4.6 Article

Fabrication of Z-Scheme Heterojunction by Anchoring Mesoporous γ-Fe2O3 Nanospheres on g-C3N4 for Degrading Tetracycline Hydrochloride in Water

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 6, Issue 12, Pages 16437-16447

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.8b03500

Keywords

gamma-Fe2O3/g-C3N4; Photocatalytic degradation activity; Z-scheme heterojunction; Tetracycline hydrochloride; Reaction mechanism

Funding

  1. National Natural Science Foundation of China [21606114, 21576112, 2157061352]
  2. Natural Science Fund of Jiangsu Province [BK20150536]
  3. Postdoctoral Science Foundation of China [2017M611712, 2017M611717]
  4. Six Talents Peaks Project in Jiangsu Province [XNY-009]
  5. Talent Introduction Project of Jiangsu University [17JDG020]

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A photocatalyst with Z-scheme heterostructure is synthesized through anchoring mesoporous gamma-Fe2O3 nanospheres on a g-C3N4 nanosheet surface. The fabricated Z-scheme gamma-Fe2O3/g-C3N4 heterojunction exhibits a mesoporous feature and possesses improved specific surface area, which can provide a mass of reaction active sites for pollutant molecules to improve photocatalytic activity. More importantly, the Z-scheme heterostructure constructed between gamma-Fe2O3 and g-C3N4 efficiently extends the response range at the visible region and speeds up the transfer and separation of photoinduced charge carriers, which is beneficial to boosting photocatalytic activity. Compared to the original g-C3N4 sample, the Z-scheme gamma-Fe2O3/g-C3N4 heterojunction exhibits remarkably improved photocatalytic degradation activity for mineralizing tetracycline hydrochloride (TCHC1) under the visible-light irradiation. Moreover, the photocatalytic degradation mechanism of TC-HCl is put forward and investigated in depth, the results of which identify that center dot OH, center dot O-2(-), and photogenerated h(+) all play a vital function and have the order center dot OH > center dot O-2(-) > h(+) during the TC-HCl degradation reaction.

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