Diffuse x-ray scattering of misfit dislocations at Si1−xGex/Si interfaces by triple crystal diffractometry

1997 ◽  
Vol 82 (3) ◽  
pp. 1172-1177 ◽  
Author(s):  
G. Bhagavannarayana ◽  
P. Zaumseil
1991 ◽  
Vol 237 ◽  
Author(s):  
K. S. Liang ◽  
C. H. Lee

ABSTRACTUsing grazing incidence x-ray scattering, we have studied incommensurate structures of Pb adlayers on Cu(110) surface and epitaxial Al films grown on Si(111) surface. Similar diffuse scattering profiles were found in both cases, which can be fitted with a Gaussian-plus-Lorentzian lineshape. The results are attributed to a overlayer structure with pinned misfit dislocations at the interface.


1990 ◽  
Vol 202 ◽  
Author(s):  
P. F. Miceli ◽  
K. W. Moyers ◽  
C. J. Palmstrøm

ABSTRACTThe results of a high resolution x-ray scattering study of [001]ErAs epitaxial layers grown on [001]GaAs is presented. ErAs is pseudomorphic on GaAs for thicknesses below 70Å and, for thicker films, lattice relaxation is oberved concomitant with an Increase of the In-plane mosaic due to the formation of misfit dislocations. Above 300Å, the out-of-plane transverse scattering from the ErAs lattice planes Is no longer specular and further relaxation Is related to the out-of-plane mosaic. The ratio of elastic constants, C12/C11, Is determined to be 0.126 and the thermal expansion was measured. Thin film Interference oscillations are observed and modeled. ErAs/GaAs Is an Ideal system for x-ray scattering studies of lattice relaxation and structure in epitaxial layers. Films as thin as 20Å have been studied.


1995 ◽  
Vol 78 (8) ◽  
pp. 5013-5021 ◽  
Author(s):  
V. Holý ◽  
J. H. Li ◽  
G. Bauer ◽  
F. Schäffler ◽  
H.‐J. Herzog

2001 ◽  
Vol 673 ◽  
Author(s):  
Kaile Li ◽  
Paul F. Miceli ◽  
Christian Lavoie ◽  
Tom Tiedje ◽  
Karen L. Kavanagh

ABSTRACTMotivated by x-ray scattering experiments on heteroepitaxially grown thin films, we present model calculations of the diffuse x-ray scattering arising from misfit dislocations. The model is based on the elastic displacements from dislocations whose positions are spatially uncorrelated. These numerical results give support to a phenomenological model [Phys. Rev. B 51, 5506 (1995)] that predicts the scaling of diffuse scattering intensity with perpendicular wavevector, Qz. At low Qz the diffuse width scales inversely with the defect size, which is given by the film thickness due to the effect of the elastic image field, whereas at high Qz the diffuse width is mosaic-like, scaling with Qz. New experimental results for InxGa1−xAs/GaAs are also presented and compared to the model. The calculations are in good agreement with these experiments, as well as other measurements in the literature for high and low dislocation density.


1995 ◽  
Vol 28 (4A) ◽  
pp. A92-A96 ◽  
Author(s):  
M S Goorsky ◽  
M Meshkinpour ◽  
D C Streit ◽  
T R Block

2018 ◽  
Vol 51 (4) ◽  
pp. 969-981 ◽  
Author(s):  
Václav Holý ◽  
Marcin Kryśko ◽  
Michał Leszczyński

Diffuse X-ray scattering from random chemical inhomogeneities in epitaxial layers of InGaN/GaN was simulated using linear elasticity theory and kinematical X-ray diffraction. The simulation results show the possibility of determining the r.m.s. deviations of the local In content and its lateral correlation length from reciprocal-space maps of the scattered intensity. The reciprocal-space distribution of the intensity scattered from inhomogeneities is typical and it can be distinguished from other sources of diffuse scattering such as threading or misfit dislocations.


2001 ◽  
Vol 78 (4) ◽  
pp. 443-445 ◽  
Author(s):  
R. I. Barabash ◽  
W. Donner ◽  
H. Dosch

Author(s):  
Eva-Maria Mandelkow ◽  
Eckhard Mandelkow ◽  
Joan Bordas

When a solution of microtubule protein is changed from non-polymerising to polymerising conditions (e.g. by temperature jump or mixing with GTP) there is a series of structural transitions preceding microtubule growth. These have been detected by time-resolved X-ray scattering using synchrotron radiation, and they may be classified into pre-nucleation and nucleation events. X-ray patterns are good indicators for the average behavior of the particles in solution, but they are difficult to interpret unless additional information on their structure is available. We therefore studied the assembly process by electron microscopy under conditions approaching those of the X-ray experiment. There are two difficulties in the EM approach: One is that the particles important for assembly are usually small and not very regular and therefore tend to be overlooked. Secondly EM specimens require low concentrations which favor disassembly of the particles one wants to observe since there is a dynamic equilibrium between polymers and subunits.


Author(s):  
Eva-Maria Mandelkow ◽  
Ron Milligan

Microtubules form part of the cytoskeleton of eukaryotic cells. They are hollow libers of about 25 nm diameter made up of 13 protofilaments, each of which consists of a chain of heterodimers of α-and β-tubulin. Microtubules can be assembled in vitro at 37°C in the presence of GTP which is hydrolyzed during the reaction, and they are disassembled at 4°C. In contrast to most other polymers microtubules show the behavior of “dynamic instability”, i.e. they can switch between phases of growth and phases of shrinkage, even at an overall steady state [1]. In certain conditions an entire solution can be synchronized, leading to autonomous oscillations in the degree of assembly which can be observed by X-ray scattering (Fig. 1), light scattering, or electron microscopy [2-5]. In addition such solutions are capable of generating spontaneous spatial patterns [6].In an earlier study we have analyzed the structure of microtubules and their cold-induced disassembly by cryo-EM [7]. One result was that disassembly takes place by loss of protofilament fragments (tubulin oligomers) which fray apart at the microtubule ends. We also looked at microtubule oscillations by time-resolved X-ray scattering and proposed a reaction scheme [4] which involves a cyclic interconversion of tubulin, microtubules, and oligomers (Fig. 2). The present study was undertaken to answer two questions: (a) What is the nature of the oscillations as seen by time-resolved cryo-EM? (b) Do microtubules disassemble by fraying protofilament fragments during oscillations at 37°C?


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