Jian Peng, Dengxu Wu, Fengmei Song, Shuo Wang, Quanhai Niu, Jieru Xu, Pushun Lu, Hong Li, Liquan Chen, Fan Wu
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引用次数: 35
摘要
金属锂是理想的阳极候选材料,但面临着巨大的挑战,包括液体有机电解质的热力学稳定性差,以及在连续电镀/剥离过程中枝晶的成核/生长。为了解决上述困难,本文提出了一种由液态锂溶液阳极、硫化物固体电解质和界面保护层组成的电池配置,以防止两组分之间的界面反应。这种结构结合了液体-锂溶液阳极(溶解锂,基本上防止锂成核)和硫化物固体电解质(所有固体电解质中室温离子电导率最高,只需冷压即可实现完全致密层的理想机械延展性)的优点,从而实现了创纪录的高电流密度(17.78 mA cm−2)和长循环寿命(近3000 h)。同时,系统地研究了金属锂在液态锂阳极中的溶解度和液态锂阳极的电化学性能,以找到室温电导率最高(12.2 mS cm−1)的最佳液态锂阳极浓度。这项工作为实现高比容量、高能量/功率密度和长循环寿命的二次电池提供了一种有前途的方法和电池配置。
High Current Density and Long Cycle Life Enabled by Sulfide Solid Electrolyte and Dendrite-Free Liquid Lithium Anode
Lithium metal is the ideal anode candidate but suffers from great challenges including poor thermodynamic stability in liquid organic electrolytes and dendrite nucleation/growth during the continuous plating/stripping process. To solve the difficulties listed above, here, a battery configuration combining a liquid lithium solution anode, a sulfide solid electrolyte, and an interfacial protection layer is proposed to prevent interfacial reaction between the two components. This configuration combines the advantages of liquid-lithium-solution anode (dissolve lithium to essentially prevent lithium nucleation) and sulfide solid electrolyte (highest room-temperature ionic conductivity among all solid electrolytes and ideal mechanical ductility for fully compact layer simply by cold pressing), so that a record-high current density (17.78 mA cm−2) and long cycle life (nearly 3000 h) are realized. At the same time, the solubility of lithium metal in the liquid Li anode and electrochemical properties of liquid Li anode are systematically studied to find the most suitable liquid Li anode concentration with the highest room-temperature conductivity (12.2 mS cm−1). This work provides a promising approach and battery configuration for achieving high-specific-capacity, high-energy/power-density and long-cycle-life secondary batteries.
期刊介绍:
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