López-Cartes C, Rojas T C, Litrán R, Martínez-Martínez D, de la Fuente J M, Penadés S, Fernández A
Instituto de Ciencia de Materiales de Sevilla, and Grupo Carbohidratos, Laboratory of Glyconanotechnology IIQ, CSIC-Universidad Sevilla, Américo Vespucio nr. 49, 41092-Sevilla, Spain.
J Phys Chem B. 2005 May 12;109(18):8761-6. doi: 10.1021/jp050184+.
Gold nanoparticles (NPs) have been prepared with three different capping systems: a tetralkylammonium salt, an alkanethiol, and a thiol-derivatized neoglycoconjugate. Also gold NPs supported on a porous TiO(2) substrate have been investigated. X-ray absorption spectroscopy (XAS) has been used to determine the electronic behavior of the different capped/supported systems regarding the electron/hole density of d states. Surface and size effects, as well as the role of the microstructure, have been also studied through an exhaustive analysis of the EXAFS (extended X-ray absorption fine structure) data. Very small gold NPs functionalized with thiol-derivatized molecules show an increase in d-hole density at the gold site due to Au-S charge transfer. This effect is overcoming size effects (which lead to a slightly increase of the d-electron density) for high S:Au atomic ratios and core-shell microstructures where an atomically abrupt Au-S interface likely does not exist. It has been also shown that thiol functionalization of very small gold NPs is introducing a strong distortion as compared to fcc order. To the contrary, electron transfer from reduced support oxides to gold NPs can produce a higher increase in d-electron density at the gold site, as compared to naked gold clusters.
已使用三种不同的封端体系制备了金纳米颗粒(NPs):四烷基铵盐、链烷硫醇和硫醇衍生的新糖缀合物。还研究了负载在多孔TiO(2)基底上的金纳米颗粒。X射线吸收光谱(XAS)已用于确定不同封端/负载体系关于d态电子/空穴密度的电子行为。通过对扩展X射线吸收精细结构(EXAFS)数据的详尽分析,还研究了表面和尺寸效应以及微观结构的作用。用硫醇衍生分子功能化的非常小的金纳米颗粒由于金-硫电荷转移而在金位点处显示出d空穴密度增加。对于高硫:金原子比和可能不存在原子级突变金-硫界面的核壳微观结构,这种效应克服了尺寸效应(尺寸效应导致d电子密度略有增加)。还表明,与面心立方有序相比,非常小的金纳米颗粒的硫醇功能化引入了强烈的畸变。相反,与裸金簇相比,从还原的载体氧化物到金纳米颗粒的电子转移可在金位点处产生更高的d电子密度增加。