Chemical engineering of cationic distribution in spinel ferrite nanoparticles: the effect on the magnetic properties

A set of similar to 9 nm CoFe2O4 nanoparticles substituted with Zn2+ and Ni2+ was prepared by thermal decomposition of metallic acetylacetonate precursors to correlate the effects of replacement of Co2+ with the resulting magnetic properties. Due to the distinct selectivity of these cations for the spinel ferrite crystal sites, we show that it is possible to tailor the magnetic anisotropy, saturation magnetization, and interparticle interactions of the nanoparticles during the synthesis stage. This approach unlocks new possibilities for enhancing the performance of spinel ferrite nanoparticles in specific applications. Particularly, our study shows that the replacement of Co2+ by 48% of Zn2+ ions led to an increase in saturation magnetization of approximately 40% from similar to 103 A m2 kg-1 to similar to 143 A m2 kg-1, whereas the addition of Ni2+ at a similar percentage led to an similar to 30% decrease in saturation magnetization to 68-72 A m2 kg-1. The results of calculations based on the two-sublattice Neel model of magnetization match the experimental findings, demonstrating the model's effectiveness in the strategic design of spinel ferrite nanoparticles with targeted magnetic properties through doping/inversion degree engineering.A set of similar to 9 nm CoFe2O4 nanoparticles substituted with Zn2+ and Ni2+ was prepared by thermal decomposition of metallic acetylacetonate precursors to correlate the effects of the replacement of Co2+ with the resulting magnetic properties.