2014 Volume 61 Issue S1 Pages S266-S269
We have measured the 57Fe Mössbauer spectra of Sr1-xLaxFe12-xNixO19 (x=0, 0.1 and 0.2) at room temperature using the powder and the single crystalline samples. All observed spectra were well fitted using the five subspectra, which correspond to the five nonequivalent Fe sites. In Sr1-xLaxFe12-xNixO19 (x=0.1 and 0.2), the substitutions of Ni2+ ions for Fe3+ ions are required by the electric charge balance. For SrFe12O19, the relative absorption intensities in the spectrum observed using the single crystalline sample are much different from those observed using the powder one. This result shows large anisotropies of the recoilless fractions at the Fe sites. The refined hyperfine interaction parameters of the 4f1, 2a, and 2b sites decrease linearly with increasing x. The substitution of a Ni2+ ion for a Fe3+ ion changes hyperfine interaction parameters by the perturbation of the Fe-O-Ni hybridizations. Accordingly, the Fe ions in the vicinity of the 4f1, 2a, and 2b sites are replaced by the Ni2+ ions.