PTFE nanocoating on Cu nanoparticles through dry processing to enhance electrochemical conversion of CO2 towards multi-carbon products

Polymer modified copper (Cu) catalysts have demonstrated an increased production of multi-carbon (C2+) products during the electrochemical CO2 reduction reaction (CO2RR). Herein, a solvent-free processing method has been developed to cover commercial Cu nanoparticles with a porous nanocoating of polytetrafluoroethylene (PTFE) that greatly improved the production of C2+ products. The PTFE coating created a large interfacial surface area that facilitated the transport of CO2 to the solid-liquid-gas interface. The optimal catalyst achieved a faradaic efficiency of 78% for C2+ products and a notably large C2+ to C-1 product ratio of similar to 13 at current densities ranging from 400 to 500 mA cm(-2). In comparison, catalysts prepared by a conventional solvent-based method only achieved a faradaic efficiency of 56% for C2+ products and a small C2+ to C-1 product ratio of similar to 2 in the same current density range. Density functional theory (DFT) calculations suggested that the physisorbed PTFE coating on Cu catalysts plays a more significant role than the most frequently studied chemisorbed PTFE. The physisorbed PTFE is predicted to increase the binding energy of CO intermediates on Cu and lower the activation energy for C-C coupling steps, leading to significantly higher C2+ product selectivity of the Cu catalysts.

Automated summary

A solvent-free processing method was developed to improve the production of multi-carbon (C2+) products in the electrochemical CO2 reduction reaction. By coating commercial Cu nanoparticles with a porous nanocoating of polytetrafluoroethylene (PTFE), a large interfacial surface area was created, facilitating the transport of CO2 and leading to significantly higher C2+ product selectivity of the Cu catalysts.