Stay hydrated! Impact of solvation phenomena on the CO2 reduction reaction on Pb (100) and Ag(100) surfaces.

Abstract

This article presents a comprehensive computational study of the impact of solvation on the reduction reaction of CO2to formic acid (HCOOH) and carbon monoxide (CO) at Pb(100) and Ag(100) surfaces. Results further the understanding of how solvation phenomena influence the adsorption energies of reaction intermediates. We applied an explicit solvation scheme harnessing a combined density functional theory (DFT)/microkinetic modeling approach for the CO2reduction reaction. This approach reveals high selectivities for CO formation at Ag and HCOOH formation at Pb, successfully reconciling the disparity between ab initio calculations and experimental observations. Furthermore, the detailed analysis of adsorption energies of relevant reaction intermediates shows that the total number of hydrogen bonds formed by HCOO plays a primary role for the adsorption strength of intermediates and the electrocatalytic activity. Results emphasize the importance of explicit solvation for adsorption and electrochemical reaction phenomena on metal surfaces.