A molecular view of single-atom catalysis toward carbon dioxide conversion

被引:9
|
作者
Shang, Xin [1 ,2 ]
Yang, Xiaofeng [1 ]
Liu, Guodong [1 ]
Zhang, Tianyu [3 ]
Su, Xiong [1 ]
机构
[1] Chinese Acad Sci, State Key Lab Catalysis, Dalian Inst Chem Phys, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Beijing Forestry Univ, Coll Environm Sci & Engn, Beijing 100083, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
ELECTROCATALYTIC CO2 REDUCTION; METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYSTS; ELECTROCHEMICAL REDUCTION; SELECTIVE CO2; PHOTOCATALYTIC REDUCTION; SCHEME HETEROJUNCTION; SUPPORT INTERACTIONS; TUNING SELECTIVITY; FORMIC-ACID;
D O I
10.1039/d3sc06863c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon dioxide (CO2) conversion has attracted much interest recently owing to its importance in both scientific research and practical applications, but still faces a bottleneck in selectivity control and mechanism understanding owing to diversified active sites. Single-atom catalysts (SACs) featuring isolated and well-defined active centers are proved to not only exhibit unparalleled performances in various processes of CO2 conversion but also provide excellent research paradigms by circumventing the heterogeneity of active sites. Herein, we will not only critically review recent progress on the application of SACs in chemical CO2 conversion based on previous comprehension of general thermodynamics and kinetics, but also try to offer a multi-level understanding of SACs from a molecular point of view in terms of the central atom, coordination environment, support effect and synergy with other active centers. Meanwhile, crucial scientific issues of research methods will be also identified and highlighted, followed by a future outlook that is expected to present potential aspects of further developments. We present critical advances in single-atom catalysis toward CO2 transformation and address crucial issues about SACs from a molecular point of view.
引用
收藏
页码:4631 / 4708
页数:78
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