In situ loading of Ag2WO4 on ultrathin g-C3N4 nanosheets with highly enhanced photocatalytic performance

被引:148
作者
Li, Yunfeng [1 ]
Jin, Renxi [1 ]
Fang, Xu [1 ]
Yang, Yang [1 ]
Yang, Man [1 ]
Liu, Xianchun [1 ]
Xing, Yan [1 ]
Song, Shuyan [2 ]
机构
[1] NE Normal Univ, Dept Chem, Jilin Prov Key Lab Adv Energy Mat, Changchun 130024, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Photocatalysis; Heterojunction; Nanosheets; g-C3N4; Composite materials; VISIBLE-LIGHT PHOTOCATALYSIS; PHOTODEGRADATION PERFORMANCE; HYDROGEN-PRODUCTION; REACTION-MECHANISM; FABRICATION; IRRADIATION; COMPOSITES; OXIDATION; HETEROJUNCTION; STABILITY;
D O I
10.1016/j.jhazmat.2016.04.011
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The g-C3N4 nanosheets (g-C3N4-NS) exhibit more excellent property than common bulk g-C3N4 (g-C3N4-B) due to their large surface areas, improved electron transport ability and well dispersion in water. In this work, ultrathin g-C3N4-NS with a thickness of about 2.7 nm have been synthesized by a simple thermal exfoliation of bulk g-C3N4, and then Ag2WO4 nanoparticles are in situ loaded on their surface to construct the Ag2WO4/g-C3N4-NS heterostructured photocatalysts. Due to their unique physicochemical properties, the as-prepared heterostructures possess a fast interfacial charge transfer and increased lifetime of photo-excited charge carriers, and exhibit much higher photocatalytic activity. Under visible light irradiation, the optimum photocatalytic activity of Ag2WO4/g-C3N4-NS composites is almost 53.6 and 26.5 times higher than that of pure g-C3N4-B and Ag2WO4/g-C3N4-B heterostructures towards the degradation of rhodamine B, respectively, and is almost 30.6 and 9.8 times higher towards the degradation of methyl orange, respectively. In addition, the natural sunlight photocatalytic activities of the as-prepared samples are also investigated. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:219 / 228
页数:10
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