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Breaking insulating barriers in solid-phase conversion reactions with dual-atom catalysts for high-energy lithium batteries

  • Tong Yu
  • , Ru Xiao
  • , Pei Tang
  • , Nan Piao
  • , Ruopian Fang
  • , Bo Quan Li
  • , Zhuangnan Li
  • , Hui Ming Cheng*
  • , Zhenhua Sun*
  • , Feng Li*
  • *Corresponding author for this work
  • CAS - Institute of Metal Research
  • University of Science and Technology of China
  • Shenzhen University of Advanced Technology
  • Beijing Institute of Technology
  • Zhejiang University
  • University of Cambridge
  • Shenzhen Institute of Advanced Technology

Research output: Contribution to journal › Article › peer-review

Abstract

Batteries based on redox chemistry, such as lithium–sulfur and lithium–oxygen, can store more energy than conventional lithium-ion batteries. However, their chemical reactions are limited by sluggish and incomplete conversion reactions, especially those involving insulating solid intermediates (for example, Li2S2 and Li2O2), in which electrocatalysts play a decisive role. Here, through a large-scale theoretical analysis, we propose an electronic property criterion that emphasizes the efficient conduction of ions and electrons as essential for high catalytic activity. Guided by this insight, we have designed a CoCo dual-atom catalyst that accelerates the conversion of solid insulating Li2S2 and Li2O2 intermediates by effective orbital coupling, making these intermediates conductive and catalytically active. This strategy enables the fabrication of high-energy lithium–sulfur pouch cells at the ampere hour scale, achieving a specific energy of 459 Wh kg−1. Our results extend the fundamental understanding of rate-determining solid-phase reactions in redox chemistry and provide principles for the design of electrocatalysts for use in energy storage systems. (Figure presented.)

Original languageEnglish
Pages (from-to)460-470
Number of pages11
JournalNature Catalysis
Volume9
Issue number4
DOIs
Publication statusPublished - Apr 2026
Externally publishedYes

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