Synthesis and Characterization of Pt Dendrimer-Encapsulated Nanoparticles: Effect of the Template on Nanoparticle Formation

被引:133
作者
Knecht, Marc R. [2 ]
Weir, Michael G. [2 ]
Myers, V. Sue [2 ]
Pyrz, William D. [3 ]
Ye, Heechang [2 ]
Petkov, Valeri [1 ]
Buttrey, Douglas J. [3 ]
Frenkel, Anatoly I. [4 ]
Crooks, Richard M. [2 ]
机构
[1] Cent Michigan Univ, Dept Phys, Mt Pleasant, MI 48859 USA
[2] Univ Texas Austin, Dept Chem & Biochem, Texas Mat Inst, Ctr Nano & Mol Sci & Technol, Austin, TX 78712 USA
[3] Univ Delaware, Dept Chem Engn, Ctr Catalyt Sci & Technol, Newark, DE 19716 USA
[4] Yeshiva Univ, Dept Phys, New York, NY 10016 USA
基金
美国国家科学基金会;
关键词
D O I
10.1021/cm8004198
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this article, we provide a detailed description of the synthesis and properties of Pt dendrimer-encapsulated nanoparticles (DENs) prepared using sixth-generation, hydroxyl-terminated, poly(amidoamine) (PAMAM) dendrimers (G6-OH) and three different PtCl42-/G6-OH ratios: 55, 147, and 240. Results obtained from UV-vis spectroscopy, X-ray photoelectron spectroscopy, electron microscopy, X-ray absorption spectroscopy, and high-energy X-ray diffraction show that only a fraction of the Pt2+/dendrimer precursors are reduced by BH4- and that the reduction process is highly heterogeneous. That is, after reduction each Pt2+/dendrimer precursor complex is either fully reduced, to yield a DEN having a size and structure consistent with the original PtCl42-/dendrimer ratio used for the synthesis, or the precursor is not reduced at at all. This result is consistent with an autocatalytic process that entails slow formation of a nascent catalytic Pt seed within the dendrimer, followed by rapid, catalytic reduction of nearby Pt2+ ions. Details concerning the formation of the Pt2+/dendrimer precursor are also discussed.
引用
收藏
页码:5218 / 5228
页数:11
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