In Situ Lithiophilic Layer from H+/Li+ Exchange on Garnet Surface for the Stable Lithium-Solid Electrolyte Interface

ACS Appl Mater Interfaces. 2019 Sep 25;11(38):35030-35038. doi: 10.1021/acsami.9b13190. Epub 2019 Sep 12.

Abstract

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 ∼4.5 Ω cm2, accompanying with long-cycling stability for ∼3500 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.

Keywords: AgNO3 aqueous solution; H+/Li+ exchange; garnet electrolytes; in situ modification; interfacial stability; solid-state Li batteries.