X-Ray Study of Non-Periodic Si/SiGe Multilayers

1991 ◽  
Vol 220 ◽  
Author(s):  
H. -J. Herzog ◽  
H. Kibbel ◽  
F. Schäffler

ABSTRACTX-ray diffraction is applied for the assessment of structural data such as lattice mismatch and layer thickness of MBE grown Si/Si1−xGex heterobipolar transistor and double-barrier resonant-tunneling structures. Rocking curves from the former structure show distinct features which are obviously correlated to the individual layer parameters. The diffraction profile of the resonant tunneling structure is not only more complicated because of the larger number of parameters but also due to the strong interference effects resulting from the layer set-up. For a determination of the structural parameters a comparison of the experimental diffraction pattern with simulated rocking curves is performed.

1994 ◽  
Vol 351 ◽  
Author(s):  
Astrid C. Zeppenfeld ◽  
Catherine J. Page

ABSTRACTIn order to investigate the influence of substrate functionalization on the subsequent selfassembly of multilayer films, multilayers composed of alternating hafnium and 1,10-decanediylbis(phosphonic) acid (DBPA) have been grown on three different substrates. Substrates studied include gold wafers functionalized with 4-mercaptobutylphosphonic acid, silicon wafers functionalized using a hafnium oxychloride solution, and silicon wafers coated with an octadecylphosphonate LB-template layer. The nature of these films is probed using ellipsometry and grazing angle x-ray diffraction. These studies indicate that the overall order and the individual layer thickness can vary substantially from sample to sample and depend strongly on the initial surface functionalization prior to multilayer growth.


2018 ◽  
Vol 386 ◽  
pp. 394-399
Author(s):  
Nikita S. Saenko ◽  
Albert M. Ziatdinov

This paper outlines the procedure for determining the sizes, structural parameters and percentage content of various particle types in nanographite powders by full-profile approximation of the X-ray diffractogram of sample with using a set of X-ray diffraction profiles for powders of model nanographites. It was shown that taking into account the model nanographites with the radial dependence of interatomic distances within the layer and the dependence of interlayer distances on average number of atoms in the layer allows to describe the X-ray diffraction profile of nanographite powder in the wide angular range including so-called γ-band in small angles without assumptions on presence of other structures in it.


1995 ◽  
Vol 403 ◽  
Author(s):  
J. D. Jarratt ◽  
J. A. Barnard

AbstractGiant magnetoresistance (GMR), structure, and magnetic properties of sputtered (Co90Fe10 X Å/Ag Y Å) multilayer films have been investigated. Distinct GMR behaviors including granulartype (GGMR) and ‘discontinuous’ (DGMR) are observed which are strongly dependent on the individual CoFe and Ag layer thicknesses; however, standard multilayer GMR and the associated antiferromagnetic (AFM) coupling is absent. The multilayer structure, individual layer thicknesses, and growth texture were investigated using high and low angle x-ray diffraction (HXRD & LXRD).


1987 ◽  
Vol 31 ◽  
pp. 155-160
Author(s):  
S. Bates ◽  
P.D. Hatton ◽  
C.A. Lucas ◽  
T.W. Ryan ◽  
S.J. Miles ◽  
...  

AbstractX-ray scattering techniques at grazing incidence have been used to characterize single quantum well hetero–structures. Double–and triple-axis diffractometry has been used to determine lattice mismatch and layer thickness of a 250Å thick layer of AlInAs grown by MBE on an InP substrate and capped by a 45Å GaAs layer. Reflectivity measurements in the triple – crystal mode permit accurate measurement of individual layer thicknesses, relative electron density and interface roughnesses on the Angstrom level.


2009 ◽  
Vol 43 (1) ◽  
pp. 151-153 ◽  
Author(s):  
Fumiko Kimura ◽  
Tsunehisa Kimura ◽  
Wataru Oshima ◽  
Masataka Maeyama ◽  
Kazuaki Aburaya

A pseudo single crystal (a composite of matrix resin and powder crystallites, wherein the individual crystallites are aligned three-dimensionally) was prepared from a powder of sucrose, and its X-ray diffraction pattern was studied. A powder of sucrose crystals suspended in a UV-curable resin precursor was subjected to magnetic alignment in order to align the individual crystallites three-dimensionally, and then the resin precursor was photopolymerized to maintain this orientation. The pseudo single crystal thus obtained produced a well resolved X-ray diffraction profile that is similar to that produced by a twin crystal. The origin of the twin orientation was explained in terms of the interplay between the symmetry of magnetic susceptibility axes and the crystal symmetry (point group 2) of sucrose. The crystal structure of sucrose solved using the pseudo single crystal was in excellent agreement with that solved using a single crystal.


1989 ◽  
Vol 160 ◽  
Author(s):  
L.M. Goldman ◽  
H.A. Atwater ◽  
F. Spaepen

AbstractX-ray diffraction is one of the main methods of determining the structure of multilayers. Low angle reflectivity measurements are particulary useful for multilayers containing polycrystalline or amorphous constituents, and for obtaining specific structural data. We present a method based on both kinematic and dynamic scattering calculations, and use it to extract specific structural parameters such as the roughness or diffuseness of the external surface, the thickness of the constituent layers, and the roughness or diffuseness of the internal interfaces. Results are given for a sputtered A1/A12O3 multilayer.


