Citation: WANG Rong, YANG Cheng-Xu, SHI Ying-Guo, SUN Yu-Zeng, LI Guo-Bao, JIN Tou-Nan, QIN Gao-Wu, LIAO Fu-Hui, LIN Jian-Hua. Phase Relationship, Structure and Cationic Distribution of Oxides in the Mn3O4-Fe2O3 System Synthesized at 1200 ℃[J]. Acta Physico-Chimica Sinica, ;2012, 28(05): 1021-1029. doi: 10.3866/PKU.WHXB201202271
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A series of oxides in the Mn3O4-Fe2O3 system have been synthesized at 1200 ℃ in air, followed by quenching to room temperature. Three solid solutions, Mn3-3xFe3xO4 (0.00≤x≤0.278), Mn3-3xFe3xO4(0.291≤x≤0.667), and Mn2-2xFe2xO3 (0.89≤x≤1.00), have been identified by powder X-ray diffraction (XRD). Rietveld refinement of the XRD data show that the solids belong to the hausmannite phase with the space group I41/amd, the spinel phase with the space group Fd3m, and the hematite phase with the space group R3c, respectively. Between these are two-phase regions. 57Fe Mössbauer spectra indicate that the valence state of Fe in the three solid solutions is +3; in addition, there are two crystallographically independent Fe3+ ions in the unit cells of the hausmannite and spinel phases, and one Fe3+ in the hematite phase. Analyses of 57Fe Mössbauer spectra and X-ray photoelectron spectra (XPS) revealed that a formula of Mn1-x2+Fex3+[Mnx3+Fex3+Mn2-3x3+]O4 describes the cation distribution of both the hausmannite and spinel phases, but that for the hematite phase is Mn2-2x3+Fe2x3+O3.
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