4.7 Article

Nonpolar ZnO film growth and mechanism for anisotropic in-plane strain relaxation

期刊

ACTA MATERIALIA
卷 58, 期 3, 页码 1097-1103

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.actamat.2009.10.026

关键词

Epitaxy; Nonpolar; Anisotropic strain; X-ray; TEM

资金

  1. National Science Foundation
  2. DOE Office of Science, Division of Material Sciences & Engineering under contract with ORNL
  3. Directorate For Engineering
  4. Div Of Electrical, Commun & Cyber Sys [921517] Funding Source: National Science Foundation

向作者/读者索取更多资源

Using high-resolution transmission electron microscopy (HRTEM) and X-ray diffraction, we investigated the strain relaxation mechanisms for nonpolar (1 1 -2 0) a-plane ZnO epitaxy on (1 -1 0 2) r-plane sapphire, where the in-plane misfit ranges from -1.5% for the [0 0 0 1]ZnO parallel to[1 -1 0 -1]sapphire to -18.3% for the [-1 1 0 0]ZnO parallel to[-1 -1 2 0]sapphire direction. For the large misfit [-1 1 0 0]ZnO direction the misfit strains are fully relaxed at the growth temperature, and only thermal misfit and defect strains, which cannot be relaxed fully by slip dislocations, remain on cooling. For the small misfit direction, lattice misfit is not fully relaxed at the growth temperature. As a result, additive unrelaxed lattice and thermal misfit and defect strains contribute to the measured strain. Our X-ray diffraction measurements of lattice parameters show that the anisotropic in-plane biaxial strain leads to a distortion of the hexagonal symmetry of the ZnO basal plane. Based on the anisotropic strain relaxation observed along the orthogonal in-plane [-1 1 0 0] and [0 0 0 1]ZnO stress directions and our HRTEM investigations of the interface, we show that the plastic relaxation occurring in the small misfit direction [0 0 0 1]ZnO by dislocation nucleation is incomplete. These results are consistent with the domain-matching paradigm of a complete strain relaxation for large misfits and a difficulty in relaxing the film strain for small misfits. (C) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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