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Calcium ferroelectric

Moriyoshi C, Kuroiwa Y, Masuno A, Inoue H (2012) Site-selective calcium substitution in BaTi205 effect on the crystal structure tmd the ferroelectric phase transition. J Phys Soc Jpn... [Pg.64]

Calzada, M.L. and Sirera, R. (1996) Chemically derived ferroelectric calcium modified lead titanate thin films deposited from aquo-diol solvent solutions. /. Mater. Set Mater. Electron., 7, 39. [Pg.878]

Fig. 1.16 Some ferroelectric compounds and their phase transition types and temperatures. Different thermal expansion of calcium barium niobate in [hfcO] and [001] direction. Cracking along [hkO) faces In potassium lithium niobate caused by crossing the phase transition temperature at about 450°C. Fig. 1.16 Some ferroelectric compounds and their phase transition types and temperatures. Different thermal expansion of calcium barium niobate in [hfcO] and [001] direction. Cracking along [hkO) faces In potassium lithium niobate caused by crossing the phase transition temperature at about 450°C.
In addition to the studies on PZT, Glower et al. examined the ionic conduction in a ferroelectric material, Cao.iBao.9Ti03, by means of the same method as that used for PTZ [9]. They showed that the conduction in this oxide is ionie below 300°C, but electronic conduction appears sharply near 300°C and becomes predominant above 500°C. They identified the mobile ions as calcium ions by using so-called activation analysis, which was a kind of irradiation analysis of the surface of the solid after passing DC ciurent across the soUd conductor. [Pg.51]

Perovskite materials (ABX3) exhibit many fascinating properties from both theoretical and application perspectives, including ferroelectricity, superconductivity, charge ordering, and spin-dependent transport. The interplay of compositional, structural, optical, and transportation properties is commonly observed in this family, making them promising candidates as photocatalysts. Perovskites are characterised by a crystal structure similar to that of calcium titanium oxide (CaTiOs). Normally A and B sites are occupied by two cations with very different sizes (dA > dfi), whereas X (normally O) is an anion that bonds to both. In the ideal cubic-symmetry structure, the A and B cations are 12- and sixfold coordinated in bulk and surrounded by cuboctahedron and octahedron of anions, respectively. [Pg.120]


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