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Reversible electrochemical conversion from selenium to cuprous selenide
Sean K Sandstrom1, Heng Jiang1, Marcos Lucero2
1Department of Chemistry, Oregon State University, Corvallis, OR, 97331, USA. david.ji@oregonstate.edu.
Abstract:
Using elemental selenium as an electrode, the redox-active Cu2+/Cu+ ion is reversibly hosted via the sequential conversion reactions of Se → CuSe → Cu3Se2 → Cu2Se. The four-electron redox process from Se to Cu2Se 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 Cu2Se, the fully discharged product.
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