Nanoscopic Porous Iridium/Iridium Dioxide Superstructures (15 nm): Synthesis and Thermal Conversion by In Situ Transmission Electron Microscopy

Kevin Pappert, Kateryna Loza, Meital Shviro, Ulrich Hagemann, Marc Heggen, Rafal E. Dunin-Borkowski, Roland Schierholz, Takuya Maeda, Kenji Kaneko, Matthias Epple

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Porous particle superstructures of about 15 nm diameter, consisting of ultrasmall nanoparticles of iridium and iridium dioxide, are prepared through the reduction of sodium hexachloridoiridate(+IV) with sodium citrate/sodium borohydride in water. The water-dispersible porous particles contain about 20 wt % poly(N-vinylpyrrolidone) (PVP), which was added for colloidal stabilization. High-resolution transmission electron microscopy confirms the presence of both iridium and iridium dioxide primary particles (1–2 nm) in each porous superstructure. The internal porosity (≈58 vol%) is demonstrated by electron tomography. In situ transmission electron microscopy up to 1000 °C under oxygen, nitrogen, argon/hydrogen (all at 1 bar), and vacuum shows that the porous particles undergo sintering and subsequent compaction upon heating, a process that starts at around 250 °C and is completed at around 800 °C. Finally, well-crystalline iridium dioxide is obtained under all four environments. The catalytic activity of the as-prepared porous superstructures in electrochemical water splitting (oxygen evolution reaction; OER) is reduced considerably upon heating owing to sintering of the pores and loss of internal surface area.

Original languageEnglish
Pages (from-to)11048-11057
Number of pages10
JournalChemistry - A European Journal
Volume25
Issue number47
DOIs
StatePublished - 22 Aug 2019
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Funding

M.E. and M.H. acknowledge financial support of this work by the Deutsche Forschungsgemeinschaft (DFG) in the projects EP 22/44-1 and HE 7192/2-1, 7192/1-1, and 7192/1-2. We thank Martin Gocyla for extensive assistance with the TEM experiments. We thank the Interdisciplinary Center for Analytics at the Nanoscale (ICAN; Duisburg) for the XPS measurements. K.L. is grateful to the Japanese Society for the Promotion of Science for a scholarship. K.K. thanks the Japan Science and Technology Agency (JST) for support (JST-CREST Grant Number JPMJCR18R2). M.E. and M.H. acknowledge financial support of this work by the Deutsche Forschungsgemeinschaft (DFG) in the projects EP 22/44‐1 and HE 7192/2‐1, 7192/1‐1, and 7192/1‐2. We thank Martin Gocyla for extensive assistance with the TEM experiments. We thank the Interdisciplinary Center for Analytics at the Nanoscale (ICAN; Duisburg) for the XPS measurements. K.L. is grateful to the Japanese Society for the Promotion of Science for a scholarship. K.K. thanks the Japan Science and Technology Agency (JST) for support (JST‐CREST Grant Number JPMJCR18R2).

FundersFunder number
Interdisciplinary Center for Analytics
JST-CREST
JST‐CRESTJPMJCR18R2
Deutsche Forschungsgemeinschaft7192/1‐1, HE 7192/2‐1, 7192/1‐2, EP 22/44‐1
Japan Society for the Promotion of Science
Japan Science and Technology Agency

    Keywords

    • catalysis
    • electrochemistry
    • electron tomography
    • iridium
    • transmission electron microscopy

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