堆积
光催化
材料科学
共价键
聚乙二醇
共价有机骨架
氢键
分解水
介孔材料
部分
化学工程
催化作用
纳米技术
多孔性
化学
复合材料
有机化学
分子
工程类
作者
Ting Zhou,Lei Wang,Xingye Huang,Junjuda Unruangsri,Hualei Zhang,Rong Wang,Qingliang Song,Qingyuan Yang,Weihua Li,Changchun Wang,Kaito Takahashi,Hangxun Xu,Jia Guo
标识
DOI:10.1038/s41467-021-24179-5
摘要
Two-dimensional covalent organic frameworks (2D COFs) featuring periodic frameworks, extended π-conjugation and layered stacking structures, have emerged as a promising class of materials for photocatalytic hydrogen evolution. Nevertheless, the layer-by-layer assembly in 2D COFs is not stable during the photocatalytic cycling in water, causing disordered stacking and declined activity. Here, we report an innovative strategy to stabilize the ordered arrangement of layered structures in 2D COFs for hydrogen evolution. Polyethylene glycol is filled up in the mesopore channels of a β-ketoenamine-linked COF containing benzothiadiazole moiety. This unique feature suppresses the dislocation of neighbouring layers and retains the columnar π-orbital arrays to facilitate free charge transport. The hydrogen evolution rate is therefore remarkably promoted under visible irradiation compared with that of the pristine COF. This study provides a general post-functionalization strategy for 2D COFs to enhance photocatalytic performances.
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