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      Green synthesis of a silver nanoparticle–graphene oxide composite and its application for As(iii) detection

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          Abstract

          We report a facile and green synthetic approach to synthesize a silver nanoparticle (AgNPs)–graphene oxide (GO) composite using beta cyclodextrin as a stabilizing agent and ascorbic acid as a reducing agent.

          Abstract

          We report a facile and green synthetic approach to synthesize a silver nanoparticle (AgNPs)–graphene oxide (GO) composite using beta cyclodextrin as a stabilizing agent and ascorbic acid as a reducing agent. Further, we demonstrate its application as a highly sensitive and selective electrochemical sensor for selective determination of As( iii) in the presence of other elements, such as Cu and some organic and inorganic molecules. The GO sheets provided the surface for the reduction of silver ions. The composite can be easily used for the construction of a disposable electrochemical sensor on a glassy carbon electrode (GCE) using a drop deposition method. The composite was characterized by scanning and transmission electron microscopies, energy dispersive X-ray spectroscopy, X-ray diffraction and electrochemical impedance spectroscopy. Cyclic voltammetry and anodic stripping voltammetry measurements were employed to evaluate the electrochemical properties of beta cyclodextrin stabilized AgNPs–GO/GCE towards arsenic( iii) detection. The AgNPs–GO film exhibited distinctly higher activity for the anodic stripping analysis of As( iii) compared to the GO film alone with approximately three times enhancement of the peak current. This nanostructured electrode applied for As( iii) analysis displayed a wide linear range (13.33–375.19 nM), a high sensitivity (180.5(μA μM −1)) including a 0.24 nM detection limit. We demonstrate the real-life application of the developed sensor by selectively determining the As content in ground and river water samples.

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          Preparation of Graphitic Oxide

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            Preparation and characterization of graphene oxide paper.

            Free-standing paper-like or foil-like materials are an integral part of our technological society. Their uses include protective layers, chemical filters, components of electrical batteries or supercapacitors, adhesive layers, electronic or optoelectronic components, and molecular storage. Inorganic 'paper-like' materials based on nanoscale components such as exfoliated vermiculite or mica platelets have been intensively studied and commercialized as protective coatings, high-temperature binders, dielectric barriers and gas-impermeable membranes. Carbon-based flexible graphite foils composed of stacked platelets of expanded graphite have long been used in packing and gasketing applications because of their chemical resistivity against most media, superior sealability over a wide temperature range, and impermeability to fluids. The discovery of carbon nanotubes brought about bucky paper, which displays excellent mechanical and electrical properties that make it potentially suitable for fuel cell and structural composite applications. Here we report the preparation and characterization of graphene oxide paper, a free-standing carbon-based membrane material made by flow-directed assembly of individual graphene oxide sheets. This new material outperforms many other paper-like materials in stiffness and strength. Its combination of macroscopic flexibility and stiffness is a result of a unique interlocking-tile arrangement of the nanoscale graphene oxide sheets.
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              Graphene-based composite materials.

              Graphene sheets--one-atom-thick two-dimensional layers of sp2-bonded carbon--are predicted to have a range of unusual properties. Their thermal conductivity and mechanical stiffness may rival the remarkable in-plane values for graphite (approximately 3,000 W m(-1) K(-1) and 1,060 GPa, respectively); their fracture strength should be comparable to that of carbon nanotubes for similar types of defects; and recent studies have shown that individual graphene sheets have extraordinary electronic transport properties. One possible route to harnessing these properties for applications would be to incorporate graphene sheets in a composite material. The manufacturing of such composites requires not only that graphene sheets be produced on a sufficient scale but that they also be incorporated, and homogeneously distributed, into various matrices. Graphite, inexpensive and available in large quantity, unfortunately does not readily exfoliate to yield individual graphene sheets. Here we present a general approach for the preparation of graphene-polymer composites via complete exfoliation of graphite and molecular-level dispersion of individual, chemically modified graphene sheets within polymer hosts. A polystyrene-graphene composite formed by this route exhibits a percolation threshold of approximately 0.1 volume per cent for room-temperature electrical conductivity, the lowest reported value for any carbon-based composite except for those involving carbon nanotubes; at only 1 volume per cent, this composite has a conductivity of approximately 0.1 S m(-1), sufficient for many electrical applications. Our bottom-up chemical approach of tuning the graphene sheet properties provides a path to a broad new class of graphene-based materials and their use in a variety of applications.
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                Author and article information

                Journal
                RSCACL
                RSC Adv.
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2014
                2014
                : 4
                : 28
                : 14432-14440
                Affiliations
                [1 ]Department of Chemistry
                [2 ]University of Mumbai
                [3 ]Mumbai-400098, India
                [4 ]US Army Research Laboratory
                [5 ]Vehicle Technology Directorate, RDRL-VTM
                [6 ]Aberdeen Proving Ground, USA
                [7 ]Weapons and Materials Research laboratory, RDRL-WM
                Article
                10.1039/C4RA00934G
                1e541fdb-56ca-4d33-bae2-9e9a5b5bb814
                © 2014
                History

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