过电位
电解质
锂(药物)
阳极
电流密度
材料科学
快离子导体
化学工程
化学
电化学
电极
物理化学
工程类
物理
内分泌学
医学
量子力学
作者
Zeyu Ge,Nanshan Chen,Rui Wang,Rui Ma,Bo Fan,David Le Coq,Xianghua Zhang,Hongli Ma,Xue Bai
标识
DOI:10.1016/j.cej.2023.143409
摘要
All-solid-state lithium metal batteries (ASSLMBs) have received much attention because of their potential for high energy density and high safety performance. However, the poor compatibility of the lithium/solid electrolytes (SEs) interface and the penetration of lithium dendrites during cycling prevent them from achieving current densities that are capable of commercialization. In this work, a lithium-metastable solid electrolyte and a lithium-unstable solid electrolyte have been mixed to obtain mix-structured solid electrolyte. In particular, Li5.5PS4.5Cl1.5 acts as a lithium-compatible matrix, and Li10SnP2S12 as a dendrite-scavenger. The synergy between the two generates a stable interface with the Li anode and effectively suppresses the penetration of lithium dendrites. Li symmetric cells can operate stably for 160 h at a current density of 0.5 mA cm-2 at room temperature. The critical current density can reach 5 mA cm-2 and the overpotential is less than 0.5 V. The Li/SEs/Li4Ti5O12 all-solid-state cells show a high capacity of 174 mAh g-1 at 0.2 C and 148 mAh g-1 at 2 C. High-capacity retentions of 97.3% and 94.4% are shown after 75 cycles at 1 C and 2 C at room temperature, respectively. This work highlights the advantages of the electrolyte with mixed structure and provides a new strategy to resist lithium dendrites and improve the critical current density and cycle life of ASSLMBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI