合成和改性 g-C3N4 以改善可见光驱动的抗生素光催化降解的最新进展

Kingsley Igenepo John, Goen Ho, Dan Li
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摘要

氮化石墨碳(g-C3N4)是一种被广泛研究的可见光活性光催化剂,具有成本低、无毒、易于合成等优点。然而,由于电荷载流子的快速重组、低表面积和对可见光的吸收能力不足,其光催化效率低于标准。因此,以提高光催化性能为目标的 g-C3N4 改性研究引起了广泛关注。有关 g-C3N4 应用改性的综述文章已经发表了不少。然而,在概述和比较可用的改性策略以提高 g-C3N4 基催化剂在去除抗生素方面的光催化活性方面,所做的努力还很有限。目前还没有人尝试比较改性 g-C3N4 和其他已知催化剂在去除抗生素方面的光催化性能。针对这些问题,我们的研究回顾了已报道的 g-C3N4 改性策略,包括金属/非金属掺杂、缺陷调整、结构工程、异质结构形成等,并比较了它们在去除抗生素方面的性能。异质结构形成是研究最广泛、最有前景的 g-C3N4 改性途径,它具有卓越的活性。与其他已知光催化剂相比,异质结 g-C3N4 在降解特定抗生素方面表现出了竞争力。我们讨论了相关机理,最后揭示了目前在实际应用中面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent progresses in synthesis and modification of g-C3N4 for improving visible-light-driven photocatalytic degradation of antibiotics
Graphitic carbon nitride (g-C3N4) is a widely studied visible-light-active photocatalyst for low cost, non-toxicity, and facile synthesis. Nonetheless, its photocatalytic efficiency is below par, due to fast recombination of charge carriers, low surface area, and insufficient visible light absorption. Thus, the research on the modification of g-C3N4 targeting at enhanced photocatalytic performance has attracted extensive interest. A considerable amount of review articles have been published on the modification of g-C3N4 for applications. However, limited effort has been specially contributed to providing an overview and comparison on available modification strategies for improved photocatalytic activity of g-C3N4-based catalysts in antibiotics removal. There has been no attempt on the comparison of photocatalytic performances in antibiotics removal between modified g-C3N4 and other known catalysts. To address these, our study reviewed strategies that have been reported to modify g-C3N4, including metal/non-metal doping, defect tuning, structural engineering, heterostructure formation, etc. as well as compared their performances for antibiotics removal. The heterostructure formation was the most widely studied and promising route to modify g-C3N4 with superior activity. As compared to other known photocatalysts, the heterojunction g-C3N4 showed competitive performances in degradation of selected antibiotics. Related mechanisms were discussed, and finally, we revealed current challenges in practical application.
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