Regulating the Electron Distribution of Metal‐Oxygen for Enhanced Oxygen Stability in Li‐rich Layered Cathodes

Author:

Yin Zijia12ORCID,Zhao Jun3,Luo Dong1,Chin Yi‐Ying4,Chen Chien‐Te5,Chen Huaican6,Yin Wen6,Tang Yu1,Yang Tingting1,Ren Jincan1,Li Tianyi7,Wiaderek Kamila M.7,Kong Qingyu8,Fan Jun3,Zhu He29,Ren Yang12,Liu Qi12ORCID

Affiliation:

1. Department of Physics City University of Hong Kong Hong Kong 999077 P. R. China

2. Shenzhen Research Institute City University of Hong Kong Shenzhen Guangdong 518057 P. R. China

3. Department of Materials Science and Engineering City University of Hong Kong Hong Kong 999077 P. R. China

4. Department of Physics National Chung Cheng University No.168, Sec. 1, University Rd., Minhsiung Chiayi 621301 Taiwan

5. National Synchrotron Radiation Research Center 101 Hsin‐Ann Road Hsinchu 30076 Taiwan

6. Institute of High Energy Physics Chinese Academy of Sciences (CAS) Beijing 100049 P. R. China

7. X‐Ray Science Division Argonne National Laboratory Lemont IL 60439 USA

8. Société Civile Synchrotron SOLEIL L'Orme des Merisiers Saint‐Aubin, BP 48 GIF‐sur‐Yvette Cedex 91192 France

9. Herbert Gleiter Institute of Nanoscience School of Materials Science and Engineering Nanjing University of Science and Technology Nanjing 210094 P. R. China

Abstract

AbstractLi‐rich Mn‐based layered oxides (LLO) hold great promise as cathode materials for lithium‐ion batteries (LIBs) due to their unique oxygen redox (OR) chemistry, which enables additional capacity. However, the LLOs face challenges related to the instability of their OR process due to the weak transition metal (TM)‐oxygen bond, leading to oxygen loss and irreversible phase transition that results in severe capacity and voltage decay. Herein, a synergistic electronic regulation strategy of surface and interior structures to enhance oxygen stability is proposed. In the interior of the materials, the local electrons around TM and O atoms may be delocalized by surrounding Mo atoms, facilitating the formation of stronger TM─O bonds at high voltages. Besides, on the surface, the highly reactive O atoms with lone pairs of electrons are passivated by additional TM atoms, which provides a more stable TM─O framework. Hence, this strategy stabilizes the oxygen and hinders TM migration, which enhances the reversibility in structural evolution, leading to increased capacity and voltage retention. This work presents an efficient approach to enhance the performance of LLOs through surface‐to‐interior electronic structure modulation, while also contributing to a deeper understanding of their redox reaction.

Funder

National Key Research and Development Program of China

Glaucoma Research Foundation

Shenzhen Research Institute, City University of Hong Kong

Shenzhen Science and Technology Innovation Program

Innovative Research Group Project of the National Natural Science Foundation of China

Publisher

Wiley

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