Résumé
NaSICON-type materials, such as Li1.3Al0.3Ti1.7(PO4)3 (LATP), are considered promising solid electrolytes due to their good total ionic conductivity of 10-4 S.cm-1 at room temperature and their stability at high potentials (4.1 V vs Li/Li+). However, decreasing their densification temperature is crucial for their integration into all-solid-state batteries (ASSBs). The minimum required heat treatment temperature for densification of LATP is 900 °C, which is incompatible with its integration in composite electrode of ASSBs due to reactivity with the positive electrode material (cathode). To lower this temperature, lithium salts are often proposed as sintering aids to promote liquid-phase sintering. However, the systematic formation of impurities, such as LiTiOPO4 and Li4P2O7, suggests that chemical reactivity plays a significant role in LATP densification. In this work, the chemical reactivity mechanism of lithium salts with LATP during densification and sintering was investigated. Various characterization techniques, including in situ and ex situ X-ray diffraction, TGA-DTA-MS, DSC, ex situ Raman and solid-state NMR spectroscopy (7Li, 27Al, 31P), were employed to elucidate the mechanism. The formation of intermediate decomposition products Li3PO4 and TiO2 is identified for the first time via the reactivity of the lithium salt with LATP prior to the melting temperature of the salt. These intermediates subsequently react with LATP at higher temperature, resulting in the formation of final impurities LiTiOPO4 and Li4P2O7. This unified mechanism provides important insights on the enhanced densification of LATP at lower temperatures with the use of Li salt sintering aids.