Oxygen functional groups in graphitic carbon nitride for enhanced photocatalysis

被引:112
作者
Liu, Shizhen [1 ,2 ]
Li, Degang [1 ,2 ,3 ]
Sun, Hongqi [1 ,2 ]
Ang, Ha Ming [1 ,2 ]
Tade, Moses O. [1 ,2 ]
Wang, Shaobin [1 ,2 ]
机构
[1] Curtin Univ, Dept Chem Engn, GPO Box U1987, Perth, WA 6845, Australia
[2] Curtin Univ, CRC Contaminat Assessment & Remediat Environm CRC, GPO Box U1987, Perth, WA 6845, Australia
[3] Shandong Univ Technol, Sch Chem Engn, Zibo 255049, Peoples R China
基金
澳大利亚研究理事会;
关键词
Water treatment; Oxygen modification; Metal-free catalyst; Graphitic carbon nitride; Photodegradation; TITANIUM-DIOXIDE; HYDROTHERMAL SYNTHESIS; ELECTRONIC-STRUCTURE; HYDROGEN-PRODUCTION; AIR PURIFICATION; FACILE APPROACH; CO2; REDUCTION; DOPED G-C3N4; GRAPHENE; HYBRID;
D O I
10.1016/j.jcis.2016.01.051
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
Metal-free semiconductors offer a new opportunity for environmental photocatalysis toward a potential breakthrough in high photo efficiency with complete prevention of metal leaching. In this study, graphitic carbon nitride (GCN) modified by oxygen functional groups was synthesized by a hydrothermal treatment of pristine GCN at different temperatures with H2O2. Insights into the emerging characteristics of the modified GCN in photocatalysis were obtained by determining the optical properties, band structure, electrochemical activity and pollutant degradation efficiency. It was found that the introduction of GCN with oxygen functional groups can enhance light absorption and accelerate electron transfer so as to improve the photocatalytic reaction efficiency. The photoinduced reactive radicals and the associated photodegradation were investigated by in situ electron paramagnetic resonance (EPR). The reactive radicals,O-center dot(2)- and (OH)-O-center dot, were responsible for organic degradation. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 182
页数:7
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