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      An ultrafast rechargeable aluminium-ion battery.

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          Abstract

          The development of new rechargeable battery systems could fuel various energy applications, from personal electronics to grid storage. Rechargeable aluminium-based batteries offer the possibilities of low cost and low flammability, together with three-electron-redox properties leading to high capacity. However, research efforts over the past 30 years have encountered numerous problems, such as cathode material disintegration, low cell discharge voltage (about 0.55 volts; ref. 5), capacitive behaviour without discharge voltage plateaus (1.1-0.2 volts or 1.8-0.8 volts) and insufficient cycle life (less than 100 cycles) with rapid capacity decay (by 26-85 per cent over 100 cycles). Here we present a rechargeable aluminium battery with high-rate capability that uses an aluminium metal anode and a three-dimensional graphitic-foam cathode. The battery operates through the electrochemical deposition and dissolution of aluminium at the anode, and intercalation/de-intercalation of chloroaluminate anions in the graphite, using a non-flammable ionic liquid electrolyte. The cell exhibits well-defined discharge voltage plateaus near 2 volts, a specific capacity of about 70 mA h g(-1) and a Coulombic efficiency of approximately 98 per cent. The cathode was found to enable fast anion diffusion and intercalation, affording charging times of around one minute with a current density of ~4,000 mA g(-1) (equivalent to ~3,000 W kg(-1)), and to withstand more than 7,500 cycles without capacity decay.

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          Most cited references22

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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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            Dialkylimidazolium chloroaluminate melts: a new class of room-temperature ionic liquids for electrochemistry, spectroscopy and synthesis

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              • Record: found
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              The rechargeable aluminum-ion battery.

              We report a novel aluminium-ion rechargeable battery comprised of an electrolyte containing AlCl(3) in the ionic liquid, 1-ethyl-3-methylimidazolium chloride, and a V(2)O(5) nano-wire cathode against an aluminium metal anode. The battery delivered a discharge capacity of 305 mAh g(-1) in the first cycle and 273 mAh g(-1) after 20 cycles, with very stable electrochemical behaviour.
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                Author and article information

                Journal
                Nature
                Nature
                1476-4687
                0028-0836
                Apr 16 2015
                : 520
                : 7547
                Affiliations
                [1 ] 1] Department of Chemistry, Stanford University, Stanford, California 94305, USA [2] Green Energy and Environment Research Laboratories, Industrial Technology Research Institute, Hsinchu 31040, Taiwan.
                [2 ] Department of Chemistry, Stanford University, Stanford, California 94305, USA.
                [3 ] 1] Department of Chemistry, Stanford University, Stanford, California 94305, USA [2] School of Physics and Electronics, Hunan University, Changsha 410082, China.
                [4 ] 1] Department of Chemistry, Stanford University, Stanford, California 94305, USA [2] Department of Chemistry, National Taiwan Normal University, Taipei 11677, Taiwan [3] Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 10617, Taiwan.
                [5 ] Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan.
                Article
                nature14340
                10.1038/nature14340
                25849777
                ca42aeb5-7fc4-4305-8b1f-7a6590d1d641
                History

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