Electrocatalytic Conversion of CO<sub>2</sub> to Formate at Low Overpotential by Electrolyte Engineering in Model Molecular Catalysis
Elli Vichou, Albert Solé‐Daura, Caroline Mellot‐Draznieks, Yun Li, María Gómez-Mingot, Marc Fontecave, Carlos M. Sánchez‐Sánchez
Abstract
Abstract An electrolyte engineering strategy was developed for CO 2 reduction into formate with a model molecular catalyst, [Rh(bpy)(Cp*)Cl]Cl, by modifying the solvent (organic or aqueous), the proton source (H 2 O or acetic acid), and the electrode/solution interface with imidazolium‐ and pyrrolidinium‐based ionic liquids (ILs). Experimental and theoretical density functional theory investigations suggested that π + ‐π interactions between the imidazolium‐based IL cation and the reduced bipyridine ligand of the catalyst improved the efficiency of the CO 2 reduction reaction (CO 2 RR) by lowering the overpotential, while granting partial suppression of the hydrogen evolution reaction. This allowed tuning the selectivity towards formate, reaching for this catalyst an unprecedented faradaic efficiency (FE HCOO −) ≥90 % and energy efficiency of 66 % in acetonitrile solution. For the first time, relevant CO 2 conversion to formic acid/formate was reached at low overpotential (0.28 V) using a homogeneous catalyst in acidic aqueous solution (pH=3.8). These results open up a new strategy based on electrolyte engineering for enhancing carbon balance in CO 2 RR.