ABSTRACT
The facile and selective synthesis of small crystalline Pt(3)Sn alloy nanoparticles was performed at room temperature under H(2), using a colloidal approach without the use of extra-stabilizing ligands. The Pt(3)Sn alloy was found to be obtained spontaneously as the unique phase regardless of the number of tin equivalents introduced.
ABSTRACT
Well-defined and perfectly dispersed [( identical withSiO)Au(I)] surface species supported on silica have been obtained via surface organometallic chemistry and transformed upon mild reduction (H(2), 300 degrees C) into small (1.8 +/- 0.6 nm) Au particles supported on silica passivated with SiMe(3) functionalities. Improved performance in liquid-phase aerobic epoxidation has been achieved, and the intrinsic activity of gold in oxidation is revealed.
ABSTRACT
X-ray absorption near-edge structure (XANES) suffers from core-hole lifetime broadening at a higher energy absorption edge, such as Sn K (29 keV, Gamma(K) = 8.49 eV). To overcome this problem, emitted Sn Kalpha1 fluorescence from sample was counted using high-energy-resolution fluorescence spectrometer in the XANES measurements. Experimental energy resolution (5.0 eV) was consistent with theoretical values based on the Rowland configuration of the spectrometer. The absorption edge became steeper compared to conventional spectra. The white-line peak due to Sn(II) species became remarkably sharper and more intense in the Sn Kalpha1-detecting Sn K-edge XANES for Pt-Sn/SiO2. To support the semiclassical theory of resonant Raman scattering for the explanation of observed elimination of lifetime width, more resolved XANES data at Cu K, Pb L3, and Sn K in this work were convoluted (filtered) with a Lorentzian of each core-hole lifetime width. The processed data resembled generally well corresponding XANES spectrum measured in transmission mode. The verification based on ab initio XANES calculations was also performed.
