Regulating the Electrochemical Performance of A2Ni2TeO6 (A = Na, K) as a Cathode of Alkali Metal Ion Battery by 3d Transition Metal Substitution from a Theoretical Perspective

Abstract

With its unique honeycomb layered structure, P2-type A₂Ni₂TeO₆ (A = Na, K) exhibits remarkable cycling stability and ionic diffusion capability, making it a promising cathode material for sodium-ion batteries (SIBs) and potassium-ion batteries (PIBs). However, the high operating voltage of A₂Ni₂TeO₆ (A = Na, K) leading to surface degradation and CEI formation limits the capacity of A₂Ni₂TeO₆ (A = Na, K), where only 2/3 of Na⁺ and 1/2 K⁺ can be reversibly extracted at a high charge rate. To enhance the capacity of A₂Ni₂TeO₆ (A = Na, K) while maintaining its cycling stability, we delved into the impacts of 3d transition metal substitution on sodium and potassium storage chemistry through first-principles calculations. Our investigation includes multiple facets: lattice structure, substituting formation energy, electronic properties, ionic diffusion, average open-circuit voltage, transition metal migration, and intermediate phases in the high-voltage region. After comprehensive consideration, Mn- and Fe-substituted Na₂Ni₂TeO₆ and Fe-substituted K₂Ni₂TeO₆ emerged as the most promising candidates, exhibiting exceptional electrochemical performance. Furthermore, we discovered that the energy difference between alkali metal ions occupying substitution sites and active transition metal sites dominates the ionic diffusion behavior in TM-substituted A₂Ni₂TeO₆ (A = Na, K), and the nonuniform distribution of alkali metal ions significantly contributes to the large volume change during ionic extraction. The findings of this work not only underscore the intricate structure–activity relationship of P2-type A₂Ni₂TeO₆ (A = Na, K) substitution but also provide theoretical insights for future application of honeycomb layered transition metal oxides (HLOs) in SIB and PIB cathodes.