Edge-Functionalized g-C3N4 Nanosheets as a Highly Efficient Metal-free Photocatalyst for Safe Drinking Water

被引:275
作者
Teng, Zhenyuan [1 ]
Yang, Nailiang [2 ,5 ]
Lv, Hongying [1 ]
Wang, Sicong [1 ]
Hu, Maozhi [4 ]
Wang, Chengyin [1 ]
Wang, Dan [2 ,5 ]
Wang, Guoxiu [1 ,3 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, 180 Si Wang Ting Rd, Yangzhou 225002, Jiangsu, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, 1 Beiertiao, Beijing 100190, Peoples R China
[3] Univ Technol Sydney, Ctr Clean Energy Technol, City Campus, Sydney, NSW 2007, Australia
[4] Yangzhou Univ, Test Ctr Yangzhou Univ, 48 Wen Hui Dong Rd, Yangzhou 225009, Jiangsu, Peoples R China
[5] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHITIC CARBON NITRIDE; VISIBLE-LIGHT; HYDROGEN EVOLUTION; ESCHERICHIA-COLI; HYBRID PHOTOCATALYST; HALF-METALLICITY; GRAPHENE; DISINFECTION; INACTIVATION; PERFORMANCE;
D O I
10.1016/j.chempr.2018.12.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solar water disinfection catalyzed by metal-free photocatalyst has emerged as a promising approach for clean water production. By using the edge-functionalized graphitic carbon nitride (g-C3N4) as photocatalytic disinfectants, we find that the pathogen-rich water can be rapidly purified in 30 min with a disinfection efficiency of over 99.9999% under visible-light irradiation, which meets the requirement for drinking water. The edge-functionalized g-C3N4 shows a first-order disinfection rate that is five times higher than the previously reported best metal-free photocatalyst but only consumes 1/10 of the catalyst. The catalytic activity is also comparable to that of the best metal-based photocatalyst. Results of the highest occupied molecular orbitals and Mulliken charge distribution reveal that the exposed -COOH and C=O groups at the edges of g-C3N4 nanosheets not only significantly promote charge separation but also induce the upward bending of the surface band, facilitating the generation of hydrogen peroxide.
引用
收藏
页码:664 / 680
页数:17
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