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Advanced catalytic performance of Au-Pt double-walled nanotubes and their fabrication through galvanic replacement reaction.
- Source :
-
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2013 Aug 26; Vol. 19 (35), pp. 11753-8. Date of Electronic Publication: 2013 Jul 12. - Publication Year :
- 2013
-
Abstract
- Bimetallic tubular nanostructures have been the focus of intensive research as they have very interesting potential applications in various fields including catalysis and electronics. In this paper, we demonstrate a facile method for the fabrication of Au-Pt double-walled nanotubes (Au-Pt DWNTs). The DWNTs are fabricated through the galvanic displacement reaction between Ag nanowires and various metal ions, and the Au-Pt DWNT catalysts exhibit high active catalytic performances toward both methanol electro-oxidation and 4-nitrophenol (4-NP) reduction. First, they have a high electrochemically active surface area of 61.66 m(2) g(-1), which is close to the value of commercial Pt/C catalysts (64.76 m(2) g(-1)), and the peak current density of Au-Pt DWNTs in methanol oxidation is recorded as 138.25 mA mg(-1), whereas those of Pt nanotubes, Au/Pt nanotubes (simple mixture), and commercial Pt/C are 24.12, 40.95, and 120.65 mA mg(-1), respectively. The Au-Pt DWNTs show a markedly enhanced electrocatalytic activity for methanol oxidation compared with the other three catalysts. They also show an excellent catalytic performance in comparison with common Au nanotubes for 4-nitrophenol (4-NP) reduction. The attractive performance exhibited by these prepared Au-Pt DWNTs can be attributed to their unique structures, which make them promising candidates as high-performance catalysts.<br /> (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
Details
- Language :
- English
- ISSN :
- 1521-3765
- Volume :
- 19
- Issue :
- 35
- Database :
- MEDLINE
- Journal :
- Chemistry (Weinheim an der Bergstrasse, Germany)
- Publication Type :
- Academic Journal
- Accession number :
- 23852858
- Full Text :
- https://doi.org/10.1002/chem.201301490