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Mitigating Reaction Barriers in Ni-Rich Cathodes via Surface-Bulk Coupling Strategy for Fast-Charging

  • Yingjie Sun
  • , Xudong Li*
  • , Peng Gao
  • , Wenhao Jia
  • , Shumin Liu
  • , Robson Monteiro
  • , Zhongzhu Liu*
  • , Luanna Parreira
  • , Ruichen Zhu
  • , Yongming Zhu*
  • , Liguang Wang*
  • *Corresponding author for this work
  • Harbin Institute of Technology Weihai
  • Companhia Brasileira de Metalurgia e Mineração
  • CITC Metal
  • Zhejiang University

Research output: Contribution to journalArticlepeer-review

Abstract

Material degradation in layered oxide cathodes, particularly mechanical degradation, presents a “chicken or egg” dilemma as it may originate from either the surface or the bulk. Surface-only or bulk-only modifications have proven insufficient to resolve these intrinsic issues. While combined surface-bulk strategies can mitigate degradation, they often require complex processes that increase costs and limit scalability. Here, we report a design that couples bulk structural stabilization with the in situ formation of a fast conductive interphase on Ni-rich layered oxides. This dual approach yields a robust bulk framework and a stable surface with accelerated reaction kinetics, enabling a high-rate capability of over 160 mAh g−1 at the current of 5 C and stable cycling over 200 cycles. Beyond performance gains, our results reveal atomic-scale insights into the interplay between structural evolution, ionic transport, and electrochemical stability, offering a practical pathway to durable high-nickel cathodes for fast-charging batteries.

Original languageEnglish
Article numbere72943
JournalSmall
Volume22
Issue number22
DOIs
StatePublished - 17 Apr 2026
Externally publishedYes

Keywords

  • bifunctional coupling design
  • high-rate Ni-rich cathodes
  • in situ self-formed interphase
  • mechano-electrochemical stability

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