无定形固体
电解水
催化作用
材料科学
分解水
纳米技术
电化学
析氧
耐久性
合理设计
化学工程
非晶态金属
边疆
氢
氧气
氧还原反应
工艺工程
催化效率
作者
Gaihong Wang,Zhijie Chen,Jinliang Zhu,Jiangzhou Xie,Wei Wei,Yi‐Ming Yan,Bing‐Jie Ni
出处
期刊:Nano-micro Letters
[Springer Science+Business Media]
日期:2025-10-20
卷期号:18 (1): 77-77
被引量:3
标识
DOI:10.1007/s40820-025-01936-5
摘要
Abstract High‐entropy amorphous catalysts (HEACs) integrate multielement synergy with structural disorder, making them promising candidates for water splitting. Their distinctive features—including flexible coordination environments, tunable electronic structures, abundant unsaturated active sites, and dynamic structural reassembly—collectively enhance electrochemical activity and durability under operating conditions. This review summarizes recent advances in HEACs for hydrogen evolution, oxygen evolution, and overall water splitting, highlighting their disorder-driven advantages over crystalline counterparts. Catalytic performance benchmarks are presented, and mechanistic insights are discussed, focusing on how multimetallic synergy, amorphization effect, and in‐situ reconstruction cooperatively regulate reaction pathways. These insights provide guidance for the rational design of next‐generation amorphous high‐entropy electrocatalysts with improved efficiency and durability.
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