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Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media

The design of active and durable catalysts for the H(2)O/O(2) interconversion is one of the major challenges of electrocatalysis for renewable energy. The oxygen evolution reaction (OER) is catalyzed by SrRuO(3) with low potentials (ca. 1.35 V(RHE)), but the catalyst’s durability is insufficient. He...

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Autores principales: Retuerto, María, Pascual, Laura, Calle-Vallejo, Federico, Ferrer, Pilar, Gianolio, Diego, Pereira, Amaru González, García, Álvaro, Torrero, Jorge, Fernández-Díaz, María Teresa, Bencok, Peter, Peña, Miguel A., Fierro, José Luis G., Rojas, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499887/
https://www.ncbi.nlm.nih.gov/pubmed/31053713
http://dx.doi.org/10.1038/s41467-019-09791-w
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author Retuerto, María
Pascual, Laura
Calle-Vallejo, Federico
Ferrer, Pilar
Gianolio, Diego
Pereira, Amaru González
García, Álvaro
Torrero, Jorge
Fernández-Díaz, María Teresa
Bencok, Peter
Peña, Miguel A.
Fierro, José Luis G.
Rojas, Sergio
author_facet Retuerto, María
Pascual, Laura
Calle-Vallejo, Federico
Ferrer, Pilar
Gianolio, Diego
Pereira, Amaru González
García, Álvaro
Torrero, Jorge
Fernández-Díaz, María Teresa
Bencok, Peter
Peña, Miguel A.
Fierro, José Luis G.
Rojas, Sergio
author_sort Retuerto, María
collection PubMed
description The design of active and durable catalysts for the H(2)O/O(2) interconversion is one of the major challenges of electrocatalysis for renewable energy. The oxygen evolution reaction (OER) is catalyzed by SrRuO(3) with low potentials (ca. 1.35 V(RHE)), but the catalyst’s durability is insufficient. Here we show that Na doping enhances both activity and durability in acid media. DFT reveals that whereas SrRuO(3) binds reaction intermediates too strongly, Na doping of ~0.125 leads to nearly optimal OER activity. Na doping increases the oxidation state of Ru, thereby displacing positively O p-band and Ru d-band centers, weakening Ru-adsorbate bonds. The enhanced durability of Na-doped perovskites is concomitant with the stabilization of Ru centers with slightly higher oxidation states, higher dissolution potentials, lower surface energy and less distorted RuO(6) octahedra. These results illustrate how high OER activity and durability can be simultaneously engineered by chemical doping of perovskites.
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spelling pubmed-64998872019-05-06 Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media Retuerto, María Pascual, Laura Calle-Vallejo, Federico Ferrer, Pilar Gianolio, Diego Pereira, Amaru González García, Álvaro Torrero, Jorge Fernández-Díaz, María Teresa Bencok, Peter Peña, Miguel A. Fierro, José Luis G. Rojas, Sergio Nat Commun Article The design of active and durable catalysts for the H(2)O/O(2) interconversion is one of the major challenges of electrocatalysis for renewable energy. The oxygen evolution reaction (OER) is catalyzed by SrRuO(3) with low potentials (ca. 1.35 V(RHE)), but the catalyst’s durability is insufficient. Here we show that Na doping enhances both activity and durability in acid media. DFT reveals that whereas SrRuO(3) binds reaction intermediates too strongly, Na doping of ~0.125 leads to nearly optimal OER activity. Na doping increases the oxidation state of Ru, thereby displacing positively O p-band and Ru d-band centers, weakening Ru-adsorbate bonds. The enhanced durability of Na-doped perovskites is concomitant with the stabilization of Ru centers with slightly higher oxidation states, higher dissolution potentials, lower surface energy and less distorted RuO(6) octahedra. These results illustrate how high OER activity and durability can be simultaneously engineered by chemical doping of perovskites. Nature Publishing Group UK 2019-05-03 /pmc/articles/PMC6499887/ /pubmed/31053713 http://dx.doi.org/10.1038/s41467-019-09791-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Retuerto, María
Pascual, Laura
Calle-Vallejo, Federico
Ferrer, Pilar
Gianolio, Diego
Pereira, Amaru González
García, Álvaro
Torrero, Jorge
Fernández-Díaz, María Teresa
Bencok, Peter
Peña, Miguel A.
Fierro, José Luis G.
Rojas, Sergio
Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
title Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
title_full Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
title_fullStr Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
title_full_unstemmed Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
title_short Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
title_sort na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499887/
https://www.ncbi.nlm.nih.gov/pubmed/31053713
http://dx.doi.org/10.1038/s41467-019-09791-w
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