化学
催化作用
选择性
光催化
密度泛函理论
金属salen络合物
光化学
过渡金属
可见光谱
选择性还原
营业额
还原(数学)
计算化学
有机化学
物理
光电子学
几何学
数学
作者
Chao Su,Zi‐Lu Chen,Feng Qin,Fangsha Wei,Mingling Zhang,Anna Mo,Hai‐Hua Huang,Huancheng Hu,Dongcheng Liu
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-11-23
卷期号:61 (49): 19748-19755
被引量:3
标识
DOI:10.1021/acs.inorgchem.2c02515
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 Co-salen 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.
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