双金属片
催化作用
分解水
析氧
贵金属
电化学
Atom(片上系统)
氧化还原
电催化剂
制氢
纳米技术
化学
化学工程
材料科学
工程类
计算机科学
无机化学
物理化学
电极
有机化学
光催化
嵌入式系统
作者
Nasar Alam,Tayyaba Nооr,Naseem Iqbal
出处
期刊:Chemical Record
[Wiley]
日期:2024-02-19
卷期号:24 (3): e202300330-e202300330
被引量:9
标识
DOI:10.1002/tcr.202300330
摘要
Electrochemical water splitting for sustainable hydrogen and oxygen production have shown enormous potentials. However, this method needs low-cost and highly active catalysts. Traditional nano catalysts, while effective, have limits since their active sites are mostly restricted to the surface and edges, leaving interior surfaces unexposed in redox reactions. Single atom catalysts (SACs), which take advantage of high atom utilization and quantum size effects, have recently become appealing electrocatalysts. Strong interaction between active sites and support in SACs have considerably improved the catalytic efficiency and long-term stability, outperforming their nano-counterparts. This review's first section examines the Hydrogen Evolution Reaction (HER) and the Oxygen Evolution Reaction (OER). In the next section, SACs are categorized as noble metal, non-noble metal, and bimetallic synergistic SACs. In addition, this review emphasizes developing methodologies for effective SAC design, such as mass loading optimization, electrical structure modulation, and the critical role of support materials. Finally, Carbon-based materials and metal oxides are being explored as possible supports for SACs. Importantly, for the first time, this review opens a discussion on waste-derived supports for single atom catalysts used in electrochemical reactions, providing a cost-effective dimension to this vibrant research field. The well-known design techniques discussed here may help in development of electrocatalysts for effective water splitting.
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