3D ordered macroporous sulfur-doped g-C3N4 /TiO2 S-scheme photocatalysts for efficient H2O2 production in pure water

被引:84
|
作者
Jiang, Zicong [1 ]
Long, Qing [1 ]
Cheng, Bei [1 ]
He, Rongan [2 ]
Wang, Linxi [3 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Changsha Univ, Hunan Key Lab Appl Environm Photocatalysis, Changsha 410022, Peoples R China
[3] China Univ Geosci, Fac Mat Sci & Chem, Lab Solar Fuel, Wuhan 430074, Peoples R China
来源
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY | 2023年 / 162卷
基金
中国国家自然科学基金;
关键词
Photocatalysis; Step-scheme heterojunction; Three dimensionally ordered macroporous; Hydrogen peroxide; O 2 reduction reaction; LIGHT HYDROGEN-PRODUCTION; CARBON NITRIDE; CHARGE-TRANSFER; HETEROJUNCTION; PEROXIDE; OXYGEN; NANOSHEETS; PHOSPHORUS; NITROGEN;
D O I
10.1016/j.jmst.2023.03.045
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Photocatalytic hydrogen peroxide (H2O2) production offers a clean and cost-efficient alternative to the traditional anthraquinone oxidation approach. Herein, a step-scheme (S-scheme) heterojunction photocat-alyst is fabricated by coupling TiO2 with three dimensionally ordered macroporous sulfur-doped graphitic carbon nitride (3DOM SCN/T) by electrostatic self-assembly. The optimized photocatalyst achieved a high photocatalytic H2O2 production activity with a yield of 2128 mu mol h -1g -1 without the addition of hole scavengers. The remarkable performance was attributed to the synergy between the 3DOM framework and the S-scheme heterojunction. The former enhances light harvesting and provides abundant active sites for surface reactions, while the latter promotes the spatial separation of photogenerated carriers and enhances the redox power. Finally, the mechanism of photocatalytic H2O2 production over the 3DOM SCN/T S-scheme composite is proposed. This work provides novel insights into the development of effi-cient photocatalysts for H2O2 production from water and O 2 .(c) 2023 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:1 / 10
页数:10
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