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The O3-type NaNi1/3Fe1/3Mn1/3O2 (NFM) has emerged as a highly promising cathode material for sodium-ion batteries due to its facile synthesis and high theoretical capacity. However, it suffers from severe capacity and rate capability degradation caused by multiple coupled failure mechanisms, including irreversible phase transitions, structural deterioration at high voltages, and electrolyte-induced surface corrosion. This work addresses the challenge of high-voltage stability in NFM cathodes via a synergistic bulk-phase and interface engineering strategy. Firstly, Li, Ti, and Co are co-doped into the bulk lattice structure to suppress the Mn3+-induced Jahn-Teller distortion and improve Na+ diffusion kinetics. And then, an AlPO4 protective coating layer is fabricated to mitigate electrolyte corrosion and interfacial side reactions. Consequently, the as-designed composite cathode (AP@NFMLTC) can effectively suppress the P3 to O3’ phase transition within the voltage range of 2.0 to 4.2 V, resulting in a highly reversible sodium storage mechanism. After 100 cycles at a rate of 1 C, the capacity retention rate significantly improves from 45.6% to 83.6%, with a minimal voltage decay of just 0.08 V. The dual bulk-interface synergistic strategy in this work provides valuable insights into achieving high stable operation for SIBs cathodes under enhanced voltage.
© The Author(s) 2025. Published by Tsinghua University Press.
This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/)