Neutron diffraction intensity enhancement of ∝-LiIO3 single crystal under DC voltage at elevated temperatures

1989 ◽  
Vol 69 (3) ◽  
pp. 201-202 ◽  
Author(s):  
Yang Zhen ◽  
Cheng Yu-fen
Keyword(s):  
Neutron Diffraction ◽  
Single Crystal ◽  
Elevated Temperatures ◽  
Diffraction Intensity ◽  
Dc Voltage ◽  
Intensity Enhancement

Mechanical Properties and Dislocation Structure of Single Crystal Cdte Deformed in Compression at 300°C

1976 ◽  
Vol 34 ◽  
pp. 592-593
Author(s):  
Ernest L. Hall ◽  
J. B. Vander Sande
Keyword(s):  
Mechanical Properties ◽  
Single Crystal ◽  
Dislocation Structure ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Strain Curve ◽  
Optical Devices ◽  
Semiconductor Compound ◽  
Wide Range ◽  
Sample Orientation

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.

SINGLE CRYSTAL NEUTRON DIFFRACTION STUDIES OF HCP RARE EARTH THORIUM ALLOYS

1971 ◽  
Vol 32 (C1) ◽  
pp. C1-1128-C1-1129
Author(s):  
H. R. CHILD ◽  
W. C. KOEHLER
Keyword(s):  
Rare Earth ◽  
Neutron Diffraction ◽  
Single Crystal

NEUTRON DIFFRACTION AND MAGNETIZATION STUDY OF THE MAGNETIC PHASE DIAGRAM OF UAs0.75Se0.25 SINGLE CRYSTAL

1988 ◽  
Vol 49 (C8) ◽  
pp. C8-479-C8-480 ◽  
Author(s):  
M. Kuznietz ◽  
P. Burlet ◽  
J. Rossat-Mignod ◽  
O. Vogt ◽  
K. Mattenberger ◽  
...  
Keyword(s):  
Phase Diagram ◽  
Neutron Diffraction ◽  
Single Crystal ◽  
Magnetic Phase ◽  
Magnetic Phase Diagram ◽  
Magnetization Study

Single crystal neutron diffraction studies of antiferromagnets at low temperatures in applied magnetic fields

1959 ◽  
Vol 20 (2-3) ◽  
pp. 180-184 ◽  
Author(s):  
W.C. Koehler ◽  
M. K. Wilkinson ◽  
J.W. Cable ◽  
E.O. Wollan
Keyword(s):  
Magnetic Fields ◽  
Neutron Diffraction ◽  
Single Crystal ◽  
Low Temperatures

Water Molecule Dispositions in the Cesium Sulfate α- and β-Alums: Single-Crystal Neutron Diffraction Studies of CsM(SO4)2.12H2O (M=V, Rh)

1993 ◽  
Vol 46 (9) ◽  
pp. 1337 ◽  
Author(s):  
JK Beattie ◽  
SP Best ◽  
FH Moore ◽  
BW Skelton ◽  
AH White
Keyword(s):  
Neutron Diffraction ◽  
Water Molecule ◽  
Single Crystal ◽  
Tilt Angle ◽  
Room Temperature ◽  
Bond Angle ◽  
Sulfate Salt ◽  
Cell Dimensions ◽  
Coordinated Water ◽  
Unit Cell Dimensions

Room-temperature single-crystal neutron diffraction studies are recorded for two alums, Cs( Rh /V)(SO4)2.12H2O [cubic, Pa3, a 12.357(5) ( Rh ), 12.434(1)Ǻ (V)], residuals 0.037 and 0.068 for 328 and 164 'observed' reflections, with the intention of defining water molecule hydrogen atom orientations. Whereas the two tervalent hexaaqua cations are similar in size [ rM -O = 2.010(6)Ǻ (M = V) and 2.006(2)Ǻ (M = Rh )] the vanadium salt adopts the β alum modification while rhodium gives an α alum. Significantly, the water coordination geometry is different in the two cases with the tilt angle between the plane of the water molecule and the M-O bond vector being 1° (M = V) and 35° (M = Rh ). The tilt angle for water coordinated to rhodium in CsRh (SeO4)2.12H2O is inferred from the unit cell dimensions to be similar to that of the corresponding sulfate salt and not that which generally pertains for caesium selenate alums. Significant differences in the H-O-H bond angle are found for trigonal planar and trigonal pyramidal water coordination, suggesting that differences in the metal(III)-water interaction are a determinant of the geometry of the coordinated water molecule in the caesium sulfate/ selenate alum lattices.

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