二甲氧基乙烷
电解质
溶剂化
无机化学
溶剂
材料科学
锂(药物)
电池(电)
离子
阴极
乙醚
硝酸锂
金属
化学
离子键合
有机化学
物理化学
电极
功率(物理)
内分泌学
物理
医学
量子力学
作者
Dandan Chai,Haotian Yan,Xin Wang,Xiang Li,Yongzhu Fu
标识
DOI:10.1002/adfm.202310516
摘要
Abstract Ether‐based electrolytes have good compatibility for lithium metal, which is widely used in lithium metal batteries (LMBs). However, the electrolyte is not suitable for high voltage (>4.0 V) due to its poor anti‐oxidation behavior. Herein, an anion chemistry strategy is designed for a typical 1,2‐dimethoxyethane (DME)‐based electrolyte with 1 m lithium bis(fluorosulfonyl)imide (LiFSI), by using nitrate anion (NO 3 − ) with a high donor number (DN) value to regulate the coordination of DME and FSI – . It is evidenced that the interaction between them is weakened due to the competitive advantage of NO 3 − , therefore a weakly solvating electrolyte is achieved. It promotes the formation of an inorganic‐rich passivation layer on the cathode and facilitates the de‐solvation process, thus it is suitable for high voltage even at 4.5 V. The anion‐regulated weakly solvating electrolyte (ARWSE) designed here is different from the high‐concentration electrolyte (HCE), localized HCE, and WSE which are of high cost and complexity. The ARWSE is demonstrated to be an adjustable electrolyte system, effectively improving the interfacial chemistry of LMBs.
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