Heteroatoms binary-doped hierarchical porous g-C3N4 nanobelts for remarkably enhanced visible-light-driven hydrogen evolution

被引:151
作者
Wu, Jiaojiao [1 ]
Li, Nan [1 ]
Zhang, Xiao-Hong [1 ]
Fang, Hua-Bin [1 ]
Zheng, Yan-Zhen [2 ]
Tao, Xia [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Res Ctr, Minist Educ High Grav Engn & Technol, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; photocatalyst; C; O co-doping; Hierarchical porous nanobelt; Visible photocatalytic H-2 evolution; GRAPHITIC CARBON NITRIDE; PHOTOCATALYTIC H-2 EVOLUTION; EFFICIENT PHOTOCATALYST; CODOPED G-C3N4; NANOSHEETS; OXYGEN; WATER; PHOTOREACTIVITY; SEMICONDUCTORS; SEPARATION;
D O I
10.1016/j.apcatb.2017.12.045
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
The heteroatoms C, O binary-doped g-C3N4 (C-O/CN) with hierarchical porous nanobelt architecture was synthesized via a straightforward template-free self-assembly method using dicyandiamide as g-C3N4 precursor and glutathione as C, O doping source. The as-prepared C-O/CN exhibits well-defined hierarchical nanobelt structure composed of porous nanosheets, resulting in obvious enhanced specific surface area (120 m(2) g(-1)). Particularly, C, O heteroatoms, introduced into the structure of g-C3N4 by substituting N atoms, induce narrowed bandgap for more effective visible-light harvesting and negatively shifted conduction band position for stronger reducibility of electrons for H-2 production. Such hierarchical porous C-O/CN nanobelts are demonstrated to be highly efficient in charge separation and transfer. Under optimal mass ratio of glutathione to dicyandiamide (0.1%), C-O/CN-0.1 shows a highest H-2 evolution rate of 18.38 mmol h(-1) g(-1) under visible-light (lambda > 420 nm) irradiation (about 79.9 times higher than that of the bulk g-C3N4) and a remarkable apparent quantum efficiency of 9.83% at 420 nm, which can be used as a promising low-cost photocatalyst for H-2 evolution.
引用
收藏
页码:61 / 70
页数:10
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