光催化
材料科学
X射线光电子能谱
扫描电子显微镜
电子顺磁共振
傅里叶变换红外光谱
光致发光
异质结
光谱学
带隙
漫反射红外傅里叶变换
可见光谱
分析化学(期刊)
光化学
核化学
化学工程
复合材料
光电子学
核磁共振
催化作用
化学
有机化学
工程类
物理
量子力学
作者
Zhanyao Gao,Binghua Yao,Fan Yang,Tiantian Xu,Yangqing He
标识
DOI:10.1016/j.mssp.2019.104882
摘要
A new kind of BiOBr-Bi composite with improved photocatalytic capabilities was successfully prepared by in-situ reduction. The X-ray diffraction (XRD), Scanning electron microscopy (SEM), Ultraviolet–visible spectroscopy (UV–VisDRS), X-ray photoelectron spectroscopy (XPS), Brunner-Emmet-Teller measurements (BET), Fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) and the electron paramagnetic resonance (EPR) were used to characterize the morphological structures, physical properties and surface element composition of the photocatalysts. In addition, photocatalytic activity was evaluated by degrading the antibiotic norfloxacin (NOR). The results showed that the BiOBr-Bi (40 mmol/L NaBH4) had the highest activity. The degradation rate reached 97.2%. The half-life of NOR was shortened to 25 min. Moreover, the results of capture experiments indicated that the main active groups involved in the photocatalytic process under visible light conditions were ·O2- and h+. The reason why the activity of the BiOBr-Bi material photocatalyst increased is that the heterojunction formed by BiOBr with wider bandgap and Bi metal with a lower Fermi level effectively inhibits the recombination of holes and photogenerated electrons, which leads to the enhancement of oxidation capacity.
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