光催化
X射线光电子能谱
可见光谱
扫描电子显微镜
材料科学
漫反射红外傅里叶变换
降级(电信)
电子顺磁共振
光谱学
化学工程
光化学
复合材料
催化作用
化学
光电子学
有机化学
物理
核磁共振
电信
量子力学
计算机科学
工程类
作者
Wenran Wang,Xueru Yu,Yutong Zhang,Liuqing Huang,Hongyi Wang,Cheng Gu,Zhanghao Chen
标识
DOI:10.1007/s00128-022-03629-w
摘要
Novel visible-light-driven Ag3PO4/AgBr/AgI photocatalysts were prepared via a simple self-assembly strategy combined with in-situ anion-exchanging process. The photocatalytic activity of Ag3PO4 was significantly improved by constructing double-Z system. Specifically, the obtained materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and UV-vis diffuse reflectance spectroscopy (DRS). Under visible light irradiation (λ > 420 nm), the Ag3PO4/AgBr/AgI photocatalysts showed much higher photocatalytic activity than bulk Ag3PO4 for the degradation of formaldehyde (HCHO), and 100% HCHO degradation could be obtained within 28 min. The degradation efficiency could be maintained in five cycles. Further electron paramagnetic resonance (ESR) tests demonstrated that both •OH and •O2- generated in the system. This study provides new insights into the fabrication of highly efficient visible-light-driven photocatalysts and facilitates their practical application in emerging environment issues.
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