电解质
肿胀 的
阳极
阴极
材料科学
电化学
化学工程
箔法
锂(药物)
金属
复合材料
电极
化学
冶金
物理化学
内分泌学
工程类
医学
作者
Chaojiang Niu,Hongkyung Lee,Shuru Chen,Qiuyan Li,Jason Du,Wu Xu,Ji‐Guang Zhang,M. Stanley Whittingham,Jie Xiao,Jun Liu
出处
期刊:Nature Energy
[Springer Nature]
日期:2019-05-13
卷期号:4 (7): 551-559
被引量:554
标识
DOI:10.1038/s41560-019-0390-6
摘要
Lithium metal anodes have attracted much attention as candidates for high-energy batteries, but there have been few reports of long cycling behaviour, and the degradation mechanism of realistic high-energy Li metal cells remains unclear. Here, we develop a prototypical 300 Wh kg−1 (1.0 Ah) pouch cell by integrating a Li metal anode, a LiNi0.6Mn0.2Co0.2O2 cathode and a compatible electrolyte. Under small uniform external pressure, the cell undergoes 200 cycles with 86% capacity retention and 83% energy retention. In the initial 50 cycles, flat Li foil converts into large Li particles that are entangled in the solid-electrolyte interphase, which leads to rapid volume expansion of the anode (cell thickening of 48%). As cycling continues, the external pressure helps the Li anode maintain good contact between the Li particles, which ensures a conducting percolation pathway for both ions and electrons, and thus the electrochemical reactions continue to occur. Accordingly, the solid Li particles evolve into a porous structure, which manifests in substantially reduced cell swelling by 19% in the subsequent 150 cycles. Much has been said about the high-energy, long-lasting potential of Li metal batteries, and yet little has been demonstrated at the cell scale. Here, Jun Liu and colleagues demonstrate a Li metal pouch cell with a 300 Wh kg−1 energy density and a 200-cycle lifetime.
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