Surface engineering of inorganic solid-state electrolytes via interlayers strategy for developing long-cycling quasi-all-solid-state lithium batteries.

Lithium metal batteries (LMBs) with inorganic solid-state electrolytes are considered promising secondary battery systems because of their higher energy content than their Li-ion counterpart. However, the LMB performance remains unsatisfactory for commercialization, primarily owing to the inability of the inorganic solid-state electrolytes to hinder lithium dendrite propagation. Here, using an Ag-coated Li6.4La3Zr1.7Ta0.3O12 (LLZTO) inorganic solid electrolyte in combination with a silver-carbon interlayer, we demonstrate the production of stable interfacially engineered lab-scale LMBs. Via experimental measurements and computational modelling, we prove that the interlayers strategy effectively regulates lithium stripping/plating and prevents dendrite penetration in the solid-state electrolyte pellet. By coupling the surface-engineered LLZTO with a lithium metal negative electrode, a high-voltage positive electrode with an ionic liquid-based liquid electrolyte solution in pouch cell configuration, we report 800 cycles at 1.6 mA/cm2 and 25 °C without applying external pressure. This cell enables an initial discharge capacity of about 3 mAh/cm2 and a discharge capacity retention of about 85%.

Grain Boundary Engineering Enabled High-Performance Garnet-Type Electrolyte for Lithium Dendrite Free Lithium Metal Batteries.

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.

High-energy and durable lithium metal batteries using garnet-type solid electrolytes with tailored lithium-metal compatibility.

Lithium metal batteries using solid electrolytes are considered to be the next-generation lithium batteries due to their enhanced energy density and safety. However, interfacial instabilities between Li-metal and solid electrolytes limit their implementation in practical batteries. Herein, Li-metal batteries using tailored garnet-type Li7-xLa3-aZr2-bO12 (LLZO) solid electrolytes is reported, which shows remarkable stability and energy density, meeting the lifespan requirements of commercial applications. We demonstrate that the compatibility between LLZO and lithium metal is crucial for long-term stability, which is accomplished by bulk dopant regulating and dopant-specific interfacial treatment using protonation/etching. An all-solid-state with 5 mAh cm-2 cathode delivers a cumulative capacity of over 4000 mAh cm-2 at 3 mA cm-2, which to the best of our knowledge, is the highest cycling parameter reported for Li-metal batteries with LLZOs. These findings are expected to promote the development of solid-state Li-metal batteries by highlighting the efficacy of the coupled bulk and interface doping of solid electrolytes.

Method Using Water-Based Solvent to Prepare Li7La3Zr2O12 Solid Electrolytes.

Li-garnet Li7La3Zr2O12 (LLZO) is a promising candidate of solid electrolytes for high-safety solid-state Li+ ion batteries. However, because of its high reactivity to water, the preparation of LLZO powders and ceramics is not easy for large-scale amounts. Herein, a method applying water-based solvent is proposed to demonstrate a possible solution. Ta-doped LLZO, that is, Li6.4La3Zr1.4Ta0.6O12 (LLZTO), and its LLZTO/MgO composite ceramics are made by attrition milling, followed by a spray-drying process using water-based slurries. The impacts of parameters of the method on the structure and properties of green and sintered pellets are studied. A relative density of ∼95%, a Li-ion conductivity of ∼3.5 × 10-4 S/cm, and uniform grain size LLZTO/MgO garnet composite ceramics are obtained with an attrition-milled LLZTO/MgO slurry that contains 40 wt % solids and 2 wt % polyvinyl alcohol binder. Li-sulfur batteries based on these ceramics are fabricated and work under 25 °C for 20 cycles with a Coulombic efficiency of 100%. This research demonstrates a promising mass production method for the preparation of Li-garnet ceramics.