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Dopant effect and cell-configuration-dependent dielectric properties of nematic liquid crystals.

1. Introduction

Nematic liquid crystals (NLCs) have ubiquitously been exploited in photonic devices, especially in current flat panel displays. Regardless of their origins, impurity ions existing in liquid-crystal (LC) cells have long been a nuisance to the global LC display (LCD) industry. It is well known that the cumulative impurity ions produce an internal, counteracting electric field in an LC cell under voltage application, causing many problems such as the reduction of voltage holding ratio, increase in threshold voltage, image sticking, gray-level shift, image flickering, and the slowdown of switching response [1-4]. In order to solve these issues, some research groups have adopted a postsynthetic approach [5] and demonstrated that doping an adequate amount of carbon nanotubes (CNTs) into NLCs can help suppress the unwanted field-screening effect [6]. The fact that the impurity ions can be effectively trapped by CNTs via charge transfer substantially improves the electrooptical performance of an LC device [7, 8]. With a compatible shape to the rodlike molecules of NLCs, tubular CNTs are known as a one-dimensional nanomaterial, possessing unique material characteristics to be promisingly applied in modern photonic and semiconductor devices. As a matter of fact, recent laboratory studies have demonstrated their potential for flat panel display applications, permitting their roles in electrodes, thin-film transistors, alignment layers, and field-emission devices.

The quality of an LC material for photonic applications can be examined by low-frequency dielectric spectroscopy [9]. It has been established that the LC dielectric behavior at low frequencies is dictated by the charge carrier transport process and is susceptible to the material properties of the alignment layers if any [10]. Interestingly but not surprisingly, Costa et al. revealed that impurity ions in the NLC E7 travel to electrodes faster in homeotropic cells than in homogeneous cells due to the anisotropy in diffusion constant [11]. Thus, the underlying mechanisms depend upon the materials used and the properties of the cell.

In this comparative study we used a low-resistivity NLC (E7) and a high-resistivity NLC (CYLC-01) to observe their low-frequency polarizations contributed by mobile ions. The dielectric spectra of the two eutectic NLC materials were compared between 10 Hz and 10 kHz. The dopant effects of CNTs on the dielectric properties of the two NLCs were investigated. In addition, by expanding the frequency range to [10.sup.-1]-[10.sup.4] Hz, the ionic transport behaviors were analyzed for three distinctive (homogeneous, twisted-nematic, and homeotropic) cell configurations for the ion-rich NLC E7.

2. Experimental

Both low- and high-resistivity NLC materials were employed for comparison; they were E7 and CYLC-01, respectively. With a typical bulk resistivity of ~[10.sup.11] [OMEGA]-cm, E7 is a well-known commercial eutectic mixture (from Merck), consisting of primarily 4'-n-pentyl-4-cyanobiphenyl and three other cyano compounds. Owing to its high polarity, E7 exhibits a strong permanent dipole moment along the molecular axis, possesses large dielectric anisotropy ([DELTA][epsilon]' ~14 at 1 kHz and 20[degrees]C [12]), and is notorious for its vulnerability to ionic contamination. On the other hand, the mixture CYLC-01 is an ultrapure C[F.sub.2]O-based TFT-grade NLC. Its excellent material quality, including high bulk resistivity of ~[10.sup.14] [OMEGA]-cm, allows its appearance in the modern active-matrix LC displays. Both the LC substances are of positive dielectric anisotropy (defined as the difference between the parallel component [epsilon][parallel] and perpendicular component e[perpendicular to] of the real dielectric constant). The dopant material used was ultrapure multiwalled carbon nanotubes (CNTs) with inner diameters of 2-3 nm and ~21 graphene layers (from SRS Research). According to our prior experience, the optimal CNT concentration of 0.05 wt% was adopted [13]. Four material samples were prepared, including pure E7, E7/CNT, pure CYLC01, and CYLC-01/CNT, which were individually injected into empty homogeneous-alignment cells by capillary action in the isotropic phase. The cell gap was 11.3 [micro]m between the conducting glass substrates, and the effective electrode area was 1 [cm.sup.2]. For the second part of the experiment concerning the influence of cell configuration, we prepared five pristine E7 samples for each type of cell structure. The cell configurations investigated in this work included the homogeneous (i.e., planar alignment), 90[degrees] twisted-nematic, and homeotropic (i.e., vertical alignment) structures. The alignment layers for the 6.2 [micro]m thick homogeneous and twisted cells were the same polyimide (Nissan SE-2170). The homeotropic cells of ~5 [micro]m in thickness were purchased from EHC, Japan, and the aligning material is unknown.

