Magnesium Mitigation Behavior in P2-Layered Sodium-Ion Battery Cathode

Heteroatom incorporation can effectively suppress the phase transition of layered sodium-ion battery cathode, but heteroatom behaviors during operating conditions are not completely understood at the atomic scale. Here, density functional theory calculations are combined with experiments to explore the mitigation behavior of Mg dopant and its mechanisms under operating conditions in P2-Na0.67Ni0.33Mn0.67O2. The void formed by Na extraction will pump some Mg dopants into Na layers from TM layers, and the collective diffusion of more than one Mg ion most likely occurs when the Mg content is relatively high in the TM layer, finally aggregating to form Mg-enrich regions (i.e., Mg segregation) apart from Ni vacancies. The void-pump-effect-induced Mg segregation effectively suppresses the P2-O2 phase transition owing to the stronger Mg-O electrostatic attraction that enhances the integrate of two adjacent oxygen layers and prevents the crack growth by mitigating the lattice volume variation under high-voltage cycling. Our work provides a fundamental understanding of heteroatom mitigation behavior in layered cathodes at the atomic level for next-generation energy storage technologies.

Automated summary

This study combines density functional theory calculations with experiments to explore the mitigation behavior of Mg dopant in layered sodium-ion battery cathodes. The study reveals that Mg dopants are pumped into Na layers from TM layers during the void formation caused by Na extraction, forming Mg-enrich regions in the TM layer. This void-pump effect effectively suppresses the phase transition and improves the cycling performance of the battery.