Modifying g-C3N4 with oxidized Ti3C2 MXene for boosting photocatalytic U(VI) reduction performance

被引:32
作者
Li, Shutong [1 ,2 ]
Wang, Yun [1 ,2 ]
Wang, Jingjing [1 ,2 ]
Liang, Jianjun [1 ,2 ]
Li, Yuqiang [1 ,2 ]
Li, Ping [1 ,2 ]
机构
[1] Chinese Acad Sci, Northwest Inst Ecoenvironm & Resources, Lanzhou 730000, Peoples R China
[2] Key Lab Petr Resources, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Uranium; Reduction; g-C3N4; Ti3C2; GRAPHITIC CARBON NITRIDE; STATE Z-SCHEME; AQUEOUS-SOLUTION; HYDROGEN EVOLUTION; URANIUM EXTRACTION; VISIBLE-LIGHT; TIO2; REMOVAL; SPECTROSCOPY; NANOSHEETS;
D O I
10.1016/j.molliq.2021.117937
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
The photocatalytic reduction of U(VI) has been regarded as an efficient method for separating uranium from aqueous solution. This study is devoted to develop a catalyst with high photocatalytic efficiency for the reduction of U(VI). The decoration of Ti3C2 on carbon nitride (CN) remarkably improved the adsorption affinity for U(VI), the optical absorbance, and the separation efficiency of the photo-generated electrons and holes, which subsequently enhanced the photocatalytic performance for U(VI) reduction. Compared to pristine CN, the reaction constant of CN/TC-2 for the reduction of U(VI) improved by 14.05 times fold. Owing to the formation of TiO2 on Ti3C2 surface, an all-solid-state Z-scheme hetero-junction was formed, which was key for the efficient separation of charge carriers and the enhancement of the photocatalytic reactivity of CN/TC composites. During the photocatalytic reactions, U(VI) was reduced to U(IV), forming UO2+x (x < 0.25) deposits, and center dot O-2 acted as the dominant reduction species. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:8
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