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Updated: May 12, 2026

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
Published on: August 12, 2013
Synergistic Pore Architecture and Surface Lithiation Enable Li3PO4-Dominated Interphases for Ultrahigh-Rate Graphite
Zhikun Huang1,2, Chenghao Cui1,3, Kai Wang4
1State Key Laboratory of High Performance Ceramics, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050, P. R. China.
Abstract:
Designing high-rate anodes for lithium-ion batteries (LIBs) remains a critical challenge due to the sluggish ion dynamics and capacity degradation of graphite-based materials under high-rate cycling. Here, we present a surface-lithiated porous graphite (LPG) anode designed through synergistic structural and interfacial modifications. Micron-scale pores introduced on graphite basal planes reduce Li+ diffusion distance while maintaining a low specific surface area (≤ 2 m2·g-1), ensuring an initial Coulombic efficiency exceeding 90%. Surface lithium-containing groups are identified as a key factor in inducing the formation of a Li3PO4-enriched solid electrolyte interface (SEI), which effectively mitigates Li+-solvent interactions and enhances desolvation kinetics. As a result, LPG anodes exhibit good high-rate capabilities, delivering a delithiated capacity of 327 mAh·g-1 at 50 C and retaining 88.9% initial capacity after 2000 cycles at 5 C. With kilogram-scale production and soft-pack battery verification, this strategy positions LPG as a scalable, high-rate anode solution for next-generation LIBs, achieving a good balance between rate performance and capacity retention. Surface-lithiated porous graphite achieves a good balance in balancing rate performance and capacity retention for lithium-ion batteries.

