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Autor(en) / Beteiligte
Titel
Pt Nanoparticles Supported on Mesoporous CeO2 Nanostructures Obtained through Green Approach for Efficient Catalytic Performance toward Ethanol Electro-oxidation
Ist Teil von
  • ACS sustainable chemistry & engineering, 2017-12, Vol.5 (12), p.11290-11299
Ort / Verlag
American Chemical Society
Erscheinungsjahr
2017
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • In this report, an easy and green approach to the synthesis of mesoporous cerium oxide (CeO2) nanostructures and followed by supporting platinum nanoparticles (NPs) on CeO2 nanostructures (Pt/CeO2) and their application as versatile electrocatalysts for ethanol electrooxidation has been established. The synthesis of mesoporous Pt/CeO2 nanostructures involves two steps. First, mesoporous CeO2 nanostructures were synthesized via macroalgae polymer mediated approach and followed by supporting of PtNPs of ca. 5–10 nm over the mesoporous CeO2 nanostructures using seed-mediated chemical reduction process. The structural and spectroscopic characterization techniques such as transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman, X-ray photoelectron spectroscopy (XPS), and small-angle X-ray scattering (SAXS) studies confirm the strong coupling between PtNPs and the mesoporous CeO2 support resulting in the generation of more oxygen vacancies, which can facilitate the enhanced charge transport at their functional interface. Significantly, the synthesized mesoporous Pt/CeO2 nanostructures were found to show enhanced electrocatalytic activity for ethanol electrooxidation reaction. The enhanced performance is attributed to the synergistic effect of both mesoporous structure and the formation of more oxygen vacancies in the resultant Pt/CeO2 nanostructures. Our facile and eco-friendly approach to the synthesis of mesoporous CeO2 nanostructures that supports PtNPs with an excellent catalytic activity is validated as a promising strategy for potential applications in fuel cells.
Sprache
Englisch
Identifikatoren
ISSN: 2168-0485
eISSN: 2168-0485
DOI: 10.1021/acssuschemeng.7b02019
Titel-ID: cdi_acs_journals_10_1021_acssuschemeng_7b02019
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