Tuesday, 26 June 2007 - 4:00 PM
Clayton 128
308

Thin polymer film structure using resonant soft X-ray scattering and reflectometry

Cynthia F. Welch1, Rex P. Hjelm1, Joseph T. Mang1, Marilyn E. Hawley1, Debra A. Wrobleski1, E. Bruce Orler1, and Jeffrey B. Kortright2. (1) Los Alamos National Laboratory, Los Alamos, NM, (2) Lawrence Berkeley National Laboratory, Berkeley, CA

Thin films of carbon-containing materials are found in a pervasive number of applications, ranging from well-established industrial binders and coatings to novel biomedical and optoelectronic devices based on recent advances in nanotechnology. Phase separation through self-assembly gives these films their desirable properties; thus, determining the film structure and understanding its formation are key to unravelling the structure-property relationships. However, determining the morphology of thin, carbon-based films via traditional x-ray and neutron scattering techniques is often difficult due to weak contrast between phases and small scattering volumes. Consequently, standard scattering techniques often require either heavy atom, for x-rays, or deuterium labelling, for neutrons, to locate the various chemical constituents in the structure. Here we develop soft x-ray scattering and reflectometry techniques that allow us to analyze the morphology of thin polymer films whose phase-separated domains are distinguishable without resorting to chemical modification or isotopic labelling. With these techniques, we achieve significant, x-ray energy-dependent contrast between carbon atoms in different chemical environments using soft x-ray resonance at the carbon edge. We demonstrate the use of this contrast mechanism on the phase-separated structure of a model thin polymer film. While the realization of these methods represents a significant advance in our ability to probe the morphology of thin polymer films, we expect that they will also find extensive use in the analysis of other thin, carbon-containing films often found in biological systems and new nanocomposite devices.