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Screen printed porous La0.20Sr0.25Ca0.45TiO3 fuel electrode scaffold microstructures : Optimisation of interaction with impregnated catalysts for more durable performance

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Irvine_2015_ECS_Screen.pdf (1.877Mb)
Date
2015
Author
Price, Robert
Cassidy, Mark
Schuler, J.A.
Mai, A.
Irvine, John Thomas Sirr
Keywords
QD Chemistry
NDAS
Metadata
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Abstract
La0.20Sr0.25Ca0.45TiO3 (LSCTA-) shows promise as a novel Solid Oxide Fuel Cell anode backbone material (to replace Ni-based cermets). Thick film ceramic processing techniques have been used as the primary method in controlling the characteristics of the fuel electrode (layer thickness, porosity, grain connectivity and the ultimate interaction with catalyst particles) in order to produce a microstructural architecture which has the potential to deliver higher electronic (and ionic) conductivity, improved current distribution and more durable performance in fuel cell testing. Results of preliminary studies into the ceramic processing of LSCTA- are presented here.
Citation
Price , R , Cassidy , M , Schuler , J A , Mai , A & Irvine , J T S 2015 , Screen printed porous La 0.2 0Sr 0.25 Ca 0.45 TiO 3 fuel electrode scaffold microstructures : Optimisation of interaction with impregnated catalysts for more durable performance . in K Eguchi & S C Singhal (eds) , 14th International Symposium on Solid Oxide Fuel Cells, SOFC 2015 . ECS Transactions , no. 1 , vol. 68 , Electrochemical Society , pp. 1499-1508 . DOI: 10.1149/06801.1499ecst
Publication
14th International Symposium on Solid Oxide Fuel Cells, SOFC 2015
DOI
http://dx.doi.org/10.1149/06801.1499ecst
ISSN
1938-5862
Type
Conference item
Rights
© The Electrochemical Society, Inc. [year]. All rights reserved. Except as provided under U.S. copyright law, this work may not be reproduced, resold, distributed, or modified without the express permission of The Electrochemical Society (ECS). The archival version of this work was published here: https://dx.doi.org/10.1149/06801.1499ecst
Collections
  • University of St Andrews Research
  • Chemistry Research
URI
http://hdl.handle.net/10023/7368

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