4.7 Article

Mesoporous structure and amorphous Fe-N sites regulation in Fe-g-C3N4 for boosted visible-light-driven photo-Fenton reaction

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 608, Issue -, Pages 2515-2528

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.10.168

Keywords

Photo-Fenton system; Mesoporous Fe-g-C3N4; Fe-N active sites; Ferrikinetics; Green synthesis

Funding

  1. National Natural Science Foundation of China [51671136, 21804008]
  2. Ministry of Science and Technology of China [2021YFE0111300]

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Heterogeneous photo-Fenton catalysts, such as mesoporous Fe-gC(3)N(4), have shown enhanced catalytic activity for the degradation of pollutants under visible light. The highly uniformly dispersed Fe-Nx active sites in the catalysts play a critical role in accelerating the Fenton reaction. These catalysts demonstrate high recyclability and excellent photo-Fenton performance.
Heterogeneous photo-Fenton catalysts prepared by doping metal ions in g-C3N4 are promising alternatives to traditional homogeneous Fenton catalysts, but are restricted by poor mesoporous structure and agglomerate of metal species. Recently, the highly uniformly dispersed metal-N active sites in various photocatalysts have been proved to be the critical reason for their enhanced catalytic activity. In this study based on reasonable control of mesoporous structure and metal-N active sites, mesoporous Fe-gC(3)N(4) was synthesized using a simple one-step thermal shrinkage polymerization method using ferrous oxalate as iron source and pore-forming agent. The Fe and N elements in the triazine ring skeleton of Fe-g-C3N4 form a sigma-pi bond, thus the photogenerated electrons can be quickly transferred to Fe3+ to form Fe2+ under the interaction of chemical bonds, accelerating the Fenton reaction rate. Density functional theory calculations results demonstrate that the energy band structure and electron cloud density distribution of Fe-Nx active structure are better than that of routine FeOx crystal structure with metal species agglomeration. In addition, the excellent mesoporous structure of Fe-g-C3N4 creates conditions for the high exposure of Fe-Nx active sites in the photo-Fenton reaction under visible light. The as-developed Fe-g-C3N4 system shows high recyclability and excellent photo-Fenton performance for removal of typical intractable pollutants (The degradation rate of dye and tetracycline reaches 98.2% and 98.7% at 60 and 120 min, respectively). This work provides a facile and sustainable route to develop mesoporous highly-active heterogeneous Fenton-like catalysts and even further general the design of general catalyst with ideal metal-N active sites, thereby promoting a feasible and efficient wastewater remediation solution. (C) 2021 Elsevier Inc. All rights reserved.

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