{"title":"pH-Sensitive and Self-Regenerative Honeycomb Polymer Membrane-Electrode Assembly for CO<sub>2</sub> Reduction: Shifting Selectivity toward C<sub>2</sub> Molecules.","authors":"Sandra Castanié, Léonard Curet, Emilio Palomares, Aurélien Viterisi, Laurent Billon","doi":"10.1002/cssc.202501620","DOIUrl":null,"url":null,"abstract":"<p><p>The electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) selectivity toward C<sub>2</sub> molecules presents several challenges, ranging from the chemical nature of catalysts to the hydrophobization of electrodes. In this study, a simple and versatile concept is presented based on a honeycomb polymer membrane-electrode assembly (HMEA). By covering copper foil electrodes with a PMMA-b-P4VP porous pH-sensitive polymer membrane, the electrode selectivity in the CO<sub>2</sub>RR shifts to C<sub>2</sub> molecules. It is reported that both the bio-inspired honeycomb structure of the polymer and its pH-sensitivity lead to a Cassie-Baxter behavior in KHCO<sub>3</sub> aqueous electrolyte, which limits the hydrogen evolution reaction and concentrates the CO<sub>2</sub> and intermediates in the vicinity of the electrode surface. A systematic and drastic shift in selectivity is observed when using the porous polymer, toward formate at potentials below 0.9 V<sub>RHE</sub>, and toward ethanol and ethylene for potentials above this value. After 24 h of electrocatalysis, the selectivity and efficiency of the HMEA can be restored by simple drying at room temperature. The versatility of the HMEA concept is also extended to silver foil electrodes, showing the decrease of hydrogen production and the shift of the electrode selectivity in the CO<sub>2</sub>RR toward carbon monoxide, formate, and ethanol.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202501620"},"PeriodicalIF":6.6000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202501620","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The electrochemical CO2 reduction reaction (CO2RR) selectivity toward C2 molecules presents several challenges, ranging from the chemical nature of catalysts to the hydrophobization of electrodes. In this study, a simple and versatile concept is presented based on a honeycomb polymer membrane-electrode assembly (HMEA). By covering copper foil electrodes with a PMMA-b-P4VP porous pH-sensitive polymer membrane, the electrode selectivity in the CO2RR shifts to C2 molecules. It is reported that both the bio-inspired honeycomb structure of the polymer and its pH-sensitivity lead to a Cassie-Baxter behavior in KHCO3 aqueous electrolyte, which limits the hydrogen evolution reaction and concentrates the CO2 and intermediates in the vicinity of the electrode surface. A systematic and drastic shift in selectivity is observed when using the porous polymer, toward formate at potentials below 0.9 VRHE, and toward ethanol and ethylene for potentials above this value. After 24 h of electrocatalysis, the selectivity and efficiency of the HMEA can be restored by simple drying at room temperature. The versatility of the HMEA concept is also extended to silver foil electrodes, showing the decrease of hydrogen production and the shift of the electrode selectivity in the CO2RR toward carbon monoxide, formate, and ethanol.
期刊介绍:
ChemSusChem
Impact Factor (2016): 7.226
Scope:
Interdisciplinary journal
Focuses on research at the interface of chemistry and sustainability
Features the best research on sustainability and energy
Areas Covered:
Chemistry
Materials Science
Chemical Engineering
Biotechnology