US20110198729A1 - Methods and Compositions for Preparing Tensile Strained Ge on Ge1-ySNy Buffered Semiconductor Substrates - Google Patents
Methods and Compositions for Preparing Tensile Strained Ge on Ge1-ySNy Buffered Semiconductor Substrates Download PDFInfo
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- H—ELECTRICITY
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
- H01L21/02439—Materials
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- H01L21/0245—Silicon, silicon germanium, germanium
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- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
- H01L21/02439—Materials
- H01L21/02441—Group 14 semiconducting materials
- H01L21/02452—Group 14 semiconducting materials including tin
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/02365—Forming inorganic semiconducting materials on a substrate
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- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/02631—Physical deposition at reduced pressure, e.g. MBE, sputtering, evaporation
Definitions
- the direct band gap of Ge can be reduced by alloying with Sn and by applying stress.
- thermal expansion process includes lack of precise strain control and a maximum predicted strain value of 0.3% for growth at 900° C. (see, Cannon, et al., supra).
- high temperatures 800-900° C.
- spatial confinement requires abrupt interfaces, which are precluded using this high temperature process due to the inherent elemental intermixing at the interface.
- precise and systematic control of the final strain state has not been demonstrated using this method, and this hampers the design of devices.
- the present invention provides methods for preparing a semiconductor structure comprising:
- the present invention provides semiconductor structures made by the methods of the first aspect of the invention.
- the present invention provides semiconductor structures comprising a semiconductor substrate; a Ge 1-y Sn y buffer layer formed over the substrate, and a tensile strained Ge layer formed over the Ge 1-y Sn y buffer layer.
- the present invention provides compositions comprising (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between 1:10 and 1:30.
- FIG. 1 shows the electronic band structure of Ge near the lowest direct band gap E 0 .
- k is the wave vector along the ⁇ 100> direction, and a the cubic lattice constant.
- the bands are indicated as cb (conduction band), hh (heavy hole band), lh (light hole), and so (split off band).
- the right panel shows the bands calculated for a tensile strain of 1% using absolute deformation potentials as in Ref. 15. The strain dependence of the effective masses was ignored. The zero of energy is chosen at the top of the valence band in the unstrained case (left panel).
- FIG. 2 is a high resolution image of the corresponding an Ge/GeSn interface (arrow) for an embodiment of the invention showing perfect commensuration of the (111) lattice planes.
- FIG. 3 is a diffraction contrast XTEM image of an entire Ge/GeSn/Si structure according to an embodiment of the invention.
- FIG. 4 is a room temperature Raman spectrum comparing a tensile-strained Ge film (solid line) and a bulk Ge crystal (dotted line). The spectra were obtained with 514.5 nm
- FIG. 5 is a room temperature Raman spectrum comparing a tensile-strained Ge film (solid line) and a bulk Ge crystal (dotted line). The spectra were obtained with 514.5 nm
- FIG. 6 is a graph illustrating the plane strain induced Raman shifts in tensile-strained Ge/GeSn films (solid line) as a function of the in-plane strain measured via XRD.
- FIG. 7 is an XRD reciprocal space map of the (224) reflections, showing a Ge epilayer and a Ge 0.975 Sn 0.025 buffer relative to the Si substrate peak for an embodiment of the invention.
- the Ge peak falls above the relaxation line connecting the Si peaks and the origin, indicating tensile strain.
- FIG. 8 is an XRD reciprocal space map of the (135) reflections, showing a Ge epilayer and a Ge 0.975 Sn 0.025 buffer relative to the Si substrate peak for an embodiment of the invention.
- the (135) Ge peak lies above the relaxation line connecting the Si peaks and the origin, indicating tensile strain.
- FIG. 9 is an XRD reciprocal space map of the (224) reflections, showing the Ge epilayer and the Ge 0.965 Sn 0.035 buffer relative to the Si substrate peak for an embodiment of the invention.
- the Ge peak falls above the relaxation line connecting the Si peaks and the origin, indicating tensile strain of ⁇ 0.45%.
- FIG. 10 is a strain equilibration in the Ge/Ge 0.965 Sn 0.035 bilayer.
- the relaxed Ge and GeSn in-plane lattice parameters are shifted (arrows) towards a common minimum (open circle) to minimize the combined strain energy. Note that the buffer layer is only slightly compressed.
- FIG. 11 is a diffraction contrast XTEM image of the Ge/Ge 0.965 Sn 0.035 /Si (100) heterostructure:
- FIG. 12 is a high resolution XTEM micrograph of the corresponding interface of FIG. 11 .
- FIG. 13 is a 2 ⁇ 2 ⁇ m 2 AFM scan showing a smooth surface created by the coalescence of atomically flat terraces.
- Inset is a 0.5 ⁇ 0.5 ⁇ m 2 AFM scan with RMS roughness of 0.2 nm.
- the tensile-strained Ge layers of the invention display homogeneous compositional and strain profiles, low threading dislocation densities and atomically planar surfaces, and the resulting semiconductor structure and methods for making it are compatible with, for example, selective growth, optical fiber communication applications, and back-end CMOS telecommunication applications.
- the Ge 1-y Sn y buffer layer can be a single layer, or can be a plurality of layers, such as a graded layer, and can be formed with a thickness ranging between 50 nm and several microns.
- the semiconductor buffer layer has a thickness in a range from 50 nm to 10 microns. In various other embodiments, the semiconductor buffer layer has a thickness in a range from about 50 nm to 1 micron. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 500 nm or in a range from about 20 nm to 300 nm.
- the Sn content varies between 1.5% and 3.5% (i.e., y is between 0.015 and 0.035).
- the method further comprises in situ thermal cycling (i) at a temperature of between 500° C. and 600° C. for a period of time ranging from about 1 sec. to 120 minutes; or (ii) by rapid thermal annealing at temperatures ranging up to about 850-900° C. for 1-100 seconds, following forming of the Ge 1-y Sn y buffer layer on a semiconductor substrate, to reduce residual strain.
- the Ge 1-y Sn y buffer layer is at least 90% relaxed; in various further embodiments, at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, or more relaxed.
- the Ge layer can be formed as a single layer, and can be formed over or formed directly on the one or more Ge 1-y Sn y buffer layers (as noted above) with a thickness ranging between 30-200 nm or thicker depending on the critical thickness of the sample.
- the Ge layer can be formed as a single layer, and can be formed over or formed directly on the one or more Ge 1-y Sn y buffer layers (as noted above) with a thickness ranging between about 50-200 nm or thicker depending on the critical thickness of the sample.
- the Ge layer can be formed as a single layer directly on the one or more Ge 1-y Sn y buffer layers. In certain other embodiments, the Ge layer can be formed as a single layer formed directly on the one or more Ge 1-y Sn y buffer layers (as noted above) with a thickness ranging between about 30-200 nm or about 50-200 nm or thicker depending on the critical thickness of the sample. It should be understood that when a layer is referred to as being “on” or “over” another layer or substrate, it can be directly on the layer or substrate, or an intervening layer may also be present.
- a layer when a layer is referred to as being “on” or “over” another layer or substrate, it may cover the entire layer or substrate, or a portion of the layer or substrate. It should be further understood that when a layer is referred to as being “directly on” another layer or substrate, the two layers are in direct contact with one another with no intervening layer. It should also be understood that when a layer is referred to as being “directly on” another layer or substrate, it may cover the entire layer or substrate, or a portion of the layer or substrate.
- the Ge layer has a tunable tensile strain of between 0.15% and 0.45%
- the Ge layer is tetragonal; tetragonal distortion leads to the split of the heavy/light hole bands which ultimately leads to novel optoelectronic properties such as direct gaps and high mobilities in doped systems.
- tensile strain refers to deformation along a layer segment that increases in length and width when a load/perturbation is applied that stretches the layer within the horizontal pane and reduces its vertical dimension.
- the semiconductor substrate can be any substrate suitable for semiconductor use, including but not limited to silicon, silicon on insulator, SiO 2 , Si:Ge alloys, and Si:C alloys.
- the substrate comprises silicon, including but not limited to Si(100).
- the semiconductor substrates can be n- or p-doped as is familiar to those skilled in the art; for example, n- or p-doped Si(100).
- the semiconductor buffer layer has a thickness in a range from 50 nm to several microns. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 10 microns. In various other embodiments, the semiconductor buffer layer has a thickness in a range from about 50 nm to 1 micron. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 500 nm or in a range from about 20 nm to 300 nm. In further embodiments, the semiconductor buffer layers have a density of threading defects of 10 6 /cm 2 or less.
- the semiconductor substrates of the invention comprise a Ge 1-y Sn y buffer layer and/or a Ge layer having a substantially atomically planar surface morphology (i.e., essentially atomically flat).
- substantially atomically planar and “essentially atomically flat” means that the referenced surface has an RMS roughness value of less than about 1.0 nm as measured by atomic force microscopy according to methods familiar to one skilled in the art.
- the referenced surface has an RMS roughness value of less than about 0.75 nm or an RMS roughness value ranging from about 0.2 to 1.0 nm or about 0.3 to about 0.75 nm.
