Cerium and carbon-sulfur codoped mesoporous TiO2 nanocomposites for boosting visible light photocatalytic activity

被引:9
|
作者
Zheng, Fei [1 ,2 ,3 ]
Dong, Faqin [1 ,3 ]
Zhou, Lin [1 ,3 ]
Yu, Jieyu [1 ,3 ]
Luo, Xijie [1 ,3 ]
Zhang, Xingyu [1 ,3 ]
Lv, Zhenzhen [1 ,3 ]
Jiang, Luman [1 ,3 ]
Chen, Yuheng [1 ,3 ]
Liu, Mengqing [1 ,3 ]
机构
[1] Southwest Univ Sci & Technol, Key Lab Solid Waste Treatment & Resource Recycle, Mianyang 621010, Peoples R China
[2] Xichang Univ, Coll Sci, Xichang 615000, Peoples R China
[3] Southwest Univ Sci & Technol, Sch Environm & Resource, Mianyang 621010, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Mesoporous TiO 2; C -S codoping; Ce doping; Water remediation; Rare earths; HYDROTHERMAL SYNTHESIS; FACILE SYNTHESIS; PERFORMANCE; DEGRADATION; PHOTOELECTRODE; NANOPARTICLES; ENHANCEMENT; IRRADIATION; OXIDATION; NITROGEN;
D O I
10.1016/j.jre.2022.02.016
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ce and C-S codoped mesoporous TiO2 nanocomposites were synthesized via a sol-gel method integrated with an evaporation-induced self-assembly approach. The basic physicochemical characteristics of the synthetic samples were analyzed via a series of characterization techniques. The results reveal that C-S and Ce codoping on mesoporous TiO2 enhances the photocatalytic activity owing to the synergistic effect caused by narrowing the band gap, enhancing adsorption, trapping and transferring the excited e-/h+ pairs and suppressing the recombination of e-/h+ pairs. Furthermore, the obtained C,S-TiO2/CeO2 materials exhibit large specific surface areas and numerous pores which not only effectively improve the adsorption-enrichment capability, but also supply multi-dimensional mass and electron transfer channels. The photodegradation efficiency of RhB by C,S-TiO2/CeO2 within 40 min is nearly 100%, and its degradation efficiency is 6.63 times that of undoped TiO2. Recycling experiments show that mesoporous C,S-TiO2/CeO2 shows excellent recoverability and stability. Furthermore, by trapping experiments, .O2-, h+ and .OH are the predominant active species and a possible reaction mechanism is proposed.(c) 2022 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:539 / 549
页数:11
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