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O3-type sodium-layered oxides (such as antimony-based O3 structures) have been suggested as one of the most fascinating cathode materials for sodium-ion batteries (SIBs). Honeycomb-ordered antimony-based O3 structures, however, unsatisfactorily exhibit complex phase transitions and sluggish Na + kinetics during cycling. Herein, we prepared a completely cationic-disordered O3-type Na 0.8 Ni 0.6 Sb 0.4 O 2 compound by composition regulation for SIBs. Surprisingly, the measured redox potentials for typical O3–P3 phase transition are located at 3.4 V. Operando X-ray diffraction confirms a reversible phase transition process from the O3 to P3 structure accompanied with a very small volume change (1.0%) upon sodium extraction and insertion. The low activation barrier energy of 400 meV and the fast Na + migration of 10 –11 cm 2 ·s –1 are further obtained by first-principles calculations and galvanostatic intermittent titration technique, respectively. As a result, the O3-Na 0.8 Ni 0.6 Sb 0.4 O 2 cathode displays a reversible capacity of 106 mA h g –1 at 0.1C (12 mA g –1 ), smooth charge–discharge curves, and a high average working voltage of 3.5 V during battery cycling. The results highlight the importance of searching for a new O3-type structure with cation-disordering and high working voltage for realizing high energy SIBs.
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Yu et al. (2021) studied this question.
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