4.7 Article

Rapid sun-light driven photocatalytic functions of 3D rGO/ZnO/Ag heterostructures via improved charge transfer kinetics

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出版社

ELSEVIER
DOI: 10.1016/j.jmrt.2020.12.062

关键词

Graphene; Heterostructures; Photocatalysis; Sunlight; ZnO

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2018R1D1A1B07051474, 2018R1D1A1B07051461]

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This study presents a novel three-dimensional (3D) rGO/ZnO/Ag heterostructure processed via solvothermal and photoreduction techniques, showing enhanced photon absorption in the visible region and reduced band gap values. Photocatalytic performance evaluation through dye degradation reactions under sunlight illumination demonstrated rapid and enhanced photocatalytic activity. The established schematic mechanism illustrated enhanced charge transfer kinetics in the reactions, with the heterostructure showing 99% efficiency towards recycled photocatalytic reactions.
Enhancing photon absorption across visible region could be of great significance in visualizing rapid photocatalytic reactions. In this regard, we report on a novel three-dimensional (3D) rGO/ZnO/Ag heterostructure processed via solvothermal and photoreduction techniques. The structural studies revealed the formation of a complete rGO/ZnO/Ag heterostructure. The microscopic images revealed ZnO on rGO specimens and Ag on both ZnO and rGO surface. Enhanced visible region photon absorption and lowering in band gap values was realized in rGO/ZnO/Ag specimens over rGO/ZnO. The photocatalytic performance evaluated through dye degradation reactions under sunlight illumination indicated 3D heterostructure to exhibit rapid and enhanced photocatalytic activity. A schematic mechanism was established to illustrate the enhanced charge transfer kinetics involved in the reactions. Additionally, studies on increased photocatalytic reaction rate for addition of H2O2 and role of reaction temperature was also made. The obtained heterostructure also demonstrated 99% efficiency towards recycled photocatalytic reactions. (C) 2020 The Author(s). Published by Elsevier B.V.

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