Orera, A. and Baikie, T. and Panchmatia, P. and White, T. J. and Hanna, John V. and Smith, Mark E. and Islam, M. S. and Kendrick, E. and Slater, P. R. (2010) Strategies for the optimisation of the oxide ion conductivities of apatite-type germanates. Fuel Cells, 11 (1). pp. 10-16.Full text not available from this repository.
Recently, apatite-type germanates La(9.33?) xGe(6)O(26? 3x?2) have attracted considerable interest due to their high oxide ion conductivities. Research has shown that the key defects are oxide ion interstitials which lead to the conversion of some of the GeO(4) units to GeO(5). Consequently there has been a large interest in the preparation of high oxygen excess samples with high defect concentration. This strategy, however, leads to a reduction in symmetry from hexagonal to triclinic for x > 0.4, and consequently to reduced oxide ion conductivity at low temperatures. We present doping strategies to stabilise the hexagonal lattice, while maintaining high oxygen content. In particular, partial substitution of La by smaller rare earths (Y, Yb) is shown to be successful in preparing x = 0.67 samples with hexagonal symmetry and hence high conductivities. In addition, doping on the Ge site with Ti, Nb or W, has been shown to be similarly successful, leading to very high oxygen contents for W doping, e. g. La(10)Ge(5.5)W(0.5)O(27.5). In the case of Ti doping, however, there was some evidence for trapping of the interstitial oxide ions around the Ti. Preliminary results on the effect of similar doping strategies on Pr, Nd germanates (Pr?Nd)(9.33?x)Ge(6)O(26?3x?2), are also discussed.
|Journal or Publication Title:||Fuel Cells|
|Uncontrolled Keywords:||Apatite ; Defect Trapping ; Electrolyte ; Germanate ; Oxide-Ion Conductivity ; Solid Oxide Fuel Cells|
|Deposited On:||28 Feb 2012 11:05|
|Last Modified:||09 Apr 2014 23:09|
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