Tailoring the super-paramagnetic nature of MgFe2O4 nanoparticles by In3+ incorporation

•In3+ doped MgFe2O4 nanoparticles are prepared by sol-gel method.•XRD and IR showed the formation of pure spinel ferrites.•XPS confirmed the valance states as Fe3+, Mg2+, In3+ and O2−.•Super-paramagnetic nature of nanoparticles is observed.•Blocking temperature is obtained at RT under applied field...

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Veröffentlicht in:Materials science & engineering. B, Solid-state materials for advanced technology Solid-state materials for advanced technology, 2016-09, Vol.211, p.37-44
Hauptverfasser: Naik, M.Z., Salker, A.V.
Format: Artikel
Sprache:eng
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Zusammenfassung:•In3+ doped MgFe2O4 nanoparticles are prepared by sol-gel method.•XRD and IR showed the formation of pure spinel ferrites.•XPS confirmed the valance states as Fe3+, Mg2+, In3+ and O2−.•Super-paramagnetic nature of nanoparticles is observed.•Blocking temperature is obtained at RT under applied field of 250 Oe. MgFe1−xInxO4 nanoparticles (where x=0.00, 0.04, 0.08, 0.12 and 0.16) have been prepared by sol-gel method using citric acid. The appearance of two distinct bands corresponding to tetrahedral and octahedral occupied MO bonds has been demonstrated in Fourier Transform Infra Red spectra (FT-IR). X-ray powder pattern confirmed the presence of a cubic spinel phase. X-ray Photoelectron Spectroscopy (XPS) has been employed to confirm the valence states of the metal ions present. Mössbauer spectroscopy shows the sextet for pristine sample and on In3+ doping the super-paramagnetic doublet becomes prominent. AC susceptibility profiles shows transition from single domain structure to super-paramagnetic particles on doping. The magnetic properties have been studied using Vibrating Sample Magnetometer (VSM), here the M-H and M-T curves showed the formation of super-paramagnetic nanoparticles at room temperature, where the saturation magnetisation (Ms), remnant magnetisation (Mr) and coercivity (Hc) values decreased with In3+ incorporation.
ISSN:0921-5107
1873-4944
DOI:10.1016/j.mseb.2016.05.019