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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 76 (1994), S. 5748-5753 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Single domain GaAs layers have been grown by atmosphere pressure metal-organic vapor phase epitaxy on Ge(100) substrates misoriented to (111) with different angles of 0°–4°, under various growth conditions. Epilayers have been studied by transmission electron microscopy, molten KOH etch and optical interference contrast microscopy. It is found that at an initial growth temperature of 550 °C the sublattice location of the GaAs layers grown on substrates with small misorientation angles (less than 3°) is reversed as compared to that of the layers grown on substrates with larger misorientation angles, independent of the initial growth rates and V/III ratios. When the initial growth temperature is increased the transition from one type of sublattice location to the other occurs at a lower misorientation angle, while at an initial growth temperature of 700 °C the sublattice location of the layers grown on the different substrates becomes the same. These results can hardly be explained by the existing theories and a new model is proposed based on a concept that the sublattice location of GaAs on Ge is defined by the relative intensity of nucleation at steps and on terraces between steps, taking into account the effects of the growth temperature and the step density of the substrate surface on the nucleation mode, and the fact that single domain GaAs can be obtained by the self-annihilation of antiphase boundaries.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 79 (1996), S. 1357-1364 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Localized {100} fiber textured diamond films were grown by addition of 20–200 ppm nitrogen into the gas phase during hot-filament chemical-vapor deposition (CVD). Cathodoluminescence indicates the presence of the nitrogen-vacancy system in the {100} textured diamond, whereas a blue "band A'' luminescence is normally observed in diamond films grown without nitrogen addition. The results demonstrate that the nature of the substrates used for growth has no appreciable influence on the {100} texture, which implies that this fiber texture is obtained by competitive growth and selection of facets. The interaction of nitrogen with the {100} surface is a highly important factor in this process. Homoepitaxial growth shows that the addition of a small amount of nitrogen greatly enhances the growth rate of the {100} faces, making 〈100〉 the fastest growth direction in comparison with the 〈110〉 and 〈111〉 directions. This is attributed to breaking of a part of the dimers on the (2×1) reconstructed {100} surface by nitrogen compounds. The {100} texture in narrow, ring-shaped areas on diamond layers grown by the flame technique can also be attributed to the occurrence of a certain amount of nitrogen in the gas phase. It is demonstrated that the flame grown polycrystalline diamond layers have morphologies and cathodoluminescence features that are consistent with those observed in the hot-filament CVD diamond films grown with the addition of nitrogen. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 2376-2384 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The homoepitaxial deposition of diamond layers on {111} and {001} type-IIa natural diamond substrates, by both laminar and turbulent acetylene-oxygen flames, is described. Using the same gas flows, temperatures, and supersaturations of 4%, a higher growth rate was obtained on a {001} substrate with a turbulent flame than with a laminar flame. Layers grown at the same temperature on {111} substrates with a supersaturation of 3% show no significant difference in growth rate. Due to the large differences in geometry between both types of flames it is not possible to relate the substrate positions in the acetylene feathers to each other and compare the growth results at any location. However, it is shown that the application of turbulent flames for single-crystal growth does not lead to a dramatic change in quality of the diamond as was previously reported in the literature. It is demonstrated by microscopic and spectroscopic techniques that the crystallographic orientation of the substrates, the deposition temperature, and the gas velocity all have a larger influence on the crystal morphology and impurity incorporation of the grown single crystals than the introduction of turbulence. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 3125-3131 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Homoepitaxial diamond films codoped with phosphorus and nitrogen have been grown on natural diamond substrates using phosphine and nitrogen as doping sources by hot-filament chemical-vapor deposition. The experiments show that the incorporation of nitrogen enhances both the phosphorus incorporation and the film growth rate. The former is attributed to the local lattice dilatation caused by nitrogen, while the latter can be explained by defects induced on the surface of diamond by nitrogen or by a change in gaseous composition. The highest concentrations of phosphorus and nitrogen in the epitaxial films are approximately 3×1019 and 6×1019 atoms/cm3, respectively, determined by secondary-ion-mass spectrometry; however, these epilayers are highly resistive. Furthermore, cathodoluminescence and photoluminescence studies show that despite the variety of luminescence features related to nitrogen, no indication of phosphorus induced luminescence is found in the infrared to visible range. