Nickel zinc ferrite nanoparticles (Ni0.20Zn0.44Fe2.36O4) have been produced at room temperature, without calcination, using a reverse micelle process. Particle size is approximately 7 nm as determined by x-ray powder diffraction and transmission electron microscopy. Saturation magnetization values are lower than anticipated, but are explained by elemental analysis, particle size, and cation occupancy within the spinel lattice. Extended x-ray absorption fine structure analysis suggests that a significant amount of Zn2+, which normally occupies tetrahedral sites, actually resides in octahedral coordination in a zinc-enriched outer layer of the particles. This “excess” of diamagnetic Zn can thus contribute to the overall decrease in magnetism. Further, this model can also be used to suggest a formation mechanism in which Zn2+ is incorporated at a later stage in the particle growth process.
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Morrison et al. (2004) studied this question.
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