Mg anode interface engineering in KNO3 electrolyte with sodium 5-sulfosalicylate as an additive for enhanced performance of Mg-air batteries

The Mg-air batteries face limitations with pronounced hydrogen evolution and low anodic utilization efficiency from Mg anodes in conventional NaCl electrolytes. The corrosion performance, surface composition, and discharge properties of commercial purity Mg anodes were thoroughly investigated in KNO3 electrolytes with and without sodium 5-sulfosalicylate and compared to NaCl electrolyte. The addition of sodium 5-sulfosalicylate to KNO3 -based electrolyte results in efficient inhibition of H2 evolution, consequently enhancing anodic utilization efficiency to 84% and specific capacity to 1844 mAh/g, compared to NaCl (24% and 534 mAh/g, respectively) under discharge condition of 10 mA/cm2 in half cell. Furthermore, the chelating ability of sodium 5-sulfosalicylate can significantly improve the Mg surface dissolution kinetics and discharge product deposition rate at the Mg anode / electrolyte interface, yielding formation of a thinner discharge layer as confirmed by time-of-flight secondary ion mass spectrometry. The discharge voltage is increased to 1.60 V, compared to 1.35 V in KNO3 at 0.5 mA/cm2 in full cell. However, higher concentration of sodium 5-sulfosalicylate can accelerate Mg anode dissolution, impeding the improvement of anodic utilization efficiency, specific capacity, and energy density. Hence, determining optimal additive concentration and current density is crucial for enhancing the discharge properties of Mg-air batteries and mitigating excessive Mg dissolution in chloride-free electrolytes. (c) 2024 Chongqing University. Publishing services provided by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ) Peer review under responsibility of Chongqing University