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      High-Performance Porous Silicon/Nanosilver Anodes from Industrial Low-Grade Silicon for Lithium-Ion Batteries

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          Building better batteries.

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            High-performance lithium battery anodes using silicon nanowires.

            There is great interest in developing rechargeable lithium batteries with higher energy capacity and longer cycle life for applications in portable electronic devices, electric vehicles and implantable medical devices. Silicon is an attractive anode material for lithium batteries because it has a low discharge potential and the highest known theoretical charge capacity (4,200 mAh g(-1); ref. 2). Although this is more than ten times higher than existing graphite anodes and much larger than various nitride and oxide materials, silicon anodes have limited applications because silicon's volume changes by 400% upon insertion and extraction of lithium which results in pulverization and capacity fading. Here, we show that silicon nanowire battery electrodes circumvent these issues as they can accommodate large strain without pulverization, provide good electronic contact and conduction, and display short lithium insertion distances. We achieved the theoretical charge capacity for silicon anodes and maintained a discharge capacity close to 75% of this maximum, with little fading during cycling.
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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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                Author and article information

                Contributors
                Journal
                ACS Applied Materials & Interfaces
                ACS Appl. Mater. Interfaces
                American Chemical Society (ACS)
                1944-8244
                1944-8252
                October 28 2020
                October 14 2020
                October 28 2020
                : 12
                : 43
                : 49080-49089
                Affiliations
                [1 ]State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization and Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming 650093, China
                [2 ]Nanomaterials Centre, Australian Institute for Bioengineering and Nanotechnology and School of Chemical Engineering, The University of Queensland, St. Lucia, Queensland, 4072, Australia
                [3 ]School of Photovoltaic and Renewable Energy Engineering and Australian Centre for Advanced Photovoltaics, University of New South Wales, Sydney 2052, Australia
                [4 ]Institution of Materials Science and Engineering, Yunnan University, Kunming 650091, China
                Article
                10.1021/acsami.0c14157
                1435f03d-fd26-412e-8fc1-da7f248b0980
                © 2020

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-045

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