成核
溶解
锂(药物)
材料科学
电解质
化学工程
硫化铅
纳米尺度
硫化铁
硫黄
硫化物
散射
相(物质)
化学物理
纳米技术
化学
电极
物理化学
冶金
工程类
内分泌学
有机化学
量子点
物理
光学
医学
作者
Christian Prehal,Jean-Marc von Mentlen,Sara Drvarič Talian,Alen Vižintin,Robert Dominko,Heinz Amenitsch,Lionel Porcar,Stefan A. Freunberger,Vanessa Wood
标识
DOI:10.1038/s41467-022-33931-4
摘要
The inadequate understanding of the mechanisms that reversibly convert molecular sulfur (S) into lithium sulfide (Li2S) via soluble polysulfides (PSs) formation impedes the development of high-performance lithium-sulfur (Li-S) batteries with non-aqueous electrolyte solutions. Here, we use operando small and wide angle X-ray scattering and operando small angle neutron scattering (SANS) measurements to track the nucleation, growth and dissolution of solid deposits from atomic to sub-micron scales during real-time Li-S cell operation. In particular, stochastic modelling based on the SANS data allows quantifying the nanoscale phase evolution during battery cycling. We show that next to nano-crystalline Li2S the deposit comprises solid short-chain PSs particles. The analysis of the experimental data suggests that initially, Li2S2 precipitates from the solution and then is partially converted via solid-state electroreduction to Li2S. We further demonstrate that mass transport, rather than electron transport through a thin passivating film, limits the discharge capacity and rate performance in Li-S cells.
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