可扩展性
催化作用
路径(计算)
计算机科学
电化学储能
生化工程
钥匙(锁)
系统工程
过程集成
材料科学
能量转移
系统集成
能量转换
纳米技术
工艺工程
原子能
数码产品
储能
工程类
高效能源利用
多相催化
环境修复
能源消耗
过程(计算)
控制(管理)
理论(学习稳定性)
过程控制
清洁能源
化学能
化学过程
作者
Haojie Chen,Yu Wu,Jiajie Wang,Yuqi Zhu,Xi Liu,Gaoxia Zhang,Qianhui Li,Huihui Dai,Suhua Chen,Hongda Liu,Ziwei Wang,Jianping Zou
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-02-07
卷期号:16 (4): 2976-2997
被引量:9
标识
DOI:10.1021/acscatal.5c08694
摘要
Single-atom catalysts (SACs) demonstrate immense potential in energy conversion and environmental remediation due to their extreme atomic utilization and well-defined active sites. However, transitioning SACs from laboratory research to industrial applications remains challenging because scalable and controllable synthesis must be achieved while ensuring stability and seamless integration into functional devices. This review systematically summarizes recent advances in large-scale synthesis strategies for SACs, with a focus on the scientific principles governing precursor design, coordination environment modulation, and support interactions in determining the final atomic dispersion, metal loading, and stability across various synthesis routes, such as pyrolysis, molten salt templating, and ball-milling. Furthermore, the advantages of emerging techniques, such as Joule heating, microwave, and low-temperature synthesis, in the precise construction of active sites are thoroughly examined. Importantly, this review prospectively outlines design pathways for industrial applications, scalable synthesis routes utilizing waste materials, and integration strategies of SACs into catalytic membranes and electrochemical devices. These approaches effectively address key bottlenecks, including mass transfer limitations, catalyst recovery, and process scale-up. This review aims to provide a framework and theoretical guidance for the structure–function relationship from atomic structure to macroscopic performance, facilitating the transition of SACs from laboratory applications to industrial applications.
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