2009
DOI: 10.1016/j.electacta.2008.03.015
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Synthesis and characterization of MoOx-Pt/C and TiOx-Pt/C nano-catalysts for oxygen reduction

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Cited by 79 publications
(49 citation statements)
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“…Clear and welldefined voltammetric profiles of the MoO x -C materials were observed ( Figure S4), that were in accordance with the well-established MoO x profiles reported in the literature. [12][13][14][24][25][26][27][28][29] For the Pt-containing materials, the cyclic voltammograms ( Figure 3a nd Figure S4) exhibit the typical hydrogen adsorption-desorption features of aP ts urface at 0.05-0.40 V( H UPD ), followed by the double-layer( 0.40-0.80 V) and the Pt oxide regions (0.80-1.2 V). The electrochemically active surfacea reas (ECSAs) of the electrodes were obtainedf rom the chargei nvolved in the Pt-H ads desorption process (Supporting Information), and the values are presented in Ta ble 3f or all catalysts.…”
Section: Resultsmentioning
confidence: 98%
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“…Clear and welldefined voltammetric profiles of the MoO x -C materials were observed ( Figure S4), that were in accordance with the well-established MoO x profiles reported in the literature. [12][13][14][24][25][26][27][28][29] For the Pt-containing materials, the cyclic voltammograms ( Figure 3a nd Figure S4) exhibit the typical hydrogen adsorption-desorption features of aP ts urface at 0.05-0.40 V( H UPD ), followed by the double-layer( 0.40-0.80 V) and the Pt oxide regions (0.80-1.2 V). The electrochemically active surfacea reas (ECSAs) of the electrodes were obtainedf rom the chargei nvolved in the Pt-H ads desorption process (Supporting Information), and the values are presented in Ta ble 3f or all catalysts.…”
Section: Resultsmentioning
confidence: 98%
“…This effect was attributedt ot he strong metalsupport interaction existingb etween Pt and Ws pecies, which involves the spillover of primary oxides from the WO x to Pt, facilitating CO 2 formation.I na nother study,Çakar and co-authors showedt hat the dispersion of Pt NPs on MoO x resultsi n al argers urface area and an increase of catalytic activity towards the ORR. [11] Likewise, Elezović et al [12,13] found that the increaseo fc atalytic activity of ORR electrocatalysts based on Pt/C doped with MoO x can be explained by ag reater number of ORRa ctive sites or by synergic effects ascribed to the PtMoO x interface. Furthermore, Yane tal.…”
Section: Introductionmentioning
confidence: 97%
“…It needs to bind platinum strongly enough to shift the dissolution potentials to higher values in order to prevent Pt corrosion during stop-and-go runs. In addition, it needs to maintain or improve the assets of carbonaceous supports, such as the electron conductivity, porosity and surface area size [ [18,19,20,21,22]. All of these supports are stable under corrosive conditions required for PEMFC operation, apart from WO 3 which dissolves moderately [23],and in most cases the specific activities, that is, the activities normalized per surface area, were higher than for the state-of-the-art, Pt deposited on Vulcan-C, catalyst.…”
Section: Introductionmentioning
confidence: 99%
“…The results of Pt/C and Pt-MOx/C catalysts are presented in Fig. 5, the voltammograms shape is the typical shape of that of Pt nanoparticles in acid medium [57,58]. Pt/C, Pt-TiO 2 /C and Pt-CeO 2 /C electrocatalysts show:…”
Section: Cyclic Voltammetry Resultsmentioning
confidence: 99%