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Ferroelectric Solids

In this book those ferroelectric solids that respond to shock compression in a purely piezoelectric mode such as lithium niobate and PVDF are considered piezoelectrics. As was the case for piezoelectrics, the pioneering work in this area was carried out by Neilson [57A01]. Unlike piezoelectrics, our knowledge of the response of ferroelectric solids to shock compression is in sharp contrast to that of piezoelectric solids. The electrical properties of several piezoelectric crystals are known in quantitative detail within the elastic range and semiquantitatively in the high stress range. The electrical responses of ferroelectrics are poorly characterized under shock compression and it is difficult to determine properties as such. It is not certain that the relative contributions of dominant physical phenomena have been correctly identified, and detailed, quantitative materials descriptions are not available. [Pg.113]

The contrast in knowledge is a result of the degree of complexity of materials properties elastic piezoelectric solids have perhaps the least complex behaviors, whereas ferroelectric solids have perhaps the most complex mechanical and electrical behaviors of any solid under shock compression. This complexity is further compounded by the strong coupling between electrical and mechanical states. Unfortunately, much of the work studying ferroelectrics appears to have underestimated the difficulty, and it has not been possible to carry out careful, long range, systematic efforts required to develop an improved picture. [Pg.113]

From the mechanical viewpoint, ferroelectrics exhibit unsteady, evolving waves at low stresses. Waves typical of well defined mechanical yielding are not observed. Such behavior is sensitive to the electrical boundary conditions, indicating that electromechanical coupling has a strong influence. Without representative mechanical behavior, it is not possible to quantitatively define the stress and volume compression states exciting a particular electrical response. [Pg.113]

From the electrical viewpoint, stress-induced changes in remanent polar- [Pg.113]

114 Chapter 5. Physical Properties Under Elastic-Plastie Compression [Pg.114]


In this chapter studies of physical effects within the elastic deformation range were extended into stress regions where there are substantial contributions to physical processes from both elastic and inelastic deformation. Those studies include the piezoelectric responses of the piezoelectric crystals, quartz and lithium niobate, similar work on the piezoelectric polymer PVDF, ferroelectric solids, and ferromagnetic alloys which exhibit second- and first-order phase transformations. The resistance of metals has been investigated along with the distinctive shock phenomenon, shock-induced polarization. [Pg.136]

Studies of the electrical and mechanical responses of ferroelectric solids under shock compression show this technical problem to be the most complex of any investigated. The combination of rate-dependent mechanical and electrical processes along with strong electromechanical coupling has clouded physical interpretation of the numerous investigations. [Pg.137]

Egami T (2005) Electron-Phonon Coupling in High-Tc Superconductors 114 267-286 Egami T (2007) Local Structure and Dynamics of Ferroelectric Solids. 124 69-88 Eisenstein O, see Clot E (2004) 113 1-36... [Pg.220]

There is considerable interest in developing new types of magnetic materials, with a particular hope that ferroelectric solids and polymers can be constructed— materials having spontaneous electric polarization that can be reversed by an electric field. Such materials could lead to new low-cost memory devices for computers. The fine control of dispersed magnetic nanostructures will take the storage and tunability of magnetic media to new levels, and novel tunneling microscopy approaches allow measurement of microscopic hysteresis effects in iron nanowires. [Pg.130]

In addition, many of the ferroelectric solids are mixed ions systems, or alloys, for which local disorder influences the properties. The effect of disorder is most pronounced in the relaxor ferroelectrics, which show glassy ferroelectric behavior with diffuse phase transition [1]. In this chapter we focus on the effect of local disorder on the ferroelectric solids including the relaxor ferroelectrics. As the means of studying the local structure and dynamics we rely mainly on neutron scattering methods coupled with the real-space pair-density function (PDF) analysis. [Pg.70]

Barium titanate is one example of a ferroelectric material. Other oxides with the perovskite structure are also ferroelectric (e.g., lead titanate and lithium niobate). One important set of such compounds, used in many transducer applications, is the mixed oxides PZT (PbZri-Ji/Ds). These, like barium titanate, have small ions in Oe cages which are easily displaced. Other ferroelectric solids include hydrogen-bonded solids, such as KH2PO4 and Rochelle salt (NaKC4H406.4H20), salts with anions which possess dipole moments, such as NaNOz, and copolymers of poly vinylidene fluoride. It has even been proposed that ferroelectric mechanisms are involved in some biological processes such as brain memory and voltagedependent ion channels concerned with impulse conduction in nerve and muscle cells. [Pg.392]

There are certain crystals in which dipoles are spontaneously aligned in a particular direction, even in the absence of electric field. Such substances are called ferroelectric substances and the phenomenon is called ferroelectricty. The direction of polarisation in these substances can be changed by applying electric field. Baruion titanate (BaTi03), sodium potassium tartarate (Rochelle salt), and potassium hydrozen phosphate (KH2I04) are ferroelectric solids. If the alternate dipoles are in opposite directions, then the net dipole moment will be zero and the crystal is called anti-ferroelectric. Lead zirconate (PbZr03) is an anti-ferroelectric solid. [Pg.140]

The discussion in this section is applicable to any polar solid (i.e., one that has a permanent dipole) in which relaxation of the permanent dipoles occurs. In principle this approach could be applicable to piezoelectric and ferroelectric solids at temperatures above their transition temperature as well (see next chapter). However, the same response, as shown in Fig. 14.11, can also occur as a result of heavily damped resonance. This is easily seen in Fig. 14.7a as /. which is a measure of the damping, increases, the resultant resonance curves become flatter. Experimentally it is not easy to distinguish between the two phenomena. [Pg.487]

Curie temperature (T, ) - For a ferromagnetic material, the critical temperature above which the material becomes paramagnetic. Also applied to the temperature at which the spontaneous polarization disappears in a ferroelectric solid. [1]... [Pg.100]

Figure 11.18 The Curie-Weiss behaviour of a ferroelectric solid above the Curie temperature T. Note relative permittivity T, absolute temperature... Figure 11.18 The Curie-Weiss behaviour of a ferroelectric solid above the Curie temperature T. Note relative permittivity T, absolute temperature...
How can a ferroelectric solid be made from a polycrystalline aggregate ... [Pg.357]

In the second group, the diffuse peak in relative permittivity is steeper on the low-temperature side compared to the canonical relaxors, and at a temperature generally similar to the value of for a canonical relaxor, the PNRs amalgamate into domains and form a ferroelectric solid (Figure 6.20e). In these materials, no non-ergodic state forms. [Pg.205]

An estimate of the field strength, appearing at the cell surface and due to the natural rf dipole can also be made from the properties of BaTi03. This is a ferroelectric solid. It has a hysteresis of polarization and requires a certain minimum E, override its internal intrinsic... [Pg.366]

Figure 4.26. Hysteresis in the polarization and in the mechanical strain of ferroelectric solids in an external electric held. [Pg.139]


See other pages where Ferroelectric Solids is mentioned: [Pg.113]    [Pg.113]    [Pg.297]    [Pg.69]    [Pg.69]    [Pg.69]    [Pg.70]    [Pg.71]    [Pg.73]    [Pg.75]    [Pg.76]    [Pg.77]    [Pg.79]    [Pg.81]    [Pg.83]    [Pg.85]    [Pg.87]    [Pg.229]    [Pg.541]    [Pg.355]    [Pg.358]    [Pg.314]    [Pg.202]    [Pg.139]   


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Ferroelectric solids, role

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