Gradual carbon doping of graphitic carbon nitride towards metal-free visible light photocatalytic hydrogen evolution

被引:125
作者
Chen, Zhou [1 ]
Fan, Ting-Ting [1 ]
Yu, Xiang [1 ]
Wu, Qiu-Ling [1 ]
Zhu, Qiu-Hui [2 ]
Zhang, Li-Zhong [2 ]
Li, Jian-Hui [1 ]
Fang, Wei-Ping [1 ]
Yi, Xiao-Dong [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Natl Engn Lab Green Chem Prod Alcohols, Ethers & Esters, Xiamen 361005, Peoples R China
[2] Changji Univ, Dept Chem & Appl Chem, Changji 831100, Peoples R China
基金
中国国家自然科学基金;
关键词
POROUS G-C3N4; ARTIFICIAL PHOTOSYNTHESIS; H-2; GENERATION; NANOSHEETS; WATER; SEMICONDUCTORS; NANOPARTICLES; HETEROJUNCTIONS; CONSTRUCTION; TRANSITIONS;
D O I
10.1039/c8ta03303j
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
Efficient and economical photocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are required to replace expensive metal-based catalysts used in water splitting devices. Herein, we have developed an inexpensive route to synthesize a carbon-rich graphitic carbon nitride (C-rich g-C3N4) with both nitrogen vacancies and a porous structure, which, as a highly efficient photo-induced water splitting catalyst, can meet current demands. The effects of the porous structure, nitrogen vacancies and rich amount of carbon on the electronic band structure and charge transport of g-C3N4 are systematically elucidated. The C-rich g-C3N4 can not only effectively enhance the absorption of visible light, but can also improve the majority carrier mobility and promote photoelectron transport through the defect-induced mid-gap and multiple conductive carbon rings, thus synergistically elongating the diffusion length and lifetime of the photocarriers. Importantly, the metal-free C-rich g-C3N4 photocatalyst not only demonstrates a higher solar-driven hydrogen production performance, which is over 20.5 times that of pristine g-C3N4, but also exhibits an outstanding stability with minimal loss of catalytic activity.
引用
收藏
页码:15310 / 15319
页数:10
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