成核
法拉第效率
阳极
化学工程
材料科学
纳米颗粒
电化学
电解质
合金
钠
电镀(地质)
剥离(纤维)
金属
图层(电子)
纳米技术
化学
冶金
电极
复合材料
物理化学
工程类
地质学
有机化学
地球物理学
作者
Guanyao Wang,Ying Zhang,Bingkun Guo,Liang Tang,Gang Xu,Yuanjun Zhang,Minghong Wu,Huan Liu,Shi Xue Dou,Chao Wu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-05-06
卷期号:20 (6): 4464-4471
被引量:113
标识
DOI:10.1021/acs.nanolett.0c01257
摘要
Sodium metal anode (SMA) is one of the most favored choices for the next-generation rechargeable battery technologies owing to its low cost and natural abundance. However, the poor reversibility resulted from dendrite growth and formation of unstable solid electrolyte interphase has significantly hindered the practical application of SMAs. Herein, we report that a nucleation buffer layer comprising elaborately designed core-shell C@Sb nanoparticles (NPs) enables the homogeneous electrochemical deposition of sodium metal for long-term cycling. These C@Sb NPs can increase active sites for initial sodium nucleation through Sb-Na alloy cores and keep these cores stable through carbon shells. The assembled cells with this nucleation layer can deliver continuously repeated sodium plating/stripping cycles for nearly 6000 h at a high areal capacity of 4 mA h cm-2 with an average Coulombic efficiency 99.7%. This ingenious structure design of alloy-based nucleation agent opens up a promising avenue to stabilize sodium metal with targeted properties.
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