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Scientific Reports logoLink to Scientific Reports
. 2018 Mar 15;8:4597. doi: 10.1038/s41598-018-22918-1

Analytical prediction of the piezoelectric d33 response of fluoropolymer arrays with tubular air channels

Sergey Zhukov 1,, Dagmar Eder-Goy 2, Sergey Fedosov 3, Bai-Xiang Xu 2, Heinz von Seggern 1
PMCID: PMC5854664  PMID: 29545636

Abstract

The present study is focused on tubular multi-channel arrays composed of commercial fluoropolymer (FEP) tubes with different wall thickness. After proper charging in a high electric field, such tubular structures exhibit a large piezoelectric d33 coefficient significantly exceeding the values of classical polymer ferroelectrics and being even comparable to conventional lead-free piezoceramics. The quasistatic piezoelectric d33 coefficient was theoretically derived and its upper limits were evaluated considering charging and mechanical properties of the arrays. In order to optimize the d33 coefficient the remanent polarization and the mechanical properties were taken into account, both being strongly dependent on the air channel geometry as well as on the wall thickness of the FEP tubes. The model predictions are compared with experimental d33 coefficients for two particular arrays with equal air gaps of 250 μm, but with different wall thickness of utilized FEP tubes of 50 μm and 120 μm, respectively. Analytical modeling allows for the prediction that arrays made of FEP tubes with a wall thickness of 10 μm are foreseen to exhibit a superb piezoelectric response of up to 600 pC/N if the height of stadium-like shaped air channels is reduced down to 50 μm, making them potentially interesting for application as highly sensitive sensors and energy harvesting.

Introduction

New polymer materials called ferroelectrets or piezoelectrets, with internally charged air voids possess high piezoelectric activity and has gained interest in the scientific community in recent years1,2. Being initially completely non-polar, ferroelectrets exhibit a strong piezoelectric effect only after symmetry breaking during poling in high electric fields due to positive and negative charge separation in microplasma discharges (the onset of which is governed by Paschen’s law) and subsequent trapping at the polymer/air interface24. Piezoelectricity originates from thereby engineered dipoles/polarization in the air-filled voids by forming layers with opposite surface charges ±σint at the polymer/air interfaces, which can be considered as creating a polarization Pint. Applying an electric field of opposite sign leads to the polarization reversal like in real ferroelectric materials. The corresponding switching process is described by a hysteresis loop2,5 regarded as a typical property of ferroelectrics6,7. Moreover, like all piezoelectrically active materials, ferroelectrets also belong to a class of smart materials that allow converting electrical energy into mechanical one and vice versa68. Since the initially very promising films of cellular polypropylene (PP) ferroelectrets were not sufficiently stable at temperatures above +60 °C9, the development of new thermally stable polymers with voids1018 and hybrid structures with artificial air cavities1924 is still ongoing.

One of the promising structures is a fluoropolymer array with tubular air channels2530. The tubular channels may be introduced either artificially using a template-based lamination technique25,26 or be directly formed from fluorinated ethylene propylene (FEP) tubes30. In the latter approach, a set of individual FEP tubes is compressed between two heated metal plates. Under this condition, squeezed FEP tubes are welded together at +270 °C, resulting in a flat array with regular distributed tubular air channels, as shown in Fig. 1(a). The array fabricated from FEP tubes with 1 mm diameter and a wall thickness of 50 µm has a stable and high piezoelectric d33 coefficient in the range from 120 pC/N to 160 pC/N with a flat frequency response between 0.1 Hz and 10 kHz30. However, the tubular array produced from tubes with the thicker wall of 120 µm shows a more than twofold decrease in the piezoelectric response because of the increased stiffness. Rather high d33 coefficients from 70 pC/N up to 350 pC/N were reported for tubular structures obtained by template-based lamination, and several approaches for increasing the charging efficiency of the structure were also discussed2528. All above mentioned reports have shown that ferroelectrets composed of tubular air channels are very promising for piezoelectric applications. However, a theoretical estimation of the potential limits of such arrays and ways for optimizing the tubular structure have not been studied so far.

Figure 1.

Figure 1

(a) A cross section micrograph of fragments of resulting array fabricated at +270 °C from FEP tubes with wall thickness of 50 µm, (b) Schematic representation of the tubular array with regular plane-parallel air channels. The thickness of the walls is greatly exaggerated for clarity. (c) A photograph of the array with sputtered electrodes.

The present paper is an attempt to theoretically analyse the quasistatic piezoelectric d33coefficient in dependence on the main array parameters, such as wall thickness and air channel height. For this purpose, previously developed models for cellular polymers3135, as well as for sandwiched arrangements3639 and for hybrid structures21,24 have been adapted for the used multi-channel structures. The validity of the proposed model is verified by comparing theoretical and experimental data for the interfacial charge densities and accompanying quasistatic d33 coefficients. The paper is organized as follows: First, a theoretical model for obtaining the d33 coefficients is introduced. Second, it is shown how the accumulated interface charge and effective stiffness of the tubular arrays can be derived from the experimental hysteresis loop and measurements of the mechanical response, respectively. Third, theoretical predictions for the piezoelectric d33 coefficient are compared with the experimental results and fourth, the proposed model is used to estimate d33 coefficients for hypothetical tubular devices in order to predict the maximum d33 value and related parameters. Finally, the sample preparation and description of the experimental methods are presented.

