Please use this identifier to cite or link to this item: http://hdl.handle.net/1783.1/30537

Preparation of Stable Exfoliated Pt-Clay Nanocatalyst

Authors Zhang, Wenjing
Li, Martin Ka Shing HKUST affiliated (currently or previously)
Wang, Rujie HKUST affiliated (currently or previously)
Yue, Po-Lock View this author's profile
Gao, Ping View this author's profile
Issue Date 2009
Source Langmuir , v. 25, (14), 21 July 2009, Pages 8226-8234
Summary In this paper, we report a novel experimental protocol for the preparation of stable and exfoliated nano-Pt catalysts supported oil layered silicate clay surfaces. Uniformly dispersed highly crystalline Pt nanoparticles with diameters between 2 and 5 nm were chemically adsorbed oil to the layered silicate surfaces using a chemical vapor deposition (CVD) method employing organoclay as the initial support, The as-prepared catalysts were found to be extremely stable against both intensive mechanical agitation and high temperature treatment. No Pt loading or morphology changes were observed after ultrasonication under a sonication power density of 6 MW/m(3) for up to 72 h at room temperature or annealing at 700 degrees C for I h under Ar flow. On the other hand, Pt catalysts prepared using the inorganic clay as the initial support were found to be highly unstable against both mechanical agitation and high temperature treatment. Significant leaching and catalyst restructuring or sintering was observed. Exfoliation of catalysts and the nature of Pt adsorption were elucidated by systematic analysis using wide-angle X-ray diffraction (WAXD) analysis, Brunauer-Emmett-Teller (BET) surface area analysis, and time-of-flight secondary ion mass spectroscopy (ToF-SIMS) analysis. No low angle diffraction peak was observed in the WAXD pattern, and a 700\% increase in BET surface area was observed after Pt deposition on clay surfaces. Depth profiling ToF-SIMS on Pt deposited on SiO2 wafer surfaces showed the presence of PtSiO ion at the Pt and SiO2 interface. This ion group was also detected in the bulk of Pt-OrC catalyst, confirming chemisorption of Pt on layered silicate clays. A much lower concentration of PtSiO ion was observed in the Pt-NaC with a similar Pt loading. In addition, X-ray photoelectron spectroscopy (XPS) shows that the binding energy of Pt4f(7/2) in Pt-OrC is much higher than that in the Pt-NaC. The protocol reported in this paper can also be applicable to other clay supported stable metallic catalysts.
ISSN 0743-7463
Language English
Format Article
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