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Ruthenium containing molecular electrocatalyst on glassy carbon for electrochemical water splitting
Stockholm University, Faculty of Science, Department of Organic Chemistry. Shanghai Tech University, China.ORCID iD: 0000-0001-6360-2197
Stockholm University, Faculty of Science, Department of Organic Chemistry.ORCID iD: 0000-0003-1256-501x
Stockholm University, Faculty of Science, Department of Organic Chemistry.ORCID iD: 0000-0003-3092-2631
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Number of Authors: 132022 (English)In: Dalton Transactions, ISSN 1477-9226, E-ISSN 1477-9234, Vol. 51, no 20, p. 7957-7965Article in journal (Refereed) Published
Abstract [en]

Electrochemical water splitting constitutes one of the most promising strategies for converting water into hydrogen-based fuels, and this technology is predicted to play a key role in the transition towards a carbon-neutral energy economy. To enable the design of cost-effective electrolysis cells based on this technology, new and more efficient anodes with augmented water splitting activity and stability will be required. Herein, we report an active molecular Ru-based catalyst for electrochemically-driven water oxidation (overpotential of ∼395 mV at pH 7 phosphate buffer) and two simple methods for preparing anodes by attaching this catalyst onto glassy carbon through multi-walled carbon nanotubes to improve stability as well as reactivity. The anodes modified with the molecular catalyst were characterized by a broad toolbox of microscopy and spectroscopy techniques, and interestingly no RuO2 formation was detected during electrocatalysis over 4 h. These results demonstrate that the herein presented strategy can be used to prepare anodes that rival the performance of state-of-the-art metal oxide anodes.

Place, publisher, year, edition, pages
2022. Vol. 51, no 20, p. 7957-7965
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Chemical Sciences
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URN: urn:nbn:se:su:diva-205241DOI: 10.1039/d2dt00824fISI: 000793892800001PubMedID: 35546321OAI: oai:DiVA.org:su-205241DiVA, id: diva2:1663031
Available from: 2022-06-01 Created: 2022-06-01 Last updated: 2022-06-01Bibliographically approved

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Li, LinDas, BiswanathRahaman, AhiburVerho, OscarÅkermark, Björn

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