WO1998033220A1

WO1998033220A1 - Relaxor ferroelectric single crystals for ultrasound transducers

Info

Publication number: WO1998033220A1
Application number: PCT/US1998/001521
Authority: WO
Inventors: Seung-Eek Park; Thomas R. Shrout; Patrick D. Lopath
Original assignee: The Penn State Research Foundation
Priority date: 1997-01-28
Filing date: 1998-01-27
Publication date: 1998-07-30
Also published as: US5998910A; EP1018172A1; EP1018172A4; AU6043898A; JP2001509312A

Abstract

∫001⊃ oriented crystals of lead zinc niobate - lead titanate solid solution (0 to 5 mole % lead titanate) have high electromechanical coupling > 85 % and exhibit electric field induced phase transition at electric field levels > 10 x Ec (where Ec is the coercive field), resulting in increased transducer driving voltages, decreased fabrication degradation, and high sensitivity/large bandwidth transducer characteristics due to high electromechanical couplings, up to 92 %. ∫001⊃ oriented crystals of lead magnesium niobate - lead titanate solid solution (20 to 50 mole % lead titanate) also exhibit high electromechanical couplings > 85 % and up to 94 %, and thereby can be formed into transducers which exhibit both high sensitivity and large bandwidth.

Description

Relaxor Ferroelectric Single Crystals for Ultrasound Transducers

This Application is a Continuation in Part of U S Patent Application Serial No 08/789,589, filed January 28, 1997, and further claims priority from Provisional Application Serial No

60/039.61 1 , filed March 12, 1997

FIELD OF THE INVENTION

This invention relates to transducers which employ ferroelectπcs and, more particularly, to an electromechanical transducer that is constructed using single crystals of lead zmc niobate - lead titanate or lead magnesium niobate - lead titanate solid solutions The compositions exhibit increased phase transition field values, allowing increased transducer driving voltages, decreased fabrication degradation and high electromechanical couplings, > 85 % and up to a maximum of 94%

BACKGROUND OF THE INVENTION

Piezoelectric Transducers

Piezoelectric ceramics are currently the material of choice for ultrasonic transducer applications offering relatively high coupling (kij), a wide range of dielectric constants (K), and low dielectric loss These merits translate into transducer performance in the form of relatively high sensitivity, broad bandwidth, impedance matching and minimal thermal heating

Pb(Zr, _x,Tι_x)0₃ (PZT) ceramics have been a mainstay for high pertormance transducer applications Compositionally, PZT ceramics lie near the morphotropic phase boundary (MPB) between the tetragonal and rhombohedral phases MPB compositions have anomalously high dielectric and piezoelectric properties as a result of enhanced polaπzabihty arising from coupling between two equivalent energy states, I e the tetragonal and rhombohedral phases, allowing optimum domain reorientation during the poling process Further modifications, using acceptor and donor dopants, give a wide range of piezoelectric compositions

Alternative MPB systems can be found in relaxor-based ferroelectπcs and their solid solutions with PbTι0₃ (PT) Lead based relaxor materials are complex perovskites with the general formula Pb(B,B,)0₃, (B, =Mg²⁺ , Zn²⁺, Nr\ Sc³⁺ , B₂ = Nb^s+, Ta⁵⁺, W⁶⁺ ) Characteristic of relaxors is a broad and frequency dispersive dielectric maxima Some relaxor-PT compositions such as modified Pb(Sc, ,Nb, _:)0₃ -PbTι0₃ (PSN-PT) seem to possess superior dielectric and piezoelectric properties compared to that of PZT ceramics However, if analyzed with respect to the ferroelectric transition temperature Tc (the temperature at which the material transforms from the prototypical non- ferroelectπc to ferroelectric phase being associated with a spontaneous polarization and large dielectric anomaly), no one type of ceramic offers significant advantages in overall transducer performance

Enhanced piezoelectric activity of MPB-based ceramics by compositionally adjusting the

Curie temperature (Tc) downward relative to room temperature, comes with the expense of more temperature dependent properties and less polarization stability, 1 e aging and loss of piezoelectric activity

Though relaxor- PT ceramics do not offer enhanced dielectric and piezoelectric properties comparable to PZT ceramics of similar T_c's, it is the single crystal form of relaxor-PT ceramics that exhibits ultrahigh piezoelectric properties not currently available with piezoelectric MPB ceramics This key distinction was first realized by Yonezawa et al (Journal of Japanese Society of Powder Metallurgy. Vol 16, pp 253-258, 1969) and later by Kuwata et al (Ferroelectπcs, Vol 37, pp 579- 582, 1981) for MPB compositions of Pb(Zn,_/3Nb_1/3)0₃ - PbTι0₃ (PZN PT) systems with k₃₃ values ranging 80 to 90%, followed by crystal growth and evaluation of Pb(Mg_1/3Nb_2/3)0₃ - PbTι0₃ (PMN- PT)

Although high coupling and piezoelectric properties of the PZN-PT system, first reported in 1969 and later in the PMN-PT system (1989), have been known for several years, their potential for high performance biomedical ultrasound transducers and related devices has only been recognized recently Serious efforts on the development of Pb(B_!B₂)0₃-PT crystals for high performance transducers is disclosed m US Patents 5,402,791 and 5,295,487 to Saitoh et al Therein are disclosed relaxor based ferroelectric single crystals of lead zinc niobate - lead titanate (Pb(Zn, ₃Nb_{2 3}), _xTι_x0₃) and lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb,_/3)_{l y}Ti_y0₃ ) solid solutions, where

0 05 <x ≤0 2 and 0 05 ≤y ≤0 2, respectively It should be noted that the range 0 OS ≤y ≤O 2 for

Pb(Mg_ι;3Nb,_/3)_{! y}Tι_y0₃ solid solutions described by Saitoh et al includes the non piezoelectric relaxor

(microdomain) region (0 05 ≤y <0 15) at room temperature For 0 15 ≤y <0 20, according to this invention, crystals of Pb(Mgj_/3Nb_1/3), _yTι_y0₃ solid solutions exhibit longitudinal coupling < 80%, only comparable to MPB ceramics

When optimum crystallographic cuts, in this case pseudocubic <001 > , are utilized for rhombohedral crystals, an electric field induced phase transformation from rhombohedral to tetragonal phase can occur under dc bias, because the polar axis in the rhombohedral phase is < 111 > The phase transition field is strongly dependent upon composition, I e , the closer to MPB, the lower the transition electric field level because two crystallographic states (rhombohedral and tetragonal) energetically become closer to each other and finally coexist at room temperature when the composition lies on a MPB (0 09 ≤x ≤ 1 0 and 0 35 ≤y ≤0 40, for Pb(Zn_1/3Nb,_/3), ι_x0₃ and Pb(Mg,_/3Nb_2/3), _yTι_y0₃, respectively)

