Excess Cations Alter *CO Intermediate Configuration and Product Selectivity of Cu in Acidic Electrochemical CO 2 Reduction Reaction

High Resolution Image Download MS PowerPoint Slide Concentrated cations are often employed to promote electrochemical CO 2 reduction reaction (CO 2 RR) selectivity in acidic electrolytes. Here, we investigate the influence of excess cations on the *CO adsorption configuration and the product distribution of the CO 2 RR. Operando attenuated total reflectance surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) reveals that increasing the Cs + concentration shifts the preference of the *CO intermediate on the Cu surface from the atop (*CO atop ) to the bridge (*CO bridge ) configuration. This transition leads to a sharp decline in C–C coupling and an increase in the hydrogen evolution reaction at high Cs + concentrations (0.7 and 1.0 M) under acidic conditions. Time-resolved SEIRAS scans show that *CO atop is kinetically dominant and the proportion of *CO bridge increases gradually only at high cation concentrations. Density functional theory simulations confirm that Cs + on the Cu surface can interact electrostatically with *CO and stabilize *CO bridge over *CO atop on the Cu surface. The evolution of *CO bridge is also observed on Ag catalysts, indicating that the effect at high concentrations is not limited to Cu. Furthermore, polymeric binders on the Cu surface mitigate these detrimental effects on the CO 2 RR and restore C 2 H 4 production by preventing the cation from altering the *CO adsorption sites on the catalyst surface. This study provides new insights into the effects of cations on catalyst performance, with implications for catalyst design and operation.