Cookies Policy
X

This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies.

I accept this policy

Find out more here

Platinum submonolayer–monolayer electrocatalysts: an electrochemical and X-ray absorption spectroscopy study

No metrics data to plot.
The attempt to load metrics for this article has failed.
The attempt to plot a graph for these metrics has failed.
The full text of this article is not currently available.

Brill’s MyBook program is exclusively available on BrillOnline Books and Journals. Students and scholars affiliated with an institution that has purchased a Brill E-Book on the BrillOnline platform automatically have access to the MyBook option for the title(s) acquired by the Library. Brill MyBook is a print-on-demand paperback copy which is sold at a favorably uniform low price.

Access this article

+ Tax (if applicable)
Add to Favorites
You must be logged in to use this functionality

A new Pt monolayer electrocatalyst concept is described and the results of electrochemical and X-ray absorption spectroscopy (XAS) studies are presented. Two new methods that facilitate the application of this concept in obtaining ultra-low-Pt-content electrocatalysts have been developed. One is the electroless (spontaneous) deposition of a Pt submonolayer on Ru nanoparticles, and the other is a deposition of a Pt monolayer on Pd nanoparticles by redox displacement of a Cu adlayer. The Pt submonolayer on Ru (PtRu20) electrocatalyst demonstrated higher CO tolerance than commercial catalysts under conditions of rotating disk experiments. The long-term stability test showed no loss in performance over 870 h using a fuel cell operating under real conditions, even though the Pt loading was approximately 10% of that of the standard Pt loading. In situ XAS indicated an increase in d-band vacancy of deposited Pt, which may facilitate partly the reduced susceptibility to CO poisoning for this catalyst. The kinetics of O2 reduction on a Pt monolayer on Pd nanoparticles showed a small enhancement in comparison with that from a Pt nanoparticle electrocatalyst. The increase in catalytic activity is partly attributed to decreased formation of PtOH, as shown by XAS experiments.

10.1163/156856706777973646
/content/journals/10.1163/156856706777973646
dcterms_title,pub_keyword,dcterms_description,pub_author
6
3
Loading
Loading

Full text loading...

/content/journals/10.1163/156856706777973646
Loading

Data & Media loading...

http://brill.metastore.ingenta.com/content/journals/10.1163/156856706777973646
Loading

Article metrics loading...

/content/journals/10.1163/156856706777973646
2006-05-01
2016-12-08

Sign-in

Can't access your account?
  • Tools

  • Add to Favorites
  • Printable version
  • Email this page
  • Subscribe to ToC alert
  • Get permissions
  • Recommend to your library

    You must fill out fields marked with: *

    Librarian details
    Your details
    Why are you recommending this title?
    Select reason:
     
    Research on Chemical Intermediates — Recommend this title to your library
  • Export citations
  • Key

  • Full access
  • Open Access
  • Partial/No accessInformation