The complex dielectric constant was acquired with an LCR meter (HIOKI 3522-50 LCR HiTESTER) having capability of measurement in the frequency range from 1 mHz to 100 kHz and basic measurement accuracy of [+ or -] 0.08%. The probe voltage adopted in this study was 50 m[V.sub.rms] in the sinusoidal waveform, which was much smaller than the LC threshold voltage. The voltage holding ratio (VHR) experiment [14] was carried out to simulate the charging and discharging properties of E7 cells, by which the cell performance of the doped one was examined. The temperatures for the first part and second part of the experiment were 303 K and 296 K, respectively.

3. Results and Discussion

Figure 1 shows the frequency dependence of the real and imaginary parts of the complex dielectric function ([epsilon]' - i[epsilon]") of pure E7 and pure CYLC-01. In the low-frequency region (f < [10.sup.2] Hz), the dielectric behavior was attributable to the space-charge polarization. Both frequency-varying [epsilon]' and [epsilon]", dominated by the ionic effect in this frequency region, are proportional to [f.sup.-3/2] and [f.sup.-1] respectively. Taking the diffusive motion of the impurity ions into account, the expressions for the ionic contributions to the dielectric dispersion e' and dielectric loss e" in the appropriate frequency range in the nematic LC cell are [15]

[epsilon]' (f) = [n[q.sup.2] [D.sup.3/2]/[[pi].sup.3/2] [[epsilon].sub.0] L[k.sub.B]T] [f.sup.-3/2] + [[epsilon]'.sub.b], (1)

[epsilon]" (f) = [n[q.sup.2] D/[pi][[epsilon].sub.0][k.sub.B]T] [f.sup.-1], (2)

respectively, where n is the mobile ion concentration, q is the charge of an ion, D is the diffusion constant of the ion, L is the thickness of the cells, [[epsilon].sub.0] is the permittivity in free space, [k.sub.B] is the Boltzmann constant, T is the absolute temperature, and [[epsilon]'.sub.b] is the intrinsic dielectric constant of the NLC bulk. The ionic contribution decreased with increasing frequency. At low frequencies the impurity ions had enough time to reach the electrodes to form dipole moments, while at high frequencies the space-charge polarization could not keep up with the polarity alteration of the electric field, which, in turn, led to the dielectric relaxation. The constant value of [epsilon]' between [10.sup.3] and [10.sup.4] Hz was mainly contributed by the intrinsic LC dielectric term [[epsilon]'.sub.b]. It is clear from Figure 1 that the dielectric relaxation in the low-frequency region (10 Hz < f < 100 Hz) was not evident in the dielectric spectrum of the superfluorinated LC mixture CYLC-01. As mentioned above, CYLC-01 was a high-resistivity NLC, connoting that it contained a very limited amount of impurity ions. Consequently, the ionic contribution was not as significant at low frequencies compared with the E7 counterpart.

Figure 2 depicts the dielectric spectra of pure as well as CNT-doped CYLC-01 samples. Since their real parts almost coincide with each other and imaginary parts are virtually identical, the dopant effect on the dielectric behavior (in the frequency range studied) was trivial in the TFT-grade NLC. In contrast, the impact of the dopant on the low-frequency dielectric spectrum was very pronounced for the E7 host as shown in Figure 3.One can see from this figure that, after doping 0.05-wt% CNTs in E7, the dielectric permittivity ([epsilon]') decreased in the low-frequency region and the relaxation frequency shifted to the lower frequency. Again, E7 is a low resistivity NLC, which contains a large amount of impurity ions. The CNTs as an additive in the ion-rich nematic host effectively trapped mobile ions [5] to give rise to the reduction in space-charge polarization.

The VHR is an important measure of the LCD performance. It is conventionally defined as

VHR (%) = [V.sub.t]/[V.sub.i] x 100%, (3)

where [V.sub.i] is the initial (or input) pulse voltage (5 V in this study) and [V.sub.t] is the terminal voltage of the LC cell during a frame time of 16.67 ms. One can see from Figure 4 that, by adding an adequate amount of CNTs in E7, the VHR was promoted from 48% to 61%, yielding a substantial increase by 26%. In order to monitor the degradation of the cell manifested by the decrease in VHR over time, a four-day observation was made. Figure 5 illustrates the time-evolved VHR curves for the doped and undoped cells. The monotonic fall of the VHR in both cells can be explained by the ascending ionic concentration after the cell fabrication [16]. Using the monoexponential decay expression VHR(t) = A[e.sup.-t/[tau]], where A is the VHR at time i = 0 and t is the characteristic lifetime, one can fit the experimental data and obtain a lifetime of 118 h for the doped cell compared with that of 59 h for the un doped counterpart. Obviously, the addition of CNTs in E7 prolonged the cell lifetime before degradation.

