Silver Electrodes Are Highly Selective for CO in CO2 Electroreduction due to Interplay between Voltage Dependent Kinetics and Thermodynamics

Electrochemical reduction is a promising way to make use of CO₂ as feedstock for generating renewable fuel and valuable chemicals. Several metals can be used as the electrocatalyst to generate CO and formic acid, but hydrogen formation is an unwanted side reaction that can even be dominant. The lack of selectivity is, in general, a significant problem, but silver-based electrocatalysts have been shown to be highly selective, with faradaic efficiency of CO production exceeding 90%, when the applied voltage is below -1 V vs RHE. In this voltage range, only a small amount of hydrogen and formate is formed. We present calculations of the activation free energy for the various elementary steps as a function of applied voltage at the three low index facets, Ag(111), Ag(100) and Ag(110), as well as experimental measurements on polycrystalline electrodes, to identify the reason for this high selectivity. The formation of formic acid is suppressed, even though it is thermodynamically favored, because of the low coverage of adsorbed hydrogen and kinetic hindrance to the formation of the HCOO* intermediate, while *COOH, a key intermediate in CO formation, is thermodynamically unstable until the applied voltage reaches -1 V vs RHE, at which point the kinetics for its formation are more favorable than for hydrogen. The calculated results are consistent with experimental measurements carried out for acidic conditions and provide an atomic scale insight into the high CO selectivity of silver-based electrocatalysts.