电解质
晶界
电化学
相(物质)
电导率
金属
化学工程
化学
锂(药物)
电化学窗口
材料科学
电极
阴极
快离子导体
离子电导率
阳极
分析化学(期刊)
复合材料
冶金
微观结构
内分泌学
物理化学
医学
有机化学
工程类
色谱法
作者
Yutao Li,Xi Chen,Andrei Dolocan,Zhiming Cui,Sen Xin,Leigang Xue,Henghui Xu,Kyu‐Sung Park,John B. Goodenough
摘要
Garnet-structured Li7La3Zr2O12 is a promising solid Li-ion electrolyte for all-solid-state Li-metal batteries and Li-redox-flow batteries owing to its high Li-ion conductivity at room temperature and good electrochemical stability with Li metal. However, there are still three major challenges unsolved: (1) the controversial electrochemical window of garnet, (2) the impractically large resistance at a garnet/electrode interface and the fast lithium-dendrite growth along the grain boundaries of the garnet pellet, and (3) the fast degradation during storage. We have found that these challenges are closely related to a thick Li2CO3 layer and the Li–Al–O glass phase on the surface of garnet materials. Here we introduce a simple method to remove Li2CO3 and the protons in the garnet framework by reacting garnet with carbon at 700 °C; moreover, the amount of the Li–Al–O glass phase with a low Li-ion conductivity in the grain boundary on the garnet surface was also reduced. The surface of the carbon-treated garnet pellets is free of Li2CO3 and is wet by a metallic lithium anode, an organic electrolyte, and a solid composite cathode. The carbon post-treatment has reduced significantly the interfacial resistances to 28, 92 (at 65 °C), and 45 Ω cm2 at Li/garnet, garnet/LiFePO4, and garnet/organic-liquid interfaces, respectively. A symmetric Li/garnet/Li, an all-solid-state Li/garnet/LiFePO4, and a hybrid Li–S cell show small overpotentials, high Coulombic efficiencies, and stable cycling performance.
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