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Solid-state sodium metal batteries (SSSBs) hold promise for achieving high energy density and safety in next-generation energy storage systems. However, practical implementation of the Na metal anode is severely hindered by poor interfacial contact and rampant dendrite growth. Here, we design a bilayer solid-electrolyte interphase (SEI), comprising an inner Sn-enriched NaF layer and an outer NaF-organic composite layer through an in situ reaction enabled by SnF 2 -asymmetric modification of NASICON/PVDF-HFP hybrid solid electrolytes (HSEs). The in situ-formed metallic Sn within the SEI not only enhances interfacial Na + transport kinetics but also dynamically homogenizes the electric field distribution, enabling uniform Na + flux and deposition. Consequently, the Na/Na symmetric cell achieves a critical current density (CCD) of 2 mA cm –2, which is a significant advantage over previously reported HSEs. When paired with the Na 3 V 2 (PO 4 ) 3 (NVP) cathode, the Na metal anode equipped with the Sn-rich SEI delivers outstanding rate capability, stable cycling behavior, and remarkable capacity retention. This study provides new insights into the scalable interfacial design and modification in solid-state sodium metal batteries.
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Yang et al. (2025) studied this question.
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