A Crystalline Partially Fluorinated Triazine Covalent Organic Framework for Efficient Photosynthesis of Hydrogen Peroxide

被引:263
作者
Wang, Haozhen [1 ]
Yang, Chao [2 ,3 ]
Chen, Fangshuai [1 ]
Zheng, Gengfeng [2 ,3 ]
Han, Qing [1 ]
机构
[1] Beijing Inst Technol, Key Lab Cluster Sci, Key Lab Photoelect Electrophoton Convers, Minist Educ China,Sch Chem & Chem Engn, Beijing 100081, Peoples R China
[2] Fudan Univ, Fac Chem & Mat Sci, Lab Adv Mat, Dept Chem, Shanghai 200438, Peoples R China
[3] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Fac Chem & Mat Sci, Shanghai 200438, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorination; Hydrogen Peroxide; Oxygen Reduction; Photocatalysis; Triazine Covalent Organic Frameworks; GRAPHITIC CARBON NITRIDE; PHOTOCATALYSTS; INSIGHTS;
D O I
10.1002/anie.202202328
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A partially fluorinated, metal-free, imine-linked two-dimensional triazine covalent organic framework (TF50-COF) photocatalyst was developed. Fluorine (F)-substituted and nonsubstituted units were integrated in equimolar amounts on the edge aromatic units, where they mediated two-electron O-2 photoreduction. F-substitution created an abundance of Lewis acid sites, which regulated the electronic distribution of adjacent carbon atoms and provided highly active sites for O-2 adsorption, and widened the visible-light-responsive range of the catalyst, while enhancing charge separation. Varying the proportion of F maximized the interlayer interactions of TF50-COF, resulting in improved crystallinity with faster carrier transfer and robust photostability. The TF50-COF catalyst demonstrates high selectivity and stability in O-2 photoreduction into H2O2, with a high H2O2 yield rate of 1739 mu mol h(-1) g(-1) and a remarkable apparent quantum efficiency of 5.1 % at 400 nm, exceeding the performance of previously reported nonmetal COF-based photocatalysts.
引用
收藏
页数:6
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