In this paper, we report on a novel α-VPO phosphate adopting the α-CrPO type structure as a promising anode material for rechargeable metal-ion batteries. Obtained by heat treatment of a structurally related hydrothermally prepared KTiOPO-type NHVOPO precursor under reducing conditions, the α-VPO material appears stable in a wide temperature range and possesses an interesting "sponged" needle-like particle morphology. The electrochemical performance of α-VPO as the anode material was examined in Li-, Na-, and K-based cells. The carbon-coated α-VPO/C composite exhibits 185, 110, and 37 mA h/g specific capacities respectively at the first discharge and around 120, 80, and 30 mA h/g at consecutive cycles at a C/10 rate. The considerable capacity drop after the first cycle in Li and Na cells is presumably due to irreversible alkali ion consumption taking place upon alkali-ion de/insertion. The EDX analysis of the recovered electrodes revealed an uptake of ∼23% of Na after the first discharge with significant cell parameter alteration validated by operando XRD measurements. In contrast to the known β-VPO anode materials, both Li and Na de/insertion into the new α-VPO proceed via an intercalation mechanism with the parent structural framework preserved but not via a conversion mechanism. The dimensionality of alkali-ion migration pathways and diffusion energy barriers was analyzed by the BVEL approach. Na-ion diffusion coefficients measured by the potentiostatic intermittent titration technique are in the range of (0.3-1.0)·10 cm/s, anticipating α-VPO as a prospective high-power anode material for Na-ion batteries.

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http://dx.doi.org/10.1021/acsami.8b21272DOI Listing

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