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Ruthenium containing molecular electrocatalyst on glassy carbon for electrochemical water splitting
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0000-0002-7249-7437
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2022 (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
Royal Society of Chemistry (RSC) , 2022. Vol. 51, no 20, p. 7957-7965
Keywords [en]
Cost effectiveness, Electrocatalysis, Electrocatalysts, Fuel cells, Glass, Glass membrane electrodes, Glassy carbon, Hydrogen fuels, Multiwalled carbon nanotubes (MWCN), Ruthenium, Ruthenium compounds, A-carbon, Carbon neutrals, Cell-based, Cost effective, Efficient anode, Electrochemicals, Electrolysis cell, Energy economy, Ru based catalysts, Water splitting, Anodes
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Materials Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-324159DOI: 10.1039/d2dt00824fISI: 000793892800001PubMedID: 35546321Scopus ID: 2-s2.0-85130863989OAI: oai:DiVA.org:kth-324159DiVA, id: diva2:1739729
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QC 20230227

Available from: 2023-02-27 Created: 2023-02-27 Last updated: 2023-02-27Bibliographically approved

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Shatskiy, AndreyFei, YeKärkäs, Markus D.Dutta, Joydeep

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