Novel modification of anode microstructure for proton-conducting solid oxide fuel cells with BaZr0.8Y0.2O3-δ electrolytes

被引:23
|
作者
Bae, Hongyeul [1 ,2 ]
Choi, Gyeong Man [1 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Fuel Cell Res Ctr, Dept Mat Sci & Engn, Pohang 790784, South Korea
[2] Res Inst Ind Sci & Technol RIST, Pohang 790330, South Korea
基金
新加坡国家研究基金会;
关键词
Solid oxide fuel cells; Proton conductor; Y-doped barium zirconate; Anode functional layer; Phase transformation; DOPED BARIUM ZIRCONATE; AEROSOL DEPOSITION METHOD; THIN-FILMS; ELECTROCHEMICAL PROPERTIES; YTTRIUM; PERFORMANCE; FABRICATION; MEMBRANES;
D O I
10.1016/j.jpowsour.2015.03.090
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Proton-conducting BaZr0.8Y0.2O3-delta (BZY) electrolyte is hard to sinter and the good anode material has not yet been found. In this study, a BZY electrolyte layer is deposited using aerosol deposition (AD) method on top of a Ni-YSZ (yttria-stabilized zirconia) anode. A novel technique using phase transformation is developed for the modification of microstructure of Ni-YSZ. The Ni-YSZ of the anode functional layer (AFL) is transformed into Ni-BZY by heat treatment with atmospheric powder at temperature (1200 degrees C) substantially lower than the normal sintering temperature of cell fabrication. By the reaction of BaO vapor with YSZ particles in AFL, very fine BZY particles are homogeneously formed on large Ni particles and thus largely increase the triple-phase-boundaries (TPB). This results in a dramatic decrease of areaspecific polarization resistance (0.21 SI cm(2) at 600 degrees C) and increase of peak power density (246 mW cm(-2) at 600 degrees C) compared to those values (1.19 0 cm(2) and 84 mW cm(-2)) without the novel heat treatment. This is one of the best performances among the reported values of cells with BZY-based electrolyte. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:431 / 438
页数:8
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