过电位
阳极
电化学
电解质
阴极
电池(电)
枝晶(数学)
相(物质)
锂(药物)
材料科学
电流密度
金属
化学工程
电极
化学
热力学
物理化学
冶金
有机化学
工程类
内分泌学
功率(物理)
物理
医学
量子力学
数学
几何学
作者
Xin Dong,Ziqin Liu,Kaiquan He,Pu Hu,Chaoqun Shang
标识
DOI:10.1016/j.jcis.2023.05.196
摘要
Li metal is a potential anode material for the next generation high-energy-density batteries because of its high theoretical specific capacity. However, the inhomogeneous lithium dendrite growth restrains corresponding electrochemical performance and brings safety concerns. In this contribution, the Li3Bi/Li2O/LiI fillers are generated by the in-situ reaction between Li and BiOI nanoflakes, which promises corresponding Li anodes (BiOI@Li) showing favorable electrochemical performance. This can be attributed to the bulk/liquid dual modulations: (1) The three-dimensional Bi-based framework in the bulk-phase lowers the local current density and accommodates the volume variation; (2) The LiI dispersed within Li metal is slowly released and dissolved into the electrolyte with the consumption of Li, which will form I-/I3- electron pair and further reactivate the inactive Li species. Specifically, the BiOI@Li//BiOI@Li symmetrical cell shows small overpotential and enhanced cycle stability over 600 h at 1 mA cm-2. Matched with an S-based cathode, the full Li-S battery demonstrates desirable rate performance and cycling stability.
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