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Updated: May 13, 2026

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Using Synchrotron Radiation Microtomography to Investigate Multi-scale Three-dimensional Microelectronic Packages
Published on: April 13, 2016
Three-dimensional imaging of copper pillars using x-ray tomography within a scanning electron microscope: a
N Martin1, J Bertheau, P Bleuet
1ST Microelectronics, 850 Rue Jean Monnet, 38920 Crolles, France.
The Review of Scientific Instruments
|March 8, 2013
Summary
This study introduces a 3D X-ray nanotomography system for analyzing copper pillars in 3D integration. The system enables precise quantification of intermetallic volumes within these critical microelectronic interconnections.
Area of Science:
- Materials Science
- Microscopy
- Nanotechnology
Background:
- Surface-sensitive techniques lack penetration depth for 3D microelectronic interconnections.
- 3D integration demands high-resolution, deep-penetrating imaging methods.
- X-ray tomography offers a suitable solution for characterizing complex 3D structures.
Purpose of the Study:
- To assess a versatile, turn-key 3D X-ray nanotomography system.
- To enable high-resolution 3D imaging of copper pillars for 3D integration.
- To quantify intermetallic volumes within copper pillars.
Main Methods:
- Utilized a scanning electron microscope (SEM) with a thin electron beam for X-ray generation.
- Employed cone beam tomography with sample rotation to acquire radiographs.
- Developed a 3D numerical model of a copper pillar, including intermetallics, for simulation.
- Reconstructed 3D data from simulated and experimental radiographs.
Main Results:
- Successfully reconstructed 3D images of copper pillars.
- Demonstrated the system's capability to quantify 3D intermetallic volumes.
- Validated the 3D numerical model against experimental data.
Conclusions:
- The developed 3D X-ray nanotomography system is effective for characterizing copper pillars.
- The system allows for accurate quantification of intermetallic phases in 3D.
- Further discussion on resolution limitations and future improvements is provided.
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