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Surface and bulk oxygen non-stoichiometry and bulk chemical expansion in gadolinium-doped cerium oxide
被引:98
作者:
Bishop, S. R.
[1
]
Duncan, K. L.
[1
]
Wachsman, E. D.
[1
]
机构:
[1] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32611 USA
关键词:
Ceria;
Defect equilibria;
Chemical expansion;
Thermogravimetry;
Surface chemistry;
PHASE RELATIONSHIPS;
LATTICE-PARAMETERS;
VACANCY FORMATION;
FLUORITE OXIDES;
SOLID-SOLUTIONS;
POINT-DEFECTS;
ELECTROLYTES;
CONDUCTIVITY;
TEMPERATURES;
SUBLATTICE;
D O I:
10.1016/j.actamat.2009.04.017
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
Doped and undoped cerium(IV) oxides are ceramics commonly used as catalysts and as solid oxide fuel cell materials. In low oxygen partial pressure, ceria-based materials become non-stoichiometric and can form defect complexes that hinder ionic conductivity. In addition, oxygen non-stoichiometry induces strain (chemical expansion) that can result in stresses for composite or constrained applications. In this paper the non-stoichiometry and chemical expansion behavior has been measured in the temperature range 600-900 degrees C and in a wide oxygen partial pressure range. Surface oxygen non-stoichiometry has also been measured by comparing low surface area to high surface area samples. The bulk non-stoichiometry and chemical expansion behavior have been successfully modeled using a mass action formalism with defect complex formation to account for defect interactions. It has been found that surface defect concentration, previously ignored in the literature, can result in erroneous non-stoichiometry measurements. (C) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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页码:3596 / 3605
页数:10
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