Abstract

Lithium-ion batteries (LIBs) present the advantages of long cycle life, high voltage, and energy density and are widely made in the field of energy storage. LiVOPO4 (LVOP), a cathode material used in LIBs, has a high conceptual capacity of 159 mAh g−1 and high operating voltage of 3.9 V. However, its low electrical conductivity and cycle performance limit its commercial applications. According to the X-ray diffraction results, orthogonal crystal LVOP and monoclinic crystal Li3V2(PO4)3 (LVP) coexisted in the synthesised composite material. The transmission electron microscopy results also indicated that the LVOP and LVP phases coexist, which were coated by carbon layer of about 2.5 nm. The discharge of LVOP–LVP composite material initially was 143.2 mAh g−1, and that after 120 cycles was 132.2 mAh g−1 (at 0.1 C and 3–4.5 V). Thus, the electronic conductivity and first discharge specific capacity of the material enhanced due to the introduction of fast ion conductor LVP into LVOP. Electrochemical performance improved because the introduction of LVP led to an increase in Li+ pervasion channels in the original material and the acceleration of the Li+ transmission speed.

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