Application of electroless plating process for multiscale Ni-La0.8Sr0.2Ga0.8Mg0.2O3-σ SOFC anode fabrication

被引:4
作者
Kang, Juhyun [1 ]
Lee, Kunho [1 ]
Yoo, Jae Young [1 ]
Bae, Joongmyeon [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mech Engn, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
Solid oxide fuel cell; Multiscale electrode structure; Nickel electroless plating; Nanoscale catalyst; Ni-LSGM; OXIDE FUEL-CELLS; METAL-SUPPORTED SOFCS; NANOPARTICLES; INFILTRATION; PERFORMANCE; DEPOSITION; HYDRAZINE; STABILITY;
D O I
10.1016/j.ijhydene.2018.01.147
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
An electroless plating process of nickel is introduced to solve the drawbacks of impregnation for developing the multiscale anode of a solid oxide fuel cell (SOFC). Impregnation is the conventional fabrication method of the electrode. The process is not favorable for depositing nanoscale metal catalysts due to severe problems including agglomeration of the catalysts while reducing metal oxides. Thus, as an alternative, we propose electroless plating of nickel to fabricate a multiscale nickel-based SOFC anode. A Ni-LSGM (La0.8Sr0.2-Ga0.8Mg0.2O3-sigma) anode is selected. The low chemical compatibility of LSGM with nickel emphasizes the advantage of the electroless plating process. First, nanoscale nickel particles are successfully applied as the main catalyst of the SOFC anode by plating nickel to the surface of the LSGM scaffold substrate near the triple phase boundary region. Thin film X-ray diffraction and image analysis confirm that pure nanoscale nickel particles form on the entire substrate, even at a low temperature (60 degrees C) without secondary phase formation. Electrochemical impedance spectroscopy analysis is then performed to verify the possibility of implementing an efficient Ni-LSGM anode through nickel electroless plating. As a result, the new Ni-LSGM anode shows similar to 50 times higher electrochemical performance than that of an impregnated Ni-LSGM anode. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6400 / 6405
页数:6
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