1983 Volume 52 Issue 1 Pages 254-262
Mössbauer spectroscopy has been applied to a random mixture with orthogonal spin anisotropies, Fe1−xCoxCl2·2H2O. The direction of an “individual Fe spin” of Co(Fe)-rich samples determined from the Mössbauer spectra was tilted even in the antiferromagnetic (AF) phase as well as in the mixed ordering phase. This means that, in the Co(Fe)-rich AF phase, although the spin component parallel to the easy axis of FeCl2·2H2O (CoCl2·2H2O) has no long-range order according to the neutron scattering measurement, the component exists on each lattice site statically at least in the time scale of 57Fe Mössbauer spectroscopy (∼10−8 s).
The direction of an “individual Fe spin” has been shown to be strongly affected by the local environment around the Fe spin.
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