Results and Discussion

A theoretical model for the piezoelectric d33 coefficient

The longitudinal piezoelectric d33 coefficient is used to characterize the piezoelectric response when the external force F is applied in the direction perpendicular to the plane of the array. It is expected that the resulting piezoelectric d33 coefficient of the array shown in Fig. 1(a) is determined by the utilized geometric, dielectric and mechanical parameters of the material used and also strongly depends on the amount of stored charge at the wall/air interfaces introduced by poling3139. To simplify the model, the tubular structure depicted in Fig. 1(a) is represented by two planar FEP films separated by a gap as shown in Fig. 1(b). In order to consider the influence of the necking of the structure indicated by the area between the two dotted lines in Fig. 1(a) and (b), a correction factor α is introduced. We note that an analogous approximation for the tubular structure was used in refs22,25. For the upcoming calculations it is also assumed that the electric field strengths are constant in the air-filled channel as well as in the walls. In other words, there are only charges existing at the interfaces between air and FEP31. Another assumption is that the elastic deformation of the array obeys Hooke’s law with a constant Young’s modulus. Additionally, the wall thickness d1 is assumed to remain constant, and only the air-filled channel d2 is deformed under the external stress. Under such conditions, the mechanical stress σmech can be defined as:

σmech=FA=Ytotal[Δd22d1+d2], 1

where F is the externally applied force to the tubular structure with the sample area A, Ytotal the Young’s modulus of the whole device, and Δd2 the thickness change of the air layer under the applied force F.

The piezocoefficient d33 is defined as:

d33=ΔQF=ΔQ/AF/A=ε0ε1ΔE1Ytotal[Δd22d1+d2], 2

where ΔQ is the measured change of the electrode charge, and ΔE1 the electric field change in the FEP wall adjacent to the electrode caused by the external mechanical force F.

Under the assumption of a sandwich consisting of one air layer of thickness d2 and two equally thick solid FEP layers of thickness d1 without edge effects, the electric fields E1 and E2 in the FEP layers and in the air gap, respectively, are obtained by using Gauss’ law and Kirchhoff’s second law under short-circuit conditions as follows:

ε0ε1E1=ε0ε2E2+σint, 3
2d1E1+d2E2=0, 4

where σint are the trapped areal charge density at the air/FEP interfaces. Under these conditions one obtains for the electric field E1 in the solid walls from Equations (3) and (4):

E1=σintε0ε1+ε0ε22d1d2. 5

The expression ΔE1/Δd2 as needed in Equation (2) is obtained by differentiation of Equation (5):

ΔE1Δd2=ε0ε22d1d22σint(ε0ε1+ε0ε22d1d2)2. 6

Consequently, the d33 piezocoefficient of a planar structure without edges becomes:

d33=αε1ε2σintYtotal1+(d2/2d1)(ε2+ε1(d2/2d1))2. 7

where α is introduced as a correction factor taking care of the differences between the idealized sandwich structure neglecting edge effects and the experimental sample structure as shown in Fig. 1(a) and (b). The fasciated area in Fig. 1(b) resembles thereby the deviating structure from the experimental sample of Fig. 1(a) which is responsible for the correction factor α. Equation (7) without the correction factor can also be deduced from ref.31 modeling the piezoelectric response of cellular PP by a larger number of layers. It is obvious that σint and Ytotal have to be optimized to obtain the highest possible piezoelectric activity.

How this can be achieved and how the deviations from the idealized structure assumed for Equation (7) can be taken into account will briefly be reviewed. First, the interface charge density σint has to be optimized. For a structure displayed in Fig. 1(b), there is no piezoelectric activity in the areas without air gap connecting adjacent channels as marked by the dashed lines. Therefore, the above introduced correction factor α is needed to describe the air-filled array to the total area ratio of the array24. Below it will be shown how α can be determined experimentally. According to theoretical models describing similar devices5,3638 with two solid blocking layers separated by an air gap, an increase of the poling voltage V across the entire structure results in the increase of an electric field E2 in the air gap and E1 in the walls as shown in Fig. 1(b). When E2 reaches the threshold value EB for air, breakdown starts in the air channels. This occurs at a surface potential VB. Taking again into account Equations (3) and (4), the interface charge density dependence on poling voltage V can be solved as5,36,37:

σint(V)={0VVBε0[ε12d1V(ε2+ε1d22d1)EB]VVB, 8

where the threshold voltage VB is related to the breakdown field EB by:

VB=(d2+2ε2d1ε1)EB. 9

In Equation (8) for V>VB the breakdown field EB stays constant in the air channel since a linear increase of voltage will results in a linear increase in σint with the slope ε0ε12d1. This slope is determined solely by the wall thickness and its dielectric constant. During the measurement of the hysteresis, the poling voltage changes from +V to V, while the accumulated interface charge σint initially remains constant due to stable charge trapping until the electric field in the air channel E2 resumes the value E2=EB. At this point, a renewed breakdown allows for the reversal of the interface charge. As a result, σint(V) follows a parallelogram-like hysteresis loop during the charging cycle5,36,37.

It should be noted that for practical purpose the remanent interface charge σrem is important, i.e. the interfacial charge σint after an applied voltage has been turned off or the sample was short-circuited. This parameter can be expressed as5,36,37:

σrem(V)={0VVBε0[ε12d1V(ε2+ε1d22d1)EB]VBV2VB(ε2ε0+ε1ε0d22d1)EB=σremmaxV2VB. 10

where σremmax is the maximum remanent interface charge obtained during short-circuiting after the poling voltage has been at least 2VB. Further increase of the poling voltage would not result in higher remanent polarization due to the back-switching during short-circuiting the sample5,37,40.

