Elucidation of Critical Catalyst Layer Phenomena toward High Production Rates for the Electrochemical Conversion of CO to Ethylene.

ABSTRACT: This work utilizes EIS to elucidate the impact of catalyst-ionomer interactions and cathode hydroxide ion transport resistance (R_CL,_OH^-) on cell voltage and product selectivity for the electrochemical conversion of CO to ethylene. When using the same Cu catalyst and a Nafion ionomer, varying ink dispersion and electrode deposition methods results in a change of 2 orders of magnitude for R_CL,_OH^- and ca. a 25% change in electrode porosity. Decreasing R_CL,_OH^- results in improved ethylene Faradaic efficiency (FE), up to ∼57%, decrease in hydrogen FE, by ∼36%, and reduction in cell voltage by up to 1 V at 700 mA/cm². Through the optimization of electrode fabrication conditions, we achieve a maximum of 48% ethylene with >90% FE for non-hydrogen products in a 25 cm² membrane electrode assembly at 700 mA/cm² and <3 V. Additionally, the implications of optimizing R_CL,_OH^- is translated to other material requirements, such as anode porosity. We find that the best performing electrodes use ink dispersion and deposition techniques that project well into roll-to-roll processes, demonstrating the scalability of the optimized process.

SUBMITTER: Henckel D 

PROVIDER: S-EPMC10811620 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature