CO <inf>2</inf> activation and methanol synthesis on novel Au/TiC and Cu/TiC catalysts
Abstract:
Small Cu and Au particles in contact with a TiC(001) surface undergo a charge polarization that makes them very active for CO 2 activation and the catalytic synthesis of methanol. The binding energy of CO 2 on these systems is in the range of 0.6 to 1.1 eV, much larger than those observed on surfaces or nanoparticles of Cu and Au. Thus, in spite of the poor CO 2 hydrogenation performance of Cu(111) and Au(111), the Cu/TiC(001) and Au/TiC(001) systems display a catalytic activity for methanol synthesis substantially higher than that of conventional Cu/ZnO catalysts. The turnover frequencies for methanol production on Cu/TiC(001) are 170-500 times much larger than on Cu(111). The present study moves away from the typical approach of using metal/oxide catalysts for the synthesis of methanol via CO 2 hydrogenation. This work shows that metal carbides can be excellent supports for enhancing the ability of noble metals to bond and activate CO 2. © 2012 American Chemical Society.
Año de publicación:
2012
Keywords:
Fuente:
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Tipo de documento:
Article
Estado:
Acceso restringido
Áreas de conocimiento:
- Catálisis
- Catálisis
Áreas temáticas:
- Tecnología de productos químicos industriales