Synthesis and characterization of nano-LaFeO3 powders by a soft-chemistry method and corresponding ceramics

The preparation of a nano-sized LaFeO3 powder by a soft-chemistry method using starch as complexing agent is described herein. Phase evolution and development of the specific surface area during the decomposition process of (LaFe)-gels were monitored up to 1000°C. A phase-pure nano-sized LaFeO3 powd...

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Veröffentlicht in:Solid state ionics 2013-02, Vol.231, p.43-48
Hauptverfasser: Köferstein, Roberto, Ebbinghaus, Stefan G.
Format: Artikel
Sprache:eng
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Zusammenfassung:The preparation of a nano-sized LaFeO3 powder by a soft-chemistry method using starch as complexing agent is described herein. Phase evolution and development of the specific surface area during the decomposition process of (LaFe)-gels were monitored up to 1000°C. A phase-pure nano-sized LaFeO3 powder with high specific surface area of 25.7m2/g and a crystallite size of 37nm was obtained after calcining at 570°C. TEM investigations reveal a porous powder with particles in the range of 20 to 60nm. Calcinations to 1000°C result in crystallite sizes up to 166nm. The dilatometric measurements of the sintering behaviour show that the beginning of shrinkage of pellets from the nano-sized powder is downshifted by more than 300°C compared to the coarse-grained mixed-oxide powder. The orthorhombic⇆rhombohedral phase transition was observed at 980°C in DTA measurements for the coarse-grained ceramic bodies. The enthalpy change (ΔH) during the phase transition and the thermal expansion coefficient (αdil) for the ceramics were determined as 410J/mol and 11.8·10−6K−1, respectively. Whereas the enthalpy changes during the phase transition of the nano-sized LaFeO3 powders are ≤200J/mol. ► Novel, eco-friendly and simple synthesis route for nano LaFeO3 powders using starch as complexation agent ► Monitoring the phase evolution during the synthesis ► Nano LaFeO3 powder with high sintering activity obtained after calcination at 570°C ► Dense ceramic bodies even at 1250°C without any sintering additive ► Investigations of phase transition and the thermal expansion coefficient
ISSN:0167-2738
1872-7689
DOI:10.1016/j.ssi.2012.10.017