Reflection electron energy loss spectroscopy during initial stages of Ge growth on Si by molecular beam epitaxy

Using a conventional reflection high-energy electron diffraction gun together with an electron energy loss spectrometer, we have combined in situ measurements of inelastic scattering intensities from Si L2,3 and Ge L2,3 core losses with reflection electron diffraction data in order to analyze the initial stages of Ge heteroepitaxy on Si(001). Diffraction data indicate an initial layer-by-layer growth mode followed by island formation for Ge thicknesses greater than 0.8–1.1 nm. The electron energy core loss data are consistent with a simple model of grazing incidence electron scattering from the growing Ge film. Reflection electron energy loss spectroscopy is found to be highly surface sensitive, and the energy resolution and data rate are also sufficiently high to suggest that reflection electron energy loss spectroscopy may be a useful real-time, in situ surface chemical probe during growth by molecular beam epitaxy

Nonlithographic epitaxial Sn_xGe_(1–x) dense nanowire arrays grown on Ge(001)

We have grown 1-µm-thick Sn_xGe_(1–x)/Ge(001) epitaxial films with 0 < x < 0.085 by molecular-beam epitaxy. These films evolve during growth into a dense array of Sn_xGe_(1–x) nanowires oriented along [001], as confirmed by composition contrast observed in scanning transmission electron microscopy in planar view. The Sn-rich regions in these films dominate optical absorption at low energy; phase-separated Sn_xGe_(1–x) alloys have a lower-energy band gap than homogeneous alloys with the same average Sn composition

Temperature‐dependent transmission extended electron energy‐loss fine structure of aluminum

Inelastic electron scattering experiments in a transmission electron microscope provide a probe of core electron excitations that have binding energies below 2 keV, and that are localized within submicron diameter sample volumes. Extended electron energy‐loss fine‐structure measurements which show the variation with temperature of the mean squared relative displacement of aluminum yield a localized measurement of the Debye temperature which is in excellent agreement with macroscopic measurements

Local order measurement in SnGe alloys and monolayer Sn films on Si with reflection electron energy loss spectrometry

Measurements of local order are demonstrated in Sn-containing alloys and epitaxial monolayer thickness films by analysis of extended-edge energy loss fine structure (EXELFS) data obtained by reflection electron energy loss spectrometry (REELS). These measurements of short-range order provide a complement to the chemical information obtained with REELS and long-range order obtained using reflection high energy electron diffraction. The results suggest that EXELFS measurements are practical for samples mounted on the growth manipulator in a molecular beam epitaxy chamber. Advantages and limitations of reflection EXELFS are discussed

Facet modulation selective epitaxy–a technique for quantum-well wire doublet fabrication

The technique of facet modulation selective epitaxy and its application to quantum-well wire doublet fabrication are described. Successful fabrication of wire doublets in the AlxGa1–xAs material system is achieved. The smallest wire fabricated has a crescent cross section less than 140 Å thick and less than 1400 Å wide. Backscattered electron images, transmission electron micrographs, cathodoluminescence spectra, and spectrally resolved cathodoluminescence images of the wire doublets are presented

In situ reflection electron energy loss spectroscopy measurements of low temperature surface cleaning for Si molecular beam epitaxy

In situ analysis of hydrocarbon desorption from hydrogen terminated Si(100) surfaces was performed in a silicon molecular beam epitaxy system, using reflection electron energy loss spectroscopy, in conjunction with conventional reflection high energy electron diffraction analysis. Measurements of C K edge core loss intensities demonstrate that this method is sufficiently sensitive to enable in situ analysis of hydrocarbon desorption at fractional monolayer coverages during low-temperature isothermal anneals. Hydrocarbon desorption was found to begin at 115 °C, and at 200 °C complete desorption occurred within 10 min. Hydrocarbon coverage was not measurably affected by operation of ionization gauge filaments during low temperature anneals, but was increased by transient outgassing of the sample holder, and its environs

A Generalized Law of Corresponding States for the Physisorption of Classical Gases with Cooperative Adsorbate-Adsorbate Interactions

The Law of Corresponding States for classical gases is well established. Recent attempts at developing an analogous Law of Corresponding States for gas physisorption, however, have had limited success, in part due to the omission of relevant adsorption considerations such as the adsorbate volume and cooperative adsorbate-adsorbate interactions. In this work, we modify a prior Law of Corresponding States for gas physisorption to account for adsorbate volume, and test it with experimental data and a generalized theoretical approach. Furthermore, we account for the recently-reported cooperative adsorbate-adsorbate interactions on the surface of zeolite-templated carbon (ZTC) with an Ising-type model, and in doing so, show that the Law of Corresponding States for gas physisorption remains valid even in the presence of atypically enhanced adsorbate-adsorbate interactions

Anomalous Isosteric Enthalpy of Adsorption of Methane on Zeolite-Templated Carbon

A thermodynamic study of the enthalpy of adsorption of methane on high surface area carbonaceous materials was carried out from 238 to 526 K. The absolute quantity of adsorbed methane as a function of equilibrium pressure was determined by fitting isotherms to a generalized Langmuir-type equation. Adsorption of methane on zeolite-templated carbon, an extremely high surface area material with a periodic arrangement of narrow micropores, shows an increase in isosteric enthalpy with methane occupancy; i.e., binding energies are greater as adsorption quantity increases. The heat of adsorption rises from 14 to 15 kJ/mol at near-ambient temperature and then falls to lower values at very high loading (above a relative site occupancy of 0.7), indicating that methane/methane interactions within the adsorption layer become significant. The effect seems to be enhanced by a narrow pore-size distribution centered at 1.2 nm, approximately the width of two monolayers of methane, and reversible methane delivery increases by up to 20% over MSC-30 at temperatures and pressures near ambient

SiGeC/Si superlattice microcoolers

Monolithically integrated active cooling is an attractive way for thermal management and temperature stabilization of microelectronic and optoelectronic devices. SiGeC can be lattice matched to Si and is a promising material for integrated coolers. SiGeC/Si superlattice structures were grown on Si substrates by molecular beam epitaxy. Thermal conductivity was measured by the 3omega method. SiGeC/Si superlattice microcoolers with dimensions as small as 40×40 µm^2 were fabricated and characterized. Cooling by as much as 2.8 and 6.9 K was measured at 25 °C and 100 °C, respectively, corresponding to maximum spot cooling power densities on the order of 1000 W/cm^2

A Thermodynamic Investigation of Adsorbate-Adsorbate Interactions of Carbon Dioxide on Nanostructured Carbons

A thermodynamic study of carbon dioxide adsorption on a zeolite-templated carbon (ZTC), a superactivated carbon (MSC-30) and an activated carbon (CNS-201) was carried out at temperatures from 241 to 478 K and pressures up to 5.5•10^6 Pa. Excess adsorption isotherms were fitted with generalized Langmuir-type equations, allowing the isosteric heats of adsorption and adsorbed-phase heat capacities to be obtained as a function of absolute adsorption. On MSC-30, a superactivated carbon, the isosteric heat of carbon dioxide adsorption increases with occupancy from 19 to 21 kJ•mol^(−1), before decreasing at high loading. This increase is attributed to attractive adsorbate-adsorbate intermolecular interactions as evidenced by the slope and magnitude of the increase in isosteric heat and the adsorbed-phase heat capacities. An analysis of carbon dioxide adsorption on ZTC indicates a high degree of binding-site homogeneity. A generalized Law of Corresponding States analysis indicates lower carbon dioxide adsorption than expected