2D Ti3C2 decorated Z-scheme BiOIO3/g-C3N4 heterojunction for the enhanced photocatalytic CO2 reduction activity under visible light

被引:39
|
作者
Hong, Long-fei [1 ]
Guo, Rui-tang [1 ,2 ]
Yuan, Ye [1 ]
Ji, Xiang-yin [1 ]
Lin, Zhi-dong [1 ]
Yin, Xue-feng [3 ]
Pan, Wei-guo [1 ,2 ]
机构
[1] Shanghai Univ Elect Power, Coll Energy & Mech Engn, Shanghai, Peoples R China
[2] Shanghai Engn Res Ctr Power Generat Environm Prot, Shanghai, Peoples R China
[3] Inner Mongolia Univ, Sch Ecol & Environm, Hohhot, Peoples R China
关键词
Z-scheme heterojunction; Photocatalysis; Ti3C2; MXene; BiOIO3; G-C3N4; COMPOSITE; COCATALYST; PERFORMANCE;
D O I
10.1016/j.colsurfa.2022.128358
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 development of photocatalytic technology can not only reduce CO2 emissions, but also realize the effective utilization of solar energy, thus alleviating the global energy crisis. In this work, BiOIO3/g-C3N4 Z-scheme heterojunction modified by Ti3C2 nanosheets was designed and fabricated through hydrothermal method and electrostatic self-assembly strategy. The g-C3N4/BiOIO3/Ti3C2 (4 wt%) photocatalytic system exhibited the optimal photocatalytic efficiency, reaching 5.88 and 1.55 mu mol/g/h for CO and CH4, respectively, and the CO production rate was 6.6 folds as high as that of bare g-C3N4. Various characterization techniques were utilized to research the physicochemical properties of as-prepared photocatalysts. Z-scheme heterojunction formed between g-C3N4 and BiOIO3 and the decorating of 2D Ti3C2 co-catalyst were responsible for the boosted photocatalytic behavior. Z-scheme heterojunction could prevent the recombination of charge carriers, the co-catalyst Ti3C2 acted as electron sink could achieve quick shift of photo-induced electrons and supply numerous active sites for photocatalytic reaction.
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页数:10
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