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Beyond Half-Cell Success: Cathode-Electrolyte Reactivity Driving Magnesium Battery Full-Cell Degradation at Elevated
Dedy Setiawan1, Omar Falyouna1, Toshihiko Mandai1
1Research Center for Energy and Environmental Materials (GREEN), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.
None:
Rechargeable magnesium battery (RMB) is gaining attention as a promising alternative to lithium-ion batteries, offering advantages such as low cost and high theoretical capacity of magnesium metal anodes. Yet, realizing stable, high-voltage RMB full cells remains a considerable challenge. In this study, a full-cell configuration is explored combining a vanadium oxide (VO2) cathode with a weakly coordinating anion-based electrolyte. While encouraging performance is observed in half-cell setups, translating it into full-cell operation proves complex, particularly at elevated temperatures. At 60 °C, the initial discharge capacity of 77 mAh g-1 decreases notably to 28 mAh g-1 in the second cycle, whereas performance at 30 °C remains more stable ≈25 mAh g-1. Three-electrode measurement suggests increasing overpotentials at the Mg anode as a key factor in the capacity degradation. Further analysis points to issues such as uneven Mg plating/stripping, surface pitting, and minor vanadium dissolution, contributing to impedance growth and cross-over effects. These are linked to cathode-electrolyte side reactions, particularly under high-voltage. Overall, the results emphasize the importance of developing stable interphases to enhance the long-term performance of RMB full cells, especially at elevated temperatures.
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