Thermal Exfoliation and Phosphorus Doping in Graphitic Carbon Nitride for Efficient Photocatalytic Hydrogen Production

被引:0
作者
Chen, Lu [1 ]
Zhang, Linzhu [1 ]
Xia, Yuzhou [1 ]
Huang, Renkun [1 ]
Liang, Ruowen [1 ]
Yan, Guiyang [1 ]
Wang, Xuxu [2 ]
机构
[1] Ningde Normal Univ, Fujian Prov Univ, Key Lab Green Energy & Environm Catalysis, Ningde 352100, Peoples R China
[2] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
来源
MOLECULES | 2024年 / 29卷 / 15期
关键词
graphitic carbon nitride; P doped; hydrogen evolution; thermal exfoliation; G-C3N4; NANOSHEETS; DOPED G-C3N4; COCATALYST; EVOLUTION; DEGRADATION; PERFORMANCE; PROMOTE;
D O I
10.3390/molecules29153666
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Photocatalytic H2 evolution has been regarded as a promising technology to alleviate the energy crisis. Designing graphitic carbon nitride materials with a large surface area, short diffusion paths for electrons, and more exposed reactive sites are beneficial for hydrogen evolution. In this study, a facile method was proposed to dope P into a graphitic carbon nitride framework by calcining melamine with 2-aminoethylphosphonic acid. Meanwhile, PCN nanosheets (PCNSs) were obtained through a thermal exfoliation strategy. Under visible light, the PCNS sample displayed a hydrogen evolution rate of 700 mu mol<middle dot>g-1<middle dot>h-1, which was 43.8-fold higher than that of pure g-C3N4. In addition, the PCNS photocatalyst also displayed good photostability for four consecutive cycles, with a total reaction time of 12 h. Its outstanding photocatalytic performance was attributed to the higher surface area exposing more reactive sites and the enlarged band edge for photoreduction potentials. This work provides a facile strategy to regulate catalytic structures, which may attract great research interest in the field of catalysis.
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页数:11
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