电解质
锂(药物)
电化学
化学工程
阳极
金属锂
材料科学
锂电池
阴极
电极
化学
离子键合
物理化学
有机化学
离子
内分泌学
工程类
医学
作者
Yi‐Chen Hsieh,Johannes Helmut Thienenkamp,Chen−Jui Huang,Hsien‐Chu Tao,Uta Rodehorst,Bing‐Joe Hwang,Martin Winter,Gunther Brunklaus
标识
DOI:10.1021/acs.jpcc.0c09771
摘要
Because of the high specific capacity and low redox potential, lithium metal constitutes a promising material and might be an option for high energy density next-generation battery technologies, though application of lithium metal batteries (LMBs) is currently limited by poor long-term performance and severe safety issues when liquid electrolytes are used. These challenges arise from formation of "dead" lithium or inhomogeneous lithium deposits as well as ineffective solid electrolyte interphase (SEI) layers on lithium metal electrodes. Notably, lithium consumed by SEI formation and fractions of "dead" lithium was derived from in situ 7Li nuclear magnetic resonance (NMR) of pouch-type cells, while 19F 1D magnetic resonance imaging (MRI) profiling along with operando optical microscopy analysis revealed the nature of lithium deposits, considering the impact of electrode kinetics on the occurrence of dendritic lithium microstructures, governed by processes of electrodeposition and electrodissolution. Various electrolyte formulations were compared in view of different cell configurations, including Li||Li symmetric cells as well Li||Cu cells, Cu||NMC cells, and finally NMC||Li full cell systems, establishing the origin and likely contributions to irreversible capacity losses while systematically evaluating different active materials (including electrolyte formulations, cathode material, and lithium metal anodes). Indeed, a mixture of film-forming additives—fluoroethylene carbonate (FEC) and lithium difluorophosphate (LiPO2F2)—was demonstrated to afford both "better" interfacial/interphasial properties and more homogeneous lithium deposition, thus exhibiting promising electrochemical performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI