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基于流动的多吸附质椭偏孔隙率测定法用于表征介孔Pt-TiO2和Au-TiO2纳米复合材料

Flow-based multiadsorbate ellipsometric porosimetry for the characterization of mesoporous Pt-TiO2 and Au-TiO2 nanocomposites.

作者信息

May R Alan, Patel Mehul N, Johnston Keith P, Stevenson Keith J

机构信息

Department of Chemistry and Biochemistry, Center for Nano and Molecular Science and Technology, Texas Materials Institute, The University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Langmuir. 2009 Apr 21;25(8):4498-509. doi: 10.1021/la8038158.

Abstract

Au and Pt nanoparticle distributions within hierarchically ordered mesoporous TiO2 were explored using a combination of techniques including ellipsometric porosimetry (EP) and X-ray photoelectron spectroscopy (XPS). EP studies were used to examine adsorbate-TiO2 interactions and the influence of adsorbate polarity upon adsorption isotherms for mesoporous TiO2 films with and without Pt and Au nanoparticles. In particular, methods are described for modeling EP data to estimate the surface area and porosity of mesoporous TiO2 films and for estimating the pore size distribution (PSD) directly from the ellipsometry parameters Psi and Delta when fitting parameters alone are unable to extract reliable optical constants from the ellipsometry data. This approach reveals that mesoporous TiO2 films of approximately 200 nm thickness and approximately 10 nm pore diameter can be loaded with 1.7 nm diameter Pt and 3.9 nm diameter Au nanoparticles up to 26 and 21 wt %, respectively. The BET surface area of a representative mesoporous TiO2 sample using toluene as the adsorbate was found to be 44 m2/g with a mean pore diameter of 8.8 nm. EP and XPS depth profiling experiments indicate that 1.7 nm diameter Pt nanoparticles are well dispersed through the mesoporous TiO2 film, while 3.9 nm diameter Au nanoparticles are concentrated at the top of the film, blocking a significant portion of the available TiO2 pore volume. UV irradiation of the TiO2 films indicates that adsorbate-TiO2 interactions and surface wetting effects can play a critical role in the resulting isotherm and in evaluation of PSD.

摘要

采用包括椭偏测孔法(EP)和X射线光电子能谱(XPS)在内的多种技术组合,研究了分级有序介孔TiO₂ 中Au和Pt纳米颗粒的分布情况。EP研究用于考察吸附质与TiO₂ 的相互作用,以及吸附质极性对含和不含Pt及Au纳米颗粒的介孔TiO₂ 薄膜吸附等温线的影响。特别地,本文描述了一些方法,用于对EP数据进行建模,以估计介孔TiO₂ 薄膜的表面积和孔隙率,以及在拟合参数无法从椭偏测量数据中提取可靠光学常数时,直接根据椭偏参数Psi和Delta估计孔径分布(PSD)。该方法表明,厚度约为200 nm、孔径约为10 nm的介孔TiO₂ 薄膜,可分别负载直径为1.7 nm的Pt纳米颗粒和直径为3.9 nm的Au纳米颗粒,负载量分别高达26 wt%和21 wt%。以甲苯作为吸附质时,一个代表性介孔TiO₂ 样品的BET表面积为44 m²/g,平均孔径为8.8 nm。EP和XPS深度剖析实验表明,直径为1.7 nm的Pt纳米颗粒在介孔TiO₂ 薄膜中分散良好,而直径为3.9 nm的Au纳米颗粒则集中在薄膜顶部,占据了相当一部分TiO₂ 的可用孔体积。TiO₂ 薄膜的紫外线照射表明,吸附质与TiO₂ 的相互作用以及表面润湿效应在所得等温线和PSD评估中可能起关键作用。

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