Isabel Rodríguez, Francisco J. Pérez-Alonso, José Luis Gómez de la Fuente, Álvaro Tolosana-Moranchel, Laura Pascual, Dalia Liuzzi, Cristina Peinado, Sergio Rojas, María Retuerto
{"title":"Dy2NiRu0.5Ir0.5O6:酸性析氧反应的催化剂前驱体","authors":"Isabel Rodríguez, Francisco J. Pérez-Alonso, José Luis Gómez de la Fuente, Álvaro Tolosana-Moranchel, Laura Pascual, Dalia Liuzzi, Cristina Peinado, Sergio Rojas, María Retuerto","doi":"10.1016/j.electacta.2025.146543","DOIUrl":null,"url":null,"abstract":"This article presents the synthesis and evaluation of a novel double perovskite Dy<sub>2</sub>NiRu<sub>0.5</sub>Ir<sub>0.5</sub>O<sub>6</sub>, as a promising catalyst precursor for the oxygen evolution reaction (OER) in acidic electrolyte. In this perovskite, which was synthesised by a simple sol-gel process, there are two different B sites, one with Ni<sup>2+</sup> atoms, and the other in which half of the Ir<sup>4+</sup> atoms are replaced by Ru<sup>4+</sup>.Electrochemical measurements revealed and exceptional OER activity, with an Ir-normalised mass activity 5–7 times higher than the state-of-the-art IrO<sub>2</sub> benchmarks. The catalyst also exhibited remarkable stability, maintaining a stable performance for at least 36,000 OER cycles. Structural and compositional analyses during cycling revealed a transformation of the pristine double perovskite structure into a 3D-hollow Ir<sub>0.9</sub>Ru<sub>0.1</sub>O<sub>x</sub> framework. The reconstruction, which is driven by the dissolution of Dy<sup>3+</sup>, Ni<sup>2+</sup> and part of Ru<sup>4+</sup>, results in a highly active and durable electrocatalyst. The enhanced OER performance is attributed to the composition and increased surface area of the reconstructed Ir<sub>0.9</sub>Ru<sub>0.1</sub>O<sub>x</sub> hollow structure.","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"149 1","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dy2NiRu0.5Ir0.5O6: A Catalyst Precursor for Acidic Oxygen Evolution Reaction\",\"authors\":\"Isabel Rodríguez, Francisco J. Pérez-Alonso, José Luis Gómez de la Fuente, Álvaro Tolosana-Moranchel, Laura Pascual, Dalia Liuzzi, Cristina Peinado, Sergio Rojas, María Retuerto\",\"doi\":\"10.1016/j.electacta.2025.146543\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This article presents the synthesis and evaluation of a novel double perovskite Dy<sub>2</sub>NiRu<sub>0.5</sub>Ir<sub>0.5</sub>O<sub>6</sub>, as a promising catalyst precursor for the oxygen evolution reaction (OER) in acidic electrolyte. In this perovskite, which was synthesised by a simple sol-gel process, there are two different B sites, one with Ni<sup>2+</sup> atoms, and the other in which half of the Ir<sup>4+</sup> atoms are replaced by Ru<sup>4+</sup>.Electrochemical measurements revealed and exceptional OER activity, with an Ir-normalised mass activity 5–7 times higher than the state-of-the-art IrO<sub>2</sub> benchmarks. The catalyst also exhibited remarkable stability, maintaining a stable performance for at least 36,000 OER cycles. Structural and compositional analyses during cycling revealed a transformation of the pristine double perovskite structure into a 3D-hollow Ir<sub>0.9</sub>Ru<sub>0.1</sub>O<sub>x</sub> framework. The reconstruction, which is driven by the dissolution of Dy<sup>3+</sup>, Ni<sup>2+</sup> and part of Ru<sup>4+</sup>, results in a highly active and durable electrocatalyst. The enhanced OER performance is attributed to the composition and increased surface area of the reconstructed Ir<sub>0.9</sub>Ru<sub>0.1</sub>O<sub>x</sub> hollow structure.\",\"PeriodicalId\":305,\"journal\":{\"name\":\"Electrochimica Acta\",\"volume\":\"149 1\",\"pages\":\"\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-05-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Electrochimica Acta\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.electacta.2025.146543\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.electacta.2025.146543","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
Dy2NiRu0.5Ir0.5O6: A Catalyst Precursor for Acidic Oxygen Evolution Reaction
This article presents the synthesis and evaluation of a novel double perovskite Dy2NiRu0.5Ir0.5O6, as a promising catalyst precursor for the oxygen evolution reaction (OER) in acidic electrolyte. In this perovskite, which was synthesised by a simple sol-gel process, there are two different B sites, one with Ni2+ atoms, and the other in which half of the Ir4+ atoms are replaced by Ru4+.Electrochemical measurements revealed and exceptional OER activity, with an Ir-normalised mass activity 5–7 times higher than the state-of-the-art IrO2 benchmarks. The catalyst also exhibited remarkable stability, maintaining a stable performance for at least 36,000 OER cycles. Structural and compositional analyses during cycling revealed a transformation of the pristine double perovskite structure into a 3D-hollow Ir0.9Ru0.1Ox framework. The reconstruction, which is driven by the dissolution of Dy3+, Ni2+ and part of Ru4+, results in a highly active and durable electrocatalyst. The enhanced OER performance is attributed to the composition and increased surface area of the reconstructed Ir0.9Ru0.1Ox hollow structure.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.