It is important to note that Equation (10) indicates that each voided structure has a certain limit for the stored interface charge density. If now Equation (10) is substituted into Equation (7), the corresponding maximum value of the piezoelectric coefficient can be written as:

d33max=αε0ε1ε2EB(2d1+d2)Ytotal(2ε2d1+ε1d2) 11

It should be noted that Equation (11) is applicable only in the case that the applied poling voltage has reached or exceeded the value of 2VB. For lower poling voltages, Equation (7) should be used.

Interfacial charge density σint and its hysteresis in tubular-channel ferroelectrets

In order to investigate the evolution of the interfacial charge density σint on applied voltage, measurements of electrical hysteresis loops of the fabricated arrays were conducted with the Sawyer-Tower circuit41,42. To this end, the voltage Vout built on the large capacitor C0 in series with the sample was measured by means of a Keithley 2000 multimeter, and the charge flowing through the circuit was determined as:

Q(t)=C0Vout(t)=CSVS(t)+Aσ0(t) 12

where Vout(t) is the actually measured potential across C0, A the sample area and CS geometric capacitance of the array, whileσ0 is the electrode charge induced by the interfacial charge σint at the wall/air interface as introduced previously. Figure 2(a) displays the measured displacement D=Q/A at an applied peak voltage of ±3.5 kV, and the derived hysteresis loops for σ0 and σint for the array composed from 50 µm thick walls.

Figure 2.

Figure 2

(a) Experimentally determined D and calculated σ0 and σint hysteresis loops at a peak voltage of ±3.5 kV for a 350 µm thick array fabricated from tubes of 50 µm thick walls and having a geometric capacitance CS of 12 pF, (b) σint hysteresis loops recorded for the same specimen for different peak voltages as indicated. The measurements were carried out at a frequency of 1 Hz.

Hysteresis loops for the charge density σ0 in the metal electrodes are obtained from the measured displacement D by subtracting the term CSVS(t) (see Equation (12)) whereby the geometric capacity CS of the arrays was determined independently with an LCR Meter (HP Model 4332 A). For the studied arrays, the geometric capacitance varied from 8 pF to 12 pF due to the utilized wall thickness. As a next step, the interfacial charge density σint was calculated from the charge density σ0by considering the thickness of the air channel d2 and the wall thickness d1, and the respective dielectric constants ε1 and ε2. Then, application of second Kirchhoff’s law (Equation (4)) for short-circuit and Gauss’ law (Equation (3)) yields:

σ0=ε1d22ε2d1+ε1d2σint=kσint, 13

where k is a geometry dependent factor of proportionality. Taking into account that ε1=2.1 and ε2=1, d2=250µm and d1=50µm (thin-wall array) or 120 µm (thick-wall array), the factor k is 0.84 and 0.69, respectively.

One can also see from Fig. 2(a) that hysteresis loops for σ0 and σint exhibit the shape of a tilted parallelogram exactly as predicted by the model described above. A certain deviation of the curves from ideal parallelograms can be caused by deviations of the geometry of the air channels from the assumed rectangular or plane-parallel shape (compare Fig. 1(a) and (b)). Calculated σint loops for the same sample but at different peak voltages are displayed in Fig. 2(b). In accordance with Equations (8) and (9), all the loops for the selected tubular array have the same slope and the same width equal to 2VB, but different amplitudes which are proportional to the peak voltage. No hysteresis loop for σ0 and σint could be recorded for the peak voltage less than 1.4 kV, which indicates that the breakdown voltage VB is equal VB=1.4kV for the particular array. This experimentally determined value will be used for further estimates, but it is somewhat less than 1.78 kV, calculated from formula (9) using the prediction of the Paschen law3 for an air gap of 250 μm. The main reason for this discrepancy is probably due to the fact that the actual thickness of the air gap in the individual channels can vary and deviate to smaller values due to an inwards bending of the horizontal cell walls as can be seen from Fig. 1(a). Consequently, the experimental air breakdown is initialized at a lower voltage than predicted by the model for the nominal air gap thickness. Despite this fact, it can be concluded that the experimental hysteresis loops for arrays with tubular air channels generally follow the model predictions proposed in the above section.

In the following, this model will additionally be used to analyse the remanent polarization σrem as a function of the peak voltage for the above structure. Corresponding theoretical (see Equation (10)) and experimental results obtained for different peak voltages are depicted in Fig. 3 by the red line and blue squares, respectively. As the model predicted, the theoretically obtained polarization σrem increases linearly with increasing peak voltages until it reaches a saturation value σremmax=0.029µC/cm2 at a peak voltage of 2.75 kV. The experimentally obtained σremmax is smaller and amounts to σremmax=0.025μC/cm2. The difference can be used to determine the above introduced correction factor α as the ratio of the experimental and theoretical charge density, which amounts to α=0.86. Another way to look at the correction factor α is to interpret it as the ratio of the array area with air channels to the total area of the array22,24. For the array with 50 µm thick walls, such a coefficient can be estimated to α~0.90 (see Fig. 1(b)) which is slightly larger than the previous derivation. The reason can be seen in the rounded ends of the stadium-shaped tubes, whose influence on the deposited charge density and thereby the d33 coefficient is not yet understood completely. The follow-up investigations in the near future will focus on this issue. It can be seen in Fig. 3 that the corrected model reliably describes the overall behaviour of the remanent charge density σrem for different peak voltages.

Figure 3.

