Fabrication of C/X-TiO2@C3N4 NTs (X=N, F, Cl) composites by using phenolic organic pollutants as raw materials and their visible-light photocatalytic performance in different photocatalytic systems

被引:63
作者
Li, Kexin [1 ,2 ]
Zeng, Zhenxing [2 ]
Yan, Liushui [2 ]
Huo, Mingxin [1 ]
Guo, Yihang [1 ]
Luo, Shenglian [2 ]
Luo, Xubiao [2 ]
机构
[1] NE Normal Univ, Sch Environm, Jilin Engn Res Ctr Municipal Wastewater Treatment, Changchun 130117, Peoples R China
[2] NanChang Hangkong Univ, Key Lab Jiangxi Prov Persistent Pollutants Contro, Nanchang 330063, Peoples R China
基金
中国国家自然科学基金;
关键词
Heterojunction; Carbon nitride nanotubes; Co-doped titanium dioxide; Degradation; Hydrogen evolution; CARBON NITRIDE SEMICONDUCTORS; MILL WASTE-WATER; HYDROGEN EVOLUTION; PHOTOREDOX CATALYSIS; TREATMENT STRATEGY; DEGRADATION; G-C3N4; TIO2; NANOSHEETS; REMOVAL;
D O I
10.1016/j.apcatb.2016.01.046
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
A series of nonmetallic elements co-doped titanium dioxide coated carbon nitride nanotubes (C/X-TiO2@C3N4 NTs, X=N, F, Cl) was successfully prepared by a simple sol-gel-pyrolysis process using phenolic organic pollutants, titanium butoxide, and carbon nitride nanotubes as precursors. The morphology, porosity, phase and chemical structure, and optical and electronic property of as-prepared C/X-TiO2@C3N4 NTs were well characterized. The as-prepared C/X-TiO2@C3N4 NTs exhibited excellent visible-light photocatalytic activity in the conventional degradation and hydrogen evolution systems compared with traditional TiO2/g-C3N4 heterojunction, which is attributed to their unique tubular nanostructure and nonmetallic elements co-doped TiO2 component. Subsequently, the visible-light photocatalytic activity of C/X-TiO2@C3N4 NTs was further studied in the simultaneous hydrogen evolution with organic pollutant degradation system on the basis of our previous work. The reaction mechanisms in different photocatalytic systems were further discussed in detail. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 280
页数:12
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