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  IrOx core-shell nanocatalysts for cost- and energy-efficient electrochemical water splitting

Nong, H. N., Gan, L., Willinger, E., Teschner, D., & Strasser, P. (2014). IrOx core-shell nanocatalysts for cost- and energy-efficient electrochemical water splitting. Chemical Science, 5(8), 2955-2963. doi:10.1039/C4SC01065E.

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 Creators:
Nong, Hong Nhan1, Author
Gan, Lin1, Author
Willinger, Elena2, Author           
Teschner, Detre2, Author           
Strasser, Peter1, Author
Affiliations:
1The Electrochemical Energy, Catalysis and Materials Science Laboratory, Department of Chemistry, Chemical and Materials Engineering Division, Technical University Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany , ou_persistent22              
2Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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 Abstract: A family of dealloyed metal–oxide hybrid (M1M2@M1Ox) core@shell nanoparticle catalysts is demonstrated to provide substantial advances toward more efficient and less expensive electrolytic water splitting. IrNi@IrOx nanoparticles were synthesized from IrNix precursor alloys through selective surface Ni dealloying and controlled surface oxidation of Ir. Detailed depth-resolved insight into chemical structure, composition, morphology, and oxidation state was obtained using spectroscopic, diffraction, and scanning microscopic techniques (XANES, XRD, STEM-EDX, XPS), which confirmed our structural hypotheses at the outset. A 3-fold catalytic activity enhancement for the electrochemical oxygen evolution reaction (OER) over IrO2 and RuO2 benchmark catalysts was observed for the core-shell catalysts on a noble metal mass basis. Also, the active site-based intrinsic turnover frequency (TOF) was greatly enhanced for the most active IrNi@IrOx catalyst. This study documents the successful use of synthetic dealloying for the preparation of metal-oxide hybrid core-shell catalysts. The concept is quite general, can be applied to other noble metal nanoparticles, and points out a path forward to nanostructured proton-exchange-electrolyzer electrodes with dramatically reduced noble metal content.

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Language(s): eng - English
 Dates: 2014-04-112014-04-282014-05-232014-08-01
 Publication Status: Issued
 Pages: 9
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/C4SC01065E
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Title: Chemical Science
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: 5 (8) Sequence Number: - Start / End Page: 2955 - 2963 Identifier: ISSN: 2041-6520
CoNE: https://pure.mpg.de/cone/journals/resource/2041-6520