The study employed in situ X-ray total scattering (TS) with pair distribution function (PDF) analysis and in situ synchrotron powder X-ray diffraction (PXRD) with Rietveld analysis to investigate the nucleation, crystallization, and growth mechanisms of spinel ferrite nanoparticles under hydrothermal conditions.
The in situ TS experiments revealed that the nucleation of the spinel ferrite nanoparticles involves the formation of edge-sharing octahedrally coordinated transition metal (TM) hydroxide units in the aqueous precursor, which then nucleate through linking by tetrahedrally coordinated TMs. This nucleation mechanism was found to be equivalent for the four studied spinel ferrite compositions (MnFe2O4, CoFe2O4, NiFe2O4, and ZnFe2O4).
The in situ PXRD experiments showed that the crystallization and growth of the nanocrystallites progressed via different processes depending on the specific TMs and synthesis temperatures. MnFe2O4 and CoFe2O4 nanocrystallites rapidly grew to equilibrium sizes of 20-25 nm and 10-12 nm, respectively, regardless of the applied temperature in the 170-420°C range, indicating limited possibility of targeted size control. However, varying the reaction time and temperature allowed different sizes to be obtained for NiFe2O4 (3-30 nm) and ZnFe2O4 (3-12 nm) nanocrystallites. The mechanisms controlling the crystallization and growth (nucleation, growth by diffusion, Ostwald ripening, etc.) were examined by qualitative analysis of the evolution in refined scale factor and mean crystallite volume.
Interestingly, lower kinetic barriers were observed for the formation of the mixed spinels (MnFe2O4 and CoFe2O4) compared to the inverse (NiFe2O4) and normal (ZnFe2O4) spinel structured compounds, suggesting that the energy barrier for formation may be lowered when the TMs have no site preference.
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