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.
Authors
- Yongrong Sun (ORCID: https://orcid.org/0000-0003-1421-2330)
- Chengrong Xu
- Bo Peng (ORCID: https://orcid.org/0000-0002-0668-8542)
- Junjie Du (ORCID: https://orcid.org/0000-0002-9693-0610)
- Tianze Shi
- Shaohua Guo
- Sheng Xu
- Daxian Zuo
- Jie Yang
- Yu Shi
- Jiaming Tian
- Yiwen Liu
- Haoshen Zhou
Institutions
- University Town of Shenzhen (CN)
- Collaborative Innovation Center of Advanced Microstructures (CN)
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