Abstract

The pure phase α-LiAlO2 is synthesized by a solid-state reaction. The obtained product has nanocrystalline structure with the Li deficient regions near the surfaces. Combining X-ray diffraction (XRD) and thermogravimetry-differential scanning calorimetry (TG-DSC), the synthesis mechanism is revealed. The measured room-temperature ionic conductivity of the α-LiAlO2 ceramic pellet is as low as 10−21S·cm−1. This could be caused by the absence of conduction pathways, as calculated from the bond-valence (BV) method. In addition, a first-principles calculation is performed. The calculated result suggests that although the α-LiAlO2 bulk has the extremely low ionic conductivity, its ionic conductivity could be increased significantly when applied the bias voltage, which is due to the introduction of external lithium sources (lithium reservoirs of interstitials/vacancies) and external charge sources (electrons/holes). This may explain why α-LiAlO2 as the coating layer on cathode for Li-ion batteries does not block the transport of lithium ions.

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