首页|期刊导航|实验技术与管理|钒酸铋/氧化铜异质结的可控构筑及其光催化降解四环素性能研究

钒酸铋/氧化铜异质结的可控构筑及其光催化降解四环素性能研究OA

Construction and photocatalytic tetracycline degradation performance of a bismuth vanadate-copper oxide heterojunction

中文摘要英文摘要

采用水热法构筑了BiVO4/CuO异质结光催化剂.XRD确认获得单斜相BiVO4和CuO复合结构;HRTEM显示界面晶格间距为0.308 nm和0.252 nm,对应BiVO4(121)和CuO(-111)晶面;EDS分析表明Bi∶V∶Cu原子比为1.02∶0.98∶1.05;XPS证实形成异质结结构.最优条件下(催化剂0.5 g/L,四环素20 mg/L,pH 7.0),BC-1样品对四环素的表观速率常数为 0.021 6 min-1,120 min 内降解率为 90.3%,矿化率为 85.6%,表观活化能为28.6 kJ/mol,·O2-和·OH是主要活性物种.

[Objective]To address the high carrier recombination rate and low degradation efficiency of traditional single-component photocatalysts,this study aims to construct efficient bismuth vanadate-copper oxide(BiVO4-CuO)heterojunction photocatalysts and investigate their performance in tetracycline degradation.[Methods]BiVO4-CuO heterojunction photocatalysts with different component ratios were prepared via a hydrothermal method and characterized using various analytical techniques to analyze their structural properties.The photocatalytic performance was evaluated using tetracycline as the target pollutant under visible light irradiation(λ>420 nm).The degradation mechanism was elucidated through kinetic analysis,active species trapping experiments,and electrochemical measurements.The effects of reaction temperature,pH,catalyst dosage,and initial tetracycline concentration on degradation efficiency were systematically investigated.[Results]The experimental results showed that 1)X-ray diffraction and high-resolution transmission electron microscopy confirmed the successful construction of a heterojunction structure with intimate contact between BiVO4(121)and CuO(-111)facets;2)under optimal conditions(catalyst dosage of 0.5 g/L;tetracycline concentration of 20 mg/L;pH 7.0),the BC-1 sample achieved an apparent rate constant of 0.021 6 min-1,with 90.3%degradation and 85.6%mineralization rates within 120 min;3)Mott-Schottky and X-ray photoelectron spectroscopy analyses verified the formation of a Z-scheme band structure favorable for carrier migration,extending the carrier lifetime to 15.6 ns;4)electron spin resonance and electrochemical tests revealed·O2-and·OH as the primary active species,achieving degradation through C—N and amide bond cleavage;5)after five cycles,the catalyst maintained 91.8%of its initial activity.[Conclusions]Through facet control and interface engineering,an efficient BiVO4-CuO heterojunction photocatalyst was successfully constructed.The Z-scheme band structure significantly enhanced the separation efficiency of photogenerated carriers,achieving effective degradation and mineralization of tetracycline.This work provides valuable insights for the development of high-performance composite photocatalytic materials.

党铭铭

湖南有色金属职业技术学院 资源环境系,湖南 株洲 412006

化学化工

BiVO4/CuO异质结晶面调控界面电荷转移光催化降解反应动力学活性物种

BiVO4/CuO heterojunctionfacet controlinterfacial charge transferphotocatalytic degradationreaction kineticsactive species

《实验技术与管理》 2026 (5)

98-104,7

2024年度湖南省自然科学基金项目(2024JJ8069)2024年度湖南省教育厅科学研究优秀青年项目(24B1108)2022年度湖南省普通高校青年骨干教师培养项目(湘教通[2022]287号)

10.16791/j.cnki.sjg.2026.05.013

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