1984 ◽  
Vol 17 (5) ◽  
pp. 297-306 ◽  
Author(s):  
R. J. Hill ◽  
I. C. Madsen

Crystal structure parameters have been obtained for α-Al2O3, β-PbO2 and (Mg, Fe)2SiO4 by Rietveld analysis of Cu Kα X-ray powder diffraction data collected on a conventional diffractometer using counting times ranging from 0.01 to 5 s per step. For all but the 0.01 s data collected on (Mg, Fe)2SiO4 the structural parameters obtained at different counting times are statistically identical at the 3 σ level, and the spread in the values is essentially the same as that obtained by sample repacking at a fixed counting time of 1 s per step. The parameter e.s.d.'s and conventional agreement indices Rwp and RB decrease to values limited by residual model errors as the counting time increases, but the goodness-of-fit parameter becomes unacceptably larger than its ideal value of unity. When more than a few thousand counts are accumulated for the maximum step intensity in the diffraction profile a weighting scheme based solely on counting variance is inappropriate and the parameter e.s.d.'s are no longer a reflection of their accuracy.


2018 ◽  
Vol 51 (5) ◽  
pp. 1387-1395 ◽  
Author(s):  
Ali Al Hassan ◽  
Arman Davtyan ◽  
Hanno Küpers ◽  
Ryan B. Lewis ◽  
Danial Bahrami ◽  
...  

Typically, core–shell–shell semiconductor nanowires (NWs) made from III–V materials with low lattice mismatch grow pseudomorphically along the growth axis, i.e. the axial lattice parameters of the core and shell materials are the same. Therefore, both the structural composition and interface strain of the NWs are encoded along directions perpendicular to the growth axis. Owing to fluctuations in the supplied growth species during molecular beam epitaxy (MBE) growth, structural parameters such as local shell thickness, composition and strain may differ between NWs grown onto the same substrate. This requires structural analysis of single NWs instead of measuring NW ensembles. In this work, the complete structure of single GaAs/(In,Ga)As/GaAs core–shell–shell NW heterostructures is determined by means of X-ray nanodiffraction using synchrotron radiation. The NWs were grown by MBE on a prepatterned silicon (111) substrate with a core diameter of 50 nm and an (In,Ga)As shell thickness of 20 nm with a nominal indium concentration of 15%, capped by a 30 nm GaAs outer shell. In order to access single NWs with the X-ray nanobeam being incident parallel to the surface of the substrate, a single row of holes with a separation of 10 µm was defined by electron-beam lithography to act as nucleation centres for MBE NW growth. These well separated NWs were probed sequentially by X-ray nanodiffraction, recording three-dimensional reciprocal-space maps of Bragg reflections with scattering vectors parallel (out-of-plane) and perpendicular (in-plane) to the NW growth axis. From the out-of-plane 111 Bragg reflection, deviations from hexagonal symmetry were derived, together with the diameters of probed NWs grown under the same conditions. The radial NW composition and interface strain became accessible when measuring the two-dimensional scattering intensity distributions of the in-plane 2{\overline 2}0 and 22{\overline 4} reflections, exhibiting well pronounced thickness fringes perpendicular to the NW side planes (truncation rods, TRs). Quantitative values of thickness, composition and strain acting on the (In,Ga)As and GaAs shells were obtained via finite-element modelling of the core–shell–shell NWs and subsequent Fourier transform, simulating the TRs measured along the three different directions of the hexagonally shaped NWs simultaneously. Considering the experimental constraints of the current experiment, thicknesses and In content have been evaluated with uncertainties of ±2 nm and ±0.01, respectively. Comparing data taken from different single NWs, the shell thicknesses differ from one to another.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
J. Y. Xie ◽  
F. Wang ◽  
P. Huang ◽  
T. J. Lu ◽  
L. F. Zhang ◽  
...  

Nanoscale Al/W multilayers were fabricated by DC magnetron sputtering and characterized by transmission electron microscopy and high-resolution electron microscopy. Despite the large lattice mismatch and significantly different lattice structures between Al and W, a structural transition from face-centered cubic to body-centered cubic in Al layers was observed when the individual layer thickness was reduced from 5 nm to 1 nm, forming coherent Al/W interfaces. For potential mechanisms underlying the observed structure transition and forming of coherent interfaces, it was suggested that the reduction of interfacial energy and high stresses induced by large lattice-mismatch play a crucial role.


2021 ◽  
Author(s):  
Rosa Diego ◽  
Olivier Roubeau ◽  
Guillem Aromí

Spin crossover (SCO) active solid solutions with formula [FexZn1-x(Me1,3bpp)2](ClO4)2 (x = 0.10, 0.15, 0.22, 0.33, 0.41, 0.48, 0.56 and 0.64, Me1,3bpp is a bis-pyrazolylpyridine) and the complex [Zn(Me1,3bpp)2](ClO4)2 have been prepared and characterized by single crystal X-ray diffraction. The structural data and the powder diffraction patterns of all the compounds have been compared with the reported isostructural molecular crystal [Fe(Me1,3bpp)2](ClO4)2. Increasing amounts of Zn diminishes monotonically the cooperativity of the SCO of the parent Fe(II) complex (T1/2=183 K) and cause a decrease of T1/2 in line with the negative chemical pressure exerted by the Zn(II) complexes on the Fe(II) lattice. The gradual variation of the magnetic properties as the composition changes are paralleled by the evolution of the structural parameters at the molecular, intermolecular and crystal lattice scales. Thermal trapping of a portion of the Fe(II) centers of these alloys by quenching the crystals to 2 K unveils that, upon warming, the temperature of relaxation of the metastable states is almost constant for all compositions.


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