Bimetallic Au@Pt nanoparticles (NPs) with Pt monolayer shell are of much interest for applications in heterogeneous catalysts because of enhanced catalytic activity and very low Pt-utilization. However, precisely controlled synthesis with uniform Pt-monolayers and stability on the AuNPs seeds remain elusive. Herein, we report the controlled deposition of Pt-monolayer onto uniform AuNPs seeds to obtain Au@Pt core–shell NPs and their Pt-coverage dependent electrocatalytic activity for methanol electro-oxidation. The atomic ratio between Au/Pt was effectively tuned by varying the precursor solution ratio in the reaction solution. The morphology and atomic structure of the Au@Pt NPs were analyzed by high-resolution scanning transmission electron microcopy (HR-STEM) and X-ray diffraction (XRD) techniques. The results demonstrated that the Au@Pt core–shell NPs with Pt-shell thickness (atomic ratio 1:2) exhibit higher electrocatalytic activity for methanol electro-oxidation reaction, whereas higher and lower Pt ratios showed less overall catalytic performance. Such higher catalytic performance of Au@Pt NPs (1:2) can be attributed to the weakened CO binding on the Pt/monolayers surface. Our present synthesis strategy and optimization of the catalytic activity of Au@Pt core–shell NPs catalysts provide promising approach to rationally design highly active catalysts with less Pt-usage for high performance electrocatalysts for applications in fuel cells.
1 February 2019 in Journal of Solid State Chemistry
In this investigation, time-dependent carbon nanostructures were prepared by high-energy ball milling in the air from elemental graphite powders. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy (RS), and high-resolution transmission electron microscopy (HRTEM) characterized the ball-milled powders. XRD analysis showed that the crystal size decreased with the milling time. Raman spectra confirmed the presence of carbon nanostructures with sp2 hybridization. Meanwhile, HRTEM images revealed different carbon morphologies during the milling time. During the different stages, it appears distortion of layers, large tapes, polyhedral morphologies, nanocapsules, and nano-onions. These carbon nanostructures occur in regions where there is carbon accumulation. In this way, the ball milling process in air conditions can promote distorted carbon and different morphologies.