材料科学
过电位
电镀(地质)
法拉第效率
双层
相间
电解质
成核
剥离(纤维)
化学工程
扫描电子显微镜
纳米技术
电流密度
复合材料
电极
锂离子电池的纳米结构
冶金
镁
作者
Ruixin Wu,Sufu Liu,Ruihao Deng,Ru Xiao,Keng Xu,Chengyin Fu,Andrea Ingenito,Fudong Han
标识
DOI:10.1021/acsami.6c01094
摘要
The development of anode-free solid-state batteries can significantly improve the energy density of today’s lithium-ion batteries, but it has proven difficult due to challenges in regulating Li deposition/dissolution. Here, we report a Mg/C bilayer interphase for anode-free batteries. We observed the lithiation of both Mg and C prior to the initial plating process. Moreover, a larger nucleation overpotential can be observed on lithiated carbon (Li–C) than on lithiated magnesium (Li–Mg). As a result, instead of plating at the interface between Li–C and the solid electrolyte (SE), Li will penetrate through the Li–C and the plate at the interface between Li–C and Li–Mg. The regulated Li plating was also validated through cross-sectional scanning electron microscopy images. As a result, a uniform Li plating and stripping can be achieved underneath the Li–C. The effective separation of the SE and the plated Li enabled stable plating/stripping cycles at an areal capacity of 2 mAh/cm 2 at room temperature with an average Coulombic efficiency of >99%. The results provide important insights into understanding and designing interlayers for anode-free solid-state batteries.
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