Bicarbonate Electroreduction to Multicarbon Products Enabled by Cu/Ag Bilayer Electrodes and Tailored Microenviroments.

Abstract

Bicarbonate electrolyzer can achieve the direct conversion of CO2 capture solutions that bypasses energy-intensive steps of CO2 regeneration and pressurization. However, only single-carbon chemicals (i. e., CO, formate, CH4 ) were reported as the major products so far. Herein, bicarbonate conversion to multicarbon (C2+ ) products (i. e., acetate, ethylene, ethanol, propanol) was achieved on rationally designed Cu/Ag bilayer electrodes with bilayer cation- and anion-conducting ionomers. The in-situ generated CO2 was first reduced to CO on the Ag layer, followed by its favorable further reduction to C2+ products on the Cu layer, benefiting from the locally high concentration of CO. Through optimizing the bilayer configurations, metal compositions, ionomer types, and local hydrophobicity, a microenvironment was created (high local pH, low water content, etc.) to enhance bicarbonate-to-C2+ conversion and suppress the hydrogen evolution reaction. Subsequently, a maximum C2+ faradaic efficiency of 41.6±0.39 % was achieved at a considerable current density of 100 mA cm-2 .