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In-situ Measurement of Self-Atom Diffusion in Solids Using Amorphous Germanium as a Model System
Erwin Hüger1, Florian Strauß2,3, Jochen Stahn4
1AG Mikrokinetik, Institut für Metallurgie, TU Clausthal, Clausthal-Zellerfeld, Germany. erwin.hueger@tu-clausthal.de.
Scientific Reports
|December 6, 2018
Summary
New in-situ neutron reflectometry experiments reveal time-dependent self-diffusion in amorphous germanium. This method accelerates measurements and reduces errors, uncovering structural relaxation effects on diffusion rates.
Area of Science:
- Materials Science
- Solid-State Physics
- Neutron Scattering
Background:
- Classical ex-situ diffusion measurements are time-consuming and have limitations.
- Understanding self-diffusion in amorphous materials is crucial for their technological applications.
Purpose of the Study:
- To introduce and validate an in-situ self-diffusion measurement technique using Focussing Neutron Reflectometry.
- To investigate the time and temperature dependence of self-diffusion in amorphous germanium.
- To determine the activation energy for self-diffusion in amorphous germanium.
Main Methods:
- In-situ self-diffusion experiments on isotope multilayers.
- Focussing Neutron Reflectometry (FNR).
- Isothermal annealing at various temperatures.
Main Results:
- Identified time-dependent diffusivities with reduced error limits and experimental time.
- Measured unknown self-diffusivities in amorphous germanium quasi-continuously.
- Observed a one-order-of-magnitude decrease in diffusivity due to structural relaxation and defect annihilation.
- Determined Arrhenius behavior between 375–412°C with an activation energy of (2.11 ± 0.12) eV.
- Found diffusivities five orders of magnitude higher than in germanium single crystals.
Conclusions:
- In-situ FNR is a powerful technique for studying time-dependent diffusion in solids.
- Structural relaxation significantly impacts self-diffusion in amorphous germanium.
- Amorphous germanium exhibits much higher self-diffusivity than crystalline germanium due to lower activation energy.
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