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 60 (1986), S. 3735-3745 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Photoluminescence studies have been performed on undoped and silicon-doped GaAs crystals, which were annealed between 650 and 1000 °C under different arsenic pressures. Samples were also heat treated with the addition of pure elemental Ga, Mn, or Cu. Spectra were taken in the energy range 1.15–1.55 eV at the surfaces of the annealed crystals and at various depths below the surface. Newly observed zero-phonon emissions at 1.31 and 1.347 eV are concluded to be related to CuGa-(VAs)2 and CuGa-VAs, respectively. An emission at 1.467 eV also was found to be related to a CuGa-containing complex. A new emission at 1.342 eV was found to be related to a fast diffusing MnGa-containing complex. Most likely, the emission originates from a MnAs center. The nature of these defects is discussed on the basis of their emission characteristics, diffusion behavior, and dependence on annealing parameters. Through this study it appeared that arsenic vacancies play a crucial role both in the establishment of defect equilibria and in the formation of complexes with MnGa and CuGa. A new luminescence peak at 1.448 eV was found to be related to the VAs defect. Most probably, it has to be associated with the GaAs antisite. The presence of arsenic vacancies also induces a shift of the 1.492-eV emission to 1.484 eV. This shift is attributed to the replacement of CAs by SiAs acceptors. Some evidence was found that a peak at 1.38 eV is associated with VGa. It is concluded that solid-state equilibrium of native defects and impurities is only established at the surfaces but not in the bulk of the crystal during the heat treatments.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The temperature-dependent behavior of the solid composition xs of AlxGa1−xAs has systematically been studied as a function of gas phase composition xg in an optimized horizontal metalorganic vapor phase epitaxy reactor at atmospheric pressure. Up to a temperature of 660 °C the Al incorporation is constant but slightly exceeds the Ga incorporation. Above this temperature the Al incorporation strongly increases with temperature. This behavior is most probably related to a change in growth mechanism from mass transport limited growth to a regime where the growth is controlled by thermodynamics, especially for the gallium species.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 60 (1986), S. 1648-1660 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The incorporation of impurities in GaAs epitaxial layers grown from trimethyl gallium (TMG) and AsH3 has been studied in detail by varying a large number of growth parameters. These include the V/III ratio, temperature, the axial position in the reactor, gas sources, substrate and susceptor material, carrier gas, substrate misorientation, and the crystallographic orientation of the substrate. As main characterization techniques photoluminescence and Hall–van der Pauw measurements have been used. Donor and acceptor concentrations in the layers have been found to vary not only with temperature and V/III ratio, but also with the axial position in the reactor, giving rise to p/n transitions and maxima in the carrier mobility. The V/III ratio is shown to be effectively constant for larger axial distances in the cell. Highly doped substrates have been found to give rise to outdiffusion of defect complexes into the layers. The main acceptor impurities found in this work are zinc, silicon, and carbon. They are shown to originate from the TMG gas source, the hot quartz parts in the cell, and the TMG growth component, respectively. Incorporation of these elements appears to be orientation, and in the case of carbon also misorientation, dependent. The results for {001} and misoriented {001} crystals are discussed on the basis of two models for impurity incorporation: CAs acceptors are concluded to be incorporated by a trapping process at growth steps, whereas ZnGa, SiAs, and residual donors most probably incorporate via equilibrium processes. The conclusions from a study of the influence of the misorientation are especially important for this interpretation.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 58 (1985), S. 219-222 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Indium phosphide samples (n and p type) have been photoetched in solutions consisting of CrO3-HF-H2O, i. e., in diluted Sirtl or Sirtl-like mixtures under laser or white light illumination. The method proved to be very sensitive for the delineation of defects and inhomogeneities in substrates and epitaxial layers. In n-type InP an etch depth of 0.05–0.3 μm is sufficient to reveal dislocations, growth striations, precipitates, and linear defects or to delineate epijunctions in cross sections. In p-type material, removal of 0.5–1 μm is required to obtain a clear picture of the defects. In contrast to n-type material the results for p-type InP are similar with and without illumination. The method has been calibrated with Huber etch.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 73 (1993), S. 7798-7803 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A detailed study of the photoluminescence (PL) and photoluminescence excitation (PLE) properties of Al0.48In0.52As is presented. A PL linewidth of 13 meV and a Stokes shift of only 9 meV at 4.2 K both indicate that the effect of clustering is minimal in our samples. The Stokes shift is three times lower than the lowest reported in the literature. No shift was observed in the position of the PL peak with changing excitation intensity. Both the PL energy and intensity showed anomalous temperature behavior: The energy first decreased, then increased, and finally decreased again with increasing temperature (the so-called inverted S shape); the intensity showed a temperature dependence similar to that of amorphous semiconductors and disordered superlattices. These two phenomena suggest strong localization of carriers in Al0.48In0.52As, even when the effect of clustering is minimal. The PLE spectra showed excitonic enhancement only above 40 K. The first observation of phonons with PL is reported in Al0.48In0.52As. Energies of 29.6 and 45.9 meV were measured for the InAs-like and the AlAs-like LO phonons, respectively. These phonons could only be detected below 40 K, which, on the basis of selection rules for LO phonon scattering, confirms the localized nature of the luminescence.
    Type of Medium: Electronic Resource
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