Abstract

In this paper, the structural evolutions of different oxidized LiVPO4F-based anode materials formed at 350, 550 and 650°C are studied and compared by in-situ X-ray diffraction technique in 0.0–3.0V. It is found that oxidized LiVPO4F-based sample obtained at 350°C not only displays stable structure upon heat-treatment but also shows the same lithium ion insertion/extraction mechanism as the one of the pristine LiVPO4F corresponding to the continuous phase transformation between LiVPO4F, Li2VPO4F and Li3VPO4F. Increasing the sintering temperature to 550°C or higher one, the pristine sample is oxidized to Li1−xVPO4F1−yOz at 550°C and Li1−xVPO4O at 650°C. In-situ X-ray diffraction data demonstrate that the electrochemical reaction of oxidized LiVPO4F-based sample at 550°C with Li continuously results in the formation of Li1.4−xVPO4F1−yOz, Li1.7−xVPO4F1−yOz, Li2.0−xVPO4F1−yOz, Li3.0−xVPO4F1−yOz, Li4.0−xVPO4F1−yOz and Li3PO4 after a lithiation reaction to 0.0V. However, these delithiation compounds for oxidized LiVPO4F-based sample at 550°C cannot return to the original Li1−xVPO4F1−yOz in the reverse recharge process. For comparison, the insertion/extraction mechanism of oxidized LiVPO4F-based sample at 650°C is associated with the highly reversible process between Li1−xVPO4O and Li4VPO4O in 0.0–3.0V.

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