Numéro |
J. Phys. IV France
Volume 104, March 2003
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Page(s) | 607 - 613 | |
DOI | https://doi.org/10.1051/jp4:20030155 |
J. Phys. IV France 104 (2003) 607
DOI: 10.1051/jp4:20030155
High resolution X-ray tomography with applications in biology and materials science
G. Schneider1, G. Denbeaux1, E. Anderson1, A. Pearson1, W. Bates1, S. Vogt2, C. Knochen2, M.A. Meyer2 and E. Zschech31 Center for X-Ray Optics, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 2-400, Berkeley, CA 94720, U.S.A.
2 Advanced Photon Source, Argonne National Laboratory, Building 432/B0006, 9700 South Cass Avenue, Argonne, IL 60439, U.S.A.
3 Institut für Röntgenphysik, Georg-August-Universität Göttingen, Geiststrasse 11, 37073 Göttingen, Germany
Abstract
With the new tomography setup developed for the x-ray microscope XM-1 installed at the Advanced Light
Source, tomography of immunolabelled frozen-hydrated cells to detect protein distributions inside of
cells was performed. The distribution of the nuclear protein, male specific lethal 1 (MSL-1) in the
Drosophila melanogaster cell was studied. Another application field for high resolution
tomography which is of fundamental interest in materials
science is electromigration in advanced copper interconnects. In this work, quantitative time-resolved
x-ray microscopy mass transport studies of the early stages of electromigration in an inlaid Cu line/via
structure were performed with 40 nm spatial resolution at 1.8 keV photon energy. Correlation of the
real time x-ray microscopy
images with post mortem high voltage electron micrographs of the sample shows that the void
nucleation occurs at the site of grain boundaries in Cu and that the voids migrate along these grain
boundaries during electromigration. To provide 3D information about the exact location
(bulk or interface) of void nucleation and migration during an EM experiment, as well as to measure
quantitatively the mass transport in the volume, future experiments must be based on time-resolved
x-ray tomography.
© EDP Sciences 2003