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具有光催化与光芬顿反应协同作用的2D/2D α-Fe2O3/g-C3N4 S型异质结用于高效降解四环素

王文亮 张灏纯 陈义钢 史海峰

物理化学学报2022,Vol.38Issue(7):87-96,10.
物理化学学报2022,Vol.38Issue(7):87-96,10.DOI:10.3866/PKU.WHXB202201008

具有光催化与光芬顿反应协同作用的2D/2D α-Fe2O3/g-C3N4 S型异质结用于高效降解四环素

Efficient Degradation of Tetracycline via Coupling of Photocatalysis and Photo-Fenton Processes over a 2D/2D α-Fe2O3/g-C3N4 S-Scheme Heterojunction Catalyst

王文亮 1张灏纯 1陈义钢 2史海峰1

作者信息

  • 1. 江南大学理学院,江苏无锡214122
  • 2. 南京医科大学附属无锡市第二人民医院普外科,江苏无锡214002
  • 折叠

摘要

Abstract

Graphitic carbon nitride(g-C3N4)has been widely used as a potential photocatalytic material for the removal of tetracycline from water.However,the poor visible light absorption ability and high recombination rate of the photogenerated charge significantly inhibit the catalytic activity of g-C3N4.Therefore,facile methods to improve the photocatalytic efficiency of g-C3N4 need to be developed.Hematite(α-Fe2O3),which has a good visible light absorption and corrosion resistance,is often used for photocatalysis and photo-Fenton reactions.Therefore,a two-dimension/two-dimension(2D/2D)S-scheme heterojunction constructed of g-C3N4 and α-Fe2O3 nanosheets could be expected to improve the degradation efficiency of tetracycline.In this study,2D/2D S-scheme α-Fe2O3/g-C3N4 photo-Fenton catalysts were prepared using a hydrothermal strategy.The photo-Fenton catalytic activity of α-Fe2O3/g-C3N4(α-Fe2O3 50%(w))was significantly improved by the addition of a small amount of H2O2,removing 78%of tetracycline within 20 min,which was approximately 3.5 and 5.8 times the removal achieved using α-Fe2O3 and g-C3N4,respectively.The high catalytic activity was attributed to the synergy between the photocatalysis and Fenton reaction promoted by the continuous Fe3+/Fe2+conversion over the 2D/2D S-scheme heterojunction.The 2D/2D S-scheme heterojunction was crucial in the fabrication of the α-Fe2O3/g-C3N4 photocatalyst with a large surface area,adequate active sites,and strong oxidation-reduction capability.Furthermore,the photo-Fenton reaction provided additional hydroxyl radicals for the degradation of tetracycline with the aid of H2O2.The excess reaction product(Fe3+)was reduced to Fe2+by the photogenerated electrons from the conduction band of α-Fe2O3.The resulting Fe2+could participate in the photo-Fenton reaction.The morphological structures of α-Fe2O3/g-C3N4 were analyzed using transmission electron microscopy to demonstrate the formation of a 2D/2D structure with face-to-face contact,and the optical properties of the composites were measured using ultraviolet-visible diffuse reflectance spectroscopy.α-Fe2O3/g-C3N4 possessed a significantly improved visible light absorption compared to g-C3N4.Five sequential cyclic degradation tests and X-ray diffraction(XRD)patterns obtained before and after the reaction showed that the α-Fe2O3/g-C3N4 composites possessed stable photo-Fenton catalytic activity and crystal structures.Transient photocurrent responses of α-Fe2O3/g-C3N4 demonstrated that the prepared composites exhibited a higher charge transfer efficiency compared to that of single α-Fe2O3 and g-C3N4.In addition,according to the photoluminescence analysis and active species trapping experiments,a possible S-scheme heterojunction charge transfer process in the photo-Fenton catalytic reaction was proposed.This study provided a promising method for the construction of a high-performance photo-Fenton catalytic system to remove antibiotics from wastewater.

关键词

光催化/芬顿反应/催化活性/S型异质结/2D/2D界面

Key words

Photocatalysis/Fenton reaction/Catalytic activity/S-scheme heterojunction/2D/2D interface

分类

化学化工

引用本文复制引用

王文亮,张灏纯,陈义钢,史海峰..具有光催化与光芬顿反应协同作用的2D/2D α-Fe2O3/g-C3N4 S型异质结用于高效降解四环素[J].物理化学学报,2022,38(7):87-96,10.

基金项目

This work was supported by the National Natural Science Foundation of China(22136002,22172064),Fundamental Research Funds for the Central Universities,China(JUSRP51716A),National Laboratory of Solid State Microstructures,Nanjing University,China(M34047),Wuxi Translational Medicine Center,China(2020ZHYB10)and Major Scientific Research Projects of Wuxi Health Committee,China(Z201901).Prof.Haifeng Shi was indebted to the Financial Support from the Qing Lan Project of Jiangsu Province,China.国家自然科学基金(22136002,22172064),中央高校基本科研业务费(JUSRP51716A),南京大学固体微结构国家重点实验室开放课题(M34047),无锡转化医学中心项目(2020ZHYB10),无锡市卫健委重大科研项目(Z201901)和江苏省青蓝工程项目资助 (22136002,22172064)

物理化学学报

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