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Spin glass behavior and enhanced but frustrated magnetization in Ho 3+ substituted Co–Zn ferrite interacting nanoparticles

Nanoparticles of Ho 3+ substituted in Co–Zn ferrites were synthesised by sol–gel method. The phase formation of these samples has been confirmed by X-ray powder diffraction technique. XRD Rietveld refinement carried out using the FULLPROF program shows that the Co–Zn ferrite retains its single phase...

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Bibliographic Details
Published in:RSC advances 2016, Vol.6 (80), p.76590-76599
Main Authors: Pawar, Ram A., Patange, Sunil M., Shirsath, Sagar E.
Format: Article
Language:English
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Summary:Nanoparticles of Ho 3+ substituted in Co–Zn ferrites were synthesised by sol–gel method. The phase formation of these samples has been confirmed by X-ray powder diffraction technique. XRD Rietveld refinement carried out using the FULLPROF program shows that the Co–Zn ferrite retains its single phase cubic structure with space group Fd 3 m for x ≤ 0.05. Occupancy of the cations is explained on the basis of site preference, size and valance of the substitution cations. The nanostructure and morphology of prepared samples were investigated by field emission scanning electron microscopy and transmission electron microscopy. The elemental percentage of the constituent ions was determined using energy dispersive spectroscopy. The magnetic interactions among the nanoparticles were analyzed by employing a temperature dependent vibration sample magnetometer, field cooled (FC)/zero field cooled (ZFC) measurements. The ZFC and FC curves diverge below the blocking temperature exhibiting a ZFC cusp at 195–225 K. The saturation magnetization of Co–Zn ferrite increased linearly with Ho 3+ substitution for x ≤ 0.05 and almost remains constant thereafter. The frequency dependence of the AC susceptibility measurements was performed on the sample. It shows a peak at around spin freezing temperature, with the peak position shifting as a function of driving frequency, indicating a spin-glass-like transition of the sample.
ISSN:2046-2069
2046-2069
DOI:10.1039/C6RA12541G