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AbstractThe 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.
chemical reaction, crystal structure, current density, surface property, synthesis, Science, low loading, PEM water electrolysis, Ruthenium, experimental study, Article, oxygen evolution, chronopotentiometry, electric conductivity, electrochemical analysis, morphology, ruthenium, crystallography, acidity, degradation, calculation, polarization, voltammetry, catalysis, X ray absorption near edge structure spectroscopy, Q, surface area, particle size, manganese derivative, structure analysis, cation, ruthenium derivative, hysteresis, oxygen evolution reaction, OER, computer model, room temperature, catalyst, extended X ray absorption fine structure spectroscopy
chemical reaction, crystal structure, current density, surface property, synthesis, Science, low loading, PEM water electrolysis, Ruthenium, experimental study, Article, oxygen evolution, chronopotentiometry, electric conductivity, electrochemical analysis, morphology, ruthenium, crystallography, acidity, degradation, calculation, polarization, voltammetry, catalysis, X ray absorption near edge structure spectroscopy, Q, surface area, particle size, manganese derivative, structure analysis, cation, ruthenium derivative, hysteresis, oxygen evolution reaction, OER, computer model, room temperature, catalyst, extended X ray absorption fine structure spectroscopy
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