Enhanced photocatalytic performance of heterostructure CNNS@Bi2WO6 photocatalysts towards degradation of organic pollution

光催化 罗丹明B X射线光电子能谱 材料科学 异质结 可见光谱 扫描电子显微镜 降级(电信) 化学工程 热液循环 吸收边 漫反射红外傅里叶变换 光化学 吸收(声学) 纳米技术 光电子学 化学 催化作用 带隙 计算机科学 复合材料 有机化学 电信 工程类
作者
Shiyun Li,Yuqiong Guo,Qiaoyu Zhang,Luxi Zhang,Pengjie Zhou,Małgorzata Aleksandrzak,Xuecheng Chen
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:48 (67): 26173-26186 被引量:8
标识
DOI:10.1016/j.ijhydene.2023.03.317
摘要

The flower-structured CNNS@Bi2WO6 heterostructure photocatalsts with enhanced photocatalytic performance were successfully fabricated by facile in-situ hydrothermal method. Compared with the g-C3N4 nanosheets (CNNS) and pure Bi2WO6, the flower-structured CNNS@Bi2WO6 heterostructure photocatalysts exhibited better photocatalytic performance and photocatalytic stability for degradation of rhodamine B (RhB) and tetracycline (TC) under visible. The effects of different CNNS contents on the photocatalytic efficiency of the heterostructure photocatalysts have been investigated. The results show that the CNNS@Bi2WO6 heterostructure photocatalst with CNNS mass ratio of 7% presents the best photocatalytic performance. The photocatalytic activity enhancement should be attributed to the effective separation of photogenerated electron-hole pairs and the efficient visible-light utilization efficiency. Compared with CNNS, the absorption of CNNS@Bi2WO6 photocatalysts in the visible region has been greatly strengthened, with red-shift absorption edge by the UV–vis diffuse reflectance spectra (DRS). The connection between CNNS and Bi2WO6 was studied by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The scavenging experiments with different trapping agents demonstrates that the photogenerated h+ in the system can play the main role during the RhB degradation process. Subsequently, the possible mechanism of photocatalytic degradation over flower-structured CNNS@Bi2WO6 heterostructure photocatalysts has been proposed.

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