钴
菲咯啉
光催化
共价键
吸附
苯甲醛
共价有机骨架
齿合度
产量(工程)
分子
配体(生物化学)
化学
化学工程
材料科学
催化作用
复合材料
结晶学
有机化学
冶金
金属
生物化学
受体
工程类
作者
Lvye Ai,Qian Wang,Xiaowen Chen,Guofang Jiang
出处
期刊:Aggregate
[Wiley]
日期:2024-05-08
卷期号:5 (5)
被引量:4
摘要
Abstract Metalated covalent organic frameworks (COFs) for 2D and 3D topologies are continuously being developed, whereas metalated COFs with 1D topologies are still in their infancy. Here, a novel 1D phenanthroline‐based COF containing 4,4‐(1,10‐phenanthroline‐2,9‐diyl)bis[benzaldehyde] (PBA) is reported (PAD‐COF). Subsequently, a metalated 1D COF, Co SAS/PAD‐COF, is constructed using the bidentate ligand properties of PBA and anchoring the single Co atoms in PAD‐COF through a post‐synthetic modification strategy. This complex significantly improved the photocatalytic performance of PAD‐COF, and the CO yield of the optimized Co SAS/PAD‐COF was stable at 3091 µmol g −1 h −1 with a selectivity of 93%, which is approximately 43.7 times that of the original PAD‐COF. Experimental and theoretical results demonstrate the excellent CO 2 photoreduction activity of Co SAS/PAD‐COF owing to the synergistic effect of single Co catalytic sites and PAD‐COF. Among them, PAD‐COF, as the host, adsorbs CO 2 molecules and loads single Co atoms. Meanwhile, Co atoms function as catalytic sites and promote the adsorption and activation of CO 2 , while reducing the reaction energy barrier formed by the *COOH intermediates. Therefore, this unique metalated 1D COF provides a fresh approach to photocatalytic CO 2 reduction.
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