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The influence of the surface modification on the magnetism of 4–14 nm sized core and core/shell gallium ferrites obtained by different preparation methods (Massart's and thermal decomposition from acetylacetonates) was studied. The physical properties of GaxFe3-xO4 were investigated in a wide range of Ga admixtures 0 ≤ x ≤ 1.5. Ga ions location at 8a or/and 16d positions of a spinel structure depends on the synthesis method and has a pronounced effect on the superparamagnetic properties of nanoparticles. Magnetization and Mössbauer experiments show the dominant superparamagnetic contribution for the nanoparticles with x > 0.8 with the blocking temperature TB significantly below 200 K. Surface-modified nanoferrites disclosed spontaneous magnetization that does not exceed 60 emu/g. [ABSTRACT FROM AUTHOR]

We have succeeded in synthesizing orthorhombic Ga(1_X)Fe(1+X)03 (-0.05 ≤ x ≤ 0.5), hexagonal GayFe(2-y)O3 (0 ≤ y ≤1.8) and cubic Ga(1+Z)Fe(2-Z)04 (--0.1 ≤ z ≤ 0.8) nanograins of gallium ferrites using conventional precursors and an organic environment of Pechini scenario under atmosphericpressure conditions (SG method). Phase composition and homogeneity were analyzed using X-ray diffraction. Small angle neutron scattering disclosed ellipsoidal particle shapes of gallium iron oxides (GFO) crystallizing in orthorhombic (o-GFO) and hexagonal (h-GFO) symmetry and parallelepiped shapes of Ga(1+y)Fe(2-y)O4 (c-GFO) grains. Despite local agglomeration among the magnetic grains, the scanning electron microscopy and transmission electron microscopy images point to faced-elliptical shapes. The Mössbauer spectroscopy with magnetization measurements was carried out in the temperature range of 5-295 K. The analysis of gallium ferrites magnetism demonstrates that iron atoms locate with various probabilities in crystallography positions and the spontaneous magnetization preserves up to room temperature (RT). [ABSTRACT FROM AUTHOR]