Orientation Relationships of SrTiO3and MgTiO3Thin Films Grown by Vapor−Solid Reactions on (100) and (110) TiO2(Rutile) Single Crystals

2007 ◽  
Vol 111 (17) ◽  
pp. 6372-6379 ◽  
Author(s):  
A. Lotnyk ◽  
S. Senz ◽  
D. Hesse
2006 ◽  
Vol 519-521 ◽  
pp. 1569-1578
Author(s):  
Dorte Juul Jensen

By 3 dimensional X-ray diffraction (3DXRD) using high energy X-rays from synchrotron sources it is possible to study in-situ the nucleation and growth during recrystallization. In this paper it is described and discussed how 3DXRD can supplement EBSP measurements of nucleation and growth. Three types of studies are considered: i) orientation relationships between nuclei and parent deformed matrix, ii) recrystallization kinetics of individual bulk grains and iii) filming of growing grains in deformed single crystals.


2002 ◽  
Vol 237-239 ◽  
pp. 730-734 ◽  
Author(s):  
Jong Kwan Park ◽  
Kwang Bo Shim ◽  
Keun Ho Auh ◽  
Isao Tanaka

1989 ◽  
Vol 170 ◽  
Author(s):  
F.-S. Shieu ◽  
S. L. Sass

AbstractThe dislocation structure of Pt-(001)NiO interfaces was studied using electron microscopy and electron diffraction techniques. Specimens were produced by hot pressing polycrystalline Pt films on to thin NiO single crystals, and bulk Pt single crystals on to bulk NiO single crystals. The polycrystalline Pt specimens were used to determine the favored orientation relationships between the NiO and Pt, while the bulk NiO-Pt specimens were used to study the detailed structure of the interface. Three categories of orientation relationships were identified: exact epitaxy with (001)Pt ║ (001)NiO, [110]Pt ║ [110]NiO; small rotations away from exact epitaxy about the common [001] direction; high index planes of Pt parallel to (001) of NiO. Theoretical calculations of the expected dislocation structures of interfaces with the first two orientation relationships were made using a Bollmann-type analysis. The experimental observations and theoretical predictions were shown to be in good agreement. The energies of the interfaces having the first two orientation relationships were shown to be similar which is believed to be the reason why they both occur.


2008 ◽  
Vol 454 (4-6) ◽  
pp. 314-317 ◽  
Author(s):  
I. Takahashi ◽  
D.J. Payne ◽  
R.G. Palgrave ◽  
R.G. Egdell

Author(s):  
M. C. Ball ◽  
H. F. W. Taylor

SummaryChrysotile fibres, and also single crystals of lizardite, were dehydrated hydrothermally, and the resulting pseudomorphs studied by X-ray rotation photographs. The initial products are normally forsterite and disordered material; talc forms more slowly. At water pressures up to 600 kg/cm2, both forsterite and talc show strong preferred orientation. At higher pressures the talc is oriented but the forsterite tends to be unoriented. The orientation of forsterite formed at 550° C and 500 kg/cm2 differs from that found when chrysotile is dehydrated by heating in air. The orientation relationships suggest that, in the dry reaction, the forsterite orientation is controlled mainly by the octahedral layers of the chrysotile, while in the hydrothermal reaction it is controlled mainly by the tetrahedral layers. This does not support the generally accepted mechanism for the dry reaction. New mechanisms are suggested, for both dry and hydrothermal reactions, similar to that already suggested by us for the dehydration of brucite. The formation of talc in the hydrothermal reaction, and of enstatite in the dry reaction above 1000°, are also discussed. The dehydration of talc, to give enstatite, has also been studied using single crystals, and the mechanism of this process is briefly discussed.


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