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Accurate engineering of hexagonal hollow carbon nitride with carbon vacancies: enhanced photocatalytic H2 evolution and its mechanism
被引:41
|作者:
Chen, Xueru
[1
]
Li, Xin
[1
]
Li, Xue
[1
]
Lu, Huimin
[1
]
Wang, Lei
[1
]
Liu, Qianqian
[2
]
Li, Hongping
[3
]
Ding, Jing
[1
]
Wan, Hui
[1
]
Guan, Guofeng
[1
]
机构:
[1] Nanjing Tech Univ, Coll Chem Engn, Jiangsu Natl Synerget Innovat Ctr Adv Mat, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
[2] Jiangsu Univ, Inst Energy Res, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Suzhou Univ Sci & Technol, Res Ctr ForNanophoton & Nanoelect Mat, Sch Mat Sci & Engn, Suzhou 215009, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CHARGE SEPARATION;
G-C3N4;
SOLAR;
REDUCTION;
HETEROJUNCTION;
OXIDATION;
ACID;
CO2;
PERFORMANCE;
GENERATION;
D O I:
10.1039/d1ta05752a
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:
Vacancy engineering and morphology construction were integrated simultaneously by the self-assembly of melamine (MA) and cyanuric acid (CA) in the presence of P123 and H2SO4, which contributed to the hexagonal hollow carbon nitride with carbon vacancies (HHCN). P123 functioned as the structure directing agent and H2SO4 acted as the hole-maker and stability-maintainer, the synergistic effect of whom contributed to the hexagonal hollow structure. Meanwhile, the chemical oxidation etching of H2SO4 brought about carbon vacancies. Combined with experiments and DFT calculations, it was found that carbon vacancy improved the separation rate of photo-induced carriers as well as the adsorption capacity of reaction substrate (H2O molecules) and negatively shifted the CB potential. Therefore, HHCN was endowed with the superior photocatalytic hydrogen evolution rate (5140 mu mol h(-1) g(-1)), which was 18.3-fold higher than g-C3N4. Furthermore, the possible formation mechanism and photocatalytic mechanism were proposed. This work offered an excellent basis for vacancy engineering and morphology construction for the modification of carbon nitride.
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页码:20664 / 20675
页数:12
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