New Ba0.5Sr0.5Co0.8Fe0.2O 3-d + Co3O4 composite electrode for IT-SOFCs with improved electrical conductivity and catalytic activity
dc.contributor.author | Chen, D. | |
dc.contributor.author | Huang, C. | |
dc.contributor.author | Ran, R. | |
dc.contributor.author | Park, H. | |
dc.contributor.author | Kwak, C. | |
dc.contributor.author | Shao, Zongping | |
dc.date.accessioned | 2017-01-30T10:44:41Z | |
dc.date.available | 2017-01-30T10:44:41Z | |
dc.date.created | 2015-10-29T04:09:58Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | Chen, D. and Huang, C. and Ran, R. and Park, H. and Kwak, C. and Shao, Z. 2011. New Ba0.5Sr0.5Co0.8Fe0.2O 3-d + Co3O4 composite electrode for IT-SOFCs with improved electrical conductivity and catalytic activity. Electrochemistry Communications. 13 (2): pp. 197-199. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/5231 | |
dc.identifier.doi | 10.1016/j.elecom.2010.12.012 | |
dc.description.abstract |
Ba0.5Sr0.5Co0.8Fe0.2O 3-d (BSCF) + Co3O4 composites with different Co3O4 contents were synthesized, and their properties and performance as cathodes in IT-SOFCs were investigated. The diffraction patterns of the composites were well indexed based on the physical mixture of the BSCF phase and the Co3O4 phase. A surprising increase in the total conductivity of the composites was observed even though Co3O4 is a p-type semiconductor with a low conductivity. Electrochemical impedance spectra of symmetric cells indicated that both the area specific resistance and the activation energy were reduced in samples with Co3O4 contents of 5-20 wt.% with minimum values reaching 10 wt.%. A synergistic effect likely occurred between BSCF and Co3O4 that led to the better performance. An anode-supported single cell with 90 wt.% BSCF + 10 wt.% Co3O 4 delivered a promising peak power density of 1150 mW cm - 2 at 600 °C. © 2011 Elsevier B.V. | |
dc.title | New Ba0.5Sr0.5Co0.8Fe0.2O 3-d + Co3O4 composite electrode for IT-SOFCs with improved electrical conductivity and catalytic activity | |
dc.type | Journal Article | |
dcterms.source.volume | 13 | |
dcterms.source.number | 2 | |
dcterms.source.startPage | 197 | |
dcterms.source.endPage | 199 | |
dcterms.source.issn | 1388-2481 | |
dcterms.source.title | Electrochemistry Communications | |
curtin.department | Department of Chemical Engineering | |
curtin.accessStatus | Fulltext not available |
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