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Formation mechanism of monodisperse Ce3+ substituted ZnFe2O4 nanoparticles
Monodisperse Ce3+ doped zinc ferrite magnetic nanoparticles (MMNPs) were fabricated by a solvothermal route. The Fe2+ formation may be the key step for the fabrication of the ferrite. This mechanism can be used to explain the formation of the unstoichiometric chemical formula of the Zn ferrite. [Dis...
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Published in: | Journal of alloys and compounds 2014-07, Vol.602, p.228-234 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Monodisperse Ce3+ doped zinc ferrite magnetic nanoparticles (MMNPs) were fabricated by a solvothermal route. The Fe2+ formation may be the key step for the fabrication of the ferrite. This mechanism can be used to explain the formation of the unstoichiometric chemical formula of the Zn ferrite. [Display omitted]
•Monodisperse Ce3+ doped zinc ferrite MMNPs were fabricated by a solvothermal route.•The formation mechanism for the Ce3+ doped zinc ferrite contains different processes.•Fe2+ formation may be the key step for the fabrication of the ferrite.
Monodisperse Ce3+ substituted zinc ferrite magnetic nanoparticles (MNPs) were synthesized. α-(Fe, Zn)OOH, α-Fe2O3, CeFeO3, and Ce3+ substituted ZnFe2O4 were synthesized at different intervals based on XRD, IR, XPS, ICP-AES, and HRTEM analysis. The lattice parameters and the average crystallite size for the samples obtained at different reaction intervals increased from 3 to 12h, and decreased from 12 to 24h. A possible mechanism was studied. The formation of Fe2+ may be the key step for the zinc ferrite production. The maximum saturation magnetization of the MNPs among these samples was determined to be 78.6emu/g. The surface area (78.3m2/g) of the MNPs is higher than the clusters aggregated by nanoparticles previously reported in our laboratory. These properties will render the MNPs ideal candidates for various applications. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2014.03.049 |