Frank J. Berry, Colin Greaves, Örn Helgason and Julia McManus
Rietveld structure refinement of the X-ray powder diffraction data recorded from tin-doped Fe3O4 prepared by heating metallic iron, α-iron(III) oxide and tin(IV) oxide in sealed evacuated quartz ampoules shows the tin to substitute on the octahedral sites of the inverse spinel-related structure. Tin-doped γ-Fe2O3, prepared by boiling a precipitate derived from iron(III), iron(II) and tin(II) under reflux, also adopts an inverse spinel-related structure containing tin on the octahedral sites and, compared to pure γ-Fe2O3, is stabilised with respect to conversion to α-Fe2O3. 57Fe Mössbauer spectroscopy shows the Neél temperature for γ-Fe1.9Sn0.1O3 to be between 750 and 820 K. Tin-doped α-Fe2O3 prepared by hydrothermal methods is shown by Rietveld structure refinement of the X-ray powder diffraction data to contain tin in both the substitutional and interstitial octahedral sites of the corundum-related structure.