The rhombohedral-tetragonal phase transition results in discontinuous changes m piezoelectric properties and dimensions This dimensional change can affect transducer performance during fabrication processes, such as mechanical clamping during poling Transducer polmg normally includes field cooling (cooling under dc-bias from the temperatures above Tc)

Figure 3 shows a plot of dielectric constant vs temperature for Pb(Zn_1/3Nb_2/3)₀₉₂Tι₀₀₈O₃, exhibiting transitions from rhombohedral to tetragonal (100°C) and from tetragonal to cubic (160°C) Apart from composition, the phase transition field decreases with increasing temperature Therefore, increasing temperature under dc bias causes the rhombohedral phase to readily* transform into the tetragonal phase

It should be noted that transducers are attached to multiple quarter wave length matching layers and/or take the form of a low impedance composite comprised of piezoelectric elements with intermediate passive polymer layers, in order to couple acoustic energy and decouple lateral modes

Therefore, successive cooling under bias will cause the crystals to transform back to a rhombohedral phase after the passive polymer becomes significantly rigid at low temperature, resulting in elastically clamped crystals, leading to internal stresses and mechanical failure Also, stability of rhombohedral phase becomes an issue as the transducer is driven at increased frequencies To increase driving frequency and thereby obtain enhanced sensitivity, the transducer must be thinner, resulting m an increased electric field at a same driving voltage Therefore, to avoid a phase transformation with a

<001 > rhombohedral crystal, the driving voltage must be limited To apply higher voltages for pulse generation, the composition of a rhombohedral crystal should be located appropriately away from the MPB

In summary, the problems exhibited by compositions of relaxor based single crystals are

1) Lead magnesium niobate - lead titanate (Pb(Mg,_;3Nb_2/3)_{1 )}Ti_y0₃) is not piezoelectric at room temperature when 0 05 ≤y < 0 15 and does not exhibit piezoelectric properties superior to conventional MPB ceramics when 0 15 ≤y <0 20

2) For compositions close to MPB for rhombohedral lead zinc niobate lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃), and lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_1/3), _yTι_y0₃), whereO 05 <x ≤0 09 and 0 33 < y <0 40,, the rhombohedral tetragonal phase transformation occurs at relatively low fields Piezoelectric Actuators

Electromechanical actuators constructed from piezoelectric or electrostπctive ceramics are used in applications requiring high generative force, high frequency operation, accurate displacement, quick response time, or small device sizes However, low field induced strain and poor reliability limit the usage of such ceramics for actuator applications

Electric field induced strain is the most important parameter for actuators This is demonstrated by the strain energy density which is a measure of the energy per unit mass an actuator can deliver,

e_max = 1/p • 1/4 • (1/2 • E( ²)

where e_max is the strain energy density E is the actuator's elastic modulus, e_max is the maximum field induced strain, and p is the actuator's density In designing an actuator, the maximum strain energy density should be as high as possible In electroactive ceramics, density and elastic modulus vary little from material to material Therefore, level of strain and maximum strain achievable with a reasonable electric field ( < 50kV/cm) dominates the energy density parameter

Strain for a given electric field is determined from a material's piezoelectric coefficient (d₃₃

) Soft lead-zirconate-titanates (PZT's) and perovskite relaxor-PT(Pb((B,,B₂)0₃-PbTi0₃, (where B, = Mg⁺², Zn⁺², Nι⁺², Sc⁺³, and B₂ = Nb^+S, Ta⁺⁵, W⁺⁶, ) based morphotropic phase boundary (MPB) ceramics offer piezoelectric coefficients — 600 to 700 pC/N However the best available actuators offer a maximum strain of not more than 0 15 % This limitation originates from the material's breakdown strength and polarization saturation

Soft PZT's and relaxor-PbTi0₃ based ceramics are compositionally engineered to have morphotrophic phase boundary (MPB) composition and further engineered to have a decreased paraelectπc-ferroelectπc transition temperature (Tc), resulting m high piezoelectric coefficients However, this increased piezoelectric activity comes with the expense of large hysteresis, ascribed to electric field induced domain motion This results in poor positioning accuracy and large heat generation Heat generation combined with decreased temperature usage range, also results in poor temperature stability of piezoelectric properties This limits the driving frequency, prohibiting the usage of these high piezoelectric coefficient ceramics for high frequency driving applications

Strain can be hysteresis minimized with hard piezoelectric ceramics, which exhibit decreased piezoelectric coefficient (d₃₃) A hard piezoelectric, such as PZT-4, exhibits piezoelectric coefficients of ~ 200 to 300 pC/N Another category of ceramic materials used in commercial actuators is electrostπctors Electrostπction strain is proportional to the square of an applied electric field A few materials such as lead magnesium niobate (PMN) or lead magnesium niobate-lead titanate (PMN-PT) solid solution ceramics with low lead titanate (PT) content exhibit a significant strain ( > 0 1 %) with virtually no hysteresis

In summary, the problems of commercially available piezoelectric and electrostπctive ceramics are

1) Low total strain __0 15 %)

2) Low strain energy density due to low piezoelectric coefficient (d₃₃) < 700pC/N and electrical breakdown strength

3) Significant hysteresis which leads to substantial heat generation and poor positioning accuracy

To achieve strains > 0 15 % , electroactive materials should possess high piezoelectric coefficients (d₃₃ > lOOOpC/N) and high breakdown strength

In the main, the prior art electroactive materials described above are based upon multi- crystalhne structures Saitoh et al in U S Patents 5,295,487 and 5,402,791 describe a range of piezoelectric single crystal materials which exhibit large electromechanical coupling coefficients and teach their use as ultrasound transducers One set of materials taught by Saitoh et al is based upon single crystals in the form of solid solutions of zmc lead niobate-lead titanate Another set of single crystals is given by the formula

Pb{(Ml _l/3Nb₍„_3HM)Ta_2z/3)_{l x y}Tι_xM2_y}0₃

where M l represents one of metals Zn, Ni and Mg, and M2 represents one of Pt, Fe, Bi, Rh and Ir, and x, y and z are defined as 0 05_< x.<.0 2, 0 00001j<yj<_.0 01 and 0^z_<0 1 , respectively

There is no teaching by Saitoh et al that only a certain subset of their materials will exhibit a high strain factor (it being known to those skilled in the art that high coupling coefficients do not necessarily equate to high strain factors) As will be apparent from the description of the invention below Applicants have discovered that a subset of the materials of Saitoh et al exhibit large strains so long as an electric field is applied thereto generally along the 001 crystalline axis SUMMARY OF THE INVENTION

