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International journal of hydrogen energy, 2013-09, Vol.38 (29), p.12838-12846
2013
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Autor(en) / Beteiligte
Titel
Investigation of AuNi/C anode catalyst for direct methanol fuel cells
Ist Teil von
  • International journal of hydrogen energy, 2013-09, Vol.38 (29), p.12838-12846
Ort / Verlag
Kidlington: Elsevier Ltd
Erscheinungsjahr
2013
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • AuNi nanoparticles supported on the activated carbon (AuNi/C) are synthesized by the impregnation method in the ethyleneglycol system using NH2NH2·H2O as a reducing agent. The alloying of Au and Ni and the removal of unalloyed Ni in the AuNi/C composition are achieved by heat and acid treatments in sequence. Research results reveal that the average size and alloying degree of the AuNi nanoparticles in the AuNi/C catalyst increase with the enhancement of the annealing temperature. However, the Ni content of the AuNi/C catalyst firstly goes up and then down with the rising of heat treatment temperature due to the AuNi system phase-separates. Moreover, the electrocatalytic activity normalized by the electrochemically active surface area of each AuNi/C catalyst is far better than that of the Au/C catalyst, because of the bifunctional mechanism and the electrocatalytic activity of the NiOOH. In particular, the AuNi/C catalyst annealed at 400 °C exhibits the most excellent activity, due to its small AuNi particles and proper alloying degree. Furthermore, its mass-specific electrochemical activity is higher than that of the Au/C catalyst, although the mean diameter of the AuNi nanoparticles in this catalyst is larger than that of the Au nanoparticles. •AuNi/C catalyst is synthesized by the impregnation method in the glycol system.•The AuNi system phase-separations are detected in the nano scale.•The Ni content in catalyst first goes up and then down with the annealing temperature.•AuNi/C catalyst has a better activity than Au/C catalyst for the methanol oxidation.
Sprache
Englisch
Identifikatoren
ISSN: 0360-3199
eISSN: 1879-3487
DOI: 10.1016/j.ijhydene.2013.07.102
Titel-ID: cdi_proquest_miscellaneous_1506389392

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