A Co-Doped Nanorod-like RuO2 Electrocatalyst with Abundant Oxygen Vacancies for Acidic Water Oxidation
Active and highly stable electrocatalysts for oxygen evolution reaction (OER) in acidic media are currently in high demand as a cleaner alternative to the combustion of fossil fuels. Herein, we report a Co-doped nanorod-like RuO2 electrocatalyst with an abundance of oxygen vacancies achieved through...
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Published in | iScience Vol. 23; no. 1; p. 100756 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
24.01.2020
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Active and highly stable electrocatalysts for oxygen evolution reaction (OER) in acidic media are currently in high demand as a cleaner alternative to the combustion of fossil fuels. Herein, we report a Co-doped nanorod-like RuO2 electrocatalyst with an abundance of oxygen vacancies achieved through the facile, one-step annealing of a Ru-exchanged ZIF-67 derivative. The compound exhibits ultra-high OER performance in acidic media, with a low overpotential of 169 mV at 10 mA cm−2 while maintaining excellent activity, even when exposed to a 50-h galvanostatic stability test at a constant current of 10 mA cm−2. The dramatic enhancement in OER performance is mainly attributed to the abundance of oxygen vacancies and modulated electronic structure of the Co-doped RuO2 that rely on a vacancy-related lattice oxygen oxidation mechanism (LOM) rather than adsorbate evolution reaction mechanism (AEM), as revealed and supported by experimental characterizations as well as density functional theory (DFT) calculations.
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•A Co-doped RuO2 electrocatalyst with an abundance of oxygen vacancies was synthesized•The compound exhibits ultra-high OER performance in acidic media•The oxygen vacancies contribute to the high OER performance
Catalysis; Electrochemical Energy Production; Nanomaterials |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Lead Contact These authors contributed equally |
ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2019.100756 |