Figure 6 shows the dielectric spectra of E7 in various cells with homogeneous, twisted, and homeotropic alignment. In the 103-104 Hz frequency region, the dielectric constant e' of E7 was the largest in the homeotropic configuration, because E7 possessed positive dielectric anisotropy. Note that the effective dielectric constant e can be expressed by [17]

[epsilon] = [[epsilon].sub.[perpendicular to]] + [DELTA][epsilon] [sin.sup.2] [theta], (4)

where [theta] is the tilt angle between the substrate plane and the LC director. Thus, the complex dielectric constant measured in a homeotropic cell is the sole contribution of the parallel component [[epsilon].sub.[parallel]]. In the frequency region of f < [10.sup.3] Hz, both [epsilon]' and [epsilon]" functions can be individually fitted by (1) and (2), respectively, for calculation of their ion density n and diffusion constant D. The results are listed in Table 1.

The impurity ions in the LC bulk can be contributed by the dissociation of the LC material itself and ion injection from the alignment or electrode layer [18, 19]. Based on the data displayed in Table 1, the ion concentration in the homeotropic cells was much (two orders of magnitude) higher than that in the other cells with different configurations. Here, the most likely explanation is the occurrence of ion injection into the LC bulk from the homeotropic alignment layers because the electrodes are identical. The ionic concentrations in the homogeneous and twisted-nematic cells are quite the same due to the use of the same aligning material.

The diffusion constant D is anisotropic and related to the viscosity and electrical conductivity of the medium [7, 11]. Table 1 reveals that D in a homeotropic cell was larger in comparison with that in a homogeneous one. This result, arising from the fact that the diffusion constant along the molecular axis is greater (namely, [D.sub.[parallel]] > [D.sub.[perpendicular to]]), is in good agreement with an earlier study by Costa et al. [11]. We also observed that D in the twisted cells is somewhat larger than that in the homogeneous cells. Since the viscosity of the LC E7 in splay and twist molecular configurations is identical [20], we believe that the difference can be ignored due to the experimental error and uncertainties in the curve-fitting process. As a result, it can be summarized that the alignment layer and molecular orientation play an important role in ionic concentration and diffusion constant, respectively. The dc conductivity can be written as

[[sigma].sub.dc] = qn[mu], (5)

where [mu] is the ion mobility. According to the Einstein relation

[mu] = [q/[k.sub.B]T] D, (6)

(5) becomes

[[sigma].sub.dc] = n[q.sup.2] D/[k.sub.B]T, (7)

indicating that the ionic dc conductivity [[sigma].sub.dc] is not only proportional to the ion concentration n, but also to the diffusion constant D. Thus, the conductivity of an LC cell changes with the variation of D in different LC alignment.

4. Conclusions

This paper presents the low-frequency (f < [10.sup.2] Hz) dielectric behaviors induced by impurity ions in LC cells under different conditions. In the high-resistivity NLC (CYLC-01) which contained a low concentration of impurity ions, we did not observe an evident sign of the mobile-ion polarization and the dielectric constant did not seem to change after doping CNTs. By contrast, the dielectric relaxation was obviously observed in the low-resistivity NLC (E7) rich in impurity ions. Our experimental results suggested that CNTs as a dopant can effectively suppress the ion effect in the low-resistivity NLC, thereby promoting the VHR substantially. In addition, the low-resistivity NLC confined in homeotropic cells, in comparison with cells in the homogeneous and twisted configurations, exhibited the highest impurity-ion concentration, implying significant ion injection from the corresponding alignment layers.


The authors are thankful for the financial support of the National Science Council of Taiwan under Grant nos. NSC 98-2112-M-033-004-MY3, NSC 101-2112-M-009-018MY3, and NSC 101-2811-M-009-059.


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Feng-Ching Lin, (1) Po-Chang Wu, (2) Bo-Ru Jian, (1) and Wei Lee (1,2,3)

(1) Department of Physics, Chung Yuan Christian University, Chung-Li 32023, Taiwan

(2) College of Photonics, National Chiao Tung University, Tainan 71150, Taiwan

(3) Center for Nanotechnology, Chung Yuan Christian University, Chung-Li 32023, Taiwan

Correspondence should be addressed to Wei Lee;

Received 12 July 2012; Revised 7 April 2013; Accepted 17 April 2013

Academic Editor: Hamit Yurtseven

TABLE 1: Ion concentration n and diffusion constant D in E7 for
homogeneous, twisted, and homeotropic cells at 296 K.

Cell type      n ([cm.sup.-3])     D ([cm.sup.2] s.sup.-1])

Homogeneous   1.80 x [10.sup.13]      2.67 x [10.sup.-7]
Twisted       1.74 x [10.sup.13]      3.55 x [10.sup.-7]
Homeotropic   5.12 x [10.sup.15]      5.72 x [10.sup.-7]
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Title Annotation:Research Article
Author:Lin, Feng-Ching; Wu, Po-Chang; Jian, Bo-Ru; Lee, Wei
Publication:Advances in Condensed Matter Physics
Date:Jan 1, 2013
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