Abstract
Aqueous manganese metal batteries have emerged as promising candidates for stationary storage due to their natural abundance, safety, and high energy density. However, the high chemical reactivity and sluggish migration kinetics of the Mn metal anode induce a severe hydrogen evolution reaction (HER) and dendrite formation, respectively. The situation deteriorates in the low-concentration electrolyte especially. Here, we propose a novel approach to construct an Mn-enriched interfacial layer (Mn@MIL) on the Mn metal anode surface to address these challenges simultaneously. The Mn@MIL acts as a physical barrier to not only suppress HER but also accelerate the Mn2+ diffusion kinetics through the Mn2+ saturated interfacial layer to inhibit dendrite growth. Therefore, in the low-concentration electrolyte (1 M MnCl2), the Mn||Mn symmetric cells and Mn||V2O5 full cells with high mass loading demonstrate promising cycling stability with minimal polarization and parasitic reactions, making them more suitable for practical applications in a smart grid.
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