阳极
氟化锂
电解质
成核
硫化物
材料科学
阴极
锂(药物)
化学工程
金属
纳米颗粒
图层(电子)
密度泛函理论
纳米技术
无机化学
电极
化学
物理化学
冶金
计算化学
有机化学
内分泌学
工程类
医学
作者
Caili Xu,Shu Zhang,Cheng Chen,Yunhui Lin,B. Qu,Haiping Zhou,Mengqiang Wu
标识
DOI:10.1016/j.cej.2024.148914
摘要
Li metal is a promising anode material for high-energy–density batteries due to its high theoretical capacity and low redox potential. However, both the uncontrolled Li dendrite growth and unstable solid electrolyte interphase (SEI) layer restricts its large-scale practical applications. Herein, an artificial protective layer consisting of Ag nanoparticles, lithium fluoride (LiF) and sulfide are innovatively designed and fabricated via the in-situ chemical reaction between Ag(I) trifluoromethylthiolate (AgSCF3) and Li metal. Density functional theory (DFT) results indicate that Ag nanoparticles has a high binding energy with Li atom and LiF/sulfide have wide band gap, which would provide plenty of nucleation sites for Li+ and reduce the direct contact between inner Li metal and the electrolyte. The co-existence of Ag and LiF/sulfide can produce a strong synergistic effect, and this is confirmed by the systematical comparison with single modified Ag-Li and double modified F/S-Li anodes. Benefitting from this synergistic effect, the Ag/F/S-Li symmetrical cells can stably work for 2000 h with low-voltage hysteresis at current density of 1 mA cm−2. Full cells assembled with LiCoO2 (LCO) and LiFePO4 (LFP) cathodes displays much better long‐term cycle performance when the Ag/F/S-Li anode is applied. Furthermore, this Ag/F/S-Li modification can significantly enhance discharge capacity, rate performance, as well as energy density of Li(or LiB alloy)||MnO2 primary cells. This promising work promotes the practical application of Li metal and provides new insight into the protective layer design in stable Li metal batteries.
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