A New Type of Strong Metal–Support Interaction and the Production of H through the Transformation of Water on Pt/CeO(111) and Pt/CeO/TiO(110) Catalysts.

The electronic properties of Pt nanoparticles deposited on CeO(111) and CeO/TiO(110) model catalysts have been examined using valence photoemission experiments and density functional theory (DFT) calculations. The valence photoemission and DFT results point to a new type of "strong metal-support int...

Descripción completa

Detalles Bibliográficos
Publicado en:Journal of the American Chemical Society Vol. 134; no. 21; pp. 8968 - 8975
Autores principales: Bruix, Albert, Rodriguez, José A., Ramírez, Pedro J., Senanayake, Sanjaya D., Evans, Jaime, Park, Joon B., Stacchiola, Dario, Liu, Ping, Hrbek, Jan, Illas, Francesc
Formato: Artículo
Publicado: American Chemical Society 5/30/2012
Materias:
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=hlh&AN=76905814&site=ehost-live
header:
  @attributes:
    shortDbName: hlh
    uiTerm: 76905814
    longDbName: Humanities International Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    jinfo:
      jid:
        00027863
        ACS
      jtl: Journal of the American Chemical Society
      issn: 00027863
      maglogo: N
    pubinfo:
      dt: 5/30/2012
      vid: 134
      iid: 21
      pid: 997
      pub: American Chemical Society
    artinfo:
      ui:
        76905814
        10.1021/ja302070k
      ppf: 8968
      ppct: 7
      formats:
      tig:
        atl: A New Type of Strong Metal–Support Interaction and the Production of H through the Transformation of Water on Pt/CeO(111) and Pt/CeO/TiO(110) Catalysts.
      aug:
        au:
          Bruix, Albert
          Rodriguez, José A.
          Ramírez, Pedro J.
          Senanayake, Sanjaya D.
          Evans, Jaime
          Park, Joon B.
          Stacchiola, Dario
          Liu, Ping
          Hrbek, Jan
          Illas, Francesc
        affil:
          Departament de Química Física and Institut de Química Teòrica i Computacional (IQTCUB), Universitat de Barcelona, Marti i Franques 1, 08028 Barcelona, Spain
          Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973, United States
          Facultad de Ciencias, Universidad Central de Venezuela, Caracas 1020-A, Venezuela
      su:
        Electric properties of nanoparticles
        Platinum nanoparticles
        Cerium oxides
        Valence (Chemistry)
        Photoelectron spectroscopy
        Density functionals
        Hydrogen production
        Dissociation (Chemistry)
      sug:
        subj:
          Electric properties of nanoparticles
          Platinum nanoparticles
          Cerium oxides
          Valence (Chemistry)
          Photoelectron spectroscopy
          Density functionals
          Hydrogen production
          Dissociation (Chemistry)
      ab: The electronic properties of Pt nanoparticles deposited on CeO(111) and CeO/TiO(110) model catalysts have been examined using valence photoemission experiments and density functional theory (DFT) calculations. The valence photoemission and DFT results point to a new type of "strong metal-support interaction" that produces large electronic perturbations for small Pt particles in contact with ceria and significantly enhances the ability of the admetal to dissociate the O-H bonds in water. When going from Pt(111) to Pt/CeO(111), the dissociation of water becomes a very exothermic process. The ceria-supported Pt appears as a fluxional system that can change geometry and charge distribution to accommodate adsorbates better. In comparison with other water-gas shift (WGS) catalysts [Cu(111), Pt(111), Cu/CeO(111), and Au/CeO(111)], the Pt/CeO(111) surface has the unique property that the admetal is able to dissociate water in an efficient way. Furthermore, for the codeposition of Pt and CeOx nanoparticles on TiO(110), we have found a transfer of O from the ceria to Pt that opens new paths for the WGS process and makes the mixed-metal oxide an extremely active catalyst for the production of hydrogen.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
    refInfo:
    copyright:
      @attributes:
        flag: Y
      dt:
        @attributes:
          year: 2012
    holdings:
      @attributes:
        islocal: N