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One-Step Nickel Foam Assisted Synthesis of Holey G-Carbon Nitride Nanosheets for Efficient Visible-Light Photocatalytic H2 Evolution
被引:85
|作者:
Fang, Zhenyuan
[1
]
Hong, Yuanzhi
[2
]
Li, Di
[3
]
Luo, Bifu
[1
]
Mao, Baodong
[1
]
Shi, Weidong
[1
]
机构:
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
[3] Jiangsu Univ, Inst Energy Res, Zhenjiang 212013, Peoples R China
基金:
中国国家自然科学基金;
关键词:
grphitic carbon nitride;
nanosheets;
ammonia decomposition;
photocatalysis;
hydrogen evolution;
HYDROGEN EVOLUTION;
G-C3N4;
NANOSHEETS;
POLYMERIC PHOTOCATALYST;
AMMONIA DECOMPOSITION;
POROUS G-C3N4;
DOPED G-C3N4;
WATER;
CATALYSTS;
SEMICONDUCTORS;
ENHANCEMENT;
D O I:
10.1021/acsami.8b04783
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Graphitic carbon nitride (g-C3N4) with layered structure represents one of the most promising metal-free photocatalysts. As yet, the direct one-step synthesis of ultrathin g-C3N4 nanosheets remains a challenge. Here, few-layered holey g-C3N4 nanosheets (CNS) were fabricated by simply introducing a piece of nickel foam over the precursors during the heating process. The as-prepared CNS with unique structural advantages exhibited superior photocatalytic water splitting activity (1871.09 mu mol h(-1) g(-1)) than bulk g-C3N4 (BCN) under visible light (lambda > 420 nm) (approximate to 31 fold). Its outstanding photocatalytic performance originated from the high specific surface area (240.34 m(2) g(-1)) and mesoporous structure, which endows CNS with more active sites, efficient exciton dissociation, and prolonged charge carrier lifetime. Moreover, the obvious upshift of the conduction band leads to a larger thermodynamic driving force for photocatalytic proton reduction. This methodology not only had the advantages for the direct and green synthesis of g-C3N4 nanosheets but also paved a new avenue to modify molecular structure and textural of g-C3N4 for advanced applications.
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页码:20521 / 20529
页数:9
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