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

Jiawen Huang, Xingguo An, Zhongling Cheng, Laiquan Li, Shi-Xue Dou (), Hua-Kun Liu and Chao Wu ()
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Jiawen Huang: University of Shanghai for Science and Technology
Xingguo An: University of Shanghai for Science and Technology
Zhongling Cheng: University of Shanghai for Science and Technology
Laiquan Li: University of Shanghai for Science and Technology
Shi-Xue Dou: University of Shanghai for Science and Technology
Hua-Kun Liu: University of Shanghai for Science and Technology
Chao Wu: University of Shanghai for Science and Technology

Nature Communications, 2025, vol. 16, issue 1, 1-16

Abstract: 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.

Date: 2025
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DOI: 10.1038/s41467-025-63593-x

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