Applied Catalysis2022,Vol.30513.DOI:10.1016/j.apcatb.2021.121018

Visible-light-responsive Cl/S co-doped carbon nitride nanotubes for photocatalytic denitrification: A new reaction pathway dominated by photo-electrons

Jiang G. You X. An B. Liu F. Wang Y. Liu C. Zhao C. Duan X.
Applied Catalysis2022,Vol.30513.DOI:10.1016/j.apcatb.2021.121018

Visible-light-responsive Cl/S co-doped carbon nitride nanotubes for photocatalytic denitrification: A new reaction pathway dominated by photo-electrons

Jiang G. 1You X. 1An B. 1Liu F. 1Wang Y. 1Liu C. 1Zhao C. 1Duan X.2
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作者信息

  • 1. College of Chemical Engineering China University of Petroleum
  • 2. School of Chemical Engineering and Advanced Materials The University of Adelaide
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Abstract

? 2021 Elsevier B.V.In this work, we first applied metal-free polymeric catalysts to drive the photocatalytic denitrification (PCDN) reaction under visible light. We developed a hydrothermal-transverse thermal stripping method to prepare Cl/S co-doped metal-free carbon nitride nanotubes as the photocatalysts (Cl/S-TCN). With larger specific surface area, stronger light response intensity and wider light absorption range, the PCDN performance of Cl/S-TCN was 19 times higher than that of carbon nitride (GCN, obtained by direct calcination of melamine) under visible light. In hole scavenger experiments, the PCDN reaction was dominated by photo-generated electrons (e-) over Cl/S-TCN in acidic solutions. DFT calculations showed that surface Cl and S dopants preferentially adsorbed the O atoms in NO3- and delivered photoinduced-e- to N atoms through O atoms, ultimately breaking the N-O bond. Such reaction pathway was rarely reported in previous studies. Hence, this work contributes to the first insight into PCDN catalyzed by atomically modified metal-free photocatalyst under visible light.

Key words

Carbon nitride/Cl/S co-doping/Hydrothermal-transverse thermal stripping/Photocatalytic denitrification/Photogenerated electrons

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出版年

2022
Applied Catalysis

Applied Catalysis

ISSN:0926-3373
被引量22
参考文献量68
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