Surface Chemistry of LLZO Garnet Electrolytes with Sulfur in Electron Pair Donor Solvents

Conventional Li–S batteries rely on liquid electrolytes based on LiNO 3 /DOL/DME mixtures that produce a quasistable interface with the lithium anode. Electron pair donor (EPD) solvents, also known as high donor number solvents, provide much higher polysulfide solubility and close-to-ideal sulfur utilization, making them solvents of choice for lean electrolyte Li–S cells. However, their instability to reduction requires incorporation of an ion-conductive membrane that is stable with Li–such as garnet LLZO and also stable with sulfur/polysulfides. We report that even trace amounts of LiOH on a LLTZO surface trigger a complex reaction with sulfur dissolved in typical EPD solvents (i.e., N, N -dimethylacetamide, DMA) to produce a highly resistive impedance layer that quickly grows with time from 1000 to 10,000 Ω cm 2 over a few hours, thus impeding Li + transport across the interface. Decorating the LLZO with protective phosphate groups to produce a modified surface provides a very low charge-transfer resistance of 40 Ω cm 2 that is maintained over time and inhibits the reaction of LiOH and dissolved sulfur. Hybrid liquid–solid electrolyte cells constructed on this concept result in a high sulfur utilization of 1400 mAh g –1 which is 85% of theoretical and remains constant over cycling even with conventional, unoptimized carbon/sulfur cathodes.