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Visible light photoactivity enhancement via CuTCPP hybridized g-C3N4 nanocomposite

Paper ID Volume ID Publish Year Pages File Format Full-Text
45730 46421 2015 8 PDF Available
Title
Visible light photoactivity enhancement via CuTCPP hybridized g-C3N4 nanocomposite
Abstract

•CuTCPP/g-C3N4 composites were prepared via ultrasonic dispersion method.•CuTCPP molecules easily hybridized with g-C3N4 mainly through π–π stacking interaction.•These composites show much higher visible-light photocatalytic activity than pure g-C3N4.•The enhanced visible light activity is due to the efficient electrons transfer from CuTCPP to g-C3N4.•CuTCPP sensitization can expand the visible light absorption of g-C3N4.

Cu (II) meso-Tetra (4-carboxyphenyl) porphyrin (CuTCPP) hybridized g-C3N4 (CuTCPP/g-C3N4) composites have been facilely synthesized through the ethanol dispersion method. CuTCPP molecules as a sensitizer could easily assemble on the surface of g-C3N4 nanosheets mainly through π–π stacking interaction. The CuTCPP/g-C3N4 composites show much higher photocatalytic activity for phenol degradation than pure g-C3N4 under visible light irradiation. The optimum photocatatlytic activity of the CuTCPP/g-C3N4 composites with weight ratio of CuTCPP at 0.75% is almost 2.2 times as high as that of pure g-C3N4 under the visible light. The enhancement of the visible light photocatalytic activity comes from the efficient electrons transfer from photoexcited CuTCPP molecules to g-C3N4 sheets and more efficiently visible-light harvesting due to the CuTCPP sensitization. Both the holes and ·O2− are main oxidative species of CuTCPP/g-C3N4 for phenol degradation under visible light irradiation. Finally, the possible charge transfer mechanism of enhanced visible light photocatalytic activity was proposed.

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Keywords
Photocatalysis; g-C3N4; Sensitization; Porphyrin
First Page Preview
Visible light photoactivity enhancement via CuTCPP hybridized g-C3N4 nanocomposite
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis B: Environmental - Volumes 166–167, May 2015, Pages 366–373
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis