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      Rechargeable aqueous zinc-manganese dioxide batteries with high energy and power densities

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          Abstract

          Although alkaline zinc-manganese dioxide batteries have dominated the primary battery applications, it is challenging to make them rechargeable. Here we report a high-performance rechargeable zinc-manganese dioxide system with an aqueous mild-acidic zinc triflate electrolyte. We demonstrate that the tunnel structured manganese dioxide polymorphs undergo a phase transition to layered zinc-buserite on first discharging, thus allowing subsequent intercalation of zinc cations in the latter structure. Based on this electrode mechanism, we formulate an aqueous zinc/manganese triflate electrolyte that enables the formation of a protective porous manganese oxide layer. The cathode exhibits a high reversible capacity of 225 mAh g −1 and long-term cyclability with 94% capacity retention over 2000 cycles. Remarkably, the pouch zinc-manganese dioxide battery delivers a total energy density of 75.2 Wh kg −1. As a result of the superior battery performance, the high safety of aqueous electrolyte, the facile cell assembly and the cost benefit of the source materials, this zinc-manganese dioxide system is believed to be promising for large-scale energy storage applications.

          Abstract

          The development of rechargeable aqueous zinc batteries are challenging but promising for energy storage applications. With a mild-acidic triflate electrolyte, here the authors show a high-performance Zn-MnO 2 battery in which the MnO 2 cathode undergoes Zn 2+ (de)intercalation.

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          Most cited references57

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          Research development on sodium-ion batteries.

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            What Are Batteries, Fuel Cells, and Supercapacitors?

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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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                Author and article information

                Contributors
                fycheng@nankai.edu.cn
                chenabc@nankai.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                1 September 2017
                1 September 2017
                2017
                : 8
                : 405
                Affiliations
                [1 ]ISNI 0000 0000 9878 7032, GRID grid.216938.7, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) and State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, , Nankai University, ; Tianjin, 300071 China
                [2 ]ISNI 0000 0000 9878 7032, GRID grid.216938.7, Collaborative Innovation Center of Chemical Science and Engineering, , Nankai University, ; Tianjin, 300071 China
                [3 ]ISNI 0000000119573309, GRID grid.9227.e, State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, , Chinese Academy of Sciences, ; Shanghai, 200050 China
                Author information
                http://orcid.org/0000-0002-6176-7278
                http://orcid.org/0000-0002-9400-1500
                http://orcid.org/0000-0002-1298-0267
                Article
                467
                10.1038/s41467-017-00467-x
                5581336
                28864823
                7267caa1-b444-42ef-96eb-73adef89048a
                © The Author(s) 2017

                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
                : 6 January 2017
                : 27 June 2017
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