- the Ge layers formed according to the present methods of the invention are Ge layer epitaxial.
- epitaxial means that a material is crystalline and fully commensurate with the substrate.
- epitaxial means that the material is monocrystalline, as defined herein.
- monocrystalline as used herein, means a solid in which the crystal lattice of the entire sample is continuous with no grain boundaries or very few grain boundaries, as is familiar to those skilled in the art.
- the methods comprise depositing the Ge layer on the buffer layer, which may involve introducing into a reaction chamber a gaseous precursor comprising or consisting of an admixture of (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between 1:10 and 1:30 (or, in other embodiments, 1:10 to 1:25; 1:11 to 1:25, 1:12 to 1:25; 1:13 to 1:25; 1:14 to 1:25; 1:15 to 1:25; 1:10 to 1:20; 1:10 to 1:19; 1:10 to 1:18, 1:10 to 1:17; 1:10 to 1:16, 1:10 to 1:15), under conditions whereby the Ge layer material is formed on the buffer layer.
- the admixture comprises (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between 1:15 and 1:25.
- the methods comprise depositing the Ge layer on the buffer layer, which may involve introducing into a reaction chamber a gaseous precursor comprising or consisting of an admixture of (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between about 1:20 and 1:30 (or, in other embodiments, 1:21 to 1:30, 1:22 to 1:30, 1:23 to 1:30, 1:24 to 1:30, 1:25 to 1:30; 1:26 to 1:30, 1:27 to 1:30; 1:28 to 1:30; and 1:29 to 1:30.
- a gaseous precursor comprising or consisting of an admixture of (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between about 1:20 and 1:30 (or, in other embodiments, 1:21 to 1:30, 1:22 to 1:30, 1:23 to 1:30, 1:24 to 1:30, 1:25 to 1:30; 1:26 to 1:30, 1:27 to 1:30; 1:28 to 1:30; and 1:29 to 1:30.
- the step of introducing the gaseous precursor comprises introducing the gaseous precursor in substantially pure form.
- the step of introducing the gaseous precursor comprises introducing the gaseous precursor intermixed with an inert carrier gas.
- the inert gas can be, for example, H 2 or N 2 .
- the gaseous precursor can be deposited by any suitable technique, including but not limited to gas source molecular beam epitaxy, chemical vapor deposition, plasma enhanced chemical vapor deposition, laser assisted chemical vapor deposition, and atomic layer deposition.
- the gaseous precursor is introduced by gas source molecular beam epitaxy at between at a temperature of between 300° C. and 420° C., more preferably between 350° C. and 400° C., and even more preferably between 350° C. to 380° C.
- the gaseous precursor is introduced at a partial pressure between 10 ⁇ 8 Torr and 1000 Torr. In one embodiment, the gaseous precursor is introduced at between 10 ⁇ 8 Torr and 10 ⁇ 3 Torr for gas source molecular beam epitaxy. In another embodiment, the gaseous precursor is introduced at between 10 ⁇ 7 Torr and 10 ⁇ 4 Torr for gas source molecular beam epitaxy. In yet another embodiment, the gaseous precursor is introduced at between 10 ⁇ 6 Torr and 10 ⁇ 5 Torr for gas source molecular beam epitaxy.
- the semiconductor structures of the invention may further comprise other features as desired, including but not limited to the inclusion of dopants, such as boron, phosphorous, arsenic, and antimony. These embodiments are especially preferred for semiconductor substrates used as active devices. Inclusion of such dopants into the semiconductor substrates can be carried out by standard methods in the art.
- dopants such as boron, phosphorous, arsenic, and antimony.
- the present invention provides composition, comprising (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between 1:10 and 1:30.
- the composition comprises the individual components in a ratio of 1:10 to 1:25; 1:11 to 1:25, 1:12 to 1:25; 1:13 to 1:25; 1:14 to 1:25; 1:15 to 1:25; 1:10 to 1:20; 1:10 to 1:19; 1:10 to 1:18, 1:10 to 1:17; 1:10 to 1:16, 1:10 to 1:15.
- the composition is in a gaseous form.
- the composition comprises (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between 1:15 and 1:25.
- the present invention provides composition, comprising (GeH 3 ) 2 CH 2 and Ge 2 H 6 in a ratio of between about 1:20 and 1:30 (or, in other embodiments, 1:21 to 1:30, 1:22 to 1:30, 1:23 to 1:30, 1:24 to 1:30, 1:25 to 1:30; 1:26 to 1:30, 1:27 to 1:30; 1:28 to 1:30; and 1:29 to 1:30.
- the as-grown Ge 1-y Sn y films were ⁇ 93-95% relaxed (even for thicknesses less than 100 nm) and achieve strain relief from the substrate by generating Lomer dislocations that run parallel to the film/substrate interface.
- the residual strain was relieved by in situ thermal cycling for 30 minutes at 500-600° C. or by rapid thermal annealing up to 850° C. for several seconds, depending on composition.
- Atomic force microscopy shows planar surfaces for both the as-grown and annealed Ge 1-y Sn y buffers that provide an ideal platform for subsequent growth.
- the typical RMS roughness was in the range of 0.5-0.8 nm for 10 ⁇ 10 ⁇ m 2 areas.
- MBE gas-source molecular beam epitaxy
- This combination of compounds was designed to provide built-in pseudo surfactant growth behavior enabling the fabrication of dislocation free, and atomically flat Ge films with no measurable carbon incorporation.
- SIMS measurements indicate C content at the detection limit ( ⁇ 3 ⁇ 10 17 cm ⁇ 3 ) (see, Wistey et al., Appl. Phys. Lett., 90, 082108 (2007)).
- the reaction mixture of (GeH 3 ) 2 CH 2 in Ge 2 H 6 was prepared prior to each deposition by combining the pure compounds in a 100 mL vacuum flask.
- the total pressure was 115 Torr, which is well below the vapor pressure of (GeH 3 ) 2 CH 2 (248 Torr at 25° C.).
- the flask was connected to a gas injection manifold which was pumped to ⁇ 10 ⁇ 8 Torr on the gas source MBE chamber.
- the Ge 1-y Sn y /Si(100) substrates Prior to Ge growth, the Ge 1-y Sn y /Si(100) substrates were sonicated for 5 minutes in methanol, dried by flowing N 2 over their surface, inserted through a load lock into an ultra high vacuum (UHV) chamber at a base pressure of 5 ⁇ 10 ⁇ 10 Torr, and then heated on the sample holder for one hour at 250° C. to desorb any volatile surface contaminants until the chamber pressure was restored to the base value of 10 ⁇ 10 Torr. Under these conditions we find that the Ge 1-y Sn y surfaces exhibit the typical (2 ⁇ 1) to (1 ⁇ 2) reconstruction, indicating a well-ordered crystallographic state suitable for subsequent heteroepitaxial growth.
- UHV ultra high vacuum
- the temperature was then increased to 360-380° C. and the reactant gases were admitted at a final pressure of 5 ⁇ 10 ⁇ 5 Torr to commence film growth.
- the pressure was maintained constant (5 ⁇ 10 ⁇ 5 Torr) during growth via dynamic pumping using a corrosion resistant turbomolecular pump.
- Typical growth times from 30-60 minutes yielded films of thickness in the range 30-60 nm, respectively, at a fixed growth temperature of 360° C.
- the Ge films were deposited at a rate of 2 nm/min. Under these conditions Ge growth was observed to proceed via nucleation of nanoscale atomically-flat mesas which gradually coalesce to produce continuous films with planar surfaces as evidence by AFM characterizations.
- the samples prepared according to Example 1 were extensively characterized for morphology, microstructure, purity and crystallographic properties by atomic force microscopy (AFM), Rutherford backscattering (RBS), secondary ion mass spectrometry (SIMS), cross sectional transmission electron microscopy (XTEM) and high resolution x-ray diffraction (XRD).
- the threading defects densities were estimated using an etch pit technique (EPD).
- the precise strain state of the Ge epilayers case can be systematically manipulated by varying the thickness and composition of the underlying template, for example, via tuning of the Sn content in the Ge 1-y Sn y buffer.
- Growth of Ge layers on buffers with smaller/larger lattice constants, such as Ge 1-y Sn y with y 0.015-0.035,) systematically produced larger strains in the Ge overlayers with increasing y, within the 1.5-3.5% range.
- FIG. 1 shows the quantitative changes in the band structure for 1% tensile strain in Ge.
- Small reductions in E 0 can dramatically improve the detection performance of this material at 1.55 ⁇ m and beyond to cover the technologically important near-IR telecom bands for use in optical fiber communications.
- For sufficiently large tensile strain it has been predicted that Ge may become a direct gap system, with potential applications as an active lasing material (see, Menendez and Kouvetakis, J. Appl. Phys. Lett. 2004, 85, 1175).
- the diffraction contrast image of the entire film thickness in (110) projection shows an atomically flat surface and a film devoid of threading dislocations within the field of view.
- the typical RBS spectra (in random and channeled modes) showed consistently monocrystalline and perfectly aligned materials.