Figure 3

Theoretical (solid line) σrem and experimental (symbols) σrem versus peak voltage for a 350 µm thick array fabricated from tubes of 50 µm thick walls. The dashed line resembles the corrected charge density of the plane parallel sandwich utilizing α=0.86.

To estimate the effective switching rate of the polarization in the array, σrem was analyzed from the obtained hysteresis loops for peak voltage of ±3.5 kV for different loop cycle frequencies varying from 10 mHz to 100 Hz. Figure 4 displays σrem gained from the corresponding cycle frequencies. One realizes that the reversed charge σrem is nearly constant up to 1 Hz while at higher frequencies it decreases. Obtained results prove that the polarization switching in the present arrays is a rather fast process. Full reversal can be completed in just one second. This experimental result also indicates that the utilized time of one minute for polarization of virgin samples by the contact method is more than sufficient to reach the maximum polarization or charge density.

Figure 4.

Figure 4

Interfacial charge density σrem vs. frequency of the hysteresis cycle for the thin-wall array with air gap of 250 µm.

In order to study the differences in the hysteresis behaviour of thin- and thick-wall arrays the polarization hysteresis has been measured for an equal air channel height of 250 μm utilizing a peak voltage of ±4 kV. The resulting σint loops are displayed in Fig. 5(a). As expected from Equation (10), the thicker wall results in a lower slope ε0ε1/2d1 of the hysteresis loop, thereby reducing σremmax. Additionally, the use of thicker walls is accompanied by an increase in critical voltage VB, and thus broadens the loop. It was previously established that the parameter EB in Equation (10) should not depend on the wall thickness and therefore is equal for both arrays36,37. Like in the case of a thin-wall array, the experimentally determined value of VB= 1.90 kV for the thick-wall specimen is a little bit lower than 2.07 kV, calculated from Equation (9) using the breakdown prediction of Paschen’s law for a corresponding air gap3. For a thick-wall array at an elevated peak voltage, the saturation value σremmax = 0.011 µC/cm2 is obtained at a peak voltage of about 4 kV. The model provides the same value for the remanent charge density, if the correction factor of about 0.80 is used for the ratio of the area occupied by the air channels to the total area of the sample.

Figure 5.

Figure 5

(a) Experimental hysteresis σint for thin- and thick-wall arrays, as indicated. Both arrays have air channels with the same height of 250 µm. (b) Theoretical hysteresis loops calculated from the above theory for the different wall thickness and the respective correction factors α=0.86andα=0.80.

The σint theoretical hysteresis loops for both arrays are displayed in Fig. 5(b). A direct comparison of the experimental and theoretical loops in Fig. 5 reveals that the proposed model for the hysteresis behaviour provides reliable results for the stored interface charge density σint for various tubular arrays. For both structures it is also confirmed that the devices have a limit of the remanent charge, which is reached at the poling voltage V=2VB. The amount of remanent charges is determined by the geometrical and dielectric properties, as well as by the threshold field EB.

Mechanical properties of tubular arrays

Besides the interfacial charge density σint, Young’s modulus Ytotal of the whole tubular array plays a crucial role for the final piezoelectric d33 coefficient (see Equations (7) and (11)). To determine the mechanical properties of the two tubular arrays, the quasistatic stress-strain curves were measured at room temperature. Both arrays revealed slightly non-linear mechanical responses for strain levels εmech below 15%30. Figure 6 displays Ytotal determined from the derivative σmech/εmechat different stress levels. As can be seen from Fig. 6, the minimum values for Young’s modulus are about 0.3 MPa and 0.6 MPa for arrays with wall thickness of 50 μm and 120 μm, respectively, indicating that the wall thickness of utilized FEP tubes have a strong impact on the actual stiffness of the fabricated arrays. Moreover, both values remain almost constant for a stress up to about 0.01 MPa, indicating that for such stress level Hooke’s law is valid. For increasing stress, the stiffness for both arrays shows a clear tendency to increase. To obtain a mathematical description of Ytotal(σmech), the experimental results for σmech>0.01MPa were fitted by a power function43 Ytotal=aσmechn, whereas for lower stress the stiffness was maintained constant at about 0.3 MPa or 0.6 MPa depending on the wall thickness. The corresponding fits are shown in Fig. 6 as solid lines. It can be seen that such description of Ytotal(σmech) provides an appropriate fit to the experimental results for both arrays.

Figure 6.

Figure 6

Effective Young’s modulus versus stress for arrays with air gap of 250 µm and different wall thickness as indicated. For σmech>0.01MPa solid lines represent fits by the function Ytotal=aσmechn, where a=0.073 and n=0.17 for thin-wall and a=0.061 and n=0.25 for thick-wall arrays, respectively, while for lower stress the stiffness was kept constant.

The piezoelectric d33 coefficient: model vs. experiment

Utilizing the experimentally determined values for σremmax and fit function for Ytotal(σmech), the theoretical d33 coefficient as function of applied stress σmech can be calculated utilizing Equation (7). The results of such calculation for two tubular arrays are displayed as dashed lines in Fig. 7. As expected for both arrays, the d33 coefficient is virtually constant up to 0.01 MPa while at higher applied stress it decreases.

Figure 7.

Figure 7

Theoretical (dashed lines) and experimental (closed symbols) piezoelectric d33 coefficients versus stress for two arrays with air gap of 250 µm and different wall thickness as indicated.

