Affiliation:
1. Department of Nanotechnology Engineering Pukyong National University Busan 48547 Republic of Korea
2. Department of Energy Science and Engineering DGIST Daegu 42988 Republic of Korea
3. Department of Chemistry and Chemical Biology University of New Mexico New Mexico 87131 United States
Abstract
AbstractAqueous rechargeable metal batteries have recently garnered considerable attention owing to their low cost, sufficient capacity, and the use of non‐flammable water‐based electrolytes. Among them, manganese batteries are particularly favored because of their stability, abundance, affordability, and high energy density. Despite their advantages, Mn storage host structures remain underexplored. Therefore, developing innovative host materials is crucial for advancing this field. In this paper, the study reports for the first time, the use of Ag0.33V2O5 as a cathode material in aqueous manganese batteries. The study explains the displacement/intercalation behavior of manganese and silver using electrochemical, structural, and spectroscopic analyses. Additionally, it is shown that cation (Ag+, Mn2+, H+) diffusion pathways can be simulated using diffusion‐barrier calculations. Finally, the study demonstrates high‐performance manganese batteries that exhibit a remarkable reversible capacity of ≈261.9 mAh g−1 at a current of 0.1 A g−1 and an excellent cycle retention of 69.1% after 2000 cycles at a current density of 1.5 A/g. The findings of this study contribute to the advancement of aqueous manganese battery technology, offering a promising pathway for developing safer, more cost‐effective, and high‐performance energy storage systems.
Funder
Pukyong National University