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      Strengthening of Graphene Aerogels with Tunable Density and High Adsorption Capacity towards Pb 2+

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          Abstract

          Graphene aerogels (GAs) with high mechanical strength, tunable density and volume have been prepared only via soaking graphene hydrogels (GHs) in ammonia solution. The density and volume of the obtained GAs are controlled by adjusting the concentration of ammonia solution. Although volume of the GAs decreases with increasing the concentration of ammonia solution, its specific surface area maintains at about 350 m 2 g −1, and the inner structure changes to radial after ammonia solution treatment. Thus, GAs are particularly suitable for the adsorption and energy storage applications owing to their high specific surface area and unique porous structure. The adsorption capacity of GAs for Pb 2+ from aqueous solution maintains at about 80 mg g −1, which could reach as high as 5000 g m −3 per unit volume and they can be separated easily from water after adsorption.

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          Three-dimensional flexible and conductive interconnected graphene networks grown by chemical vapour deposition.

          Integration of individual two-dimensional graphene sheets into macroscopic structures is essential for the application of graphene. A series of graphene-based composites and macroscopic structures have been recently fabricated using chemically derived graphene sheets. However, these composites and structures suffer from poor electrical conductivity because of the low quality and/or high inter-sheet junction contact resistance of the chemically derived graphene sheets. Here we report the direct synthesis of three-dimensional foam-like graphene macrostructures, which we call graphene foams (GFs), by template-directed chemical vapour deposition. A GF consists of an interconnected flexible network of graphene as the fast transport channel of charge carriers for high electrical conductivity. Even with a GF loading as low as ∼0.5 wt%, GF/poly(dimethyl siloxane) composites show a very high electrical conductivity of ∼10 S cm(-1), which is ∼6 orders of magnitude higher than chemically derived graphene-based composites. Using this unique network structure and the outstanding electrical and mechanical properties of GFs, as an example, we demonstrate the great potential of GF/poly(dimethyl siloxane) composites for flexible, foldable and stretchable conductors. © 2011 Macmillan Publishers Limited. All rights reserved
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            Chemical reduction of graphene oxide: a synthetic chemistry viewpoint.

            The chemical reduction of graphene oxide is a promising route towards the large scale production of graphene for commercial applications. The current state-of-the-art in graphene oxide reduction, consisting of more than 50 types of reducing agent, will be reviewed from a synthetic chemistry point of view. Emphasis is placed on the techniques, reaction mechanisms and the quality of the produced graphene. The reducing agents are reviewed under two major categories: (i) those which function according to well-supported mechanisms and (ii) those which function according to proposed mechanisms based on knowledge of organic chemistry. This review will serve as a valuable platform to understand the efficiency of these reducing agents for the reduction of graphene oxide.
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              Three-dimensional nitrogen and boron co-doped graphene for high-performance all-solid-state supercapacitors.

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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                22 May 2014
                2014
                : 4
                : 5025
                Affiliations
                [1 ]School of Materials Science and Engineering, University of Shanghai for Science and Technology , Shanghai 200093, China
                [2 ]Department of Mechanical Engineering and Shenzhen Research Institute, Hong Kong Polytechnic University , Hung Hom, Kowloon, Hong Kong, China
                Author notes
                Article
                srep05025
                10.1038/srep05025
                4030256
                24848100
                43a7035c-d431-49b9-bb9e-4071201f1c31
                Copyright © 2014, Macmillan Publishers Limited. All rights reserved

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. The images in this article are included in the article's Creative Commons license, unless indicated otherwise in the image credit; if the image is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the image. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 15 January 2014
                : 06 May 2014
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