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dc.contributor.authorZhou, W.
dc.contributor.authorShao, Zongping
dc.contributor.authorKwak, C.
dc.contributor.authorPark, H.
dc.date.accessioned2018-02-01T05:25:04Z
dc.date.available2018-02-01T05:25:04Z
dc.date.created2018-02-01T04:59:50Z
dc.date.issued2012
dc.identifier.citationZhou, W. and Shao, Z. and Kwak, C. and Park, H. 2012. Advanced Cathodes for Solid Oxide Fuel Cells. In Materials for High-Temperature Fuel Cells, 49-95. Singapore: Wiley.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/62690
dc.identifier.doi10.1002/9783527644261.ch2
dc.description.abstract

© 2013 Wiley-VCH Verlag GmbH & Co. KGaA. All rights reserved. As highly efficient energy conversion devices with negligible impact on environment, solid oxide fuel cells (SOFCs) have received considerable attention recently as a keystone of the future energy economy. Current developments in SOFCs focus on increasing the durability and lowering the cost of the system and the materials therein. It is generally recognized that these goals can be realized by lowering the SOFC operating temperature to the low- to intermediate-temperature (LIT) region (500-750°C). The main barrier to achieving acceptable chemical to electrical conversion efficiency in LIT-SOFCs is the sluggish oxygen reduction reaction (ORR) kinetics of the cathode. In this chapter, we review the electrochemical performance of cathodes with different crystal structures, that is, perovskite, double perovskite, and K2NiF4. We focus on the application of these cathodes on oxide ion- and proton-conducting electrolytes. In addition, we introduce some advanced techniques for cathode fabrication (wet impregnation, surfactant-assisted assembly, and spray pyrolysis).

dc.publisherWiley
dc.titleAdvanced Cathodes for Solid Oxide Fuel Cells
dc.typeBook Chapter
dcterms.source.startPage49
dcterms.source.endPage95
dcterms.source.titleMaterials for High-Temperature Fuel Cells
dcterms.source.isbn9783527644261
dcterms.source.placeSingapore
dcterms.source.chapter9
curtin.accessStatusFulltext not available


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