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.
引用
收藏
页码:20521 / 20529
页数:9
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