<001 > oriented crystals of lead zinc niobate - lead titanate solid solution (0 to 5 mole% lead titanate) have high electromechanical coupling > 85 % and exhibit electric field induced phase transitions at electric field levels > 10 x Ec (where Ec is the coercive field), resulting in increased transducer driving voltages, decreased fabrication degradation, and high sensitivity /large bandwidth transducer characteristics due to high electromechanical couplings, up to 92% <001 > oriented crystals of lead magnesium niobate - lead titanate solid solution (20 to 50 mole% lead titanate) also exhibit high electromechanical couplings > 85 % and up to 94 % , and thereby can be formed into transducers which exhibit both high sensitivity and large bandwidth

BRIEF DESCRIPTION OF THE DRAWINGS

Figs la and lb show ultrasound transducers, in accordance with the invention, comprising single crystal piezoelectric elements and intervening polymers

Figs 2a and 2b show the phase diagrams of lead zinc niobate -lead titanate and lead magnesium niobate-lead titanate solid solutions, respectively

Fig 3 shows a dielectric constant vs temperature curve for Pb(Zn_1/3Nb_2/3)_{0 92}Tι₀₀₈O₃, exhibiting transitions from rhombohedral to tetragonal (100°C) and tetragonal to cubic (160°C)

Fig 4 shows longitudinal couplings as a function of composition and crystal orientation for lead zmc niobate - lead titanate (Pb(Zn, ₃Nb_2/3), _xTι_x0₃)

Fig 5 shows longitudinal couplings as a function of composition and crystal orientation for lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_2/3), _xTι_x0₃)

Figs 6a, 6b, 6c show P= (E) curves of <001 > oriented lead zinc niobate lead titanate (Pb(Zn,_;3Nb_2/3), _xTι_x0₃) crystals for x=0, x=0 045, and x=0 08, respectively

Fig 7 shows P= (E) curves for < 111 > and <001 > oriented lead zinc niobate - lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃) crystals for x=0, with applied unipolar electric fields, after poling (applying lO xEc at room temperature)

Fig 8 shows P=/(E) curves for <001 > oriented lead zinc niobate - lead titanate (Pb(Zn_1/3Nb_2/3)_{! x}Tι_x0₃) crystals for x=0, x=0 045, and x=0 08, respectively, with unipolar electric field applied after polmg (applying 10 x Ec at room temperature) Fig 9 shows strain vs electric field curves for <001 > oriented lead zinc niobate lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃) crystals for x=0, x=0 02, x=0 045, x=0 06 and x=0 08, respectively, with unipolar electric field applied after poling (applying lOx Ec at room temperature)

Fig 10 shows Ec and phase transition fields as a function of composition, for <001 > oriented lead zinc niobate - lead titanate (Pb(Zn_1/3Nb_2/3)_{l x}Ti_x0₃) crystals

Fig 11 shows Ec and phase transition fields as a function of composition for <001 > oriented lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb,_/3), _yTι_y0₃) crystals

Fig 12 shows a perspective view of an actuator incorporating a single crystalline ferroelectric wherein an electric field is applied along the <001 > crystallographic axis

Figs 13a, 13b shows phase diagrams of lead zmc niobate-lead titanate and lead magnesium niobate-lead titanate solid solutions

Fig 14 shows a plot of strain as a function of electric field for <001 > oriented rhombohedral crystals Pb(Zn_1/3Nb_2/3)_{l x}Tι_x0₃, (x=0 0, 0 045, 0 08) and Pb(Mg_1/3Nb_2;3), _yTι_y0₃, (y =0 24)

Fig 15 shows plots of strain vs electric field for samples with different crystal orientations

Fig 16 shows plots of strain vs electric field for <001 > oriented Pb(Zn_1/3Nb_1/3)₀₉₀₅Tι₀₀₉₅O₃ crystal as an example of MPB behavior

Fig 17 shows plots of strain as a function of electric field for various <001 > oriented rhombohedral crystals (Pb(Zn_1/3Nb_2/3), _xTι_x0₃, (x=0,0 045,0 08) and Pb(Mg_1/3Nb„₃), _yTι_y0₃, (y=0 24), where hysteresis is low up to the maximum applied electric field

Fig 18 shows plots of strain as a function of electric field for various < 001 > oriented rhombohedral crystals (Pb(Zn_1/3Nb_2/3), _xTι_x0₃, (x=0,0 045,0 08) and Pb(Mg,_/3Nb_9/3)_{l y}Tι_y0₃, (y =0 24)), where electric field is applied until the samples electrically break down

Fig 19 shows representative Pb(Zn_1/3Nb_2/3)₀₉₅₅Tι₀₀₄₅O₃ crystals oriented along <001 > +α direction, where is the degree of deviation toward < 111 > from the exact <001 > direction

Figs 20, 21 show plots of low field ( <40kV/cm) strain behavior for Pb(Zn,_/3Nb_2/3)₀₉₅₅Tι₀₀₄₅0₃ crystals oriented along <001 > +α direction, where is the degree of deviation toward < 111 > from the exact <001 > direction, for various values of

Fig 22 shows plots of high field (≡ lOOkV/cm) strain behavior for Pb(Zn_1/3Nb_2/3)₀₉₅₅Tι₀₀₄₅O₃ crystals oriented along <001 > +a direction, where a is the degree of deviation toward < 111 > from the exact <001 > direction, for various values of

Fig 23 shows a plot of hysteresis as a function of for Pb(Zn_l/3Nb_2/3)₀₉₅₅Tι₀₀₄₅O₃ crystals oriented along <001 > +a direction, where is the degree of deviation toward < 111 > from the exact < 001 > direction

Fig 24 shows a plot of strain hysteresis as a function of a for Pb(Zn_1/3Nb_2/3)₀₉₅₅Tι₀₀₄₅O₃ crystals oriented along <001 > +a direction, where is the degree of deviation toward < 111 > from the exact < 001 > direction

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS OF THE INVENTION

Piezoelectric Transducers

This invention establishes structural property relationships, optimum compositions and crystallographic orientations for single crystals of lead zmc niobate - lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃) and lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_2/3), _yTι_y0₃) solid solutions, which obtain ultrahigh electromechanical coupling and avoid induced phase transitions during transducer fabrication and driving Based on the commonalties inherent to relaxor-PT systems, this invention considers two representative systems of lead zmc niobate - lead titanate (Pb(Zn, ₃Nb_2/3), _xTι 0₃) and lead magnesium niobate - lead titanate (Pb(Mg_!/3Nb_2/3)_{| y}Tι_y0₃) Though lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_2/3), _yTι_y0₃) crystals exhibit piezoelectric properties comparable with lead zmc niobate - lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃), more focus is given to the lead zinc niobate - lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃) system, owing to its relatively lower PT content for MPB This allows more uniform crystal growth of such solid solution materials

