The energy-density improvement for cathode materials by using the method of occupying the Li site with the lowest formation enthalpy was first presented, and successfully applied to Li9V3(P2O7)(3)(PO4)(2). Herein, the synthesis, structure and electrochemical properties (including both Li extraction and intercalation) of mixed alkali-ion phosphate Li8NaV3(P2O7)(3)(PO4)(2) were comprehensively studied, and compared with its isologue Li9V3(P2O7)(3)(PO4)(2). Both Li8NaV3(P2O7)(3)(PO4)(2) and Li9V3(P2O7)(3)(PO4)(2) were synthesized via an original two-step method for the first time. The sintering temperature of Li8NaV3(P2O7)(3)(PO4)(2) (650 degrees C) was much lower than that of Li9V3(P2O7)(3)(PO4)(2) (750 degrees C). The Rietveld structure refinement indicated that Na ions occupied the Li1(2b) site of Li9V3(P2O7)(3)(PO4)(2) as expected, and Li8NaV3(P2O7)(3)(PO4)(2) showed a single charge plateau at 4.4 V vs. Li in the 1st cycle. However, the Na ions migrated from Li1(2b) site after the initial cycle, and the charge plateau at 3.7 V vs. Li reappeared. On the other hand, both Li9V3(P2O7)(3)(PO4)(2) and Li8NaV3(P2O7)(3)(PO4)(2) can deliver a high reversible capacity (similar to 200 mAh g(-1)), and reveal excellent cycle and rate performance in 3.0-0.05 V vs. Li. The gentle structure changes along with abundant Li intercalation into the bulks suggested that Li9V3(P2O7)(3)(PO4)(2) and Li8NaV3(P2O7)(3)(PO4)(2) were also promising anode materials for Li-ion batteries. (C) 2015 Elsevier B.V. All rights reserved.