Review of Electro-catalysts Supported by Metal Oxides for Electrochemical Oxygen Reduction Reaction

被引:3
|
作者
Jo, Yoo-Jin [1 ]
Jung, Won Suk [1 ,2 ]
Lim, Boyoung [1 ]
机构
[1] Hankyong Natl Univ, Sch Food Biotechnol & Chem Engn, Anseong 17579, South Korea
[2] Hankyong Natl Univ, Res Ctr Chem Technol, Anseong 17579, South Korea
来源
关键词
metal oxide; oxygen reduction reaction; proton exchange membrane fuel cells; catalytic activity; stability; FUEL-CELLS; CARBON; NANOPARTICLES; DURABILITY; TIO2; ELECTROCATALYSTS; PERFORMANCE; STABILITY; CATHODE; DESIGN;
D O I
10.3365/KJMM.2023.61.4.231
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Global warming and air pollution have forced greater attention to new energy sources to replace fossil fuels. Among several eco-friendly energy sources, polymer electrolyte membrane fuel cells have been increasingly investigated since they have zero emissions, high energy density, and high energy efficiency. Carbon-supported Pt catalyst is generally used for the cathodic catalyst in polymer electrolyte membrane fuel cells. However, Pt/C catalysts corrode under start-up/shut-down conditions. Pt agglomeration, separation, and loss can occur due to the carbon corrosion, which results in a rapid performance loss. Metal oxide is a promising candidate as an alternative support since it shows high stability in the high potential. Of several metal oxides, titanium oxides and tin oxides have been widely investigated. Their performance is comparable to the Pt/C catalyst, and they have shown even higher durability than the Pt/C catalyst in accelerated stress tests simulating start-up/shut-down conditions. In this paper, we summarize the development of metal oxide supports for the Pt catalyst in the five most recent years. In recent studies, the characteristics of metal oxides have been varied using new synthesis methods, annealing temperature, precursors, and dopants, which results in enhanced ORR activity and durability. Advanced metal oxides have shown high durability and exhibited acceptable performance compared to the state-of-the-art Pt/C catalysts.
引用
收藏
页码:231 / 241
页数:11
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