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Rechargeable aqueous cadmium (Cd) metal batteries enabled by the Cd plating and stripping behaviors of anode show great promise for next-generation energy storage applications due to the superior corrosion resistance, high specific capacity (476.5 mAh g–1), suitable redox potential (−0.4 V vs standard hydrogen electrode), and cost-effectiveness of Cd anode. However, this field is still in its infancy, with limited scientific exploration and numerous unresolved challenges. Therefore, to bridge the existing research gap in the field of Cd metal batteries, this study conducted a comprehensive investigation into the electrochemical performance of the Cd metal, utilizing a stable and low-cost aqueous CdSO4 solution as an electrolyte. It is revealed that the solvation structure of Cd2+ transitions from Cd(H2O)92+ to Cd(H2O)6(SO4)34– as the CdSO4 concentration increases from 0.5 to 3 M. This transition reduces the activity of H2O around Cd2+, promotes charge transfer, and enhances desolvation/solvation kinetics during Cd plating/stripping processes. Consequently, when the concentration of CdSO4 reached nearly saturated 3 M, the Cd anode presents optimal corrosion-resistant and dendrite-free capabilities, reflecting in durable Cd plating/stripping performance for over 2000 h with a high Coulombic efficiency of 99.7%. Furthermore, the Cd//V2O5 full cell achieves an ultralong cycle life, maintaining stable performance for 30,000 cycles with minimal capacity degradation. The high reversibility of the Cd anode and the exceptional performance of the full cell affirm the potential of aqueous CdSO4 electrolyte as a foundation for the future development of Cd metal batteries, offering profound insights and guidance for advancing aqueous energy storage technology.
Song et al. (Wed,) studied this question.