Toward Ultrahigh Rate and Cycling Performance of Cathode Materials of Sodium Ion Battery by Introducing a Bicontinuous Porous Structure

Author:

Tang Chen1,Lu Wei2,Zhang Yixiao1,Zhang Wenwei3,Cui Congcong4,Liu Pan5,Han Lu4,Qian Xiaoshi2,Chen Liwei1,Xu Fugui1,Mai Yiyong1ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering Frontiers Science Center for Transformative Molecules Key Laboratory of Green and High‐End Utilization of Salt Lake Resources (Chinese Academy of Sciences) In‐situ Center for Physical Sciences, and Shanghai Key Laboratory of Electrical Insulation and Thermal Ageing Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China

2. School of Mechanical Engineering State Key Laboratory of Mechanical System and Vibration Interdisciplinary Research Center Institute of Refrigeration and Cryogenics and MOE Key Laboratory for Power Machinery and Engineering Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China

3. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China

4. School of Chemical Science and Engineering Tongji University 1239 Siping Road Shanghai 200092 China

5. School of Materials Science and Engineering State Key Laboratory of Metal Matrix Composites Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China

Abstract

AbstractThe emerging sodium‐ion batteries (SIBs) are one of the most promising candidates expected to complement lithium‐ion batteries and diversify the battery market. However, the exploitation of cathode materials with high‐rate performance and long‐cycle stability for SIBs has remained one of the major challenges. To this end, an efficient approach to enhance rate and cycling performance by introducing an ordered bicontinuous porous structure into cathode materials of SIBs is demonstrated. Prussian blue analogues (PBAs) are selected because they are recognized as a type of most promising SIB cathode materials. Thanks to the presence of 3D continuous channels enabling fast Na+ ions diffusion as well as the intrinsic mechanical stability of bicontinuous architecture, the resultant PBAs exhibit excellent rate capability (80 mAh g−1 at 2.5 A g−1) and ultralong cycling life (>3000 circulations at 0.5 A g−1), reaching the top performance of the reported PBA‐based cathode materials. This study opens a new avenue for boosting sluggish ion diffusion kinetics in electrodes of rechargeable batteries and also provides a new paradigm for solving the dilemma that electrodes’ failure due to high‐stress concentration upon ion storage.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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