A direct absorption edge tunable between 0.8 and approximately 1.4 eV is demonstrated in strain-free ternary Ge_{1-x-y}Si_{x}Sn_{y} alloys epitaxially grown on Ge-buffered Si. This decoupling of electronic structure and lattice parameter-unprecedented in group-IV alloys-opens up new possibilities in silicon photonics, particularly in the field of photovoltaics. The compositional dependence of the direct band gap in Ge_{1-x-y}Si_{x}Sn_{y} exhibits a nonmonotonic behavior that is explained in terms of coexisting small and giant bowing parameters in the two-dimensional compositional space.
High-quality, tensile-strained Ge layers with variable thickness (>30nm) have been deposited at low temperature (350–380°C) on Si(100) via fully relaxed Ge1−ySny buffers. The precise strain state of the epilayers is controlled by varying the Sn content of the buffer, yielding tunable tensile strains up to 0.25% for y=0.025. Combined Raman analysis and high resolution x-ray diffraction using multiple off-axis reflections reveal unequivocally that the symmetry of tensile Ge is perfectly tetragonal, while the strain state of the buffer (∼200nm thick) remains essentially unchanged. A downshift of the direct gap consistent with tensile strain has been observed.
Growth of Si1−xSnx alloys on Ge1−ySny-buffered Si(100) was achieved via reactions of SnD4 and SiH3SiH2SiH3 at 275°C. Kinetic studies indicate that unprecedented low growth temperatures are made possible by the highly reactive SiH2 groups. The authors obtain supersaturated metastable compositions (y∼25%) near the indirect to direct band gap crossover predicted by first principles simulations. Extensive characterizations of composition, structure, and morphology show that the SiSn∕GeSn films grow lattice matched via a “compositional pinning” mechanism. The initial Raman observations of Si–Sn bond vibrations in a condensed phase are discussed in the context of simulated bond distributions in the alloys.
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