A ferromagnetic-type behavior has been found in sputtered FeO and α-Fe2O3 thin films at low temperatures. This observation is in contrast to the bulk antiferromagnetic properties of FeO and α-Fe2O3. At room temperature the coercivity of the films is negligible, but below 150 K it increases rapidly and at 10 K it is larger than 3 kOe for both kinds of iron oxide films. The saturation magnetization of the films is large (with a maximum of 270 emu/cc in FeO and 140 emu/cc in α-Fe2O3 samples) and thickness dependent. Mössbauer spectra of α-Fe2O3 films could be analyzed by two magnetic components, one very close to bulk α-Fe2O3 and the other one identified as surface α-Fe2O3. Mössbauer spectra of FeO films showed that the samples were off-stoichiometric, with about 10% Fe deficiency. Clusters of tetrahedrally coordinated Fe3+ ions were observed in an environment similar to that in Fe3O4. The hysteresis behavior in FexO films can be explained by the defect clusters of Fe3+ ions, and by uncompensated spins in the surface component of α-Fe2O3 films. Shifted hysteresis loops were observed in field-cooled samples, indicating a strong exchange coupling between the regions with the net magnetic moment and the antiferromagnetic magnetic component.
No takes yet. Share an insight, caveat, or question.
Dimitrov et al. (1997) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: