Controllable States and Porosity of Cu‐Carbon for CO2 Electroreduction to Hydrocarbons

The electrocatalytic carbon dioxide reduction reaction (CO₂ RR) to value-added chemical products is an effective strategy for both greenhouse effect mitigation and high-density energy storage. However, controllable manipulation of the oxidation state and porous structure of Cu-carbon based catalysts to achieve high selectivity and current density for a particular product remains very challenging. Herein, a strategy derived from Cu-based metal-organic frameworks (MOFs) for the synthesis of controllable oxidation states and porous structure of Cu-carbon (Cu-pC, Cu₂ O-pC, and Cu₂ O/Cu-pC) is demonstrated. By regulating oxygen partial pressure during the annealing process, the valence state of the Cu and mesoporous structures of surrounding carbon are changed, leads to the different selectivity of products. Cu₂ O/CuO-pC with the higher oxidation state exhibits FE_C2H4 of 65.12% and a partial current density of -578 mA cm^-2 , while the Cu₂ O-pC shows the FE_CH4 over 55% and a partial current density exceeding -438 mA cm^-2 . Experimental and theoretical studies indicate that porous carbon-coated Cu₂ O structures favor the CH₄ pathway and inhibit the hydrogen evolution reaction. This work provides an effective strategy for exploring the influence of the various valence states of Cu and mesoporous carbon structures on the selectivity of CH₄ and C₂ H₄ products in CO₂ RR.