Record‐Breaking Discharge Capacity and Rate Capability in Li─O <sub>2</sub> Batteries Through Magnetic Field‐Induced Short‐Range Order Li <sub>2</sub> O <sub>2</sub>

L Li‐Na Song (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China) S Shuang Liang (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry) Y Yue Wang X Xing‐Yuan Du (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China) Y Yu Sun X Xin‐Yuan Yuan (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China) H Huan‐Feng Wang (College of Materials and Chemical Engineering Zhengzhou Key Laboratory of Functional Electrocatalysis and Chemical Energy Storage Zhengzhou University of Technology Zhengzhou 450044 P.R. China) J Ji‐Jing Xu (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China)

Abstract

Abstract Aprotic Li─O 2 batteries face significant challenges due to the insulating and insoluble nature of Li 2 O 2 , which hinders the redox kinetics and severely limits the overall performance. Traditional methods, such as using solid or liquid catalysts to enhance the kinetics, encounter substantial obstacles, in which solid catalysts are limited by their interface with Li 2 O 2 , while liquid catalysts may lead to shuttle corrosion of the Li anode, would diminish catalytic effectiveness. In this study, we propose a novel approach to address these issues by incorporating magnetic dopants into the discharge products and applying an external magnetic field. This approach results in magnetically assisted Li─O 2 batteries with significantly improved redox kinetics. During discharge, the magnetic field dynamically aligns Co 2+ centers within the discharge product, forming a short‐range ordered magnetic structure with alternating paramagnetic and diamagnetic domains, which enhances the formation kinetics of the discharge product. During charging, these uniformly distributed Co active centers act autocatalytically, accelerating the product decomposition kinetics. This configuration achieves a record‐breaking discharge capacity of 115 918 mAh g −1 and an exceptional rate capability of 6.7 A g −1 . Our results demonstrate that controlling the electronic and ionic transport properties of alkali peroxides can fundamentally enhance cathode reaction kinetics, providing new design principles for high‐performance Li─O 2 batteries.

Article Details

Volume / Issue Vol. 64, Issue 52
Published December 22, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

L

Li‐Na Song

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China

S

Shuang Liang

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry

Y

Yue Wang

X

Xing‐Yuan Du

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China

Y

Yu Sun

X

Xin‐Yuan Yuan

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China

H

Huan‐Feng Wang

College of Materials and Chemical Engineering Zhengzhou Key Laboratory of Functional Electrocatalysis and Chemical Energy Storage Zhengzhou University of Technology Zhengzhou 450044 P.R. China

J

Ji‐Jing Xu

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P.R. China