EBSD analysis of narrow damascene copper lines

4Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Orientation imaging microscopy by electron backscatter diffraction (EBSD) has been used to examine grain size and crystallographic orientations of damascene Cu lines nominally 25 nm to 55 nm in width and 100 nm thick. These are the smallest structures reported to have been examined by EBSD to date. This application poses significant challenges in specimen preparation, data collection, and data analysis. Most lines were deposited on a Ta diffusion barrier, and one set had a Ti barrier. Overburden thicknesses of 120 nm, 240 nm, and 480 nm were available with the Ta diffusion barrier, but only the 120 nm overburden case was analyzed for the Ti diffusion barrier. The grain structure of the lines was predominantly bamboo. The distributions of grain lengths along individual lines had large standard deviations, ranging up to greater than the average grain size value. Print-through of overburden grains into the grain structure of the lines was evident for all lines. Large grain sizes and a strong positive correlation between line width and grain size were seen for the case of the Ta barrier layer with 120 nm overburden thickness, but not for the thicker overburden cases. Specimen surface preparation of these lines was found to be much more demanding than for larger regions of copper films such as those that have been studied previously. For some lines, prepared according to the typical state of the art, we were able to find indexable diffraction signals from less than half of the 100 μm line length. © 2009 American Institute of Physics.

Author supplied keywords

Cite

CITATION STYLE

APA

Geiss, R. H., Read, D. T., Alers, G. B., & Graham, R. L. (2009). EBSD analysis of narrow damascene copper lines. In AIP Conference Proceedings (Vol. 1173, pp. 154–158). https://doi.org/10.1063/1.3251212

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free