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One-pot construction of Cu and O co-doped porous g-C(3)N(4) with enhanced photocatalytic performance towards the degradation of levofloxacin

Low visible light response and rapid recombination of photogeneration charge carriers have always been the main factors limiting the advanced application of g-C(3)N(4) (CN). Element doping has been confirmed to be an efficient method to improve the photocatalytic performance of CN. Here, a series of...

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Detalles Bibliográficos
Autores principales: Li, Feng, Zhu, Peng, Wang, Songmei, Xu, Xiuquan, Zhou, Zijun, Wu, Chundu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066014/
https://www.ncbi.nlm.nih.gov/pubmed/35515531
http://dx.doi.org/10.1039/c9ra02411e
Descripción
Sumario:Low visible light response and rapid recombination of photogeneration charge carriers have always been the main factors limiting the advanced application of g-C(3)N(4) (CN). Element doping has been confirmed to be an efficient method to improve the photocatalytic performance of CN. Here, a series of Cu and O co-doped porous g-C(3)N(4) (Cu/O-PCN) nanomaterials were successfully fabricated by a facile one-pot thermal polymerization approach for the first time. Compared to pure CN, the resulting Cu/O-PCN exhibited remarkably enhanced visible-light-driven photocatalytic activity towards levofloxacin (LEVO) degradation. The optimized sample of 0.5% Cu doped (Cu/O-PCN-3) presented the highest degradation rate constant of 0.0676 min(−1), which was about 6.2 times higher than that of CN. Furthermore, a substantial decrease in the residual toxicity against E. coli was observed after photocatalytic degradation treatment. The superior photocatalytic performance of Cu/O-PCN was mainly attributed to the synergistic advantages of stronger visible light response, larger specific surface area, and the more effective separation and transfer of photogenerated charge carriers. Moreover, according to the trapping experiments, ·O(2)(−) and h(+) were the major oxygen active species in the photocatalytic degradation process. Finally, the possible enhanced photocatalytic mechanism over Cu/O-PCN was proposed.