TY - JOUR
T1 - Decomposition and activation of Pt-dendrimer nanocomposites on a silica support
AU - Deutsch, D. Samuel
AU - Lafaye, Gwendoline
AU - Liu, Dongxia
AU - Chandler, Bert
AU - Williams, Christopher T.
AU - Amiridis, Michael D.
N1 - Funding Information:
The authors wish to acknowledge the National Science Foundation (NSF Award CTS-0103135) for financial support of this work. DSD further expresses his gratitude to the Alfred P. Sloan Foundation and the University of South Carolina African American Professors Program. Finally, GL expresses her gratitude to the French Government for the support provided through the Lavoisier Postdoctoral grant.
PY - 2004/9
Y1 - 2004/9
N2 - Zero valent platinum nanoparticles were stabilized in solution by the use of poly(amido)amine dendrimers and were subsequently deposited onto a porous silica support. The resulting materials were subjected to various thermal treatments in oxidizing, reducing, and inert environments, in order to remove the surrounding polymer and expose the Pt metal sites to gas phase reagents. The materials were characterized at several different stages during this process via Fourier-Transform Infrared (FTIR) spectroscopy and Transmission Electron Microscopy (TEM). The results suggest that the dendrimer decomposition occurs at its mono-substituted amide groups and begins at relatively low temperatures (∼50 °C). The presence of oxygen in the gas phase and the Pt particles in the Pt-dendrimer nanocomposite accelerate this process. Oxidation at 425 °C was the most successful temperature for removing the dendrimer fragments from the Pt surface, rendering the Pt sites most accessible for carbon monoxide adsorption. Limited sintering of the Pt particles is observed under these conditions, as well as during subsequent reduction steps, necessary to yield the metallic form of Pt.
AB - Zero valent platinum nanoparticles were stabilized in solution by the use of poly(amido)amine dendrimers and were subsequently deposited onto a porous silica support. The resulting materials were subjected to various thermal treatments in oxidizing, reducing, and inert environments, in order to remove the surrounding polymer and expose the Pt metal sites to gas phase reagents. The materials were characterized at several different stages during this process via Fourier-Transform Infrared (FTIR) spectroscopy and Transmission Electron Microscopy (TEM). The results suggest that the dendrimer decomposition occurs at its mono-substituted amide groups and begins at relatively low temperatures (∼50 °C). The presence of oxygen in the gas phase and the Pt particles in the Pt-dendrimer nanocomposite accelerate this process. Oxidation at 425 °C was the most successful temperature for removing the dendrimer fragments from the Pt surface, rendering the Pt sites most accessible for carbon monoxide adsorption. Limited sintering of the Pt particles is observed under these conditions, as well as during subsequent reduction steps, necessary to yield the metallic form of Pt.
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U2 - 10.1023/B:CATL.0000038575.79498.c3
DO - 10.1023/B:CATL.0000038575.79498.c3
M3 - Article
AN - SCOPUS:4344578074
SN - 1011-372X
VL - 97
SP - 139
EP - 143
JO - Catalysis Letters
JF - Catalysis Letters
IS - 3-4
ER -