光催化
共价键
活性氧
氧气
共价有机骨架
吸附
化学
析氧
光化学
密度泛函理论
选择性
材料科学
化学工程
纳米技术
催化作用
有机化学
计算化学
电极
物理化学
生物化学
工程类
电化学
作者
Suleman Suleman,Xinyu Guan,Yi Zhang,Amir Waseem,Önder Metin,Zheng Meng,Hai‐Long Jiang
标识
DOI:10.1016/j.cej.2023.146623
摘要
Regulating the generation of reactive oxygen species (ROS) impacts the selectivity and activity of photocatalytic oxidation, but the frequently concurrent formation of different types of ROS makes this process rather challenging. This study demonstrates the regulated production of two important ROS, 1O2 and O2•−, using a covalent-organic framework (COF) array with three members, which are made up of metalloporphyrin cores with embedded center metal ions from d-block transition metals sequentially arranged in the periodic table. Due to the evolution of the electronic structures in this COF array, the production of 1O2 and O2•− is controlled, which successively leads to distinct performance in photocatalytic aerobic oxidations. The electronic property study and density-functional theory (DFT) calculations revealed that the distinct excitonic behavior of three COFs in regulated 1O2 and O2•− generation is rooted in their different band energy levels and O2 adsorption ability. Our work presents an effective approach to the controlled production of ROS for improved photocatalytic performance.
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