Revealing the Active Phase of Copper during the Electroreduction of CO ₂ in Aqueous Electrolyte by Correlating In Situ X-ray Spectroscopy and In Situ Electron Microscopy

Abstract

The variation in the morphology and electronic structure of copper during the electroreduction of CO ₂ into valuable hydrocarbons and alcohols was revealed by combining in situ surface- and bulk-sensitive X-ray spectroscopies with electrochemical scanning electron microscopy. These experiments proved that the electrified interface surface and near-surface are dominated by reduced copper. The selectivity to the formation of the key C–C bond is enhanced at higher cathodic potentials as a consequence of increased copper metallicity. In addition, the reduction of the copper oxide electrode and oxygen loss in the lattice reconstructs the electrode to yield a rougher surface with more uncoordinated sites, which controls the dissociation barrier of water and CO ₂. Thus, according to these results, copper oxide species can only be stabilized kinetically under CO ₂ reduction reaction conditions.