催化作用
分解水
制氢
电解水
氧气
化学
析氧
生化工程
纳米技术
氢
电解
反应机理
过程(计算)
工艺工程
多相催化
化学工程
生产(经济)
密度泛函理论
机制(生物学)
反应条件
碱性水电解
作者
Z. Y. Deng,Minjie Hu,Chunyu Zhang,Enxian Yuan,Zhan Shen,Jiancheng Zhou,Chan Wu
出处
期刊:Chemical Record
[Wiley]
日期:2025-09-09
卷期号:25 (10): e202500079-e202500079
被引量:1
标识
DOI:10.1002/tcr.202500079
摘要
Water electrolysis for hydrogen production has become an industrial focus in the era of green chemistry due to its high purity of hydrogen production and environmentally friendly, efficient process. As the half reaction of water splitting at the anode, the oxygen evolution reaction (OER) features a complex and sluggish process that restricts the efficiency of water splitting. The mechanism of OER varies with different electrolytes. Single-atom catalysts (SACs) have become a research hotspot due to their advantages, such as nearly 100% atomic utilization efficiency and abundant, uniform active sites. Through structural optimization and coordination environment regulation, SACs can effectively enhance the efficiency of OER. This review comprehensively summarizes the OER mechanisms under both acidic and alkaline conditions, systematically compiles the performance and applications of precious-metal and nonprecious-metal SACs in OER, and provides mechanistic insights through density functional theory calculations. Finally, it provides an outlook on the research prospects of single-atom electrocatalysts, offering references and guidance for the preparation of higher-performance single-atom electrocatalysts.
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