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Please use this identifier to cite or link to this item: http://apo.ansto.gov.au/dspace/handle/10238/3001

Title: Structures, phase transitions, hydration, and ionic conductivity of Ba4Ta2O9.
Authors: Ling, CD
Avdeev, M
Kharton, VV
Yaremchenko, AA
Macquart, RB
Hoelzel, M
Keywords: Phase Transformations
Hydration
Ionic Conductivity
Perovskite
Tantalates
Annealing
Issue Date: 26-Jan-2010
Publisher: American Chemical Society
Citation: Ling, C. D., Avdeev, M., Kharton, V. V., Yaremchenko, A. A., Macquart, R. B., & Hoelzel, M. (2010). Structures, phase transitions, hydration, and ionic conductivity of Ba4Ta2O9. Chemistry of Materials, 22(2), 532-540.
Abstract: Low-temperature α-Ba4Ta2O9 is isostructural with α-Ba4Nb2O9 (Sr4Ru2O9 type), and it undergoes a reconstructive phase transition at approximately the same temperature (1400 K) to a γ form that can easily be quenched to room temperature. However, the γ forms of the two compounds are completely different. Whereas γ-Ba4Nb2O9 represents a unique structure type, γ-Ba4Ta2O9 adopts a more conventional 6H-perovskite type. The α→γ transition is virtually irreversible in the tantalate, unlike the niobate, which can be converted back to the α form by annealing slightly below the transition temperature. Quenched γ-Ba4Ta2O9 is highly strained due to the extreme size mismatch between Ba2+ (1.35 Å) and Ta5+ (0.64 Å) cations in perovskite B-sites, and undergoes a series of symmetry-lowering distortions from P63/mmc→P63/m→P21/c; the second of these transitions has not previously been observed in a 6H perovskite. Below 950 K, both α-Ba4Ta2O9 and γ-Ba4Ta2O9 hydrate to a greater extent than the corresponding phases of Ba4Nb2O9. Both hydrated forms show significant mixed protonic and oxide ionic conductivity, and electronic conductivity upon dehydration. © 2010, American Chemical Society
URI: http://dx.doi.org/10.1021/cm903170t
http://apo.ansto.gov.au/dspace/handle/10238/3001
ISSN: 0897-4756
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