“…The poor electrical conductivity of this material (∼10 −8 S.cm −1 ) can be directly linked to the large separation between V ions in the framework of LVP due to the PO 4 tetrahedra. 22,23 To enhance the overall electrochemical performance of LVP, several approaches have been adopted, such as carbon coating, 24 reducing the size of the particles [25][26][27] and most commonly used, cationic doping, such as divalent cation doping (Mg 2+ , Mn 2+ , Ni 2+ , … ), [28][29][30] trivalent (Fe 3+ , Al 3+ , Cr 3+ , Y 3+ , … ) [31][32][33][34][35] and tetravalent cation doping (Sn 4+ , Zr 4+ , Ge 4+ , Ti 4+ , … ). 23,[36][37][38][39][40][41] According to these studies, cation doping was found to influence the particle size, the electrical conductivity, structural stability and Li + mobility of the material, all of which have a significant impact on its electrochemical performance rated by the capacity, the energy density, and the cycling stability.…”