- the ratio of the aligned and random spectra ( ⁇ min ), which measures the degree of epitaxial registry was extremely low, an ⁇ min value of 10% within the Ge layer, close to the 3% limit for Si (100) wafers.
- the growth strategies herein provide controlled and reproducible Ge strain values exceeding those obtained to date, leading to values of tensile strain as high as 0.8%.
- the strain in this case can be systematically manipulated by varying the thickness and composition of the underlying template.
- FIG. 4 shows a Raman spectrum from a tensile-strained Ge-film in a Ge/Ge 0.975 Sn 0.025 structure.
- the Raman peak is clearly downshifted relative to the corresponding Raman peak in bulk Ge.
- Tetragonal strain splits the three-fold degenerate optical phonons at the center of the Ge Brillouin zone into a doublet and a singlet.
- p and q are the optical phonon anharmonic parameters, as defined, for example, in Anastassakis and Cardona in High Pressure in Semiconductor Physics II , ed. by T. Suski and W. Paul (Academic Press, New York, 1998)), and ⁇ 0 is the Raman frequency in bulk Ge.
- b ⁇ 415 ⁇ 40 cm ⁇ 1 .
- ⁇ ⁇ ⁇ 0.24 ⁇ 0.04%
- FIG. 5 shows a typical Raman spectrum of a Ge/Ge 0.965 Sn 0.035 sample compared to that of a bulk Ge reference. Again, the peak of the Ge film is shifted to lower energies, as expected for tensile strain.
- FIG. 6 shows the Raman shifts of the Ge-films with strains intermediate to 0.15 and 0.43% (with respect to the Raman shift in pure Ge) as a function of the measured in-plane strain ⁇ ⁇ obtained from XRD (infra). A monotonic and approximately linear dependence was observed, which confirms the XRD results.
- the strain state of the Ge films was further investigated by recording line scans and reciprocal space maps for the symmetric (004), and asymmetric (224) Bragg reflections. In each case the data were referenced to the corresponding reflections of the Si wafer.
- FIG. 7 shows the (224) reciprocal space map for a Ge/Ge 0.975 Sn 0.025 structure with epilayer and buffer thicknesses of 60 nm and 200 nm, respectively.
- the diffracted intensity peaks lie very close to the full relaxation line ((224) line in FIG. 7 ).
- the vertical alignment of the Ge and GeSn (224) peaks indicates a coherent heterostructure, while the considerable offset of the Ge peak with respect to the relaxation line implies a significant tensile strain.
- the larger scattering volume of the 140 nm thick sample enabled us to measure typically weak off-axis peaks such as the (135) and ( 1 35) reflections. These have h ⁇ k and accordingly they are sensitive to deviations from a tetragonal distortion. If the Ge film distortion is of lower symmetry than tetragonal, the in-plane value derived from these reflections will deviate significantly from their (224) counterpart.
- Table 1 compares both the in-plane and vertical lattice constants ( ⁇ ⁇ and ⁇ ⁇ respectively), for the Si substrate, the GeSn buffer layer and the strained Ge epilayer. In all three cases the in-plane lattice constant values obtained independently from the (135), ( 1 35) and (224) analysis are identical, within instrumental resolution.
- FIG. 9 shows the (224) spectra of a representative sample with composition Ge/Ge 0.965 Sn 0.035 , and epilayer/buffer thicknesses of ⁇ 60/230 nm.
- the plots also show a near perfect vertical alignment of the Ge and GeSn (224) peaks indicating a fully coherent stack as shown by the dotted line in FIG. 9 .
- ⁇ ⁇ ⁇ ⁇ ( 1 1 + a ⁇ / ⁇ ⁇ ⁇ a ⁇ ) ⁇ ⁇ ⁇ ⁇ 1 2 ⁇ ⁇ ⁇ ( 2 )
- FIGS. 11 and 12 shows electron micrographs of the Ge/Ge 0.965 Sn 0.035 sample indicating a 60 nm thick Ge layer grown epitaxially on a 230 nm thick Ge 1-y Sn y buffer.
- the bright field image shows essentially no penetrating threading defects over an extended lateral range of 1 ⁇ m and the high resolution micrograph near the Ge/Si interface reveals a sharp, commensurate transition between the epilayer and the buffer, AFM analysis of the sample shows that the surface is predominantly flat, with an RMS roughness of ⁇ 1.5 nm over a typical 5 ⁇ 5 ⁇ m 2 area [ FIG. 13 ].
- On a smaller 0.5 ⁇ 0.5 ⁇ m 2 scale we observe atomically smooth surfaces with a reduced RMS roughness of ⁇ 0.2 nm. The difference in these values is associated with the presence of tiny voids located at the intersection of individual coalescing terraces as described previously. In thicker films these terraces coalesce fully and such features are not longer visible.
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Abstract
The present disclosure describes methods for preparing semiconductor structures, comprising forming a Ge1-ySny buffer layer on a semiconductor substrate and forming a tensile strained Ge layer on the Ge1-ySny buffer layer using an admixture of (GeH3)2CH2 and Ge2H6 in a ratio of between 1:10 and 1:30. The disclosure further provides semiconductor structures having highly strained Ge epilayers (e.g., between about 0.15% and 0.45%) as well as compositions comprising an admixture of (GeH3)2CH2 and Ge2H6 in a ratio of between about 1:10 and 1:30. The methods herein provide, and the semiconductor structure provide, Ge epilayers having high strain levels which can be useful in semiconductor devices for example, in optical fiber communications devices.
Description
- This application is a Divisional of U.S. patent application Ser. No. 12/133,221, filed Jun. 4, 2008 which claims the benefit under 35 USC §119(e), of U.S. Provisional Application Ser. No. 60/933,013, filed 4 Jun. 2007, which is hereby incorporated by reference in its entirety.
- The invention described herein was made in part with government support under grant number FA9550-06-01-0442, awarded by AFOSR under the MURI; and under grant number DMR-0526734, awarded by the National Science Foundation. The United States Government has certain rights in the invention.
- Germanium has a direct band gap E0=0.81 eV at room temperature (see, MacFarlane and Roberts, Phys. Rev. 97, 1714 (1955)), which corresponds to an optical wavelength of 1.54 μm. Although this is barely enough to reach the telecom C-band (1.53 μm-1.56 μm), the very strong wavelength dependence of the absorption coefficient near the direct edge suggests that small perturbations that shift E0 to lower energies should dramatically improve the performance of this material for use in optical fiber communications. The direct band gap of Ge can be reduced by alloying with Sn and by applying stress. The dependence of E0 on Sn-concentration has been measured and found to be stronger than predicted, to the extent that the addition of only 2% of Sn increases the absorption coefficient at 1.55 μm by more than one order of magnitude (see, D'Costa et al., Phys. Rev. B 73, 125207 (2006)). The use of stress as a perturbation is problematic because the direct band gap can only be lowered with tensile strain.
- This strain cannot be obtained by growing epitaxial Ge on Ge1-xSix alloys because the latter have a smaller lattice parameter. In spite of this inherent limitation, tensile-strained Ge has been obtained by depositing the material directly on Si at relatively high temperatures and by exploiting the smaller thermal expansion of the substrate to induce stress in the Ge epilayer when the sample is quenched from ˜800° C. (see, Ishikawa et al., Appl. Phys. Lett. 82, 2044 (2003); Cannon, et al., Appl. Phys. Lett. 84, 906 (2004); Liu et al., Appl. Phys. Lett. 87, 103501 (2005); Wietler et al., Thin Solid Films 508, 6 (2006); and Liu et al., Phys. Rev. B 70, 155309 (2004)). This process leads to biaxial tensile strains as high as 0.25% in films as thick as 1 μm. While such tensile strain values may be sufficient for some photodetector designs, higher strain values are necessary for most optoelectronic applications which require tunable direct gaps (see, Liu et al., 2004, supra).
- Further limitations of the thermal expansion process include lack of precise strain control and a maximum predicted strain value of 0.3% for growth at 900° C. (see, Cannon, et al., supra). Moreover, the use of high temperatures (800-900° C.) typically induces inter-diffusion of the elements across the Si—Ge heterojunction, resulting in non-uniform and potentially defective interfaces. In the context of laser applications, spatial confinement requires abrupt interfaces, which are precluded using this high temperature process due to the inherent elemental intermixing at the interface. In addition, precise and systematic control of the final strain state has not been demonstrated using this method, and this hampers the design of devices.
- Thus, there exists a need in the art for improved methods of preparing tensile strained Ge on semiconductor substrates.
- In one aspect, the present invention provides methods for preparing a semiconductor structure comprising:
-
- a) forming a Ge1-ySny buffer layer on a semiconductor substrate; and
- b) forming a tensile strained Ge layer on the Ge1-ySny buffer layer using an admixture of (GeH3)2CH2 and Ge2H6 in a ratio of between 1:10 and 1:30.
- In a second aspect, the present invention provides semiconductor structures made by the methods of the first aspect of the invention.
