TY - JOUR
T1 - Identification of Active Sites in Oxidation Reaction from Real-Time Probing of Adsorbate Motion over Pd Nanoparticles
AU - Ghalgaoui, Ahmed
AU - Horchani, Ridha
AU - Wang, Jijin
AU - Ouvrard, Aimeric
AU - Carrez, Serge
AU - Bourguignon, Bernard
N1 - Funding Information:
We gratefully acknowledge The French National Agency for Research (Agence Nationale de Recherche) for financial support through the PNANO program (Project CANA ANR-06-NANO-0031).
Publisher Copyright:
Copyright © 2018 American Chemical Society.
PY - 2018/9/20
Y1 - 2018/9/20
N2 - Obtaining insight into the type of surface sites involved in a reaction is essential to understand catalytic mechanisms at the atomic level and a key for understanding selectivity in surface-catalyzed reactions. Here we use ultrafast broad-band vibrational spectroscopy to follow in real-time diffusion of CO molecules over a palladium nanoparticle surface toward an active site. Site-to-site hopping is triggered by laser excitation of electrons and followed in real-time from subpicosecond changes in the vibrational spectra. CO photoexcitation occurs in 400 fs and hopping from NP facets to edges follows within ∼1 ps. Kinetic modeling allows to quantify the contribution of different facet sites to the catalytic reaction. These results provide useful insights for understanding the mechanism of chemical reactions catalyzed by metal NPs.
AB - Obtaining insight into the type of surface sites involved in a reaction is essential to understand catalytic mechanisms at the atomic level and a key for understanding selectivity in surface-catalyzed reactions. Here we use ultrafast broad-band vibrational spectroscopy to follow in real-time diffusion of CO molecules over a palladium nanoparticle surface toward an active site. Site-to-site hopping is triggered by laser excitation of electrons and followed in real-time from subpicosecond changes in the vibrational spectra. CO photoexcitation occurs in 400 fs and hopping from NP facets to edges follows within ∼1 ps. Kinetic modeling allows to quantify the contribution of different facet sites to the catalytic reaction. These results provide useful insights for understanding the mechanism of chemical reactions catalyzed by metal NPs.
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U2 - 10.1021/acs.jpclett.8b02215
DO - 10.1021/acs.jpclett.8b02215
M3 - Article
C2 - 30111106
AN - SCOPUS:85052319969
SN - 1948-7185
VL - 9
SP - 5202
EP - 5206
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 18
ER -