静电自组装法制备P25/g-C3N4异质结复合光催化剂及其性能研究

李勇, 阿旺洛卓, 刘曼玉, 张鸣清, 赵清华

现代化工 ›› 2023, Vol. 43 ›› Issue (S1) : 164 -167,172.

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现代化工 ›› 2023, Vol. 43 ›› Issue (S1) : 164-167,172. DOI: 10.16606/j.cnki.issn0253-4320.2023.S1.033
科研与开发

静电自组装法制备P25/g-C3N4异质结复合光催化剂及其性能研究

    李勇, 阿旺洛卓, 刘曼玉, 张鸣清, 赵清华
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Preparation of P25/g-C3N4 heterojunction composite photocatalyst by electrostatic self-assembly and study on its properties

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摘要

高性能光催化剂是当前光催化技术进入实际应用的关键。g-C3N4是具有可见光活性的热门光催化材料,然而因其光生电子-空穴对易复合、光催化性能不高,目前仍难以进入实际应用。为了提升g-C3N4的光催化性能,将g-C3N4与P25采用简单的静电自组装方法复合,成功制备了P25/g-C3N4异质结复合光催化剂。研究发现,在异质结的作用下复合光催化剂中光生电子-空穴对复合得到了有效抑制,光催化性能得到了大幅提升,且其光催化降解性能随P25含量的增加呈先增大后减小的趋势,样品20% P25/g-C3N4的光催化性能最大,能在30 min内实现对RhB溶液近70%的降解。

Abstract

High performance photocatalyst is the key to the practical application of current photocatalyst technology.Graphite phase carbon nitride (g-C3N4) is a popular photocatalyst material with visible light activity.However,due to its easy recombination of photogenerated electron and hole pairs,g-C3N4 shows a low photocatalytic performance and is still difficult to enter practical applications.In order to improve the photocatalytic performance of g-C3N4,a simple electrostatic self-assembly method is used to composite g-C3N4 with P25,and P25/g-C3N4 heterojunction composite photocatalyst is successfully prepared.It is found that under the action of heterojunction,the recombination between photogenerated electron and hole pair in the composite photocatalyst is effectively inhibited,and the photocatalytic performance is greatly improved.The photocatalytic degradation performance of the composite photocatalyst increases firstly and decrease then with the increasing P25 content.The photocatalytic performance of 20%P25/g-C3N4 sample is the best,and it can degrade nearly 70% of RhB solution within 30 minutes.

关键词

光催化 / 二氧化钛 / 石墨相氮化碳 / 异质结

Key words

photocatalysis / titanium dioxide / graphite phase carbon nitride / heterojunction

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静电自组装法制备P25/g-C3N4异质结复合光催化剂及其性能研究[J]. 现代化工, 2023, 43(S1): 164-167,172 DOI:10.16606/j.cnki.issn0253-4320.2023.S1.033

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