Abstract

AbstractOxide‐derived Cu catalysts from Cu2O microcrystals are capable of electrochemically converting CO2 into various value‐added chemicals. However, their structural transformation and associated preferred products remain unclear, requiring further investigation. Herein, Cu2O microcrystals with controllable low‐ and high‐index facets exposure are fabricated to differentiate the effects of initial exposed facets on their structural reconstruction and product selectivity in electrochemical CO2 reduction reaction. Combined in situ characterizations and theoretical investigation reveal the direct correlations of Cu2O reconstruction and product selectivity to its initial facet exposure. The Cu2O low‐index facet, being more stable with a high energy barrier on material reduction, tends to partially maintain its original crystalline structure and larger Cu2O particle size throughout the transformation. The derived flatter surface and limited Cu2O/Cu interfaces result in a favorable selectivity toward 2‐electron transfer products. The chemically active Cu2O high‐index facet (311) is energetically favorable to be reduced owing to the feasible protonation process, thus experiencing a drastic reconstruction with rich newly formed Cu nanoparticles and evolved fine Cu2O grains; Such a reconstruction creates uncoordinated Cu species and abundant boundaries, benefiting charge transfer and increasing the local pH by confining OH−, thus leading to a high selectivity toward C2+ products.

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