Heterostructured S-Scheme BiOBr/Cu2O Nanocomposite for Photocatalytic Degradation of Glyphosate

被引:1
|
作者
Gonzalez, Albert [1 ]
Fionah, Abelline [1 ]
Bamiduro, Gbemisola J. [1 ]
Zahran, Elsayed M. [1 ]
机构
[1] Ball State Univ, Dept Chem, Muncie, IN 47306 USA
来源
ACS OMEGA | 2024年 / 9卷 / 49期
基金
美国国家科学基金会;
关键词
CU2O NANOPARTICLES; BISMUTH OXYHALIDES; HETEROJUNCTION; WATER; DRIVEN; GROUNDWATER; EVOLUTION; OXIDATION; FACILE; FACETS;
D O I
10.1021/acsomega.4c07304
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal oxide semiconductor-activated photocatalysis has become a promising sustainable technology for the mitigation of emerging organic pollutants. The rational design of a photocatalyst heterojunction allows the degradation of a broad range of organic contaminants. Herein, we optimized hydrothermal approaches for the facial synthesis of well-defined BiOBr/Cu2O heterojunction photocatalysts. Tuning the synthesis condition enhanced the interfacing of BiOBr and Cu2O nanostructures in the heterojunction photocatalyst, as confirmed by STEM, TEM, XPS, XRD, and BET analysis. The optimized BiOBr/Cu2O heterostructured photocatalyst demonstrated substantial activity in the degradation of both anionic and cationic dyes compared to the individual components. The enhanced nanocomposite exhibited complete degradation of glyphosate in 10 min of light irradiation and demonstrated high stability after five photocatalytic cycles. Our mechanistic and photoelectrochemical studies suggest that establishing an S-scheme heterojunction between BiOBr and Cu2O enhances the separation of photogenerated charge carriers and expands the redox potentials of the nanocomposite to allow high catalytic efficiency. These findings indicate that tuning the design of metal oxide heterojunctions promises applications in the remediation of a wide range of organic contaminants.
引用
收藏
页码:48512 / 48523
页数:12
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