Structures, Phase Transitions, Hydration, and Ionic Conductivity of Ba4Ta2O9

被引:39
|
作者
Ling, Chris D. [1 ,2 ]
Avdeev, Maxim [2 ]
Kharton, Vladislav V. [3 ]
Yaremchenko, Aleksey A. [3 ]
Macquart, Rene B. [1 ,2 ]
Hoelzel, Markus [4 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Australian Nucl Sci & Technol Org, Bragg Inst, Menai, NSW 2234, Australia
[3] Univ Aveiro, CICECO, Dept Ceram & Glass Engn, P-3810193 Aveiro, Portugal
[4] Tech Univ Darmstadt, D-64287 Darmstadt, Germany
关键词
TEMPERATURE PROTON CONDUCTIVITY; BILBAO CRYSTALLOGRAPHIC SERVER; POWDER DIFFRACTION; BA4NB2O9; POLYMORPHISM; PEROVSKITES; TANTALATE; NIOBATE; SR; MG;
D O I
10.1021/cm903170t
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Low-temperature alpha-Ba4Ta2O9 is isostructured With alpha-Ba4Nb2O9 (Sr4Ru2O9 type), and it undergoes a reconstructive phase transition at approximately the same temperature (1400 K) to a gamma form that can easily be quenched to room temperature. However, the gamma forms of the two compounds are completely different. Whereas gamma-Ba4Nb2O9 represents a unique Structure type, gamma-Ba4TaO9 adopts a more conventional 6H-perovskite type. The alpha ->gamma transition is Virtually irreversible in the tantalate, unlike the niobate, which can be converted back to the a form by annealing slightly below the transition temperature. quenched gamma-Ba4Nb2O highly strained due to tile extreme size mismatch between Ba2+ (1.35 angstrom) and Ta5+, (0.64 angstrom) cations in perovskite B-sites, and undergoes a series of symmetry-lowering distortions from P6(3)/nunc -> P6(3)/m -> P2(1)/c; the second of these transitions has not previously been observed in a 6H perovskite. Below similar to 950 K. both alpha-Ba4Ta4O9 and gamma-Ba4Ta2O9 hydrate to a greater extent than the corresponding phases of Ba4Ta4O9 Both hydrated forms show significant mixed protonic and oxide ionic conductivity, and electronic conductivity upon dehydration,
引用
收藏
页码:532 / 540
页数:9
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