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光电协同作用下Ag@AgBr/MgAl-LDH催化性能的研究

林双龙 何超 齐跃红 次立杰 周二鹏 李贺

燃料化学学报(中英文)2026,Vol.54Issue(1):31-39,9.
燃料化学学报(中英文)2026,Vol.54Issue(1):31-39,9.DOI:10.3724/2097-213X.2025.JFCT.0019

光电协同作用下Ag@AgBr/MgAl-LDH催化性能的研究

Study on the catalytic performance of Ag@AgBr/MgAl-LDH under photoelectric synergy

林双龙 1何超 2齐跃红 2次立杰 2周二鹏 2李贺3

作者信息

  • 1. 石家庄学院化工学院石家庄市低碳能源材料重点实验室,河北石家庄 050035||石家庄科佳建筑工程技术有限公司,河北石家庄 050035
  • 2. 石家庄学院化工学院石家庄市低碳能源材料重点实验室,河北石家庄 050035
  • 3. 河北华北制药华恒药业有限公司,河北石家庄 050035
  • 折叠

摘要

Abstract

In this paper,the Ag@AgBr/MgAl-LDH complex was prepared by hydrothermal,precipitation and photoreduction methods,and the target product,methylene blue(MB)solution,was catalytically degraded under the condition of photoelectric synergy,and the catalytic activity of the samples was studied by the degradation rate.By combining with Ag@AgBr,Ag@AgBr/MgAl-LDH composite photocatalytic materials can be prepared.Ag@AgBr has the surface plasmon resonance(SPR)effect,and a certain voltage is applied to it by an electrochemical workstation,which can promote the efficient separation of photogenerated electrons from holes and greatly reduce the recombination of the two,and greatly improve the activity of catalytic degradation.This study provides an effective solution to the environmental problems caused by pollution such as industrial wastewater and organic dyes,and has important research value and application prospects.During the experiment,the photocatalytic performance of the sample was studied by the difference in the degradation rate of the sample to the methylene blue solution.Through a series of chemical characterization and photoelectric activity tests such as XRD and SEM of the prepared materials,the material composition,microscopic morphology and particle size and other parameters of the samples were determined.Parameters such as the electrochemical properties of materials are characterized by the use of potentiostats;The optimal modification amount of the catalyst was determined by exploring the degradation rate of the composite under different Ag@AgBr modification amounts of the sample.The recovery performance of the catalyst was characterized by multiple test cycle experiments on the samples.The reaction mechanism of the catalyst was determined by quenching experiments;The reaction mechanism of the active substance was determined by quenching the experiment.Through experiments,it is proved that when the Ag@AgBr modification amount is 12.5%,the photoelectric synergistic degradation rate of Ag@AgBr/MgAl-LDH is the highest,and the degradation rate can reach 90.97%.Through XRD,SEM,ultraviolet-visible diffuse reflection and Fourier transform infrared(FT-IR)characterization of the material,it was proved that the Ag@AgBr was successfully modified to MgAl-LDH,and the material also had good hydrophilic properties.A series of electrochemical performance tests were carried out on Ag@AgBr/MgAl-LDH by electrochemical workstation to characterize the electrochemical properties of the materials,and the results showed that the composite electrode materials had low barrier widths and impedances,high catalytic degradation ability,and more catalytic reaction active sites.After 5 cycle experiments,the material still has a high degradation rate,so it can be found that the composite material has very good stability,less catalyst loss and no significant degradation rate.The experimental results show that the active species in the process of photoelectric synergistic degradation of Ag@AgBr/MgAl-LDH are quenched by using different quenchers,and the experimental results show that the active species in the process are h+and O2-.Finally,combined with a series of characterization and test results in this experiment,the electron transfer mechanism of the Ag@AgBr/MgAl-LDH complex during the degradation process was further explored.

关键词

亚甲基蓝/Ag@AgBr/MgAl-LDH/光电催化

Key words

methylene blue/Ag@AgBr/MgAl-LDH/electrically assisted photocatalysis

分类

化学化工

引用本文复制引用

林双龙,何超,齐跃红,次立杰,周二鹏,李贺..光电协同作用下Ag@AgBr/MgAl-LDH催化性能的研究[J].燃料化学学报(中英文),2026,54(1):31-39,9.

基金项目

Supported by the Beijing-Tianjin-Hebei Basic Research Cooperation Project(B2024106019)and Shijiazhuang Science and Technology Plan Project(2410709503).京津冀基础研究合作专项(B2024106019)和石家庄市科技计划项目(2410709503)资助 (B2024106019)

燃料化学学报(中英文)

2097-213X

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