Isotropic dielectric functions of highly disordered Al_xGa_1-xInP (0≤x≤1) lattice matched to GaAs

Authors

Mathias Schubert, University of Nebraska-LincolnFollow
John A. Woollam, University of Nebraska-LincolnFollow
G. Leibiger, University of Leipzig
B. Rheinlander, Department of Semiconductor Physics, Faculty of Physics and Geoscience, University of Leipzig
I. Pietzonka, University of Leipzig, Faculty of Chemistry and Mineralogy, Department of Solid State Chemistry
T. Sab, University of Leipzig, Faculty of Chemistry and Mineralogy, Department of Solid State Chemistry
V. Gottschalch, University of Leipzig, Faculty of Chemistry and Mineralogy, Department of Solid State Chemistry

Document Type

Article

Date of this Version

8-15-1999

Comments

Published in J. Appl. Phys., Vol. 86, No. 4, 15 August 1999. © 1999 American Institute of Physics. Used by permission.

Abstract

Determination of the complex dielectric function and the critical-point energies of (Al_xGa_1-x)_0.51In_0.49P, over the full range of composition x and for photon energies E from 0.75 to 5 eV is reported from variable angle of incidence spectroscopic ellipsometry. Native-oxide effects on the (Al_xGa_1-x)_0.51In_0.49P optical functions are removed numerically. The highly disordered state of the metalorganic vapor-phase epitaxy grown samples is analyzed by transmission electron microscopy. Optical anisotropy investigations revealed that the order-induced optical birefringence is negligible throughout. The augmentation of A. D. Rakic´ and M. L. Majewski [J. Appl. Phys. 80, 5909 (1996)] to Adachi’s critical-point model, i.e., consideration of Gaussian-like broadening function instead of Lorentzian broadening, is used for calculation of the isotropic (Al_xGa_1-x)_0.51In_0.49P dielectric function ε. The optical functions spectra consistently match the experimental data, whereas previously reported model dielectric functions fail to reproduce the correct absorption behavior of the quaternary, especially near the fundamental band-to-band transition. The results are compared to those presented previously, and influence of spontaneous chemical ordering is discussed.