Fabrication of BaTi2O5 Glass−Ceramics with Unusual Dielectric Properties during Crystallization
Source abstract
Abstract
A 2-mm-diameter glass sphere of ferroelectric BaTi 2 O 5 was fabricated from melt using containerless processing. The glass structure was analyzed by high-energy X-ray diffraction using an incident photon energy of 113.5 keV, indicating that distorted Ti−O polyhedra, with average coordination number ( N Ti - O ) of approximately 5, presented in the glass. Above the glass transition temperature (972 K), three successive phase transitions, from glass to a metastable α phase at 972 K, then to a metastable β phase at 1038 K, and finally to a stable monoclinic γ phase above 1100 K, were observed. At the crystallization temperature of the α phase, the permittivity jumped instantaneously by more than 1 order of magnitude, reaching a peak of 1.4 × 10 7 . This interesting phenomenon, occurring near the crystallization temperature, has important technical implications for obtaining an excellent dielectric glass−ceramic through controlled crystallization of BaTi 2 O 5 glass.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Glass properties and applications · Ferroelectric and Piezoelectric Materials · Microwave Dielectric Ceramics Synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Japan Aerospace Exploration Agency, ISS Science Project Office, 2-1-1 Sengen, Tsukuba, Ibaraki 305-8505, Japan, Japan Synchrotron Radiation Research Institute, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198, Japan, CREST, Japan Science and Technology Agency, Honmachi, Kawaguchi, Saitama 332-0012, Japan, Materials and Structures Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226, Japan, and Graduate School of Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi...
References (25)
Show source-provided references
1. Narasaki A. · Appl. Phys. Lett. · 1999 · 75 · 339910.1063/1.125306 ↗
2. Sakai R. · Appl. Phys. Lett. · 2000 · 77 · 211810.1063/1.1313805 ↗
3. Takahashi Y. · Appl. Phys. Lett. · 2002 · 81 · 22310.1063/1.1493667 ↗
4. Glass A. M. · Appl. Phys. Lett. · 1977 · 31 · 24910.1063/1.89670 ↗
5. Nassau K. · J. Am. Ceram. Soc. · 1979 · 62 · 7410.1111/j.1151-2916.1979.tb18810.x ↗
6. Masaaki T. · Jpn. J. Appl. Phys. · 1980 · 19 · 55510.1143/JJAP.19.L555 ↗
7. Kim S. H. · Jpn. J. Appl. Phys. · 1998 · 37 · 23410.1143/JJAP.37.234 ↗
8. Lines M. E. · Phys. Rev. B. · 1978 · 17 · 198410.1103/PhysRevB.17.1984 ↗
9. Akishige Y. · Jpn. J. Appl. Phys. · 2003 · 42 · L94610.1143/JJAP.42.L946 ↗
10. Waghmare U. · Appl. Phys. Lett. · 2004 · 84 · 491710.1063/1.1757021 ↗
11. Rase D. E. · J. Am. Ceram. Soc. · 1955 · 38 · 10210.1111/j.1151-2916.1955.tb14585.x ↗
12. Jonker G. H. · J. Am. Ceram. Soc. · 1958 · 41 · 39010.1111/j.1151-2916.1958.tb13509.x ↗
13. Negas T. · J. Solid State Chem. · 1974 · 9 · 24910.1016/0022-4596(74)90087-5 ↗
14. O'Bryan H. M. · J. Am. Ceram. Soc. · 1974 · 57 · 52210.1111/j.1151-2916.1974.tb10801.x ↗
15. Ritter J. J. · J. Am. Ceram. Soc. · 1986 · 69 · 15510.1111/j.1151-2916.1986.tb04721.x ↗
16. Yu J. · Chem. Mater. · 2004 · 16 · 397310.1021/cm0487526 ↗
17. Yu J. · Appl. Phys. Lett. · 2004 · 85 · 289910.1063/1.1799246 ↗
18. Yu J. · Jpn. J. Appl. Phys. · 2004 · 43 · 813510.1143/JJAP.43.8135 ↗
19. Paradis P.-F. · Rev. Sci. Instrum. · 1996 · 67 · 26210.1063/1.1146581 ↗
20. Isshiki M. · Nucl. Instrum. Methods Phys. Res., Sect. A · 2001 · 467 · 66310.1016/S0168-9002(01)00441-7 ↗
21. Kohara S. · Nucl. Instrum. Methods Phys. Res., Sect. A · 2001 · 467 · 103010.1016/S0168-9002(01)00630-1 ↗
22. Sakka S. · J. Non-Cryst. Solids · 1989 · 107 · 17110.1016/0022-3093(89)90459-6 ↗
23. Proffen · J. Appl. Crystallogr. · 1999 · 32 · 57210.1107/S0021889899003532 ↗
24. Kimura T. · Acta Crystallogr. · 2003 · 59 · i128
25. Kohara S. · Science · 2004 · 303 · 164910.1126/science.1095047 ↗