Highly Selective Methanol Synthesis Using Electrochemical CO2 Reduction with Defect-Engineered Cu58 Nanoclusters.

Abstract

Atomically precise copper nanoclusters (Cu NCs) exhibit significant potential as catalysts for the electrocatalytic reduction of CO₂. However, the range of products achievable with these NCs has been somewhat constrained. This study presents an innovative design strategy to enhance the catalytic activity of Cu NCs by engineering their active sites. These active sites are formed here by introducing defects on cubic Cu NCs through the partial dislocation of Cu atoms at their vertices, which creates surface ligand vacancies. This dislocation further refines the internal cationic geometry by altering cuprophilic interactions, leading to distinct modifications in the edges and vertices of the cubic geometry. These unique Cu(I) atom arrangements within the cluster effectively influence product specificity during electrochemical CO₂ reduction. Density functional theory calculations correlate the enhanced selectivity for CH₃OH in [Cu₅₈H₂₀(SPr)₃₆(PPh₃)₇]²⁺ (Pr = CH₂CH₂CH₃) NC to the increased reactivity of edge Cu atoms in binding CO and CHO intermediates, compared to [Cu₅₈H₂₀(SPr)₃₆(PPh₃)₈]²⁺ and [Cu₅₈H₂₀(SEt)₃₆(PPh₃)₆]²⁺ (Et = CH₂CH₃) NCs. Thus, this work underscores the potential of tailored structural designs of atomically precise nanocatalysts in directing electrochemical CO₂ reduction toward unconventional products.