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Synergistical Engineering of Vacancy and Doping Enables High-Rate and Ultrastable Na4Fe2Mn(PO4)2P2O7 Cathode for
Chenxi Jiang1, Qinqin Yu2, Chunyang Wu3
1School of Biology, Food and Environment, Anhui Key Laboratory of Sewage Purification and Ecological Rehabilitation Materials, Hefei University, Hefei, 230601, China.
Abstract:
Iron-manganese-based polyanionic compounds (Na4Fe3-xMnx(PO4)2P2O7) have attracted extensive interest as cathode for sodium ion batteries (SIBs) owing to higher working voltage, and higher energy density compared to Na4Fe3(PO4)2P2O7. However, such cathode suffers from sluggish Na+ diffusion, severe voltage hysteresis, and large structural strain caused by Jahn-Teller distortion of Mn3+. Taking Na4Fe2Mn(PO4)2P2O7 (NFMPP) as an example, herein, a synergistic engineering strategy of vacancy and doping for constructing Na4Fe2Mn1-5y/3Nb2y/3□y(PO4)2P2O7 cathodes (□: vacancy) is developed where vacancies endow rigid MnO6 octahedra more flexible for boosting Na+ mobility while Nb doping stabilize crystal structure. Based on theoretical calculations and electrochemical characterizations, the optimized Na4Fe2Mn0.9Nb0.04□0.06(PO4)2P2O7 exhibits the lowest Na+ diffusion energy barrier, the best rate capability and cyclability at both room temperature and elevated temperature than those of NFMPP with only vacancy/doping. Such cathode shows a specific capacity of 63.6 mAh g-1 at 50 C, a capacity retention of 91.0% after 10 000 cycles at 10 C, and a capacity retention of 70.1% after 3 000 cycles at 10 C (50 °C) in half cell, and also delivers a reversible capacity of 96.5 mAh g-1 at 0.1 C and a capacity retention of 88.2% after 300 cycles in full cell.

