Metal-free activation of H2O2 by g-C3N4 under visible light irradiation for the degradation of organic pollutants

被引:535
作者
Cui, Yanjuan [1 ]
Ding, Zhengxin [1 ]
Liu, Ping [1 ]
Antonietti, Markus [2 ]
Fu, Xianzhi [1 ]
Wang, Xinchen [1 ]
机构
[1] Fuzhou Univ, State Key Lab Breeding Base Photocatalysis, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
[2] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany
基金
中国国家自然科学基金;
关键词
HYDROGEN-PEROXIDE; RHODAMINE-B; PHOTOASSISTED DEGRADATION; OXIDATION; PHOTODEGRADATION; WATER; DYES; MORPHOLOGY; CATALYSIS; BENZENE;
D O I
10.1039/c1cp22820j
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
Semiconducting carbon nitride materials were successfully prepared via a thermal poly-condensation of dicyandiamide as a precursor at > 500 degrees C. The resulting materials were investigated as metal-free catalysts for the activation of H2O2 with visible light under mild conditions, using the decomposition of Rhodamine B (RhB) in aqueous solution as a model reaction. Results revealed that carbon nitride catalysts can activate H2O2 to generate reactive oxy-radicals under visible light irradiation without employment of any metal additives, leading to the mineralization of the dye. Factors affecting the degradation of organic compounds are pH values and the concentration of H2O2. Recycling of the catalyst indicated no obvious deactivation during the entire catalytic reaction, indicating good (photo) chemical stability of metal-free polymeric carbon nitride photocatalysts for environmental purification. This study demonstrated a promising approach for the activation of green oxidant, hydrogen peroxide, by the newly-developed polymer photocatalysts for environmental remediation and oxidation catalysis.
引用
收藏
页码:1455 / 1462
页数:8
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