- In a third aspect, the present invention provides semiconductor structures comprising a semiconductor substrate; a Ge1-ySny buffer layer formed over the substrate, and a tensile strained Ge layer formed over the Ge1-ySny buffer layer.
- In a fourth aspect, the present invention provides compositions comprising (GeH3)2CH2 and Ge2H6 in a ratio of between 1:10 and 1:30.
- Herein is provided an approach based for the generation of tensile-strained Ge epilayers based on the creation of Ge1-ySny alloys with tunable lattice dimensions above that of Ge which serve as the critical facilitating platforms for the subsequent tensile-Ge growth. In addition this approach subsumes the following distinctive features: (i) low growth temperature that promotes the assembly of highly-strained tetragonally-distorted Ge structures that remain robust despite the inherent metastability. (ii) layer-by-layer growth mechanisms leading to flat surfaces, chemically abrupt interfaces devoid of chemical intermixing and relatively defect free layer microstructures. Both features are enabled by exploiting the high reactivity and the pseudo-surfactant behavior of the (GeH3)2CH2 species. Collectively this methodology has allowed the systematic production of Ge layers with very high tensile strains and all of the desired morphological and structural properties as discussed below. Thereby, the utility of Ge can be extended into the wider infrared optoelectronic domain by tuning its fundamental optical properties using strain as a main parameter
-
FIG. 1 shows the electronic band structure of Ge near the lowest direct band gap E0. Here, k is the wave vector along the <100> direction, and a the cubic lattice constant. The bands are indicated as cb (conduction band), hh (heavy hole band), lh (light hole), and so (split off band). The valence band spin-orbit splitting at k=0 is Δ0. The right panel shows the bands calculated for a tensile strain of 1% using absolute deformation potentials as in Ref. 15. The strain dependence of the effective masses was ignored. The zero of energy is chosen at the top of the valence band in the unstrained case (left panel). -
FIG. 2 is a high resolution image of the corresponding an Ge/GeSn interface (arrow) for an embodiment of the invention showing perfect commensuration of the (111) lattice planes. -
FIG. 3 is a diffraction contrast XTEM image of an entire Ge/GeSn/Si structure according to an embodiment of the invention. -
FIG. 4 is a room temperature Raman spectrum comparing a tensile-strained Ge film (solid line) and a bulk Ge crystal (dotted line). The spectra were obtained with 514.5 nm -
FIG. 5 is a room temperature Raman spectrum comparing a tensile-strained Ge film (solid line) and a bulk Ge crystal (dotted line). The spectra were obtained with 514.5 nm -
FIG. 6 is a graph illustrating the plane strain induced Raman shifts in tensile-strained Ge/GeSn films (solid line) as a function of the in-plane strain measured via XRD. -
FIG. 7 is an XRD reciprocal space map of the (224) reflections, showing a Ge epilayer and a Ge0.975Sn0.025 buffer relative to the Si substrate peak for an embodiment of the invention. The Ge peak falls above the relaxation line connecting the Si peaks and the origin, indicating tensile strain. -
FIG. 8 is an XRD reciprocal space map of the (135) reflections, showing a Ge epilayer and a Ge0.975Sn0.025 buffer relative to the Si substrate peak for an embodiment of the invention. As for the (224) peak, the (135) Ge peak lies above the relaxation line connecting the Si peaks and the origin, indicating tensile strain. -
FIG. 9 is an XRD reciprocal space map of the (224) reflections, showing the Ge epilayer and the Ge0.965Sn0.035 buffer relative to the Si substrate peak for an embodiment of the invention. The Ge peak falls above the relaxation line connecting the Si peaks and the origin, indicating tensile strain of ˜0.45%. -
FIG. 10 is a strain equilibration in the Ge/Ge0.965Sn0.035 bilayer. The relaxed Ge and GeSn in-plane lattice parameters (dotted lines) are shifted (arrows) towards a common minimum (open circle) to minimize the combined strain energy. Note that the buffer layer is only slightly compressed. -
FIG. 11 is a diffraction contrast XTEM image of the Ge/Ge0.965Sn0.035/Si (100) heterostructure: -
FIG. 12 is a high resolution XTEM micrograph of the corresponding interface ofFIG. 11 . -
FIG. 13 is a 2×2 μm2 AFM scan showing a smooth surface created by the coalescence of atomically flat terraces. Inset is a 0.5×0.5 μm2 AFM scan with RMS roughness of 0.2 nm. - As demonstrated herein, the tensile-strained Ge layers of the invention display homogeneous compositional and strain profiles, low threading dislocation densities and atomically planar surfaces, and the resulting semiconductor structure and methods for making it are compatible with, for example, selective growth, optical fiber communication applications, and back-end CMOS telecommunication applications.
- In the case of pure Ge, increasing the tensile strain beyond the values allowed by the thermal expansion method is highly desirable. The so-called telecom U-band can be covered with a biaxial tensile strain of 0.4%. Our approach has provided strains as high as 0.45% which is suitable for generating U-bands and represents the highest value ever observed. As described below, the availability of Sn-based buffers allows the growth of strained Ge films to be conducted at unprecedented low temperatures (350-380° C.) which are compatible with selective growth and back-end CMOS telecommunication applications.
- The Ge1-ySny buffer layer can be a single layer, or can be a plurality of layers, such as a graded layer, and can be formed with a thickness ranging between 50 nm and several microns. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 10 microns. In various other embodiments, the semiconductor buffer layer has a thickness in a range from about 50 nm to 1 micron. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 500 nm or in a range from about 20 nm to 300 nm.
- In various embodiments, the Sn content varies between 1.5% and 3.5% (i.e., y is between 0.015 and 0.035). In a further embodiment, the method further comprises in situ thermal cycling (i) at a temperature of between 500° C. and 600° C. for a period of time ranging from about 1 sec. to 120 minutes; or (ii) by rapid thermal annealing at temperatures ranging up to about 850-900° C. for 1-100 seconds, following forming of the Ge1-ySny buffer layer on a semiconductor substrate, to reduce residual strain. In a further embodiment, the Ge1-ySny buffer layer is at least 90% relaxed; in various further embodiments, at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, or more relaxed.
- The Ge layer can be formed as a single layer, and can be formed over or formed directly on the one or more Ge1-ySny buffer layers (as noted above) with a thickness ranging between 30-200 nm or thicker depending on the critical thickness of the sample. In certain embodiments, the Ge layer can be formed as a single layer, and can be formed over or formed directly on the one or more Ge1-ySny buffer layers (as noted above) with a thickness ranging between about 50-200 nm or thicker depending on the critical thickness of the sample.
- In certain embodiments, the Ge layer can be formed as a single layer directly on the one or more Ge1-ySny buffer layers. In certain other embodiments, the Ge layer can be formed as a single layer formed directly on the one or more Ge1-ySny buffer layers (as noted above) with a thickness ranging between about 30-200 nm or about 50-200 nm or thicker depending on the critical thickness of the sample. It should be understood that when a layer is referred to as being “on” or “over” another layer or substrate, it can be directly on the layer or substrate, or an intervening layer may also be present. It should also be understood that when a layer is referred to as being “on” or “over” another layer or substrate, it may cover the entire layer or substrate, or a portion of the layer or substrate. It should be further understood that when a layer is referred to as being “directly on” another layer or substrate, the two layers are in direct contact with one another with no intervening layer. It should also be understood that when a layer is referred to as being “directly on” another layer or substrate, it may cover the entire layer or substrate, or a portion of the layer or substrate.
- In various embodiments, the Ge layer has a tunable tensile strain of between 0.15% and 0.45% In a further embodiment, the Ge layer is tetragonal; tetragonal distortion leads to the split of the heavy/light hole bands which ultimately leads to novel optoelectronic properties such as direct gaps and high mobilities in doped systems. As used herein, “tensile strain” refers to deformation along a layer segment that increases in length and width when a load/perturbation is applied that stretches the layer within the horizontal pane and reduces its vertical dimension.
- The semiconductor substrate can be any substrate suitable for semiconductor use, including but not limited to silicon, silicon on insulator, SiO2, Si:Ge alloys, and Si:C alloys. In a preferred embodiment, the substrate comprises silicon, including but not limited to Si(100). The semiconductor substrates can be n- or p-doped as is familiar to those skilled in the art; for example, n- or p-doped Si(100).
- In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to several microns. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 10 microns. In various other embodiments, the semiconductor buffer layer has a thickness in a range from about 50 nm to 1 micron. In various embodiments, the semiconductor buffer layer has a thickness in a range from 50 nm to 500 nm or in a range from about 20 nm to 300 nm. In further embodiments, the semiconductor buffer layers have a density of threading defects of 106/cm2 or less.
- In a further embodiment, the semiconductor substrates of the invention comprise a Ge1-ySny buffer layer and/or a Ge layer having a substantially atomically planar surface morphology (i.e., essentially atomically flat). As used herein, the terms “substantially atomically planar” and “essentially atomically flat” means that the referenced surface has an RMS roughness value of less than about 1.0 nm as measured by atomic force microscopy according to methods familiar to one skilled in the art. Preferably, that the referenced surface has an RMS roughness value of less than about 0.75 nm or an RMS roughness value ranging from about 0.2 to 1.0 nm or about 0.3 to about 0.75 nm.
