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               <dc:title>CeO2-promoted Cu2O-based catalyst sprayed on the gas diffusion layer for the electroreduction of carbon dioxide to ethylene</dc:title>
               <dc:creator>Alarcón, Aristides de</dc:creator>
               <dc:creator>Andreu Arbella, Teresa</dc:creator>
               <dc:creator>Ponce de León, Carlos</dc:creator>
               <dc:subject>Electroquímica</dc:subject>
               <dc:subject>Diòxid de carboni</dc:subject>
               <dc:subject>Reacció d'oxidació-reducció</dc:subject>
               <dc:subject>Electrochemistry</dc:subject>
               <dc:subject>Carbon dioxide</dc:subject>
               <dc:subject>Oxidation-reduction reaction</dc:subject>
               <dc:description>The development of efficient and selective catalysts for the carbon dioxide reduction reaction (CO2RR) is crucial for sustainable energy and chemical synthesis. In this work, CeO2-y (y = C (cubic) and R (rod)) was incorporated into Cu2O nanocube electrocatalyst as a promoter for ethylene (C2H4) production. The results demonstrate that the catalyst with a loading of 5 wt% crystalline CeO2-C exhibits competitive activity and stability for ethylene production compared to pristine Cu2O. Under optimized reaction conditions of −250 mA cm−2 current density and 1 M KOH electrolyte, the Cu2O–5CeO2-C catalyst achieved a faradaic efficiency (FE) of ∼53% for C2H4 production, while maintaining stability over a period of 120 minutes. In contrast, non-promoted Cu2O exhibited a lower FE for C2H4 (∼38%) and experienced partial deactivation after 45 minutes. The characterization of the catalysts before and after the reaction revealed that the interaction between Cu2O and CeO2-C creates intrinsic sites (Cux–CeO2−x; Cux = Cu2+, Cu+, and Cu0) for the binding of CO2 and H2O molecules. Moreover, the Cu2O–5CeO2-C catalyst outperforms other reported systems in terms of FE and partial current density for C2H4 production. It requires a lower potential (−0.98 V vs. RHE) to operate at the same electrolyte concentration. This finding highlights the promising nature of Cu2O–5CeO2-C as an efficient and cost-effective catalyst for C2H4 production.</dc:description>
               <dc:date>2024-04-05T13:21:15Z</dc:date>
               <dc:date>2024-04-05T13:21:15Z</dc:date>
               <dc:date>2024-12-01</dc:date>
               <dc:date>2024-04-05T13:21:20Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1039/D3MA01009K</dc:relation>
               <dc:relation>Materials Advances, 2024, vol. 5, p. 2377-2387</dc:relation>
               <dc:relation>https://doi.org/10.1039/D3MA01009K</dc:relation>
               <dc:rights>cc-by-nc (c)  Alarcón, A. et al., 2024</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Royal Society of Chemistry</dc:publisher>
               <dc:source>Articles publicats en revistes (Ciència dels Materials i Química Física)</dc:source>
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