Correlation of Oxygen Anion Redox Activity to In-Plane Honeycomb Cation Ordering in NaxNiyMn1-yO2 Cathodes

Sodium-ion batteries (SIBs) are one of the most promising next-generation energy storage systems because of their abundant and low-cost component materials. However, the lower energy density of SIBs compared with lithium-ion batteries diminishes their practical value proposition. Among the many sodium-based cathodes, layered transition metal oxides with high sodium content have energy densities comparable with the lithium-ion battery technology. When charged above 4.1 V, the sodium-based cathodes often undergo transformations because the activation of oxygen anion redox causes irreversible oxygen release, transition metal ion migration, lattice distortion, and rapid capacity decay. Here, in situ gas analysis is performed to evaluate the lattice oxygen anion redox activity in NaxNiyMn1-yO2 cathodes with P2 and O3 structural orderings. Operando X-ray diffraction and neutron diffraction are performed to assess the structural changes related to lattice oxygen redox and transition metal ion migration in NaxNiyMn1-yO2 cathodes. The results unveil that in-plane honeycomb cationic ordering can help suppress oxygen anion redox activity, which is critical for the future design of layered transition metal oxide cathodes that are prone to achieve high-energy for durable SIBs.

Automated summary

Sodium-ion batteries (SIBs) are a promising energy storage system due to their low-cost materials, but their lower energy density compared to lithium-ion batteries limits their practical value. This study investigates the lattice oxygen anion redox activity in NaxNiyMn1-yO2 cathodes and suggests that a honeycomb cationic ordering can suppress this activity, providing insights for the design of high-energy and durable SIBs.