首页|改性g-C3N4光催化降解双酚A的研究进展

改性g-C3N4光催化降解双酚A的研究进展

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光催化技术可源源不断地利用清洁的太阳能来实现对内分泌干扰物双酚A(BPA)的有效降解,从而在众多降解方法中脱颖而出。类石墨相氮化碳(g-C3N4)作为经典的半导体材料,具有合成简单、热稳定性和化学稳定性好、经济无污染等优点,广泛应用于光催化降解领域。但是本体g-C3N4由于高的光生电子-空穴对复合率、较窄的可见光吸收范围以及较低的氧化电位,使得其降解BPA的性能大大降低。为了提高g-C3N4对BPA的降解能力,研究者采用多种改性方法对g-C3N4进行改性。本文主要综述了元素掺杂、形貌调控、异质结的构建以及共聚等手段对g-C3N4进行改性的进展,从电子结构、能带结构和光学性能等角度出发,详细总结了改性后g-C3N4对BPA的降解性能以及降解机理;其次,总结了 BPA常见的降解路径及安全性分析;最后针对改性g-C3N4降解BPA的有效选择性进行了展望。
Progress of photocatalytic degradation of bisphenol A by modified g-C3N4
Photocatalysis technology can continuously use clean solar energy to achieve effective degradation of the endocrine disruptor,bisphenol A(BPA),which stands out among many degradation methods.Graphite-like carbon nitride(g-C3N4),as a classic semiconductor material,has the advantages of simple synthesis,good thermal and chemical stability,economic and pollution-free,and is widely used in the field of photocatalytic degradation.However,due to the high recombination rate of photogenerated electron hole pairs,weak visible light absorption range and low oxidation potential of bulk g-C3N4,the performance of BPA degradation by bulk g-C3N4 is not high.In order to improve the degradation ability of g-C3N4 to BPA,a variety of modification methods are used to modify g-C3N4.This paper mainly reviewed the modification of g-C3N4 by means of element doping,morphology control,heterojunction construction and copolymerization.From the perspective of electronic structure,band structure and optical properties,the degradation performance and mechanism of modified g-C3N4 for BPA were summarized in detail.Secondly,the common degradation pathways and safety analysis of BPA were also summarized.Finally,effective selectivity for the degradation of BPA by modified g-C3N4 was prospected.

photocatalysisdegradationbisphenol Ag-C3N4modificationmechanismdegradation pathway

马香港、丁远、张俊格、刘应良、徐慎刚、曹少魁

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郑州大学材料科学与工程学院,河南郑州 450001

华东交通大学材料科学与工程学院,江西南昌 330013

光催化 降解 双酚A 类石墨相氮化碳 改性 机理 降解路径

2024

化工进展
中国化工学会,化学工业出版社

化工进展

CSTPCD北大核心
影响因子:1.062
ISSN:1000-6613
年,卷(期):2024.43(11)