It should be noted that the mechanical compression of the soft tubular channels leads to a redistribution of the electric fields inside the arrays. For an extremely high compression level, it can be expected that the electric field across the air channels may exceed the critical value limited by Paschen’s law3. This can cause an unwanted electric breakdown in the air channels, which leads to a partial depolarization of the sample thus lowering σrem. In turn, this will also lower the piezoelectric response permanently. However, for low compression levels used in the current work, this factor can be neglected. Under this condition, the behaviour of the d33 coefficient on external stress, shown in Fig. 7, is basically controlled by Ytotal(σmech) as displayed in Fig. 6.

The measured d33 coefficients vs. stress for both arrays are also shown in Fig. 7. There is a good correspondence between the calculated and measured values. The decrease of the d33 coefficients with stress is explained by the increase of the elastic modulus of the structure due to an obvious densification of the structure at higher stress. Such a behaviour is typical not only for the tubular structures26 but also for cellular43,44 and open-porous17,18 ferroelectrets.

The piezoelectric d33 coefficient: arrays with varied d1 and d2

To explore future potential of tubular channel arrays, the piezoelectric d33 coefficient for hypothetical devices with smaller wall thickness and air channel heights will be analysed using Equation (11). Therefore, it is assumed that the sample is poled to its maximal interface charge density σremmax, while the parameter α is fixed at 0.85. Further simplifications were used to perform such calculations. First, a linear extrapolation for the d2 dependence of low stress Ytotal for arrays with a common air gap thickness of 250 µm is used on the basis of the wall thickness of 50 μm and 120 μm. The linear extrapolation is shown in Fig. 8(a) and is used to evaluate the stiffness of the samples for d1 smaller than 50 μm. The values obtained are about 0.25 MPa and 0.20 MPa for the 25 µm and 12.5 µm wall thickness, respectively. Note that FEP solid films with mentioned thickness are available on the market and can in principle be used for the production of such ferroelectrets with tubular channels by template-based lamination25,26. It was also assumed that arrays made of tubes with fixed wall thickness, but different air channel heights of 50 μm, 100 μm and 250 μm, virtually have the same Young’s modules. However, it has to be taken into account that the breakdown strength EB in Equation (11) depends on d2. Recent detailed experiments have shown that EB in ferroelectrets with air voids with a height of the order of tens of microns exactly follows the prediction of Paschen’s law45, while in earlier publications some deviations from this law have been reported36,37. For the present estimation the values for EB of 110 kV/cm, 86 kV/cm and 60 kV/cm were used for air gaps of 50 μm, 100 μm and 250 μm, respectively.

Figure 8.

Figure 8

(a) Measured (grey squares) and extrapolated (red squares) Ytotal values as a function of wall thickness d1 for arrays with a common air channel height of d2=250µm. (b) Theoretical d33 coefficients for tubular arrays as a function of d1 for various d2 values as indicated. Dashed lines are guides to the eye.

The estimates of the piezoelectric d33 coefficients obtained under the above mentioned assumptions for different hypothetical devices with different wall thickness d1 and air channel heights d2 are shown in Fig. 8(b). It can be recognized that the theoretical piezoelectric coefficients vary from about 100 pC/N to about 600 pC/N, indicating that the tubular structure can be efficiently optimized to maximize the piezoelectric response. One promising way of such an optimization is to reduce the wall thickness d1, keeping the thickness of the air channel d2 constant. Such a modification of the structure is accompanied by a decrease in Young’s modulus, as shown in Fig. 8(a), which leads to a significant increase in d33. At the same time, the EB parameter does not or only slightly depend on d1, while the term 2d1+d22ε2d1+ε1d2 in Equation (11) varies insignificantly. Therefore, mainly the function Ytotal(d1) seems to be dominant for the piezoelectric response of the array when only the wall thickness is changed.

The second possible way to optimize the tubular structure involves regulating the height of the air channel. It can be seen from Fig. 8(b) that a decrease in d2 from 250 µm to 50 µm enhances d33 approximately twice. This is valid for all wall thickness used. The main reason for this effect is related to the dependence of EB on d2, since the breakdown field in the air channel increases in accord with Paschen’s law with decreasing d23,45. Once again, we note that possible changes in the stiffness of the array by modification of the air channel height in the current study are not taken into account.

Before concluding, it should be emphasized that the present study has once again demonstrated that the outstanding piezoelectric properties of tubular arrays in particular and ferroelectrets in general originate from a unique combination of mechanical and electrical properties of polymer structures with voids. On the one hand, polymer dielectrics with air cavities can accumulate a quasi-remanent polarization with relatively low charge density up to approximately 0.1 µC/cm2 22,27,3739,46 significantly lower than the typical values for classical bulk ferroelectric polymers (5–15 µC/cm2)7,47 and conventional piezoceramics (10–100 µC/cm2)6,48,49. But on the other hand, ferroelectrets, like all porous polymers1,50, have an extremely low Young modulus ranging from 0.2 MPa to 10 MPa, depending on the mechanical properties of the polymer matrix and the pore geometry10,22,30,33,44,51.

Conclusion

A theoretical model is proposed for the quasistatic piezoelectric d33 coefficient of tubular channel arrays. The model takes into account the polarization through interfacial charge densities stored at the wall/air interfaces, as well as mechanical properties through the Young’s modulus of the investigated arrays. Comparison of theoretical results based on model calculations with experimental data contributes to a deeper understanding of involved physics of ferroelectrets with regular tubular air channels. It is shown that the geometry of the produced arrays, mainly the thickness of the wall of the FEP tubes and the air channels, affect the piezoelectric d33 coefficient. It has been demonstrated that a future increase of d33 through optimizing the geometry is possible, e.g. by adjusting the thickness of d1 and d2. Model predictions suggest that arrays produced by FEP tubes with down to about 10 μm thick walls will exhibit a piezoelectric d33 coefficient comparable to conventional PZT piezoceramics.

