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Comparative study of Ce(0.85)Sm(0.075)Nd(0.075)O(2-delta) electrolyte synthesized by different routes
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
2011 (English)In: Journal of Alloys and Compounds, ISSN 0925-8388, E-ISSN 1873-4669, Vol. 509, no 35, 8720-8727 p.Article in journal (Refereed) Published
Abstract [en]

In this work, four different methods, including polyvinyl alcohol (PVA)-assisted sol-gel process, polyethylene glycol (PEG)-assisted sol-gel process, citrate sol-gel process and oxalate coprecipitation process (OCP) are employed to synthesize the Sm and Nd co-doped ceria electrolyte with the composition of Ce(0.85)Sm(0.075)Nd(0.075)O(2-delta) (SNDC). The phase structure of the powders can be well indexed with the fluorite-type CeO(2) structure. The morphology of sintered samples indicates that the ceramics can be highly densified. The relative density and the average grain size vary with the synthesis processes and the sintering temperatures. The bulk conductivities are quite close and the OCP-SNDC yields highest grain-boundary conductivities and total conductivities. The results indicate that the OCP process for the powder synthesis results in higher relative density and conductivities, lower grain-boundary resistance and activation energy. Grain-boundary space charge potentials for different specimens are calculated based on the Mott-Schottky model. The synthesis process and sintering temperature have significant effect on the space charge potential and the specific grain-boundary conductivity.

Place, publisher, year, edition, pages
2011. Vol. 509, no 35, 8720-8727 p.
Keyword [en]
Solid oxide fuel cells, Electrolyte, Co-doped, Ceria, Conductivity
National Category
Natural Sciences
Identifiers
URN: urn:nbn:se:su:diva-68022DOI: 10.1016/j.jallcom.2011.06.040ISI: 000293824600022OAI: oai:DiVA.org:su-68022DiVA: diva2:471891
Note
authorCount :4Available from: 2012-01-03 Created: 2012-01-02 Last updated: 2017-12-08Bibliographically approved

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