ClAg14 (C≡Ct Bu)12 Nanoclusters as Efficient and Selective Electrocatalysts Toward Industrially Relevant CO2 Conversion.

Abstract

Atomically precise metal nanoclusters (NCs) have emerged as a promising frontier in the field of electrochemical CO2 reduction reactions (CO2 RR) because of their distinctive catalytic properties. Although numerous metal NCs are developed for CO2 RR, their use in practical applications has suffered from their low-yield synthesis and insufficient catalytic activity. In this study, the large-scale synthesis and electrocatalytic performance of ClAg14 (C≡Ct Bu)12 + NCs, which exhibit remarkable efficiency in catalyzing CO2 -to-CO electroreduction with a CO selectivity of over 99% are reported. The underlying mechanisms behind this extraordinary CO2 RR activity of ClAg14 (C≡Ct Bu)12 + NCs are investigated by a combination of electrokinetic and theoretical studies. These analyses reveal that different active sites, generated through electrochemical activation, have unique adsorption properties for the reaction intermediates, leading to enhanced CO2 RR and suppressed hydrogen production. Furthermore, industrially relevant CO2 -to-CO electroreduction using ClAg14 (C≡Ct Bu)12 + NCs in a zero-gap CO2 electrolyzer, achieving high energy efficiency of 51% and catalyst activity of over 1400 A g-1 at a current density of 400mAcm-2 is demonstrated.