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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 1336-1348 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: In this article, domain wall motion and the extrinsic contributions to the dielectric and piezoelectric responses in sol–gel derived lead zirconate titanate (PZT) films with compositions near the morphotropic phase boundary were investigated. It was found that although the films had different thicknesses, grain sizes, and preferred orientations, similar intrinsic dielectric constants were obtained for all films between 0.5 and 3.4 μm thick. It was estimated that about 25%–50% of the dielectric response at room temperature was from extrinsic sources. The extrinsic contribution to the dielectric constant of PZT films was mainly attributed to 180° domain wall motion, which increased with both film thickness and grain size. In studies on the direct and converse longitudinal piezoelectric coefficients of PZT films as a function of either stress or electric driving field, it was found that the ferroelastic non-180° domain wall motion was limited. Thus extrinsic contributions to the piezoelectric response were small in fine grain PZT films (especially those under 1.5 μm in thickness). However, as the films became thicker (〉5μm), nonlinear behavior between the converse piezoelectric coefficient and the electric driving field was observed. This indicated that there was significant ferroelectric non-180° domain wall motion under high external excitation in thicker films. The activity of the non-180° domain walls was studied through non-180° domain switching. For fine grain films with film thicknesses less than 2 μm, non-180° switching was negligible. Transmission electron microscopy plan-view micrographs evidenced non-180° domain fringes in these films, where the vast majority of grains were 50–100 nm in diameter and showed a single set of domain fringes. Taken together, these measurements suggest that the pinning of non-180° domain walls is very strong in films with thickness less than 2 μm. In thicker films, non-180° domain switching was evidenced when the poling field exceeded a threshold field. The threshold field decreased with an increase in film thickness, suggesting more non-180° domain wall mobility in thicker films. Non-180° domain switching in large grained PZT films was found to be much easier and more significant than in the fine grained PZT films. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 75 (1994), S. 7211-7219 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Nonlinear optical polymers contain molecular dipoles with very large hyperpolarizabilities in a glassy polymer matrix. Two typical examples—a guest-host system with dispersed polar dye molecules and a side-chain material with chemically attached molecular dipoles—were investigated by means of poling experiments, dielectric spectroscopy, thermally stimulated depolarization, and electro-optical thermal analysis. The dielectric behavior of both polymers can be described by the phenomenological Havriliak–Negami equation, and the existence of master curves for both materials demonstrates the validity of the time-temperature superposition principle above the respective glass transitions. Temperature-dependent mean relaxation times and relaxation-time distributions calculated from the dielectric data allow for an optimization of poling times. The dielectric relaxation strengths obtained from poling current and field, from dielectric measurements, and from thermally stimulated depolarization are in very good agreement and thus represent a useful measure of the polarization in poled polymers. From the temperature dependence of the polarization, optimal poling temperatures may be derived. Electro-optical thermal analysis yields the same temperature-stability curves as thermally stimulated depolarization and is therefore a valuable tool for investigating the stability of poled polymers, especially since it is not sensitive to charge effects. Optimal poling fields and currents must be selected as a compromise between high dipole mobilities (short relaxation times) and low bulk conductivities.
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  • 3
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Stable polymers with nonlinear optical side groups were synthesized from maleic anhydride copolymers and the azo dye Disperse Red 1 via esterification. After electrode poling under 135 V/μm at 185 °C, thermal stabilities were measured by pyroelectric and electro-optic thermal analysis and compared to a guest/host polymer of polymethylmethacrylate and the same dye. The pyroelectrically detected dipole orientation and the electro-optic activity of the side-chain polymers decreased only above 150 °C, and electro-optic r33 coefficients of up to 6 pm/V were achieved at 780 nm even without optimizing the dye content.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 64 (1994), S. 22-24 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Electron beams with an energy of 10 keV were employed for selectively poling only the lower part of a typical nonlinear optical guest/host polymer at a temperature of 90 °C. The resulting dipole orientation was examined by means of electro-optical measurements and thermally stimulated depolarization, while the nonuniform charge and polarization profiles were probed with laser-induced pressure pulses and thermal waves. The concept of nonlinear optical frequency conversion with simultaneous mode conversion is described as an example for the advantages of such a selective poling process.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 80 (2002), S. 3174-3176 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Electric-field-induced phase transitions and piezoelectric properties of 〈001〉-oriented Pb(Zn1/3Nb2/3)O3–xPbTiO3 single crystals for x=4.5% and 8% (PZN–4.5%PT and PZN–8%PT) have been investigated as a function of temperature. It was found that the piezoelectric properties and phase transitions for both crystals are strongly dependent on temperature. The measurements of polarization and strain as a function of unipolar electric field show that the field for the rhombohedral–tetragonal phase transition decreases linearly with temperature in the range between 25 and 105 °C. Thus, raising the temperature can stabilize the tetragonal phase in 〈001〉-oriented PZN–PT crystals. Longitudinal piezoelectric constant d33 in the rhombohedral phase increases with temperature for both crystals; in PZN–4.5%PT the slope itself increases significantly at temperatures over 60 °C. In the field-induced tetragonal phase, there is little change in d33 for PZN–8%PT within the temperature range investigated, while in PZN–4.5%PT a slight increase of d33 with temperature was observed at temperatures above 80 °C. © 2002 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Crystal Growth 101 (1990), S. 454-457 
    ISSN: 0022-0248
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 163 (1989), S. 215-219 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 201 (1993), S. 247-249 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Engineering and Design. Fusion 3 (1986), S. 309-318 
    ISSN: 0167-899X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Vacuum 42 (1991), S. 1071 
    ISSN: 0042-207X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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