769 research outputs found
Monte Carlo study of Si(111) homoepitaxy
An attempt is made to simulate the homoepitaxial growth of a Si(111) surface
by the kinetic Monte Carlo method in which the standard Solid-on-Solid model
and the planar model of the (7x7) surface reconstruction are used in
combination.
By taking account of surface reconstructions as well as atomic deposition and
migrations, it is shown that the effect of a coorparative stacking
transformation is necessary for a layer growth.Comment: 4 pages, 5 figures. For Fig.1 of this article, please see Fig.2 of
Phys.Rev. B56, 3583 (1997). To appear in Phys.Rev.B. (June 1998
Structure analysis of the Ga-stabilized GaAs(001)-c(8x2) surface at high temperatures
Structure of the Ga-stabilized GaAs(001)-c(8x2) surface has been studied
using rocking-curve analysis of reflection high-energy electron diffraction
(RHEED). The c(8x2) structure emerges at temperatures higher than 600C, but is
unstable with respect to the change to the (2x6)/(3x6) structure at lower
temperatures. Our RHEED rocking-curve analysis at high temperatures revealed
that the c(8x2) surface has the structure which is basically the same as that
recently proposed by Kumpf et al. [Phys. Rev. Lett. 86, 3586 (2001)]. We found
that the surface atomic configurations are locally fluctuated at high
temperatures without disturbing the c(8x2) periodicity.Comment: 14 pages, 4 figures, 1 tabl
Magic Islands and Barriers to Attachment: A Si/Si(111)7x7 Growth Model
Surface reconstructions can drastically modify growth kinetics during initial
stages of epitaxial growth as well as during the process of surface
equilibration after termination of growth. We investigate the effect of
activation barriers hindering attachment of material to existing islands on the
density and size distribution of islands in a model of homoepitaxial growth on
Si(111)7x7 reconstructed surface. An unusual distribution of island sizes
peaked around "magic" sizes and a steep dependence of the island density on the
growth rate are observed. "Magic" islands (of a different shape as compared to
those obtained during growth) are observed also during surface equilibration.Comment: 4 pages including 5 figures, REVTeX, submitted to Physical Review
Diffusion of hydrogen in crystalline silicon
The coefficient of diffusion of hydrogen in crystalline silicon is calculated
using tight-binding molecular dynamics. Our results are in good quantitative
agreement with an earlier study by Panzarini and Colombo [Phys. Rev. Lett. 73,
1636 (1994)]. However, while our calculations indicate that long jumps dominate
over single hops at high temperatures, no abrupt change in the diffusion
coefficient can be observed with decreasing temperature. The (classical)
Arrhenius diffusion parameters, as a consequence, should extrapolate to low
temperatures.Comment: 4 pages, including 5 postscript figures; submitted to Phys. Rev. B
Brief Repor
Sector logic implementation for the ATLAS endcap level-1 muon trigger
We present development of the Sector Logic for the ATLAS endcap Level-1 (LVL1) muon trigger. The muon tracks from the interaction point (IP) are bent by the magnetic fields induced by the ATLAS toroidal magnets. The Sector Logic reconstructs three dimensional muon tracks with six levels of transverse momentum (pT) by combining two sets (R-Z and φ-Z) of information from the Thin Gap Chamber (TGC) detectors. Then, it selects two highest pT tracks in each trigger sector. The Sector Logic module is designed in pipelined structure to achieve no-dead-time operation and shorter latency. Look-Up-Tables (LUTs) are used so that any pT threshold level can be set. To achieve these, we adopted SRAM embedded type FPGA devices. The design and its performance are given in this presentation
Differing roles of CD1d2 and CD1d1 proteins in type I natural killer T cell development and function
MHC class I-like CD1 molecules have evolved to present lipid-based antigens to T cells. Differences in the antigen-binding clefts of the CD1 family members determine the conformation and size of the lipids that are presented, although the factors that shape CD1 diversity remain unclear. In mice, two homologous genes, CD1D1 and CD1D2, encode the CD1d protein, which is essential to the development and function of natural killer T (NKT) cells. However, it remains unclear whether both CD1d isoforms are equivalent in their antigen presentation capacity and functions. Here, we report that CD1d2 molecules are expressed in the thymus of some mouse strains, where they select functional type I NKT cells. Intriguingly, the T cell antigen receptor repertoire and phenotype of CD1d2-selected type I NKT cells in CD1D1−/− mice differed from CD1d1-selected type I NKT cells. The structures of CD1d2 in complex with endogenous lipids and a truncated acyl-chain analog of α-galactosylceramide revealed that its A′-pocket was restricted in size compared with CD1d1. Accordingly, CD1d2 molecules could not present glycolipid antigens with long acyl chains efficiently, favoring the presentation of short acyl chain antigens. These results indicate that the two CD1d molecules present different sets of self-antigen(s) in the mouse thymus, thereby impacting the development of invariant NKT cells
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