多硫化物
电解质
电极
X射线光电子能谱
锂(药物)
氧化物
无机化学
金属
电池(电)
材料科学
化学
化学工程
物理化学
有机化学
医学
功率(物理)
物理
量子力学
工程类
内分泌学
作者
Kie Hankins,Venkateshkumar Prabhakaran,Sungun Wi,Vaithiyalingam S. Shutthanandan,Grant E. Johnson,Swadipta Roy,Hui Wang,Yuyan Shao,Suntharampillai Thevuthasan,Perla B. Balbuena,Karl Todd Mueller,Vijayakumar Murugesan
标识
DOI:10.1021/acs.jpclett.1c01930
摘要
Delineating intricate interactions between highly reactive Li-metal electrodes and the diverse constituents of battery electrolytes has been a long-standing scientific challenge in materials design for advanced energy storage devices. Here, we isolated lithium polysulfide anions (LiS 4 – ) from an electrolyte solution based on their mass-to-charge ratio and deposited them on Li-metal electrodes under clean vacuum conditions using ion soft landing (ISL), a highly controlled interface preparation technique. The molecular level precision in the construction of these model interfaces with ISL, coupled with in situ X-ray photoelectron spectroscopy and ab initio theoretical calculations, allowed us to obtain unprecedented insight into the parasitic reactions of well-defined polysulfides on Li-metal electrodes. Our study revealed that the oxide-rich surface layer, which is amenable to direct electron exchange, drives multielectron sulfur oxidation (S 0 → S 6+ ) processes. Our results have substantial implications for the rational design of future Li–S batteries with improved efficiency and durability.
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