光催化
材料科学
漫反射红外傅里叶变换
扫描电子显微镜
光谱学
傅里叶变换红外光谱
拉曼光谱
掺杂剂
溶剂热合成
带隙
光致发光
分析化学(期刊)
红外光谱学
核化学
化学工程
兴奋剂
无机化学
催化作用
化学
有机化学
光学
复合材料
光电子学
工程类
量子力学
物理
作者
Khirbet López-Velázquez,Jorge Luis Guzmán-Mar,Aracely Hernández-Ramírez,Edgar González-Juárez,Minerva Villanueva-Rodríguez
标识
DOI:10.1016/j.mssp.2020.105499
摘要
In this work, BiOBr photocatalyst co-doped with Fe and N (Fe–BiOBr–N) was synthesized by a microwave-assisted solvothermal method. This material was characterized by X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, N2 adsorption-desorption, X-ray photoelectronic spectrometry, UV–Vis diffuse reflectance spectroscopy, atomic absorption spectroscopy, elemental analysis, and photoluminescence techniques. The characterization of this material revealed the formation of flower-like structures and the successful incorporation of Fe and N in BiOBr. The incorporation of Fe and N in BiOBr caused a decrease of the band gap (from 2.87 to 1.92 eV), the crystal size (from 12.93 to 8.43 nm), and the recombination rate of photogenerated charges compared with unmodified BiOBr. Likewise, these dopants caused an increase in specific surface area (from 7 to 16 m2/g). The photocatalytic activity was assessed on the elimination of bisphenol A (BPA) under visible radiation. Fe–BiOBr–N exhibited higher photocatalytic activity than pristine BiOBr on the BPA degradation, allowing complete degradation and 65% of mineralization in 240 min, while using pristine BiOBr 40% of degradation and 20% of mineralization were obtained. Fe–BiOBr–N is a promising option for the effective elimination of persistent contaminants such as BPA in the aqueous medium, under visible radiation.
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