Tuning local chemistry of P2 layered-oxide cathode for high energy and long cycles of sodium-ion battery

Layered transition-metal oxides have attracted intensive interest for cathode materials of sodium-ion batteries. However, they are hindered by the limited capacity and inferior phase transition due to the gliding of transition-metal layers upon Na(+) extraction and insertion in the cathode materials. Here, we report that the large-sized K(+) is riveted in the prismatic Na(+) sites of P2-Na(0.612)K(0.056)MnO(2) to enable more thermodynamically favorable Na(+) vacancies. The Mn-O bonds are reinforced to reduce phase transition during charge and discharge. 0.901 Na(+) per formula are reversibly extracted and inserted, in which only the two-phase transition of P2 ↔ P’2 occurs at low voltages. It exhibits the highest specific capacity of 240.5 mAh g(−1) and energy density of 654 Wh kg(−1) based on the redox of Mn(3+)/Mn(4+), and a capacity retention of 98.2% after 100 cycles. This investigation will shed lights on the tuneable chemical environments of transition-metal oxides for advanced cathode materials and promote the development of sodium-ion batteries.