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      Electrochemically primed functional redox mediator generator from the decomposition of solid state electrolyte

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          Abstract

          Recent works into sulfide-type solid electrolyte materials have attracted much attention among the battery community. Specifically, the oxidative decomposition of phosphorus and sulfur based solid state electrolyte has been considered one of the main hurdles towards practical application. Here we demonstrate that this phenomenon can be leveraged when lithium thiophosphate is applied as an electrochemically “switched-on” functional redox mediator-generator for the activation of commercial bulk lithium sulfide at up to 70 wt.% lithium sulfide electrode content. X-ray adsorption near-edge spectroscopy coupled with electrochemical impedance spectroscopy and Raman indicate a catalytic effect of generated redox mediators on the first charge of lithium sulfide. In contrast to pre-solvated redox mediator species, this design decouples the lithium sulfide activation process from the constraints of low electrolyte content cell operation stemming from pre-solvated redox mediators. Reasonable performance is demonstrated at strict testing conditions.

          Abstract

          The decomposition of solid state electrolyte material has been well-known in the literature. Here the authors report that the same decomposition process can be leveraged to act as a source of redox mediator that is only activated at certain voltages for application in Li 2S based cathodes.

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          Most cited references43

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          Origin of Outstanding Stability in the Lithium Solid Electrolyte Materials: Insights from Thermodynamic Analyses Based on First-Principles Calculations.

          First-principles calculations were performed to investigate the electrochemical stability of lithium solid electrolyte materials in all-solid-state Li-ion batteries. The common solid electrolytes were found to have a limited electrochemical window. Our results suggest that the outstanding stability of the solid electrolyte materials is not thermodynamically intrinsic but is originated from kinetic stabilizations. The sluggish kinetics of the decomposition reactions cause a high overpotential leading to a nominally wide electrochemical window observed in many experiments. The decomposition products, similar to the solid-electrolyte-interphases, mitigate the extreme chemical potential from the electrodes and protect the solid electrolyte from further decompositions. With the aid of the first-principles calculations, we revealed the passivation mechanism of these decomposition interphases and quantified the extensions of the electrochemical window from the interphases. We also found that the artificial coating layers applied at the solid electrolyte and electrode interfaces have a similar effect of passivating the solid electrolyte. Our newly gained understanding provided general principles for developing solid electrolyte materials with enhanced stability and for engineering interfaces in all-solid-state Li-ion batteries.
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            Interface Stability in Solid-State Batteries

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              First principles study on electrochemical and chemical stability of solid electrolyte–electrode interfaces in all-solid-state Li-ion batteries

              This study provides the understanding and design strategy of solid electrolyte–electrode interfaces to improve electrochemical performance of all-solid-state Li-ion batteries. All-solid-state Li-ion batteries based on ceramic solid electrolyte materials are a promising next-generation energy storage technology with high energy density and enhanced cycle life. The poor interfacial conductance is one of the key limitations in enabling all-solid-state Li-ion batteries. However, the origin of this poor conductance has not been understood, and there is limited knowledge about the solid electrolyte–electrode interfaces in all-solid-state Li-ion batteries. In this study, we performed first principles calculations to evaluate the thermodynamics of the interfaces between solid electrolyte and electrode materials and to identify the chemical and electrochemical stabilities of these interfaces. Our computation results reveal that many solid electrolyte–electrode interfaces have limited chemical and electrochemical stability, and that the formation of interphase layers is thermodynamically favorable at these interfaces. These formed interphase layers with different properties significantly affect the electrochemical performance of all-solid-state Li-ion batteries. The mechanisms of applying interfacial coating layers to stabilize the interface and to reduce interfacial resistance are illustrated by our computation. This study demonstrates a computational scheme to evaluate the chemical and electrochemical stability of heterogeneous solid interfaces. The enhanced understanding of the interfacial phenomena provides the strategies of interface engineering to improve performances of all-solid-state Li-ion batteries.
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                Author and article information

                Contributors
                baizhengyu@htu.cn
                zhwchen@uwaterloo.ca
                junlu@anl.gov
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                23 April 2019
                23 April 2019
                2019
                : 10
                : 1890
                Affiliations
                [1 ]ISNI 0000 0004 0605 6769, GRID grid.462338.8, School of Chemistry and Chemical Engineering, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, , Henan Normal University, ; 453007 Xinxiang, China
                [2 ]ISNI 0000 0000 8644 1405, GRID grid.46078.3d, Department of Chemical Engineering, Waterloo Institute of Nanotechnology, , University of Waterloo, ; 200 University Avenue West, Waterloo, ON N2L 3G1 Canada
                [3 ]ISNI 0000 0001 1939 4845, GRID grid.187073.a, Chemical Sciences and Engineering Division, , Argonne National Laboratory, ; 9700 Cass Avenue, Lemont, IL 60439 USA
                [4 ]ISNI 0000 0001 2107 4242, GRID grid.266100.3, Department of NanoEngineering, , University of California San Diego, ; 9500 Gilman Drive, La Jolla, CA 92093 USA
                [5 ]ISNI 0000 0001 1939 4845, GRID grid.187073.a, X-ray Science Division, Advanced Photon Source, , Argonne National Laboratory, ; 9700 Cass Avenue, Lemont, IL 60439 USA
                [6 ]ISNI 0000 0001 2164 3847, GRID grid.67105.35, Department of Macromolecular and Science and Engineering, School of Engineering, , Case Western Reserve University, ; 2100 Adelbert Road, Cleveland, OH 44106 USA
                Author information
                http://orcid.org/0000-0001-9646-0738
                http://orcid.org/0000-0002-1488-1668
                http://orcid.org/0000-0001-9206-3719
                http://orcid.org/0000-0003-3463-5509
                http://orcid.org/0000-0003-0858-8577
                Article
                9638
                10.1038/s41467-019-09638-4
                6478822
                31015408
                6081e88e-584a-4c8f-b929-460fadf69b07
                © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2019 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
                : 16 February 2019
                : 17 March 2019
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                © The Author(s) 2019

                Uncategorized
                batteries,electrochemistry
                Uncategorized
                batteries, electrochemistry

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