Polymer-driven proton regulation in CO2R
Barbara Polesso a, Eman Ahmed b, Adrián Pinilla-Sánchez a, Blanca Belsa a, Viktoria Holovanova a, Lu Xia a, F. Pelayo Garcia de Arquer a
a ICFO - Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, 08860, Castelldefels, Spain
b NRC - National Research Centre Egypt
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Spring 2024 Conference (MATSUS24)
#InOpCat - In situ and operando characterization of electrocatalytic interfaces
Barcelona, Spain, 2024 March 4th - 8th
Organizers: Esther Alarcon-Llado, Jesus Barrio Hermida and Paula Sebastian Pascual
Oral, Barbara Polesso, presentation 228
DOI: https://doi.org/10.29363/nanoge.matsus.2024.228
Publication date: 18th December 2023

CO2 reduction reaction (CO2R) in acidic media is one of the alternatives to overcome low carbon utilization efficiencies and energy penalties due to the carbonate formation in an alkaline/neutral environment. In acid electrolytes the hydrogen evolution reaction (HER) is kinetically more favorable, limiting the conversion of CO2 in C2+ products. Modulating the reaction microenvironment at the catalyst-electrolyte interface with inorganic and organic components is a strategy to promote the reaction activity, selectivity, and stability [1-3]. Here, we report a CO2R reaction environment modulation strategy consisting of a polymer heterojunction coating that (1) increases local CO2 availability; (2) stabilizes CO2 reaction intermediates, leading to a high *CO coverage and improved C-C coupling in acid; and (3) regulates local proton activity with dedicated functional groups – as demonstrated by a combination of operando Raman spectroscopy and electrochemical characterizations. The polymer-coated PTFE/copper electrodes achieve a multicarbon Faradaic efficiency of 60% at 300 mA cm−2 in acidic media.

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