Unusual cation coordination in nanostructured mullites

Abstract

Abstract Nanocrystalline mullite-type bismuth-bearing complex oxides Bi2(M0.5Al0.5)4O9 (M=Fe3+, Ga3+) are prepared by high-energy ball milling of the corresponding microcrystalline counterparts. An unusual five-fold coordination of metal cations is revealed in nanostructured Bi2(M0.5Al0.5)4O9 by means of 27Al magic angle spinning nuclear magnetic resonance and 57Fe Mössbauer spectroscopies. The concentration of five-fold coordinated cations increases with decreasing crystallite size of a material at the expense of octahedrally coordinated ones. In addition to the nuclear spectroscopic methods, Rietveld analyses of the X-ray diffraction data of the as-prepared nanooxides show that the constituent tetrahedra, octahedra, and the newly formed structural units with five-fold cation coordination are strongly distorted. With decreasing crystallite size of mullites, the average volume of their octahedra increases whereas this parameter decreases for tetrahedra. The macroscopic behaviour of the non-equilibrium nanomullites is characterised by SQUID magnetometry. The Fe-containing mullites exhibit a superposition of a dominant antiferromagnetism and a weak ferromagnetism. The increase in both the remanent magnetization and the coercive field with decreasing crystallite size is attributed to the effect of spin canting. The latter is confined to the interfacial and surface regions of the nanomaterials, and arises due to both the mechanically induced deformation of constituent structural units and the formation of cation sites with the unusual five-fold coordination.