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dc.contributor.authorYou, Futian
dc.contributor.authorUrrego Ortiz, Ricardo
dc.contributor.authorPan, Steve Shao Wei
dc.contributor.authorCalle Vallejo, Federico
dc.contributor.authorYeo, Boon Siang
dc.date.accessioned2025-01-03T17:49:33Z
dc.date.available2025-01-03T17:49:33Z
dc.date.issued2024-03-28
dc.identifier.citationApplied Catalysis B: Environment and Energy 352 : (2024) // Article ID 124008es_ES
dc.identifier.issn0926-3373
dc.identifier.issn1873-3883
dc.identifier.urihttp://hdl.handle.net/10810/71109
dc.description.abstractCO electroreduction (COR), powered by renewable electricity, shows promise for producing green chemicals at the industrial scale. Here, we aim to understand why amongst C2 products, acetate is formed with relatively greater selectivity on Cu catalysts mounted in flow cells, as compared to in H-cells. We attribute this to improved CO transport in flow cells, which increases local pH and *CO coverage (θ_(*CO)). The effect of local pH was verified through COR in different electrolytes, which shows a significant increase in the Faradaic efficiency (FE) of acetate as local pH rose. Higher CO concentrations in flow cells under similar local pH also substantially increased the FEacetate, as compared to FEethylene and FEethanol. This suggests that acetate formation is most sensitive to θ_(*CO). DFT calculations emphasize the importance of θ_(*CO) in favoring acetate formation from the *CHCO intermediate, and reveals the role of lateral interactions in the production of C2 molecules.es_ES
dc.description.sponsorshipThe authors acknowledge financial support from the National Research Foundation of Singapore (Urban Solutions and Sustainability, Industry Alignment Fund (Pre-Positioning) Programme, A-0004543-00-00). The project that gave rise to these results also received the support of a PhD fellowship from “la Caixa” Foundation (ID 100010434, fellowship code LCF/BQ/DI22/11940040). This work also received financial support from grants PID2021-127957NB-I00 and TED2021-132550B-C21, which are funded by MCIN/AEI/ 10.13039/501100011033 and by the European Union. We also acknowledge financial support through grant IT1453-22 “Grupos Consolidados UPV/EHU del Gobierno Vasco”. The use of supercomputing facilities at SURFsara was sponsored by NWO Physical Sciences, with financial support by NWO. We also thank Dr. Xiaofei Zhao, Dr. Evon Ong and Ms. Li Jun Lim from NUS Chemistry for assisting with the Cu deposition and Dr. Gaolei Zhan from NUS Chemistry for assisting with the AFM measurements.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/MCIN/PID2021-127957NB-I00es_ES
dc.relationinfo:eu-repo/grantAgreement/MCIN/TED2021-132550B-C21es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.titleAdsorbate Coverage Effects on the Electroreduction of CO to Acetatees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND licensees_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.apcatb.2024.124008es_ES
dc.identifier.doi10.1016/j.apcatb.2024.124008
dc.departamentoesPolímeros y Materiales Avanzados: Física, Química y Tecnologíaes_ES
dc.departamentoeuPolimero eta Material Aurreratuak: Fisika, Kimika eta Teknologiaes_ES


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© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license
Except where otherwise noted, this item's license is described as © 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license