电解质
电化学
材料科学
离子电导率
电导率
锂(药物)
复合数
化学工程
电流密度
自行车
相(物质)
涂层
硫化物
纳米技术
电极
化学
复合材料
冶金
物理化学
医学
工程类
物理
考古
量子力学
有机化学
历史
内分泌学
作者
Yuzhe Zhang,Haolong Chang,Aiguo Han,Shijie Xu,Xinyu Wang,Shunjin Yang,Xiaohu Hu,Yujiang Sun,Xiao Sun,Xing Chen,Yongan Yang
标识
DOI:10.1016/j.gee.2024.07.001
摘要
Li6PS5Cl is a highly wanted sulfide-solid-electrolyte (SSE) for developing all-solid-state lithium batteries, due to its high ionic conductivity, good processability and abundant compositional elements. However, its cyclability is poor because of harmful side reactions at the Li6PS5Cl/Li interface and growth of lithium dendrites inside Li6PS5Cl phase. Herein, we report a simple interface-engineering remedy to boost the electrochemical performance of Li6PS5Cl, by coating its surface with a Li-compatible electrolyte Li3OCl having low electronic conductivity. The obtained Li6PS5Cl@Li3OCl core@shell structure exhibits a synergistic effect. Consequently, compared with the bare Li6PS5Cl, this composite electrolyte exhibits great performance improvements: 1) In Li|electrolyte|Li symmetric cells, the critical current density at 30 °C gets increased from 0.6 mA cm−2 to 1.6 mA cm−2, and the lifetime gets prolonged from 320 h to 1400 h at the cycling current of 0.2 mA cm−2 or from 10 h to 900 h at the cycling current of 0.5 mA cm−2; 2) In Li|electrolyte|NCM721 full cells running at 30 °C, the cycling capacity at 0.2 C (or 0.5 C) gets enhanced by 20% (or from unfeasible to be feasible) for 100 cycles and the rate capability reaches up to 2 C from 0.2 C; and in full cells running at 60 °C, the cycling capacity is increased by 7% at 0.2 C and the rate capability is enhanced to 3.0 C from 0.5 C. The experimental studies and theoretical computations show that the performance enhancements are due to the confined electron penetration and suppressed lithium dendrites growth at the Li6PS5Cl@Li3OCl interface.
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