Dipole-dipole interaction-induced dense primitive solid-electrolyte interphase for high-power Ah-level anode-free sodium metal batteries

偶极-偶极相互作用诱导的致密原始固态电解质界面用于高功率安时级无阳极钠金属电池

阅读:1

Abstract

High-energy and resource-abundant anode-free sodium metal batteries suffer from limited lifespan owing to dendrite growth and rapid capacity fading at early stages, particularly at high rate and high capacity. Here we report a preliminary surface-passivation strategy by highly fluorinated electrolyte, instantly forming a dense inorganic-dominant primitive solid-electrolyte interphase. Driven by dipole-dipole interaction, the spontaneously formed solid-electrolyte interphase is sufficiently dense to resist solvent decomposition and moisture attack, meanwhile regulating Na plating/stripping at high current densities and areal capacities up to 8 mA cm(-2) and 5 mAh cm(-2), respectively. The fabricated anode-free batteries demonstrate long-term stability at high cathode loadings (10-15 mg cm(-2)) and high rates (1-3 C), even with moisture contained. Impressively, fast-charging Ah-level anode-free pouch cells deliver energy density up to 150 Wh kg(-1) (0.5 C) based on total cell weight, achieving power density as high as 152 W kg(-1) and long lifespan up to 700 cycles at 1 C.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。