The crystals were fabricated as follows High purity ( > 99 9%) powders of Pb₃0₄, ZnO, MgC0₃, Nb,0₅ and TiO-, were used as starting materials Raw powders were weighed in desired molar ratios with excess Pb₃0₄ as a flux The powder was dry mixed for a desired period of time using a tumbling mill Mixed powder was loaded into a platinum crucible, which was then placed an alumina crucible sealed with an alumina lid and alumina cement to minimize PbO volatilization

The crucible and powder were then placed in a tube furnace and held at an appropriate soak temperature above the melting temperature, followed by slow cooling The crucible was then furnace- cooled to room temperature Hot HN0₃ was used to separate the crystals from of the rest of the melt The crystals of lead zinc niobate - lead titanate and lead magnesium niobate - lead titanate solid solutions can similarly be fabricated using, 1 e , the top seeded solution growth method (TSSG), the submerged seeded solution growth method, Kyropoulous method, the hydro thermal method, the Bndgman method, and the solid state growth technique (exaggerated gram growth), in addition to the flux method described above Other crystal forms can be used For example, material bodies comprising a textured structure or epitaxially grown films also show superior behavior Further, the crystals can contain certain amounts of impurities from chemicals and crucibles, 1 e Pt, Ir, Rh, Fe, and Bi

The piezoelectric properties were measured as follows For longitudinal coupling (k₃₃) determinations, bar shape samples with lengths ranging from 3 mm to 5 mm were used The piezoelectric coefficient (k₃₃) was calculated based on IEEE standards Individual crystals were oriented along their pseudocubic axes < 111 > and <001 > using a Laue back reflection camera For electrical characterization, samples were prepared by polishing with silicon carbide and alumina polishing powders to achieve flat and parallel surfaces, onto which gold electrodes were sputtered

High-field measurements, including polarization and strain hysteresis, were made using a modified Sawyer-Tower circuit and linear variable differential transducer (LVDT), driven by a lock in amplifier (Stanford Research Systems, Model SR830) Plate shaped samples with thicknesses ranging from 0 2 mm to 0 5 mm were used The voltage was supplied using a Trek 609C-6 high voltage DC amplifier Through use of the LVDT sensor, sample strain was measured when a field was applied Electric fields as high as - 140 kV/cm could be applied using an amplified unipolar waveform at 0 2 Hz During testing the samples were submerged in Fluoπnert (FC-40, 3M, St Paul, MN), an insulating liquid, to prevent arcing

Piezoelectric single crystals according to the present invention are expressed by formulae 1-4 below

Pb(Zn_1/3Nb_2/3)_{1 x}Tι_x0₃ (1)

where x is defined as 0 ≤ < 0 05 With these compositions, crystals have a rhombohedral structure and crystals oriented along pseudocubic <001 > direction exhibit longitudinal couplings > 85 % If x >0 05, <001 > oriented rhombohedral Pb(Zn_1/3Nb_2/3), _xTι_x0₃ crystals transform into a tetragonal phase at electric fields lower than a 10 x coercive field (Ec), limiting transducer driving voltage and increasing fabrication degradation

Pb(Mg,_/3Nb_2/3)_{1 y}Tι_y0₃ (2)

where y is defined as 0 20 <y ≤0 50 With these compositions, crystals oriented along the pseudocubic <001 > direction exhibit longitudinal coupling > 80% If0 ≤y <0 15, Pb(Mg_1/3Nb,_/3)₁ _yTι_y0₃ crystals are not piezoelectric without a dc-bias at room temperature If 0 15 <y <0 2, Pb(Mg_1/3Nb,_/3)i _yTι_y0₃ crystals exhibits longitudinal couplings lower than 80%

Pb(Mg_l/3Nb_2/3)_{l y}Ti_y0₃ (3)

where y is defined as 0 20 <y <0 35 With these compositions, crystals have rhombohedral structure and crystals oriented along pseudocubic <001 > direction exhibit longitudinal couplings > 80%

Pb(Mg_1/3Nb_2/3), _yTι_y0₃ (4)

where y is defined as 0 35 <y ≤0 50 With these compositions, crystals have MPB or tetragonal structure and crystals oriented along pseudocubic < 001 > direction exhibit longitudinal couplings > 85 % , comparable to those observed with formula 1

It is more preferable to use the crystals with the compositions of

Pb(M_gl/3Nb_7/3), _yTι_y0₃ (5)

where, y is defined as 0 25 ≤y ≤0 33 With these rhombohedral compositions, <001 > oriented crystals possess longitudinal couplings > 85% with a maximum value of — 94% However, if 0 33 <y ≤0 40, the resulting composition is close to the MPB or lies on the MPB, resulting in < 001 > oriented rhombohedral Pb(Mg _1/3Nb_2/3) , _xTι_x0₃ crystals which transform into a tetragonal phase at significantly lower electric fields, e g , < 10 x coercive field (Ec)

Fig la shows an exploded view of 2-2 composite ultrasound transducer 100, comprising plural single crystal piezoelectric elements 102, encompassing polymer layers 104 and electrodes 106 and 108 Fig lb shows an exploded view of 1 3 composite ultrasound transducer 110, comprising plural single crystal piezoelectric elements 112, encompassing polymer layers 114 and electrodes 116 and 118

Ultrasound transducer 100 is manufactured by the following method Transducer fabrication from an as-grown single crystal began with orientation using a Laue back reflection camera Once a reference face parallel to the (001) plane was polished into the crystal, the crystal was sliced parallel to the reference face to approximately 1 mm This slice was then polished flat and gold sputtered on both sides An electric field, as high as lOx the coercive field (Ec), was applied to pole the slice Kerfs were cut into the material parallel to < 100 > , using standard dicing technology, such as a Kulicke and Soffa 782 wafer dicing saw The cut spaces were then filled with polymer such as Hysol 2038/3404 epoxy The composite was polished again down to a determined thickness and gold was sputtered on both sides To make sure poling was complete, electric fields as high as 10 x Ec were then applied at temperatures above the polymer softening temperature (in this case ~60°C) The composite was then cooled, under dc-bias, to room temperature

