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Facile synthesis of BiOI/CdWO4 p-n junctions: enhanced photocatalytic activities and photoelectrochemistry

机译:BioI / CDWO4 P-N结合合成:增强的光催化活动和光电化学

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摘要

In this work, a series of novel BiOI/CdWO4 p-n junction photocatalysts were successfully fabricated via a facile ultrasonic and stirring process. The photodegradation tests showed that the BiOI/CdWO4 p-n junction photocatalysts show enhanced efficiencies compared to pure BiOI and CdWO4. The best photocatalytic performance was obtained for the BC-2.0 sample, and the as prepared samples were studied by XRD, TEM, HRTEM, XPS, UV-vis DRS and photoluminescence (PL) spectroscopy. This enhancement may be predominantly attributed to the improvement of the photogenerated electronhole separation and migration efficiency of the synergy impact between BiOI and CdWO4. The efficient separation of electron-hole pairs because of the synergy impact between BiOI and CdWO4. Radical scavenger experiments and ESR indicated that holes (h(+)) and superoxide radicals (O-center dot(2)) were the main active species in the photocatalytic process.
机译:在这项工作中,通过容易的超声波和搅拌方法成功制造了一系列新型的BioI / Cdwo4 P-N结光催化剂。 光降解试验表明,与纯BIOI和CDWO4相比,BIOI / CDWO4 P-N结光催化剂显示出增强的效率。 为BC-2.0样品获得最佳的光催化性能,并通过XRD,TEM,HRTEM,XPS,UV-VIS DRS和光致发光(PL)光谱来研究作为制备的样品。 这种增强可以主要归因于改善BioI和CdWO4之间的协同撞击的光发化电子孔分离和迁移效率。 电子孔对的有效分离,因为生物和CDWO4之间的协同效应。 自由基清除剂实验和ESR表示孔(H(+))和超氧化物自由基(O-Center Dot(2))是光催化过程中的主要活性物质。

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  • 来源
    《RSC Advances》 |2016年第44期|共10页
  • 作者单位

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

    Jiangsu Univ Sch Chem &

    Chem Engn Zhenjiang 212013 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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