Manipulated Fluoro‐Ether Derived Nucleophilic Decomposition Products for Mitigating Polarization‐Induced Capacity Loss in Li‐Rich Layered Cathode

Author:

Zhang Baodan12,Zhang Haitang1,Luo Haiyan1,Hua Haiming1,Wu Xiaohong3,Chen Yilong1,Zhou Shiyuan1,Yin Jianhua1,Zhang Kang1,Liao Hong‐Gang1,Wang Qingsong4,Zou Yeguo12,Qiao Yu12ORCID,Sun Shi‐Gang1

Affiliation:

1. State Key Laboratory of Physical Chemistry of Solid Surfaces Collaborative Innovation Center of Chemistry for Energy Materials (iChEM) Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 P. R. China

2. Fujian Science & Technology Innovation Laboratory for Energy Materials of China (Tan Kah Kee Innovation Laboratory) Xiamen 361005 P. R. China

3. Fujian Provincial Key Laboratory of Functional Materials and Applications Institute of Advanced Energy Materials School of Materials Science and Engineering Xiamen University of Technology Xiamen 361024 P. R. China

4. Bavarian Center for Battery Technology (BayBatt) Department of Chemistry University of Bayreuth 95447 Bayreuth Germany

Abstract

AbstractElectrolyte engineering is a fascinating choice to improve the performance of Li‐rich layered oxide cathodes (LRLO) for high‐energy lithium‐ion batteries. However, many existing electrolyte designs and adjustment principles tend to overlook the unique challenges posed by LRLO, particularly the nucleophilic attack. Here, we introduce an electrolyte modification by locally replacing carbonate solvents in traditional electrolytes with a fluoro‐ether. By benefit of the decomposition of fluoro‐ether under nucleophilic O‐related attacks, which delivers an excellent passivation layer with LiF and polymers, possessing rigidity and flexibility on the LRLO surface. More importantly, the fluoro‐ether acts as “sutures”, ensuring the integrity and stability of both interfacial and bulk structures, which contributed to suppressing severe polarization and enhancing the cycling capacity retention from 39 % to 78 % after 300 cycles for the 4.8 V‐class LRLO. This key electrolyte strategy with comprehensive analysis, provides new insights into addressing nucleophilic challenge for high‐energy anionic redox related cathode systems.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

National Synchrotron Radiation Laboratory

Publisher

Wiley

Subject

General Chemistry,Catalysis

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