电解质
材料科学
离子
链条(单位)
无机化学
铝
固态
化学工程
纳米技术
化学
电极
有机化学
冶金
物理化学
物理
天文
工程类
作者
Ke Guo,Wei Wang,Handong Jiao,Wei‐Li Song,Shuqiang Jiao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-04
卷期号:19 (36): 32595-32605
被引量:1
标识
DOI:10.1021/acsnano.5c09979
摘要
Aluminum-ion batteries (AIBs) have garnered significant attention due to their high safety and environmental compatibility. However, their practical development has been hindered by conventional liquid electrolytes, which suffer from a narrow electrochemical stability window and interfacial instability. Here, we develop a hypercoordinated chloroaluminate electrolyte (HCCAE) for low-cost and long-life solid-state AIBs, featuring a chain-assisted ion transport mechanism. Different from traditional ionic liquid electrolytes (ILs) that rely on AlCl4- and Al2Cl7- for ion conduction, the HCCAE forms a network where chloride ions from minimal 1-ethyl-3-methylimidazolium chloride (EMIC) migrate through a hypercoordinated AlCl3-rich framework, enabling a continuous, fast and stable solid-state conduction pathway [AlCl3-(AlCl3)n-AlCl3-AlCl4-]. The electrolyte exhibits ionic conductivity of 0.89 mS cm-1, an electrochemical window of >2.6 V, and electrolyte-electrode stability with Al plating/stripping over 900 h. The full battery demonstrates excellent cycling performance over 2000 cycles with high Coulombic efficiency. This work provides insights into ion transport mechanisms in aluminum-based solid electrolytes, which helps to achieve low-cost, high-safety, and long-life AIBs.
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