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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Novel Z-scheme heterogeneous photo-Fenton-like g-C3N4/FeOCl for the pollutants degradation under visible light irradiation
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Novel Z-scheme heterogeneous photo-Fenton-like g-C3N4/FeOCl for the pollutants degradation under visible light irradiation

机译:新型Z形方案非均相光 - 芬顿般的G-C3N4 / FeoCl用于污染物下可见光照射下的降解

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Effective electron-hole separation efficiency is an important factor for enhanced photocatalytic activity. In this work, the Z-scheme heterogeneous photo-Fenton-like (HPF-like) g-C3N4/FeOCl catalysts were synthesized successfully by calcination method. The composites were applied for the photo-Fenton (PF) degradation of water pollutants with the assistance of H2O2. During this process, the color-less antibiotic tetracycline and dye rhodamine B were used as the target pollutants. Compared with pure FeOCl material, the Z-scheme g-C3N4/FeOCl composites reveal a higher PF catalytic activity under the irradiation of visible light. According to the experimental results, the enhanced catalytic activity of g-C3N4/FeOCl material was attributed to the formation of Z-scheme between g-C3N4 and FeOCl, which could promote the separation efficiency of electron-hole pairs induced by hybridization. Moreover, with the addition of g-C3N4, the increased specific surface area would further promoted the decomposition of H2O2 to form more (OH)-O-center dot. The results of radical trapping experiments and ESR confirmed the hydroxyl radical was the main active group in this process, indicating the Z-scheme was generated between g-C3N4 and FeOCl. Therefore, a possible mechanism of this HPF-like g-C3N4/FeOCl material was presented. This work may promote the development and application of FeOCl-based materials in the field of PF-like water pollutants treatment.
机译:有效的电子空穴分离效率是增强光催化活性的重要因素。在这项工作中,通过煅烧方法成功地合成了Z形方案非均相光芬顿样(HPF样)G-C3N4 / FeoCl催化剂。在H 2 O 2的辅助下,将复合材料施用于水污染物的水污染物的劣化。在此过程中,使用着色的抗生素四环素和染料罗丹明B作为目标污染物。与纯FeoCl材料相比,Z样方G-C3N4 / FeoCl复合材料揭示了可见光照射下的较高PF催化活性。根据实验结果,G-C3N4 / FeoCl材料的增强催化活性归因于G-C3N4和FeoC1之间的Z方案的形成,其可以促进通过杂交诱导的电子空穴对的分离效率。此外,随着G-C3N4的添加,增加的比表面积将进一步促进H2O2的分解形成更多(OH)-O中心点。自由基捕获实验和ESR的结果证实羟基是该过程中的主要活性基团,表明在G-C3N4和FeoCl之间产生Z方案。因此,提出了这种类似HPF样G-C3N4 / FeoCl材料的可能机制。这项工作可以促进PF样水污染物处理领域的FeoCl基材料的开发和应用。

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