阴极
电解质
介电谱
溶解
材料科学
电极
X射线光电子能谱
化学工程
多孔性
基质(化学分析)
硫黄
溶解度
纳米技术
电化学
化学
复合材料
冶金
工程类
有机化学
物理化学
作者
Rezan Demir-Çakan,Mathieu Morcrette,Gangulibabu,Aurélie Guéguen,Rémi Dedryvère,Jean‐Marie Tarascon
摘要
Although promising improvements have been made in the field of Li–S rechargeable batteries, they are still far from reaching the market place due to several drawbacks. To combat the solubility of polysulphides, confinement approaches aiming to trap sulphur within the cathode side have been pursued, but success has been limited. Herein, we drastically deviate from this approach and use a liquid cathode obtained either by dissolving polysulphides within the electrolyte or by placing sulphur powders in contact with the Li negative electrode. Such approaches are shown to result in greater performance than confinement approaches. Such a strategy eliminates the detrimental Li2S formation inside a porous carbon matrix and moreover leads to the formation of a protective SEI layer at the Li electrode, as deduced by impedance spectroscopy and XPS, which seems beneficial to the cell cycling performance.
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