Carbon nitride with simultaneous porous network and O-doping for efficient solar-energy-driven hydrogen evolution

被引:589
作者
Huang, Zhen-Feng [1 ,2 ]
Song, Jiajia [1 ,2 ]
Pan, Lun [1 ,2 ]
Wang, Ziming [1 ]
Zhang, Xueqiang [1 ]
Zou, Ji-Jun [1 ,2 ]
Mi, Wenbo [3 ]
Zhang, Xiangwen [1 ,2 ]
Wang, Li [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Minist Educ, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[3] Tianjin Univ, Fac Sci, Tianjin Key Lab Low Dimens Mat Phys & Preparat Te, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Carbon nitride; Porous network; O-doping; Hydrogen evolution; MESOPOROUS TIO2; METAL; G-C3N4; WATER; PHOTOANODE; NANOWIRES; OXIDATION; STRATEGY; SPACE; SHELL;
D O I
10.1016/j.nanoen.2015.01.043
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Efficient charge separation and broaden light absorption are of crucial importance for solar-driven hydrogen evolution reaction (HER), and graphitic carbon nitride (g-C3N4) is a very promising photocatalyst for this reaction. Here we report a facile precursor pre-treatment method, by forming hydrogen bond-induced supramolecular aggregates, to fabricate g-C3N4 with simultaneous novel porous network and controllable O-doping. Experimental and DFT computation identified that O doping preferentially occurs on two-coordinated N position, and the porous network and O-doping synergetically promote the light harvesting and charge separation. As a result, this material shows 6.1 and 3.1 times higher HER activity (with apparent quantum efficiency of 7.8% at 420 nm) than bulk and even 3D porous g-C3N4. This work highlights that simply pre-treating the precursor can not only control the architecture but also introduce helpful foreign atoms or monomer in the matrix, which provides a useful strategy to design and fabricate highly efficient g-C3N4 photocatalyst. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:646 / 656
页数:11
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