Methods

In order to fabricate two structures with regular air channels, the fusion bonding technique was used29. The arrays were fabricated from FEP tubes with the same outer diameter of 1 mm but with different wall thickness of 50 μm and 120 μm. Both types of FEP tubes were provided by ZEUS Ltd., USA. Figure 1(a) shows a photomicrograph of a cross section of a tubular array composed from tubes with 50 µm thick walls. The dimensions of the manufactured arrays were limited to approximately 30 × 40 mm2, due to the fabrication device while the thickness of the air channels in both structures was fixed at 250 μm. The arrays were first metallized on both sides with Al electrodes, which have the shape of a square with a side length of 15 mm. A micrograph of the device with sputtered electrodes is shown in Fig. 1(c). Electrical poling was then conducted by a direct-contact charging in ambient air at room temperature by application of a bias voltage of up to ±5 kV from the power supply HSN-35 (FUG GmbH). Typically, one minute was more than enough to fully polarize such arrays.

The quasistatic measurements of the direct piezoelectric d33 coefficient were performed by rapid loading with a mass m. The temporal charge response ΔQ of the sample was measured for 10 s by means of a Keithley 610 C electrometer in the charge mode. The d33 coefficients then were determined from the relation d33=ΔQ/(mg), where g denotes the acceleration of gravity.

The rheometer AR 2000 Ex from TA Instruments was used to determine the mechanical properties. During the measurement, the specimen was compressed between two parallel bars at a rate of 10 μm/s, and the resultant force was measured by a force gauge. Using this technique, quasistatic stress-strain curves were recorded at room temperature which allowed for the determination of Young’s modulus Ytotal.

The polarization hysteresis loops of ferroelectrets were obtained by utilizing the Sawyer-Tower circuit where a large standard capacitor C0 (455 nF) was connected in series with the sample. An AC triangular voltage with a frequency between 10 mHz and 100 Hz was applied by a high voltage amplifier (Trek, Model 20/20 C) controlled by an arbitrary waveform generator. All the experiments were carried out at room temperature.

Acknowledgements

The authors would like to thank the Deutsche Forschungsgemeinschaft (DFG) for financial support through the grants SE 941/19-1, SE 941/17-1 and XU 121/5-1.

Author Contributions

H.v.S. and B.X. initiated the project and designed the experiments with S.F. and S.Z. Samples were prepared by S.Z. and S.F. and experiments performed by S.Z. and D.E. Data analysis was done by S.Z. who also interpreted the results with H.v.S., S.F., D.E. and B.X. The manuscript draft was prepared by S.Z. and H.v.S. All authors contributed to the final version.

Competing Interests

The authors declare no competing interests.

