Ultra-Shallow Chemical Characterization of Organic Thin Films Deposited by Plasma and Vacuum-Ultraviolet, Using Angle- and Excitation Energy-Resolved XPS

被引:14
|
作者
Girard-Lauriault, Pierre-Luc [2 ]
Ruiz, Juan-Carlos [1 ]
Gross, Thomas [2 ]
Wertheimer, Michael R. [1 ]
Unger, Wolfgang E. S. [2 ]
机构
[1] Ecole Polytech, Dept Engn Phys, Montreal, PQ H3C 3A7, Canada
[2] BAM Bundesanstalt Mat Forsch & Prufung, D-12200 Berlin, Germany
关键词
Plasma polymers; Vacuum ultraviolet photopolymers; Synchrotron XPS; Depth profile; MEAN FREE PATHS; POLYMER-FILMS; PHOTOELECTRON-SPECTROSCOPY; ATMOSPHERIC-PRESSURE; SURFACE; POLYSTYRENE; RADIATION; PROFILE; PHOTOPOLYMERIZATION; MODEL;
D O I
10.1007/s11090-011-9306-3
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Nitrogen (N)-rich organic thin films were deposited using both low-pressure plasma- and vacuum-ultraviolet-based techniques, from mixtures of ammonia (NH3) and ethylene (C2H4). These films were investigated using angle-resolved and excitation energy resolved X-ray photoelectron spectroscopy (ARXPS and ERXPS, respectively) in order to determine their sub-surface chemical profiles. These two techniques enable one to tune the "XPS 95%" information depth, z (95%), by varying either the angle or the excitation energy. Using a combination of both techniques, z (95%) can be varied continuously from 0.7 to 11 nm. The surface-near chemistry is investigated using both high-resolution C 1s spectra and elemental concentrations derived from elemental peak intensities. Results show that while laboratory XPS, and even ARXPS, suggest homogenous surface chemistries, the novel combination of ARXPS and ERXPS points to the existence of a compositional profile in the extreme outer surface layer. Our conclusions are supported by simulations using SESSA software.
引用
收藏
页码:535 / 550
页数:16
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    Pierre-Luc Girard-Lauriault
    Juan-Carlos Ruiz
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    Michael R. Wertheimer
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