Photoinduced Hydration Boosts O2 Evolution on Co-Chelating Covalent Organic Framework

被引:42
作者
He, Yajun [2 ]
Liu, Guoyu [2 ]
Liu, Zheyuan [2 ]
Bi, Jinhong [1 ]
Yu, Yan [2 ]
Li, Liuyi [2 ]
机构
[1] Fuzhou Univ, Dept Environm Sci & Engn, Fuzhou 350108, Peoples R China
[2] Fuzhou Univ, Coll Mat Sci & Engn, Key Lab Adv Mat Technol, Fuzhou 350108, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE NI SITES; WATER OXIDATION; SELECTIVE PHOTOREDUCTION; REDUCTION;
D O I
10.1021/acsenergylett.3c00228
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The achievement of artificial photosynthesis relies on successful water oxidation and a detailed mechanistic understanding. Here, we demonstrate a photoinduced hydration pathway for O-2 evolution from water oxidation over an imine-linked covalent organic framework (COF) comprising electron-rich benzotrithiophene and electron-deficient benzothiadiazole units with atomically chelated Co sites. The experimental and theoretical results suggest that the water oxidation starts with the photoinduced hydration of imine groups. The subsequent oxidative deprotonation and intramolecular hydroxyl attack lead to O-O bond formation. The hydration path significantly averages the energy barriers of water oxidation, thus promoting O-2 evolution. Inspired by this fact, we fabricate a COF-based heterostructure, which realizes overall water splitting with H-2 and O-2 evolution rates of 450 and 212 mu mol center dot g(-1) h(-1), respectively.
引用
收藏
页码:1857 / 1863
页数:7
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