Cation Disordered Anti‐Perovskite Cathode Materials with Enhanced Lithium Diffusion and Suppressed Phase Transition

Author:

Deng Zhi1ORCID,Chen Diancheng1,Ou Mingyang2,Zhang Yuanpeng3ORCID,Xu Jia2,Ni Dixing1,Ji Zhaoran1,Han Jiantao2ORCID,Sun Yang4,Li Shuai1ORCID,Ouyang Chuying5ORCID,Wang Zhaoxiang67

Affiliation:

1. Department of Physics and Institute for Applied Optics and Precision Engineering Southern University of Science and Technology Shenzhen 518055 China

2. School of Materials Science and Engineering Huazhong University of Science and Technology Wuhan 430074 China

3. Neutron Scattering Division Oak Ridge National Laboratory (ORNL) Oak Ridge TN 37831 USA

4. School of Materials Sun Yat‐sen University Guangzhou 510275 China

5. Fujian Science and Technology Innovation Laboratory for Energy Devices of China (21C‐LAB) Contemporary Amperex Technology Ltd. (CATL) Ningde 352100 China

6. Key Laboratory for Renewable Energy Chinese Academy of Sciences Beijing Key Laboratory for New Energy Materials and Devices Institute of Physics Chinese Academy of Sciences Beijing 100190 China

7. College of Materials Science and Opto‐Electronic Technology and School of Physical Sciences University of Chinese Academy of Sciences Beijing 100190 China

Abstract

AbstractRecently, a new family of anti‐perovskite Li2TMSO was discovered as promising cathode materials for Li‐ion batteries (LIBs) with superiorities in high specific capacity, low cost, and environmental friendliness. However, the applications of these anti‐perovskite materials meet severe challenges in the cyclability and rate performance. Herein, a cation‐disordered anti‐perovskite type solid solution Li2Fe1−xMnxSO (LFMSO, x = 0, 0.2, 0.5) with excellent electrochemical performance is reported. On the basis of comprehensive structural characterizations, the role of the cation disordering in LFMSO is clarified. In comparison with Li2FeSO (LFSO), the reduced Li‐ion diffusion barrier and the increased Li‐rich octahedral configurations in LFMSO with higher configurational entropy imply the facilitated long‐range Li‐ion diffusion and the suppressed phase transition, which favor the high‐rate capability and cycling stability. In addition, the large lattice distortion and Coulombic interaction between the anions and cations lead to the breathing of the unit cell during charge/discharge. The variation of the unit cell volume decreases to 2.5% upon Li‐ion delithiation. A superstructure is observed in LFMSO for the first time. These findings help to pave the way for the research and development of novel cathode materials for the next generation LIBs.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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