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Spinel cobalt ferrite/hexagonal strontium hexaferrite (2CoFe2O4/SrFe12−2xSmxLaxO19; x = 0.2, 0.5, 1.0, 1.5) nanocomposites were fabricated using the tartaric acid precursor pathway, and the effects of La3+–Sm3+ double substitution on the formation, structure, and magnetic properties of CoFe2O4/SrFe12−2xSmxLaxO19 nanocomposite at different annealing temperatures were assayed through X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry. A pure 2CoFe2O4/SrFe12O19 nanocomposite was obtained from the tartrate precursor complex annealed at 1100 °C for 2 h. The substitution of Fe3+ ion by Sm3–+La3+ions promoted the formation of pure 2CoFe2O4/SrFe12O19 nanocomposite at 1100 °C. The positions and intensities of the strongest peaks of hexagonal ferrite changed after Sm3+–La3+ substitution at ≤1100 °C. In addition, samples with an Sm3+–La3+ ratio of ≥1.0 annealed at 1200 °C for 2 h showed diffraction peaks for lanthanum cobalt oxide (La3Co3O8; dominant phase) and samarium ferrite (SmFeO3). The crystallite size range at all constituent phases was in the nanocrystalline range, from 39.4 nm to 122.4 nm. The average crystallite size of SrFe12O19 phase increased with the number of Sm3+–La3+ substitutions, whereas that of CoFe2O4 phase decreased with an x of up to 0.5. La–Sm co-doped ion substitution increased the saturation magnetization (Ms) value and the subrogated ratio to 0.2, and the Ms value decreased with the increasing number of double substitutions. A high saturation magnetization value (Ms = 69.6 emu/g) was obtained using a La3+–Sm3+ co-doped ratio of 0.2 at 1200 for 2 h, and a high coercive force value (Hc = 1192.0 Oe) was acquired using the same ratio at 1000 °C.

materials

Boost the Crystal Installation and Magnetic Features of Cobalt Ferrite/M-Type Strontium Ferrite Nanocomposites Double Substituted by La3+ and Sm3+ Ions (2CoFe2O4/SrFe12−2xSmxLaxO19)