Edge electronic vacancy on ultrathin carbon nitride nanosheets anchoring O2 to boost H2O2 photoproduction

被引:97
|
作者
Liu, Lian-Lian [1 ]
Chen, Fei [1 ,2 ]
Wu, Jing-Hang [1 ]
Ke, Ming-Kun [1 ]
Cui, Chao [1 ]
Chen, Jie-Jie [1 ]
Yu, Han-Qing [1 ]
机构
[1] Univ Sci & Technol China, Dept Environm Sci & Engn, CAS Key Lab Urban Pollutant Convers, Hefei 230026, Peoples R China
[2] Chongqing Univ, Coll Environm & Ecol, Minist Educ, Key Lab Three Gorges Reservoir Reg Ecoenvironm, Chongqing 400045, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金; 中国博士后科学基金;
关键词
Electronic vacancy; H2O2; production; Oxygen reduction; Photocatalysis; Selectivity; HYDROGEN-PEROXIDE; ENERGY-CONVERSION; DOPED G-C3N4; WATER; NITROGEN; PHOTOCATALYST;
D O I
10.1016/j.apcatb.2021.120845
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 utilization of solar energy for hydrogen peroxide (H2O2) production using graphitic carbon nitride (g-C3N4) under visible light irradiation has attracted increasing interests due to its high efficiency and cost-effectiveness. However, this process is still limited by slow charge carrier migration. In this work, continuous regulation of band structure inside g-C3N4 is obtained by defect engineering through gradient calcination. The H2O2 production rate (4980 mu mol g-1 h-1) of nitrogen-defective g-C3N4 is 18 times higher than that of pristine g-C3N4. The pi*C--N-C signals in X-ray absorption near-edge structure spectrum decline, indicating an increased N-defects. The N-defects with the electronic vacancies in the heptazine intensifies its light-harvesting on g-C3N4 and also improve the selectivity of 2-electron O2 reduction. A quantitative structure-activity relationship between Ndefects and band structure is unveiled. This work offers an accessible strategy to design photocatalysts with desirable defect structures for energy conservation.
引用
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页数:12
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