Please use this identifier to cite or link to this item: https://doi.org/10.1002/smll.200500253
Title: Segmented Pt/Ru, Pt/Ni, and Pt/RuNi nanorods as model bifunctional catalysts for methanol oxidation
Authors: Liu, F.
Lee, J.Y. 
Zhou, W.J. 
Keywords: Alloys
Catalysis
Electrooxidatlon
Methanol
Nanorods
Issue Date: Jan-2006
Citation: Liu, F., Lee, J.Y., Zhou, W.J. (2006-01). Segmented Pt/Ru, Pt/Ni, and Pt/RuNi nanorods as model bifunctional catalysts for methanol oxidation. Small 2 (1) : 121-128. ScholarBank@NUS Repository. https://doi.org/10.1002/smll.200500253
Abstract: Five-segment (Pt-Ru-Pt-Ru-Pt, Pt-Ni-Pt-Ni-Pt, and Pt-RuNi-Pt-RuNi-Pt) nanorods with the same overall rod length and the same total Pt segment length were prepared by sequential electrodeposition of the metals into the pores of commercially available anodic aluminum oxide (AAO) membranes. Field-emission scanning electron microscopy (FESEM) showed that the nanorods were about 210 nm in diameter and about 1.5 μm in length. The alternating Pt and oxophilic metal(s) segments could be easily differentiated in backscattered-electron images. X-ray diffraction (XRD) analysis of the nanorods indicated that Pt and Ni were polycrystalline with fcc structures, Ru was hcp, and the co-deposited RuNi adopted the nickel fcc structure with some negative shifts in the Bragg angles. The chemical states of Pt, Ru, and Ni on the nanorod surface were assayed by X-ray photoelectron spectroscopy (XPS), and the presence of Pt, PtII, PtIV, Ru, RuVI, Ni, and NiII was observed. The nanorods were catalytically active for the room-temperature electrooxidation of methanol in acidic solutions. The relative rates of reaction showed the Pt-RuNi pair sites as having the lowest overpotential to dissociate water, the highest catalytic activity in methanol oxidation, and the strongest CO-tolerance in the potential window employed. The use of segmented nanorods with identifiable Pt-oxophilic metal(s) interfaces removes many of the ambiguities in the interpretation of experimental data from conventional alloy catalysts, thereby enabling a direct comparison of the activities of various types of pair sites in methanol oxidation. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
Source Title: Small
URI: http://scholarbank.nus.edu.sg/handle/10635/90088
ISSN: 16136810
DOI: 10.1002/smll.200500253
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