阳极
电解质
锂(药物)
金属锂
材料科学
介电谱
电化学
电极
电化学电池
化学工程
化学
医学
工程类
内分泌学
物理化学
作者
A. J. Louli,A. Eldesoky,Jack deGooyer,Matt Coon,C. P. Aiken,Zachary Simunovic,Michael Metzger,J. R. Dahn
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2022-03-30
卷期号:169 (4): 040517-040517
被引量:42
标识
DOI:10.1149/1945-7111/ac62c4
摘要
With a potential to deliver 60% greater energy density than conventional lithium-ion batteries, the simple design of anode-free lithium metal cells with liquid electrolytes has generated significant research interest. However, without excess lithium, the short lifetime and safety concerns for cells cycling lithium metal with liquid electrolytes make the development of anode-free cells particularly challenging. Herein, we investigate the effect of four different positive electrode materials on the performance of anode-free cells—LiNi 0.5 Mn 0.3 Co 0.2 O 2 (NMC532), LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NMC811), LiCoO 2 (LCO), and LiFePO 4 (LFP). In-situ electrochemical impedance spectroscopy and electrolyte degradation measurements were performed on cells with dual-salt LiDFOB/LiBF 4 electrolyte to elucidate cell failure. Additional state-of-the-art electrolyte systems as well as other testing conditions (temperature, pressure, depth of discharge) were also explored, along with nail safety tests and calendar aging cycle-hold experiments. We show that the rate of lithium inventory loss and impedance growth differs amongst these cell chemistries, ultimately resulting in the shortest lifetime for NMC811 and the longest lifetime for LCO anode-free cells of 200 cycles.
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