4.7 Article

α-MnO2 modified exfoliated porous g-C3N4 nanosheet (2D) for enhanced photocatalytic oxidation efficiency of aromatic alcohols

Journal

INORGANIC CHEMISTRY COMMUNICATIONS
Volume 130, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.inoche.2021.108717

Keywords

Heterojunction; Visible light; Z scheme; Charge transfer; Photocatalytic oxidation

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The introduction of MnO2 onto the g-C3N4 nanosheets significantly enhances the photocatalytic performance, with 3 wt% MnO2 modification showing the highest oxidation efficiency towards aromatic alcohols. This enhancement is attributed to heterojunction formation and the generation of active charged species responsible for the oxidation of aromatic alcohols through a free radical mechanism under visible light.
Porous graphitic carbon nitride (g-C3N4) was synthesized by taking melamine and ammonium bicarbonate through single-step calcination method followed by ultrasonication to obtain exfoliated porous g-C3N4 (2D) nanosheets. Further enhancement of photocatalytic performance, g-C3N4 nanosheet (2D) was further modified with different weight percentage of (1, 3, 5, and 7) of MnO2. The introduction of alpha-MnO2 onto the g-C3N4 nanosheet establishes an interlayer channels to promote the migration of charge carriers through the valence band and conduction band of the prepared composite MnO2@g-C3N4. The transformation of photo induced charge carriers adopt the Z-scheme mechanism rather band-transfer mechanism. The accumulated photo generated electrons in conduction band of g-C3N4 is more electro negative than the potential of (O2/O2-.) and able to reduce oxygen to superoxide (O2-.) radical. At the same time, the holes in valence band of alpha-MnO2 are more electro positive than the potential of (OH-/OH.) and help in oxidate OH- to hydroxyl (OH.) radical. Among all the composites, 3 wt% MnO2 modified g-C3N4 shows the best photocatalytic oxidation efficiency towards all the aromatic alcohols. In presence of visible light, heterojuction formation, and formation of active charged species (OH. and O2-.) were mostly responsible for photocatalytic oxidation of aromatic alcohols through free radical mechanism.

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