电解质
阳极
合金
材料科学
薄膜
金属
纹理(宇宙学)
电化学
结晶
箔法
兴奋剂
冶金
化学工程
电极
纳米技术
复合材料
化学
光电子学
物理化学
计算机科学
人工智能
工程类
图像(数学)
作者
Yuhang Hu,Hao Li,Zidong Chen,Wanglai Cen,Qiang Wang,Yungui Chen,Ali Davoodi,Wei Liu
标识
DOI:10.1016/j.cej.2023.143084
摘要
A thin Li metal anode is imperative for practical lithium metal batteries (LMBs). Fabricating and stabilizing <50 μm Li-metal anode is daunting due to the poor processability of Li and its inherent instability in liquid electrolytes. Here, we found that doping Li with 8.9 at% Sn yields a Li-Li22Sn5 dual-phase alloy with impressive processability that allows rolling of <40 μm thin foils. Intriguingly, in the thin Li-Sn foil, the rolling process built a strong Li22Sn5(822) texture that can regulate Li electro-crystallization along the densely packed Li(110) facets. Such in-built Li(110) epitaxy is a result of >99% lattice match of Li(110)-Li22Sn5(822) and gives rise to a greatly stabilized Li growth front due to the low binding energy of solvated-Li+ with Li(110) surface. Partial de-alloy treatment can fully activate the in-built Li(110) epitaxy, achieving stable plate-strip cycling in symmetric cells over 300 h at 80% depth-of-discharge (DOD). Stable 2.5 mAh/cm2 full pouch cells in carbonate electrolyte (EC:EMC: DEC = 1:1:1, 5 % FEC) were achieved at a low N:P ratio of 2.1. Conversely, conventional Li-Sn and neat Li, even possessing more abundant active Li, quickly failed. The uncovered critical crystallography-electrochemistry correlation in textured Li-alloys sheds light on thin Li-metal anode development.
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