Enhanced electron separation on in-plane benzene-ring doped g-C3N4 nanosheets for visible light photocatalytic hydrogen evolution

被引:117
作者
Liu, Jian [1 ,2 ]
Yu, Yu [3 ]
Qi, Ruilian [1 ,2 ]
Cao, Changyan [1 ,2 ]
Liu, Xiaoyan [4 ]
Zheng, Yujun [4 ]
Song, Weiguo [1 ,2 ]
机构
[1] Chinese Acad Sci, CAS Res Educ Ctr Excellence Mol Sci, Lab Mol Nanostruct & Nanotechnol, Beijing Natl Lab Mol Sci,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Beijing Jiaotong Univ, Sch Sci, Beijing 100044, Peoples R China
[4] Shandong Univ, Sch Phys, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; In-plane; Benzene-ring doping; Hydrogen evolution; Photocatalysis; GRAPHITIC CARBON NITRIDE; IN-SITU; Z-SCHEME; WATER; PHOSPHORUS; GRAPHENE; NITROGEN;
D O I
10.1016/j.apcatb.2018.11.070
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
Solar-to-chemical energy conversion by photocatalytic hydrogen evolution (PHE) is critical for reduction of the pollution and storage of clean energy. To improve the solar conversion efficiency, it is highly imperative to accelerate the photocarrier separation and transportation through materials design. Herein, we describe a highly effective PHE catalyst based on in-plane benzene-ring doped g-C3N4 nanosheets heterostructure through the thermal co-polymerization of urea and 4, 4'-sulfonyldiphenol (BPS) followed by a controlled heat-etching step. The solid-state C-13 NMR confirms the existence of benzene-ring structure in g-C3N4 nanosheets. Experimental results and theoretical calculations show that the energy and electronic structure of the catalyst are optimally regulated, inducing increased light absorption and effectively accelerated separation of the photo-driven charge carriers. It exhibits enhanced photocatalytic hydrogen evolution efficiency with a PHE rate of 12.3 mmol h(-1) g(-1) (almost 12 times higher than that of pure g-C3N4 nanosheets) and the quantum efficiency of 17.7% at 420 nm.
引用
收藏
页码:459 / 464
页数:6
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