journal article·2017-05-01Open access

Thermal stability and magnetic properties of MgFe2O4@ZnO nanoparticles

S. Mallesh, D. Prabu, V. Srinivas

AIP Advances· Volume 7· Issue 5

Abstract

Magnesium ferrite, MgFe2O4, (MgFO) nanoparticles (NPs) have been synthesized through sol-gel process. Subsequently, as prepared particles were coated with Zinc-oxide (ZnO) layer(s) through ultrasonication process. Thermal stability, structure and magnetic properties of as-prepared (AP) and annealed samples in the temperature range of 350 °C-1200 °C have been investigated. Structural data suggests that AP MgFO NPs and samples annealed below 500 °C in air exhibit stable ferrite phase. However, α-Fe2O3 and a small fraction of MgO secondary phases appear along with ferrite phase on annealing in the temperatures range 500 °C- 1000 °C. This results in significant changes in magnetic moment for AP NPs 0.77 μB increases to 0.92 μB for 1200 °C air annealed sample. The magnetic properties decreased at intermediate temperatures due to the presence of secondary phases. On the other hand, pure ferrite phase could be stabilized with an optimum amount of ZnO coated MgFO NPs for samples annealed in the temperature range 500 °C-1000 °C with improvement in magnetic behavior compared to that of MgFO samples.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Magnetic Properties and Synthesis of Ferrites · Electromagnetic wave absorption materials · Magnesium Oxide Properties and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Indian Institute of Technology Madras 1 Department of Physics, , Chennai 600036, India

International Advanced Research Centre for Powder Metallurgy and New Materials 2 Centre for Automotive Energy Materials, , Chennai 600113, India

References (19)

Show source-provided references
1. J. Appl Phys. · 2010 · 107 · 04352510.1063/1.3319563 ↗
2. Mater. Chem. Phys. · 2013 · 139 · 56610.1016/j.matchemphys.2013.01.058 ↗
3. Acta. Pharmacol. Sin. · 2009 · 30 · 168810.1038/aps.2009.158 ↗
4. Dalton Trans. · 2013 · 42 · 124910.1039/C2DT31114C ↗
5. Chem. Mater. · 2006 · 18 · 305710.1021/cm0514894 ↗
6. J. Aust. Ceram. Soc. · 2010 · 46 · 1110.1142/s0219581x09005967 ↗
7. J. Mol. Catal. A. Chem. · 2011 · 335 · 3110.1016/j.molcata.2010.11.007 ↗
8. J. Sol-gel Sci Technol. · 2009 · 51 · 30110.1007/s10971-009-1962-x ↗
9. Cent. Eur. J. Chem. · 2013 · 11 · 1330
10. Physica B. · 2014 · 448 · 31210.1016/j.physb.2014.03.086 ↗
11. J. Alloys Compd. · 2010 · 508 · 43310.1016/j.jallcom.2010.08.083 ↗
12. J. Magn. Magn. Mater. · 2007 · 310 · 237810.1016/j.jmmm.2006.10.737 ↗
13. IEEE Trans. Magn. · 2014 · 50 · 200820410.1109/TMAG.2014.2327694 ↗
14. J. Magn. Magn. Mater. · 2016 · 418 · 11210.1016/j.jmmm.2016.03.017 ↗
15. RSC Adv. · 2014 · 4 · 5796710.1039/C4RA10659H ↗
16. J. Nano. Struct. · 2015 · 5 · 289
17. Mater. Lett. · 2014 · 122 · 20110.1016/j.matlet.2013.12.106 ↗
18. J. Mater. Chem. C. · 2013 · 1 · 313810.1039/c3tc00082f ↗
19. Phys. Rev. · 1956 · 102 · 146010.1103/PhysRev.102.1460 ↗