Chemical Modifications of Ag Catalyst Surfaces with Imidazolium Ionomers Modulate H-2 Evolution Rates during Electrochemical CO2 Reduction

Bridging polymer design with catalyst surface science is a promising direction for tuning and optimizing electrochemical reactors that could impact long-term goals in energy and sustainability. Particularly, the interaction between inorganic catalyst surfaces and organic-based ionomers provides an avenue to both steer reaction selectivity and promote activity. Here, we studied the role of imidazolium-based ionomers for electrocatalytic CO2 reduction to CO (CO2R) on Ag surfaces and found that they produce no effect on CO2R activity yet strongly promote the competing hydrogen evolution reaction (HER). By examining the dependence of HER and CO2R rates on concentrations of CO2 and HCO3-, we developed a kinetic model that attributes HER promotion to intrinsic promotion of HCO3- reduction by imidazolium ionomers. We also show that varying the ionomer structure by changing substituents on the imidazolium ring modulates the HER promotion. This ionomerstructure dependence was analyzed via Taft steric parameters and density functional theory calculations, which suggest that steric bulk from functionalities on the imidazolium ring reduces access of the ionomer to both HCO3- and the Ag surface, thus limiting the promotional effect. Our results help develop design rules for ionomer-catalyst interactions in CO2R and motivate further work into precisely uncovering the interplay between primary and secondary coordination in determining electrocatalytic behavior.

Automated summary

Integrating polymer design with catalyst surface science can impact the long-term goals in energy and sustainability by tuning and optimizing electrochemical reactors. Specifically, the role of imidazolium-based ionomers in electrocatalytic CO2 reduction has been studied, showing no effect on CO2R activity but promoting the competing hydrogen evolution reaction. Varying the ionomer structure by changing substituents on the imidazolium ring modulates the promotion of the hydrogen evolution reaction.