电解质
材料科学
离子电导率
锂(药物)
铟
电化学窗口
化学工程
介电谱
电化学
快离子导体
阳极
反应性(心理学)
电导率
相(物质)
离子键合
合金
化学稳定性
金属
放松(心理学)
复合数
降级(电信)
电化学电池
钛酸锂
电阻式触摸屏
结构稳定性
硝酸锂
电极
作者
Camilla Rosa,Arianna Pesce,Pierre Lannelongue,Marco Ravalli,Juan Miguel López del Amo,Pedro López‐Aranguren,Eliana Quartarone,Cristina Tealdi
标识
DOI:10.1016/j.jpcs.2025.113327
摘要
The development of safe, high-energy-density all-solid-state batteries (ASSBs) hinges on solid electrolytes that combine high ionic conductivity with chemical and electrochemical stability. In this work, we investigate the physico-chemical and interfacial properties of Li 3 InCl 6 synthesized via an ethanol-mediated route, offering a scalable, low-energy alternative to conventional processing methods. The resulting material exhibits high phase purity and relatively high room-temperature ionic conductivity (0.73 mS·cm -1 ), being readily densifiable under cold pressing and maintaining structural integrity. Interfacial reactivity with lithium and indium metal anodes was systematically studied using electrochemical impedance spectroscopy (EIS), distribution of relaxation times (DRT) analysis, and X-ray diffraction (XRD). While lithium induces rapid formation of a resistive solid electrolyte interphase (SEI), indium significantly mitigates interface degradation by forming a Li-In alloy that enhances chemical stability and cycling performance. Symmetric stripping/plating tests demonstrate stable long-term cycling under pressure and elevated temperature in cells employing Li-In composite anodes. This work highlights the importance of interfacial engineering for halide-based solid electrolytes and introduces DRT as a valuable analysis tool to resolve and monitor dynamic degradation processes at buried interfaces in ASSBs.
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