- In other embodiments, the Ge layers formed according to the present methods of the invention are Ge layer epitaxial. The term “epitaxial” as used herein, means that a material is crystalline and fully commensurate with the substrate. Preferably, epitaxial means that the material is monocrystalline, as defined herein. The term “monocrystalline” as used herein, means a solid in which the crystal lattice of the entire sample is continuous with no grain boundaries or very few grain boundaries, as is familiar to those skilled in the art.
- The methods comprise depositing the Ge layer on the buffer layer, which may involve introducing into a reaction chamber a gaseous precursor comprising or consisting of an admixture of (GeH3)2CH2 and Ge2H6 in a ratio of between 1:10 and 1:30 (or, in other embodiments, 1:10 to 1:25; 1:11 to 1:25, 1:12 to 1:25; 1:13 to 1:25; 1:14 to 1:25; 1:15 to 1:25; 1:10 to 1:20; 1:10 to 1:19; 1:10 to 1:18, 1:10 to 1:17; 1:10 to 1:16, 1:10 to 1:15), under conditions whereby the Ge layer material is formed on the buffer layer. In a particular embodiment, the admixture comprises (GeH3)2CH2 and Ge2H6 in a ratio of between 1:15 and 1:25.
- In another embodiment, the methods comprise depositing the Ge layer on the buffer layer, which may involve introducing into a reaction chamber a gaseous precursor comprising or consisting of an admixture of (GeH3)2CH2 and Ge2H6 in a ratio of between about 1:20 and 1:30 (or, in other embodiments, 1:21 to 1:30, 1:22 to 1:30, 1:23 to 1:30, 1:24 to 1:30, 1:25 to 1:30; 1:26 to 1:30, 1:27 to 1:30; 1:28 to 1:30; and 1:29 to 1:30.
- In various embodiments, the step of introducing the gaseous precursor comprises introducing the gaseous precursor in substantially pure form. In another embodiment, the step of introducing the gaseous precursor comprises introducing the gaseous precursor intermixed with an inert carrier gas. In this embodiment, the inert gas can be, for example, H2 or N2.
- In the methods of the invention, the gaseous precursor can be deposited by any suitable technique, including but not limited to gas source molecular beam epitaxy, chemical vapor deposition, plasma enhanced chemical vapor deposition, laser assisted chemical vapor deposition, and atomic layer deposition. In a further embodiment, the gaseous precursor is introduced by gas source molecular beam epitaxy at between at a temperature of between 300° C. and 420° C., more preferably between 350° C. and 400° C., and even more preferably between 350° C. to 380° C. Practical advantages associated with this low temperature/rapid growth process include (i) short deposition times compatible with preprocessed Si wafers, (ii) selective growth for application in high frequency devices, and (iii) negligible mass segregation of dopants, which is particularly critical for thin layers.
- In various further embodiments, the gaseous precursor is introduced at a partial pressure between 10−8 Torr and 1000 Torr. In one embodiment, the gaseous precursor is introduced at between 10−8 Torr and 10−3 Torr for gas source molecular beam epitaxy. In another embodiment, the gaseous precursor is introduced at between 10−7 Torr and 10−4 Torr for gas source molecular beam epitaxy. In yet another embodiment, the gaseous precursor is introduced at between 10−6 Torr and 10−5 Torr for gas source molecular beam epitaxy.
- All definitions and embodiments described above for the methods of the invention apply to the semiconductor structure aspects of the invention.
- The semiconductor structures of the invention may further comprise other features as desired, including but not limited to the inclusion of dopants, such as boron, phosphorous, arsenic, and antimony. These embodiments are especially preferred for semiconductor substrates used as active devices. Inclusion of such dopants into the semiconductor substrates can be carried out by standard methods in the art.
- In another aspect, the present invention provides composition, comprising (GeH3)2CH2 and Ge2H6 in a ratio of between 1:10 and 1:30. In various preferred embodiments, the composition comprises the individual components in a ratio of 1:10 to 1:25; 1:11 to 1:25, 1:12 to 1:25; 1:13 to 1:25; 1:14 to 1:25; 1:15 to 1:25; 1:10 to 1:20; 1:10 to 1:19; 1:10 to 1:18, 1:10 to 1:17; 1:10 to 1:16, 1:10 to 1:15. In a further embodiment of each of these embodiments, the composition is in a gaseous form. In particular embodiment, the composition comprises (GeH3)2CH2 and Ge2H6 in a ratio of between 1:15 and 1:25.
- In another embodiment, the present invention provides composition, comprising (GeH3)2CH2 and Ge2H6 in a ratio of between about 1:20 and 1:30 (or, in other embodiments, 1:21 to 1:30, 1:22 to 1:30, 1:23 to 1:30, 1:24 to 1:30, 1:25 to 1:30; 1:26 to 1:30, 1:27 to 1:30; 1:28 to 1:30; and 1:29 to 1:30.
- Ge1-ySny buffer layers (y=0.02-0.04) were deposited on hydrogen-passivated Si(100) wafers at 330-350° C., as described previously (see, Bauer et al., Appl. Phys. Lett. 81, 2992 (2002), which is hereby incorporated by reference in its entirety). The as-grown Ge1-ySny films were ˜93-95% relaxed (even for thicknesses less than 100 nm) and achieve strain relief from the substrate by generating Lomer dislocations that run parallel to the film/substrate interface. The residual strain was relieved by in situ thermal cycling for 30 minutes at 500-600° C. or by rapid thermal annealing up to 850° C. for several seconds, depending on composition. These steps also reduces the density of threading defects penetrating to the surface to levels below 106/cm2. Atomic force microscopy (AFM) shows planar surfaces for both the as-grown and annealed Ge1-ySny buffers that provide an ideal platform for subsequent growth. The typical RMS roughness was in the range of 0.5-0.8 nm for 10×10 μm2 areas.
- Growth of Ge epilayers was conducted ex situ on the relaxed Ge1-ySny buffers (y=0.02-0.04) via gas-source molecular beam epitaxy (MBE) at 340-380° C. and 5×10−5 Torr using 1:15 admixtures of (GeH3)2CH2 and Ge2H6. This combination of compounds was designed to provide built-in pseudo surfactant growth behavior enabling the fabrication of dislocation free, and atomically flat Ge films with no measurable carbon incorporation. SIMS measurements indicate C content at the detection limit (<3×1017 cm−3) (see, Wistey et al., Appl. Phys. Lett., 90, 082108 (2007)).
- The reaction mixture of (GeH3)2CH2 in Ge2H6 was prepared prior to each deposition by combining the pure compounds in a 100 mL vacuum flask. The total pressure was 115 Torr, which is well below the vapor pressure of (GeH3)2CH2 (248 Torr at 25° C.). The flask was connected to a gas injection manifold which was pumped to ˜10−8 Torr on the gas source MBE chamber.
- Prior to Ge growth, the Ge1-ySny/Si(100) substrates were sonicated for 5 minutes in methanol, dried by flowing N2 over their surface, inserted through a load lock into an ultra high vacuum (UHV) chamber at a base pressure of 5×10−10 Torr, and then heated on the sample holder for one hour at 250° C. to desorb any volatile surface contaminants until the chamber pressure was restored to the base value of 10−10 Torr. Under these conditions we find that the Ge1-ySny surfaces exhibit the typical (2×1) to (1×2) reconstruction, indicating a well-ordered crystallographic state suitable for subsequent heteroepitaxial growth.
- The temperature was then increased to 360-380° C. and the reactant gases were admitted at a final pressure of 5×10−5 Torr to commence film growth. The pressure was maintained constant (5×10−5 Torr) during growth via dynamic pumping using a corrosion resistant turbomolecular pump. Typical growth times from 30-60 minutes yielded films of thickness in the range 30-60 nm, respectively, at a fixed growth temperature of 360° C. The Ge films were deposited at a rate of 2 nm/min. Under these conditions Ge growth was observed to proceed via nucleation of nanoscale atomically-flat mesas which gradually coalesce to produce continuous films with planar surfaces as evidence by AFM characterizations.
- At growth temperatures of 380° C. and higher, a significant increase in growth rate and a surface morphology consisting of two-dimensional tiling formations based on rectangular mesas with variable shape and size were observed. On the length scale of the mesas (˜1 μm) the film surface is atomically flat; however, on the scale of 2-5 μm the surface roughness is higher due the presence of vertical steps between the mesas.
- The samples prepared according to Example 1 were extensively characterized for morphology, microstructure, purity and crystallographic properties by atomic force microscopy (AFM), Rutherford backscattering (RBS), secondary ion mass spectrometry (SIMS), cross sectional transmission electron microscopy (XTEM) and high resolution x-ray diffraction (XRD). The threading defects densities were estimated using an etch pit technique (EPD).
