Abstract

It is shown that under ambient atmospheric conditions heating causes the crystal structure of βFeOOH (synthetic akaganeite) to degenerate gradually into a quasi amorphous intermediate state, before the final phase transformation to αFe2O3 (hematite) takes place. Using X-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Mossbauer Spectroscopy, this amorphization process is monitored and the structural, morphological and magnetic features of the intermediate phase as a function of the isochronal heating temperature are discussed: the crystallites develop macropores on their surface, the adsorption capacity raises up to 10 percent of the initial mass, a third type of Fe3+ coordination, having an extremely large quadrupole splitting, is created and the Neel temperature, after an initial decrease, exhibits a sharp increase at higher heating temperatures. The magnetic behaviour of this intermediate phase at low temperatures and in high external fields suggests this antiferromagnet undergoes magnetic phase transitions (metamagnetism and spin flop) at unusually low critical fields.

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