Carbon ring and molecular scaffold co-doped g-C3N4 heterostructural nanosheets for highly efficient hydrogen evolution

被引:6
|
作者
Zhou, Ling [1 ,2 ,3 ]
Hu, Kan [1 ,2 ,3 ]
Dong, Tengguo [1 ,2 ,3 ]
Wang, Qian [1 ,2 ,3 ]
Huang, Hengming [1 ,2 ,3 ]
Lu, Chunhua [1 ,2 ,3 ]
Kou, Jiahui [1 ,2 ,3 ]
Xu, Zhongzi [1 ,2 ,3 ]
机构
[1] Nanjing Tech Univ, Coll Mat Sci & Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
[2] Nanjing Tech Univ, Jiangsu Collaborat Innovat Ctr Adv Inorgan Funct, Nanjing 210009, Peoples R China
[3] Nanjing Tech Univ, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Graphitic carbon nitride; Carbon ring; Molecular scaffold; Copolymerization; Hydrogen evolution; PHOTOCATALYTIC ACTIVITY; NITRIDE; WATER; FABRICATION; ENHANCEMENT; ACTIVATION;
D O I
10.1016/j.materresbull.2021.111482
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Copolymerization is an efficient method to modulate the intrinsic properties of graphitic carbon nitride (g-C3N4). Herein, carbon ring and stereo molecular scaffold co-doped g-C3N4 heterostrcutural nanosheets are constructed for simultaneously enhanced photocatalytic hydrogen evolution under ordinary pressure. The carbon ring changes the in-plane connection of g-C3N4 by the sp(2)-hybridized C-N bonds, extending the delocalization of pi electrons. The stereo molecular scaffold loses the interlayer stacking of bulk g-C3N4 for easier exfoliation. The synergistic effect of the above two aspects can greatly improve the photocatalytic performance of AGCN. After thermal exfoliation, the highest photocatalytic hydrogen generation activity of A(0)(.2)G(0)(.3)CN-E sample is 12.9 times higher than that of MCN. This work provides a strategy to design g-C3N4 photocatalysts with enhanced photocatalytic activity by using synergistic effect.
引用
收藏
页数:8
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