Source abstract
Abstract
Industrial activities lead to a substantial share of current anthropogenic CO2 emissions and are some of the most challenging to abate. Direct utilization of industrial flue gases to produce fuels or value-added chemicals is challenging due to the presence of impurities and low concentrations of CO2. Herein, we demonstrate a rational assembly of a permselective gas diffusion electrode (PGDE) for direct CO2 conversion from quasi flue gas (i.e., 10–15% CO2, 4% O2, and N2 balance at 100% relative humidity). The electrode design consists of a metal–organic framework (MOF) based mixed matrix membrane (MMM) that enables the selective permeation of CO2 to a silver electrocatalyst. The MOF is CALF-20, notable for the ability to physisorb CO2 in wet gas streams. Applying this approach, we convert N2-diluted CO2 streams to CO at a faradaic efficiency of 95% compared to 58% for the nonmodified counterpart electrode with MMM. The PGDE retained its electrochemical performance when introducing O2 by preventing ∼84% loss of current toward parasitic oxygen reduction reaction (ORR) and reported 30 mA cm–2 CO partial current density. Further, wetting the gas stream showed a negligible effect on the MOF and the electrochemical performance. Using our PDGE, we report nearly constant CO selectivity over 19 h in a membrane electrode assembly electrolyzer. This approach offers the potential for direct utilization of low-concentration CO2 while avoiding the economic and environmental costs of obtaining purified CO2 feedstocks.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Drive NW, Calgary, ABT2N 1N4, Canada
Department of Mechanical and Industrial Engineering, University of Toronto, 5 King’s College Road, Toronto, OntarioM5S 3G8, Canada
Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, New York14260, United States
Department of Materials Science and NanoEngineering, Rice University, 6100 Main St., Houston, Texas77005, United States
Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, ABT2N 1N4, Canada
Funding
University of Toronto · Government of Alberta · Canada First Research Excellence Fund · Natural Sciences and Engineering Research Council of Canada · Alberta Innovates · Hatch Ltd.