The possibility to finely control nanostructured cubic ferrites (M(II)Fe2O4) paves the way to design materials with the desired magnetic properties for specific applications. However, the strict and complex interrelation among the chemical composition, size, polydispersity, shape and surface coating renders their correlation with the magnetic properties not trivial to predict. In this context, this work aims to discuss the magnetic properties and the heating abilities of Zn-substituted cobalt ferrite nanoparticles with different zinc contents (ZnxCo1-xFe2O4 with 0 < x < 0.6), specifically prepared with similar particle sizes (∼7 nm) and size distributions having the crystallite size (∼6 nm) and capping agent amount of 15%. All samples have high saturation magnetisation (Ms) values at 5 K (>100 emu g(-1)). The increase in the zinc content up to x = 0.46 in the structure has resulted in an increase of the saturation magnetisation (Ms) at 5 K. High Ms values have also been revealed at room temperature (∼90 emu g(-1)) for both CoFe2O4 and Zn0.30Co0.70Fe2O4 samples and their heating ability has been tested. Despite a similar saturation magnetisation, the specific absorption rate value for the cobalt ferrite is three times higher than the Zn-substituted one. DC magnetometry results were not sufficient to justify these data, the experimental conditions of SAR and static measurements being quite different. The synergic combination of DC with AC magnetometry and (57)Fe Mössbauer spectroscopy represents a powerful tool to get new insights into the design of suitable heat mediators for magnetic fluid hyperthermia.
The magnetic properties of cobalt ferrite nanoparticles dispersed in a silica matrix in samples with different concentrations (5 and 10 wt% CoFe2O 4) and same particle size (3 nm) were studied by magnetization, DC and AC susceptibility, and Mossbauer spectroscopy measurements. The results indicate that the particles are very weakly interacting. The magnetic properties (saturation magnetization, anisotropy constant, and spin-canting) are discussed in relation to the cation distribution.
Molecular coating of nanoparticles represents probably
the most
important and, at the same time, critical step to design new nanostructured
magnetic materials. The interaction between molecules and surface
atoms leads to a strong modification of surface magnetic properties,
that are one of the key points in the physics of magnetic nanoparticles.
In this paper the magnetic properties of CoFe2O4 nanoparticles (⟨D⟩ ≅ 4–8 nm) coated
with oleic acid have been investigated in order to clarify the role
of the molecular coating on the interparticle interactions and surface
anisotropy. An increase of magnetic anisotropy (i.e., coercive field
and anisotropy constant) with particle size is observed in coated
nanoparticles, indicating that the magnetic anisotropy is governed
mainly by its magneto-crystalline component. The removal of molecular
coating induces a strong increase of anisotropy, because of the increase
of its surface component, as indicated by the increase of exchange
bias field.
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