Copper–Supramolecular Pair Catalyst Promoting C<sub>2+</sub>Product Formation in Electrochemical CO<sub>2</sub>Reduction
Lin‐Jun Zhu, Duan‐Hui Si, Fa‐Xue Ma, Meng-Jiao Sun, Teng Zhang, Rong Cao
Abstract
Electrochemical CO 2 reduction (ECR) into value-added multicarbon products is a promising approach for a carbon-neutral economy. Heterogeneous molecular catalysts consist of atomic-precise, controllable active sites with the potential to improve catalytic activity by ligand design and engineering, yet most reported molecular ECR catalysts do not exhibit multicarbon product selectivity. Herein, we report the use of a copper–supramolecular pair as a crystalline molecular catalyst to promote the formation of multicarbon products. A combination of experimental and theoretical studies reveal that the paired Cu sites work collaboratively to activate the CO 2 substrate and facilitate the coupling of adsorbed CO species although they are not bonded or bridged directly. The van der Waals interactions between the substrate and the secondary coordination sphere also play a crucial role in multicarbon product selectivity.