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Synthesis of visible-light-driven BiOBrxI1-xsolid solution nanoplates by ultrasound-assisted hydrolysis method with tunable bandgap and superior photocatalytic activity

机译:具有可调带隙和优异光催化活性的超声辅助水解法合成可见光驱动的BiOBrxI1-x固溶体纳米板

摘要

In this study, a series of visible-light-driven BiOBrxI1-xsolid solution nanoplates photocatalysts are successfully prepared by an ultrasound-assisted hydrolysis method, which does not use organic reagents, with advantages of cost-effectiveness and non-toxicity. Under visible-light irradiation, all of the as-prepared BiOBrxI1-xnanoplates exhibit superior photocatalytic activities compared to those of pure BiOBr and BiOI for the degradation of methyl orange (MO). BiOBr0.3I0.7exhibits the highest photocatalytic activity, corresponding to the degradation of 92% MO in 40 min under visible-light irradiation. The structures and elemental composition of the as-prepared BiOBrxI1-xnanoplates samples are characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, and high-resolution transmission electron microscopy. From the results obtained from X-ray photoelectron spectroscopy, UV–vis diffuse reflectance spectroscopy, and transient time-resolved luminescence decay, it is suggested that the enhanced photocatalytic activity of BiOBrxI1-xis possibly related to the narrowing of the band gap and high separation of the photo-generated electron–hole pairs. Electron paramagnetic resonance and mechanistic experiments indicated that [rad]O2−and h+are active radicals for photocatalytic degradation. In conclusion, an ultrasound-assisted hydrolysis method which is free of organic reagents is developed for synthesizing BiOBrxI1-xnanoplates photocatalysts with tunable bandgap and enhanced photocatalytic activity.
机译:本研究通过超声辅助水解法成功制备了一系列可见光驱动的BiOBrxI1-x固溶体纳米板光催化剂,该方法不使用有机试剂,具有成本效益高,无毒的优点。在可见光照射下,与纯BiOBr和BiOI相比,所有制备的BiOBrxI1-xnanoplates均具有优异的光催化活性,可降解甲基橙(MO)。 BiOBr0.3I0.7表现出最高的光催化活性,对应于可见光照射下40分钟内92%MO的降解。通过X射线粉末衍射,扫描电子显微镜,透射电子显微镜和高分辨率透射电子显微镜对制备的BiOBrxI1-xnanoplate样品的结构和元素组成进行表征。从X射线光电子能谱,紫外可见漫反射光谱和瞬态时间分辨发光衰减获得的结果表明,BiOBrxI1-xis的增强的光催化活性可能与带隙变窄和高分离度有关。光生电子-空穴对的数量。电子顺磁共振和机理实验表明,[rad] O2-和h +是光催化降解的活性基团。总之,开发了一种不含有机试剂的超声辅助水解方法,用于合成带隙可调且光催化活性增强的BiOBrxI1-xnanoplates光催化剂。

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