4.6 Article

Fingerprinting Lithium-Sulfur Battery Reaction Products by X-ray Absorption Spectroscopy

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 161, Issue 6, Pages A1100-A1106

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.078406jes

Keywords

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Funding

  1. Office of Vehicle Technologies of the U.S. Department of Energy [DE-AC02-05CH11231]
  2. DOE Office of Biological and Environmental Research
  3. National Institutes of Health, National Institute of General Medical Sciences [P41GM103393]
  4. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]

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Lithium-sulfur batteries have a theoretical specific energy that is a factor of five greater than that of current lithium-ion batteries, but suffer from consequences of the solubility of lithium polysulfide reaction intermediates that form as the batteries are charged and discharged. These species can react with each other and diffuse out of the cathode, causing battery capacity to fade and ultimately, cell failure. In spite of work that has spanned four decades, fingerprints of polysulfides have not yet been established, precluding a systematic study of lithium-sulfur chemistry. Herein we demonstrate the use of principal component analysis of X-ray absorption spectroscopy (XAS) to obtain fingerprints of lithium polysulfides. This approach enables interpretation of spectral data without any assumptions regarding the origin of the observed spectral features or knowledge of the stability of the polysulfide species of interest. We show that in poly(ethylene oxide)-based solid electrolytes containing polysulfides made by chemically reacting Li2S and elemental sulfur, Li2S2 and Li2S6 spontaneously disproportionate to give binary Li2S/Li2S4 and Li2S4/Li2S8 mixtures, respectively, while Li2S4 and Li2S8 exist as single molecular species. XAS fingerprints of Li2S4 and Li2S8 are thus presented. (C) 2014 The Electrochemical Society. All rights reserved.

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