材料科学
电解质
阳极
复合数
成核
电镀(地质)
功率密度
化学工程
枝晶(数学)
电池(电)
纳米纤维
电流密度
电极
复合材料
工程类
几何学
地球物理学
化学
有机化学
功率(物理)
物理化学
地质学
物理
数学
量子力学
作者
Jingyi Wu,Zhixiang Rao,Xueting Liu,Yue Shen,Lixia Yuan,Zhen Li,Xiaolin Xie,Yunhui Huang
标识
DOI:10.1002/adfm.202009961
摘要
Abstract The practical application of lithium metal anode has been hindered by safety and cyclability issues due to the uncontrollable dendrite growth, especially during fast cycling and deep plating/stripping process. Here, a composite Li metal anode supported by periodic, perpendicular, and lithiophilic TiO 2 /poly(vinyl pyrrolidone) (PVP) nanofibers via a facial rolling process is reported. TiO 2 /PVP nanofibers with good Li affinity provide low‐tortuosity and directly inward Li + transport paths to facilitate Li nucleation and deposition under high areal capacities and current densities. The micrometer‐scale interspaces between TiO 2 /PVP walls offer enough space to circumvent the huge volume variation and avoid structure collapsing during the repeated deep Li plating/stripping. The unique structure enables stable cycling under ultrahigh currents (12 mA cm −2 ), and ultra‐deep plating/stripping up to 60 mAh cm −2 with a long cycle life in commercial carbonate electrolytes. The gassing behavior in operating pouch cells is observed using ultrasonic transmission mapping. When paired with LiFePO 4 (5 mAh cm −2 ), sulfur (3 mAh cm −2 ), and high‐voltage LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathodes, the composite Li anodes deliver remarkably improved rate performance and cycling stability, demonstrating that it could be a promising strategy for balancing high‐energy density and high‐power density in Li metal batteries.
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