4.7 Article

Enhanced photocatalytic degradation of sulfamethoxazole by stable hierarchical Fe2O3/Co3O4 heterojunction on nickel foam

Journal

CHINESE CHEMICAL LETTERS
Volume 32, Issue 11, Pages 3431-3434

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2021.05.022

Keywords

Photocatalysis; Sulfamethoxazole; Ni foam; Fe2O3; CO3O4

Funding

  1. Postdoctoral Science Foundation of Jiangsu Province [2020Z299]
  2. China Postdoctoral Science Foundation [2020M671443]

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A facile approach was employed to prepare Fe2O3/Co3O4 nanosheet arrays on nickel foams, exhibiting high efficiency in photocatalytic degradation of SMZ. The introduction of Ni foam helped with electron transfer, and Fe2O3/Co3O4 @NF showed effective and stable catalytic performance for SMZ.
A facile approach was successfully employed to prepare Fe2O3/Co3O4 nanosheet arrays on nickel foams (Fe2O3/Co3O4 @NF), which owned such advantages as narrow band gap energies and high separation rate of photoexcited electron-hole pairs. The combination of Fe2O3 and Co3O4 dramatically enhanced the photocatalytic activity towards sulfamethoxazole (SMZ) degradation, with the highest catalytic efficiency of k = 0.0538 min(-1), which was much higher than that of Fe2O3 @NF (0.0098 min(-1)) and Co3O4 @NF (0.0094 min(-1)). The introduction of Ni foam could not only act as the support to anchor photocatalyst, but also work as the electron mediator to promote the transition of electron-hole pairs. Reactive species trapping experiments combined with electron paramagnetic resonance analysis confirmed O-center dot(2)- was primarily responsible for SMZ degradation. Furthermore, Fe2O3/Co3O4 @NF was effective and almost unaffected by inorganic cations and anions in aqueous solution. This study could provide a facile and promising path for the construction of self-supported metal oxide-based heterojunction with high efficiency and strong stability. (C) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.

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