TiO₂-engineered polyurethane gel electrolyte enabling dendrite-free Na metal cycling and high-fidelity state estimation

Sodium-ion batteries (SIBs) are promising alternatives to lithium-ion batteries due to their low cost and abundant sodium resources; however, conventional liquid electrolytes suffer from safety issues and interfacial instability. Herein, a gel polymer electrolyte (TPU–TiO₂ GPE) was developed by incorporating 5 wt% TiO₂ nanoparticles into a thermoplastic polyurethane (TPU) matrix. The Lewis acidic centers of TiO₂ interact synergistically with polyurethane chain segments, reducing polymer crystallinity and enhancing chain mobility. As a result, the TPU–TiO₂ GPE exhibits higher room-temperature ionic conductivity (2.91 × 10 −4 S·cm −1 ) and tensile strength (32.7 MPa) than pristine TPU. Moreover, the TPU–TiO₂ GPE forms a stable and uniform solid–electrolyte interphase (SEI) on sodium metal, effectively suppressing dendrite growth. Na||Na symmetric cells demonstrate stable cycling for over 250 h at 0.2 mA·cm −2 , while Na||Na₃V₂(PO₄)₃ full cells retain 93.84% of their capacity after 280 cycles at 0.5C. The state of charge (SOC) of the full cells was estimated using a second-order RC equivalent circuit model combined with an extended Kalman filter (EKF). Compared with the pristine TPU system, the TPU–TiO₂ GPE exhibits smoother OCV–SOC characteristics and reduced polarization, leading to significantly improved SOC estimation accuracy. The voltage-model fitting RMSE is reduced from approximately 2.4 mV to 1.3 mV. This improvement enables more reliable SOC tracking across the entire SOC range. These results indicate that the TPU–TiO₂ GPE enhances both electrochemical performance and SOC predictability, providing a viable strategy for safe and intelligently managed sodium-ion batteries. • A TiO₂-modified TPU gel electrolyte achieves 3× higher ionic conductivity and improved strength. • TiO₂ incorporation improves Na + transport by reducing crystallinity and enhancing segmental mobility. • A stable and uniform SEI effectively suppresses Na dendrite growth, enabling >250 h symmetric-cell cycling. • Na||NVP full cells show 93.84% capacity retention after 280 cycles at 0.5C. • Improved OCV–SOC smoothness enables accurate SOC estimation under a 2RC–EKF framework.

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Publication Details

Journal
Journal of Energy Storage
Published
2026-04-13
DOI
https://doi.org/10.1016/j.est.2026.122171
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.00

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article

TiO₂-engineered polyurethane gel electrolyte enabling dendrite-free Na metal cycling and high-fidelity state estimation

Rongzheng Ren, Chengyi Lu, Chunming Xu, Yuhan Li et al.
Journal of Energy Storage
Advanced Battery Materials and Technologies
article

TiO₂-engineered polyurethane gel electrolyte enabling dendrite-free Na metal cycling and high-fidelity state estimation

Rongzheng Ren, Chengyi Lu, Chunming Xu, Yuhan Li, Shaowei Zhang, Wang Sun, Guang Pan, Siyuan Liu, Juchen Li, Silun Luo
article en

Abstract

Sodium-ion batteries (SIBs) are promising alternatives to lithium-ion batteries due to their low cost and abundant sodium resources; however, conventional liquid electrolytes suffer from safety issues and interfacial instability. Herein, a gel polymer electrolyte (TPU–TiO₂ GPE) was developed by incorporating 5 wt% TiO₂ nanoparticles into a thermoplastic polyurethane (TPU) matrix. The Lewis acidic centers of TiO₂ interact synergistically with polyurethane chain segments, reducing polymer crystallinity and enhancing chain mobility. As a result, the TPU–TiO₂ GPE exhibits higher room-temperature ionic conductivity (2.91 × 10 −4 S·cm −1 ) and tensile strength (32.7 MPa) than pristine TPU. Moreover, the TPU–TiO₂ GPE forms a stable and uniform solid–electrolyte interphase (SEI) on sodium metal, effectively suppressing dendrite growth. Na||Na symmetric cells demonstrate stable cycling for over 250 h at 0.2 mA·cm −2 , while Na||Na₃V₂(PO₄)₃ full cells retain 93.84% of their capacity after 280 cycles at 0.5C. The state of charge (SOC) of the full cells was estimated using a second-order RC equivalent circuit model combined with an extended Kalman filter (EKF). Compared with the pristine TPU system, the TPU–TiO₂ GPE exhibits smoother OCV–SOC characteristics and reduced polarization, leading to significantly improved SOC estimation accuracy. The voltage-model fitting RMSE is reduced from approximately 2.4 mV to 1.3 mV. This improvement enables more reliable SOC tracking across the entire SOC range. These results indicate that the TPU–TiO₂ GPE enhances both electrochemical performance and SOC predictability, providing a viable strategy for safe and intelligently managed sodium-ion batteries. • A TiO₂-modified TPU gel electrolyte achieves 3× higher ionic conductivity and improved strength. • TiO₂ incorporation improves Na + transport by reducing crystallinity and enhancing segmental mobility. • A stable and uniform SEI effectively suppresses Na dendrite growth, enabling >250 h symmetric-cell cycling. • Na||NVP full cells show 93.84% capacity retention after 280 cycles at 0.5C. • Improved OCV–SOC smoothness enables accurate SOC estimation under a 2RC–EKF framework.

Journal of Energy StorageVol. 163
Northwestern Polytechnical University (CN), Ningbo Polytechnic (CN), Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 24%
Advanced Battery Materials and Technologies
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