- As detailed below, the precise strain state of the Ge epilayers case can be systematically manipulated by varying the thickness and composition of the underlying template, for example, via tuning of the Sn content in the Ge1-ySny buffer. Growth of Ge layers on buffers with smaller/larger lattice constants, such as Ge1-ySny with y=0.015-0.035,) systematically produced larger strains in the Ge overlayers with increasing y, within the 1.5-3.5% range.
- We have used the Ge1-ySny buffer layers (y=0.015-0.035) to demonstrate that the highest reported tensile strains on Ge can be easily reproduced within this composition range, although record strains as high as 0.45% have already been achieved by our method. Advantageously, these buffer compositions have been shown to possess high thermal stability (up to 800° C.) and to be compatible with conventional CMOS processing.
- Combined Raman analysis and high-resolution x-ray diffraction using multiple off-axis reflections revealed unequivocally that the symmetry of tensile Ge was perfectly tetragonal. A downshift of the direct gap consistent with tensile strain has been observed.
- The degree of tensile strain alters the Ge band structure and induces a tunable redshift of the direct gap E0 absorption edge
FIG. 1 shows the quantitative changes in the band structure for 1% tensile strain in Ge. Small reductions in E0 can dramatically improve the detection performance of this material at 1.55 μm and beyond to cover the technologically important near-IR telecom bands for use in optical fiber communications. For sufficiently large tensile strain it has been predicted that Ge may become a direct gap system, with potential applications as an active lasing material (see, Menendez and Kouvetakis, J. Appl. Phys. Lett. 2004, 85, 1175). - In XTEM studies of the materials prepared according to Example 1 revealed monocrystalline Ge epilayer films possessing commensurate interfaces and atomically smooth surfaces regardless of the epilayer thickness. Electron micrographs demonstrated heteroepitaxial growth of a 60 nm thick Ge film on a 200 nm thick Ge1-ySny buffer with ε∥=0.25% (see,
FIGS. 2 & 3 ). The diffraction contrast image of the entire film thickness in (110) projection (FIG. 3 ) shows an atomically flat surface and a film devoid of threading dislocations within the field of view. - Surface flatness was confirmed on a larger 10×10 μm2 scale by AFM scans, which show RMS roughness values of 0.5 nm. A corresponding high resolution image showed a sharp interface between the two materials that is fully commensurate and defect-free. Occasional threading defects are observed to propagate, however, from the Si interface through the buffer and terminate at the Ge/GeSn interface, suggesting that deflection and bending of dislocations into the plane of this interface may be taking place.
- The typical RBS spectra (in random and channeled modes) showed consistently monocrystalline and perfectly aligned materials. The ratio of the aligned and random spectra (χmin), which measures the degree of epitaxial registry was extremely low, an χmin value of 10% within the Ge layer, close to the 3% limit for Si (100) wafers.
- Combined Raman analysis and high-resolution x-ray diffraction using multiple off-axis reflections reveal unequivocally that the symmetry of tensile Ge epilayers, with varying thickness, prepared according to Example 1 are perfectly tetragonal, while the strain state of the buffer remains essentially unchanged. A downshift of the direct gap consistent with tensile strain has been observed.
- The growth strategies herein provide controlled and reproducible Ge strain values exceeding those obtained to date, leading to values of tensile strain as high as 0.8%. The strain in this case can be systematically manipulated by varying the thickness and composition of the underlying template.
-
FIG. 4 shows a Raman spectrum from a tensile-strained Ge-film in a Ge/Ge0.975Sn0.025 structure. The Raman peak is clearly downshifted relative to the corresponding Raman peak in bulk Ge. Tetragonal strain splits the three-fold degenerate optical phonons at the center of the Ge Brillouin zone into a doublet and a singlet. For the (001) backscattering configuration used here, only the singlet is observable, and its shift relative to bulk Ge is given by Δω=bεp, with b=[q−p(C12/C11)]/ω0. Here p and q are the optical phonon anharmonic parameters, as defined, for example, in Anastassakis and Cardona in High Pressure in Semiconductor Physics II, ed. by T. Suski and W. Paul (Academic Press, New York, 1998)), and ω0 is the Raman frequency in bulk Ge. Using values from Anastassakis (supra), we obtain b=−415±40 cm−1. Thus from the observed Raman shift Δω=−1.0±0.1 cm−1, we deduce ε∥=−0.24±0.04%, in excellent agreement with the X-ray analysis. Moreover, initial photoreflectance experiments on this sample confirm the downshift of the direct gap induced by the tensile strain. -
FIG. 5 shows a typical Raman spectrum of a Ge/Ge0.965Sn0.035 sample compared to that of a bulk Ge reference. Again, the peak of the Ge film is shifted to lower energies, as expected for tensile strain. The results for this and similar samples are summarized inFIG. 6 , where we plot the Raman shifts of the Ge-films with strains intermediate to 0.15 and 0.43% (with respect to the Raman shift in pure Ge) as a function of the measured in-plane strain ε∥ obtained from XRD (infra). A monotonic and approximately linear dependence was observed, which confirms the XRD results. A fit with Eq. (1) yields bG e=436±18 cm−1. This overlaps considerably with the earlier results of Cerdeira et al. (see,Phys. Rev. B 1972, 5, 580). Thus we conclude that, as in the case of Si, the original strain shift coefficients determined in the 70's are sufficiently accurate to characterize strain using Raman spectroscopy. Finally we note that preliminary photoreflectance studies of selected samples have shown a downshift of the direct gap consistent with tensile strain. - The strain state of the Ge films was further investigated by recording line scans and reciprocal space maps for the symmetric (004), and asymmetric (224) Bragg reflections. In each case the data were referenced to the corresponding reflections of the Si wafer.
- The data were acquired with a PANalytical™ X′Pert MRD system (PANalytical B.V., Almelo, Netherlands) and were referenced for each sample to the corresponding reflections of the Si wafer.
FIG. 7 shows the (224) reciprocal space map for a Ge/Ge0.975Sn0.025 structure with epilayer and buffer thicknesses of 60 nm and 200 nm, respectively. - For the Ge0.975Sn0.025 layer, the diffracted intensity peaks lie very close to the full relaxation line ((224) line in
FIG. 7 ). A numerical fit yields α∥=5.6742 Å and α⊥,Ge=5.6794 Å, which corresponds to a compressive strain of −0.05%. The vertical alignment of the Ge and GeSn (224) peaks indicates a coherent heterostructure, while the considerable offset of the Ge peak with respect to the relaxation line implies a significant tensile strain. The measured in-plane (α∥,Ge=5.6719 Å) and vertical (α⊥,Ge=5.6476 Å) lattice parameters are related by the tetragonal strain relation ε⊥=2C12/C11ε∥, where C11 and C12 are bulk Ge elastic constants, and the strain is defined as ε∥=(π∥−α0)/α0 and ε⊥=(α⊥−α0)/α0. By averaging published experimental values for the elastic constants (see, O. Madelung, in Semiconductors, Landolt Borstein New Series III (Springer-Verlag, Berlin, N.Y., 2001), Vol. 41-A), we obtain 2C12/C11=0.72±0.04, from which we calculate α0=5.6578 Å. This is in excellent agreement with measurements in relaxed Ge films and with published values for the lattice constant of bulk Ge (see, Madelung, supra). Using the calculated relaxed lattice constant, we estimate for our sample a strain value ε∥=−0.25±0.02%, where the error arises from the scattering of the elastic constant data and the uncertainty in the determination of the maxima in the reciprocal space maps. - In previous work we showed that Ge1-ySny alloys display a compliant behavior when used as buffer layers for the growth of lattice-mismatched Ge1-x-ySixSny alloys (see, Tolle, et al., Appl. Phys. Lett. 88, 252112 (2006)). The lattice constant α∥ for the buffer and epilayer was found to approach the value predicted from a simple strain energy minimization expression that neglects the interaction with the Si substrate. For the sample in
FIG. 7 such a model predicts a compressive buffer strain ε∥=−0.08, in reasonably agreement with the observed value. To exp incorporate the same buffer layer but a much thicker Ge film (140 nm) than the previously discussed sample (60 nm). Then the compressive strain on the buffer layer should increase to ε∥=−0.14. - XRD data including the (224) and (004) reflections indicated that the buffers remain virtually unchanged with α∥,GeSn=5.6731 Å and α⊥,GeSn=5.6794 Å, which correspond to ε∥=−0.06. The lattice constants α∥,GeSn=5.6704 Å and α∥,GeSn=5.6731 Å are again very close, indicating the same degree of coherency as in the previous structure. The calculated unstrained Ge lattice constant (α0=5.6576 Å) is virtually identical to the one obtained for the previous sample. The strain analysis yields ε∥˜0.23%, which is nearly the same as that of the 60 nm thick Ge sample. This value is within the 0.02% error shown above. Therefore, these experiments do not show evidence for a compliant buffer behavior. It is interesting to point out, however, that in the present case the strain energy densities are smaller than in Tolle et al. (supra) by up to one order of magnitude, so that neglecting the buffer-substrate interaction may no longer be a good approximation.
