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Use of Nanoscale Carbon Layers on Ag-Based Gas Diffusion Electrodes to Promote CO Production

A promising strategy for the inhibition of the hydrogen evolution reaction along with the stabilization of the electrocatalyst in electrochemical CO2 reduction cells involves the application of a nanoscale amorphous carbon layer on top of the active catalyst layer in a gas diffusion electrode. Witho...

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Bibliographic Details
Published in:ACS applied nano materials 2022-06, Vol.5 (6), p.7723-7732
Main Authors: Pacquets, Lien, Van den Hoek, Järi, Arenas-Esteban, Daniel, Ciocarlan, Radu-George, Cool, Pegie, Baert, Kitty, Hauffman, Tom, Daems, Nick, Bals, Sara, Breugelmans, Tom
Format: Article
Language:English
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Summary:A promising strategy for the inhibition of the hydrogen evolution reaction along with the stabilization of the electrocatalyst in electrochemical CO2 reduction cells involves the application of a nanoscale amorphous carbon layer on top of the active catalyst layer in a gas diffusion electrode. Without modifying the chemical nature of the electrocatalyst itself, these amorphous carbon layers lead to the stabilization of the electrocatalyst, and a significant improvement with respect to the inhibition of the hydrogen evolution reaction was also obtained. The faradaic efficiencies of hydrogen could be reduced from 31.4 to 2.1% after 1 h of electrolysis with a 5 nm thick carbon layer. Furthermore, the impact of the carbon layer thickness (5–30 nm) on this inhibiting effect was investigated. We determined an optimal thickness of 15 nm where the hydrogen evolution reaction was inhibited and a decent stability was obtained. Next, a thickness of 15 nm was selected for durability measurements. Interestingly, these durability measurements revealed the beneficial impact of the carbon layer already after 6 h by suppressing the hydrogen evolution such that an increase of only 37.9% exists compared to 56.9% without the use of an additional carbon layer, which is an improvement of 150%. Since carbon is only applied afterward, it reveals its great potential in terms of electrocatalysis in general.
ISSN:2574-0970
2574-0970
DOI:10.1021/acsanm.2c00473