Polarization dependent EXAFS study of Bi[sub 2]Sr[sub 2]Ca[sub 0.4]Pr[sub 0.6]Cu[sub 2]O[sub 8−δ] insulating single crystal

2001 ◽  
Author(s):  
S. Dalela
Keyword(s):  
2000 ◽  
Vol 14 (29n31) ◽  
pp. 3432-3437
Author(s):  
S. Dalela ◽  
B. Dalela ◽  
D. Chaturvedi ◽  
R. K. Singhal ◽  
D. C. Jain ◽  
...  

Polarised EXAFS measurements on the Cu K edge in a Pr-doped BSCCO (2212) insulating single crystal have been made at room temperature at the SRRC, Taiwan. Measurements have been confined to only the E//a, E//a∧45 and E//b directions within the Cu- O 2 plane as most of the action is here. While the spectra in the E//a and E//b look very similar, the E//a∧45 spectrum does look a little different. EXAFS analysis shows that Cu-O (planar) distances as well as the Debye Waller factor values in different directions turn out to be slightly different indicating a possibility of presence of some in-plane distortion. This appears to be very much in agreement with our XANES results on this system and our EXAFS results on Pr-doped YBCO (123) system reported earlier, which also indicate the presence of some distortion. Presence of Pr is speculated to be the cause for producing this distortion. This would be discussed in some detail taking into account the possibility that Pr, besides quenching holes, may also be displacing the in-plane oxygens.


2020 ◽  
Vol 127 (11) ◽  
pp. 115106
Author(s):  
X. Biquard ◽  
E. G. Víllora ◽  
K. Shimamura ◽  
K. Lorenz

2011 ◽  
Vol 471 (5-6) ◽  
pp. 137-142 ◽  
Author(s):  
S. Dalela ◽  
B. Dalela ◽  
Neena D ◽  
P.A. Alvi

1994 ◽  
Vol 339 ◽  
Author(s):  
D. P. Pappas ◽  
V. G. Harris ◽  
H. A. Hoff ◽  
G. L. Watena ◽  
J. W. Glesener

ABSTRACTCopper films were grown on a single crystal diamond substrate using an iron seed layer. The effect of the crystalline structure of the iron seed on the Cu films was studied with extended x-ray absorption fine structure (EXAFS) and scanning electron microscopy (SEM). The EXAFS study shows that the 10 Å Fe seed layer is in an fee structure, and has collapsed into a bec structure by the time 20 Å of Fe has been deposited. In the SEM pictures it is observed that subsequent layers of Cu grow as continuous films for thin fcc-Fe seeds, and grow in an island mode for the thick, bcc-Fe seeds.


Author(s):  
Akira Tanaka ◽  
David F. Harling

In the previous paper, the author reported on a technique for preparing vapor-deposited single crystal films as high resolution standards for electron microscopy. The present paper is intended to describe the preparation of several high resolution standards for dark field microscopy and also to mention some results obtained from these studies. Three preparations were used initially: 1.) Graphitized carbon black, 2.) Epitaxially grown particles of different metals prepared by vapor deposition, and 3.) Particles grown epitaxially on the edge of micro-holes formed in a gold single crystal film.The authors successfully obtained dark field micrographs demonstrating the 3.4Å lattice spacing of graphitized carbon black and the Au single crystal (111) lattice of 2.35Å. The latter spacing is especially suitable for dark field imaging because of its preparation, as in 3.), above. After the deposited film of Au (001) orientation is prepared at 400°C the substrate temperature is raised, resulting in the formation of many square micro-holes caused by partial evaporation of the Au film.