- The larger scattering volume of the 140 nm thick sample enabled us to measure typically weak off-axis peaks such as the (135) and (135) reflections. These have h<k and accordingly they are sensitive to deviations from a tetragonal distortion. If the Ge film distortion is of lower symmetry than tetragonal, the in-plane value derived from these reflections will deviate significantly from their (224) counterpart. Table 1 compares both the in-plane and vertical lattice constants (α∥ and α⊥ respectively), for the Si substrate, the GeSn buffer layer and the strained Ge epilayer. In all three cases the in-plane lattice constant values obtained independently from the (135), (135) and (224) analysis are identical, within instrumental resolution.
-
TABLE 1 In-plane and perpendicular lattice constants for the Si substrate, Ge0.975Sn0.025 buffer layer and strained Ge epilayer as determined from independent x-ray reflections (004), (224), (135) and (135) Reflection a (Å) c (Å) Si (004) 5.4306 (224) 5.4305 5.4305 (135) 5.4306 5.4307 ( 1 35)5.4305 5.4305 5.4305 5.4306 GeSn (004) 5.6801 (224) 5.6731 5.6794 (135) 5.6735 5.6798 ( 1 35)5.6730 5.6800 5.6702 5.6798 Ge (004) 5.6484 (224) 5.6703 5.6482 (135) 5.6704 5.6485 ( 1 35)5.6702 5.6484 5.6703 5.6484
A similar independent analysis of the (004), (135), (135) and (224) peaks also yields vertical lattice constants that are virtually identical within experimental error. Collectively these data demonstrate that the Ge epilayer displays a perfect tetragonal distortion, verifying the underlying assumption in our strain analysis above. In addition, Table 1 shows that Si is perfectly cubic as expected, and that the buffer is only slightly compressed, as shown inFIG. 8 , where the diffraction maps for the (135) peaks of the Ge epilayer and GeSn buffer are shown. It should be noted that for samples grown on unrelaxed GeSn buffers we consistently observe discrepancies in the α∥ parameter derived from the (224), (135) and (135) reflections, demonstrating a non-tetragonal deformation. This indicates that residual compressive strains in the as grown buffers lead to tensile strained Ge layers possessing complicated lower symmetries associated with monoclinic or orthorhombic distortions. This emphasizes the crucial need to relax the buffers prior to any subsequent depositions. Interestingly, we find that a combination of X-ray diffraction and Raman spectroscopy provided (see, Example 2b) a quick way to identify non-tetragonal distortions. If we use the (224) reciprocal space maps and assume a tetragonal distortion to deduce the strain, the value obtained from the X-ray analysis and from Raman spectroscopy agree within experimental error for perfectly tetragonal samples, but differ by factors as high as two if the sample distortion is of lower symmetry than tetragonal. -
FIG. 9 shows the (224) spectra of a representative sample with composition Ge/Ge0.965Sn0.035, and epilayer/buffer thicknesses of ˜60/230 nm. The thicker Ge0.965Sn0.035 layer was also found to be essentially relaxed and nearly cubic (α∥,GeSn=5.6872 Å, α⊥,GeSn=5.6955 Å). This was further confirmed by the close proximity of the GeSn peak maximum to the relaxation line connecting the corresponding Si (224) peak to the origin of the plot. The plots also show a near perfect vertical alignment of the Ge and GeSn (224) peaks indicating a fully coherent stack as shown by the dotted line inFIG. 9 . Note the considerable vertical offset of the Ge peak with respect to the relaxation line, indicating a significant tensile strain which is manifested as a tetragonal distortion that accommodates the large lattice mismatch with the buffer. The ideal strain equilibration behavior of the Ge/Ge0.965Sn0.035 sample is plotted inFIG. 10 which shows that most of the strain energy minimization is accounted for by the expansion of the Ge epilayer in the a-b plane. This indicates that for thick (>200 nm) buffers very little change in the dimensions of the buffer is expected. - To derive the precise values of the in-plane (ε∥) and perpendicular (ε⊥) strain values we conducted a quantitative analysis of the XRD data assuming that the epitaxial Ge films adopt a purely tetragonal distortion, relative to their unstrained cubic form, in which ε∥=(a∥−a0)/a0 and ε⊥=(a⊥−a0)/a0 (where a∥, a⊥ and a0 are the measured in-plane, vertical and relaxed lattice constants). The two strains are related by ε⊥=2C12/C11ε∥, which we can write ε⊥=−ξε∥, with ξ=2C12/C11 (where C12 and C11 are the elastic constants). The strain relation can be inverted to obtain the unstrained lattice constant a0=(a⊥+ξa∥)/(1+ξ), the ε∥=(a∥−a⊥)/(a⊥+ξa∥) and the ε⊥=ξ(a⊥−a∥)/(a⊥+ξa∥) of the film. For the elastic constants we adopt the values C11=128.5 GPa, C12=48.3 GPa from Madelung (supra). while for strained Ge film we use a∥,Ge=5.6802 Å and a⊥,Ge=5.6416 Å obtained from XRD. These data yield parallel and perpendicular strain values of ε∥˜+0.40% and ε⊥˜−0.30%, and an unstrained Ge lattice constant of a0=5.658 Å, in excellent agreement with the known bulk Ge value. Taking differentials of the strain relations above yields the following expression:
-
- Thus a fractional error in the elastic ratio ξ=2C12/C11 produces half this error in the in-plane strain. For instance, if C11=129±3 GPa and C12=48±3 GPa, (see, Madelung, supra), then ξ=0.75±0.07 (±9.3%) which implies a corresponding fractional error of only ˜5% in the in-plane strain. So, for the Ge/Ge0.965Sn0.035 we obtain ε∥˜0.40±0.03%. The corresponding strain value obtained by Raman (see below) is ε∥˜0.43 well within the 0.03% error. This value represents the highest tensile strain observed in elemental Ge semiconductors to date.
- Extensive XRD studies of a wide range of tensile strained Ge films grown on Ge1-ySny (y=0.015-0.035) indicated strain states between 0.15-0.43%, respectively. The XTEM data of these samples revealed monocrystalline films possessing commensurate interfaces and atomically smooth surfaces regardless of the epilayer thickness.
FIGS. 11 and 12 shows electron micrographs of the Ge/Ge0.965Sn0.035 sample indicating a 60 nm thick Ge layer grown epitaxially on a 230 nm thick Ge1-ySny buffer. The bright field image shows essentially no penetrating threading defects over an extended lateral range of 1 μm and the high resolution micrograph near the Ge/Si interface reveals a sharp, commensurate transition between the epilayer and the buffer, AFM analysis of the sample shows that the surface is predominantly flat, with an RMS roughness of ˜1.5 nm over a typical 5×5 μm2 area [FIG. 13 ]. On a smaller 0.5×0.5 μm2 scale we observe atomically smooth surfaces with a reduced RMS roughness of ˜0.2 nm. The difference in these values is associated with the presence of tiny voids located at the intersection of individual coalescing terraces as described previously. In thicker films these terraces coalesce fully and such features are not longer visible. In contrast, the growth of pure Ge2H6 in the absence of the organic additive (GeH3)2CH2 produces defective and rough films with classic island-like surface morphology consistent with a mismatched heteroepitaxy growth mode. This observation confirms the notion that the organic additives significantly alter the surface energetics, promoting organized assembly of planar Ge films at conditions that would normally preclude their growth directly on GeSn on the basis of surface energy differences. Note that analogous differences in surface energetics prevent the heteroepitaxial growth of silicon films directly on a Ge surface. However, as we have demonstrated above, the pseudosurfactant properties of the organic additives enable the remarkable and unconventional growth of fully strained and perfectly planar Si layers on Ge buffers. - In one example of Ge epilayer strain tuning via Sn content in the buffer, we conducted growth of Ge layers on buffers with smaller/larger lattice constants such as Ge1-ySny with y=0.015-0.035. For samples with the similar Ge/GeSn film thickness ratio we find ε∥=0.17% for y=0.015 and ε∥=0.45% for y=0.035 (see,
FIG. 3 ). Increasing y (within the 1.5-3.5% range) produces systematically larger strains in the Ge overlayers. - In summary, we have demonstrated the growth of tensile strained Ge films on Ge1-ySny/Si composite substrates. Our approach is straightforward and suitable for large-scale integration. Contrary to the thermal expansion processes, our growth proceeds at low temperatures (˜380° C.) compatible with selective growth.
Claims (9)
1. A semiconductor structure produced by a method comprising:
a) forming a Ge1-ySny buffer layer on a semiconductor substrate; and
b) forming a tensile strained Ge layer on the Ge1-ySny buffer layer using an admixture of (GeH3)2CH2 and Ge2H6 in a ration of between 1:10 and 1:30.
2. A semiconductor structure comprising:
a semiconductor substrate,
a Ge1-ySny buffer layer formed over the substrate, and
a tensile strained Ge layer formed over the Ge1-ySny buffer layer.
3. The semiconductor structure of claim 2 , wherein the tensile strained Ge layer has an essentially atomically flat surface.
