4.7 Article

Designing water/air-stable Co-free high-entropy oxide cathodes with suppressed irreversible phase transition for sodium-ion batteries

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APPLIED SURFACE SCIENCE
卷 636, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apsusc.2023.157856

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High entropy oxide; Layered cathode; Air stability; Phase transition; Co free; Sodium-ion batteries

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In this study, a new Co-free high-entropy oxide layered cathode NaFe0.2Cu0.1Ni0.2Mn0.3Ti0.2O2 is proposed, which enhances reversible phase transition, improves air stability, and reduces cost. The HEO cathode shows excellent sodium-ion storage performance and cycling stability, as well as enhanced water resistance. The high-entropy design suppresses irreversible phase transformation and exhibits fast Na+ diffusion kinetics.
Layered transitional metal oxides are promising cathode materials for sodium-ion batteries that benefit from their high energy densities. Nevertheless, the complicated irreversible phase transitions and poor air stability limit their energy efficiency and implementation in practical devices. Here, a new Co-free high-entropy oxide (HEO) layered cathode NaFe0.2Cu0.1Ni0.2Mn0.3Ti0.2O2 is proposed to enhance the reversible phase transition, improve the air stability, and further decrease the cost. The HEO cathode displays excellent sodium-ion storage performance with a capacity of 121 mAh g � 1, competitive cycling stability (-83.8% capacity retention after 200 cycles at 2 C), and enhanced water resistance (capacity of 105.2 mAh g � 1 after soaking in water for 2 h and capacity retention of 83% after 200 cycles at 1 C). Moreover, the as-obtained NFCNMT||hard carbon full cells exhibit superior performance with reversible specific capacity 115 mAh g � 1 and approximately -73% capacity retention after 100 cycles at 1C. Ex-situ X-ray diffraction and transmission electron microscopy reveal the completely reversible O3 -* P3 -* O3 structure evolution and suppressed violent changes in lattice parameters owing to the high-entropy design. Furthermore, the galvanostatic intermittent titration technique and in-situ electrochemical impedance spectroscopy reveal that the HEO cathode exhibits fast Na+ diffusion kinetics. For sodium-ion batteries, this work provides a new strategy for suppressing irreversible phase transformation and enhancing air stability.

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