阳极
材料科学
金属锂
金属
纳米技术
电极
化学工程
冶金
物理化学
化学
工程类
作者
Xuefeng Wang,Gorakh Pawar,Yejing Li,Xiaodi Ren,Minghao Zhang,Bingyu Lu,Abhik Banerjee,Ping Liu,Eric J. Dufek,Ji‐Guang Zhang,Jie Xiao,Jun Liu,Ying Shirley Meng,Bor Yann Liaw
出处
期刊:Nature Materials
[Springer Nature]
日期:2020-07-27
卷期号:19 (12): 1339-1345
被引量:65
标识
DOI:10.1038/s41563-020-0729-1
摘要
Lithium metal has been considered an ideal anode for high-energy rechargeable Li batteries, although its nucleation and growth process remains mysterious, especially at the nanoscale. Here, cryogenic transmission electron microscopy was used to reveal the evolving nanostructure of Li metal deposits at various transient states in the nucleation and growth process, in which a disorder–order phase transition was observed as a function of current density and deposition time. The atomic interaction over wide spatial and temporal scales was depicted by reactive molecular dynamics simulations to assist in understanding the kinetics. Compared to crystalline Li, glassy Li outperforms in electrochemical reversibility, and it has a desired structure for high-energy rechargeable Li batteries. Our findings correlate the crystallinity of the nuclei with the subsequent growth of the nanostructure and morphology, and provide strategies to control and shape the mesostructure of Li metal to achieve high performance in rechargeable Li batteries. Lithium metal is considered an ideal anode for high-energy rechargeable lithium batteries, but understanding its nucleation and growth at the nanoscale remains challenging. Using cryogenic transmission electron microscopy and simulations, a structural and morphological evolution scenario for Li deposits is proposed.
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