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Self-Diffusion in Amorphous Silicon by Local Bond Rearrangements
J Kirschbaum1, T Teuber1, A Donner1
1Institute of Materials Physics, Westfälische Wilhelms-Universität Münster, 48149 Münster, Germany.
Self-diffusion in amorphous silicon (Si) was studied. Results show self-diffusion occurs via local bond rearrangements, not extended defects, before recrystallization.
Area of Science:
- Materials Science
- Solid-State Physics
- Semiconductor Research
Background:
- Amorphous silicon (a-Si) is a crucial material in semiconductor technology.
- Understanding diffusion mechanisms in a-Si is vital for device fabrication and reliability.
- Previous studies suggested extended defects mediate self-diffusion in a-Si.
Purpose of the Study:
- To investigate self-diffusion in amorphous silicon (a-Si) at elevated temperatures.
- To determine the mechanism governing self-diffusion in a-Si.
- To compare the activation enthalpy of self-diffusion with other related processes.
Main Methods:
- Preparation of amorphous silicon using Si ion implantation of isotope multilayers.
- Annealing experiments at temperatures ranging from 460 to 600°C.
- Analysis of Si isotope profiles using secondary ion mass spectrometry (SIMS).
Main Results:
- Structural relaxation did not cause significant intermixing.
- Significant self-diffusion was observed before recrystallization.
- The temperature dependence of self-diffusion followed an Arrhenius law with Q=(2.70±0.11) eV.
Conclusions:
- Self-diffusion in amorphous silicon is primarily mediated by local bond rearrangements.
- The activation enthalpy for self-diffusion matches that of hydrogen diffusion and bond defect migration.
- Findings challenge previous hypotheses attributing self-diffusion to extended defect migration.
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