Figs 2a and 2b show phase diagrams of lead zinc niobate - lead titanate and lead magnesium niobate lead titanate solid solutions, respectively The dots reflect the crystal compositions tested in the process of making this invention, and the solid dots represent the compositions that fall within the claimed ranges of this invention

Fig 3 shows variations of dielectric constant vs temperature for Pb(Zn_1/3Nb_2/3)_{0 92}Tι₀₀₈O₃, exhibiting transitions from rhombohedral to tetragonal (100°C) and tetragonal to cubic (160°C) Increased temperature, together with dc bias, cause the rhombohedral phase to readily transform to the tetragonal phase This occurs for all <001 > oriented rhombohedral crystals of lead zmc niobate - lead titanate (Pb(Zn_1/3Nb_2/3), _xTι_x0₃) and lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb, ₃), _yTι_y0₃

) solid solutions, where 0 ≤x <0 09 and 0 15 ≤y ≤0 35, respectively

Stability of the rhombohedral phase during poling becomes an issue for 0 05 < x <0 09 and 0 33 ≤y <0 35, as transition fields are less than 10 x Ec at room temperature (where the rhombohedral tetragonal transition occurs at much lower field intensities with increased temperature)

Also, rhombohedral phase stability issues limit transducer driving voltage, especially at high driving frequencies To increase the driving frequency for enhanced sensitivity, the transducer must be thinner, resulting in an increased electric field at the same driving voltage Therefore, use of a <001 > rhombohedral crystal limits the transducer driving voltage, unless composition of the rhombohedral crystal is adjusted to be appropriately distant from the MPB

Table 1 presents dielectric and piezoelectric properties, calculated based on IEEE standards, as a function of composition and crystal orientation High longitudinal couplings (k₃₃ > 85 %) can be observed with crystals oriented along the pseudocubic <001 > direction < 111 > oriented rhombohedral crystals of lead zinc niobate - lead titanate (Pb(Zn_1/3Nb,_/3)_{! x}Tι_x0₃) and lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_2/3), _yTι_y0₃ ), where 0 ≤x <0 9 and 0 2 <y <0 35, exhibited inferior couplings < 40% If 0 15 ≤y <0 2, lead magnesium niobate - lead titanate (Pb(Mg,_/3Nb_1/3), _yTι_y0₃ ) solid solutions possess longitudinal coupling < 80%, only comparable to the conventional MPB ceramics such as PZT Table 1 Piezoelectric Properties of various PZN-PT and PMN-PT crystals (longitudinal mode)

Composition Crystal Orient coupling s_M ^b (10 loss <1₃₃ (pC/N)

Structure ^,2m²/N) FZN Rhom' 111 0₃8 74 900 0012 83

001 0.85 48 3600 0008 1100

PZN-2%PT Rhom 111 038 77 900 0004 90

001 0.87 74 3800 0010 1550

PZN-4.5%PT Rhom 111 03₅ 90 1500 0004 110

001 0.92 102 4000 0004 2000

PZN-6 PT Rhom 111 033 73 710 0004 74

001 093 130 500 0012 2400

PZN-8%PT Rhom 111 039 74 2150 0012 82

001 094 130 ₄200 0012 2400

PZN-9 ₅%PT MPB² 111 064 104 ₄300 0007 600

001 089 77 1600 0004 1600

PZN 12%PT Tetra³ 001 0 86 900 0 004 500

PlviN-24 PT Rhom 001 0.84 54 3700 0009 900

PMN-33%PT Rhom 001 0.94 79 4500 0012 1700

PMN-35%PT MPB 001 0.92 67 3100 0014 1240

PMN-40%PT Tetra 001 0.85 1000 0005

¹ rhombohedral

² morphotropic phase boundary - coexistence of both rhombohedral and tetragonal phases

³ tetragonal

From Table 1 , it can be concluded that compositions of lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_2/3)_{1 y}Tι_y0₃ ) crystals must be 0 20 <y ≤0.50, in order to obtain ultrahigh couplings > 80% More particularly, compositions of lead magnesium niobate - lead titanate (Pb(Mg,_/3Nb_2/3), _vTι_y0₃) crystals should preferably be 0 25 ≤ y ≤ 0 50 to have longitudinal couplings higher than 85 % , comparable to lead zmc niobate - lead titanate (Pb(Zn,_/3Nb_2/3), _xTι_x0₃) High couplings > 85% with low dielectric constants ( < 1000) for tetragonal lead magnesium niobate - lead titanate (Pb(Mg_1/3Nb_2/3), _yTι_y0₃ ) crystals 0 38 <y ≤O 50) illustrate significant usefulness for single element transducers, as this type of transducer requires high electromechanical coupling, with a low dielectric constant for electrical impedence matching

Fig 4 shows plots of longitudinal coupling as a function of composition and crystal orientation, for lead zinc niobate - lead titanate (Pb(Znι_/3Nb_2/3), _xTι_x0₃) It can be seen that closeness to the MPB is not essential to obtain ultrahigh coupling, if rhombohedral crystals are oriented along the <001 > axis Solid dots indicate coupling values as a function of compositions that are within the scope of the invention

Fig 5 shows plots of longitudinal coupling as a function of composition and crystal orientation for lead magnesium niobate - lead titanate (Pb(Mg„₃Nb_2/3), _xTι 0₃) Couplings > 80% can be observed for the compositions 0 2 <y <0 5 Solid dots indicate coupling values as a function of compositions that are within the scope of the invention

Figs 6a, 6b, 6c show P=/(E) curves of <001 > oriented lead zmc niobate - lead titanate (Pb(Zn_l/3Nb, ₃), _xTι_x0₃) crystals for x=0, x=0 045, and x =0 08, respectively All <001 > oriented crystals exhibited ferroelectric hysteresis similar to those observed with single domain switching, implying a stable domain configuration Coercive fields (Ec), where orientation of ferroelectric domains occurs by application of an electric field, were found to be almost the same ( ~ 3kV/cm) for all <001 > oriented rhombohedral crystals The larger Ps (35 μC/cm²) and hump in P=/(E) curve observed with <001 > oriented Pb(Zn,_/3Nb_2/3)_{0 92}Tι₀₀₈O₃) crystals are related to the rhombohedral to tetragonal phase transition

Fig 7 shows P=/(E) curves for < 111 > and <001 > oriented lead zmc niobate lead titanate (Pb(Zn_1/3Nb-,_/3), _xTι_x0₃) crystals for x=0, with a unipolar electric field applied, after poling (applying 10 x Ec at room temperature) All <001 > oriented rhombohedral crystals exhibited hysteresis-free behavior, resulting from a stable domain configuration However, domain instability with < 111 > oriented rhombohedral crystals resulted in hysteresis in P =/(E) curves and inferior piezoelectric properties, as presented in Table 1

