In vacuo XPS investigation of surface engineering for lithium metal anodes with plasma treatment

X射线光电子能谱 钝化 锂(药物) 电解质 阳极 手套箱 材料科学 图层(电子) 金属 分析化学(期刊) 原子层沉积 电化学 等离子体 表面改性 化学工程 电极 表层 化学 无机化学 纳米技术 冶金 物理化学 内分泌学 工程类 有机化学 物理 医学 量子力学 色谱法
作者
Bo Zhao,Jin Li,Maxime Guillaume,Jolien Dendooven,Christophe Detavernier
出处
期刊:Journal of Energy Chemistry [Elsevier BV]
卷期号:66: 295-305 被引量:47
标识
DOI:10.1016/j.jechem.2021.08.032
摘要

Lithium (Li) metal is an attractive anode material with high capacity (3860 mAh g−1) and low potential (−3.04 V vs. standard hydrogen electrode) that shows highly promising for applications requiring high energy density. However, the low electrochemical potential of Li metal makes it extremely reactive and inevitably forming a native oxidized layer in the ambient environment and repeatedly being consumed when exposed to liquid electrolytes. It is therefore beneficial to replace the poorly controlled native passivation layer with a tailored artificial SEI to improve interface management between Li and electrolyte and enhance the stability of Li metal battery. Here, we use an integrated glovebox-atomic layer deposition (ALD)- X-ray photoelectron spectroscopy (XPS) setup to in-situ investigating the pristine Li surface and the surface composition after Ar, H2, O2, N2 and NH3 plasma treatment processes. We find that the pristine Li foil is naturally being covered with a native oxidized layer, which is mainly composed of LiOH, Li2O and Li2CO3. These investigated plasmas can efficiently remove the oxidized layer from the Li metal surface, in which metallic Li surface is obtained after Ar or H2 plasma treatments, where Ar plasma is more efficient. While O2 plasma treatment produces a Li2O layer, and N2 or NH3 plasma treatment leads to a Li3N (including a certain amount of LiON) layer on the Li surface. When employing the representative metallic Li (by Ar plasma treatment), Li2O layer coated Li (by O2 plasma treatment) and Li3N layer coated Li (by N2 plasma treatment) foils as electrodes in symmetric Li metal batteries, the Li3N coated Li electrode exhibits much higher stability than that of metallic and Li2O layer coated Li foils. Improved electrochemical performance has also been achieved in LiMn2O4 (LMO)||Li full cells using Li anode with Li3N protective coating layer. Our work reveals the detailed process of surface engineering of Li metal anodes with plasma treatments by in vacuo XPS, which may also be extended to other gas-treatment or plasma-treatment for stabilization of high energy density Li metal anodes and other metal-based anodes.
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