Gonzalez Albert, Fionah Abelline, Bamiduro Gbemisola J, Zahran Elsayed M
Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.
ACS Omega. 2024 Nov 21;9(49):48512-48523. doi: 10.1021/acsomega.4c07304. eCollection 2024 Dec 10.
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/CuO heterojunction photocatalysts. Tuning the synthesis condition enhanced the interfacing of BiOBr and CuO nanostructures in the heterojunction photocatalyst, as confirmed by STEM, TEM, XPS, XRD, and BET analysis. The optimized BiOBr/CuO 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 CuO 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.
金属氧化物半导体激活的光催化已成为一种有前景的可持续技术,用于减轻新兴有机污染物的影响。光催化剂异质结的合理设计能够降解多种有机污染物。在此,我们优化了水热法,以便简便合成结构明确的BiOBr/CuO异质结光催化剂。通过扫描透射电子显微镜(STEM)、透射电子显微镜(TEM)、X射线光电子能谱(XPS)、X射线衍射(XRD)和比表面积分析(BET)证实,调节合成条件增强了异质结光催化剂中BiOBr和CuO纳米结构的界面结合。与单个组分相比,优化后的BiOBr/CuO异质结构光催化剂在降解阴离子和阳离子染料方面均表现出显著活性。这种增强的纳米复合材料在光照10分钟内实现了草甘膦的完全降解,并且在五个光催化循环后仍表现出高稳定性。我们的机理和光电化学研究表明,在BiOBr和CuO之间建立S型异质结可增强光生电荷载流子的分离,并扩展纳米复合材料的氧化还原电位,从而实现高催化效率。这些发现表明,调整金属氧化物异质结的设计有望应用于多种有机污染物的修复。