材料科学
电解质
相间
阳极
金属
化学工程
无机化学
纳米技术
冶金
电极
物理化学
化学
遗传学
工程类
生物
作者
Wanxia Li,Yulin Jie,Zixu He,Zhanwu Lei,Zhihao Ma,Yehu Han,Xiaodi Ren,Jianbin Zhou,Ruiguo Cao,Shuhong Jiao
标识
DOI:10.1021/acsami.5c03673
摘要
Solid electrolyte interphases (SEIs) play essential roles in lithium metal batteries by dictating the deposition morphology and Coulombic efficiency (CE) of lithium metal anodes. However, the understanding of the formation and evolution of SEIs remains elusive so far. Herein, we present an operando investigation of the formation and evolution dynamics of LiNO3-induced SEI under liquid electrolytes using high-resolution electrochemical atomic force microscopy (EC-AFM). For the first time, we discovered the in situ formation of an ultrathick SEI (∼648 nm) under liquid electrolytes, which far exceeded the thicknesses observed via ex situ characterization techniques. This ultrathick SEI formed through a sequential reduction process, wherein an inorganic-rich inner layer was initially formed, followed by the deposition of a soft outer layer with a modulus of approximately 24 MPa. We also observed that the outer SEI layer was metastable and susceptible to dissolution in liquid electrolytes. Our findings provide a comprehensive investigation of the formation and evolution processes of the LiNO3-induced SEI, deepening the understanding of the in situ structure of SEIs under liquid electrolytes.
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