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Sol–Gel Synthesis of Ruthenium Oxide Nanowires To Enhance Methanol Oxidation in Supported Platinum Nanoparticle Catalysts

[Image: see text] A template-directed, sol–gel synthesis is utilized to produce crystalline RuO(2) nanowires. Crystalline nanowires with a diameter of 128 ± 15 nm were synthesized after treating the nanowires at 600 °C in air. Analysis of these nanowires by X-ray powder diffraction revealed the majo...

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Detalles Bibliográficos
Autores principales: Sztaberek, Lukasz, Mabey, Hannah, Beatrez, William, Lore, Christopher, Santulli, Alexander C., Koenigsmann, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733171/
https://www.ncbi.nlm.nih.gov/pubmed/31508545
http://dx.doi.org/10.1021/acsomega.9b01489
Descripción
Sumario:[Image: see text] A template-directed, sol–gel synthesis is utilized to produce crystalline RuO(2) nanowires. Crystalline nanowires with a diameter of 128 ± 15 nm were synthesized after treating the nanowires at 600 °C in air. Analysis of these nanowires by X-ray powder diffraction revealed the major crystalline phase to be tetragonal RuO(2) with a small quantity of metallic ruthenium present. Further analysis of the nanowire structures by high-resolution transmission electron microscopy reveals that they are polycrystalline and are composed of interconnected, highly crystalline, nanoparticles having an average size of ∼25 nm. Uniform 3 nm Pt nanoparticles were dispersed on the surface of RuO(2) nanowires using an ambient, solution-based technique yielding a hybrid catalyst for methanol oxidation. Linear sweep voltammograms (LSVs) and chronoamperometry performed in the presence of methanol in an acidic electrolyte revealed a significant enhancement in the onset potential, mass activity, and long-term stability compared with analogous Pt nanoparticles supported on commercially available Vulcan XC-72R carbon nanoparticles. Formic acid oxidation LSVs and CO stripping voltammetry revealed that the RuO(2)-supported Pt nanoparticles exhibit significantly higher CO tolerance, which leads to higher catalytic stability over a period of several hours. X-ray photoelectron spectroscopy results suggest that crystalline RuO(2) leads to less-significant oxidation of the Pt surface relative to more widely studied hydrous RuO(2) supports, thereby increasing catalytic performance.