Low-loading IrO2 supported on Pt for catalysis of PEM water electrolysis and regenerative fuel cells

被引:67
|
作者
Lim, Ahyoun [1 ,2 ]
Kim, Junyoung [1 ]
Lee, Hye Jin [1 ]
Kim, Hyoung-Juhn [1 ,3 ]
Yoo, Sung Jong [1 ,3 ]
Jang, Jong Hyun [1 ,3 ]
Park, Hee Young [1 ]
Sung, Yung-Eun [2 ]
Park, Hyun S. [1 ,3 ]
机构
[1] Korea Inst Sci & Technol KIST, Ctr Hydrogen Fuel Cell Res, Seoul 02792, South Korea
[2] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
[3] Univ Sci & Technol UST, KIST Sch, Div Energy & Environm Technol, Seoul 02792, South Korea
基金
新加坡国家研究基金会;
关键词
Proton exchange membrane water electrolysis; Unitized regenerative fuel cell; Electrodeposition; Oxygen evolution catalysts; GAS-DIFFUSION LAYER; OXYGEN REDUCTION REACTION; ENERGY-STORAGE; IRIDIUM OXIDE; EVOLUTION REACTION; MASS-TRANSPORT; ELECTROCATALYSTS; ELECTRODES; FABRICATION; CORROSION;
D O I
10.1016/j.apcatb.2020.118955
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
A unitized regenerative fuel cell (URFC), an electrochemical device operated in both water electrolysis (WE) and fuel cell (FC) modes, is a promising technology in interconverting renewable electricity and chemical fuels within a compact system. However, Proton-exchange membrane-based URFCs usually employ a significant amount of precious metal catalysts, e.g., up to 4 mg((Pt+IrO2)) cm(-2), to achieve high efficiency in round-trip operations. Here, we present a PEM-URFC electrode that uses only 0.8 mg((Pt+Ir)) cm(-2) without compromising the performance of URFC. IrO2-shells (70 nm) layered upon hemispherical Pt particles (Pt@IrO2) are formed using sequential electrodeposition over Ti-felt electrodes. A 100 % improvement in WE compared to performance without Pt supports and superior mass activity (44 A mg(Ir)(-1) at 2 V-cell) with an insignificant degradation rate of 155 mu V h(-1) at 0.4 A cm(-2) are demonstrated. In addition, high round-trip efficiency of 49 % at 0.4 A cm(-2) in URFC is achieved.
引用
收藏
页数:10
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