study of the powdered ferrites. Energy Dispersive Spectroscopy (EDS) gave the compositional analysis of the samples. Two major vibrational frequencies from the Fourier Transform Infrared (FT-IR) Spectroscopy validate the spinel cubic ferrite structure. Raman spectroscopy exposes a doublet-like peak behaviour in A
1
g
and E
g
modes as a result of different ionic radius of ions belonging to Mg/Co and Fe. The magnetic parameters like saturation magnetization, coercivity, and remanent were also thoroughly analysed against the increase in the Mg-density in cobalt ferrite. The DC electrical resistivity is found to increase with Mg concentration. The room temperature, electrical and dielectric properties were investigated in the frequency range between 100 and 5 MHz. The observed results were related to the microstructural characteristic and amount of Mg dopants. |
---|---|
ISSN: | 0947-8396 1432-0630 |
DOI: | 10.1007/s00339-020-04048-6 |