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In Situ NMR Observation of the Temporal Speciation of Lithium Sulfur Batteries during Electrochemical Cycling
Author(s) -
Hao Wang,
Niya Sa,
Meinan He,
Xiao Liang,
Linda F. Nazar,
Mahalingam Balasubramanian,
Kevin G. Gallagher,
Baris Key
Publication year - 2017
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.7b01922
Subject(s) - polysulfide , disproportionation , sulfur , electrochemistry , lithium (medication) , dissolution , electrolyte , anode , inorganic chemistry , chemistry , in situ , precipitation , electrode , materials science , organic chemistry , catalysis , medicine , physics , meteorology , endocrinology
The understanding of the reaction mechanism and temporal speciation of the lithium–sulfur batteries is challenged by complex polysulfide disproportionation chemistry coupled with the precipitation and dissolution of species. In this report, for the first time, we present a comprehensive method to investigate lithium sulfur electrochemistry using in situ 7Li NMR spectroscopy, a technique that is capable of quantitatively capturing the evolution of the soluble and precipitated lithium (poly)sulfides during electrochemical cycling. Through deconvolution and quantification, every lithium-bearing species was closely tracked and four-step soluble lithium polysulfide-mediated lithium sulfur electrochemistry was demonstrated in never before seen detail. Significant irreversible accumulation of Li2S is observed on the Li metal anode after four cycles because of sulfur shuttling. The application of the method presented here to study electrolyte/additive development and lithium protection research can be readily env...

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