Abstract
The 57Fe Mössbauer spectra of deerites of different chemical composition, taken at several temperatures, show that Fe2+ and Fe3+ occupy all the six-coordinated lattice sites with a preference of Fe3+ probably for the M(1) to M(3) positions, and a preference of Fe2+ probably for the M(4) to M(6) and the M(7) to M(9) sites. The room and high temperature spectra reveal absorption patterns due to thermally activated Fe2+ → Fe3+ electron delocalization. The extent of electron delocalization is dependent on the chemical composition, e.g., the amount of ions (Mg, Mn, Al) substituting for Fe.
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Amthauer, G., Langer, K. & Schliestedt, M. Thermally activated electron delocalization in deerite. Phys Chem Minerals 6, 19–30 (1980). https://doi.org/10.1007/BF00308390
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DOI: https://doi.org/10.1007/BF00308390