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dc.contributor.authorSong, J.
dc.contributor.authorRan, R.
dc.contributor.authorShao, Zongping
dc.date.accessioned2017-01-30T13:44:33Z
dc.date.available2017-01-30T13:44:33Z
dc.date.created2016-09-12T08:36:55Z
dc.date.issued2010
dc.identifier.citationSong, J. and Ran, R. and Shao, Z. 2010. Hydrazine as efficient fuel for low-temperature SOFC through ex-situ catalytic decomposition with high selectivity toward hydrogen. International Journal of Hydrogen Energy. 35 (15): pp. 7919-7924.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/34615
dc.identifier.doi10.1016/j.ijhydene.2010.05.094
dc.description.abstract

Hydrazine is a promising fuel for portable fuel cells because it is a liquid, it is carbon free and it has a high energy density. In this work, hydrazine was investigated as an efficient fuel for low temperature solid-oxide fuel cells (SOFCs) with a traditional nickel anode. A catalytic system with high selectivity toward hydrogen was developed using Ba0.5Sr 0.5Co0.8Fe0.2O3-d (BSCF) as the main catalyst and potassium hydroxide as the promoter. The result of compositional analysis of the products showed that the hydrazine can be decomposed into hydrogen and nitrogen with 100% selectivity when an appropriate amount of KOH promoter is used. Acceptable power densities were achieved for a thin-film samaria-doped ceria (SDC) electrolyte cell operating on hydrazine decomposition products and hydrogen over a complete operation temperature range of 650-450 °C. In addition, a similar cell with ammonia as the fuel displayed a much lower performance. © 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.

dc.publisherElsevier Ltd
dc.titleHydrazine as efficient fuel for low-temperature SOFC through ex-situ catalytic decomposition with high selectivity toward hydrogen
dc.typeJournal Article
dcterms.source.volume35
dcterms.source.number15
dcterms.source.startPage7919
dcterms.source.endPage7924
dcterms.source.issn0360-3199
dcterms.source.titleInternational Journal of Hydrogen Energy
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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