We studied the structural, chemical and magnetic properties of non-doped ceria (CeO(2)) thin films electrodeposited on silicon substrates. Experimental results confirm that the observed room temperature ferromagnetism is driven by both cerium and oxygen vacancies. We investigated ceria films presenting vacancy concentrations well above the percolation limit. Irradiation experiments with neon ions were employed to generate highly oxygen defective CeO(2-δ) structures. X-ray photoelectron spectroscopy and x-ray absorption near-edge structure spectroscopy were used to estimate the concentration of Ce(3+) sites in the films, which can reach up to 50% of Ce(3+) replacing Ce(4+), compared to a stoichiometric CeO(2) structure. Despite the increment of structural disorder, we observe that the saturation magnetization continuously increases with Ce(3+) concentration. Our experiments demonstrate that the ferromagnetism observed in ceria thin films, highly disordered and oxygen-deficient, preserving the fluorite-type structure only in a nanometer scale, remains intrinsically stable at room temperature.
This study evaluates the structural, microstructural, electric and magnetic properties of nickel ferrite samples prepared through the solid state reaction. It was observed that an increase in the sintering temperature produces a higher cation concentration in the A site when compared to the B site. The assessment of magnetic properties showed that an increase in grain size leads to a decrease in the coercive fields verging on superparamagnetic values, while the saturation magnetization increases up to 46.5 Am 2 .kg -1 for samples sintered at 1200 °C. The dc electric resistivity behavior of samples was attributed to the increase in the cross-sectional area of grains as well as the different oxidation states and distribution of cations amongst the lattice sites of the spinel structure.
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