Directly-Deposited Ultrathin Solid Polymer Electrolyte for Enhanced CO2 Electrolysis
Kibria Md Golam a
a Department of Chemical and Petroleum Engineering, University of Calgary, University Drive Northwest, 2500, Calgary, Canada
Materials for Sustainable Development Conference (MATSUS)
Proceedings of Materials for Sustainable Development Conference (MAT-SUS) (NFM22)
#SolarFuels - Solar fuels through emerging system approaches
Barcelona, Spain, 2022 October 24th - 28th
Organizer: F. Pelayo Garcia de Arquer
Invited Speaker, Kibria Md Golam, presentation 315
DOI: https://doi.org/10.29363/nanoge.nfm.2022.315
Publication date: 11th July 2022

Carbon capture, conversion and utilization (CCU) is gaining attention from the worldwide community for its ability to minimize CO2 accumulation in the atmosphere. Electroreduction of CO2 (eR-CO2) in combination with renewable electricity sources can be one of routes to achieve the target. Economic viability of eR-CO2 relies on improved performance accompanied with scalable system design. Membranes are commonly used for the separation of reduction and oxidation products as well as to provide a suitable micro-environment for CO2R. Commercial membranes often address only one of the key challenges in CO2R: either they offer suitable micro-environment for CO2R (e.g., anion exchange membrane) or suppress carbonate cross-over (e.g., cation exchange membrane and bipolar membrane). Here, we present a cation-infused ultrathin (~3 µm) solid polymer electrolyte (CISPE) that concomitantly addresses both of these challenges via bidirectional ion transport mechanism and suppressed anolyte diffusion. The CISPE was directly deposited into the copper cathode catalyst, eliminating the requirement of a standalone membrane. Our demonstrated system offers high selectivity towards CO2 electrolysis (~90%) and a single-pass CO2 utilization of ~18% at 200 mA/cm2 with the primary product being ethylene (faradaic efficiency of 65%). Our directly-deposited CISPE enabled record low energy consumption of 294 GJ/ton C2H4 along with ~110 hours of stable operation with C2H4 as the primary product. The present work offers a versatile design paradigm for functional polymer electrolyte, opening doors towards stable, and efficient electrolysis for high-value feedstock chemicals and fuels production using low-cost catalysts.

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