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 language | English |
---|---|
Pages (from-to) | 11048-11057 |
Number of pages | 10 |
Journal | Chemistry - A European Journal |
Volume | 25 |
Issue number | 47 |
DOIs | |
State | Published - 22 Aug 2019 |
Externally published | Yes |
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).
Funders | Funder number |
---|---|
Interdisciplinary Center for Analytics | |
JST-CREST | |
JST‐CREST | JPMJCR18R2 |
Deutsche Forschungsgemeinschaft | 7192/1‐1, 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