Sulfone-Modified Covalent Organic Frameworks Enabling Efficient Photocatalytic Hydrogen Peroxide Generation via One-Step Two-Electron O2 Reduction

被引:316
作者
Luo, Yu [1 ]
Zhang, Beiping [1 ]
Liu, Chenchen [1 ]
Xia, Dehua [2 ]
Ou, Xinwen [3 ]
Cai, Yanpeng [1 ]
Zhou, Yang [1 ]
Jiang, Jin [1 ]
Han, Bin [1 ]
机构
[1] Guangdong Univ Technol, Sch Ecol Environm & Resources, Key Lab City Cluster Environm Safety & Green Dev, Minist Educ, Guangzhou 510006, Peoples R China
[2] Sun Yat Sen Univ, Sch Environm Sci & Engn, Guangzhou 510275, Peoples R China
[3] Zhejiang Univ, Sch Phys, Zheda Rd 38, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
COFs; H2O2; Generation; Oxygen Reduction Reaction; Photosynthesis; Sulfone Units; G-C3N4; NANOSHEETS; CARBON NITRIDE; SINGLE-ATOM; H2O2; CATALYST;
D O I
10.1002/anie.202305355
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photocatalytic oxygen reduction reaction (ORR) offers a promising hydrogen peroxide (H2O2) synthetic strategy, especially the one-step two-electron (2e(-)) ORR route holds great potential in achieving highly efficient and selectivity. However, efficient one-step 2e(-) ORR is rarely harvested and the underlying mechanism for regulating the ORR pathways remains greatly obscure. Here, by loading sulfone units into covalent organic frameworks (FS-COFs), we present an efficient photocatalyst for H2O2 generation via one-step 2e(-) ORR from pure water and air. Under visible light irradiation, FS-COFs exert a superb H2O2 yield of 3904.2 mu mol h(-1) g(-1), outperforming most reported metal-free catalysts under similar conditions. Experimental and theoretical investigation reveals that the sulfone units accelerate the separation of photoinduced electron-hole (e(-)-h(+)) pairs, enhance the protonation of COFs, and promote O-2 adsorption in the Yeager-type, which jointly alters the reaction process from two-step 2e(-) ORR to the one-step one, thereby achieving efficient H2O2 generation with high selectivity.
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页数:8
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