Electrochemical Activation Inducing Rocksalt‐to‐Spinel Transformation for Prolonged Service Life of LiMn2O4 Cathodes

Author:

Li Fangyan1ORCID,Jiao Yiding1ORCID,Yang Shuo1ORCID,Mao Wei1,Tao Qiantu2,Bai Chenyu1ORCID,He Er1ORCID,Li Luhe1,Ye Tingting1ORCID,Li Yiran1ORCID,Wang Jiacheng1ORCID,Ren Junye1ORCID,Wang Yuanzhen1ORCID,Gao Rui1ORCID,Li Qianming1ORCID,Lu Jiang1ORCID,Song Jie1ORCID,Ma Jing2ORCID,Deng Yu1,Wang Peng123,Zhang Ye1ORCID

Affiliation:

1. National Laboratory of Solid State Microstructures Jiangsu Key Laboratory of Artificial Functional Materials Chemistry Biomedicine Innovation Center Collaborative Innovation Center of Advanced Microstructures College of Engineering and Applied Sciences Nanjing University Nanjing 210023 China

2. Key Laboratory of Mesoscopic Chemistry School of Chemistry and Chemical Engineering Nanjing University Nanjing 210023 China

3. Department of Physics University of Warwick Coventry CV4 7AL UK

Abstract

AbstractLiMn2O4 spinel is emerging as a promising cathode material for lithium‐ion batteries, largely due to its open framework that facilitates Li+ diffusion and excellent rate performance. However, the charge–discharge cycling of the LiMn2O4 cathode leads to severe structural degradation and rapid capacity decay. Here, an electrochemical activation strategy is introduced, employing a facile galvano‐potentiostatic charging operation, to restore the lost capacity of LiMn2O4 cathode without damaging the battery configuration. With an electrochemical activation strategy, the cycle life of the LiMn2O4 cathode is extended from an initial 1500 to an impressive 14 000 cycles at a 5C rate with Li metal as the anode, while increasing the total discharge energy by ten times. Remarkably, the electrochemical activation enhances the diffusion kinetics of Li+, with the diffusion coefficient experiencing a 37.2% increase. Further investigation reveals that this improvement in capacity and diffusion kinetics results from a transformation of the redox‐inert LiMnO2 rocksalt layer on the surface of degraded cathodes back into active spinel. This transformation is confirmed through electron microscopy and corroborated by density functional theory simulations. Moreover, the viability of this electrochemical activation strategy has been demonstrated in pouch cell configurations with Li metal as the anode, underscoring its potential for broader application.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

China Postdoctoral Science Foundation

Publisher

Wiley

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