Solvation‐Regulated PVDF Solid Polymer Electrolytes Enabled by Borates for Dendrite‐Resistant Lithium Metal Batteries

Despite their mechanical robustness and high‐voltage stability, poly(vinylidene fluoride) (PVDF) solid polymer electrolytes are hindered by sluggish Li + transport, stemming from anion‐dominated conduction and residual solvent‐induced interfacial degradation. This study addresses these issues by introducing zinc borate (ZB) as a filler into the PVDF electrolyte and preparing the composite electrolyte PVZB, thereby reconstructing the lithium‐ion solvation structure and stabilizing the electrode interface, elevating the Li + transference number to 0.49, and boosting room‐temperature ionic conductivity to 3.3 × 10 −4 S cm −1 . Crucially, a rich inorganic solid electrolyte interphase enables stable cycling of Li/PVZB/Li cells for 3000 h at 0.1 mA cm −2 . NCM811/PVZB/Li cells deliver 78.5% capacity retention after 400 cycles at 4.3 V with excellent Coulombic efficiency (99.2%).

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Publication Details

Journal
Batteries & Supercaps
Published
2026-05-01
DOI
https://doi.org/10.1002/batt.70320
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.00

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article

Solvation‐Regulated PVDF Solid Polymer Electrolytes Enabled by Borates for Dendrite‐Resistant Lithium Metal Batteries

Aoyuan Chen, Wujie Yang, Taiyu Yang, H Pan et al.
Batteries & Supercaps
Advanced Battery Materials and Technologies
article

Solvation‐Regulated PVDF Solid Polymer Electrolytes Enabled by Borates for Dendrite‐Resistant Lithium Metal Batteries

Aoyuan Chen, Wujie Yang, Taiyu Yang, H Pan, Ping He, Zhenjie Zhang
article en

Abstract

Despite their mechanical robustness and high‐voltage stability, poly(vinylidene fluoride) (PVDF) solid polymer electrolytes are hindered by sluggish Li + transport, stemming from anion‐dominated conduction and residual solvent‐induced interfacial degradation. This study addresses these issues by introducing zinc borate (ZB) as a filler into the PVDF electrolyte and preparing the composite electrolyte PVZB, thereby reconstructing the lithium‐ion solvation structure and stabilizing the electrode interface, elevating the Li + transference number to 0.49, and boosting room‐temperature ionic conductivity to 3.3 × 10 −4 S cm −1 . Crucially, a rich inorganic solid electrolyte interphase enables stable cycling of Li/PVZB/Li cells for 3000 h at 0.1 mA cm −2 . NCM811/PVZB/Li cells deliver 78.5% capacity retention after 400 cycles at 4.3 V with excellent Coulombic efficiency (99.2%).

Batteries & SupercapsVol. 9(5)
Collaborative Innovation Center of Advanced Microstructures (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 8%
Advanced Battery Materials and Technologies
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