材料科学
相间
阳极
电解质
电化学
储能
原位
化学工程
金属锂
金属
电极
催化作用
电化学能量转换
快离子导体
离解(化学)
锂(药物)
纳米技术
电化学储能
电化学电位
温度梯度
化学反应
能量转换
电化学电池
枝晶(数学)
化学能
电位梯度
阴极
单排替反应
相容性(地球化学)
表征(材料科学)
氧化还原
金属有机骨架
表面能
作者
Xuanyi Zhou,Shihao Fang,Yuxuan Liu,Lin Dai,Xupeng Xu,Lei Xi,Jüjun Yuan,Chao Peng,Min Zhu,Jun Liu
摘要
ABSTRACT All‐solid‐state lithium‐metal batteries utilizing inorganic solid electrolytes are viewed as a promising alternative for electrochemical energy storage systems. Nevertheless, compatibility issues as for the anode‐electrolytes interface hinder their practical implementation due to the uncontrollable Li dendrite growth and undesirable side reactions. By regulating the reaction pathways, the composition and structure of the interface can be precisely tailored, thereby enhancing the anode interface compatibility. Here, a gradient F‐rich multiphase interphase was constructed through precise control over the in situ “catalytic conversion” reactions of metal fluorides at the Li/electrolyte interface. Through advanced characterization and detailed calculation, we found that metal fluorides can act as catalytic centers, promoting the dissociation of lithium salts due to the strong Lewis acid‐alkali base electrostatic interaction. Subsequently, Li‐alloy phases were generated through thermodynamic spontaneous reaction at low potentials. Finally, the gradient lipophilic‐lipophobic SEI composed of co‐grown LiF, Li 3 N, and Li‐alloy effectively enhances the Li + transport and promotes uniform Li + flux. The reaction driven F‐rich multiphase SEI enable the Li symmetric cell an impressive CCD performance of up to 4.6 mA cm −2 , and the NCM811/Li full cell an excellent cycling performance with a capacity retention of 80.4% after 800 cycles, demonstrating the practical application potential in energy storage field.
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