𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Self-Diffusion in Selenium

✍ Scribed by P. Brätter; H. Gobrecht


Publisher
John Wiley and Sons
Year
1970
Tongue
English
Weight
613 KB
Volume
37
Category
Article
ISSN
0370-1972

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Self‐diffusion measurements have been carried out in single crystals of the semiconductor element selenium using a residual activity method and Se‐75 as the tracer in the temperature range 152 to 215 °C. In the direction of the trigonal axis (| c‐axis) the data of the lattice diffusion can be represented by D⟂ = 0.2 exp (—1.2 eV/kT) cm^2^ s^−1^. The diffusion along the short circuit paths can be approximately described by the values Q≈︁ 0.5 eV and Q≈︁ 0.7 eV for the activation energy and by diffusion coefficients between 5 × 10^−10^ and 10^−8^ cm^2^ s^−1^ in the temperature range considered. The vacancy formation enthalpy in selenium is estimated to be about 0.75 eV. From the diffusion data determined the vacancy migration enthalpy is estimated to be about 0.5 eV along the c‐axis and 0.7 eV perpendicular to the c‐axis. It is possible to explain the self‐diffusion in selenium on the basis of a vacancy mechanism. The anomalous self‐diffusion behaviour of the elemental semiconductors and correlation considerations are discussed. Several typical features were found and the presented results for selenium are shown to be in agreement.


📜 SIMILAR VOLUMES


Diffusion of Sulfur in Selenium
✍ P. Brätter; H. Gobrecht 📂 Article 📅 1970 🏛 John Wiley and Sons 🌐 English ⚖ 414 KB
Self-Diffusion in liquids
✍ C. J. Vadovic; C. P. Colver 📂 Article 📅 1972 🏛 American Institute of Chemical Engineers 🌐 English ⚖ 175 KB 👁 2 views
Self-diffusion in indium
✍ J.E Dickey 📂 Article 📅 1959 🏛 Elsevier Science ⚖ 461 KB

Self-diffusion coefficients parallel (D,) and perpendicular (01) to the tetragonal axis were measured in paired samples of single-crystal indium in the range from 44" to 144°C. The ratio D,,/DL was found to be ~0.75 + 0.05 and was not noticeably temperature dependent. Thus the activation energies Q,