Sodium-deficient nickel-manganese oxides exhibit a layered structure, which is flexible enough to acquire different layer stacking. The effect of layer stacking on the intercalation properties of P3-Nax Ni0.5 Mn0.5 O2 (x=0.50, 0.67) and P2-Na2/3 Ni1/3 Mn2/3 O2 , for use as cathodes in sodium- and lithium-ion batteries, is examined. For P3-Na0.67 Ni0.5 Mn0.5 O2 , a large trigonal superstructure with 2√3 a×2√3 a×2 c is observed, whereas for P2-Na2/3 Ni1/3 Mn2/3 O2 there is a superstructure with reduced lattice parameters. In sodium cells, P3 and P2 phases intercalate sodium reversibly at a well-expressed voltage plateau. Preservation of the P3-type structure during sodium intercalation determines improving cycling stability of the P3 phase within an extended potential range, in comparison with that for the P2 phase, for which a P2-O2 phase transformation has been found. Between 2.0 and 4.0 V, P3 and P2 phases display an excellent rate capability. In lithium cells, the P3 phase intercalates lithium, accompanied by a P3-O3 structural transformation. The in situ generated O3 phase, containing lithium and sodium simultaneously, determines the specific voltage profile of P3-Nax Ni0.5 Mn0.5 O2 . The P2 phase does not display any reversible lithium intercalation. The P3 phase demonstrates a higher capacity at lower rates in lithium cells, whereas in sodium cells P3-Nax Ni0.5 Mn0.5 O2 operates better at higher rates. These findings reveal the unique ability of sodium-deficient nickel-manganese oxides with a P3-type structure for application as low-cost electrode materials in both sodium- and lithium-ion batteries.
Keywords: electrochemistry; intercalations; lithium; sodium; transition metals.
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