Abstract

Mn-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 141mA 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.

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