Microenvironments of Cu catalysts in zero-gap membrane electrode assembly for efficient CO2 electrolysis to C2+ products

Abstract

A zero-gap membrane-electrode assembly (MEA) electrolyzer is a promising design for electrochemical CO₂ reduction reactions (eCO₂RRs), where gaseous CO₂ is directly fed without catholyte. The zero-gap junction between the catalyst and the membrane can have distinct chemical environments and mass transfer properties from the conventional H-type cell but is rarely studied. In this work, we designed an integrated experimental-simulation study in MEA to understand the zero-gap junction and factors to determine the eCO₂RR activity to multi-carbon production. We developed a simple synchronous ionomer/catalyst activation step under alkaline conditions to form jagged CuO nanoparticles whose unique morphological evolution facilitates the C₂₊ chemical production for the zero-gap MEA electrolyzer. Moreover, under gas-fed and high–current density conditions, computational fluid dynamics suggests that the mass transfer limitation of water as a proton source across the catalyst-membrane layer and cathode kinetic overpotential are critical to determining C₂₊ chemical production in the range of several micrometers. From the chemical-physical understanding, we achieved a high partial current density of 336.5 mA cm⁻² and a faradaic efficiency of 67.3% towards C₂₊ chemicals.