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      Ultra-high Areal Capacity Realized in Three-Dimensional Holey Graphene/SnO 2 Composite Anodes

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          Summary

          Nanostructured alloy-type electrode materials and its composites have shown extraordinary promise for lithium-ion batteries (LIBs) with exceptional gravimetric capacity. However, studies to date are usually limited to laboratory cells with too low mass loading (and thus too low areal capacity) to exert significant practical impact. Herein, by impregnating micrometer-sized SnO 2/graphene composites into 3D holey graphene frameworks (HGF), we show that a well-designed 3D-HGF/SnO 2 composite anode with a high mass loading of 12 mg cm −2 can deliver an ultra-high areal capacity up to 14.5 mAh cm −2 under current density of 0.2 mA cm −2 and stable areal capacity of 9.5 mAh cm −2 under current density of 2.4 mA cm −2, considerably outperforming those in the state-of-art research devices or commercial devices. This robust realization of high areal capacity defines a critical step to capturing the full potential of high-capacity alloy-type electrode materials in practical LIBs.

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          Highlights

          • 3D holey graphene framework/SnO 2 composite electrode was designed and prepared

          • Micrometer-sized SnO 2/graphene was impregnated into 3D holey graphene frameworks

          • The 3D composite anode can deliver an ultra-high areal capacity up to 14.5 mAh cm −2

          • This study defines a critical step in exploring the alloy-type electrode for LIBs

          Abstract

          Energy Storage; Nanomaterials; Energy Materials

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          Most cited references24

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          Stable cycling of double-walled silicon nanotube battery anodes through solid-electrolyte interphase control.

          Although the performance of lithium ion-batteries continues to improve, their energy density and cycle life remain insufficient for applications in consumer electronics, transport and large-scale renewable energy storage. Silicon has a large charge storage capacity and this makes it an attractive anode material, but pulverization during cycling and an unstable solid-electrolyte interphase has limited the cycle life of silicon anodes to hundreds of cycles. Here, we show that anodes consisting of an active silicon nanotube surrounded by an ion-permeable silicon oxide shell can cycle over 6,000 times in half cells while retaining more than 85% of their initial capacity. The outer surface of the silicon nanotube is prevented from expansion by the oxide shell, and the expanding inner surface is not exposed to the electrolyte, resulting in a stable solid-electrolyte interphase. Batteries containing these double-walled silicon nanotube anodes exhibit charge capacities approximately eight times larger than conventional carbon anodes and charging rates of up to 20C (a rate of 1C corresponds to complete charge or discharge in one hour).
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            Multidimensional materials and device architectures for future hybrid energy storage

            Electrical energy storage plays a vital role in daily life due to our dependence on numerous portable electronic devices. Moreover, with the continued miniaturization of electronics, integration of wireless devices into our homes and clothes and the widely anticipated ‘Internet of Things', there are intensive efforts to develop miniature yet powerful electrical energy storage devices. This review addresses the cutting edge of electrical energy storage technology, outlining approaches to overcome current limitations and providing future research directions towards the next generation of electrical energy storage devices whose characteristics represent a true hybridization of batteries and electrochemical capacitors.
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              Graphene/metal oxide composite electrode materials for energy storage

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                Author and article information

                Contributors
                Journal
                iScience
                iScience
                iScience
                Elsevier
                2589-0042
                20 August 2019
                27 September 2019
                20 August 2019
                : 19
                : 728-736
                Affiliations
                [1 ]Department of Materials Science and Engineering, University of California, Los Angeles, CA 90095, USA
                [2 ]Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA
                [3 ]School of Energy and Power Engineering, North University of China, Shanxi, Taiyuan 030051, P. R. China
                [4 ]Department of Industrial and Manufacturing Engineering, The Pennsylvania State University, University Park, PA 16802-4400, USA
                [5 ]College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China
                [6 ]School of Chemistry, Beihang University, Beijing 100191, China
                [7 ]California NanoSystems Institute, University of California, Los Angeles, CA 90095, USA
                Author notes
                []Corresponding author linguo@ 123456buaa.edu.cn
                [∗∗ ]Corresponding author yhuang@ 123456seas.ucla.edu
                [∗∗∗ ]Corresponding author xduan@ 123456chem.ucla.edu
                [8]

                These authors contributed equally

                [9]

                Lead Contact

                Article
                S2589-0042(19)30303-7
                10.1016/j.isci.2019.08.025
                6726882
                31476619
                eb6a2d6f-e744-4fca-a130-d92cabcb833c
                © 2019 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 25 March 2019
                : 25 June 2019
                : 13 August 2019
                Categories
                Article

                energy storage,nanomaterials,energy materials
                energy storage, nanomaterials, energy materials

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