In situ ionic-liquid-assisted synthesis of plasmonic photocatalyst Ag/AgBr/g-C3N4 with enhanced visible-light photocatalytic activity

被引:58
作者
Chen, Daimei [1 ]
Wang, Zhihong [1 ]
Du, Yue [1 ]
Yang, Gaolin [1 ]
Ren, Tiezhen [1 ]
Ding, Hao [1 ]
机构
[1] China Univ Geosci, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
g-C3N4; Organic compound; Photocatalysis; AgBr; Surface plasmon resonance; CARBON NITRIDE SEMICONDUCTORS; HIGHLY EFFICIENT; HYDROGEN-PRODUCTION; PHOTODEGRADATION; DEGRADATION; PERFORMANCE; FABRICATION; EVOLUTION; HYBRID; G-C3N4;
D O I
10.1016/j.cattod.2015.03.031
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of visible-light-induced Ag/AgBr/g-C3N4 nanocomposites were fabricated vis a one-pot and simple approach. The ionic liquid 1-octyl-3-methylimidazolium bromide ([Omim]Br) was introduced into the synthesis system, and served not only as the Br source but also as a dispersant. The Ag/AgBr nanoparticles were found to be highly dispersed on the sheets of g-C3N4. The Ag/AgBr/g-C3N4 nanocomposites showed much higher visible-light-driven photocatalytic activity than individual g-C3N4 and Ag/AgBr for organic compound degradation. The optimal Ag/AgBr content with the highest photocatalytic activity is determined to be 40%, which is almost 2.4 and 1.9 times higher than that those of individual g-C3N4 and Ag/AgBr for the degradation of methylene blue (MB), and 18.8 and 1.6 folds for the degradation of phenol. The enhancement in photocatalytic activity should be assigned to the extended light-absorption range and efficient charge separation as a result of the surface plasmon resonance effect of Ag-0 and the well-matched overlapping band-structure between Ag/AgBr and g-C3N4. Finally, the possible mechanism for the charge separation and transformation among Ag, AgBr and g-C3N4 ternary system under the visible light is proposed. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
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