Vol.:(0123456789)
Research on Chemical Intermediates
https://doi.org/10.1007/s11164-018-3686-4
1 3
Surface reconstruction of Pt–Sn nanoparticles supported
on Al
2
O
3
in the presence of carbon monoxide
Abdellah Arrahli
2
· Abdelhak Kherbeche
2
· Daniel Bianchi
1
Received: 27 September 2018 / Accepted: 20 November 2018
© Springer Nature B.V. 2018
Abstract
FTIR spectroscopy and volumetric measurements are used to study the adsorption
of CO (mainly 1% CO/He) in the temperature range 300–713 K on a 1.2% Pt–2.7%
Sn/Al
2
O
3
solid reduced in H
2
at 713 K leading from XRD to PtSn bimetallic par-
ticles. This reveals the changes in the adsorption properties of the Pt sites for CO
adsorption by comparison with monometallic Pt/Al
2
O
3
solids and the stability of
the Pt–Sn bimetallic particles in the presence of CO. At 300 K, FTIR spectroscopy
shows that the insertion of Sn leads to (a) the total disappearance of the Pt sites
forming bridged CO species (ascribed to a geometric efect of Sn) and (b) a signif-
cant shift in the position of the IR band of linear CO species on Pt sites from 2066
to 2044 cm
−1
on Pt and Pt–Sn particles, respectively, ascribed to diferent adsorbed
species, namely L
Pt
and L1
Pt–Sn,
respectively. Moreover, it is shown that the insertion
of Sn is associated with the decrease in the amount (in µmol/g of platinum) of Pt
adsorption sites for CO adsorption. The evolution of the IR band of the L1
Pt–Sn
CO
species with the increase in T
a
in isobaric conditions reveals a modifcation of the
surface of the Pt–Sn particles for T
a
> ≈ 460 K ascribed to enrichment in Pt° due to
a surface reconstruction. The Pt sites of the reconstructed surface are characterized
by an IR band at 2057 cm
−1
after adsorption of CO at 300 K ascribed to a linear CO
species named L2
Pt–Sn
. The reconstructed surface is stable in the presence of CO in
the range 300–713 K and disappears by hydrogen reduction at 713 K. Successive
surface reconstruction/hydrogen reduction at 713 K cycles lead to an ageing of the
Pt–Sn particles associated with a progressive decrease in the amount of Pt° sites on
the freshly prepared and reconstructed Pt–Sn particles. It is shown that the recon-
struction of the Pt–Sn particles is probably due to the formation of SnO
x
species via
oxygen species coming mainly from the hydroxyls groups of the support.
* Abdelhak Kherbeche
abdelhak.kherbeche@usmba.ac.ma
1
Institut de Recherches sur la Catalyse et l’Environnement de Lyon (IRCELYON), UMR 5256,
CNRS, Université Claude Bernard Lyon I, Bat. Chevreul, 43 Boulevard du 11 Novembre 1918,
69622 Villeurbanne, France
2
Laboratoire de Catalyse, Matériaux et Environnement (LCME), Université Sidi Mohammed Ben
Abdellah, Fès, Route d’Imouzzer, BP 2427, Fes, Morocco