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      The synergetic effect of lithium polysulfide and lithium nitrate to prevent lithium dendrite growth.

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          Abstract

          Lithium metal has shown great promise as an anode material for high-energy storage systems, owing to its high theoretical specific capacity and low negative electrochemical potential. Unfortunately, uncontrolled dendritic and mossy lithium growth, as well as electrolyte decomposition inherent in lithium metal-based batteries, cause safety issues and low Coulombic efficiency. Here we demonstrate that the growth of lithium dendrites can be suppressed by exploiting the reaction between lithium and lithium polysulfide, which has long been considered as a critical flaw in lithium-sulfur batteries. We show that a stable and uniform solid electrolyte interphase layer is formed due to a synergetic effect of both lithium polysulfide and lithium nitrate as additives in ether-based electrolyte, preventing dendrite growth and minimizing electrolyte decomposition. Our findings allow for re-evaluation of the reactions regarding lithium polysulfide, lithium nitrate and lithium metal, and provide insights into solving the problems associated with lithium metal anodes.

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          Author and article information

          Journal
          Nat Commun
          Nature communications
          2041-1723
          2041-1723
          2015
          : 6
          Affiliations
          [1 ] Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, USA.
          [2 ] Department of Chemical Engineering, Stanford University, Stanford, California 94305, USA.
          [3 ] Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
          [4 ] 1] Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, USA [2] Stanford Institute for Materials and Energy Sciences, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park, California 94025, USA.
          Article
          ncomms8436
          10.1038/ncomms8436
          26081242
          9e4cf966-d2c2-48c9-a358-55a8f2468035
          History

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