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Nanoscaled Sm-doped CeO2 buffer layers for intermediate-temperature solid oxide fuel cells
被引:53
|作者:
Chen, Dengjie
[1
]
Yang, Guangming
[3
]
Shao, Zongping
[3
]
Ciucci, Francesco
[1
,2
]
机构:
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem & Biomol Engn, Kowloon, Hong Kong, Peoples R China
[3] Nanjing Univ Technol, Coll Chem &Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
基金:
美国国家科学基金会;
关键词:
Pulsed laser deposition;
Buffer layer;
Phase reaction;
Thin film;
Solid oxide fuel cells;
THIN-FILMS;
PERFORMANCE;
ELECTROLYTE;
DEPOSITION;
SOFCS;
CERIA;
INTERLAYERS;
CATHODE;
D O I:
10.1016/j.elecom.2013.08.017
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
dense and crack-free nanoscaled Sm-doped CeO2 (SDC) thin film as a buffer layer for intermediate-temperature solid oxide fuel cells has been successfully deposited onto the polycrystalline yttria-stabilized zirconia (YSZ) electrolyte by pulsed laser deposition (PLD). SEM and XRD results reveal that the dense and crack-free buffer layer effectively prevents the formation of the insulating layer between the Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) cathode and the YSZ electrolyte. The fuel cell with the as-deposited buffer layer exhibits high peak power density (e.g., 2016 mW cm(-2) at 700 degrees C) and low resistance. In contrast, at 700 degrees C the fuel cell with an optimized SDC layer prepared by spray deposition or the fuel cell without interlayer have lower peak power densities, 1132 mW cm(-2) and 60 mW cm(-2) respectively, and higher resistances. The significant enhancement in peak power densities with the adoption of the SDC buffer layer by PLD is likely due to the combination of three factors: the lack of solid-state reaction between BSCF and YSZ, the thinner thickness in comparison to the SDC layer by spray deposition, as well as the improvement of the charge-transfer process. (C) 2013 Elsevier B.V. All rights reserved.
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页码:131 / 134
页数:4
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