金属锂
电解质
材料科学
锂(药物)
电镀(地质)
电池(电)
剥离(纤维)
锂离子电池
金属
溶剂
离子
无机化学
化学工程
冶金
有机化学
化学
电极
复合材料
物理化学
热力学
功率(物理)
内分泌学
工程类
地质学
物理
医学
地球物理学
作者
Qian Li,Gang Liu,Yinghua Chen,Jia Wang,Pushpendra Kumar,Hongliang Xie,Wandi Wahyudi,Hao Yu,Zexu Wang,Zheng Ma,Jun Ming
标识
DOI:10.1002/adfm.202420327
摘要
Abstract Electrolyte engineering plays a critical role in tuning lithium plating/stripping behaviors, thereby enabling safer operation of lithium metal anodes in lithium metal batteries (LMBs). However, understanding how electrolyte microstructures influence the lithium plating/stripping process at the molecular level remains a significant challenge. Herein, using a commonly employed ether‐based electrolyte as a model, the role of each electrolyte component is elucidated and a relationship between electrolyte behavior and the lithium plating/stripping process is established by investigating the effects of electrolyte compositions, including solvents, salts, and additives. The variations in Li + deposition kinetics are not only analyzed by characterizing the lithium deposition overpotential and exchange current density but it is also identified that the intermolecular interactions are the previously unexplored cause of these variations by 2D nuclear overhauser effect spectroscopy (NOESY). An interfacial model is developed to explain how solvent interactions, distinct roles of anions, and critical effects of additives influence Li + desolvation kinetics and the thermodynamic stability of desolvation clusters during lithium plating/stripping process. This model clarifies how these configurations of solvents and ions are related to the macroscopic properties of lithium plating/stripping chemistry. These findings contribute to more uniform and controllable lithium deposition, providing valuable insights for designing advanced electrolyte systems for LMBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI