Synergistic Hybrid Interfaces for Ultrastable Sodium Anode via Spontaneous Conversion of Tin Fluoride in Polymer Matrix

We report a synergistic hybrid organic–inorganic artificial solid–electrolyte-interphase (SEI) engineered to stabilize sodium metal anodes for high-performance sodium metal batteries, achieved via the spontaneous conversion of tin fluoride (SnF2) in a polymer matrix. A composite protective layer is fabricated by integrating poly(ethylene oxide) (PEO) and tin fluoride (SnF2) in a dimethyl carbonate solution, forming a hybrid interphase that synergistically combines the flexibility of organic polymers with the mechanical robustness of inorganic fluorides. The optimized coating, particularly at an 11 wt % PEO:SnF2 (10:1) ratio, develops a uniform and chemically stable barrier interphase that effectively suppresses dendrite formation, minimizes electrolyte decomposition, and maintains a low interfacial impedance. Comprehensive morphological and chemical analysis confirm that this protective layer undergoes spontaneous conversion to generate a NaF-rich phase and a Na–Sn alloy network, both of which facilitate uniform sodium deposition and enhance interphase stability. Atomistic ReaxFF molecular-dynamics simulations of the PEO/SnF2/Na interface further reveal the in situ formation of NaF clusters and a Na–Sn alloy network that homogenizes Na+ flux and fortifies the hybrid layer, providing mechanistic insight into the observed electrochemical stability. Most importantly, electrochemical testing in symmetric cells with such artificial SEI layer demonstrates a dramatic extension of cycle life from approximately 190 h for bare sodium to nearly 2000 h (at a current density of 0.25 mA/cm2 in 1 M NaPF6 in ethylene carbonate/dimethyl carbonate (EC/DMC), and from less than 100 h for bare sodium to over 2000 h at a current density of 1.0 mA/cm2 in 1 M NaPF6 in tetraethylene glycol dimethyl ether, representing a (10–20×) in enhancement in cycling performance and stability. This work presents a promising strategy for enabling safer, longer-lasting, and higher energy density sodium metal batteries through the design of hybrid interfaces with spontaneous inorganic conversion.

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Journal
ACS Applied Energy Materials
Published
2026-02-19
DOI
https://doi.org/10.1021/acsaem.5c03683
Primary Topic
Advanced Battery Materials and Technologies
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article
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article

Synergistic Hybrid Interfaces for Ultrastable Sodium Anode via Spontaneous Conversion of Tin Fluoride in Polymer Matrix

Roya Damircheli, Tanmay Sarkar Akash, Chuan-Fu Lin, Siddhartha Das et al.
ACS Applied Energy Materials
Advanced Battery Materials and Technologies
article

Synergistic Hybrid Interfaces for Ultrastable Sodium Anode via Spontaneous Conversion of Tin Fluoride in Polymer Matrix

Roya Damircheli, Tanmay Sarkar Akash, Chuan-Fu Lin, Siddhartha Das, Amrit P. Kafle, Binh Hoang, David M. Stewart, Sukanya Goswami, Tai-Feng Hung
article en

Abstract

We report a synergistic hybrid organic–inorganic artificial solid–electrolyte-interphase (SEI) engineered to stabilize sodium metal anodes for high-performance sodium metal batteries, achieved via the spontaneous conversion of tin fluoride (SnF2) in a polymer matrix. A composite protective layer is fabricated by integrating poly(ethylene oxide) (PEO) and tin fluoride (SnF2) in a dimethyl carbonate solution, forming a hybrid interphase that synergistically combines the flexibility of organic polymers with the mechanical robustness of inorganic fluorides. The optimized coating, particularly at an 11 wt % PEO:SnF2 (10:1) ratio, develops a uniform and chemically stable barrier interphase that effectively suppresses dendrite formation, minimizes electrolyte decomposition, and maintains a low interfacial impedance. Comprehensive morphological and chemical analysis confirm that this protective layer undergoes spontaneous conversion to generate a NaF-rich phase and a Na–Sn alloy network, both of which facilitate uniform sodium deposition and enhance interphase stability. Atomistic ReaxFF molecular-dynamics simulations of the PEO/SnF2/Na interface further reveal the in situ formation of NaF clusters and a Na–Sn alloy network that homogenizes Na+ flux and fortifies the hybrid layer, providing mechanistic insight into the observed electrochemical stability. Most importantly, electrochemical testing in symmetric cells with such artificial SEI layer demonstrates a dramatic extension of cycle life from approximately 190 h for bare sodium to nearly 2000 h (at a current density of 0.25 mA/cm2 in 1 M NaPF6 in ethylene carbonate/dimethyl carbonate (EC/DMC), and from less than 100 h for bare sodium to over 2000 h at a current density of 1.0 mA/cm2 in 1 M NaPF6 in tetraethylene glycol dimethyl ether, representing a (10–20×) in enhancement in cycling performance and stability. This work presents a promising strategy for enabling safer, longer-lasting, and higher energy density sodium metal batteries through the design of hybrid interfaces with spontaneous inorganic conversion.

ACS Applied Energy MaterialsVol. 9(5)
Ming Chi University of Technology (TW), Battery Park (US), University of Maryland, College Park (US), Catholic University of America (US)
Openalex Percentile: Top 51%
Advanced Battery Materials and Technologies
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