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      Harnessing the concurrent reaction dynamics in active Si and Ge to achieve high performance lithium-ion batteries

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          Abstract

          A composite anode of Cu/Si/Ge nanowire arrays grown on a porous Ni foam enables the outstanding capacity, rate capability and cycle stability of Li-ion batteries.

          Abstract

          Advanced composite electrodes containing multiple active components are often used in lithium-ion batteries for practical applications. The performance of such heterogeneous composite electrodes can in principle be enhanced by tailoring the concurrent reaction dynamics in multiple active components for promoting their collective beneficial effects. However, the potential of this design principle has remained uncharted to date. Here we develop a composite anode of Cu/Si/Ge nanowire arrays, where each nanowire consists of a core of Cu segments and a Si/Ge bilayer shell. This unique electrode architecture exhibited a markedly improved electrochemical performance over the reference Cu/Si systems, demonstrating a stable capacity retention (81% after 3000 cycles at 2C) and doubled specific capacity at a rate of 16C (1C = 2 A g −1). By using in situ transmission electron microscopy and electrochemical testing, we unravel a novel reaction mechanism of dynamic co-lithiation/co-delithiation in the active Si and Ge bilayer, which is shown to effectively alleviate the electrochemically induced mechanical degradation and thus greatly enhance the long-cycle stability of the electrode. Our findings offer insights into a rational design of high-performance lithium-ion batteries via exploiting the concurrent reaction dynamics in the multiple active components of composite electrodes.

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          Most cited references48

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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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              High-performance lithium-ion anodes using a hierarchical bottom-up approach.

              Si-based Li-ion battery anodes have recently received great attention, as they offer specific capacity an order of magnitude beyond that of conventional graphite. The applications of this transformative technology require synthesis routes capable of producing safe and easy-to-handle anode particles with low volume changes and stable performance during battery operation. Herein, we report a large-scale hierarchical bottom-up assembly route for the formation of Si on the nanoscale--containing rigid and robust spheres with irregular channels for rapid access of Li ions into the particle bulk. Large Si volume changes on Li insertion and extraction are accommodated by the particle's internal porosity. Reversible capacities over five times higher than that of the state-of-the-art anodes (1,950 mA h g(-1)) and stable performance are attained. The synthesis process is simple, low-cost, safe and broadly applicable, providing new avenues for the rational engineering of electrode materials with enhanced conductivity and power.
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                Author and article information

                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                2018
                2018
                : 11
                : 3
                : 669-681
                Affiliations
                [1 ]Department of Materials Science and Engineering
                [2 ]Xiamen University
                [3 ]Xiamen
                [4 ]Fujian 361005
                [5 ]China
                [6 ]State Key Laboratory for Physical Chemistry of Solid Surfaces
                [7 ]Department of Chemistry
                [8 ]Xiamen 361005
                [9 ]Environmental Molecular Sciences Laboratory
                [10 ]Pacific Northwest National Laboratory
                [11 ]Richland
                [12 ]Washington 99352
                [13 ]USA
                [14 ]School of Materials Science and Engineering
                [15 ]Georgia Institute of Technology
                [16 ]Atlanta
                [17 ]Woodruff School of Mechanical Engineering
                [18 ]Semiconductor Photonics Research Center
                [19 ]Department of Physics
                [20 ]Center of Electron Microscopy and State Key Laboratory of Silicon Materials
                [21 ]Zhejiang University
                [22 ]Hangzhou 310027
                Article
                10.1039/C8EE00239H
                e1cb4e18-b349-44d6-849b-a453cbbc3205
                © 2018

                http://rsc.li/journals-terms-of-use

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