AVS 61st International Symposium & Exhibition | |
Biomaterial Interfaces | Tuesday Sessions |
Session BI+AS-TuA |
Session: | Characterization of Biointerfaces |
Presenter: | Daniel Graham, University of Washington |
Authors: | D.J. Graham, University of Washington L.J. Gamble, University of Washington |
Correspondent: | Click to Email |
The development of argon cluster sources has opened up new opportunities for ToF-SIMS depth profiling. These sources have enabled depth profiling of a wide range of materials that previously could not be accurately depth profiled. In addition, due to the low damage accumulation and sputtering efficiency of these sources, it is now possible to depth profile through microns of material. This in turn has opened up new opportunities for exploring the 3D chemical environments of a wide range of samples including drug eluting polymers, thick multilayer polymer films and porous tissue scaffolds. However, the ability to dig deeper into samples also results in significant challenges in 3D image reconstruction. For example, due to the fixed geometry of the analysis beam (at 45 deg from the surface normal in our instrument), sputtering away 1 micron of the surface will shift the analysis position by 1 micron. This means that if one were to depth profile 50 microns into a surface, the final image would be shifted by 50 microns. Traditional image registrations methods can be used to accommodate for these shifts, however when digging to depths larger than 10 microns, this requires significantly increasing the initial image size in order to end up with a usable image stack after the image shifting and cropping.
In this presentation we will summarize methods we have been developing to reconstruct deep depth profiles including adjusting the sample height during data acquisition and post acquisition image shifting. We will also show results from a new 3D image overlay tool that enables localization of different chemical environments in 3D and that can show areas of overlap between selected peak area images. These methods and tools will be demonstrated on data from control samples made from polymer beads on silicon and from data taken from polymer tissue scaffolds.