http://www.cnr.it/ontology/cnr/individuo/prodotto/ID53889
Structure and the metal-support interaction of the Au/Mn oxide catalysts (Articolo in rivista)
- Type
- Label
- Structure and the metal-support interaction of the Au/Mn oxide catalysts (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/cm100697b (literal)
- Alternative label
A. Longo, L.F. Liotta, G. Di Carlo, F. Giannici, A.M. Venezia, A. Martorana (2010)
Structure and the metal-support interaction of the Au/Mn oxide catalysts
in Chemistry of materials
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- A. Longo, L.F. Liotta, G. Di Carlo, F. Giannici, A.M. Venezia, A. Martorana (literal)
- Pagina inizio
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- Rivista
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Consiglio Nazionale delle Ricerche, Istituto per lo Studio dei Materiali Nanostrutturati, Sezione di Palermo,
Via Ugo La Malfa, 153, I-90146 Palermo, Italy, and ?Dipartimento di Chimica Inorganica e Analitica \"Stanislao Cannizzaro\", Università di Palermo,Viale delle Scienze, I-90128 Palermo, Italy (literal)
- Titolo
- Structure and the metal-support interaction of the Au/Mn oxide catalysts (literal)
- Abstract
- Gold catalysts with loading 1 and 10 wt % were prepared by deposition-precipitation method
with urea over mesoporous manganese oxide, obtained through a surfactant-assisted procedure by
using cetyltrimethylammonium bromide (CTAB), followed by treatment with sulphuric acid. For
comparison, Au(10 wt %) was also deposited over commercial CeO2 and SiO2 supports. The
materials were characterized by XRD and EXAFS at the Mn K and Au LIII edges and XPS.
Moreover, the analyses were performed on the samples treated under 1%CO/He, at 250 ?C for
90min. The structural and surface results of the as preparedmanganese oxide confirmed the formation
of ?-MnO2 along with some amorphous Mn3O4 upon treatment of the precursor oxide with sulphuric
acid. The CO treatment induces the formation of reduced phases, Mn3O4 (Hausmannite) and Mn2O3
(Bixbyite). Gold particles have a positive effect in promoting the reduction ofmanganese oxide and this
effect is more pronounced in the Au(10 wt %) catalyst, which exhibits an enhanced CO oxidation
activity with respect to both the Au(1 wt %) sample and the metal-free manganese oxide. The higher
efficiency of Au(10 wt %) catalyst is attributed to a strong metal-support interaction between gold
nanoparticles and support, as demonstrated by the presence of a component Au-O at 2.1 A ° in the
Fourier transform of the EXAFS signal of both the fresh and the CO-treated samples. (literal)
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