Understanding the Role of Mn Substitution for Boosting High-Voltage Na4Fe3-xMnx(PO4)2P2O7 Cathode in Sodium-Ion Batteries

Na4Fe3(PO4)(2)P2O7 is regarded as the most promising polyanionic cathode for sodium-ion batteries (SIBs) due to its superior structural stability, cost-effectiveness, and environmental benignity. However, the low operating voltage inevitably weakens its competitiveness in energy density. Previous works have tried to enhance its operating voltage by Mn doping, which draws on the design idea of LiFexMn1-xPO4 cathode for lithium-ion batteries, but with little success. In this context, uncovering the role of Mn substitution in Na4Fe3-xMnx(PO4)(2)P2O7 (NFMxPP) cathode is urgently needed. This work discloses the effect of Mn contents on the structure, sodium storage property, and reaction mechanism of NFMxPP cathode for the first time. Introducing a moderate amount of Mn (0.6 <= x <= 1.2) into NFMxPP can weaken the Fe-O bonding interaction, thus leading to the full utilization of Mn3+/Mn2+ redox couple. As the representative, NFM1.2PP cathode exhibited a high operating voltage of approximate to 3.3 V with a reversible capacity of 109.2 mAh g(-1). Note that a Hard carbon||NFM1.2PP full battery manifests considerably high-capacity retention of 92.3% over 1600 cycles. It is believed that an understanding of the role of Mn substitution in this work will promote the practical application of high voltage NFMxPP cathodes for SIBs.