4. The semiconductor structure of claim 2 , wherein the substrate comprises silicon.
5. The semiconductor structure of claim 2 , wherein y is between 0.015-0.045.
6. The semiconductor structure of claim 2 , wherein the Ge1-ySny buffer layer is at least 95% relaxed.
7. The semiconductor structure of claim 2 , wherein the symmetry of the tensile Ge layer is tetragonal.
8. The semiconductor structure of claim 2 , wherein the Ge layer has a tunable tensile strain of between 0.15% and 0.45%
9. The semiconductor structure of claim 2 , wherein the Ge layer is formed directly on the Ge1-ySny buffer layer.
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US20190113468A1 (en) * | 2017-10-13 | 2019-04-18 | Infineon Technologies Austria Ag | Method for Determining the Concentration of an Element of a Heteroepitaxial Layer |
WO2020243831A1 (en) * | 2019-06-03 | 2020-12-10 | Moutanabbir Oussama | Quantum heterostructures, related devices and methods for manufacturing the same |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8647439B2 (en) * | 2012-04-26 | 2014-02-11 | Applied Materials, Inc. | Method of epitaxial germanium tin alloy surface preparation |
US20140077339A1 (en) * | 2012-09-14 | 2014-03-20 | Radek Roucka | DELTA DOPING AT Si-Ge INTERFACE |
US9330907B2 (en) | 2013-10-10 | 2016-05-03 | The Board Of Trustees Of The Leland Stanford Junior University | Material quality, suspended material structures on lattice-mismatched substrates |
US9299566B2 (en) * | 2014-02-25 | 2016-03-29 | Tsinghua University | Method for forming germanium-based layer |
CN105895727B (en) * | 2016-04-22 | 2017-07-28 | 西安电子科技大学 | Photodetector based on relaxation GeSn materials |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2988427A (en) * | 1957-07-17 | 1961-06-13 | Kali Chemie Ag | Method for the purification of hydrides of silicon and germanium group of the periodic system |
US4777023A (en) * | 1986-02-18 | 1988-10-11 | Solarex Corporation | Preparation of silicon and germanium hydrides containing two different group 4A atoms |
US4910153A (en) * | 1986-02-18 | 1990-03-20 | Solarex Corporation | Deposition feedstock and dopant materials useful in the fabrication of hydrogenated amorphous silicon alloys for photovoltaic devices and other semiconductor devices |
US6897471B1 (en) * | 2003-11-28 | 2005-05-24 | The United States Of America As Represented By The Secretary Of The Air Force | Strain-engineered direct-gap Ge/SnxGe1-x heterodiode and multi-quantum-well photodetectors, laser, emitters and modulators grown on SnySizGe1-y-z-buffered silicon |
US7238596B2 (en) * | 2003-06-13 | 2007-07-03 | Arizona Board of Regenta, a body corporate of the State of Arizona acting for and on behalf of Arizona State University | Method for preparing Ge1-x-ySnxEy (E=P, As, Sb) semiconductors and related Si-Ge-Sn-E and Si-Ge-E analogs |
US20070297967A1 (en) * | 2004-09-14 | 2007-12-27 | Arizona Board Of Regents | Hydride Compounds With Silicon And Germanium Core Atoms And Method Of Synthesizing Same |
US20080113186A1 (en) * | 2004-09-14 | 2008-05-15 | John Kouvetakis | Method for Growing Si-Ge Semiconductor Materials and Devices on Substrates |
US20090050935A1 (en) * | 2005-11-23 | 2009-02-26 | The Arizona Board Ofg Regents, A Body Corporate Acting On Behalf Of Arizona State University | Silicon-Germanium Hydrides and Methods for Making and Using Same |
US7589003B2 (en) * | 2003-06-13 | 2009-09-15 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University, A Corporate Body Organized Under Arizona Law | GeSn alloys and ordered phases with direct tunable bandgaps grown directly on silicon |
US7594967B2 (en) * | 2002-08-30 | 2009-09-29 | Amberwave Systems Corporation | Reduction of dislocation pile-up formation during relaxed lattice-mismatched epitaxy |
US7598513B2 (en) * | 2003-06-13 | 2009-10-06 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University, A Corporate Body Organized Under Arizona Law | SixSnyGe1-x-y and related alloy heterostructures based on Si, Ge and Sn |
US20100012972A1 (en) * | 2005-11-23 | 2010-01-21 | The Arizona Board of Regents, a body corparate acting onbehalf of Arizona State University | Silicon-Germanium Hydrides and Methods for Making and Using Same |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5202284A (en) | 1989-12-01 | 1993-04-13 | Hewlett-Packard Company | Selective and non-selective deposition of Si1-x Gex on a Si subsrate that is partially masked with SiO2 |
DE4306106A1 (en) | 1993-02-27 | 1994-09-01 | Thomas Dipl Chem Lobreyer | Method for preparing silylgermanes |
AU2002368035A1 (en) * | 2002-06-19 | 2004-01-06 | Massachusetts Institute Of Technology | Ge photodetectors |
US7540920B2 (en) | 2002-10-18 | 2009-06-02 | Applied Materials, Inc. | Silicon-containing layer deposition with silicon compounds |
KR101060372B1 (en) | 2004-09-14 | 2011-08-29 | 아리조나 보드 오브 리전트스, 아리조나주의 아리조나 주립대 대행법인 | Growth method of Si-Si semiconductor material and device on substrate |
US7596158B2 (en) * | 2005-10-28 | 2009-09-29 | Massachusetts Institute Of Technology | Method and structure of germanium laser on silicon |
-
2008
- 2008-06-04 US US12/133,221 patent/US7915104B1/en not_active Expired - Fee Related
-
2011
- 2011-02-23 US US13/033,361 patent/US20110198729A1/en not_active Abandoned
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2988427A (en) * | 1957-07-17 | 1961-06-13 | Kali Chemie Ag | Method for the purification of hydrides of silicon and germanium group of the periodic system |
US4777023A (en) * | 1986-02-18 | 1988-10-11 | Solarex Corporation | Preparation of silicon and germanium hydrides containing two different group 4A atoms |
US4910153A (en) * | 1986-02-18 | 1990-03-20 | Solarex Corporation | Deposition feedstock and dopant materials useful in the fabrication of hydrogenated amorphous silicon alloys for photovoltaic devices and other semiconductor devices |
US7594967B2 (en) * | 2002-08-30 | 2009-09-29 | Amberwave Systems Corporation | Reduction of dislocation pile-up formation during relaxed lattice-mismatched epitaxy |
US7238596B2 (en) * | 2003-06-13 | 2007-07-03 | Arizona Board of Regenta, a body corporate of the State of Arizona acting for and on behalf of Arizona State University | Method for preparing Ge1-x-ySnxEy (E=P, As, Sb) semiconductors and related Si-Ge-Sn-E and Si-Ge-E analogs |
US7589003B2 (en) * | 2003-06-13 | 2009-09-15 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University, A Corporate Body Organized Under Arizona Law | GeSn alloys and ordered phases with direct tunable bandgaps grown directly on silicon |
US7598513B2 (en) * | 2003-06-13 | 2009-10-06 | Arizona Board Of Regents, Acting For And On Behalf Of Arizona State University, A Corporate Body Organized Under Arizona Law | SixSnyGe1-x-y and related alloy heterostructures based on Si, Ge and Sn |
US6897471B1 (en) * | 2003-11-28 | 2005-05-24 | The United States Of America As Represented By The Secretary Of The Air Force | Strain-engineered direct-gap Ge/SnxGe1-x heterodiode and multi-quantum-well photodetectors, laser, emitters and modulators grown on SnySizGe1-y-z-buffered silicon |
US20070297967A1 (en) * | 2004-09-14 | 2007-12-27 | Arizona Board Of Regents | Hydride Compounds With Silicon And Germanium Core Atoms And Method Of Synthesizing Same |
US20080113186A1 (en) * | 2004-09-14 | 2008-05-15 | John Kouvetakis | Method for Growing Si-Ge Semiconductor Materials and Devices on Substrates |
US20090050935A1 (en) * | 2005-11-23 | 2009-02-26 | The Arizona Board Ofg Regents, A Body Corporate Acting On Behalf Of Arizona State University | Silicon-Germanium Hydrides and Methods for Making and Using Same |
US20100012972A1 (en) * | 2005-11-23 | 2010-01-21 | The Arizona Board of Regents, a body corparate acting onbehalf of Arizona State University | Silicon-Germanium Hydrides and Methods for Making and Using Same |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190113468A1 (en) * | 2017-10-13 | 2019-04-18 | Infineon Technologies Austria Ag | Method for Determining the Concentration of an Element of a Heteroepitaxial Layer |
US10718726B2 (en) * | 2017-10-13 | 2020-07-21 | Infineon Technologies Austria Ag | Method for determining the concentration of an element of a heteroepitaxial layer |
WO2020243831A1 (en) * | 2019-06-03 | 2020-12-10 | Moutanabbir Oussama | Quantum heterostructures, related devices and methods for manufacturing the same |
US20220310793A1 (en) * | 2019-06-03 | 2022-09-29 | Oussama Moutanabbir | Quantum heterostructures, related devices and methods for manufacturing the same |
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