Footnotes

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Bauer S, Gerhard-Multhaupt R, Sessler GM. Ferroelectrets: soft electroactive foams for transducers. Phys. Today. 2004;57:37–43. doi: 10.1063/1.1688068. [DOI] [Google Scholar]
  • 2.Wegener M, Bauer S. Microstorms in cellular polymers: a route to soft piezoelectric transducer materials with engineered macroscopic dipoles. Chem Phys Chem. 2005;6:1014–1025. doi: 10.1002/cphc.200400517. [DOI] [PubMed] [Google Scholar]
  • 3.Raizer, Y. P. Gas Discharge Physics (ed. Allen, J. E.) 128–137 (Berlin: Springer, 1991).
  • 4.Lindner M, Bauer-Gogonea S, Bauer S, Paajanen M, Raukola J. Dielectric barrier microdischarges: Mechanism for the charging of cellular piezoelectric polymers. J. Appl. Phys. 2002;91:5283–5287. doi: 10.1063/1.1459751. [DOI] [Google Scholar]
  • 5.Zhukov S, von Seggern H. Polarization hysteresis and piezoelectricity in open-porous fluoropolymer sandwiches. J. Appl. Phys. 2007;102:044109. doi: 10.1063/1.2764024. [DOI] [Google Scholar]
  • 6.Lines, M. E. & Glass, A. M. Principles and Applications of Ferroelectrics and Related Materials 559–607 (Oxford: Clarendon, 1977).
  • 7.Wang, T., Herbert, J. & Glass, A. The Application of Ferroelectric Polymers (Glasgow: Blackie, 1988).
  • 8.Ramadan KS, Sameoto D, Evoy S. A review of piezoelectric polymers as functional materials for electromechanical transducers. Smart Mater. Struct. 2014;23:033001. doi: 10.1088/0964-1726/23/3/033001. [DOI] [Google Scholar]
  • 9.Paajanen M, Lekkala J, Kirjavainen K. Electromechanical film (EMFi) - a new multipurpose electret material. Sensors Actuators A. 2000;84:95–102. doi: 10.1016/S0924-4247(99)00269-1. [DOI] [Google Scholar]
  • 10.Wegener M, Wirges W, Gerhard-Multhaupt R. Piezoelectric polyethylene terephthalate (PETP) foams – specifically designed and prepared ferroelectret films. Adv. Eng. Mat. 2005;7:1128–1131. doi: 10.1002/adem.200500177. [DOI] [Google Scholar]
  • 11.Behrendt N, et al. Morphology and electret behaviour of microcellular high glass temperature films. Appl. Phys. A-Mater. Sci. Process. 2006;85:87–93. doi: 10.1007/s00339-006-3660-7. [DOI] [Google Scholar]
  • 12.Saarimäki E, et al. Novel heat durable electromechanical film: Processing for electromechanical and electret applications. IEEE Trans. Dielectr. Electr. Insul. 2006;13:963–972. doi: 10.1109/TDEI.2006.247820. [DOI] [Google Scholar]
  • 13.Montanari GC, et al. Charging properties and time-temperature stability of innovative polymeric cellular ferroelectrets. IEEE Trns. Dielectr. Electr. Insul. 2007;14:238–248. doi: 10.1109/TDEI.2007.302892. [DOI] [Google Scholar]
  • 14.Hu Z, von Seggern H. Breakdown-induced polarization buildup in porous fluoropolymer sandwiches: a thermally stable piezoelectret. J. Appl. Phys. 2006;99:024102. doi: 10.1063/1.2161825. [DOI] [Google Scholar]
  • 15.Zhukov S, von Seggern H. Breakdown-induced light emission and poling dynamics of porous fluoropolymers. J. Appl. Phys. 2007;101:084106. doi: 10.1063/1.2716872. [DOI] [Google Scholar]
  • 16.von Seggern H, Zhukov S, Fedosov S. Poling dynamics and thermal stability of FEP/ePTFE/FEP sandwiches. IEEE Trans. Dielectr. Electr. Insul. 2010;17:1056–1063. doi: 10.1109/TDEI.2010.5539675. [DOI] [Google Scholar]
  • 17.Huang J, Zhang X, Xia Z, Wang X. Piezoelectrets from laminated sandwiches of porous PTFE films and nonporous FEP films. J. Appl. Phys. 2008;103:084111. doi: 10.1063/1.2910773. [DOI] [Google Scholar]
  • 18.Zhang X, Zhang X, Sessler GM, Gong X. Quasi-static and dynamic piezoelectric responses of layered polytetrafluoroethylene ferroelectrets. J. Phys. D: Appl. Phys. 2014;47:015501. doi: 10.1088/0022-3727/47/1/015501. [DOI] [Google Scholar]
  • 19.Altafim RAC, et al. Piezoelectrets from thermo-formed bubble structures of fluoropolymer-electret films. IEEE Trans. Dielectr. Electr. Insul. 2006;13:979–985. doi: 10.1109/TDEI.2006.247822. [DOI] [Google Scholar]
  • 20.Zhang X, Hillenbrand J, Sessler GM. Ferroelectrets with improved thermal stability made from fused fluorocarbon layers. J. Appl. Phys. 2007;101:054114. doi: 10.1063/1.2562413. [DOI] [Google Scholar]
  • 21.Sun Z, et al. Polarization and piezoelectricity in polymer films with artificial void structure. Appl. Phys. A. 2011;105:197–205. doi: 10.1007/s00339-011-6481-2. [DOI] [Google Scholar]
  • 22.Zhang X, Hillenbrand J, Sessler GM, Haberzettl S, Lou K. Fluoroethylenepropylene ferroelectrets with patterned microstructure and high, thermally stable piezoelectricity. Appl. Phys. A. 2012;107:621–629. doi: 10.1007/s00339-012-6840-7. [DOI] [Google Scholar]
  • 23.Kachroudi A, Basrour S, Rufer L, Sylvestre A, Jomni F. Micro-structured PDMS piezoelectric enhancement through charging conditions. Smart Mater. Struct. 2016;25:105027. doi: 10.1088/0964-1726/25/10/105027. [DOI] [Google Scholar]
  • 24.Zhang X, Sessler GM, Xue Y, Ma X. Audio and ultrasonic responses of laminated fluoroethylenepropylene and porous polytetrafluoroethylene films with different charge distributions. J. Phys. D: Appl. Phys. 2016;49:205502. doi: 10.1088/0022-3727/49/20/205502. [DOI] [Google Scholar]
  • 25.Altafim RAP, et al. Template-based fluoroethylenepropylene piezoelectrets with tubular channels for transducer applications. J. Appl. Phys. 2009;106:014106. doi: 10.1063/1.3159039. [DOI] [Google Scholar]
