RESUMEN
Solid-state lithium metal batteries (SSLMBs) are attracting increasing attentions as one of the promising next-generation technologies due to their high-safety and high-energy density. Their practical application, however, is hindered by lithium dendrite growth and propagation in solid-state electrolytes (SSEs). Herein, an in situ grain boundary modification strategy relying on the reaction between Li2 TiO3 (LTO) and Ta-substituted garnet-type electrolyte (LLZT) is developed, which forms LaTiO3 along with lesser amounts of LTO/Li2 ZrO3 at the grain boundaries (GBs). The second phases of LTO/Li2 ZrO3 inhibit abnormal grain growth. The presence of LaTiO3 at the GBs reduces electronic conductivity and improves mechanical strength, which can hinder dendrite formation and block lithium dendrite penetration through the LLZT. Moreover, the adjacent grains by LaTiO3 build a continuous Li+ transport path, providing a homogeneous Li+ flux throughout the whole LLZT-4LTO. As a result, symmetric cells of Li | LLZT-4LTO | Li shows a high critical current density of 1.8 mA cm-2 and a long cycling stability up to 2000 h at 0.3 mA cm-2 . Moreover, the high-voltage full cells demonstrate remarkable cycling stability and rate performance. It is believed that this novel grain boundary modification strategy can shed light on the constructing of high-performance SSEs for practical SSLMBs.
RESUMEN
Garnet-type solid-state electrolytes (SSEs) show a promising application in solid-state Li batteries. Poor interfacial contact with lithium causing large interfacial impedance and dendrite penetration is a problem. Inspired by unique H+/Li+ exchange of garnet electrolyte, we used an AgNO3 aqueous solution induced strategy to construct a lithiophilic layer in situ on the garnet surface without any specific apparatus. Experimental analysis reveals the uniform distribution of Ag nanoparticles and significantly enhanced affinity between the solid state electrolyte (SSE) and Li anode for the Li-Ag alloying. As expected, the interfacial area specific resistance (ASR) is greatly reduced to â¼4.5 Ω cm2, accompanying with long-cycling stability for â¼3500 h at 0.2 mA cm-2 and high critical current density of 0.75 mA cm-2. With modified SSEs, quasi-solid-state batteries with a LiFePO4 or LiNi0.5Co0.2Mn0.3O2 cathode operate well at room temperature and an all-solid-state LiFePO4/garnet/Li battery displays good cycling stability for over 200 cycles at 60 °C.