Bivalent cations (M = Ni 2+ , Co 2+ , Mg 2+ ) with different doping contents (x = 0.1, 0.2, 0.3, 0.4, 0.5) were incorporated for vanadium in the Na 3+x V 2−x M x (PO 4 ) 3 (NVP), yielding enhanced rate performance and capacity retention. Successful doping of these cations in the NVP structure was confirmed by powder X-ray diffraction (PXRD), vibrational FT-IR spectroscopy, and scanning electron microscopy (SEM) techniques. The improved electrochemical performance of substituted NVP cathode has been correlated to effective Na ion migration, which improved kinetics of charging and discharging properties. Mg 2+ was possible to dope up to x = 0.5 in the NVP structure, which exhibited a superior electrochemical performance compared to that of Ni 2+ -and Co 2+ -doped NVP samples. The Mg 2+ -doped NVP electrode exhibited fast Na ion kinetics with a specific capacity of 70 mAh g −1 at a 20 C rate. The oxidation state of the vanadium in the Mg 2+ -substituted NVP was investigated by using X-ray photoelectron spectroscopy (XPS).

Enhancing the ionic conductivity and thermal stability of solid electrolytes is crucial for the development of all-solid-state batteries.

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