材料科学
阳极
电解质
阴极
化学工程
储能
剥离(纤维)
金属
电化学
电极
复合材料
冶金
化学
量子力学
物理
工程类
物理化学
功率(物理)
作者
Zhixin Tai,Yajie Liu,Zhipeng Yu,Ziyu Lu,Olekasandr Bondarchuk,Zhijian Peng,Lifeng Liu
出处
期刊:Nano Energy
[Elsevier]
日期:2022-01-13
卷期号:94: 106947-106947
被引量:28
标识
DOI:10.1016/j.nanoen.2022.106947
摘要
Rechargeable sodium (Na) batteries based on a Na metal anode are considered a promising, inexpensive alternative to their lithium (Li) counterparts, able to offer a high energy density for stationary and mobile energy storage. However, major challenges arising from dendrite growth, unstable solid-electrolyte interphase (SEI) and high reactivity of Na have severely hindered the practical implementation of Na metal anodes. Here, we report a novel strategy that allows easy preparation of nanostructured Na metal anodes with a three-dimensional non-collapsing artificial SEI, by simply grinding Na-rich sodium-potassium (Na57K) alloy with polytetrafluoroethylene (PTFE) nanoparticles, followed by casting the resultant mixture ([email protected]) onto a current collector. The high surface area of nanorod-like Na57K triggers defluorination of PTFE, resulting in a cross-linked artificial SEI layer containing inorganic NaF and KF. The in-situ spontaneously formed, cross-linked PTFE derivative remarkably enhances the stability of SEI, suppresses formation and growth of Na dendrites, and prevents over-consumption of electrolyte. Consequently, stable plating/stripping is accomplished in the [email protected]//[email protected] symmetric cells. When [email protected] is coupled with the sodium vanadium phosphate (Na3V2(PO4)3) cathode in a full cell, substantially improved cycling performance is achieved at high rates, even in a lean electrolyte. The [email protected] shows great promise for use as high-performance anode in fast-charging Na metal batteries.
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