Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201002906
Title: Visible-light-induced dye degradation over copper-modified reduced graphene oxide
Authors: Xiong, Z.
Zhang, L.L. 
Zhao, X.S. 
Keywords: catalytic degradation
copper
dyes/pigments
graphene
photochemistry
Issue Date: 18-Feb-2011
Citation: Xiong, Z., Zhang, L.L., Zhao, X.S. (2011-02-18). Visible-light-induced dye degradation over copper-modified reduced graphene oxide. Chemistry - A European Journal 17 (8) : 2428-2434. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201002906
Abstract: Previously, it was found that reduced graphene oxide (RGO) can degrade rhodamine B (RhB) under visible-light irradiation, but with an extraordinarily slow rate. It was also found that modification of RGO with gold nanoparticles can dramatically accelerate the photoreaction rate. Herein, we describe the preparation and photocatalytic properties of copper-ion-modified RGO composite materials, which display a faster photocatalytic reaction rate and better mineralization under visible-light irradiation than gold-modified RGO. The copper-ion-modified RGO composites were prepared by an immersion method. The characterization results of X-ray diffraction, transmission electron microscopy, field-emission scanning electron microscopy, and X-ray photoelectron spectroscopy show the presence of crystalline copper species Cu 2(OH)3NO3 and Cu2(OH)3Cl on the surface of RGO. Modification of RGO with the copper species greatly enhances the degradation of RhB-after 3 hours of reaction under visible-light irradiation, the total organic carbon is decreased by about 31%. The copper species act as an electron relay, passing the excited electrons from the RGO sheets to adsorbed oxygen, thus leading to continuous generation of reactive oxygen species for the degradation of RhB. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Source Title: Chemistry - A European Journal
URI: http://scholarbank.nus.edu.sg/handle/10635/90479
ISSN: 09476539
DOI: 10.1002/chem.201002906
Appears in Collections:Staff Publications

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