Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-24T08:54:05.573Z Has data issue: false hasContentIssue false
  • English
  • Français

On Extended X-Rays Absorption Fine Structure Characterisation of Iron Platinum Clusters

Published online by Cambridge University Press:  10 February 2011

G. D'Agostino ,
A. Filipponi ,
A. Verrazzani  and
G. Vitulli
G. D'Agostino
Affiliation:
Divisione Nuovi Materiali, ENEA, Centro Ricerche Casaccia - Roma (Italy)
A. Filipponi
Affiliation:
Beam Line 18, ESRF, Grenoble (France)
A. Verrazzani
Affiliation:
Dip. di Chimica e Chimica industriale, Università degli studi di Pisa and Centro di Studi del CNR per le Macromolecole stereordinate ed otticamente attive, V. Risorgimento 35 PISA (Italy)
G. Vitulli
Affiliation:
Dip. di Chimica e Chimica industriale, Università degli studi di Pisa and Centro di Studi del CNR per le Macromolecole stereordinate ed otticamente attive, V. Risorgimento 35 PISA (Italy)
Get access

Abstract

Present paper reports on Extended X-rays Absorption Fine Structure (EXAFS) Spectroscopy characterisation of Fe/Pt clusters. Samples of different nominal iron contents (FePt4 and FePt2) have been prepared and characterised by direct measurements of absorption coefficient at Pt L3 and Fe K edges. Catalysts were prepared by precipitation from suitable mixing (in the appropriate stoichiometry) of mesitylene suspentions containing small clusters of either platinum or iron. Single species suspention, in turn, were prepared by vapor metal deposition.

Catalitic activity of prepared samples was tested on cinnammic aldehyde. As a general result, platinum clusters exhibit activity in the hydrogenation of both carbon double bond and aldehyde group with a preference for the latter. Iron addition to the pure platinum catalyst reverts the selectivity while leaving the catalitic activity almost unchanged.

The present paper represents a temptative to achieve structural information on Fe and Pt short range environments, thus providing insights on the dynamics of the catalytic process.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 497: Symposium Z – Recent Advances in Catalytic Materials , 1997 , 115
Copyright
Copyright © Materials Research Society 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Hayashi, C., Physics Today 40, 44 (1987).Google Scholar
[2] Schmid, G., Chem. Rev., 92 1709 (1992).Google Scholar
[3] Andrews, M.P. and Ozin, G.A., Chem. Mater. 1, 174 (1989).Google Scholar
[4] Klabunde, K.J., Lia, Y.Y.X. and Tan, B.J., Chem. Mater. 3, 30 (1991).Google Scholar
[5] Vitulli, G., Pitzalis, E., Lazzaroni, R., Pertici, P., Salvadori, P., Salvetti, O., Coluccia, S. and Marra, G., Mat. Science Forum 15, 93 (1995).Google Scholar
[6] Delia Longa, S., Amiconi, G., Ascone, I., Bertollini, A., Bianconi, A. and Congiu Castellano, A., J. Phys. IV France 7 C2–629 (1997).Google Scholar
[7] D'Agostino, G., Pinto, A. and Mobilio, S. Phys. Rev B 48, 14447 (1993).Google Scholar
[8] Filipponi, A. and Di Cicco, A., Phys. Rev. B 52, 15135 (1995).Google Scholar