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Single-Atom Catalysts on Covalent Organic Frameworks for CO2 Reduction
被引:13
|作者:
Wang, Rui
[1
]
Yuan, Yufei
[1
]
Bang, Ki-Taek
[1
]
Kim, Yoonseob
[1
]
机构:
[1] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Clear Water Bay, Hong Kong, Peoples R China
来源:
关键词:
Single-atom catalysts;
CO2;
reduction;
Covalent organic frameworks;
Macrocycles;
Ligand coordination;
CARBON-DIOXIDE;
ELECTROREDUCTION;
SITES;
ELECTROCATALYST;
D O I:
10.1021/acsmaterialsau.2c00061
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The long-unresolved issue of CO2 release and the resulting atmospheric change can be solved through the application of effective catalysts. Thus, single-atom catalysts (SACs) have been rapidly developed for the CO2 reduction reaction (CO2RR), as they show improved catalytic metrics and enable the generation of C2+ products. Among numerous novel SACs, such as those based on graphene, metal-organic frameworks, and covalent organic frameworks (COFs), the COF-based SACs are the most promising owing to their high stability, porosity, and designability. Considering this, we describe two synthesis methods of COF-based SACs: ligand coordination and macrocycle backbone integration, and explore the pros and cons of each. We also propose routes for designing superior COF-based SACs and evaluate the factors influencing CO(2)RRs over COF-based SACs, such as metal loading and ligand types.
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页码:28 / 36
页数:9
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