Fig 8 shows P=/(E) curves for <001 > oriented lead zinc niobate - lead titanate

(Pb(Zn,_/3Nb_2/3), _xTι_x0₃) crystals for x=0, x=0 045, and x=0 08, respectively, with an applied unipolar electric field, after poling (applying 10 x Ec at room temperature) Each crystal exhibited a discontinuous increase m polarization at the electric fields, the amount of which was inversely proportional to x This discontinuous increase in P=/(E) curves and resultant hysteresis are caused by an electric field-induced phase transformation, I e , rhombohedral to tetragonal transition for

<001 > oriented rhombohedral crystals

Fig 9 shows strain vs electric field curves for <001 > oriented lead zinc niobate - lead titanate (Pb(Zn_1/3Nb,_/3)j _xTι_x0₃) crystals for x=0, x=0 02, x=0 045, x=0 06 and x=0 08, respectively, with an applied unipolar electric field, after poling (applying lOx Ec at room temperature) Associated with the phase transition, strain increased abruptly and a large hysteresis can be observed This large strain during the induced phase transition, resulted in an increased fabrication failure rate and limited the transducer driving voltage

Fig 10 shows Ec and phase transition fields as a function of composition, for <001 > oriented lead zinc niobate lead titanate (Pb(Zn,_/3Nb_2/3)_{l x}Ti_x0₃) crystals Ec ( ~ 3kV/cm) does not vary significantly as a function of composition, but the transition field is strongly dependent upon composition Electric fields > 10 X Ec can be applied without causing a phase transformation at room temperature for <001 > oriented lead zinc niobate - lead titanate (Pb(Zn_1/3Nb,_/3), _xTι_x0₃) crystals, when compositions are 0 <x <0 05 Crystals with compositions 0 ≤x <0 05 have a Tc lower than those x ≥O 05, possibly resulting in more temperature dependent properties, and less polarization stability However, as shown in the phase diagram of lead zinc niobate - lead titanate (Pb(Zn,_/3Nb-,_/3)_! χTι_x0₃, Fig 2), Tc increases with increased x, whereas the rhombohedral - tetragonal transition temperature decreases, the latter being more critical during fabrication and driving Also, transducer temperature can be maintained constant by using PTCR (positive temperature coefficient resistor) ceramics such as doped BaTι0₃

Fig 11 shows Ec and phase transition fields as a function of composition for <001 > oriented lead magnesium niobate - lead titanate (Pb(Mg,_/3N ,_/3), _yTι_y0₃) crystals Ec( ~ 3kV/cm) does not vary significantly as a function of composition, but the transition field is strongly dependent upon composition Electric fields > 10 x Ec can be applied without causing a phase transformation at room temperature for <001 > oriented lead magnesium niobate lead titanate (Pb(Mg_1/3Nb-, ₃)_{l y}Tι₎0₃) crystals when compositions are y ≤O 33

Experimental

Transducers using <001 > oriented rhombohedral Pb(Zn_1/3Nb-,_/3)_{0 955}Tι₀₀₄₅O₃ crystals and rhombohedral Pb(Zn_1/3Nb_2/3)_{0 92}Tι₀₀₈O₃ crystals were manufactured as shown in Fig 1 As-grown single crystals were oriented using a Laue back reflection camera Once a reference face parallel to the (001) plane was polished into the crystal, the crystals were sliced parallel to the reference face to approximately 1 mm The slice was then polished flat, and gold was sputtered on both sides

Electric fields as high as 10 x Ec were applied to pole the disk Kerfs were cut into the material, parallel to < 100 > , using standard dicing technology such as a Kuhcke and Soffa 782 wafer dicing saw The cut spaces were then filled with polymers such as Hysol 2038/3404 epoxy The composite was polished again down to a determined thickness and gold was sputtered on both sides To make sure poling was complete, electric fields as high as ~ 10 xEc were then applied at temperatures above the polymer softening temperature (in this case ~ 60°C) The composite was cooled under dc-bias, down to room temperature

Table 2 presents longitudinal coupling values (k₃₃) for a single element transducer and couplings measured from a 2x2 composite (k_bar ) Mechanical clamping by tall and narrow element shape (lateral clamping) and by the rigid polymer results in decreased values of k_bar However, further decreases in k_bar can be found m example 2 below, with increased mechanical failure resulting from the phase transformation during poling It should be noted that, even though a single longitudinal bar having a composition closer to the MPB exhibits higher couplings, subsequent couplings of composites are higher for the compositions that are positioned away from MPB Table 2

Composition orienk₃₃ tor single k ar for 2-2 survived tation element composite transducers example 1 Pb(Zn_1/3Nb_2/3)_{0 955}Tι₀₀₄₅O₃ <001 > 92% 89% 90% example 2 Pb(Zn_1/3Nb_2/3)_{0 92}Tι₀₀₈O₃ <001 > 94% 70% 75 %

Piezoelectric Actuators

It has been found that certain single crystal ferroelectπcs will evidence very high strain values if their constituents restrict their crystalline form to the rhombohedral structure and an electric field is applied thereacross so as to be in general alignment with the <001 > crystallographic axis Such ferroelectπcs exhibit very low levels of hysteresis and thus may be driven at relatively high frequencies without overheating The materials comprising the invention are preferably in solid solution form

Single crystalline ferroelectπcs, which exhibit large strain and low hysteresis and are usable with actuators incorporating the invention, are solid solutions of lead zinc niobate-lead titanate or lead magnesium niobate-lead titanate, which possesses a large piezoelectric coefficient (d₃₃ — 1000 pC/N to 2500 pC/N), and a maximum strain > 1 2%

In Fig 12, an actuator 10 incorporating the invention comprises a ferroelectric body 12 that is bounded by conductive electrodes 14 and 16 Body 12 comprises a single crystal solid solution of the chosen ferroelectric composition and the crystal axes of the crystal are generally aligned as shown by coordinates 20 When a voltage V is applied across electrodes 14 and 16, ferroelectric body 12 is poled as shown by arrow 24

A ferroelectric single crystal according to the present invention is described by formulae 1 and 2 below

Pb(Zn_l/3Nb_2/3)_{l x}Ti_x0₃ (6) Pb(Mg_1/3Nb_2/3), _yTι_y0₃ (7)

where x and y are defined as 0 ≤x <0 10, and O ≤y <0 40, respectively If x > 0 1 and y >0 4, the single crystals have a tetragonal structure with piezoelectric coefficients as low as 500 pC/N

A more preferred range of limits for x and y are 0 ≤x <0 09, and O ≤y <0 35, resulting in rhombohedral crystalline structure In the range of 0 09 ≤x ≤0 1 and 0 35 <y ≤0 4, crystals lie on morphotropic phase boundaries (MPB), with coexisting rhombohedral and tetragonal phases In spite of observed strain as high as 1 % and large low field piezoelectric coefficients (d₃₃ ωl500 pC/N) for MPB crystals, large hysteresis associated with domain motion and phase transition is observed when strain is plotted versus applied electric field for such MPB crystals Thus while such compositions are usable and exhibit large strain values, their range of applications is not as wide as materials in the more preferred ranges of x and y.

