• Al-Rawas, A. D.
• Moore, Elaine
• Widatallah, H. M.
• Johnson, C.
• Al-Harthi, S. H.
• Gismelseed, A. M.
• Stewart, S. J.

Abstract

The influence of mechanical milling and subsequent sintering of a 2:1 molar mixture of SrCO3 and α-Fe2O3 on the formation of SrFeO3−δ pervoskite-related nanocrystalline particles is investigated. The structural evolution during the formation process is systematically investigated using X-ray diffraction, thermal analysis, X-ray photoelectron spectroscopy and Mössbauer spectroscopy. Premilling the mixture in air for 120 h leads to the incorporation of Sr2+ in the α-Fe2O3 crystal structure thus facilitating the formation of a 2:1 nanocrystalline mixture of SrFeO3 and SrFeO2.875 by sintering the pre-milled mixture in air at 800 °C (12 h). This temperature is ∼300 °C lower than those at which SrFeO3−δ phases are synthesized by the conventional ceramic techniques. Pre-milling the precursors was found to result in a smaller oxygen deficiency (δ) relative to conventional ceramic synthesis of SrFeO3−δ. Rietveld refinement of the X-ray diffraction shows the interatomic distances in the resulting SrFeO2.875 nanocrystalline phase to be slightly different from those of the conventionally prepared bulk leading, in turn, to a crystal structure with tilted polyhedral cationic sites. This structural distortion is related to both small-size and surface effects in the nanoparticles that have no counterparts in the corresponding bulk material. The surface structure of the attained SrFeO3−δ nanocrystalline particles shows a significant partial reduction of Fe4+ to Fe3+ due to ambient conditions and the presence of an appreciable amount of SrCO3 as well.

Topics

• nanoparticle
• impedance spectroscopy
• surface
• phase
• x-ray diffraction
• x-ray photoelectron spectroscopy
• Oxygen
• grinding
• milling
• thermal analysis
• ceramic
• sintering
• Mössbauer spectroscopy