Author(s):  
L. E. Murr ◽  
G. Wong

Palladium single-crystal films have been prepared by Matthews in ultra-high vacuum by evaporation onto (001) NaCl substrates cleaved in-situ, and maintained at ∼ 350° C. Murr has also produced large-grained and single-crystal Pd films by high-rate evaporation onto (001) NaCl air-cleaved substrates at 350°C. In the present work, very large (∼ 3cm2), continuous single-crystal films of Pd have been prepared by flash evaporation onto air-cleaved (001) NaCl substrates at temperatures at or below 250°C. Evaporation rates estimated to be ≧ 2000 Å/sec, were obtained by effectively short-circuiting 1 mil tungsten evaporation boats in a self-regulating system which maintained an optimum load current of approximately 90 amperes; corresponding to a current density through the boat of ∼ 4 × 104 amperes/cm2.


Author(s):  
D. J. Barber ◽  
R. G. Evans

Manganese (II) oxide, MnO, in common with CoO, NiO and FeO, possesses the NaCl structure and shows antiferromagnetism below its Neel point, Tn∼ 122 K. However, the defect chemistry of the four oxides is different and the magnetic structures are not identical. The non-stoichiometry in MnO2 small (∼2%) and below the Tn the spins lie in (111) planes. Previous work reported observations of magnetic features in CoO and NiO. The aim of our work was to find explanations for certain resonance results on antiferromagnetic MnO.Foils of single crystal MnO were prepared from shaped discs by dissolution in a mixture of HCl and HNO3. Optical microscopy revealed that the etch-pitted foils contained cruciform-shaped precipitates, often thick and proud of the surface but red-colored when optically transparent (MnO is green). Electron diffraction and probe microanalysis indicated that the precipitates were Mn2O3, in contrast with recent findings of Co3O4 in CoO.


Author(s):  
J. M. Galbraith ◽  
L. E. Murr ◽  
A. L. Stevens

Uniaxial compression tests and hydrostatic tests at pressures up to 27 kbars have been performed to determine operating slip systems in single crystal and polycrystal1ine beryllium. A recent study has been made of wave propagation in single crystal beryllium by shock loading to selectively activate various slip systems, and this has been followed by a study of wave propagation and spallation in textured, polycrystal1ine beryllium. An alteration in the X-ray diffraction pattern has been noted after shock loading, but this alteration has not yet been correlated with any structural change occurring during shock loading of polycrystal1ine beryllium.This study is being conducted in an effort to characterize the effects of shock loading on textured, polycrystal1ine beryllium. Samples were fabricated from a billet of Kawecki-Berylco hot pressed HP-10 beryllium.


Author(s):  
G. G. Hembree ◽  
M. A. Otooni ◽  
J. M. Cowley

The formation of oxide structures on single crystal films of metals has been investigated using the REMEDIE system (for Reflection Electron Microscopy and Electron Diffraction at Intermediate Energies) (1). Using this instrument scanning images can be obtained with a 5 to 15keV incident electron beam by collecting either secondary or diffracted electrons from the crystal surface (2). It is particularly suited to studies of the present sort where the surface reactions are strongly related to surface morphology and crystal defects and the growth of reaction products is inhomogeneous and not adequately described in terms of a single parameter. Observation of the samples has also been made by reflection electron diffraction, reflection electron microscopy and replication techniques in a JEM-100B electron microscope.A thin single crystal film of copper, epitaxially grown on NaCl of (100) orientation, was repositioned on a large copper single crystal of (111) orientation.


Author(s):  
Ernest L. Hall ◽  
J. B. Vander Sande

The present paper describes research on the mechanical properties and related dislocation structure of CdTe, a II-VI semiconductor compound with a wide range of uses in electrical and optical devices. At room temperature CdTe exhibits little plasticity and at the same time relatively low strength and hardness. The mechanical behavior of CdTe was examined at elevated temperatures with the goal of understanding plastic flow in this material and eventually improving the room temperature properties. Several samples of single crystal CdTe of identical size and crystallographic orientation were deformed in compression at 300°C to various levels of total strain. A resolved shear stress vs. compressive glide strain curve (Figure la) was derived from the results of the tests and the knowledge of the sample orientation.


Sign in / Sign up

Export Citation Format

Share Document