Heterojunction construction on covalent organic frameworks for visible-light-driven H2O2 evolution in ambient air

被引:22
|
作者
Xia, Guanglu [1 ]
Qiu, Jianhao [1 ]
Zhang, Lu [1 ]
Dai, Dingliang [1 ]
Yao, Jianfeng [1 ]
机构
[1] Nanjing Forestry Univ, Coll Chem Engn, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Nanjing 210037, Peoples R China
关键词
Covalent organic frameworks; H2O2; evolution; Photocatalysis; STRATEGY; MOS2;
D O I
10.1016/j.colsurfa.2023.131124
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
Photocatalytic H2O2 production by reducing O-2 has drawn great interest, but most reactions were conducted in pure O-2 which requires extra energy input. Here, TpPa-1 was facilely decorated by ZnIn2S4 nanosheets for H2O2 production in ambient air under visible light. Profiting from the hierarchical heterostructure, efficient visible-light absorption and O-2 capture of ZnIn2S4/TpPa-1, an H2O2 yield of 516 mu mol center dot L-1 was obtained with 2 h irradiation, which is 3.0 and 3.9 times those of blank TpPa-1 and ZnIn2S4, respectively. The intimate interface contact between ZnIn2S4 and TpPa-1 also contributes to the performance improvement. It is noted that the photocatalytic H2O2 formation over ZnIn2S4/TpPa-1 hybrids experienced an indirect reduction of O-2 that center dot O-2(-) served as the key intermediate. Additionally, the reactions under different atmospheres and ethanol concentrations demonstrate that both O-2 and ethanol play important roles in the efficient evolution of H2O2. This work could enlighten the heterostructure construction and (photo)catalytic H2O2 production based on covalent organic frameworks.
引用
收藏
页数:9
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