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Enabling direct H2O2 production through rational electrocatalyst design.
Siahrostami, Samira; Verdaguer-Casadevall, Arnau; Karamad, Mohammadreza; Deiana, Davide; Malacrida, Paolo; Wickman, Björn; Escudero-Escribano, María; Paoli, Elisa A; Frydendal, Rasmus; Hansen, Thomas W; Chorkendorff, Ib; Stephens, Ifan E L S; Stephens, Ifan E; Rossmeisl, Jan.
Afiliação
  • Siahrostami S; 1] Center for Atomic-scale Materials Design, Department of Physics, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark [2].
Nat Mater ; 12(12): 1137-43, 2013 Dec.
Article em En | MEDLINE | ID: mdl-24240242
ABSTRACT
Future generations require more efficient and localized processes for energy conversion and chemical synthesis. The continuous on-site production of hydrogen peroxide would provide an attractive alternative to the present state-of-the-art, which is based on the complex anthraquinone process. The electrochemical reduction of oxygen to hydrogen peroxide is a particularly promising means of achieving this aim. However, it would require active, selective and stable materials to catalyse the reaction. Although progress has been made in this respect, further improvements through the development of new electrocatalysts are needed. Using density functional theory calculations, we identify Pt-Hg as a promising candidate. Electrochemical measurements on Pt-Hg nanoparticles show more than an order of magnitude improvement in mass activity, that is, A g(-1) precious metal, for H2O2 production, over the best performing catalysts in the literature.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article