材料科学
阳极
催化作用
钴
电解水
析氧
化学工程
电解
质子交换膜燃料电池
制氢
金属
降级(电信)
膜
电极
耐久性
氢
分解水
电化学
聚合物电解质膜电解
纳米技术
无机化学
资源回收
可扩展性
质子
碱性水电解
氢经济
相(物质)
作者
Lei Han,L. J. Yuan,Xiayu Peng,Haijing Li,Qirui Wu,Huimin Yu,Zhentao Du,Huanyu Jin
摘要
ABSTRACT Proton exchange membrane water electrolyzers (PEMWEs) are central to green hydrogen production, yet their anodic oxygen evolution reaction (OER) still relies on noble‐metal catalysts (Ir or Ru), raising concerns regarding cost and resource scarcity. Therefore, the exploration of stabilized supported materials is essential to achieve low/non‐noble metal loading anodes in PEMWEs. Recent studies indicate that Co 3 O 4 can not only serve as an efficient support for noble‐metal single atoms, but also act as a non‐noble active phase or an integral component of hybrid catalyst systems. However, its unsatisfactory long‐term stability in acidic environments remains a major barrier. In this review, we analyze the fundamental degradation mechanism of Co 3 O 4 under acidic OER and highlight the key factors underlying dissolution, lattice restructuring, and loss of electronic conductivity. In addition, strategies that improve durability are investigated. Practical considerations for device integration, such as catalyst‐layer design, dynamic‐load stability, and scalable fabrication, are also analyzed. To translate laboratory breakthroughs into commercial technologies, future research must now prioritize dynamic stability and scalable integration of membrane electrode assemblies over conventional activity metrics.
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