Local microenvironment tuning induces switching between electrochemical CO reduction pathways
Gas diffusion layers (GDL) have become a critical component in electrochemical CO 2 reduction (CO 2 R) systems because they can enable high current densities needed for industrially relevant productivity. Besides this function, it is often assumed that the choice of catalyst and electrolyte play muc...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 11; no. 25; pp. 13493 - 1351 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Published |
27.06.2023
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Online Access | Get full text |
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Summary: | Gas diffusion layers (GDL) have become a critical component in electrochemical CO
2
reduction (CO
2
R) systems because they can enable high current densities needed for industrially relevant productivity. Besides this function, it is often assumed that the choice of catalyst and electrolyte play much more important roles than the GDL in influencing the observed product selectivity. Here, we show that tuning of the GDL pore size can be used to control the local microenvironment of the catalyst and hence, effect significant changes in catalytic outcomes. This concept is demonstrated using sputtered Ag films on hydrophobic PTFE substrates with 6 different pore sizes. Although Ag is known to be a predominantly CO generating catalyst, we find that smaller pore sizes favor the generation of formate up to a faradaic efficiency of 43%. Combined experimental and simulation results show that this is due to the influence of the pore size on CO
2
mass transport, which alters the local pH at the electrode, resulting in reaction pathway switching between CO and formate. Our results highlight the importance of the local microenvironment as an experimental knob that can be rationally tuned for controlling product selectivity: a key consideration in the design of CO
2
R systems.
We show that the pore size of the gas-diffusion layer used in electrochemical CO
2
reduction affects CO
2
mass transport. This directly influences the local reaction microenvironment, controlling the selectivity between CO and formate on Ag catalysts. |
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Bibliography: | into value-added chemicals and fuels. This was followed by a postdoctoral stint at the University of Toronto where he developed new electrochemical routes for ethylene upgrading. After this, he joined the Institute of Materials Research and Engineering, A*STAR as a staff scientist in 2019 and then the Department of Chemical and Biomolecular Engineering at the National University of Singapore as an Assistant Professor in 2021. His research interests include electrocatalysis, CO conversion and hydrogen storage. 2 Dr. Yanwei Lum obtained his PhD degree in Materials Science and Engineering at the University of California, Berkeley in 2018 where he studied the electrochemical conversion of CO https://doi.org/10.1039/d3ta02558f Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta02558f |