Nitrogen vacancy induced in situ g-C3N4 p-n homojunction for boosting visible light-driven hydrogen evolution

被引:101
|
作者
Liao, Yuwei [1 ]
Wang, Guohong [1 ]
Wang, Juan [1 ]
Wang, Kai [1 ]
Yan, Suding [1 ]
Su, Yaorong [2 ]
机构
[1] Hubei Normal Univ, Inst Adv Mat, Coll Chem & Chem Engn, Hubei Key Lab Pollutant Anal & Reuse Technol, Huangshi 435002, Hubei, Peoples R China
[2] Shenzhen Technol Univ, Coll New Mat & New Energies, Shenzhen 518118, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphitic carbon nitride; Nitrogen-vacancy; p-n homojunction; Photocatalysis; H-2; evolution;
D O I
10.1016/j.jcis.2020.12.009
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
Graphitic carbon nitride (g-C3N4) as a novel photocatalyst with great potentials has been extensively employed in solar-driven energy conversion. Herein, the novel in situ g-C3N4 p-n homojunction photocatalyst with nitrogen vacancies (NV-g-C3N4) is successfully fabricated via hydrothermal synthesis followed by two-step calcination. The in situ NV-g-C3N4 homojunction can be employed as an effective photocatalyst for hydrogen generation through water splitting under visible light, and the optimum rate constant of 3259.1 mu mol.g(-1).h(-1) is achieved, which is 8.7 times as high as that of pristine g-C3N4. Moreover, the markedly increased photocatalytic performance is ascribed to the enhanced light utilization, large specific surface area and unique nitrogen-vacated p-n homojunction structure, which provides more active sites and improves the separation of photo-excited electron-hole pairs. Besides, the underlying mechanism for efficient charge transportation and separation is also proposed. This work demonstrates that the remodeling of g-C3N4 p-n homojunction with nitrogen vacancies is a feasible way as highly efficient photocatalysts and might inspire some new strategies for energy and environmental applications. (c) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:110 / 120
页数:11
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