Sodium batteries have been regarded as promising candidates for large-scale energy storage application, provided cathode hosts with high energy density and long cycle life can be found. Herein, we report… Click to show full abstract
Sodium batteries have been regarded as promising candidates for large-scale energy storage application, provided cathode hosts with high energy density and long cycle life can be found. Herein, we report NASICON-structured Na3MnZr(PO4)3 as a cathode for sodium batteries that exhibits an electrochemical performance superior to those of other manganese phosphate cathodes reported in the literature. Both the Mn4+/Mn3+ and Mn3+/Mn2+ redox couples are reversibly accessed in Na3MnZr(PO4)3, providing high discharge voltage plateaus at 4.0 and 3.5 V, respectively. A high discharge capacity of 105 mAh g-1 was obtained from Na3MnZr(PO4)3 with a small variation of lattice parameters and a small volume change on extraction of two Na+ ions per formula unit. Moreover, Na3MnZr(PO4)3 exhibits an excellent cycling stability, retaining 91% of the initial capacity after 500 charge/discharge cycles at 0.5 C rate. On the basis of structural analysis and density functional theory calculations, we have proposed a detailed desodiation pathway from Na3MnZr(PO4)3 where Mn and Zr are disordered within the structure. We further show that the cooperative Jahn-Teller distortion of Mn3+ is suppressed in the cathode and that Na2MnZr(PO4)3 is a stable phase.
               
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