Abstract
The manuscript explores the oxygen reduction activity of Mn-doped Cu oxide electrodes. Mn is redox-active within the ORR potential range, exhibiting oxidation states from +2 to +7. The Cu[Mn]Ox/Au catalyst demonstrates superior ORR performance, surpassing both pure CuOx and MnOx electrodes. In situ Raman spectroscopy shows that the peak at 612cm-1 demonstrated stark tuning ~0.7V, indicating a redox-active structural framework containing Cu-O-Mn type linkages. In general, this study reinforces the idea that mixing a first-row transition metal into a CuO system can create mixed phases with coordinative unsaturation that can enhance O-O bond breaking.
Supplementary materials
Title
Supporting Information
Description
Contains materials characterization data, electrochemical data, in situ Raman Spectroscopy data
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