Donor impurity incorporation during layer growth of Zn II-VI semiconductors

• Published in: Journal of crystal growth Vol. 479; pp. 93 - 97
• Main Author: Barlow, D.A.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 01.12.2017; Elsevier BV
• Subjects: A1. Diffusion; A1. Doping; B1. Zinc compounds; B2. Semiconducting II-VI materials; Conduction bands; Crystal growth; Crystals; Diffusion; Energy of formation; Halogens; Heat of reaction; Impurities; Lattice sites; Semiconductors; Statistical mechanics; Studies; Zinc oxide; Zinc selenide; Zinc sulfide; Zinc tellurides; A1. Doping; B2. Semiconducting II-VI materials; B1. Zinc compounds; A1. Diffusion
• ISSN: 0022-0248; 1873-5002
• DOI: 10.1016/j.jcrysgro.2017.09.012

•Diatomic bond energies are use to estimate a donor formation energy.•The Efficiency of Halogens donors within the Zn Chalcogenides is studied.•Diffusion activation energies are estimated for halogen donors in the Zn Chacogenides. The maximum halogen donor concentration in Zn II-VI semiconductors during layer growth is studied using a standard model from statistical mechanics. Here the driving force for incorporation is an increase in entropy upon mixing of the donor impurity into the available anion lattice sites in the host binary. A formation energy opposes this increase and thus equilibrium is attained at some maximum concentration. Considering the halogen donor impurities within the Zn II-VI binary semiconductors ZnO, ZnS, ZnSe and ZnTe, a heat of reaction obtained from reported diatomic bond strengths is shown to be directly proportional to the log of maximum donor concentration. The formation energy can then be estimated and an expression for maximum donor concentration derived. Values for the maximum donor concentration with each of the halogen impurities, within the Zn II-VI compounds, are computed. This model predicts that the halogens will serve as electron donors in these compounds in order of increasing effectiveness as: F, Br, I, Cl. Finally, this result is taken to be equivalent to an alternative model where donor concentration depends upon impurity diffusion and the conduction band energy shift due to a depletion region at the growing crystal's surface. From this, we are able to estimate the diffusion activation energy for each of the impurities mentioned above. Comparisons are made with reported values and relevant conclusions presented.