Cui Jinxian, Fu Yaomei, Song Jian, Meng Bo, Zhou Jie, Zhou Ziyan, Su Zhongmin
College of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong, 255000, China.
Shandong Engineering Research Center of Green and High-value Marine Fine Chemicals, Weifang University of Science and Technology Shouguang, Shandong, 262700, China.
ChemSusChem. 2023 Mar 22;16(6):e202202079. doi: 10.1002/cssc.202202079. Epub 2023 Jan 30.
The application of solar energy to convert CO into high-value chemicals and fuels has been considered a highly desirable approach to relieving the greenhouse effect and energy crisis. However, the exploration of appropriate photocatalysts remains a major challenge. Combining the respective advantages of covalent organic frameworks and metal-organic frameworks to construct covalent metal-organic frameworks (CMOFs) can be a valid strategy to provide efficient, reliable, and eco-friendly photocatalysts. In this study, a Cu cluster-based CMOF (JNM-2) is used as a photocatalyst for CO photoreduction under visible-light irradiation. JNM-2 exhibits remarkable efficiency in photocatalytic CO reduction with high production rates of HCOOH (9019 μmol g h ) and CO (835 μmol g h ). The active center, reaction intermediates, and product generation pathways are elucidated by in situ DRIFTS and DFT calculations. This work demonstrates the tremendous possibilities of CMOFs as photocatalysts for CO reduction and provides profound insights into the mechanism of CO conversion into HCOOH/CO by using a molecularly accurate structural model.
将太阳能应用于将一氧化碳转化为高价值化学品和燃料,被认为是缓解温室效应和能源危机的一种非常理想的方法。然而,探索合适的光催化剂仍然是一项重大挑战。结合共价有机框架和金属有机框架的各自优势来构建共价金属有机框架(CMOFs),可能是提供高效、可靠且环保的光催化剂的有效策略。在本研究中,一种基于铜簇的CMOF(JNM - 2)被用作可见光照射下一氧化碳光还原的光催化剂。JNM - 2在光催化一氧化碳还原方面表现出显著效率,甲酸(9019 μmol g⁻¹ h⁻¹)和一氧化碳(835 μmol g⁻¹ h⁻¹)的产率很高。通过原位漫反射红外傅里叶变换光谱(DRIFTS)和密度泛函理论(DFT)计算阐明了活性中心、反应中间体和产物生成途径。这项工作展示了CMOFs作为一氧化碳还原光催化剂的巨大潜力,并通过使用分子精确结构模型,为一氧化碳转化为甲酸/一氧化碳的机理提供了深刻见解。