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.
引用
收藏
页码:131 / 134
页数:4
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