Comparison of surface and bulk room temperature domain structure of barium titanate ceramics using x-ray diffraction

1988 ◽  
Vol 87 (1) ◽  
pp. 243-253 ◽  
Author(s):  
V. K. Seth ◽  
G. J. Gatins ◽  
W. A. Schulze
2009 ◽  
Vol 42 (3) ◽  
pp. 480-484 ◽  
Author(s):  
Dean S. Keeble ◽  
Pamela A. Thomas

The room-temperature phase of the important ferroelectric material barium titanate, BaTiO3, was re-investigated by single-crystal X-ray diffraction on a sample grown by the top-seeded solution growth method, with the intention of demonstrating once again that the structure has tetragonal symmetry consistent with the space-group assignmentP4mmand thus resolving recent controversy in the scientific community and literature [Yoshimura, Kojima, Tokunaga, Tozaki & Koganezawa (2006).Phys. Lett. A,353, 250–254; Yoshimura, Morioka, Kojima, Tokunaga, Koganezawa & Tozaki (2007).Phys. Lett. A,367, 394–401]. To this end, the X-ray diffraction pattern of a small (341 µm3) sample of top-seeded solution-grown BaTiO3was measured using an Oxford Diffraction Gemini CCD diffractometer employing Mo Kα radiation and an extended 120 mm sample-to-detector distance. More than 104individual diffraction maxima observed out to a maximum resolution of 0.4 Å were indexed on two tetragonal lattices. These were identical to within the standard deviations on the lattice parameters and were related to each other by a single rotation of 119.7° about the [11\overline1] direction of the first tetragonal lattice (the major twin component), although the actual twinning operation that explains the observed diffraction pattern both qualitatively and quantitatively is shown to be conventional 90° twinning by them[101] operation. Importantly, it is not necessary to invoke either monoclinic symmetry or a coexistence of tetragonal and monoclinic phases to explain the observed diffraction data.


2012 ◽  
Vol 463-464 ◽  
pp. 276-280 ◽  
Author(s):  
Dan Su ◽  
Yu Wang ◽  
Wan Ping Chen ◽  
Helen Lai Wah Chan ◽  
Li Na Bing

CuO has been doped solely and together with BaO and SiO2 into barium titanate by mixing and calcination. X-ray diffraction showed that the sample doped by CuO-BaO has stable second hexagonal phase while the samples doped by CuO, CuO-SiO2 were of a pure perovskite phase. For CuO-BaO doping, the Curie temperature was decreased accompanied with higher εmax; while for CuO doping and CuO-SiO2 codoping, the Curie temperature was increased with εmax decreased. The difference can be explained considering that Cu2+ ion could not only incorporate into the BaTiO3 lattice, but also assemble in the boundary phase when CuO was doped solely. Besides, the mechanisms of CuO doping and SiO2 doping could happen at one time.


2014 ◽  
Vol 608 ◽  
pp. 247-252 ◽  
Author(s):  
Md. Fakhrul Islam ◽  
Rubayyat Mahbub ◽  
Adnan Mousharraf

The main focus of the research was to correlate the composition and sintering parameters with the microstructure and dielectric properties of Ta2O5 (Tantalum Oxide) doped BaTiO3 (Barium Titanate) ceramics. Ta2O5 was doped at three different percentages viz. 0.5, 1.0 and 1.5 mole%. The doped samples were then sintered using both single and double stage sintering techniques. Thereafter field emission scanning electron microscope (FESEM) and X-ray diffraction (XRD) techniques were used to examine the structure of the samples with particular focus on the incorporation of Ta5+ions into the BaTiO3 crystal lattice. Finally, the dielectric properties were analyzed using impedence analyzer and the relationship between the properties and structure of doped BaTiO3 was established. From the research, it can be stated that double stage sintering yielded best dielectric properties. The best stable value of room temperature dielectric constant (k) of 19000 was obtained for 1.5mole % Ta2O5 doped BaTiO3 sample, sintered at 1320°C for 0 hour and 1280°C for 6 hours due to the combination of high percent theoretical density (%TD) and optimum grain size. At a temperature range of 30°C to 60°C, this combination of composition and sintering parameters yielded dielectric constant in the range of 18000-19000.


2014 ◽  
Author(s):  
Nurazila Mat Zali ◽  
Che Seman Mahmood ◽  
Siti Mariam Mohamad ◽  
Choo Thye Foo ◽  
Julie Adrianny Murshidi

2012 ◽  
Vol 6 (3) ◽  
pp. 117-122 ◽  
Author(s):  
Stanislav Slavov ◽  
Milena Krapchanska ◽  
Elena Kashchieva ◽  
Svetlin Parvanov ◽  
Yanko Dimitriev

Bismuth-titanate ceramics containing SiO2 and Nd2O3 as additives are synthesized by melt quenching method in the system Bi2O3-TiO2-Nd2O3-SiO2 in the temperature range of 1250-1500 ?C. The phase composition of the obtained materials is determined by X-ray diffraction analysis and energy dispersive spectroscopy. Using scanning electron microscopy different microstructures are observed in the samples depending on the composition. Different values of conductivity, dielectric losses and relative permittivity are obtained depending on the composition. It is established that all investigated samples are dielectric materials with conductivity between 10-9 and 10-13 (??cm)-1 at room temperature, dielectric permittivity from 1000 to 3000 and dielectric losses tg? between 0.0002 and 0.1.


2015 ◽  
Vol 815 ◽  
pp. 131-135 ◽  
Author(s):  
Nur Farahin Abdul Hamid ◽  
Rozana Aina Maulat Osman ◽  
Mohd Sobri Idris

Undoped barium titanate and lanthanum (La) doped barium titanate (BaTiO3) were studied for ferroelectric properties with the formula of Ba1-xLaxTi1-x/4O3 for x=0.1 and being prepared by using conventional solid state method reaction. The pure phase of this composition which x=0 were found at final heating temperatures starting from 1300°C and x=0.1 at 1350°C for overnight in air with intermittent grinding. The changes in the crystal structure of the composition were detected by using X-ray diffraction. Impedance Spectroscopy analysis is carried out to determine the dielectric properties for undoped BaTiO3 and La doped BaTiO3 for x=0.1.


2012 ◽  
Vol 560-561 ◽  
pp. 914-918 ◽  
Author(s):  
Da Yong Lu ◽  
Li Zhang ◽  
Dan Dan Han ◽  
Yan Dong Wang ◽  
Xue Yang ◽  
...  

For Barium Titanate Ceramics doped with the trivalent and hexavalent chromium oxides, the influence of Cr valence state on dielectric-temperature stability was investigated with Atomic force microscopy, X-ray diffraction, Raman spectroscopy, and dielectric measurements. The application of the trivalent Cr2O3 dopant can give rise to a temperature-stable X7R specification and a lower dielectric loss (< 0.02) when the sample was prepared at 1240 °C, but the dielectric permittivity is lower (~600); Cr ions exist predominantly as Cr4+ and slightly as Cr3+. Increasing sintering temperature will destroy the core-shell structure of the samples. The application of the hexavalent CrO3 dopant can not produce a temperature-stable X7R ceramic; Cr ions exist as Cr4+ and Cr5+. Cr5+ can not enter the perovskite lattice owing to the valence mismatching.


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