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Unexpected high selectivity for acetate formation from CO₂ reduction with copper based 2D hybrid catalysts at ultralow potentials.

ABSTRACT: Copper-based catalysts are efficient for CO₂ reduction affording commodity chemicals. However, Cu(i) active species are easily reduced to Cu(0) during the CO₂RR, leading to a rapid decay of catalytic performance. Herein, we report a hybrid-catalyst that firmly anchors 2D-Cu metallic dots on F-doped Cu _x O nanoplates (Cu _x OF), synthesized by electrochemical-transformation under the same conditions as the targeted CO₂RR. The as-prepared Cu/Cu _x OF hybrid showed unusual catalytic activity towards the CO₂RR for CH₃COO^- generation, with a high FE of 27% at extremely low potentials. The combined experimental and theoretical results show that nanoscale hybridization engenders an effective s,p-d coupling in Cu/Cu _x OF, raising the d-band center of Cu and thus enhancing electroactivity and selectivity for the acetate formation. This work highlights the use of electronic interactions to bias a hybrid catalyst towards a particular pathway, which is critical for tuning the activity and selectivity of copper-based catalysts for the CO₂RR.

SUBMITTER: Cai R

PROVIDER: S-EPMC8635182 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Author Correction: Dynamic transformations of cubic copper catalysts during CO2 electroreduction and its impact on catalytic selectivity.

Project description: Not available

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