材料科学
溶解
电化学
电解质
合金
锂(药物)
化学工程
金属锂
金属
纳米技术
电极
复合材料
冶金
物理化学
化学
内分泌学
工程类
医学
作者
Mengqi Li,Dong Zhou,Chao Wang,Wei Weng,Miao Jiang,Gaozhan Liu,Xiayin Yao,Hao He
标识
DOI:10.1021/acsami.1c16356
摘要
All-solid-state lithium-metal batteries (ASSLMBs) have received great interest due to their high potential to display both high energy density and safety performance. However, the poor compatibility at the Li/solid electrolyte (SE) interface and penetration of lithium dendrites during cycling strongly impede their successful commercialization. Herein, a thin Ag layer was introduced between Li and Li10GeP2S12 for the in situ formation of a Li-Ag alloy interface, thus tuning the interfacial chemistry and lithium deposition/dissolution behavior. Superior electrochemical properties and improved interfacial stability were achieved by optimizing the Ag thicknesses. The assembled symmetric cell with Li@Ag 1 μm showed a steady voltage evolution up to 1000 h with an areal capacity of 1 mAh cm-2. Moreover, a high reversible capacity of 106.5 mAh g-1 was achieved in an all-solid-state cell after 100 cycles, demonstrating the validity of the Ag layer. This work highlights the importance of the Li/SE interface re-engineering and provides a new strategy for improving the cycle life of ASSLMBs.
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