TY - JOUR
T1 - Phosphorus diffusion and deactivation during SiGe oxidation
AU - Thornton, Chappel S.
AU - Shen, Xiao
AU - Tuttle, Blair
AU - Li, Xuebin
AU - Law, Mark E.
AU - Pantelides, Sokrates T.
AU - Wang, George T.
AU - Jones, Kevin S.
N1 - Funding Information:
The project was funded by the Laboratory Directed Research and Development program at Sandia National Laboratories, a multimission laboratory managed and operated by the National Technology and Engineering Solutions of Sandia, LLC., a wholly owned subsidiary of Honeywell International, Inc., for the U.S. Department of Energy's National Nuclear Security Administration under Contract No. DE-NA-0003525. This paper describes the objective technical results and analysis. Any subjective views or opinions that might be expressed in the paper do not necessarily represent the views of the U.S. Department of Energy or the United States Government. This article has been authored by an employee of the National Technology & Engineering Solutions of Sandia, LLC under Contract No. DE-NA0003525 with the U.S. Department of Energy (DOE). The employee owns all right, title, and interest in and to the article and is solely responsible for its contents. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this article or allow others to do so, for United States Government purposes. The DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan https://www.energy.gov/downloads/doe-public-access-plan . Theoretical work at Vanderbilt University was supported, in part, by the Air Force Research Laboratory through the Hi-REV program and by the McMinn Endowment at Vanderbilt. Calculations were performed using resources provided by the University of Memphis High-Performance Computing Center (HPCC) and the Department of Defense’s High-Performance Computing Modernization Program (HPCMP). The authors would like to thank Jim Ferris at EAG for his help in assessing the SIMS data. We thank Scott Schmucker of Sandia National Laboratories for the critical reading of this manuscript.
Publisher Copyright:
© 2023 Author(s).
PY - 2023/4/7
Y1 - 2023/4/7
N2 - Dopant profiles near the semiconductor-oxide interface are critical for microelectronic device performance. As the incorporation of Si1-xGex into transistors continues to increase, it is necessary to understand the behavior of dopants in Si1-xGex. In this paper, the diffusion and electrical activation of phosphorus within a strained, single-crystal Si0.7Ge0.3 layer on Si during oxidation are reported. Both layers were uniformly doped, in situ, with an average phosphorus concentration of 4 × 1019 atoms/cm3. After high-temperature oxidation, secondary ion mass spectrometry measurements revealed that the bulk of the phosphorus diffuses out of only the SiGe layer and segregates at the oxidizing SiGe-SiO2 interface. Hall effect measurements corroborate the observed phosphorus loss and show that the phosphorus diffusing to the oxidizing interface is electrically inactive. Through density functional theory (DFT) calculations, it is shown that phosphorus interstitials prefer sites near the SiGe-SiO2 interface. Finally, based on a combination of experimental data and DFT calculations, we propose that the phosphorus atoms are displaced from their lattice sites by Ge interstitials that are generated during SiGe oxidation. The phosphorus atoms then migrate toward the SiGe-SiO2 interface through a novel mechanism of hopping between Ge sites as P-Ge split interstitials. Once they reach the interface, they are electrically inactive, potentially in the form of interstitial clusters or as part of the reconstructed interface or oxide.
AB - Dopant profiles near the semiconductor-oxide interface are critical for microelectronic device performance. As the incorporation of Si1-xGex into transistors continues to increase, it is necessary to understand the behavior of dopants in Si1-xGex. In this paper, the diffusion and electrical activation of phosphorus within a strained, single-crystal Si0.7Ge0.3 layer on Si during oxidation are reported. Both layers were uniformly doped, in situ, with an average phosphorus concentration of 4 × 1019 atoms/cm3. After high-temperature oxidation, secondary ion mass spectrometry measurements revealed that the bulk of the phosphorus diffuses out of only the SiGe layer and segregates at the oxidizing SiGe-SiO2 interface. Hall effect measurements corroborate the observed phosphorus loss and show that the phosphorus diffusing to the oxidizing interface is electrically inactive. Through density functional theory (DFT) calculations, it is shown that phosphorus interstitials prefer sites near the SiGe-SiO2 interface. Finally, based on a combination of experimental data and DFT calculations, we propose that the phosphorus atoms are displaced from their lattice sites by Ge interstitials that are generated during SiGe oxidation. The phosphorus atoms then migrate toward the SiGe-SiO2 interface through a novel mechanism of hopping between Ge sites as P-Ge split interstitials. Once they reach the interface, they are electrically inactive, potentially in the form of interstitial clusters or as part of the reconstructed interface or oxide.
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U2 - 10.1063/5.0145730
DO - 10.1063/5.0145730
M3 - Article
AN - SCOPUS:85152918805
SN - 0021-8979
VL - 133
JO - Journal of Applied Physics
JF - Journal of Applied Physics
IS - 13
M1 - 135301
ER -