Non-collapsing 3D solid-electrolyte interphase for high-rate rechargeable sodium metal batteries

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 BV]
卷期号:94: 106947-106947 被引量:45
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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