As Li-ion battery optimization approaches theoretical limits, interest has grown in designing next-generation batteries from low-cost earth-abundant materials. Mg-S batteries are promising candidates, exhibiting widespread abundance of elemental precursors and a relatively large theoretical energy density albeit at lower cell voltage. However, Mg-S batteries exhibit poor reversibility, in part due to interactions between dissolved polysulfides and the Mg anode. Herein, we employ electrochemical experiments using Ag2S quasi-reference electrodes to probe the interactions between Mg anodes and dissolved polysulfides. We show that Mg2+ reduction (charging) is impeded in the presence of polysulfides, while Mg metal oxidation (discharging) remains facile. Large reduction overpotentials arise due to the formation of a passivation layer on the anode surface, likely composed primarily of MgS. The passivation layer is removed under oxidative conditions but quickly reforms during reduction. We discover that dissolved S8 influences the rate of MgS formation by shifting the polysulfide disproportionation equilibria. Shorter-chain polysulfides react more readily than longer-chain polysulfides at the Mg electrode, and thus, film formation is mediated by the electrochemical generation of shorter-chain polysulfide species.
Keywords: Mg SEI; Mg corrosion; Mg−S battery; divalent batteries; magnesium polysulfides.