Piezoelectric single crystals of formulae 6 and 7 should be oriented and poled generally along the pseudocubic <001 > direction to obtain a large strain value with little or no hysteresis effects

EXPERIMENTAL

The piezoelectric coefficients (d₃₃) of lead zmc niobate-lead titanate and lead magnesium niobate-lead titanate solid solution single crystals were measured using direct observation of strain as a function of electric field as well as calculations based on IRE standards

The crystals were fabricated as follows High purity ( > 99 9%) powders of Pb₃0₄, ZnO, MgC0₃, Nb₂0₅ and Tι0₂ were used as starting material. Raw powders were weighed with desired molar ratio with excess Pb₃0₄ as a flux. The powder was dry mixed for a desired period of time using a tumbling mill Mixed powder was loaded into a platinum crucible, which was then placed in an alumina crucible sealed with an alumina lid and alumina cement to minimize PbO volatilization The crucible and powder were then placed in a tube furnace and held at an appropriate soak temperature above melting temperature, followed by slow cooling. The crucible was then furnace-cooled to room temperature Hot HN0₃ was used to separate the crystals out of the rest of the melt

Crystals of lead zmc niobate - lead titanate and lead magnesium niobate - lead titanate solid solutions can similarly be fabricated using a top seeded solution growth method (TSSG), a submerged seeded solution growth method, Kyropoulous method, the hydrothermal method, solid state reaction via exaggerated gram growth and the Bndgman method, in addition to the flux method described above Also, single crystals or pseudocrystals that consist of multiple single crystals of lead zinc niobate-lead titanate and lead magnesium niobate-lead titanate solid solutions can be fabricated using textured growth or epitaxial growth, that is, the growth of crystals of one material on the crystal surface of another material, such that the crystalline substrates of both materials have the same structural orientation

The piezoelectric properties were measured as follows Individual crystals were oriented along their pseudocubic < 111 > , < 110 > and <001 > directions using a Laue back reflection camera For electrical characterization, samples were prepared by polishing with silicon carbide and alumina polishing powders to achieve flat and parallel surfaces onto which gold electrodes were sputtered

High-field measurements included polarization and strain hysteresis using a linear variable differential transducer (LVDT) driven by a lock-in amplifier (Stanford Research Systems, Model SR830) Plate shape samples with the thickness ranged from 0 2 mm to 0 5 mm were used The voltage was supplied using a Trek 609C-6 high voltage DC amplifier Through the LVDT sensor the strain of the samples was measured with the application of applied fields Electric fields as high as — 140 kV/cm were applied using an amplified unipolar wave form at 0 2 Hz

During testing the samples were submerged in Fluonnert (FC-40, 3M, St Paul, MN), an insulating liquid, to prevent arcing For piezoelectric coefficιent(d₃₃) determination, bar shape samples with the lengths which ranged from 3 mm to 5 mm were used Piezoelectric coefficient (d₃₃) was calculated based on IRE standards

Figs 13a and 13b show phase diagrams of lead zmc niobate - lead titanate and lead magnesium niobate-lead titanate solid solutions, respectively The solid dots are the crystal compositions which were tested during the development of the invention

Table 3 presents low field dielectric and piezoelectric properties, calculated based on IRE standards, as a function of composition and crystal orientation High piezoelectric coefficient (d₃₃ > 1000 pC/N) crystals had a rhombohedral structure or MPB composition and orientation along pseudocubic < 001 > direction Piezoelectric coefficients as high as 2200 were measured for (001) oriented rhombohedral crystals of Pb(Zn_1/3Nb_2/3)_{0 92}Tι_00gO₃

Table 3. Low Field Piezoelectric Properties of Various PZN-PT and PMN-PT Crystals.

001 0.85 48 3600 0.008 1100

PZN-4.5%PT Rhom 111 0.35 9.0 1500 0.004 110 001 0.91 102 4000 0.004 2000

PZN-8%PT Rhom 11 1 0.39 7.4 2150 0.012 82 001 0.94 130 4200 0.012 2200

PZN-9.5%PT MPB' 111 0.64 10.4 4300 0.007 600 001 0.89 77 1600 0.004 1600

PZN-12%PT Tetra³ 001 0.86 900 0.004 500

PMN-24%PT Rhom 001 3700 0.009 900 PMN-33%PT Rhom 001 0.94 79 4500 0.012 1700 PMN-35%PT MPB 001 0.92 67 3100 0.014 1240 rhombohedral.

^" morphotropic phase boundary - coexistence of both rhombohedral and tetragonal phases. ³ tetraeonal.

Fig. 14 shows a plot of strain as a function of electric field for various <001 > oriented rhombohedral crystals (Pb(Zn_1/3Nb_2/3),._xT 0₃ (x=0, 0.045, 0.08) and Pb(Mg_1/3Nb_2/3),._yTi_y0₃ (y =0.24)). Piezoelectric coefficients (d₃₃) directly calculated from the slope of strain vs. electric field curves confirmed the values of piezoelectric coefficients presented in Table 3. A d₃₃ value >2500 pC/N was directly measured from the slope of the strain versus electric field curve for a <001 > oriented Pb(Zn,_/3Nb_2/3)_0..₎₂Ti_{u 08}O₃ crystal. Low hysteresis behaviors are apparent from the plots of Fig 14 That behavior can be ascribed to a stable domain configuration Strain behavior of piezoelectric ceramics (PZT-5H) with the largest piezoelectric coefficient (d₃₃ — 750pC/N) is compared with those of single crystals in the

Fig 15 shows examples of strain vs electric field for samples with different crystal orientations Pb(Zn,_/3Nb_2/3)_{0 92}Tι₀₀₈O₃ crystal oriented along the pseudocubic < 111 > and <001 > directions and a Pb(Znι_/3Nb_2/3)_{0 955}Tι₀₀₄₅0₃ crystal oriented along the pseudocubic < 110 > direction were chosen as examples E-field induced strain deviated from linearity and exhibited large hysteresis due to domain motion for crystals oriented along < 1 1 1 > and < 1 10 > directions It was concluded that pseudocubic <001 > was the direction resulting in a hysteresis strain

