Bi-layer oxide ferroelectrics

Compositions – Piezoelectric

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117 4, 117 5, 117 6, 117945, 501134, C30B 2922

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active

059140682

DESCRIPTION:

BRIEF SUMMARY
TECHNICAL FIELD

This invention relates to Bi-layer oxide ferroelectrics and more particularly, to Bi-layer oxide ferroelectrics which are particularly useful as capacitors, ultrasonic oscillators and the like and also to a method for making such Bi-layer oxide ferroelectrics in high accuracy.


BACKGROUND ART

Known oxide ferroelectrics which are employed as capacitors and transducers include, for example, Pb(Zr,Ti)O.sub.3 having the Perovskite structure and Bi-layer Perovskite compounds.
The term "Perovskite structure" used herein is intended to mean a crystal structure represented by the general formula, ABO.sub.3, wherein the BO.sub.6 oxygen octahedra with consists of six-coordinated octahedra of oxygen ions (O) about a given cation (B) undergo mutual corner sharings to form a three-dimensional fundamental structure in such a way that the resultant spaces are occupied with another type of cation (A). The above-indicated Pb(Zr,Ti)O.sub.3 represents a compound having the Perovskite structure wherein Pb corresponds to the A ion and the (Zr, Ti) corresponds to the B ion. In the above formula, the parentheses ( ) mean that at least one element selected from the elements included in the parentheses should be principally contained. It is a matter of course, however, that if a mixing ratio is defined, the elements being mixed are contained in such a compositional ratio.
Moreover, the term "layer Perovskite structure" is intended to mean a crystal structure wherein pseudo-Perovskite structures and intermediate layers (i.e. a layer intercalated between adjacent pseudo-Perovskite structures) are alternately located, as having such a structure as of pseudo-Perovskite structure/intermediate layer/pseudo-Perovskite structure/intermediate layer/ . . . , at a given period in one direction. The term "pseudo-Perovskite structure" means a structure which fundamentally consists of a Perovskite structure but whose elemental ratios are not exactly represented by ABO.sub.3 because the pseudo-Perovskite structure is invariably contiguous to the intermediate layers.
Further, the term "Bi-layer Perovskite structure" means such an intermediate layer as mentioned above wherein the cation in the intermediate layer consists of Bi. For instance, known compounds having a typical layer Perovskite structure include (Bi.sub.2 O.sub.2)(A.sub.n-1 B.sub.n O.sub.3n+1). In this instance, the intermediate layer consists of (Bi.sub.2 O.sub.2) and the pseudo-Perovskite structure consists of (A.sub.n-1 B.sub.n O.sub.3n+1). The suffix, n, means that corner-shared BO.sub.6 oxygen octahedral are stacked n times within the pseudo-Perovskite structure along the direction wherein the pseudo-Perovskite structures and intermediate layers are alternatively located.
FIG. 1(b) is a schematic projection view of a crystal structure, as viewed from the side of the layer, of a Bi-layer Perovskite compound of the formula wherein n=3, (Bi.sub.2 O.sub.2)(A.sub.2 B.sub.3 O.sub.10). In the figure, rectangles 11 each having a "cross" symbol therein, respectively, represent a BO.sub.6 octahedron formed by oxygen ions octahedrally coordinated about the B ion. These BO.sub.6 octahedra are three-dimensionally shared at the corners thereof to form a pseudo-Perovskite structure 18. The space between the adjacent BO.sub.6 oxygen octahedra 11 is occupied with an A ion 12. A region surrounded by a dotted line 15 indicates a Bi.sub.2 O.sub.2 intermediate layer isolating adjacent pseudo-Perovskite structures 18 from each other. This intermediate layer is constituted of Bi ions 13 and O ions 14.
A pure Perovskite structure has elemental ratios of A:B:O of 1:1:3. With the pseudo-Perovskite structure, the elemental ratios are n-1:n:3n+1, disenabling one to express the elemental composition as ABO.sub.3. As having set out hereinbefore, this is because the pseudo-Perovskite structures and the intermediate layers adjoin each other at a given period. As will be apparent from FIG. 1(b), the sites to be occupied by the A ions 12 are occupied by the Bi ions 13.
The compounds of the afor

REFERENCES:
patent: 5519566 (1996-05-01), Perino et al.
patent: 5683614 (1997-11-01), Boyle
"Structural Basis of Ferroelectricity in the Bismuth Titanate Family", R.E. Newnham, R.W. Wolfe and J.F. Dorrian, Materials Research Laboratory, pp. 1029-1039, vol. 6, No. 10, Jul. 28, 1971.
Ikegama et al, "Piezoelectricity in Ceramics of Ferroelectrics Bismuth Compound with Layer Structure" Jpn. Jr. of App. Phy. vol. 13, No. 10 Oct., 1975.

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