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首页> 外文期刊>Chemical engineering journal >Synthesis and characterization of 2D/0D g-C3N4/CdS-nitrogen doped hollow carbon spheres (NHCs) composites with enhanced visible light photodegradation activity for antibiotic
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Synthesis and characterization of 2D/0D g-C3N4/CdS-nitrogen doped hollow carbon spheres (NHCs) composites with enhanced visible light photodegradation activity for antibiotic

机译:2D / 0D G-C3N4 / Cds-氮掺杂中空碳球(NHCS)复合材料的合成与表征,具有增强的抗生素可见光光降解活性的复合材料

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摘要

Herein, the high surface area and efficient visible light (VSL) induced photocatalyst, namely 2D/0D g-C3N4/CdS-nitrogen doped hollow carbon spheres (NHCs) composites have been prepared. Firstly, the physicochemical, photoelectric and electronic structures (including band structure, density of state and charge density difference) properties of the obtained samples were studied. Then, the photocatalytic experiments indicated that the g-C3N4/CdS-NHCs composites performed a markedly improved VSL photocatalytic performance and photostability for cloxacillin antibiotic degradation compared with pure g-C3N4, CdS and g-C3N4/CdS heterojunction. The enhanced photocatalytic performance of g-C3N4/CdS-NHCs composites could ascribe to the synergy between g-C3N4/CdS heterojunction and NHCs, which obviously improved the specific surface area, the absorption of VSL, the transfer rate of electrons and the separation efficiency of photogenerated electron-hole pairs of the photocatalysts. Finally, the mechanism analysis showed that active substances h(+), center dot O-2(-), and center dot OH worked together in the photocatalytic process, which attack the beta-lactam, thiazolidine ring and amide group should be the fatal act for CLX mineralization.
机译:这里,已经制备了高表面积和高效可见光(VSL)诱导的光催化剂,即2D / 0D G-C3N4 / CDS-氮掺杂的中空碳球(NHCS)复合材料。首先,研究了所得样品的物理化学,光电和电子结构(包括带结构,状态和充电密度差)的性质。然后,光催化实验表明,与纯G-C3N4,CDS和G-C3N4 / CDS异质结相比,G-C3N4 / CDS-NHCS复合材料对克罗克里林蛋白抗生素降解进行明显改善的VSL光催化性能和光稳定性。 G-C3N4 / CDS-NHCS复合材料的增强的光催化性能可以归因于G-C3N4 / CDS异质结和NHC之间的协同作用,这明显改善了比表面积,VSL的吸收,电子传递速率和分离效率光催化剂的光静电电子空穴对。最后,机制分析表明,活性物质H(+),中心点O-2( - )和中心点OH在光催化过程中合作,攻击β-内酰胺,噻唑烷环和酰胺组应该是致命的CLX矿化法案。

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