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Ruthenium and ruthenium oxide nanofiber supports for enhanced activity of platinum electrocatalysts in the methanol oxidation reaction

Authors
An, Geon-HyoungLee, Eun-HwanAhn, Hyo-Jin
Issue Date
Jun-2016
Publisher
Royal Society of Chemistry
Citation
Physical Chemistry Chemical Physics, v.18, no.22, pp 14859 - 14866
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
Physical Chemistry Chemical Physics
Volume
18
Number
22
Start Page
14859
End Page
14866
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/73380
DOI
10.1039/c6cp01964a
ISSN
1463-9076
1463-9084
Abstract
Novel supports for the dispersion of Pt electrocatalysts in fuel cells are constantly being developed in order to improve the electrochemical performance and reduce the cost. The electrocatalytic activity and stability in fuel cells largely depend on the surface morphology and structure of the support. In this study, Ru and RuO2 nanofibers prepared by electrospinning and post-calcination have been considered as Pt-catalyst supports. The composite material loaded with 20 wt% Pt catalyst exhibited a high anodic current density of 641.7 mA mg(Pt)(-1), a high I-F/I-B ratio of 1.9, and excellent electrocatalytic stability compared to commercial Pt/C. The improved anodic current density of the composite is attributed to the high dispersion of the Pt catalyst over the large surface area of the nanosized support grains, while its low onset potential, high I-F/I-B ratio, and excellent electrocatalytic stability are ascribed to a bifunctional effect resulting from the existence of Ru atoms on the support surface. Finally, the efficient electron transfer and a rapid diffusion rate of the electrolyte are due to the unique network structure of the supports. Thus, the Ru and RuO2 nanofiber composites act as promising Pt-catalyst supports for the methanol oxidation reaction.
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