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  Microwave-Assisted Synthesis of Stable and Highly Active Ir Oxohydroxides for Electrochemical Oxidation of Water

Massue, C., Huang, X., Tarasov, A., Ranjan, C., Cap, S., & Schlögl, R. (2017). Microwave-Assisted Synthesis of Stable and Highly Active Ir Oxohydroxides for Electrochemical Oxidation of Water. ChemSusChem, 10(9), 1958-1968. doi:10.1002/cssc.201601864.

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 Creators:
Massue, Cyriac1, Author           
Huang, Xing1, Author           
Tarasov, Andrey, Author
Ranjan, Chinmoy1, Author           
Cap, Sebastian, Author
Schlögl, Robert1, Author           
Affiliations:
1Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society, ou_3023874              

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 Abstract: Water splitting for hydrogen production in acidic media has been limited by the poor stability of the anodic electrocatalyst devoted to the oxygen evolution reaction (OER). To help circumvent this problem we have synthesized a class of novel Ir oxohydroxides by rapid microwave-asisted hydrothermal synthesis, which bridges the gap between electrodeposited amorphous IrOx films and crystalline IrO2 electrocatalysts prepared by calcination routes. For electrode loadings two orders of magnitude below current standards, the synthesized compounds present an unrivalled combination of high activity and stability under commercially relevant OER conditions in comparison to reported benchmarks, without need for pretreatment. The best compound achieved a lifetime 33times longer than the best commercial Ir benchmark. Thus, the reported efficient synthesis of an Ir oxohydroxide phase with superior intrinsic OER performance constitutes a major step towards the targeted design of cost-efficient Ir based OER electrocatalysts for acidic media.

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 Dates: 2017
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 733902
ISI: 000401165900012
DOI: 10.1002/cssc.201601864
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Title: ChemSusChem
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 10 (9) Sequence Number: - Start / End Page: 1958 - 1968 Identifier: ISSN: 1864-5631
CoNE: https://pure.mpg.de/cone/journals/resource/1864-5631