析氧
催化作用
氧气
制氢
分解水
电解水
化学工程
化学
材料科学
无机化学
纳米技术
电化学
物理化学
电极
电解
有机化学
光催化
电解质
工程类
作者
Dmitry Galyamin,Jorge Torrero,Isabel Rodrı́guez-Garcı́a,Manuel J. Kolb,Pilar Ferrer,L. Pascual,Mohamed Abdel Salam,Diego Gianolio,Verónica Celorrio,Mohamed Mokhtar,Daniel García Sánchez,Aldo Gago,K. Andreas Friedrich,M.A. Peña,J. A. Alonso,Federico Calle‐Vallejo,M. Retuerto,Sergio Rojas
标识
DOI:10.1038/s41467-023-37665-9
摘要
The production of green hydrogen in water electrolyzers is limited by the oxygen evolution reaction (OER). State-of-the-art electrocatalysts are based on Ir. Ru electrocatalysts are a suitable alternative provided their performance is improved. Here we show that low-Ru-content pyrochlores (R2MnRuO7, R = Y, Tb and Dy) display high activity and durability for the OER in acidic media. Y2MnRuO7 is the most stable catalyst, displaying 1.5 V at 10 mA cm-2 for 40 h, or 5000 cycles up to 1.7 V. Computational and experimental results show that the high performance is owed to Ru sites embedded in RuMnOx surface layers. A water electrolyser with Y2MnRuO7 (with only 0.2 mgRu cm-2) reaches 1 A cm-2 at 1.75 V, remaining stable at 200 mA cm-2 for more than 24 h. These results encourage further investigation on Ru catalysts in which a partial replacement of Ru by inexpensive cations can enhance the OER performance.
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