2018
DOI: 10.1016/j.jcis.2017.11.085
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Enhanced electrocatalytic activity and stability of monodisperse Pt nanocomposites for direct methanol fuel cells

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Cited by 101 publications
(15 citation statements)
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“…According to the TEM analysis results, it is clear that the synthesized nanoparticles are spherical, isotropic in structure (Figure 1). TEM images showed that the particle size of Rc-Ag NPs was 13–21 nm (with the help of the elimination of outliers) consistent with the literature [29, 30].
Figure 1(a) TEM patterns and (b) particle size histogram of Rc-Ag NPs.
…”
Section: Resultssupporting
confidence: 86%
“…According to the TEM analysis results, it is clear that the synthesized nanoparticles are spherical, isotropic in structure (Figure 1). TEM images showed that the particle size of Rc-Ag NPs was 13–21 nm (with the help of the elimination of outliers) consistent with the literature [29, 30].
Figure 1(a) TEM patterns and (b) particle size histogram of Rc-Ag NPs.
…”
Section: Resultssupporting
confidence: 86%
“…The study showed that PtCu/C catalyst exhibits higher activity in the reactions of electrooxidation of organic substances in comparison with Pt/C at high potentials, while the Pt/(SnO 2 /C) catalyst is the most active among the studied samples and is tolerant to the resulting intermediates under conditions where electrooxidation occurs at a potential of 0.60 V. The reasons for the increased activity of Pt/(SnO 2 /C) and PtCu/C catalysts compared to Pt/C in MOR were previously discussed in [32,33,44] and [33][34][35], respectively. The presence of Pt and SnO 2 nanoparticles attached to the surface of a carbon support can facilitate the implementation of a bifunctional catalysis mechanism by facilitating the adsorption of hydroxyl groups on the surface of tin dioxide nanoparticles and their participation in the conversion of CO molecules (an intermediate product of organic substances oxidation) on the surface of neighboring platinum nanoparticles.…”
Section: Resultsmentioning
confidence: 81%
“…As evident, the oxidation currents quickly collapsed at an initial stage of CA curves and continued quietly till the end of the scanning. This decline is owing to the poisoning of electrocatalysts by PdO 2 and Pd (OH) 4 and adsorption of CO, hydrocarbons, and oxygenates 43 . The amount of exchange charge, the current density in the beginning and end of time CA are recorded in Table 1.…”
Section: Resultsmentioning
confidence: 99%