Electrocatalytic CO₂ Reduction with Atomically Precise Au₁₃ Nanoclusters: Effect of Ligand Shell on Catalytic Performance

Abstract

Supported gold nanoclusters of the formula [Au13(L)5Cl2]3+ where L = N-heterocyclic carbene (NHC) or phosphine ligands are examined in the electrocatalytic CO2 reduction reaction (eCO2RR) in a membrane electrode assembly cell configuration. Gold nanoclusters bearing bisNHC ligands are shown to exhibit improved catalytic performance compared with diphosphine-stabilized nanoclusters after activation at the optimum treatment temperatures. The thermal properties of the nanoclusters are shown to have a significant impact on their catalytic activity. Thermogravimetric analysis, UV–vis absorption spectroscopy, and X-ray photoelectron spectroscopy revealed that thermal treatment of [Au13(diphosphine)5Cl2]3+ nanoclusters results in complete loss of diphosphine ligands while [Au13(bisNHC)5Cl2]3+ nanoclusters show stepwise and partial removal of bisNHC ligands. We propose that the partial removal of bisNHC ligands enables efficient activation of [Au13(bisNHC)5Cl2]3+ clusters while conserving the core structure. This leads to the implication that intact clusters retaining at least some ligands in their coordination environment are more active than ligand-free clusters.