电解质
材料科学
离子电导率
阳极
电化学
电导率
化学工程
锂(药物)
储能
卤化物
电化学窗口
无机化学
金属锂
腐蚀
金属
降级(电信)
容量损失
电极
钛酸锂
电池(电)
锂离子电池的纳米结构
半电池
电化学电池
快离子导体
过渡金属
化学稳定性
导电体
作者
Xin Wu,Lixin Liang,Bingxuan Du,Yiwen Liu,Zhenjie Zhang,Yu Shi,Shaochun Tang,Guangjin Hou,Haoshen Zhou,Ping He
标识
DOI:10.1002/anie.202523225
摘要
All-solid-state lithium batteries (ASSLBs) are promising candidates for next-generation energy storage due to their enhanced safety and energy density. Among solid-state electrolytes (SSEs), argyrodite-type Li6PS5X compounds offer economic advantages but suffer from limited ionic conductivity and electrochemical stability. In this study, we design a novel SSE, Li5.5P0.94Ta0.06S4.5Cl0.75Br0.75, featuring dual halide (Cl-/Br-) occupation and Ta5+ substitution to enhance conductivity and interfacial compatibility. The resulting SSE exhibits a high ionic conductivity of 12 mS cm-1 at room temperature. Inspired by Al corrosion passivation, it forms in situ self-passivating interfacial layers, ensuring stability against both lithium metal anodes and high-voltage cathodes. Batteries incorporating this electrolyte achieved 100% capacity retention over 200 cycles at 0.2C, and over 81% retention after 1200 cycles at 0.5C. Under high-loading (30 mg cm-2) and N/P = 1.8 conditions, 81% capacity was maintained after 150 cycles. A 10 × 6 cm2 pouch cell retained 96.4% of its capacity after 200 cycles. This work offers a viable route toward high-performance, scalable ASSLBs using a single-passivating electrolyte.
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