Fundamental studies of hafnia-hematite nanoparticles

Abstract

xHfO2-(1-x)α-Fe2O3 (x = 0.1, 0.3, 0.5 and 0.7) nanoparticles system was obtained using mechanochemical activation by high energy ball milling for time periods ranging from 0 to 12 h. X-ray diffraction patterns revealed the presence of two phases, a hafnium-doped hematite and an iron-doped hafnia, which competed with each other to form a solid solution. The trend observed in the lattice parameters using Rietveld refinement was consistent with differences in ionic radii between Hf and Fe. Crystallite sizes for both hematite and hafnia were analyzed as function of milling time using the Scherrer method and found to decrease down to ~15 nm for all molar concentrations used. Mössbauer spectroscopy revealed the presence of 1–5 sextets corresponding to different numbers of Hf nearest neighbors of Fe in the hematite structure. The different hyperfine magnetic fields could be resolved in the model of local atomic environment. Substitutions of Fe in hafnia gave rise to a nonmagnetic phase represented by a quadrupole split doublet, whose abundance was found to increase with ball milling time. Hysteresis loops recorded at 5 K showed that the Hf-doped system does not saturate in an applied magnetic field of 5 T. The Morin transition was observed during zero-field-cooling-field cooling (ZFC-FC) in an external magnetic field of 200 Oe. Differential scanning calorimetry with thermal gravimetric analysis (DSC-TGA) evidenced an exothermic peak for the starting oxides and an endothermic peak for the solid solution.