Interfacial Modification of Ga-Substituted Li<sub>7</sub>La<sub>3</sub>Zr<sub>2</sub>O<sub>12</sub> against Li Metal via a Simple Doping Method
Cheng Xing, Qiaohong Yan, Rentai Yan, Xingrui Pu, Yue Jiang, Yi Huang, Xiaohong Zhu
Abstract
Garnet Li 7 La 3 Zr 2 O 12 (LLZO) is considered a promising solid electrolyte for all-solid-state lithium-ion batteries due to its outstanding performance in which Ga-doped LLZO particularly exhibits excellent ionic conductivity. However, the application of Ga-doped LLZO is limited by the interfacial instability between Ga-doped LLZO and Li metal. In this study, Ga 3+ - and Sb 5+ -codoped LLZO is prepared using a conventional solid-state reaction method, and the effects of dual-doping on the crystal structure, microstructure, conductivity of LLZO, and battery cycle stability are investigated. The results demonstrate that the introduction of an appropriate amount of Sb 5+ into Ga 3+ -stabilized cubic-phase LLZO promotes grain contact and enhances the total ionic conductivity. The optimized Li 6.3 Ga 0.2 La 3 Zr 1.9 Sb 0.1 O 12 solid electrolyte exhibits the highest total ionic conductivity of 4.65 × 10 –4 S cm –1 at room temperature. Additionally, the introduction of Sb 5+ suppresses the formation of the LiGaO 2 impurity phase, thereby improving the interface stability between Ga-doped LLZO and the Li metal. The assembled Li||Ga,Sb 0.1 -LLZO||Li symmetric cell demonstrates stable cycling for 500 h at room temperature under a current density of 0.13 mA cm –2 . The Li||Ga,Sb 0.1 -LLZO||LiFePO 4 full cell delivers a reversible capacity of about 140 mA h g –1, exhibiting negligible decay after 50 cycles. These findings suggest that the application of Ga-doped LLZO in all-solid-state lithium-ion batteries holds great promise by simply doping Zr sites with high-valence ions.