Mg-S batteries are promising candidates in replacing Li-ion and Li-S batteries. Mg is more abundant in the earth’s crust than Li, shows lower tendency to form dendrites and has higher theoretical volumetric capacity when coupled with sulphur cathode. The biggest challenges in Mg-S batteries development are lack of electrolytes compatible with Mg anode and sulphur cathode and diffusion of polysulfide species that are formed during discharge away from the cathode. To be able to better understand the working mechanics of Mg-S batteries, we compared battery cells with two different electrolytes regarding their electrochemistry, polysulfide species formation and their solubility. In battery cells containing electrolyte based on Mg(TFSI)2 we observed one voltage plateau and lower capacity than in battery cells containing electrolyte based on Mg[Al(hfip)4]2, where we observed higher cell capacity and two voltage plateaus that represent formation of polysulfide species and final discharge products (MgS2 and MgS), respectively. We determined concentration profile of polysulfide species during discharge with HPLC via the analysis of samples obtained from cathode and separator. In cells containing electrolyte based on Mg(TFSI)2 the concentration of polysulfide species is rising throughout the discharge while in the cells containing electrolyte based on Mg[Al(hfip)4]2 the concentration of polysulfide species is rising in the first voltage plateau and decreasing in second plateau. In the end these cells practically did not contain any polysulfide species. We observed that in both electrolytes longer polysulfide species are formed first while shorter polysulfide species are formed later. Battery cells containing electrolyte based on Mg[Al(hfip)4]2 showed better performance with higher capacity, both voltage plateaus were also visible. The cause for absence of second voltage plateau in cells containing electrolyte based on Mg(TFSI)2 is large overcharge in the beginning of discharge, which is most likely caused by passivation of anode due to the presence of impurities in electrolyte or instability of electrolyte on the anode surface.
|