Mössbauer Study of Isomer Shift, Quadrupole Interaction, and Hyperfine Field in Several Oxides ContainingFe57

Abstract
Mössbauer absorption by Fe57 was used to study isomer shift, quadrupole splitting, and hyperfine fields in several oxides containing iron. The established relations between isomer shifts and ionic states of Fe were further confirmed by measurements on Fe2+ Ti2 O5, Fe23+TiO5 and several other mixed oxides. By utilizing this relation, in turn, to identify the ionic states when these are in doubt, it has been found that (Fe,V)2 O3 incorporates the cation pair Fe3+ - V3+, rather than Fe2+ - V4+, and that "SrFeO3" contains Fe4+ and Fe3+ in the ratio of 3:1. A well-defined quadrupole splitting was observed in Fe1xO and in a number of the solid solutions (Fe,Mg)O, although their over-all symmetry is cubic. This is explained by the assumption of local asymmetry at the Fe nuclei caused either by vacancies or foreign ions. Hyperfine fields at the Fe3+ nuclei in (Fe,Cr)2 O3, (Fe,V)2 O3, and (Fe,Al)2 O3 have values between 520 and 540 koe when extrapolated to 0°K, and the results are discussed in conjunction with their magnetic properties.