材料科学
X射线光电子能谱
介电谱
法拉第效率
微晶
俄歇电子能谱
阳极
电解质
Crystal(编程语言)
金属
循环伏安法
单晶
分析化学(期刊)
电极
电化学
化学工程
结晶学
冶金
物理化学
化学
核物理学
工程类
程序设计语言
物理
色谱法
计算机科学
作者
Kohei Ishikawa,Shunta Harada,Miho Tagawa,Toru Ujihara
标识
DOI:10.1021/acsami.9b22157
摘要
Li metal anodes are plagued by low coulombic efficiency due to their interfacial instability. Many approaches were proposed to cope with this problem; however, little attention has been given to the current collector of Li anodes. In this study, we investigate the crystal orientation dependence of the cycling stability of Li anodes on single-crystal Cu(111), (101), and (001) and polycrystalline Cu current collectors. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) show that (111) and (001) achieved high current efficiency and low interfacial resistance, while (101) and polycrystalline Cu exhibited low cyclabilities. X-ray photoelectron spectroscopy (XPS) and auger electron spectroscopy (AES) analysis revealed that the thickness of the solid electrolyte interphase (SEI) varies with the Cu crystal orientation, and the SEI is the thinnest on the single-crystal Cu(111). This tendency can be explained by the orientation dependence of the surface energy of Cu, which corresponds to the chemical activity of the surfaces. Our result advocates the importance of considering Cu orientation for interfacial engineering of Li metal anodes.
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