Anchoring Single-Atomic Metal Sites in Metalloporphyrin-Based Covalent Organic Frameworks for Enhanced Photocatalytic Hydrogen Evolution

被引:0
作者
Zhang, Yue [1 ,2 ,3 ]
Chen, Zi-Ao [2 ,4 ]
Xu, Zi-Jian [2 ,4 ]
Li, Jun-Yu [2 ,4 ]
Li, Xi-Ya [2 ]
Fang, Zhi-Bin [2 ,3 ,4 ]
Zhang, Teng [2 ,3 ,4 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fuzhou 350007, Fujian, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[3] Univ Chinese Acad Sci, Fujian Coll, Fuzhou 350002, Fujian, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
covalent organic framework; photocatalysis; water splitting; metalloporphyrin; single-atomic catalyst; WATER; DESIGN; CO2;
D O I
10.1002/cssc.202400556
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A photoactive covalent organic framework (COF) was built from metalloporphyrin and bipyridine monomers and single-atomic Pt sites were subsequently installed. Integrating photosensitizing metalloporphyrin and substrate-activating Pt(bpy) moieties in a single solid facilitates multielectron transfer and accelerates photocatalytic hydrogen evolution with a maximum production rate of 80.4 mmol h-1 gPt-1 and turnover frequency (TOF) of 15.7 h-1 observed. This work demonstrates that incorporation of single-atomic metal sites with photoactive COFs greatly enhances photocatalytic activity and provides an effective strategy for the design and construction of novel photocatalysts. Integrating photoactive metalloporphyrin and single-atomic Pt(bpy) moieties in a single covalent organic framework facilitates multielectron transfer and accelerates photocatalytic hydrogen evolution. with a maximum turnover frequency of 15.7 h-1 observed. image
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页数:7
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