Local CO2 reservoir layer promotes rapid and selective electrochemical CO2 reduction

Electrochemical CO 2 reduction reaction in aqueous electrolytes is a promising route to produce added-value chemicals and decrease carbon emissions. However, even in Gas-Diffusion Electrode devices, low aqueous CO 2 solubility limits catalysis rate and selectivity. Here, we demonstrate that when assembled over a heterogeneous electrocatalyst, a film of nitrile-modified Metal-Organic Framework (MOF) acts as a remarkable CO 2 -solvation layer that increases its local concentration by ~27-fold compared to bulk electrolyte, reaching 0.82 M. When mounted on a Bi catalyst in a Gas Diffusion Electrode, the MOF drastically improves CO 2 -to-HCOOH conversion, reaching above 90% selectivity and partial HCOOH currents of 166 mA/cm 2 (at −0.9 V vs RHE). The MOF also facilitates catalysis through stabilization of reaction intermediates, as identified by operando infrared spectroscopy and Density Functional Theory. Hence, the presented strategy provides new molecular means to enhance heterogeneous electrochemical CO 2 reduction reaction, leading it closer to the requirements for practical implementation. Converting CO 2 to valuable chemicals is of high interest. Here the authors address the challenge of low CO2 solubility in water by incorporating a metal-organic framework layer to enhance CO 2 pre-concentration and activation before its electroreduction by the underlying solid electrocatalyst.