Synchrotron-radiation XPS analysis of ultra-thin silane films: Specifying the organic silicon

被引:79
作者
Dietrich, Paul M. [1 ]
Glamsch, Stephan [1 ,2 ]
Ehlert, Christopher [1 ,3 ]
Lippitz, Andreas [1 ]
Kulak, Nora [2 ]
Unger, Wolfgang E. S. [1 ]
机构
[1] Bundesanstalt Mat Forsch & Prufung BAM, Unter Eichen 87, D-12205 Berlin, Germany
[2] Free Univ Berlin, Inst Chem & Biochem, Fabeckstr 34-36, D-14195 Berlin, Germany
[3] Univ Potsdam, Inst Chem, Karl Liebknecht Str 24-25, D-14476 Potsdam, Germany
关键词
Synchrotron radiation XPS; Depth profiling; Silanes; Monolayer; Amines; Amides; SURFACE; SI; QUANTIFICATION; IMMOBILIZATION; MONOLAYERS; LAYERS; SPECTROSCOPY; MICROARRAYS; ADSORPTION; BIOSENSORS;
D O I
10.1016/j.apsusc.2015.12.052
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
The analysis of chemical and elemental in-depth variations in ultra-thin organic layers with thicknesses below 5 nm is very challenging. Energy- and angle-resolved XPS (ER/AR-XPS) opens up the possibility for non-destructive chemical ultra-shallow depth profiling of the outermost surface layer of ultra-thin organic films due to its exceptional surface sensitivity. For common organic materials a reliable chemical in-depth analysis with a lower limit of the XPS information depth z(95) of about 1 nm can be performed. As a proof-of-principle example with relevance for industrial applications the ER/AR-XPS analysis of different organic monolayers made of amino- or benzamidosilane molecules on silicon oxide surfaces is presented. It is demonstrated how to use the Si 2p core-level region to non-destructively depth-profile the organic (silane monolayer) - inorganic (SiO2/Si) interface and how to quantify Si species, ranging from elemental silicon over native silicon oxide to the silane itself. The main advantage of the applied ER/AR-XPS method is the improved specification of organic from inorganic silicon components in Si 2p core-level spectra with exceptional low uncertainties compared to conventional laboratory XPS. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:406 / 411
页数:6
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