Bifunctional Metal-Organic Layer for Selective Photocatalytic Carbon Dioxide Reduction to Carbon Monoxide

被引:2
|
作者
Liao, Yingling [1 ,2 ]
Wang, Zitong [1 ]
Li, Jinhong [1 ]
Fan, Yingjie [1 ]
Wang, David [1 ]
Shi, Li [2 ]
Lin, Wenbin [1 ]
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[2] East China Univ Sci & Technol, Int Joint Res Ctr Green Energy Chem Engn, Shanghai 200237, Peoples R China
来源
ACS CATALYSIS | 2024年 / 14卷 / 22期
关键词
metal-organic framework; two-dimensional materials; heterogeneous photocatalysis; CO2; photoreduction; synergistic catalysis; CO2; REDUCTION; FRAMEWORKS; DESIGN; PHOTOREDUCTION; PLATFORMS; CATALYSIS; CHEMISTRY;
D O I
10.1021/acscatal.4c04772
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
We report a bifunctional metal-organic layer (MOL) as a photocatalyst for CO2 reduction to CO under visible light irradiation with a turnover number of 6990 in 24 h and a CO selectivity of 99%. The fully accessible and modifiable Hf-12 secondary building units and the coordinating porphyrin linkers of the MOL allow for the integration of both Ru photosensitizers and catalytic Fe-porphyrin sites into one single platform. The close distance (similar to 11 & Aring;) between the Ru photosensitizer and the catalytic center leads to enhanced electron transfer and promotes photocatalytic CO2 reduction. This strategy leads to an increase of the CO2-to-CO turnover number for the bifunctional MOL catalyst over a combination of a homogeneous Ru photosensitizer and an Fe-porphyrin complex. The mechanism of MOL-catalyzed CO2 photoreduction was also studied by photophysical and electrochemical experiments.
引用
收藏
页码:16957 / 16962
页数:6
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