Low-temperature activation conditions for PAMAM dendrimer templated Pt nanoparticles

被引:53
作者
Singh, A [1 ]
Chandler, BD [1 ]
机构
[1] Trinity Univ, Dept Chem, San Antonio, TX 78212 USA
关键词
D O I
10.1021/la051605h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surface immobilized polyamidoamine (PAMAM) dendrimer templated Pt nanoparticles were employed as precursors to heterogeneous catalysts. CO oxidation catalysis and in situ infrared spectroscopy were used to evaluate conditions for dendrimer removal. Infrared spectroscopy showed that PAMAM dendrimer amide bonds begin decomposing at temperatures as low as 75 degrees C. Although the amide stretches are completely removed after 3 h of oxidation at 300 degrees C, 16 h were required to reach maximum catalytic activity. Further treatment under oxidizing or reducing atmospheres did not cause substantial changes in activity. Infrared spectroscopy of the activated materials indicated that organic residues, probably surface carboxylates, are formed during oxidation. These surface species passivate the Pt NPs, and their removal was required to fully activate the catalyst. Substantially less forcing activation conditions were possible by employing a CO/O(2)/He oxidation treatment. At appropriate temperatures, CO acts as a protecting group for the Pt surface, helping to prevent fouling of the nanoparticle by organic residues. CO oxidation catalysis and infrared spectroscopy of adsorbed CO indicated that the low temperature activation treatment yielded supported nanoparticles that were substantially similar to those prepared with more forcing conditions.
引用
收藏
页码:10776 / 10782
页数:7
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共 31 条
[11]  
Forzatti P, 1999, CATAL TODAY, V52, P165, DOI 10.1016/S0920-5861(99)00178-9
[12]   Automobile exhaust catalysts [J].
Heck, RM ;
Farrauto, RJ .
APPLIED CATALYSIS A-GENERAL, 2001, 221 (1-2) :443-457
[13]   THE INFLUENCE OF SURFACE-DEFECTS ON THE INFRARED-SPECTRA OF ADSORBED SPECIES [J].
HOLLINS, P .
SURFACE SCIENCE REPORTS, 1992, 16 (02) :51-94
[14]   PATHWAYS FOR CARBOXYLIC-ACID DECOMPOSITION ON TIO2 [J].
KIM, KS ;
BARTEAU, MA .
LANGMUIR, 1988, 4 (04) :945-953
[15]   Synthesis and microscopic characterization of dendrimer-derived Ru/Al2O3 catalysts [J].
Lafaye, G ;
Williams, CT ;
Amiridis, MD .
CATALYSIS LETTERS, 2004, 96 (1-2) :43-47
[16]  
Lang HF, 2005, CHEM IND-SER, V104, P243
[17]   Dendrimer-encapsulated nanoparticle precursors to supported platinum catalysts [J].
Lang, HF ;
May, RA ;
Iversen, BL ;
Chandler, BD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (48) :14832-14836
[18]   Synthesis and characterization of dendrimer templated supported bimetallic Pt-Au nanoparticles [J].
Lang, HG ;
Maldonado, S ;
Stevenson, KJ ;
Chandler, BD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (40) :12949-12956
[19]   Dendrimer-mediated formation of Cu-CuOx nanoparticles on silica and their physical and catalytic characterization [J].
Larsen, G ;
Noriega, S .
APPLIED CATALYSIS A-GENERAL, 2004, 278 (01) :73-81
[20]   Strong blue photoluminescence and ECL from OH-terminated PAMAM dendrimers in the absence of gold nanoparticles [J].
Lee, WI ;
Bae, YJ ;
Bard, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (27) :8358-8359