Fast and Reversible Four‐Electron Storage Enabled by Ethyl Viologen for Rechargeable Magnesium Batteries
Magnesium (Mg) batteries are the most promising “post‐lithium‐ion” energy storage technologies owing to their high theoretical energy density, low cost, and intrinsic safety with air and moisture. However, the development of Mg batteries has been limited to cathode materials leading to low power, lo...
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Veröffentlicht in: | Advanced energy materials 2019-12, Vol.9 (48), p.n/a |
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Sprache: | eng |
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Zusammenfassung: | Magnesium (Mg) batteries are the most promising “post‐lithium‐ion” energy storage technologies owing to their high theoretical energy density, low cost, and intrinsic safety with air and moisture. However, the development of Mg batteries has been limited to cathode materials leading to low power, low reversible energy density, and poor cycle life. Here, a new Mg cathode is reported based on ethyl viologen (EV), which not only has a fast redox couple EV2+/EV0 but also is capable of coupling with redox‐active anions, such as iodide (I−), achieving a total four‐electron storage. The EV2+/EV0 redox couple demonstrates a superior rate performance (10 C) and stable cycle life (500 cycles) owing to intrinsic fast electrode kinetics. A high material utilization (>80%) can be achieved at 1.0 C under a high areal loading of 5 mg cm−2. When coupling with iodide I−, a reversible four‐electron storage is achieved with a high energy density (304.2 Wh kg−1) and a stable cycle life (>100 cycles). This study provides effective strategies for designing reversible multielectron storage for high‐rate and high‐energy rechargeable Mg batteries.
A new redox couple ethyl viologen (EV2+/EV0) is reported for rechargeable magnesium cathodes, which demonstrates a superior rate performance (10 C) and stable cycle life (500 cycles). A high material utilization (>80%) can be achieved at 1.0 C under a high areal loading of 5 mg cm−2. Redox‐active anions I−/I3− can be coupled with EV to achieve reversible four‐electron storage. |
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ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.201903002 |