Driving force dependence of inner-sphere electron transfer for the reduction of CO2 on a gold electrode
Benjamin A. Zhang, Cyrille Costentin, Daniel G. Nocera
Abstract
The kinetics of the inner-sphere electron transfer reaction between a gold electrode and CO2 was measured as a function of the applied potential in an aqueous environment. Extraction of the electron transfer rate constant requires deconvolution of the current associated with CO2 reduction from the competing hydrogen evolution reaction and mass transport. Analysis of the inner-sphere electron transfer reaction reveals a driving force dependence of the rate constant that has similar characteristics to that of a Marcus–Hush–Levich outer-sphere electron transfer model. Consideration of simple assumptions for CO2 adsorption on the electrode surface allows for the evaluation of a CO2,ads/CO2•−ads standard potential of ∼−0.75 ± 0.05 V vs Standard Hydrogen Electrode (SHE) and a reorganization energy on the order of 0.75 ± 0.10 eV. This standard potential is considerably lower than that observed for CO2 reduction on planar metal electrodes (∼>–1.4 V vs SHE for >10 mA/cm2), thus indicating that CO2 reduction occurs at a significant overpotential and thus provides an imperative for the design of better CO2 reduction electrocatalysts.