| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 41681 | Applied Catalysis A: General | 2011 | 8 Pages |
Nanoparticle catalysts of PtRu/C for the direct methanol fuel cell anode were synthesized by a radiolytic process. Bimetallic substructures were controlled by varying irradiation dose rate and by addition of NH4OH or NaH2PO2. Material characterization was performed with the transmission electron microscopy, the X-ray diffraction, the X-ray fluorescence spectroscopy and the X-ray absorption fine structure techniques. Methanol oxidation activity was evaluated by the linear sweep voltammetry. We concluded that the structure of the radiolytically synthesized catalysts has a Pt-rich core/Ru-rich shell structure or incomplete alloy structure. A correlation between the substructures and catalytic activities was found by using a pairing factor defined from coordination numbers determined by the extend X-ray absorption fine structure analysis, which indicates the validity of the bifunctional mechanism in the PtRu nanoparticle system. This radiolytic process is promising for synthesizing advanced PtRu/C catalysts with well-mixed bimetallic substructures enhancing methanol oxidation.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (108 K)Download as PowerPoint slideResearch highlights► Highly active PtRu/C nanoparticle catalysts are synthesized by a radiolytic process, which is a simple one-pot process without any use of surfactant, solvent or heating. ► The mixed state of PtRu is controlled by using high dose rates and additives to the synthetic solution. ► A correlation between the substructure of the catalysts and the activity of methanol oxidation was found.
