材料科学
相间
电解质
电化学
水溶液
钝化
化学工程
无机化学
纳米技术
图层(电子)
物理化学
电极
有机化学
化学
工程类
生物
遗传学
作者
Zong‐Qiong Lin,Guangheng Fan,Tao Zhang,Fengwei Huo,Qiao Xi,Jie Wang,Tiantian She,Xinwei Zeng,Jiena Weng,Wei Huang
标识
DOI:10.1002/aenm.202203532
摘要
Abstract The solid‐electrolyte interphase (SEI) is the key component of the electrochemical electrode as a passivation layer, which enables a long calendar life for commercial applications. However, owing to the poor understanding of aqueous SEI in conventional aqueous electrolytes, the adoption of aqueous Li‐ion batteries (ALIBs) has been drastically limited. Herein, the construction of a robust aqueous SEI is successfully demonstrated by introducing a ladderized heterocyclic polymer electrode into a water‐in‐salt electrolyte, leading to ultra‐stable dual‐ion storage with long‐term calendar life. The sophisticated SEI composed of fluorinated/oxygenated species is revealed. Electrochemical and structural analysis confirm that such SEI formation is characterized by a proton co‐intercalation, which consumes the water in the Li + 's solvation shell to trigger the subsequent decomposition of organic anions. This new SEI formation path is expected to broaden the horizons of aqueous SEI and open new avenues for the design of versatile electrode materials for further advances in ALIBs.
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