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首页|期刊导航|武汉工程大学学报|C空位协同g-C3N4/BiOCl异质结对亚甲基蓝光催化降解性能的研究

C空位协同g-C3N4/BiOCl异质结对亚甲基蓝光催化降解性能的研究

王雪燕 袁嘉泽 何禄英

武汉工程大学学报2024,Vol.46Issue(5):490-496,542,8.
武汉工程大学学报2024,Vol.46Issue(5):490-496,542,8.DOI:10.19843/j.cnki.CN42-1779/TQ.202311012

C空位协同g-C3N4/BiOCl异质结对亚甲基蓝光催化降解性能的研究

Photocatalytic degradation of methylene blue by C-vacancy and g-C3N4/BiOCl heterojunction

王雪燕 1袁嘉泽 1何禄英1

作者信息

  • 1. 武汉工程大学化工与制药学院,绿色化工过程教育部重点实验室(武汉工程大学),湖北 武汉 430205
  • 折叠

摘要

Abstract

C-vacancy-containing g-C3N4 was synthesized using a hydrothermal method,and composite photocatalysts of g-C3N4/BiOCl with different BiOCl loadings were prepared.The structure,morphology,and light absorption properties of the photocatalysts were characterized using electron paramagnetic resonance,X-ray photoelectron spectroscopy,scanning electron microscopy,transmission electron microscopy,and ultraviolet-visible diffuse reflectance spectroscopy.Methylene blue was used as the degradation target to investigate the impact of carbon vacancies and BiOCl on the photocatalytic degradation performance of g-C3N4,along with the degradation mechanism of the composite photocatalyst.Results show that the synthesized composite photocatalyst,compared to BiOCl and g-C3N4 alone,can regulate the electronic structure and effectively separate photogenerated electrons and holes.This synergistic effect enhances the efficiency of photocatalytic degradation of methylene blue.With 70%BiOCl loading,the photocatalytic degradation efficiency of g-C3N4/BiOCl reached 88.6%after 90 minutes of light reaction,outperforming pure-phase g-C3N4 and BiOCl.

关键词

g-C3N4/BiOCl/碳空位/异质结/光催化降解

Key words

g-C3N4/BiOCl/carbon vacancy/heterojunction/photocatalytic degradation

分类

化学化工

引用本文复制引用

王雪燕,袁嘉泽,何禄英..C空位协同g-C3N4/BiOCl异质结对亚甲基蓝光催化降解性能的研究[J].武汉工程大学学报,2024,46(5):490-496,542,8.

基金项目

武汉工程大学第十四届研究生教育创新基金(CX2022026) (CX2022026)

武汉工程大学绿色化工过程教育部重点实验室创新基金(GCX2023005) (GCX2023005)

国家级大学生创新创业训练计划项目(202110490002) (202110490002)

武汉工程大学学报

1674-2869

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