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Updated: Dec 22, 2025

Quantitative Atomic-Site Analysis of Functional Dopants/Point Defects in Crystalline Materials by Electron-Channeling-Enhanced Microanalysis
Published on: May 10, 2021
Unravelling new principles of site-selective doping contrast in the dual-beam focused ion beam/scanning electron
1Centre for Advanced Photonics and Electronics, Electrical Engineering Division, Department of Engineering, University of Cambridge, 9 JJ Thomson Avenue, Cambridge CB3 0FA, United Kingdom; Department of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS, United Kingdom.
Abstract:
Doping contrast using the secondary electron (SE) signal in the scanning electron microscope (SEM) can satisfy the International Roadmap for Semiconductors (ITRS) requisites for quantitative dopant profiling of next-generation integrated circuits and devices, but only if adopting a site-selective specimen preparation procedure. In this study, site-specific dopant profiling was performed on the trench side-wall cut by a 30-kV Ga+ focused ion beam (FIB) into silicon p-n junction specimens and milled using successively lower voltages in the dual-beam FIB/SEM. Although depositing the protective platinum strap on the surface effectively controls 'curtaining' effects at low final milling voltages, significantly reduced doping contrast from the side-wall compared to that from a cleaved surface subjected to the same ion-beam energy is ascribed to the material affected by a previous milling step, as well as the dissimilar geometries of milling and imaging. New principles underpinning the doping contrast mechanism were surveyed taking into account the depth and concentration of ion implantation and amorphization damage as a linear function of the final milling voltage. Patch fields are suppressed, but the bulk doping-dependent surface band-bending fields at the amorphous-crystalline interface is crucial for doping contrast. In general, as the milling voltage decreases the doping contrast increases, which although reaches up to only half that attainable from a freshly-cleaved specimen, is usable, and demonstrates the feasibility of site-specific dopant profiling in situ in the SEM.
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