Selective reduction technique (SRT): A robust method to synthesize bioactive Ag/Au doped Graphene Oxide

We report herein the simple methodology for the synthesis of Graphene Oxide (GO)-metal nanohybrids through selective reduction technique (SRT), which eliminates the formation of undesirable reduced Graphene Oxide (rGO) by conventional method and enhances the dispersibility of GO-nanohybrids in aqueo...

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Bibliographic Details
Published in:Materials & design Vol. 102; pp. 186 - 195
Main Authors: Mondal, Maloy Kr, Banerjee, Prajna Paramita, Saha, Swadhin K., Chowdhury, Pranesh, Sengupta, Archya, Bandyopadhyay, Arindam, Bhattacharya, Shelley, Chattopadhyay, Ansuman
Format: Journal Article
Language:English
Published: Elsevier Ltd 15-07-2016
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Summary:We report herein the simple methodology for the synthesis of Graphene Oxide (GO)-metal nanohybrids through selective reduction technique (SRT), which eliminates the formation of undesirable reduced Graphene Oxide (rGO) by conventional method and enhances the dispersibility of GO-nanohybrids in aqueous medium. The dispersibility of the materials in aqueous medium has been explained from zeta (ζ) potential value. The synthesized materials are characterized well by UV–Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and various types of microscopic studies such as Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), and Atomic Force Microscopy (AFM). A preliminary attempt has been made to search its (doped materials) bioactivity towards breast cancer cells (MCF-7). The results are compared with a well known anti cancer chemotherapy drug Mitomycin-C. [Display omitted] •Graphene Oxide (GO) based metal nanohybrids has been through selective reduction technique (SRT).•SRT eliminates the formation of rGO and enhances the dispersibility of the materials in the context of biological study.•Finally a preliminary attempt has been taken to search its activity towards breast cancer cells (MCF-7).
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ISSN:0264-1275
1873-4197
DOI:10.1016/j.matdes.2016.04.017