Heterogeneous Single-Atom Catalyst for Visible-Light-Driven High-Turnover CO2 Reduction: The Role of Electron Transfer

被引:401
|
作者
Gao, Chao [1 ,2 ]
Chen, Shuangming [1 ,2 ]
Wang, Ying [1 ,2 ]
Wang, Jiawen [1 ,2 ]
Zheng, Xusheng [1 ,2 ]
Zhu, Junfa [1 ,2 ]
Song, Li [1 ,2 ]
Zhang, Wenkai [3 ]
Xiong, Yujie [1 ,2 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, iChEM Collaborat Innovat Ctr Chem Energy Mat, Sch Chem & Mat Sci,Natl Synchrotron Radiat Lab, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, CAS Ctr Excellence Nanosci, Hefei 230026, Anhui, Peoples R China
[3] Beijing Normal Univ, Dept Phys, Beijing 100875, Peoples R China
基金
中国博士后科学基金; 国家重点研发计划;
关键词
active sites; carbon dioxide conversion; electron transfer; photocatalysis; single-atom catalysts; METAL-ORGANIC FRAMEWORKS; ARTIFICIAL PHOTOSYNTHESIS; CARBON-DIOXIDE; COORDINATION CHEMISTRY; WATER OXIDATION; GRAPHENE OXIDE; EFFICIENT; COMPLEX; SOLAR; STATE;
D O I
10.1002/adma.201704624
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Visible-light-driven conversion of CO2 into chemical fuels is an intriguing approach to address the energy and environmental challenges. In principle, light harvesting and catalytic reactions can be both optimized by combining the merits of homogeneous and heterogeneous photocatalysts; however, the efficiency of charge transfer between light absorbers and catalytic sites is often too low to limit the overall photocatalytic performance. In this communication, it is reported that the single-atom Co sites coordinated on the partially oxidized graphene nanosheets can serve as a highly active and durable heterogeneous catalyst for CO2 conversion, wherein the graphene bridges homogeneous light absorbers with single-atom catalytic sites for the efficient transfer of photoexcited electrons. As a result, the turnover number for CO production reaches a high value of 678 with an unprecedented turnover frequency of 3.77 min(-1), superior to those obtained with the state-of-theart heterogeneous photocatalysts. This work provides fresh insights into the design of catalytic sites toward photocatalytic CO2 conversion from the angle of single-atom catalysis and highlights the role of charge kinetics in bridging the gap between heterogeneous and homogeneous photocatalysts.
引用
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页数:9
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