4 years ago

Ultrahigh methanol electro-oxidation activity from gas phase synthesized palladium nanoparticles optimized with three-dimensional carbon nanostructured supports

Ultrahigh methanol electro-oxidation activity from gas phase synthesized palladium nanoparticles optimized with three-dimensional carbon nanostructured supports
Pd nanoparticles with a mean diameter of 6.7nm are prepared by gas phase cluster beam deposition. The Pd nanoparticle films exhibit excellent catalytic activity and stability for methanol oxidation. 3D hybrid nanostructures combined with multi-walled carbon nanotubes and few-layer graphene sheets are used as supports to further enhance the methanol electro-oxidation activity of the Pd nanoparticle catalysts by a factor of more than 2.7. The catalytic activity towards methanol electro-oxidation is characterized with cyclic voltammetry measurements. An ultrahigh electrochemical active surface area (ECSA) as large as 311m2 g−1 pd and a mass specific current corresponding to methanol oxidation levels as high as 4038mAmg−1 pd are realized. These results can be attributed to the high electrochemical activity of the Pd nanoparticles and the unique conductive structure of the multi-walled carbon nanotubes/few-layer graphene sheets.

Publisher URL: www.sciencedirect.com/science

DOI: S0013468617318108

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.