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      Fluorine-free water-in-ionomer electrolytes for sustainable lithium-ion batteries

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          Abstract

          The continuously increasing number and size of lithium-based batteries developed for large-scale applications raise serious environmental concerns. Herein, we address the issues related to electrolyte toxicity and safety by proposing a “water-in-ionomer” type of electrolyte which replaces organic solvents by water and expensive and toxic fluorinated lithium salts by a non-fluorinated, inexpensive and non-toxic superabsorbing ionomer, lithium polyacrylate. Interestingly, the electrochemical stability window of this electrolyte is extended greatly, even for high water contents. Particularly, the gel with 50 wt% ionomer exhibits an electrochemical stability window of 2.6 V vs. platinum and a conductivity of 6.5 mS cm −1 at 20 °C. Structural investigations suggest that the electrolytes locally self-organize and most likely switch local structures with the change of water content, leading to a 50% gel with good conductivity and elastic properties. A LiTi 2(PO 4) 3/LiMn 2O 4 lithium-ion cell incorporating this electrolyte provided an average discharge voltage > 1.5 V and a specific energy of 77 Wh kg −1, while for an alternative cell chemistry, i.e., TiO 2/LiMn 2O 4, a further enhanced average output voltage of 2.1 V and an initial specific energy of 124.2 Wh kg −1 are achieved.

          Abstract

          The flammability and toxicity of the currently used electrolytes are the concerns that must be addressed. Here the authors show a non-fluorinated and non-toxic ionomeric aqueous gel electrolyte called water-in-ionomer that allows an enlargement of electrochemical stability window and design of environmentally friendly battery cell chemistries.

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          Most cited references40

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          "Water-in-salt" electrolyte enables high-voltage aqueous lithium-ion chemistries.

          Lithium-ion batteries raise safety, environmental, and cost concerns, which mostly arise from their nonaqueous electrolytes. The use of aqueous alternatives is limited by their narrow electrochemical stability window (1.23 volts), which sets an intrinsic limit on the practical voltage and energy output. We report a highly concentrated aqueous electrolyte whose window was expanded to ~3.0 volts with the formation of an electrode-electrolyte interphase. A full lithium-ion battery of 2.3 volts using such an aqueous electrolyte was demonstrated to cycle up to 1000 times, with nearly 100% coulombic efficiency at both low (0.15 coulomb) and high (4.5 coulombs) discharge and charge rates.
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            Single-ion BAB triblock copolymers as highly efficient electrolytes for lithium-metal batteries.

            Electrochemical energy storage is one of the main societal challenges of this century. The performances of classical lithium-ion technology based on liquid electrolytes have made great advances in the past two decades, but the intrinsic instability of liquid electrolytes results in safety issues. Solid polymer electrolytes would be a perfect solution to those safety issues, miniaturization and enhancement of energy density. However, as in liquids, the fraction of charge carried by lithium ions is small (<20%), limiting the power performances. Solid polymer electrolytes operate at 80 °C, resulting in poor mechanical properties and a limited electrochemical stability window. Here we describe a multifunctional single-ion polymer electrolyte based on polyanionic block copolymers comprising polystyrene segments. It overcomes most of the above limitations, with a lithium-ion transport number close to unity, excellent mechanical properties and an electrochemical stability window spanning 5 V versus Li(+)/Li. A prototype battery using this polyelectrolyte outperforms a conventional battery based on a polymer electrolyte.
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              Unusual stability of acetonitrile-based superconcentrated electrolytes for fast-charging lithium-ion batteries.

              The development of a stable, functional electrolyte is urgently required for fast-charging and high-voltage lithium-ion batteries as well as next-generation advanced batteries (e.g., Li-O2 systems). Acetonitrile (AN) solutions are one of the most promising electrolytes with remarkably high chemical and oxidative stability as well as high ionic conductivity, but its low stability against reduction is a critical problem that hinders its extensive applications. Herein, we report enhanced reductive stability of a superconcentrated AN solution (>4 mol dm(-3)). Applying it to a battery electrolyte, we demonstrate, for the first time, reversible lithium intercalation into a graphite electrode in a reduction-vulnerable AN solvent. Moreover, the reaction kinetics is much faster than in a currently used commercial electrolyte. First-principle calculations combined with spectroscopic analyses reveal that the peculiar reductive stability arises from modified frontier orbital characters unique to such superconcentrated solutions, in which all solvents and anions coordinate to Li(+) cations to form a fluid polymeric network of anions and Li(+) cations.
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                Author and article information

                Contributors
                zhangxin@mail.buct.edu.cn
                jie.li@uni-muenster.de
                e.paillard@fz-juelich.de
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                14 December 2018
                14 December 2018
                2018
                : 9
                : 5320
                Affiliations
                [1 ]GRID grid.461895.7, Helmholtz Institute Münster – Forschungszentrum Jülich GmbH (IEK 12), ; Corrensstrasse 46, 48149 Münster, D-48149 Münster, Germany
                [2 ]ISNI 0000 0000 9931 8406, GRID grid.48166.3d, State Key Laboratory of Chemical Resource Engineering, Institute of Materia Medica, College of Science, , Beijing University of Chemical Technology, ; Beijing, 100029 P. R. China
                [3 ]ISNI 0000000121885934, GRID grid.5335.0, Department of Chemistry, , University of Cambridge, Lensfield Road, ; Cambridge, CB2 1EW UK
                [4 ]GRID grid.457348.9, University Grenoble Alpes, CEA, CNRS, SyMMES, ; F-38000 Grenoble, France
                [5 ]ISNI 0000 0001 2172 9288, GRID grid.5949.1, MEET Battery Research Center, Institute of Physical Chemistry, , University of Münster, ; Corrensstraße 46, D-48149 Münster, Germany
                [6 ]ISNI 0000 0001 2297 375X, GRID grid.8385.6, Jülich Centre for Neutron Science at MLZ, , Forschungszentrum Jülich GmbH, ; Lichtenbergstrasse 1, D-85747 Garching, Germany
                [7 ]ISNI 0000000419368657, GRID grid.17635.36, Department of Chemistry, Chemical Theory Center, and Minnesota Supercomputing Institute, , University of Minnesota, ; Minneapolis, Minnesota 55455-0431 USA
                [8 ]ISNI 0000 0001 0075 5874, GRID grid.7892.4, Present Address: Karlsruhe Institute of Technology (KIT), ; Helmholtzstrasse 11, 89081 Ulm, Germany
                Author information
                http://orcid.org/0000-0002-0272-9079
                http://orcid.org/0000-0002-8812-8783
                http://orcid.org/0000-0002-7742-7294
                Article
                7331
                10.1038/s41467-018-07331-6
                6294254
                30552314
                7611a47e-55c9-40b9-aab5-f7335d082573
                © The Author(s) 2018

                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
                : 14 November 2017
                : 28 October 2018
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