Ex-solution of Ni nanoparticles in a La0.2Sr0.8Ti1-xNixO3-δ alternative anode for solid oxide fuel cell

被引:48
|
作者
Park, Byung Hyun [1 ]
Choi, Gyeong Man [1 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Fuel Cell Res Ctr, Dept Mat Sci & Engn, Pohang 790784, South Korea
基金
新加坡国家研究基金会;
关键词
SOFC; Stability; Anode; Ex-solution; AUTOMOTIVE EMISSIONS CONTROL; RARE-EARTH VANADATES; SOFC ANODE; PERFORMANCE; TEMPERATURE; PRECIPITATION; ENHANCEMENT; EXSOLUTION; CATALYST; TITANATE;
D O I
10.1016/j.ssi.2013.10.016
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
Electro-catalytic nanoparticles can be produced in oxide anodes for solid oxide fuel cell (SOFC) by an-ex-solution method, i.e., by incorporating metals into a perovskite oxide phase in air followed by the reduction of the perovskite oxide. In this study, we used a Ni ex-solution method with a La and Ni co-doped SrTiO3 (La0.2Sr0.8Ti1 - xNixO3 - delta, x = 0-02) anode for SOFC The parameters and mechanisms of the Ni ex-solution were investigated by varying the ex-solution temperature (800-1300 degrees C) and time (3-24 h). The degrees of Ni ex-solution and Ti reduction were dependent on time and temperature. Ni ex-solution reaction was relatively faster than Ti reduction which required a higher temperature or a longer time. XRD analysis was used to observe the changes in the lattice parameter of La0.2Sr0.8Ti1 - xNixO3 - delta after the ex-solution process. The electrochemical performance of an electrolyte (Sc-stabilized zirconia)-supported cell with the La0.2Sr0.8Ti1 - xNixO3 - delta anode with x = 0.1 showed that the total cell resistance is high, due mostly to the anode resistance. The maximum power density at 800 degrees C is also relatively low, similar to 150 mW/cm(2), due to the thick (similar to 300 mu m) electrolyte and the low level of anodic performance. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:345 / 348
页数:4
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