X-ray absorption study of platinum nanoparticles on an ion-irradiated carbon support

The chemical state and local structure of 2.6-nm-sized platinum (Pt) nanoparticles on an ion-irradiated glassy carbon (GC) substrate were investigated by X-ray absorption fine structure measurements. The partial oxidation of the Pt nanoparticles was confirmed by the peak intensity in the near-edge r...

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Veröffentlicht in:Radiation physics and chemistry (Oxford, England : 1993) England : 1993), 2018-12, Vol.153, p.152-155
Hauptverfasser: Kakitani, Kenta, Kimata, Tetsuya, Yamaki, Tetsuya, Yamamoto, Shunya, Matsumura, Daiju, Taguchi, Tomitsugu, Terai, Takayuki
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Sprache:eng
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Zusammenfassung:The chemical state and local structure of 2.6-nm-sized platinum (Pt) nanoparticles on an ion-irradiated glassy carbon (GC) substrate were investigated by X-ray absorption fine structure measurements. The partial oxidation of the Pt nanoparticles was confirmed by the peak intensity in the near-edge region of the absorption spectrum. The analysis of the extended region revealed a higher coordination number and shorter bond length of Pt–Pt compared to those of the Pt nanoparticles on the non-ion-irradiated GC. Thus, Pt nanoparticles on the ion-irradiated GC substrate were found to hold a rigid metallic coordination during the oxidation. •Pt nanoparticles were deposited on a 380 keV Ar+-irradiated carbon support.•The partial oxidation of Pt was confirmed by XANES measurements.•Pt on the irradiated support held a rigid metallic coordination during oxidation.
ISSN:0969-806X
1879-0895
DOI:10.1016/j.radphyschem.2018.09.017