罗丹明B
X射线光电子能谱
光催化
全氟辛酸
材料科学
降级(电信)
漫反射红外傅里叶变换
扫描电子显微镜
化学工程
吸附
激进的
光化学
电子顺磁共振
氧气
漫反射
催化作用
化学
环境化学
复合材料
有机化学
物理
工程类
光学
电信
核磁共振
计算机科学
作者
Jianping Shang,Zhiqi Xue,Bin Huang,Zhiqin Cao
标识
DOI:10.1016/j.inoche.2023.111485
摘要
In this demonstration, SiO2/BiOCl composites were fabricated by loading SiO2 nanoparticles onto the surface of BiOCl nanosheets through a conventional hydrothermal approach. SiO2/BiOCl photocatalysts were studied by specific surface area analysis, X-ray diffraction (XRD), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), UV–Vis diffuse reflection spectroscopy (UV–Vis DRS) and electron spin resonance (ESR) techniques. In light of the rich pore structures of BiOCl modified by SiO2, the photogenerated carriers separation efficiency of SiO2/BiOCl is significantly improved. Therefore, SiO2/BiOCl composite nanosheets show high efficiency towards degradation of perfluorooctanoic acid (PFOA) and rhodamine B (RhB), and the composites display exceptional stability. In comparison to the pure BiOCl, photocatalytic degradation activity of 4.4 % SiO2/BiOCl (mass ratio of SiO2/Bi(NO3)3·5H2O is 4.4 %) for RhB and PFOA increases by 100 % and 50 %, respectively. The result from the radical capture experiments suggests that holes (h+) and superoxide radicals (·O2–) play a crucial role as the primary active species in degradation of organic pollutants. The enhanced photocatalytic efficiency of the SiO2/BiOCl composites can be primarily ascribed to the construction of numerous oxygen vacancies (OVs), which effectively promote the adsorption of organic pollutants, boost light responsiveness, and expedite the separation of photoinduced e-/h+ pairs.
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