多硫化物
电解质
硫黄
溶解
电化学
材料科学
阴极
溶解度
扩散
电导率
无机化学
锂硫电池
电池(电)
化学工程
化学
冶金
电极
有机化学
物理化学
热力学
功率(物理)
工程类
物理
作者
Li Wang,Yong Xie,Xiaoqun Qi,Ruining Jiang,Kai Huang,Long Qie,Sa Li
标识
DOI:10.1021/acsami.2c10906
摘要
Due to the poor electronic conductivity of solid sulfur and sulfides, the dissolution of Sα- (α = 0, 2/8, 2/6, 2/4) into a liquid electrolyte and the vehicular diffusion of Sα- to carbon black are necessary for the electrochemical activity of a sulfur cathode in lithium-sulfur (Li-S) batteries. However, exactly how much dissolution and diffusion are required for high sulfur utilization and how this may control the minimum electrolyte/sulfur ratio, (E/S)min, have not been quantitatively settled. In this work, we show experimentally that a dissolved polysulfide concentration which is too high (>10-20 MS) may gel the liquid electrolyte, leading to catastrophic loss of Sα- mobility, a failure mode that is especially susceptible in a high-donor-number (DN) electrolyte under a lean condition (low E/S), similar to a traffic jam, resulting in high electrochemical polarization and low sulfur utilization. In contrast, we show that a low-DN electrolyte, even with a low polysulfide solubility of 0.1-0.5 MS, will never encounter a gelation catastrophe even at extremely low E/S, leading to unprecedentedly high energy density. Specifically, high sulfur utilizations of 96% (1600 mAh g-1) and 78% (1300 mAh g-1) are reached in an electrolyte as lean as E/S = 2 and 1 μL mg-1 Li-S coin cells when DME1.6LiFSI-HFE of low solvation capability (DN = 13.9) is adopted, even paired against a high-sulfur-loading cathode (5 mg cm-2).
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