电解质
材料科学
分离器(采油)
阳极
相间
金属锂
锂(药物)
金属
背景(考古学)
液态金属
化学工程
纳米技术
电极
复合材料
冶金
化学
热力学
物理化学
古生物学
遗传学
内分泌学
工程类
物理
医学
生物
作者
Dongping Lu,Yuyan Shao,Terence Lozano,Wendy D. Bennett,Gordon L. Graff,Bryant J. Polzin,Ji‐Guang Zhang,Mark Engelhard,Natalio T. Saenz,Wesley A. Henderson,Priyanka Bhattacharya,Jun Liu,Jie Xiao
标识
DOI:10.1002/aenm.201400993
摘要
In recent years, the Li metal anode has regained a position of paramount research interest because of the necessity for employing Li metal in next‐generation battery technologies such as Li‐S and Li‐O 2 . Severely limiting this utilization, however, are the rapid capacity degradation and safety issues associated with rechargeable Li metal anodes. A fundamental understanding of the failure mechanism of Li metal at high charge rates has remained elusive due to the complicated interfacial chemistry that occurs between Li metal and liquid electrolytes. Here, it is demonstrated that at high current density the quick formation of a highly resistive solid electrolyte interphase (SEI) entangled with Li metal, which grows towards the bulk Li, dramatically increases up the cell impedance and this is the actual origin of the onset of cell degradation and failure. This is instead of dendritic or mossy Li growing outwards from the metal surface towards/through the separator and/or the consumption of the Li and electrolyte through side reactions. Interphase, in this context, refers to a substantive layer rather than a thin interfacial layer. Discerning the mechanisms and consequences for this interphase formation is crucial for resolving the stability and safety issues associated with Li metal anodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI