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

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, polyethylenesulphonyl fluoride (PESF), coated on the HC surface (PolyHC) to minimize electrolyte decomposition. The PESF with the –SO2F group attached has a powerful polar feature, which simultaneously induces 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 NaNi1/3Fe1/3Mn1/3O2 cathode and PolyHC anode, displays exceptional fast-charging capability and durability. This method is compatible with various HC, offering a novel perspective for modulating the HC interface chemistry.