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      Chemical vapour deposition of freestanding sub-60 nm graphene gyroids

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          Interpretation of Raman spectra of disordered and amorphous carbon

          Physical Review B, 61(20), 14095-14107
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            Is Open Access

            The Raman Fingerprint of Graphene

            Graphene is the two-dimensional (2d) building block for carbon allotropes of every other dimensionality. It can be stacked into 3d graphite, rolled into 1d nanotubes, or wrapped into 0d fullerenes. Its recent discovery in free state has finally provided the possibility to study experimentally its electronic and phonon properties. Here we show that graphene's electronic structure is uniquely captured in its Raman spectrum that clearly evolves with increasing number of layers. Raman fingerprints for single-, bi- and few-layer graphene reflect changes in the electronic structure and electron-phonon interactions and allow unambiguous, high-throughput, non-destructive identification of graphene layers, which is critically lacking in this emerging research area.
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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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                Author and article information

                Journal
                Applied Physics Letters
                Appl. Phys. Lett.
                AIP Publishing
                0003-6951
                1077-3118
                December 18 2017
                December 18 2017
                : 111
                : 25
                : 253103
                Affiliations
                [1 ]Department of Engineering, University of Cambridge, Cambridge CB3 0FA, United Kingdom
                [2 ]Surface Engineering and Nanotechnology Institute, Cranfield University, Cranfield MK43 0AL, United Kingdom
                [3 ]Department of Physics, University of Cambridge, Cambridge CB3 0HE, United Kingdom
                [4 ]Adolphe Merkle Institute, University of Fribourg, Fribourg CH-1700, Switzerland
                [5 ]Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, United Kingdom
                [6 ]Department of Chemical and Biomolecular Engineering, Vanderbilt University School of Engineering, 2301 Vanderbilt Place PMB 351826, Nashville, Tennessee 37235-1826, USA
                [7 ]Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB3 0FS, United Kingdom
                Article
                10.1063/1.4997774
                69481bb4-2376-4688-bd55-b693aa7c6349
                © 2017
                History

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