阳极
材料科学
电解质
法拉第效率
化学工程
锂(药物)
金属
图层(电子)
碳酸乙烯酯
电池(电)
无机化学
金属锂
氧化还原
锂离子电池的纳米结构
电极
纳米技术
化学
冶金
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Jianming Zheng,Pengfei Yan,Donghai Mei,Mark Engelhard,Samuel Cartmell,Bryant J. Polzin,Chongmin Wang,Ji‐Guang Zhang,Wu Xu
标识
DOI:10.1002/aenm.201502151
摘要
Lithium (Li) metal has been extensively investigated as an anode for rechargeable battery applications due to its ultrahigh theoretical specific capacity and the lowest redox potential. However, significant challenges including dendrite growth and low Coulombic efficiency are still hindering the practical applications of rechargeable Li metal batteries. It is demonstrated that long‐term cycling of Li metal batteries can be realized by the formation of a transient high‐concentration electrolyte layer near the surface of Li metal anode during high rate discharge process. The highly concentrated Li + ions in this transient layer will immediately be solvated by the available solvent molecules and facilitate the formation of a stable and flexible solid electrolyte interphase (SEI) layer composed of a poly(ethylene carbonate) framework integrated with other organic/inorganic lithium salts. This SEI layer largely suppresses the corrosion of Li metal anode attacked by free organic solvents and enables the long‐term operation of Li metal batteries. The fundamental findings in this work provide a new direction for the development of Li metal batteries that could be operated at high current densities for a wide range of applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI