光催化
三嗪
特里斯
共价键
过氧化氢
1,3,5-三嗪
化学
组合化学
催化作用
高分子化学
有机化学
生物化学
作者
Zhenwei Zhang,Qi Zhang,Yuxin Hou,Jiali Li,Shanshan Zhu,Hong Xia,Huijuan Yue,Xiaoming Liu
标识
DOI:10.1002/anie.202411546
摘要
Abstract Two‐dimensional covalent organic frameworks (2D‐COFs) have recently emerged as fascinating scaffolds for solar‐to‐chemical energy conversion because of their customizable structures and functionalities. Herein, two tris(triazolo)triazine‐based COF materials (namely COF‐JLU51 and COF‐JLU52) featuring large surface area, high crystallinity, excellent stability and photoelectric properties were designed and constructed for the first time. Remarkably, COF‐JLU51 gave an outstanding H 2 O 2 production rate of over 4200 μmol g −1 h −1 with excellent reusability in pure water and O 2 under one standard sun light, that higher than its isomorphic COF‐JLU52 and most of the reported metal‐free materials, owing to its superior generation, separation and transport of photogenerated carriers. Experimental and theoretical researches prove that the photocatalytic process undergoes a combination of indirect 2e − O 2 reduction reaction (ORR) and 4e − H 2 O oxidation reaction (WOR). Specifically, an ultrahigh yield of 7624.7 μmol g −1 h −1 with apparent quantum yield of 18.2 % for COF‐JLU52 was achieved in a 1 : 1 ratio of benzyl alcohol and water system. This finding contributes novel, nitrogen‐rich and high‐quality tris(triazolo)triazine‐based COF materials, and also designate their bright future in photocatalytic solar transformations.
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