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Urea-modified carbon quantum dots as electron mediator decorated g-C_3N_4/WO_3 with enhanced visible-light photocatalytic activity and mechanism insight

机译:尿素修饰的碳量子点作为电子介体修饰了g-C_3N_4 / WO_3,具有增强的可见光光催化活性和机理研究

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摘要

A novel urea modified carbon quantum dots (NCDs) decorated g-C3N4/WO3 Z-scheme heterojunction was prepared through in situ calcination and physical deposition way in the article. The analysis data of UV-vis spectroscopy demonstrated that the introduction of NCDs and the construction of g-C3N4/WO3 Z-scheme heterojunction can significantly improve the visible-light utilization. The enhanced photocurrent response and the reduced fluorescence intensity indicated the recombination of photogenerated electron-hole pairs in g-C3N4/WO3/NCDs composites is significantly inhibited. In addition, the results of cyclic experiment and the XRD diffraction peak of g-C3N4/WO3/NCDs before and after the experiment declared that g-C3N4/WO3/NCDs possess strong structural stability. Obviously, the excellent photocatalytic performance of g-C3N4/WO3/NCDs can be ascribed to the above three experimental processes. Experimental analysis of free radical capture confirmed that superoxide ion radicals (center dot O-2(-)) was the main active component in photocatalytic degradation, and the possible degradation mechanism of g-C3N4/WO3/NCDs was proposed.
机译:通过原位煅烧和物理沉积的方法,制备了一种新型的修饰g-C3N4 / WO3 Z-方案异质结的尿素修饰碳量子点。紫外-可见光谱的分析数据表明,引入NCD和构建g-C3N4 / WO3 Z方案异质结可以显着提高可见光利用率。增强的光电流响应和降低的荧光强度表明,g-C3N4 / WO3 / NCDs复合材料中光生电子-空穴对的重组受到显着抑制。另外,循环实验的结果和g-C3N4 / WO3 / NCDs的XRD衍射峰在实验前后都表明g-C3N4 / WO3 / NCDs具有很强的结构稳定性。显然,g-C3N4 / WO3 / NCDs优异的光催化性能可以归因于上述三个实验过程。自由基捕获的实验分析证实超氧离子自由基(中心点O-2(-))是光催化降解的主要活性成分,并提出了可能的g-C3N4 / WO3 / NCDs降解机理。

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