4.8 Article

Ti3+ self-doped TiO2 nanotubes photoelectrode decorated with Ar-Fe2O3 derived from MIL-100(Fe): Enhanced photo-electrocatalytic performance for antibiotic degradation

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 310, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2022.121344

Keywords

Electrodeposition; Photo-electrocatalysis; Metal organic frameworks; Ti3+ self-doped; TiO2 nanotubes

Funding

  1. National Natural Science Foundation of China [51878258]
  2. National Youth Foundation of China [52000064]
  3. Changsha Municipal Natural Science Foundation [kq2014054]
  4. Special Funds for the Construction ofInnovative Provinces in Hunan [2021SK2040]
  5. Science and Technology Innovation Program of Hunan Province [2021RC3133]

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This study successfully prepared Ar-Fe2O3/Ti3+-TiO2-NTs photoelectrodes through multiple processes and achieved efficient degradation of antibiotics. The photoelectrodes exhibited excellent performance in various applications.
The low interfacial mass transfer efficiency between metal-organic framework (MOFs) and conductive substrates makes the development of MOFs-based photoelectrodes challenging. Herein, Ar-Fe2O3/Ti3+-TiO2-NTs photo electrodes are obtained through electrochemical reduction, pulsed deposition, MOFs self-assembly, and sculptural reduction processes. The target photoelectrodes achieve 100% degradation of tetracycline (TC) within 90 min, and the photo-electrocatalytic synergy factor is estimated to be 4.20. Ar-Fe2O3/Ti3+-TiO2-NTs photo electrodes also exhibit excellently in multiple antibiotics and real samples. The reduction self-doping of Ti3+ retains vertical orientation properties of nanotubes to provide a path for electronics, and heightens the light harvesting capacity. The pulse deposition improves the dispersibility of Fe, which is beneficial to the self assembly of MIL-100(Fe). After sculpture-reduction processes, Ar-Fe2O3 retains the porous structure of MIL100(Fe), and the heterojunction formed with Ti3+-TiO2-NTs can significantly enhance the interface charge transfer. This work enriches the electrochemical modification strategy of TiO2-NTs, and gives new insights into the development of MOFs-based photoelectrodes.

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