Giordano T. Paganoto; Josimar Ribeiro
Abstract
Ni and Ga elements are inexpensive compared to the Pt. Ni and NiOx have been recognized to have potential applications in ethanol electrooxidation. For these reasons and based on previous results obtained with Ga addition on Pt-based electrocatalysts we have investigated the PtSn/C electrocatalysts modified ...
Read More
Ni and Ga elements are inexpensive compared to the Pt. Ni and NiOx have been recognized to have potential applications in ethanol electrooxidation. For these reasons and based on previous results obtained with Ga addition on Pt-based electrocatalysts we have investigated the PtSn/C electrocatalysts modified with Ni and Ga. The PtSnNiGa/C electrocatalysts were characterized in acidic medium by electrochemical techniques and by physicochemical techniques such as: X-ray diffraction; Energy dispersive X-ray spectroscopy; Transmission electron microscopy. Based on the TEM analyses, the PtSnNiGa/C electrocatalysts show average particle sizes range between 3.6 – 5.5 nm, which is consistent with XRD data. The ethanol oxidation on the PtSnNiGa/C electrocatalysts occurs at lower potentials as compared to the Pt/C. The higher current normalized by Pt mass (2.62 Ag-1Pt), lower susceptibility to poisoning anodic and charge transfer resistance (245 Ω) were obtained for the Pt45Sn22Ni21Ga12/C electrocatalyst.The current normalized by Pt mass: Pt50Sn26Ni12Ga12/C (2.8 Ag -1 Pt); Pt45Sn22Ni21Ga12/C (2.62 Ag -1 Pt); Pt52Sn21Ni18Ga9/C (1.63 Ag -1 Pt) and Pt43Sn23Ni11Ga22/C (1.27 Ag -1 Pt) electrocatalysts are higher compared to binary catalysts with high Pt content. The promotion effect of PtSnNiGa/C to ethanol electrooxidation can be explained by the modification structural of Pt by incorporation of Sn, Ni and/or Ga to the face-centered cubic crystalline of Pt.

Rajesh W Raut; Bandopant T Nikam;Sahebrao B Kashid; Ansari Sana Mohd. Haroon; Yuvraj S Malghe
Abstract
The fabrication of metal nanoparticles is undergoing the revolutionary changes due to their widespread applications in the areas like selective and specific catalysis such as hydrogenation, optoelectronics, semiconductor, sensing and diagnosis. Biologically, the metal nanoparticles are produced using ...
Read More
The fabrication of metal nanoparticles is undergoing the revolutionary changes due to their widespread applications in the areas like selective and specific catalysis such as hydrogenation, optoelectronics, semiconductor, sensing and diagnosis. Biologically, the metal nanoparticles are produced using fungi, yeasts, bacteria, algae and plant biomass. The metal nanoparticles synthesized using biological methods include mainly silver and gold. The synthesis of metals like platinum and palladium is still unexplored. In this context we have synthesized Platinum and palladium metal nanoparticles using root extract of Asparagus racemosus Linn. at room temperature. The synthesized metals were characterized using UV-visible spectroscopy, Transmission Electron Microscopy (TEM) and Cyclic Voltammetry (CV) techniques. UV-Visible study revealed that in both cases nanoparticles are produced within 5 min. TEM study shows that metal nanoparticles formed are crystalline in nature and spherical in shape. It also shows that Pt and Pd nanoparticles are nearly monodispersed and having a particle size ranging between 1 to 6nm. CV of the metal nanoparticles shows reversible redox behavior. The method reported for the synthesis of metal nanoparitcles is clean, rapid and ecofriendly.
Jiagang Hou; Haoran Geng; Caixia Xu; Xiaolei Mu; Jinshui Yao
Abstract
Nanoporous platinum was fabricated by a simple dealloying method. Electron microscope characterizations show that selectively etching Al from PtAl alloy precursors in alkali or acid solution can both easily prepare three-dimensional bicontinuous network nanostructures of Pt. The resulted nanostructure ...
Read More
Nanoporous platinum was fabricated by a simple dealloying method. Electron microscope characterizations show that selectively etching Al from PtAl alloy precursors in alkali or acid solution can both easily prepare three-dimensional bicontinuous network nanostructures of Pt. The resulted nanostructure exhibited much enhanced catalytic performance towards methanol electrooxidation compared with commercial Pt/C catalyst. More importantly, CO stripping and potentiostatic tests demonstrated that nanoporous Pt has much higher long-term catalytic stability and CO resistance than the Pt/C catalyst.