Polymer-induced solid–electrolyte interphase on hard carbon enabling 5C fast-charging practical sodium-ion pouch cell

Achieving <15 min fast-charging technology for long-life sodium-ion batteries (SIBs) remains a formidable challenge, primarily due to parasitic reactions and unstable solid-electrolyte interphase (SEI) at the hard carbon (HC) interface. Here we develop a universal polymer-induced SEI strategy that enables an Ah-level SIB pouch cell to achieve <10 min fast-charging capability. We design a <4.0 nm functionalized polymer molecular layer, polyethylenesulfonyl fluoride (PESF), coated on the HC surface (PolyHC) to minimize electrolyte decomposition. The PESF with the -SO<sub>2</sub>F group attached has a powerful polar feature, which simultaneously induces an anion enriched at the PolyHC interface and tailors extra F atoms, contributing to the architecture of a ∼5.0 nm stable SEI that hybridizes polymer and NaF. This SEI with a resilient polymer skeleton permanently holds the generated inorganic component, enabling long-term structural stability during fast charging. The assembled 1.2 Ah pouch cell, paired with NaNi<sub>1/3</sub>Fe<sub>1/3</sub>Mn<sub>1/3</sub>O<sub>2</sub> cathode and PolyHC anode, displays exceptional fast-charging capability and durability. This method is compatible with various HCs, offering a novel perspective for modulating the HC interface chemistry.

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Publication Details

Journal
National Science Review
Published
2026-01-14
DOI
https://doi.org/10.1093/nsr/nwag025
Citations
2
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
43.86
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article

Polymer-induced solid–electrolyte interphase on hard carbon enabling 5C fast-charging practical sodium-ion pouch cell

Yongrong Sun, Chengrong Xu, Bo Peng, Junjie Du et al.
2 citations
National Science Review
Advancements in Battery Materials
43.86
article

Polymer-induced solid–electrolyte interphase on hard carbon enabling 5C fast-charging practical sodium-ion pouch cell

Yongrong Sun, Chengrong Xu, Bo Peng, Junjie Du, Tianze Shi, Shaohua Guo, Sheng Xu, Daxian Zuo, Jie Yang, Yu Shi, Jiaming Tian, Yiwen Liu, Haoshen Zhou
article en
2 citations

Abstract

Achieving <15 min fast-charging technology for long-life sodium-ion batteries (SIBs) remains a formidable challenge, primarily due to parasitic reactions and unstable solid-electrolyte interphase (SEI) at the hard carbon (HC) interface. Here we develop a universal polymer-induced SEI strategy that enables an Ah-level SIB pouch cell to achieve <10 min fast-charging capability. We design a <4.0 nm functionalized polymer molecular layer, polyethylenesulfonyl fluoride (PESF), coated on the HC surface (PolyHC) to minimize electrolyte decomposition. The PESF with the -SO<sub>2</sub>F group attached has a powerful polar feature, which simultaneously induces an anion enriched at the PolyHC interface and tailors extra F atoms, contributing to the architecture of a ∼5.0 nm stable SEI that hybridizes polymer and NaF. This SEI with a resilient polymer skeleton permanently holds the generated inorganic component, enabling long-term structural stability during fast charging. The assembled 1.2 Ah pouch cell, paired with NaNi<sub>1/3</sub>Fe<sub>1/3</sub>Mn<sub>1/3</sub>O<sub>2</sub> cathode and PolyHC anode, displays exceptional fast-charging capability and durability. This method is compatible with various HCs, offering a novel perspective for modulating the HC interface chemistry.

National Science ReviewVol. 13(4)
University Town of Shenzhen (CN), Collaborative Innovation Center of Advanced Microstructures (CN)
Openalex Percentile: Top 0%
Advancements in Battery Materials
43.86
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Polymer-induced solid–electrolyte interphase on hard carbon enabling 5C fast-charging practical sodium-ion pouch cell — Yongrong Sun, Chengrong Xu, et al. · National Science Review (2026) | TGRS Research Map | TGRS