Water-steam activation toward oxygen-deficient vanadium oxides for enhancing zinc ion storage.

A major limitation of vanadium oxides in aqueous Zn/V₂O₅ ion battery applications is that they suffer from strong coulombic ion–lattice interactions with divalent Zn²⁺. Correspondingly, vanadium oxides show the poor utilization of their electrochemically active surface areas and unsatisfactory structural stability. The Gibbs free energy of Zn²⁺ adsorption in the vicinity of oxygen vacancies can be reduced to a thermoneutral value, which suggests that the Zn²⁺ adsorption/desorption process on the oxygen-deficient oxide lattice is more reversible as compared to a less defective vanadium oxide. In this work, it is demonstrated that these problems can be significantly ameliorated via creating oxygen vacancies in vanadium oxide host materials. Specifically, for the first time, vanadium oxides with abundant oxygen defects (labeled V_o-V₂O₅) are fabricated via a new water-steam activation strategy. Such water-steam activation forms abundant oxygen defects, and the as-prepared materials show a 3.5-fold increase in the carrier density, together with larger electrochemically active surface areas compared to a less defective vanadium oxide. When used as a cathode material for aqueous zinc ion batteries, V_o-V₂O₅ exhibits a high specific capacity (335 mA h g⁻¹ at 0.2 A g⁻¹) and excellent cell stability (∼87.2% capacity retention after 3500 continuous charge/discharge cycles at 5.0 A g⁻¹). Thus, this water-steam activation approach for disordered metal oxides yields highly competitive cathode materials, which may also aid in the future development of advanced materials in related energy fields. [ABSTRACT FROM AUTHOR]