Activating abnormal capacity in stoichiometric NaVO3 as cathode material for sodium-ion battery.

Abstract Traditional sodium-ion battery cathodes utilize the change in oxidation state of the transition metal(s) in the structure to accommodate the electron transfer during charge and discharge. Recent researches on sodium-rich compounds such as Na 2 RuO 3 and Na 2 IrO 3 suggest that anionic reaction with oxygen can be an additional source of electrons during electrochemical reactions. Here we demonstrate for the first time that stoichiometric NaVO 3 , despite the valence of vanadium of 5+, delivers a reversible capacity by activating it beyond 4.5 V. Elemental analysis confirms Na removal and insertion from/into NaVO 3 during charge/discharge. X-ray photoelectron spectroscopy and X-ray absorption near-edge spectroscopy results show that the oxidation state of vanadium remains unchanged, while oxygen is likely to compensate for the charge transfer during charge/discharge. Theoretical calculation on spin density of electrons in the lattice also supports the involvement of oxygen during sodium removal. Our demonstration of the unique behaviors of NaVO 3 provides a new exciting direction for research in sodium-ion battery cathodes. Highlights • NaVO 3 can be charged despite vanadium in its highest oxidation state. • Capacity of NaVO 3 depends strongly on particle size and electrical conductivity. • NaVO 3 undergoes reversible charge-discharge after activation. • NaVO 3 maintains its crystal structure upon charge and discharge. • Theoretical calculation suggests the involvement of oxygen during sodium removal. [ABSTRACT FROM AUTHOR]