Reversible electrochemical conversion from selenium to cuprous selenide

Using elemental selenium as an electrode, the redox-active Cu 2+ /Cu + ion is reversibly hosted via the sequential conversion reactions of Se → CuSe → Cu 3 Se 2 → Cu 2 Se. The four-electron redox process from Se to Cu 2 Se produces a high initial specific capacity of 1233 mA h g −1 based on the mass...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2021-10, Vol.57 (82), p.173-176
Hauptverfasser: Sandstrom, Sean K, Jiang, Heng, Lucero, Marcos, Xu, Yunkai, Gallagher, Trenton C, Cao, Mengyuan, Feng, Zhenxing, Ji, Xiulei
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Sprache:eng
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Zusammenfassung:Using elemental selenium as an electrode, the redox-active Cu 2+ /Cu + ion is reversibly hosted via the sequential conversion reactions of Se → CuSe → Cu 3 Se 2 → Cu 2 Se. The four-electron redox process from Se to Cu 2 Se produces a high initial specific capacity of 1233 mA h g −1 based on the mass of selenium alone or 472 mA h g −1 based on the mass of Cu 2 Se, the fully discharged product. Using elemental selenium as an electrode, the redox-active Cu 2+ /Cu + ion is reversibly hosted via the sequential conversion reactions of Se → CuSe → Cu 3 Se 2 → Cu 2 Se.
ISSN:1359-7345
1364-548X
DOI:10.1039/d1cc03983k