Investigation of oxide ion flux at cathode/electrolyte interface in solid oxide fuel cell

被引:13
|
作者
Nagasawa, Tsuyoshi [1 ]
Hanamura, Katsunori [2 ]
机构
[1] Tokyo Inst Technol, Dept Syst & Control Engn, Sch Engn, Meguro Ku, 2-12-1 O-Okayama, Tokyo 1528550, Japan
[2] Tokyo Inst Technol, Dept Mech Engn, Sch Engn, Tokyo, Japan
基金
日本学术振兴会;
关键词
Solid oxide fuel cell; Composite cathode; Quenching; Oxygen isotope; SIMS; Oxide ion flux; OXYGEN-TRANSPORT; DIFFUSION; CATHODE; ANODE; VISUALIZATION; COEFFICIENT; SIMULATION; SITES; MODEL;
D O I
10.1016/j.jpowsour.2018.12.013
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
Oxide ion flux at cathode/electrolyte interface of solid oxide fuel cell (SOFC) is investigated through quenching reaction and oxygen isotope labeling. A YSZ (yttria-stabilized zirconia) electrolyte-supported cell with LSM (strontium-doped lanthanum manganite)/YSZ porous cathode is operated by supplying O-18(2) at 973 K and abruptly quenched to room temperature by a direct helium gas-impinging jet to the cell. The O-18 concentration distribution in the cross section of the cathode/electrolyte interface is obtained by secondary ion mass spectrometry (SIMS) with a spatial resolution of 50 nm. From the analysis of oxygen isotope diffusion profiles in YSZ electrolyte, oxide ion flux incorporated from a cathode/electrolyte interface to an electrolyte is first estimated. The obtained flux 1.01-1.43 x 10(-3) mol m(-2) s(-1) at a current density of 0.09A cm(-2) indicates that 22-31% of the overall electrochemical reaction occurs at the cathode/electrolyte interface, while the remaining 69-78% of those proceeds inside the porous cathode under the present experimental condition.
引用
收藏
页码:695 / 700
页数:6
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