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Título

Metal-doped imine frameworks for the oxygen reduction reaction in acidic media

AutorTolosana-Moranchel, Álvaro; López García, Álvaro CSIC ORCID ; García-Corral, Álvaro; Marco, J.F. CSIC ORCID CVN ; Pascual, L.; Liuzzi, Dalia; Salam, Mohamed A.; Ferrer, Pilar CSIC ORCID; Torrero, Jorge; Grinter, David C.; Held, Georg; García Sánchez, Daniel; Friedrich, K. Andreas; Retuerto, María CSIC ORCID; Rojas, Sergio
Fecha de publicación15-sep-2023
EditorElsevier
CitaciónJournal of Power Sources 578: 233223 (2023)
ResumenThe overall performance of proton exchange membrane fuel cells is limited by the sluggish kinetics of the oxygen-reduction reaction (ORR). Among the most active PGM-free ORR electrocatalysts are metal-nitrogen-carbon (M-N-C), such as Fe–N–C. The Fe–N4 ensembles in these PGM-free catalysts, present in different configurations, are proposed to be the active sites for the ORR in acid. In this work, we have synthesized a Fe/N/C catalyst via thermal treatment of a polymeric CxNy precursor obtained by the wet-polymerization of melamine (a nitrogen rich molecule) and terephthaldehyde. The materials obtained (Im-FeNC-1HT and Im-FeNC-2HT) display high ORR activity in acid electrolyte compared to other Fe–N–C catalysts prepared with precursors different than 2-methylimidazole or ZIF-8. Characterization data indicate the formation of high- and low-spin Fe-Nx ensembles, with a site density of 4.4·1019 sitesFe·g−1 estimated by electrochemical stripping of NO. The ORR activity was evaluated in a RRDE configuration in 0.1 M HClO4 and in MEA configuration in a single cell.
Descripción11 pags., 7 figs., 2 tabs.
Versión del editorhttps://doi.org/10.1016/j.jpowsour.2023.233223
URIhttp://hdl.handle.net/10261/335665
DOI10.1016/j.jpowsour.2023.233223
ISSN0378-7753
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