Fig 16 shows the strain vs electric field curve for <001 > oriented

Pb(Zn_1/3Nb_2/3)_{0 905}Tι₀₀₉₅O₃ crystal as an example of MPB behavior Strain as high as 1 % was observed, with large hysteresis due to the electric field induced domain motion It is believed that the rhombohedral -tetragonal phase transition is also related to this hysteresis It was concluded that the crystal must be rhombohedral to have low hysteresis strain behavior

Fig 17 shows the strain as a function of electric field for various <001 > oriented rhombohedral crystals (Pb(Zn_1/3Nb,_/3), _xTι_x0₃ (x=0, 0 045, 0 08) and PtyMg^Nb^), _yTι_y0₃

(y =0 24)), where hysteresis is low, up to the maximum applied electric field Low hysteresis strain up to 0 55 % was observed Strains of various piezoelectric ceramics such as soft PZT (PZT 5H), hard PZT (PZT-8) and of electrostπctive ceramics are compared m the Fig

Fig 18 shows the strain as a function of electric field for various < 001 > oriented rhombohedral crystals (Pb(Zn_1/3Nb_2/3)_{l x}Ti_x0₃ (x=0, 0 045, 0 08) and Pb(Mg,_/3Nb,_/3), _yTι_y0₃ (y=0 24)), where electric field is applied until the samples electrically break down Samples undergo an electric field induced rhombohedral-tetragonal transition, resulting in hysteresis Strains as high as 0 8% were observed for all tested crystal samples Pb(Zn_1/3Nb_2/3)₀₉₅₅Tι₀₀₄₅O₃ crystal did not experience electric break down within the voltage limit of apparatus, resulting in strain > 1 2%

Figs 19 22 are plots which demonstrate that strain values of materials having the preferred composition ratios vary when the electric field is not aligned with the <001 > crystallographic axis However it is to be noted that so long as the electric field vector is within +/ 20°, that acceptable strain values and hysteresis levels are obtained More specifically, Fig 8 shows representative

Pb(Zn,_/3Nb-,_/3)_{0 955}Tι₀ ^0₃ crystals oriented along <001 > +cv direction, where a is the degree of deviation toward < 111 > from the exact <001 > direction This Fig illustrates the deviation of the crystal orientation from an electric field applied along the <001 > axis Figs 20, 21 show plots of low field ( <40kV/cm) strain behavior for Pb(Zn_l/3Nb_2/3)₀₉₅₅Ti₀₀₄₅O₃ crystals oriented along < 001 > +CY direction, were is the degree of deviation toward < 111 > from the exact <001 > direction, for various values of It is to be noted that when exceeds 20°, the level of hysteresis increases substantially

Fig 22 shows plots of high field ( s lOOkV/cm) strain behavior for Pb(Zn_1/3Nb_2/3)_{0 95s}Tι_{0 M} 0₃ crystals oriented along <001 > + direction, where a is the degree of deviation toward < 111 > from the exact <001 > direction, for various values of a It is to be noted that when a exceeds 20°, the achievable strain value decreases markedly Further, increased breakdown strength allowed a <001 > crystal to exhibit strain as high as 1 5%

Fig 23 shows a plot of hysteresis as a function of CY for Pb(Zn_1/3Nb_2/3)o₉₅₅Tι₀₀₄₅θ₃ crystals oriented along < 001 > + direction Hysteresis values were calculated from polarization vs unipolar electric field when the maximum applied field was 20kV/cm for all crystals Fig 23 indicates that hysteresis caused by domain motion increases with increased value of , resulting in more heat generation The increased hysteresis also implies that strain values are not reproducible at the same electric field, a characteristic which is to be avoided for positioner applications

Fig 24 shows a plot relative values of strain hysteresis as a function of for Pb(Zn„₃Nb,_/3)₀ ^Tio^O_j crystals oriented along < 001 > + direction Relative values of strain hysteresis were calculated from the equation (S_d-S,)/S„ where S_d and S, are strain values at 5 kV/cm with increasing and decreasing the electric field, respectively, and when the maximum applied electric field was 20kV/cm Ideally, these values should be zero, resulting in no hysteresis of strain and perfect positional reproducibi ty From Fig 13, it is seen that strain hvsteresis increases abruptly at about α = 20°

In summary, single crystals of the preferred ferroelectric compositions were found to have a piezoelectric coefficient (d₃₃) as high as 2500 pC/N, maximum electric field induced strains of 1 3 % and very low strain-electric field hysteresis (So long as the applied electric field was applied generally along the <001 > crystallographic axis )

It should be understood that the foregoing description is only illustrative of the invention Various alternatives and modifications can be devised by those skilled in the art without departing from the invention For instance, other rhombohedral relaxor - PLbTι0₃ crystals will likely exhibit high strain so long as their <001 > crystallographic axes are oriented +/-20⁰ from a common directional orientation Also, while the invention has been described in the context of a single crystal actuator configuration, pseudocrystals that consist of multiple single crystals can be utilized so long as their < 001 > crystallographic axes are oriented +/-20^c from a common directional orientation These multiple single crystals can be fabricated using textured growth or epitaxial growth, that is, the growth of crystals of one material on the crystal surface of another material, such that the crystalline substrates of both materials have the same structural orientation. Accordingly, the present invention is intended to embrace all such alternatives, modifications and variances which fall within the scope of the appended claims.

Claims

1 A transducer comprising single crystals of a lead zinc niobate lead titanate solid solution, wherein said single crystals of lead zinc niobate lead titanate solid solution have a composition represented by the formulae

Pb(Zn_{1 3}Nb_2/3)_{l x}Ti_x0₃

where x is within the following limits 0 ≤x <0 05

2 The transducer as recited in claim 1 , wherein said single crystals are oriented along their respective pseudocubic <001 > direction

3 A transducer comprising single crystals of lead magnesium niobate-lead titanate, wherein said single crystals of lead magnesium niobate-lead titanate solid solution have composition represented by the formulae

Pb(Mg,_/3Nb,_/3), _vTι_y0₃

where y is within the following limits 0 20 <y ≤0 50

4 The transducer as recited in claim 3, wherein y is within the following limits 0 20 <y <0 35

5 The transducer as recited in claim 3, wherein y is withm the following limits 0 35 <y ≤0 50

6 The transducer as recited in claim 3, wherein y is within the following limits 0 25 < y ≤0 33

7 The transducer as recited in claim 3, wherein said single crystals are oriented along their respective pseudocubic < 001 > direction