Resonant soft x-ray reflectivity of organic thin films

被引:49
作者
Wang, Cheng
Araki, Tohru
Watts, Benjamin
Harton, Shane
Koga, Tadanori
Basu, Saibal
Ade, Harald [1 ]
机构
[1] N Carolina State Univ, Dept Phys, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[3] SUNY Stony Brook, Dept Mat Sci & Engn, Chem & Mol Engn Program, Stony Brook, NY 11794 USA
[4] Natl Inst Stand & Technol, Ctr Neutron Res, Gaithersburg, MD 20899 USA
来源
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A | 2007年 / 25卷 / 03期
关键词
D O I
10.1116/1.2731352
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
At photon energies close to absorption edges in the soft x-ray range, the complex index of refraction, n = 1 - delta- i beta, of organic materials varies rapidly as a function of photon energy in a manner that strongly depends on the chemical moieties and functionalities present in the material. The authors present details of how these molecular structure specific variations in the complex index of refraction can be utilized to enhance and tune the contrast in reflectivity experiments of organic films. This near edge contrast enhancement mimics the specific contrast achieved through deuterium labeling in neutron reflectivity (NR). This relatively new x-ray approach, resonant soft x-ray reflectivity (RSoXR), thus combines aspects of NR and conventional x-ray reflectivity (XR), yet does not require special chemical procedures. The capabilities of RSoXR are exemplified using a number of polymeric bi- and multilayers. Furthermore, a direct comparison of RSoXR to conventional x-ray reflectivity and NR for polystyrene and poly(methyl methacrylate) bilayers verifies that RSoXR is an excellent alternative tool for the characterization of organic thin films. The influence of the longitudinal and transverse coherence properties as well as the divergence of the x-ray or neutron beam on the capabilities and limitations of each reflectivity variant is discussed. (C) 2007 American Vacuum Society
引用
收藏
页码:575 / 586
页数:12
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