Highly Efficient Visible-Light-Driven CO2-to-CO Conversion by Coordinatively Unsaturated Co-Salen Complexes in a Water- Containing System

被引:7
作者
Su, Chao [1 ]
Chen, Zilu [1 ]
Feng, Qin [1 ]
Wei, Fangsha [1 ]
Zhang, Mingling [1 ]
Mo, Anna [1 ]
Huang, Hai-Hua [1 ]
Hu, Huancheng [1 ]
Liu, Dongcheng [1 ]
机构
[1] Guangxi Normal Univ, Collaborat Innovat Ctr Guangxi Ethn Med, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; COBALT COMPLEXES; ELECTROCHEMICAL REDUCTION; PHOTOCATALYTIC REDUCTION; CARBON-DIOXIDE; AQUEOUS CO2; PHOTOREDUCTION; ELECTRON; IRON; MACROCYCLES;
D O I
10.1021/acs.inorgchem.2c02515
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The development of cost-effective catalysts for CO2 reduction is highly desired but remains a significant challenge. The unsaturated coordination metal center in a catalyst is favorable for the process of catalytic CO2 reduction. In this paper, two asymmetric salen ligands were used to synthesize two coordinatively unsaturated Co-salen complexes. The two Cosalen complexes exhibit an unsaturated coordination pattern and display high activity and CO selectivity for visible-light-driven CO2 reduction in a water containing system. The photocatalytic performance of 2 is higher than that of 1 because the reduction potential of the catalytic CoII center and the energy barrier of the catalytic transition states of 2 are lower than those of 1, with turnover numbers (TONCO), turnover frequencies (TOF), and CO selectivity values of 8640, 0.24 s-1, and 97% for 2, respectively. The photocatalytic reduction of CO2 to CO for 2 is well supported by control experiments and density functional theory (DFT) calculations.
引用
收藏
页码:19748 / 19755
页数:8
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