2011
DOI: 10.1039/c0cp02167a
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Synthesis of octahedral Pt–Pd alloy nanoparticles for improved catalytic activity and stability in methanol electrooxidation

Abstract: We report Pt-Pd nanoparticles synthesized by means of a polyol process with glycerol as a reducing agent. The Pt-Pd nanoparticles exhibit dominantly exposed {111} facets in octahedral shape with complete alloy formation between Pt and Pd. Furthermore, the octahedral Pt-Pd alloy catalysts show improved catalytic activity and stability in methanol electrooxidation.

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Cited by 96 publications
(55 citation statements)
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“…In addition, less-noble metals dissolution would happen when applying potential cycling to multi-metallic alloys [32,36,37]. For np-PtRuCuW, the CV features are different from the PtC and PtRu catalysts (Figure 3a).…”
Section: Catalytic Activity Of Np-ptrucuw At Anodementioning
confidence: 99%
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“…In addition, less-noble metals dissolution would happen when applying potential cycling to multi-metallic alloys [32,36,37]. For np-PtRuCuW, the CV features are different from the PtC and PtRu catalysts (Figure 3a).…”
Section: Catalytic Activity Of Np-ptrucuw At Anodementioning
confidence: 99%
“…Moreover, the reduction peak of Pt oxides shifts to a more positive direction compared to the PtC and PtRu catalysts (as highlighted by dotted line in Figure 3a). The characteristics are typical to multi-component alloys [7,27,32,36,37]. Normally, the electrochemically active surface area (ECSA) can be obtained from the equation ECSAPt (m 2 /g) = QH/(2.1 × mPt) by integrating the hydrogen ad/desorption charge and using the value of 2.1 C m −2 for the oxidation of a monolayer of hydrogen on a polycrystalline Pt electrode [35,38] Figure 3b, the specific activity of the np-PtRuCuW is 1.8 mA cm −2 , which is 3.6 and 2.9 times that of the PtC and PtRu catalysts (0.5 and 0.63 mA cm ).…”
Section: Catalytic Activity Of Np-ptrucuw At Anodementioning
confidence: 99%
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“…The CV parameters for the electrocatalytic performance for each catalysts are summarised in Table 1. The ratio of the forward anodic peak to the backward peak current density (J f /J b ) relates to the ability of the catalyst to tolerate carbonaceous species, 47,50,51 thus it should generally be a higher value for the best-performing catalyst. The onset potential (E onset ) and peak potential for the forward reaction (E peak ) describe the ease at which electro-oxidation occurs at the catalyst, thus they should be less positive for the best-performing electrocatalysts.…”
Section: Spectroscopy and Microscopic Characterizationmentioning
confidence: 99%
“…In particular, shape-controlled metallic NPs have been synthesized with 0-dimensional (cube, octahedron, truncated cube, and tetrahedron) [6][7][8][9][10], 1-dimensional (wire, rod, and tube) [11][12][13], 2-dimensional (plate and sheet), and 3-dimensional (star, flower, and dendrite) structures [14][15][16][17]. Among them, the dendritic and flower-like nanostructures for electrochemical energy conversion devices such as fuel cells and metal-air batteries have shown much enhanced electrocatalytic activity and stability [18].…”
Section: Introductionmentioning
confidence: 99%