Selenium and selenium-sulfur cathode materials for high-energy rechargeable magnesium batteries

Magnesium (Mg) is an attractive metallic anode material for next-generation batteries owing to its inherent dendrite-free electrodeposition, high capacity and low cost. Here we report a new class of Mg batteries based on both elemental selenium (Se) and selenium-sulfur solid solution (SeS2) cathode...

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Veröffentlicht in:Journal of power sources 2016-08, Vol.323, p.213-219
Hauptverfasser: Zhao-Karger, Zhirong, Lin, Xiu-Mei, Bonatto Minella, Christian, Wang, Di, Diemant, Thomas, Behm, R. Jürgen, Fichtner, Maximilian
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Sprache:eng
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Zusammenfassung:Magnesium (Mg) is an attractive metallic anode material for next-generation batteries owing to its inherent dendrite-free electrodeposition, high capacity and low cost. Here we report a new class of Mg batteries based on both elemental selenium (Se) and selenium-sulfur solid solution (SeS2) cathode materials. Elemental Se confined into a mesoporous carbon was used as a cathode material. Coupling the Se cathode with a metallic Mg anode in a non-nucleophilic electrolyte, the Se cathode delivered a high initial volumetric discharge capacity of 1689 mA h cm−3 and a reversible capacity of 480 mA h cm−3 was retained after 50 cycles at a high current density of 2 C. The mechanistic insights into the electrochemical conversion in Mg-Se batteries were investigated by microscopic and spectroscopic methods. The structural transformation of cyclic Se8 into chainlike Sen upon battery cycling was revealed by ex-situ Raman spectroscopy. In addition, the promising battery performance with a SeS2 cathode envisages the perspective of a series of SeSn cathode materials combining the benefits of both selenium and sulfur for high energy Mg batteries. •Selenium based composites are studied as cathode materials for magnesium batteries.•The selenium composites show high volumetric capacity and rate capability.•The electrochemical mechanism of Mg–Se battery is investigated.
ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2016.05.034