A Strategy to Mitigate Jahn Teller Effect of Mn‐Rich NASICON Framework for Sodium‐Ion Batteries

Author:

Ahsan Muhammad Tayyab1,Ali Zeeshan1,Qiu Daping2,Biao Zhang1,Wang Jing jing1,Hou Yanglong134ORCID

Affiliation:

1. School of Materials Science and Engineering Peking University Beijing 100871 China

2. Hubei Provincial Collaborative Innovation Center for New Energy Microgrid College of Electrical Engineering & New Energy China Three Gorges University Yichang Hubei 443002 China

3. Beijing Key Laboratory for Magnetoelectric Materials and Devices (BKL‐MMD) School of Materials Science and Engineering Peking University Beijing 100871 China

4. School of Materials Sun Yat‐Sen University Shenzhen 518107 China

Abstract

AbstractMn‐based sodium superionic conductors have driven attention to the low‐cost advanced cathode materials for sodium‐ion batteries (SIBs). However, low‐rate capability and unsatisfactory cyclic performance due to the Jahn teller effect of Mn3+ redox couple which occurs from the change in Mn‐O bond length at the octahedral site of crystal structure during charge–discharge, eventually limiting their application. Herein, a disordered and sodium deficient NASICON Na4‐xMn(FeVCrTi)0.25(PO4)3 (termed as Na4‐xMn(HE)) is synthesized to mitigate this Jahn teller effect to achieve high rate and ultrastable cathode material. Interestingly, the as‐prepared Na3.5Mn(HE) shows five reversible electron reactions (i.e., Ti3+/Ti4+, Fe2+/Fe3+, V3+/V4+, Mn2+/Mn3+, and Mn3+/Mn4+) and demonstrates 141 mA h g−1 at 0.2 C with 80% capacity retention at 1 C after 500 cycles which is far superior to its counterparts binary Mn‐based materials. The excellent cyclic performance is due to the remediation of the Jahn teller effect in sodium‐deficient entropy‐stabilized material. The structural reversibility, enhanced kinetics, and electronic properties are further studied in detail by in situ X‐ray diffraction (XRD), ex situ X‐ray photoelectron spectroscopy (XPS), and first principal calculations. Na3.5Mn(HE)//HC full cell delivered 89.7 mAh g−1 capacity at 0.2 C. This work sheds light on designing Mn‐based cathodes with superior electrochemical performance for wide energy storage applications.

Funder

National Key Research and Development Program of China

Natural Science Foundation of Beijing Municipality

National Natural Science Foundation of China

Publisher

Wiley

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