Intrinsic and external active sites of single-atom catalysts

被引:3
|
作者
Yao, Xue [1 ]
Halpren, Ethan [1 ]
Liu, Ye Zhou [1 ]
Shan, Chung Hsuan [1 ]
Chen, Zhi Wen [1 ]
Chen, Li Xin [1 ]
Singh, Chandra Veer [1 ,2 ]
机构
[1] Univ Toronto, Dept Mat Sci & Engn, Toronto, ON M5S 3E4, Canada
[2] Univ Toronto, Dept Mech & Ind Engn, Toronto, ON M5S 3G8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
METAL-ORGANIC FRAMEWORKS; OXYGEN REDUCTION REACTION; WATER-GAS SHIFT; CO OXIDATION; ELECTROCHEMICAL REDUCTION; HYDROGEN-PRODUCTION; NITROGEN REDUCTION; RATIONAL DESIGN; PORPHYRIN SHEET; DOPED GRAPHENE;
D O I
10.1016/j.isci.2023.107275
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Active components with suitable supports are the common paradigm for industrial catalysis, and the catalytic activity usually increases with minimizing the active component size, generating a new frontier in catalysis, single-atom catalysts (SACs). However, further improvement of SACs activity is limited by the relatively low loading of single atoms (SAs, which are heteroatoms for most SACs, i.e., external active sites) because of the highly favorable aggregation of single heteroatoms during preparation. Research interest should be shifted to investigate SACs with intrinsic SAs, which could circumvent the aggregation of external SAs and consequently increase the SAs loading while maintaining them individual to further improve the activity. In this review, SACs with external or intrinsic SAs are discussed and, at last, the perspectives and challenges for obtaining high-loading SACs with intrinsic SAs are outlined.
引用
收藏
页数:21
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