法拉第效率
材料科学
阳极
相间
电化学
锂(药物)
阴极
极化(电化学)
化学工程
金属
金属锂
枝晶(数学)
电极
半电池
离子电导率
电解质
电导率
电化学窗口
纳米技术
冶金
化学
工作电极
医学
工程类
物理化学
生物
遗传学
内分泌学
几何学
数学
作者
Haoling Liu,Wen Pan,Bo Xiao,Yunke Jin,Kun Li,An Wang,Huimiao Li,Zhibin Wu,Yuejiao Chen,Shaozhen Huang,Lin Mei,Libao Chen
出处
期刊:Materials
[Multidisciplinary Digital Publishing Institute]
日期:2025-04-24
卷期号:18 (9): 1930-1930
摘要
Interfacial modification strategies for lithium metal anodes have emerged as a promising method to improve cycling stability, suppress lithium dendrite growth, and increase Coulombic efficiency. However, the reported chemical synthesis methods lead to side reactions and side products, which hinder their electrochemical performance. In this study, we propose a novel and facile red phosphorus-assisted solid-state friction method to in situ fabricate a uniform Li3P interphase directly on the surface of lithium metal. Interestingly, the as-formed artificial Li3P interphase with high ionic conductivity and lithium affinity features significantly enhanced interfacial stability and electrochemical kinetics. The symmetric cells based on Li@P with the Li3P interphase achieved a prolonged lifespan, over 1000 h, at 1 mA/cm2 with low polarization. When paired with a high-loading LiFePO4 cathode (10.5 mg/cm2), the Li@P||LiFePO4 full cell retained 88.9% of its capacity after stable cycling for 550 cycles at 2 C and further demonstrated the excellent performance and stability of the Li@P‖LiCoO2 full pouch cell. This study provides an efficient and scalable strategy for stabilizing lithium metal anodes, expanding new ideas for the development of next-generation high-energy-density batteries.
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