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 iniScience Vol. 23; no. 1; p. 100756
Main Authors Tian, Yuanyuan, Wang, Shuo, Velasco, Ever, Yang, Yueping, Cao, Lujie, Zhang, Linjuan, Li, Xing, Lin, Yichao, Zhang, Qiuju, Chen, Liang
Format Journal Article
LanguageEnglish
Published Elsevier Inc 24.01.2020
Elsevier
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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. [Display omitted] •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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These authors contributed equally
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2019.100756