Synthesis and characterization of triclinic structural LiVPO4F as possible 4.2 V cathode materials for lithium ion batteries

A potential 4.2 V cathode material LiVPO4F for lithium batteries was prepared by two-step reaction method based on a carbon-thermal reduction (CTR) process. Firstly, V2O5, NH4H2PO4 and acetylene black are reacted under an Ar atmosphere to yield VPO4. The transition-metal reduction is facilitated by the CTR based on C -> CO transition. These CTR conditions favor stabilization of the vanadium as V3+ as well as leaving residual carbon, which is useful in the subsequent electrode processing. Secondly, VPO4 reacts with LiF to yield LiVPO4F product. The property of the LiVPO4F was investigated by X-ray diffractometry (XRD), scanning electron microscopy (SEM) and electrochemical measurement. XRD studies show that LiVPO4F synthesized has triclinic structure(space group p1), isostructural with the naturally occurring mineral tavorite, LiFePO4 center dot OH. SEM image exhibits that the particle size is about 2 mu m together with homogenous distribution. Electrochemical test shows that the initial discharge capacity of LiVPO4F powder is 119 mA center dot h/g at the rate of 0.2C with an average discharge voltage of 4.2V (vs Li/Li+), and the capacity retains 89 mA center dot h/g after 30 cycles.