We report herein results concerning the solid solutions Pr 2؊x M x NiO 4؉ , M ؍ La, Sr. These two cations are larger than praseodymium and lead to a structural stabilization. The oxygen excess decreases with x for La and Sr substituted Pr 2 NiO 4؉ . Both cases suggest that structural strain is a l
Stability and oxygen transport properties of Pr2NiO4+δ ceramics
✍ Scribed by A.V. Kovalevsky; V.V. Kharton; A.A. Yaremchenko; Y.V. Pivak; E.N. Naumovich; J.R. Frade
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 406 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0955-2219
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✦ Synopsis
The oxygen permeability and stability of dense Pr 2 NiO 4+δ ceramics have been appraised in comparison with K 2 NiF 4 -type lanthanum nickelate. In oxidizing atmospheres, Pr 2 NiO 4+δ exhibit an extensive oxygen uptake and decomposition into the Ruddlesden-Popper-type Pr 4 Ni 3 O 10 and praseodymium oxide at temperatures below 900 • C. At 900-950 • C when the K 2 NiF 4 -type praseodymium nickelate is stable in the ceramic membranes placed under an oxygen partial pressure gradient, the steady-state oxygen permeability of Pr 2 NiO 4+δ is similar to La 2 NiO 4+δ . The phase changes on cooling lead to considerably higher oxygen permeability, which becomes comparable to that of perovskite-type cobaltites, and to noticeable isothermal expansion. The stability of Pr 2 NiO 4+δ in reducing atmospheres, estimated from the p(O 2 ) dependencies of total conductivity and Seebeck coefficient, is lower than that of La 2 NiO 4+δ , probably due to a smaller size of the A-site cation.
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We have studied the stability of Pr 2 NiO 4؉ under pure oxygen 6ow by in situ measurement of its weight versus T. Above 8503C a fast oxidation is observed corresponding to the ex-solution of PrO y species and to the formation of metallic Pr 4 Ni 3 O 10؊x . This reaction is not reversible. The quanti