Crystal structure of intermetallic phase in Fe–20Cr–4Al–0.5Y alloy by convergent beam electron diffraction

1987 ◽  
Vol 2 (1) ◽  
pp. 16-27 ◽  
Author(s):  
Raghavan Ayer ◽  
J. C. Scanlon ◽  
T. A. Ramanarayanan ◽  
R. R. Mueller ◽  
R. Petkovic-Luton ◽  
...  

The crystal structure and chemical composition of the intermetallic phase in a Fe-20%Cr-4%Al-0.5%Y (wt. %) alloy were investigated by electron microscopy. Convergent beam diffraction studies revealed that the intermetallic phase forms in three different crystal structures that could coexist in a single grain of the phase. The dominant crystal structure was shown to be hexagonal (a = 0.85, c = 0.84 nm) with a space group most likely to be P63/mmc. Within the hexagonal phase, regions of a rhombohedral crystal structure (a = 0.85, c = 1.26 nm) were observed that had grown in without an apparent phase boundary separating the two crystal structures. The third crystal structure was determined to be monoclinic (a = 0.97, b = 0.85, c = 1.07 nm, and beta = 97.3°) and formed by twinning on the {10$\overline 1$1} planes of the hexagonal phase. The chemical compositions of regions with different crystal structures were comparable and the stoichiometry of the intermetallic phase corresponds to (Fe,Cr)17 (Al,Y)2. The relationship of the observed crystal structures to those previously reported is discussed.

Author(s):  
A. F. Marshall ◽  
J. W. Steeds ◽  
D. Bouchet ◽  
S. L. Shinde ◽  
R. G. Walmsley

Convergent beam electron diffraction is a powerful technique for determining the crystal structure of a material in TEM. In this paper we have applied it to the study of the intermetallic phases in the Cu-rich end of the Cu-Zr system. These phases are highly ordered. Their composition and structure has been previously studied by microprobe and x-ray diffraction with sometimes conflicting results.The crystalline phases were obtained by annealing amorphous sputter-deposited Cu-Zr. Specimens were thinned for TEM by ion milling and observed in a Philips EM 400. Due to the large unit cells involved, a small convergence angle of diffraction was used; however, the three-dimensional lattice and symmetry information of convergent beam microdiffraction patterns is still present. The results are as follows:1) 21 at% Zr in Cu: annealed at 500°C for 5 hours. An intermetallic phase, Cu3.6Zr (21.7% Zr), space group P6/m has been proposed near this composition (2). The major phase of our annealed material was hexagonal with a point group determined as 6/m.


1988 ◽  
Vol 43 (12) ◽  
pp. 1567-1574 ◽  
Author(s):  
U. Schaffrath ◽  
R. Gruehn

Abstract Single crystals of the new oxochlorotantalate Nd7.33Ta8O28Cl6, could be obtained only by chemical transport reactions (T2 → T1; T2 - 1000 °C, T, = 900 °C) with mixtures of Cl2/TaCl5 as transport agent. NdTaO4 was chosen as the starting material. A direct preparative route to Nd7.33Ta8O28Cl6 from binary and ternary components, however, was not successful. Nd7.33Ta8O28Cl6 , crystallizes in the space group Cmmm with a = 10.3381(8) Å, b = 18.865(1) Å, c - 3.9152(3) A; Z = 1. The structure was refined to R - 4.42%, R w = 2.76%. Main building units are pairs of edge-sharing TaO6 -octahedra which are connected with threefold capped trigonal prisms around Nd. Especially remarkable is one Nd position with an occupation factor of 0.833. The relationship of this new structure type with Nd2Ta2O7Cl2 is considered. Furthermore, we have measured the magnetic susceptibilities of both Nd-compounds in a temperature range from 3,6 to 251,3 K. The results are compared with calculated data.


2014 ◽  
Vol 1705 ◽  
Author(s):  
Lydia Bahrig ◽  
Danny Haubold ◽  
Falk Röder ◽  
Stephen G. Hickey ◽  
Alexander Eychmüller

ABSTRACTThe relationship between nanoparticle geometry and their two dimensional assembly is investigated in order to provide insights into the three dimensional arrangement of mesocrystals. The crystal structure of the nanoparticles and their homogeneity are investigated during structure formation on the mesoscale whereby effects such as fibrillation have been observed.


MRS Bulletin ◽  
2007 ◽  
Vol 32 (2) ◽  
pp. 127-133 ◽  
Author(s):  
Kimberly A. Dick ◽  
Knut Deppert ◽  
Lisa S. Karlsson ◽  
Magnus W. Larsson ◽  
Werner Seifert ◽  
...  

AbstractWe describe the production of hierarchical branched nanowire structures by the sequential seeding of multiple wire generations with metal nanoparticles. Such complex structures represent the next step in the study of functional nanowires, as they increase the potential functionality of nanostructures produced in a self-assembled way. It is possible, for example, to fabricate a variety of active heterostructure segments with different compositions and diameters within a single connected structure. The focus of this work is on epitaxial III-V semiconductor branched nanowire structures, with the two materials GaP and In As used as typical examples of branched structures with cubic (zinc blende) and hexagonal (wurtzite) crystal structures. The general morphology of these structures will be described, as well as the relationship between morphology and crystal structure.


1999 ◽  
Vol 32 (3) ◽  
pp. 397-403 ◽  
Author(s):  
M. Leicht ◽  
T. Remmele ◽  
D. Stenkamp ◽  
H. P. Strunk

In this study, a particular type of nanoscopic twinned crystal structure which can occur in any tetragonal or orthogonal crystal structure with a ratio of lattice parameters c/a=c/b=2 is presented. This type of twinning is characterized by twin components whosecaxes are oriented perpendicular to one another, by twin-habit planes parallel to {102} planes, and by a superstructure along the twin boundaries which is described by orthogonal unit cells with lattice parameters 2a, 2a,a. Furthermore, the suitability of electron microdiffraction, a diffraction technique of transmission electron microscopy (TEM) with a moderately convergent beam, for the analysis of such twinned crystal structures is demonstrated. For this demonstration, electron microdiffraction is applied to the chalcogenide compound Cu2In3Se5, which indeed exhibits the proposed twinned crystal structure.


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