  • 26.Altafim RAP, et al. Laminated tubular-channel ferroelectret systems from low-density polyethylene films and from fluoroethylene-propylene copolymer films – A comparison. IEEE Trans. Dielectr. Electr. Insul. 2012;19:1116–1123. doi: 10.1109/TDEI.2012.6259978. [DOI] [Google Scholar]
  • 27.Qiu X. Significant enhancement of the charging efficiency in the cavities of ferroelectrets through gas exchange during charging. Appl. Phys. Lett. 2016;109:222903. doi: 10.1063/1.4971259. [DOI] [Google Scholar]
  • 28.Qiu X, Wirges W, Gerhard R. Thermal poling of ferroelectrets: How does the gas temperature influence dielectric barrier discharges in cavities? Appl. Phys. Lett. 2016;108:252901. doi: 10.1063/1.4954263. [DOI] [Google Scholar]
  • 29.Nepal N, Altafim RAP, Mellinger A. Space charge deposition in tubular channel ferroelectrets: A combined fluorescence imaging/LIMM study with finite element analysis. J. Appl. Phys. 2017;121:244103. doi: 10.1063/1.4990280. [DOI] [Google Scholar]
  • 30.Zhukov S, et al. Tubular fluoropolymer arrays with high piezoelectric response. Smart Mater. Struct. 2018;27:015010. doi: 10.1088/1361-665X/aa9a63. [DOI] [Google Scholar]
  • 31.Sessler GM, Hillenbrand J. Electromechanical response of cellular electret films. Appl. Phys. Lett. 1999;75:3405–3407. doi: 10.1063/1.125308. [DOI] [Google Scholar]
  • 32.Kacprzyk R, Motyl E, Gajewski JB, Pasternak A. Piezoelectric properties of nonuniform electrets. J. Electrostat. 1995;35:161–166. doi: 10.1016/0304-3886(95)00034-8. [DOI] [Google Scholar]
  • 33.Neugchwandtner GS, et al. Piezo- and pyroelectricity of a polymer-foam space-charge electret. J. Appl. Phys. 2001;89:4503–4511. doi: 10.1063/1.1355719. [DOI] [Google Scholar]
  • 34.Zhang, P., Xia, Z., Qiu, X., Wang, F. & Wu, X. Y. Influence of charging parameters on piezoelectricity for cellular polypropylene film electrets. Proc. IEEE 12th Int. Symp. Electrets 39–42 (Salvador, Brazil, 11–14 Sept. 2005).
  • 35.Paajanen, M., Välimäki, H. & Lekkala, J. Modeling the sensor and actuator operations of the ElectroMechanical Film EMFi. Proc. IEEE 10th Int. Symp. Electrets 735–738 (Athens, Greece, 22-24 Sept. 1999).
  • 36.von Seggern H, Zhukov S, Fedosov S. Importance of geometry and breakdown field on the piezoelectricd33 coefficient of corona charged ferroelectret sandwiches. IEEE Trans. Dielectr. Electr. Insul. 2011;18:49–56. doi: 10.1109/TDEI.2011.5704492. [DOI] [Google Scholar]
  • 37.Zhukov S, Fedosov S, von Seggern H. Piezoelectrets from sandwiched porous polytetrafluoroethylene (ePTFE) films: influence of porosity and geometry on charging properties. J. Phys. D: Appl. Phys. 2011;44:105501. doi: 10.1088/0022-3727/44/10/105501. [DOI] [Google Scholar]
  • 38.Xu B-X, von Seggern H, Zhukov S, Gross D. Continuum modeling of charging process and piezoelectricity of ferroelectrets. J. Appl. Phys. 2013;114:094103. doi: 10.1063/1.4819441. [DOI] [Google Scholar]
  • 39.Xu B-X, von Seggern H, Zhukov S, Gross D. An internal-variable-based interface model for the charging process of ferroelectrets. Eur. J. Mech. A-Solids. 2014;48:97–111. doi: 10.1016/j.euromechsol.2013.12.011. [DOI] [Google Scholar]
  • 40.Qiu X, Mellinger A, Wegener M, Wirges W, Gerhard R. Barrier discharges in cellular polypropylene ferroelectrets: How do they influence the electromechanical properties? J. Appl. Phys. 2007;101:104112. doi: 10.1063/1.2735410. [DOI] [Google Scholar]
  • 41.Sawyer CB, Tower CH. Rochelle salt as a dielectric. Phys. Rev. 1930;35:269–273. doi: 10.1103/PhysRev.35.269. [DOI] [Google Scholar]
  • 42.Qiu X, Wirges W, Gerhard R. Polarization and hysteresis in tubular-channel fluoroethylenepropylene-copolymer ferroelectrets. Ferroelectrics. 2014;472:100–109. doi: 10.1080/00150193.2014.964603. [DOI] [Google Scholar]
  • 43.Kacprzyk R. Piezoelectric properties of non-uniform polymeric structures under static load. Phase Transitions. 2017;90:104–111. doi: 10.1080/01411594.2016.1252977. [DOI] [Google Scholar]
  • 44.Gaal M, et al. Viscoelastic properties of cellular polypropylene ferroelectrets. J. Appl. Phys. 2016;119:125101. doi: 10.1063/1.4944798. [DOI] [Google Scholar]
  • 45.Harris S, Mellinger A. Towards a better understanding of dielectric barrier discharges in ferroelectrets: Paschen breakdown fields in micrometer sized voids. J. Appl. Phys. 2014;115:163302. doi: 10.1063/1.4871678. [DOI] [Google Scholar]
  • 46.Mohebbi, A., Rodrigue, D. Energy absorption capacity of ferroelectrets based on porous polypropylene. Polym. Eng. Sci. 10.1002/pen.24573 (2017).
  • 47.Schütrumpf J, Zhukov S, Genenko YA, von Seggern H. Polarization switching dynamics by inhomogeneous field mechanism in ferroelectric polymers. J. Phys. D: Appl. Phys. 2012;45:165301. doi: 10.1088/0022-3727/45/16/165301. [DOI] [Google Scholar]
  • 48.Zhukov S, et al. Effect of bipolar electric fatigue on polarization switching in lead-zirconate-titanate ceramics. J. Appl. Phys. 2010;108:014105. doi: 10.1063/1.3452326. [DOI] [Google Scholar]
  • 49.Zhukov S, et al. Fatigue effect on polarization switching dynamics in polycrystalline bulk ferroelectrics. J. Appl. Phys. 2016;120:064103. doi: 10.1063/1.4960691. [DOI] [Google Scholar]
  • 50.Gibson, L. J.& Ashby, M. F. Cellular Solids: Structure and Properties (Cambridge U. Press, New York, 1999).
  • 51.Mohebbi A, Mighri F, Ajji A, Rodrigue D. Polymer ferroelectret based on polypropylene foam: piezoelectric properties prediction using dynamic mechanical analysis. Polym. Adv. Technol. 2017;28:476–483. doi: 10.1002/pat.3908. [DOI] [Google Scholar]

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