4.6 Article

Fabrication and Characterization of Co-Doped Fe2O3 Spindles for the Enhanced Photo-Fenton Catalytic Degradation of Tetracycline

Journal

ACS OMEGA
Volume 6, Issue 49, Pages 33717-33727

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c04950

Keywords

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Funding

  1. National Natural Science Foundation of China [51802305, 52072079]
  2. Natural Science Foundation of Guangdong Province [2021A1515010445]
  3. Science and Technology Program of Guangzhou City [201904010131]
  4. Analytical & Testing Center, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, China

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The study successfully prepared Co-doped Fe2O3 spindles with different Co contents and showed their improved photocatalytic and photo-Fenton catalytic performances. The Co(5%)-Fe2O3 spindles exhibited the highest activity and best stability, attributed to the reduction of band gap, establishment of an internal electric field, and acceleration of Fe2+/Fe3+ redox cycling.
Co-doped Fe2O3 spindles with different Co contents were successfully fabricated by a facile one-step hydrothermal method. The crystalline structure, morphology, optical properties, and chemical state of the as-prepared catalysts before and after photo-Fenton reaction were characterized. Co2+ incorporated into the Fe2O3 lattice was confirmed by the above characterizations. Also, the photocatalytic and photo-Fenton catalytic performances of the samples were evaluated by the degradation of tetracycline (TC) under visible light irradiation in the absence/presence of H2O2. The results demonstrated that Co-doped Fe2O3 spindles exhibited better catalytic degradation performance in comparison with single Fe2O3 spindles, and the sample of Co(5%)-Fe2O3 spindles displayed the highest activity and best stability. The improvement of photo-Fenton activity might be attributed to two reasons: On the one hand, Co-doped Fe2O, spindles not only formed the Fe vacancies to reduce the band gap but also could build up an internal electric field, which inhibits electron/hole pair recombination and facilitates the transfer of photoexcited charge carriers. On the other hand, the intrinsic Co2+/Co3+ redox cycling can accelerate the circulation between Fe2+ and Fe3+ in Co(5%)-Fe2O3 spindles to facilitate H2O2 consumption and produce more center dot OH radicals for TC degradation.

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