Abstract
AbstractComplex oxide heterostructures on Si gain in the field of engineered Si wafers increasing interest as flexible buffer systems for developing virtual Si substrates. Strain engineering of thin epitaxial Si thin films on insulating oxide buffers is of special interest to boost charge carrier mobility for Silicon‐on‐Insulator (SOI) technologies. The single crystalline Si(111)/Y2O3 (111)/Pr2O3 (111)/Si(111) heterostructure offers, in principle, the opportunity to grow strain‐engineered epitaxial Si(111) layers, realizing compressed, fully relaxed, as well as tensile‐strained Si films. This flexibility is based on a thickness‐dependence of the Y2O3 lattice constant in the oxide bi‐layer buffer: In theory, the Y2O3 buffer lattice constant on Pr2O3/Si(111) can change from pseudomorphism (bigger than Si) over the Si lattice constant towards a fully relaxed status (smaller than Si). By a detailed interface analysis, using TEM‐EELS in combination with an in‐situ RHEED–XPS study of the isomorphic Y2O3 growth on Pr2O3/Si(111), the physical origin of this Y2O3 buffer lattice constant variation is identified. It is possible to discriminate between the contributions from chemical mixing effects between the isomorphic oxides Y2O3 and Pr2O3 on the one hand and true misfit strain relaxation mechanisms in stoichiometric Y2O3 on the other hand. Copyright © 2010 John Wiley & Sons, Ltd.
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