Electrocatalysis is central to the production of renewable fuels and high-value commodity chemicals. The electrolyte and the electrode together determine the catalytic properties of the liquid/solid interface. In particular, the cations of the electrolyte can greatly change the rates and reaction selectivity of many electrocatalytic processes. For this reason, the careful choice of the cation is an essential step in the design of catalytic interfaces with high selectivity for desired high-value products. To make such a judicious choice, it is critical to understand where in the electric double layer the cations reside and the various distinct mechanistic impacts they can have on the electrocatalytic process of interest. In this perspective, we review recent advances in the understanding of the electric double layer with a particular focus on the interfacial distribution of cations and the cations’ hydration states in the vicinity of the electrode under various experimental conditions. Furthermore, we summarize the different ways in which cations can alter the rates and selectivity of chemical processes at electrified interfaces and identify possible future areas of research in this field.

The product selectivity of many heterogeneous electrocatalytic processes is profoundly affected by the liquid side of the electrocatalytic interface. The electrocatalytic reduction of CO to hydrocarbons on Cu electrodes is a prototypical example of such a process. However, probing the interactions of surface-bound intermediates with their liquid reaction environment poses a formidable experimental challenge. As a result, the molecular origins of the dependence of the product selectivity on the characteristics of the electrolyte are still poorly understood. Herein, we examined the chemical and electrostatic interactions of surface-adsorbed CO with its liquid reaction environment. Using a series of quaternary alkyl ammonium cations (${\mathrm{m}\mathrm{e}\mathrm{t}\mathrm{h}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$, ${\mathrm{e}\mathrm{t}\mathrm{h}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$, ${\mathrm{p}\mathrm{r}\mathrm{o}\mathrm{p}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$, and ${\mathrm{b}\mathrm{u}\mathrm{t}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$), we systematically tuned the properties of this environment. With differential electrochemical mass spectrometry (DEMS), we show that ethylene is produced in the presence of ${\mathrm{m}\mathrm{e}\mathrm{t}\mathrm{h}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$ and ${\mathrm{e}\mathrm{t}\mathrm{h}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$ cations, whereas this product is not synthesized in ${\mathrm{p}\mathrm{r}\mathrm{o}\mathrm{p}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$- and ${\mathrm{b}\mathrm{u}\mathrm{t}\mathrm{y}\mathrm{l}}_4{\mathrm{N}}^{+}$-containing electrolytes. Surface-enhanced infrared absorption spectroscopy (SEIRAS) reveals that the cations do not block CO adsorption sites and that the cation-dependent interfacial electric field is too small to account for the observed changes in selectivity. However, SEIRAS shows that an intermolecular interaction between surface-adsorbed CO and interfacial water is disrupted in the presence of the two larger cations. This observation suggests that this interaction promotes the hydrogenation of surface-bound CO to ethylene. Our study provides a critical molecular-level insight into how interactions of surface species with the liquid reaction environment control the selectivity of this complex electrocatalytic process. Significance Many technologically interesting electrocatalytic reactions lead to a variety of products; that is, they exhibit poor product selectivity. Examples include the oxidations of ammonia and methane and the reductions of nitrogen and carbon dioxide. The poor selectivity hinders the adoption of these promising technologies. Improving the selectivity requires a molecular-level understanding of the factors that control these reaction processes. Herein, we investigated how the liquid reaction environment impacts the selectivity of the reduction of CO to ethylene, a prototypical process for multielectron–proton transfer reactions. We show that the intermolecular interaction between surface-adsorbed CO and interfacial water is critical for the formation of ethylene. This mechanistic insight is expected to guide the design of electrocatalytic interfaces with high product selectivity.

The catalytic selectivity and reactivity of an electrocatalytic interface can profoundly depend on the identity of the supporting electrolyte's cation. In the case of CO₂ reduction on copper electrodes, these cation effects have been utilized to suppress undesired hydrogen evolution and to promote the formation of C₂ reduction products. However, to more effectively steer the catalytic selectivity of the electrolyte/copper interface by cations, it is crucial to reveal the various physical mechanisms by which cations impact the catalytic properties of this prototypical interface for CO₂ reduction. Herein, we employ surface-sensitive infrared spectroscopy to probe how alkali cations (Li⁺, K⁺, and Cs⁺) control the coverage of CO, a key intermediate in CO₂ reduction, on a polycrystalline copper electrode. We find that surface-adsorbed CO experiences an increasingly larger interfacial electric field with increasing cation size. The reduction of CO is further promoted by the two larger cations, leading to a significant drop of the CO coverage at high cathodic potential around −1 V vs. RHE. Our results demonstrate for the first time that the coverage of CO on the electrode is very sensitive to the identity of the cation. Since the relative coverage of CO and hydrogen on the copper surface affects the catalytic rates of CO₂ reduction and hydrogen evolution, our results represent an essential step towards a better understanding of how cation effects control the product distribution.