Single crystal x-ray diffraction of lead magnesium niobate-lead titanate in the transmission mode

2006 ◽  
Vol 89 (9) ◽  
pp. 092903 ◽  
Author(s):  
Alp Sehirlioglu ◽  
David A. Payne ◽  
Scott R. Wilson ◽  
Pengdi Han
2004 ◽  
Vol 19 (2) ◽  
pp. 609-615 ◽  
Author(s):  
Raji Soundararajan ◽  
Rabindra Nath Das ◽  
Russ Tjossem ◽  
Amit Bandyopadhyay ◽  
Kelvin G. Lynn ◽  
...  

We have grown lead magnesium niobate–lead titanate (PMN–PT) single crystals, using the high-pressure vertical Bridgman (HPVB) technique, around the stoichiometric composition of 0.7 PMN–0.3PT [0.7Pb(Mg1/3Nb2/3)O3 + 0.3(PbTiO3)]. The final ingot (about 50-mm diameter, 25-mm long) was machinable using an inner diameter saw. The room-temperature x-ray diffraction on the starting powders and the final single crystal revealed a desirable perovskite structure. The natural growth direction in most of the crystals, as determined using orientation image microscopy, was (110). Examination of the final microstructures and phases/inclusions had been done using optical and infrared microscopy, energy dispersive spectroscopy, and x-ray backscatter techniques. Microstructural characterizations of the final ingots have revealed the presence of pores filled with Mg–Si–O-rich impurity phase, usually found along the cell boundary–like structures, in all the growths. We have measured some piezoelectric properties including d33 (1200 pC/N), k33 (0.85), kt (0.5), and the dielectric constant at the Curie temperature.


2013 ◽  
Vol 102 (4) ◽  
pp. 042906 ◽  
Author(s):  
Tian-Bing Xu ◽  
Laura Tolliver ◽  
Xiaoning Jiang ◽  
Ji Su

2012 ◽  
Vol 51 ◽  
pp. 07GE09 ◽  
Author(s):  
Daisuke Yamaguchi ◽  
Takefumi Kanda ◽  
Koichi Suzumori ◽  
Masataka Kuroda ◽  
Dai Takeda

2000 ◽  
Author(s):  
Jin T. Wang ◽  
Feng Tang

Abstract Ta-Doping effect on the microstructure of lead magnesium niobate-lead titanate crystalline solutions 0.9PbMg1/3(Nb(1−x)Tax)2/3O3-0.1PbTiO3(PMN-PT) have been firstly investigated in this paper. Scanning Electron Micrographs (SEM) were taken from fractured surfaces of the samples with different additives of x = 0.0, 0.1, 0.2, 0.3 and 1.0 by Hitachi F-2460N microscope operating at an accelerating voltage of 25kV. The chemical content analysis for the synthesized samples performed on JEOL Super Prob733 Energy Perspective Spectrum. The x-ray diffraction was carried out with a Siemens D5000 Dual Diffraction Meter. It is clearly evident that doping Ta in PMNTa-PT can affect the grain size and density of the compounds. Smaller grain size (3.1μm) is formed in the specimens with the additives of x = 0.1, 0.2 and 0.3 in comparison with those of the specimens without doping (6.6μm) or over doping (6.4μm). The porosity at grain intersections increase with increasing of additive tantalum for niobium site in 0.9PMNTa-0.1PT. Larger grain size (6.4μm), greater non-uniformity and more inter-granular voids are found in the compound, if tantalum completely substitutes niobium (x = 1). No non-reacted starting regents were observed in any of the compositions mentioned above.


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