材料科学
碱金属
电解质
成核
氧化物
碳纤维
阳极
碳纳米纤维
润湿
阴极
纳米纤维
化学工程
纳米技术
碳纳米管
电极
复合材料
有机化学
冶金
物理化学
工程类
化学
量子力学
物理
复合数
作者
Siyuan Li,Qilei Liu,Jiajun Zhou,Teng Pan,Lina Gao,Weidong Zhang,Lei Fan,Yingying Lü
标识
DOI:10.1002/adfm.201808847
摘要
Abstract Uncontrollable dendritic behavior and infinite volume expansion in alkali metal anode results in the severe safety hazards and short lifespan for high‐energy batteries. Constructing a stable host with superior Na/Li‐philic properties is a prerequisite for commercialization. Here, it is demonstrated that the small Gibbs free energy change in the reaction between metal oxide (Co 3 O 4 , SnO 2 , and CuO) and alkali metal is key for metal infusion. The as‐prepared hierarchical Co 3 O 4 nanofiber–carbon sheet (CS) skeleton shows improved wettability toward molten Li/Na. The 3D carbon sheet serves as a primary framework, offering adequate lithium nucleation sites and sufficient electrolyte/electrode contact for fast charge transfer. The secondary framework of Co/Li 2 O nanofibers provides physical confinement of deposited Li and further redistributes the Li + flux on each carbon fiber, which is verified by COMSOL Multiphysics simulations. Due to the uniform deposition behavior and near‐zero volume change, modified symmetrical Li/Li cells can operate under an ultrahigh current density of 20 mA cm −2 for more than 120 cycles. When paired with LiFePO 4 cathodes, the Li/Co–CS cell shows low polarization and 88.4% capacity retention after 200 cycles under 2 C. Convincing improvement can also be observed in Na/Co–CS symmetrical cells applying NaClO 4 ‐based electrolyte. These results illustrate a significant improvement in developing safe and stable alkali metal batteries.
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