Revealing the Origin of Transition‐Metal Migration in Layered Sodium‐Ion Battery Cathodes: Random Na Extraction and Na‐Free Layer Formation

Author:

Chu Shiyong12,Kim Duho3,Choi Gwanghyeon3,Zhang Chunchen1,Li Haoyu12,Pang Wei Kong4,Fan Yameng4,D'Angelo Anita M.5,Guo Shaohua12ORCID,Zhou Haoshen1

Affiliation:

1. College of Engineering and Applied Sciences Jiangsu Key Laboratory of Artificial Functional Materials National Laboratory of Solid State Microstructures Collaborative Innovation Center of Advanced Microstructures Frontiers Science Center for Critical Earth Material Cycling Nanjing University Nanjing 210023 China

2. Shenzhen Research Institute of Nanjing University Shenzhen 518000 China

3. Department of Mechanical Engineering (Integrated Engineering Program) Kyung Hee University 1732, Deogyeong-daero, Giheung-gu Yongin-si Gyeonggi-do 17104 (Republic of Korea

4. Institute for Superconducting & Electronic Materials University of Wollongong Wollongong NSW-2522 Australia

5. Australian Synchrotron, Australian Nuclear Science and Technology Organization 800 Blackburn Road Clayton Victoria 3168 Australia

Abstract

AbstractCation migration often occurs in layered oxide cathodes of lithium‐ion batteries due to the similar ion radius of Li and transition metals (TMs). Although Na and TM show a big difference of ion radius, TMs in layered cathodes of sodium‐ion batteries (SIBs) can still migrate to Na layer, leading to serious electrochemical degeneration. To elucidate the origin of TM migration in layered SIB cathodes, we choose NaCrO2, a typical layered cathode suffering from serious TM migration, as a model material and find that the TM migration is derived from the random desodiation and subsequent formation of Na‐free layer at high charge potential. A Ru/Ti co‐doping strategy is developed to address the issue, where the doped active Ru is first oxidized to create a selective desodiation and the doped inactive Ti can function as a pillar to avoid complete desodiation in Ru‐contained TM layers, leading to the suppression of the Na‐free layer formation and subsequent enhanced electrochemical performance.

Funder

National Natural Science Foundation of China

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

Subject

General Medicine

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