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Sharing electronic and ionic transfer channels for high-energy-density and stable quasi-solid-state lithium-oxygen battery

  • Yuanguo Wu
  • , Zhuojun Zhang
  • , Jiaqi Wang
  • , Hongtao Qu
  • , Jing Li
  • , Liuxi Yang
  • , Amanda Kale
  • , Xikun Zhang
  • , Xiangyu Wen
  • , Zhihong Wang
  • , Zhe Lü
  • , Yu Li*
  • , Peng Tan*
  • , Xingbao Zhu*
  • , Bao Lian Su*
  • *此作品的通讯作者
  • Universite de Namur
  • School of Physics, Harbin Institute of Technology
  • Ltd.
  • University of Science and Technology of China
  • Wuhan University of Technology
  • Beijing Institute of Technology

科研成果: 期刊稿件文章同行评审

摘要

Thick cathodes are essential for practical high-energy batteries, yet their development is hindered by sluggish charge kinetics, particularly in lithium-oxygen batteries (LOBs) where robust three-phase boundaries (TPBs) for e, Li+, and O2 are indispensable. Herein, we propose a gel polymer electrolyte (GPE) integration strategy that enables the construction of a streamlined dual-conductive network for both e and Li+ while preserving optimal porosity for rapid O2 diffusion in thick cathodes (∼2 mm). This innovative architecture creates extensive and continuous TPBs throughout the entire cathode, enabling an exceptional areal capacity of 34.6 mAh cm−2, surpassing most previously reported LOBs, and a record-breaking gravimetric capacity of 19 000 mAh g−1. Numerical simulations further validate the superiority of this approach. Our work provides a proof of concept for overcoming kinetic transport limitations in thick cathodes, paving the way for next-generation high-capacity and stable LOBs.

源语言英语
期刊National Science Review
13
9
DOI
出版状态已出版 - 5月 2026
已对外发布

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