Boosted Mg−CO 2 Batteries by Amine‐Mediated CO 2 Capture Chemistry and Mg 2+ ‐Conducting Solid‐electrolyte Interphases
Mg−CO 2 battery has been considered as an ideal system for energy conversion and CO 2 fixation. However, its practical application is significantly limited by the poor reversibility and sluggish kinetics of CO 2 cathode and Mg anode. Here, a new amine mediated chemistry strategy is proposed to reali...
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Veröffentlicht in: | Angewandte Chemie International Edition 2024-01, Vol.63 (2) |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Mg−CO
2
battery has been considered as an ideal system for energy conversion and CO
2
fixation. However, its practical application is significantly limited by the poor reversibility and sluggish kinetics of CO
2
cathode and Mg anode. Here, a new amine mediated chemistry strategy is proposed to realize a highly reversible and high‐rate Mg−CO
2
battery in conventional electrolyte. Judiciously combined experimental characterization and theoretical computation unveiled that the introduced amine could simultaneously modify the reactant state of CO
2
and Mg
2+
to accelerate CO
2
cathodic reactions on the thermodynamic‐kinetic levels and facilitate the formation of Mg
2+
‐conductive solid‐electrolyte interphase (SEI) to enable highly reversible Mg anode. As a result, the Mg−CO
2
battery exhibits boosted stable cyclability (70 cycles, more than 400 h at 200 mA g
−1
) and high‐rate capability (from 100 to 2000 mA g
−1
with 1.5 V overpotential) even at −15 °C. This work opens a newly promising avenue for advanced metal‐CO
2
batteries. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202313264 |