电解质
材料科学
阳极
硅
锂(药物)
氢氧化物
X射线光电子能谱
相间
无机化学
化学工程
电极
物理化学
冶金
工程类
内分泌学
生物
化学
医学
遗传学
作者
Steven Lam,Ankit Verma,Maxwell C. Schulze,Robert L. Sacci,Harry M. Meyer,Michael J. Lance,Khryslyn G. Araño,A.R. de L. Musgrove,Marco‐Tulio F. Rodrigues,Stephen E. Trask,Andrew M. Colclasure,Gabriel M. Veith
标识
DOI:10.1021/acsami.5c07869
摘要
Although localized high-concentration electrolytes (LHCEs) have been shown to improve the calendar lifetime of silicon anodes, the roles of the electrolyte constituents in calendar aging are not well understood. Here, we utilize a voltage hold protocol and an LHCE with varying molar ratios of lithium bis(fluorosulfonyl)imide (LiFSI), tetramethylene sulfone (TMS), and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTE) to probe the component roles during aging. Interestingly, the estimated calendar lifetime and irreversible lithium losses from the V-hold experiments are independent of the electrolyte formulations. Contrarily, the solid electrolyte interphase (SEI) composition depends on the electrolyte formulation. X-ray photoelectron spectroscopy shows that TMS-coordinated species decompose to form insoluble alkanes and lithium hydroxide (LiOH), while lithium fluoride (LiF) originates from the anion-coordination complex. The SEI composition does not appear to play a significant role in the silicon anode passivity, as measured by parasitic current, suggesting that the SEI-electrolyte interactions dictate the calendar aging mechanisms.
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