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      Diatomite derived hierarchical hybrid anode for high performance all-solid-state lithium metal batteries

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          Abstract

          Lithium metal based anode with hierarchical structure to enable high rate capability, volume change accommodation, and dendritic suppression is highly desirable for all-solid-state lithium metal battery. However, the fabrication of hierarchical lithium metal based anode is challenging due to the volatility of lithium. Here, we report that natural diatomite can act as an excellent template for constructing hierarchical silicon-lithium based hybrid anode for high performance all-solid-state lithium metal battery. This hybrid anode exhibits stable lithium stripping/plating performance over 1000 h with average overpotential lower than 100 mV without any short circuit. Moreover, all-solid-state full cell using this lithium metal composite anode to couple with lithium iron phosphate cathode shows excellent cycling stability (0.04% capacity decay rate for 500 cycles at 0.5C) and high rate capability (65 mAh g −1 at 5C). The present natural diatomite derived hybrid anode could further promote the fabrication of high performance all-solid-state lithium batteries from sustainable natural resources.

          Abstract

          Lithium metal is the anode of choice for the next-generation high energy density batteries. To address the key technological challenges, the authors report a hybrid Li anode design with hierarchical pores structure derived from natural diatomite and improved electrochemical performance in all-solid-state lithium batteries.

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          Most cited references44

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          Toward Safe Lithium Metal Anode in Rechargeable Batteries: A Review.

          The lithium metal battery is strongly considered to be one of the most promising candidates for high-energy-density energy storage devices in our modern and technology-based society. However, uncontrollable lithium dendrite growth induces poor cycling efficiency and severe safety concerns, dragging lithium metal batteries out of practical applications. This review presents a comprehensive overview of the lithium metal anode and its dendritic lithium growth. First, the working principles and technical challenges of a lithium metal anode are underscored. Specific attention is paid to the mechanistic understandings and quantitative models for solid electrolyte interphase (SEI) formation, lithium dendrite nucleation, and growth. On the basis of previous theoretical understanding and analysis, recently proposed strategies to suppress dendrite growth of lithium metal anode and some other metal anodes are reviewed. A section dedicated to the potential of full-cell lithium metal batteries for practical applications is included. A general conclusion and a perspective on the current limitations and recommended future research directions of lithium metal batteries are presented. The review concludes with an attempt at summarizing the theoretical and experimental achievements in lithium metal anodes and endeavors to realize the practical applications of lithium metal batteries.
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            Layered reduced graphene oxide with nanoscale interlayer gaps as a stable host for lithium metal anodes.

            Metallic lithium is a promising anode candidate for future high-energy-density lithium batteries. It is a light-weight material, and has the highest theoretical capacity (3,860 mAh g(-1)) and the lowest electrochemical potential of all candidates. There are, however, at least three major hurdles before lithium metal anodes can become a viable technology: uneven and dendritic lithium deposition, unstable solid electrolyte interphase and almost infinite relative dimension change during cycling. Previous research has tackled the first two issues, but the last is still mostly unsolved. Here we report a composite lithium metal anode that exhibits low dimension variation (∼20%) during cycling and good mechanical flexibility. The anode is composed of 7 wt% 'lithiophilic' layered reduced graphene oxide with nanoscale gaps that can host metallic lithium. The anode retains up to ∼3,390 mAh g(-1) of capacity, exhibits low overpotential (∼80 mV at 3 mA cm(-2)) and a flat voltage profile in a carbonate electrolyte. A full-cell battery with a LiCoO2 cathode shows good rate capability and flat voltage profiles.
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              The Impact of Elastic Deformation on Deposition Kinetics at Lithium/Polymer Interfaces

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                Author and article information

                Contributors
                yhb@ustc.edu.cn
                shyu@ustc.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                6 June 2019
                6 June 2019
                2019
                : 10
                : 2482
                Affiliations
                [1 ]ISNI 0000000121679639, GRID grid.59053.3a, Division of Nanomaterials & Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, CAS Center for Excellence in Nanoscience, Hefei Science Center of CAS, Department of Chemistry, , University of Science and Technology of China, ; 230026 Hefei, Anhui China
                [2 ]ISNI 0000000121679639, GRID grid.59053.3a, Department of Polymer Science and Engineering, , University of Science and Technology of China, ; 230026 Hefei, Anhui China
                [3 ]ISNI 0000000121679639, GRID grid.59053.3a, CAS Key Laboratory of Mechanical Behavior and Design of Materials, Department of Modern Mechanics, , University of Science and Technology of China, ; 230026 Hefei, Anhui China
                [4 ]ISNI 0000000121679639, GRID grid.59053.3a, National Synchrotron Radiation Laboratory, , University of Science and Technology of China, ; 230026 Hefei, Anhui China
                [5 ]ISNI 0000000121679639, GRID grid.59053.3a, Center for Micro- and Nanoscale Research and Fabrication, , University of Science and Technology of China, ; 230026 Hefei, Anhui China
                [6 ]ISNI 0000000419368956, GRID grid.168010.e, Department of Materials Science and Engineering, , Stanford University, ; Stanford, CA 94305 USA
                Author information
                http://orcid.org/0000-0002-7999-767X
                http://orcid.org/0000-0002-8944-5764
                http://orcid.org/0000-0002-6103-6352
                http://orcid.org/0000-0003-3732-1011
                Article
                10473
                10.1038/s41467-019-10473-w
                6554300
                31171790
                268ea54f-96e5-47ab-84e4-a891c0fdf1a6
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 November 2018
                : 10 May 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001809, National Natural Science Foundation of China (National Science Foundation of China);
                Award ID: 21501165
                Award ID: 51571184
                Award ID: 21805268
                Award Recipient :
                Funded by: the Foundation for Innovative Research Groups of the National Natural Science Foundation of China (Grants 21521001, 11472262), the Users with Excellence and Scientific Research Grant of Hefei Science Center of CAS (2015HSC-UE007, 2015SRG-HSC038), Key Research Program of Frontier Sciences, CAS (Grant QYZDJ-SSW-SLH036), the Chinese Academy of Sciences (Grant KJZD-EW-M01-1), the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDB22040502)
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                batteries,composites
                Uncategorized
                batteries, composites

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