Citation: Yujia LI, Tianyu WANG, Fuxue WANG, Chongchen WANG. Direct Z-scheme MIL-100(Fe)/BiOBr heterojunctions: Construction and photo-Fenton degradation for sulfamethoxazole[J]. Chinese Journal of Inorganic Chemistry, ;2024, 40(3): 481-495. doi: 10.11862/CJIC.20230314 shu

Direct Z-scheme MIL-100(Fe)/BiOBr heterojunctions: Construction and photo-Fenton degradation for sulfamethoxazole

  • Corresponding author: Chongchen WANG, chongchenwang@126.com
  • Received Date: 18 August 2023
    Revised Date: 6 January 2024

Figures(13)

  • A series of MIL-100(Fe)/BiOBr direct Z-scheme heterojunctions was fabricated by the in-situ precipitation method. The crystal structures, micromorphology, optical adsorption property, and chemical states were estimated by powder X-ray diffraction (PXRD), Fourier transforms infrared (FTIR) spectra, UV-Vis diffuse reflectance spectra (UV-Vis DRS), scanning electron microscopy (SEM), high-resolution transmission electron microscope (HRTEM) and X-ray photoelectron spectra (XPS). The performance of photo-Fenton degradation for sulfamethoxazole (SMX) under low-powered light emitting diode lamp irradiation was explored. The catalytic degradation efficiency of SMX (5 mg·L-1) in the optimal reaction system (MB-7/Vis/H2O2, MB-7 was prepared when the mass of MIL-100 (Fe) was 70% of the mass of BiOBr) could reach 99.8% upon 70 min illumination. Meanwhile, the effects of H2O2 concentration, catalyst dosage, pH, and co-existing inorganic anions on SMX removal over MB-7/Vis/H2O2 were studied. The removal efficiency of SMX could reach above 95% after five consecutive operations, suggesting that MB-7 had good stability and reusability. The possible catalytic mechanism was unraveled by photoluminescence (PL) spectra, electrochemical measurements, radical trapping experiments, and electronic spin resonance (ESR) technique. The enhanced photo-Fenton reactivity could be attributed to the fabrication of heterostructures accelerated separation photocarriers and then induced the generation of reactive species and Fe3+/Fe2+ redox cycle.
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