Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes
Studied in this work has been the effect of nanoparticles – magnetite and single-wall carbon nanotubes – separately and together on the conductivity of nematic liquid crystal 6CHBT dispersed in polyvinyl alcohol. Morphology of these films was analyzed using an electron microscope. When using sele...
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Інститут фізики напівпровідників імені В.Є. Лашкарьова НАН України
2014
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nasplib_isofts_kiev_ua-123456789-1184232025-02-10T01:16:34Z Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes Kopčanský, P. Timko, M. Mitrova, Z. Tomašovičová, N. Tomčo, L. Kovalchuk, O.V. Kovalchuk, T.M. Oleinikova, I.V. Lad, A.I. Studenyak, I.P. Studied in this work has been the effect of nanoparticles – magnetite and single-wall carbon nanotubes – separately and together on the conductivity of nematic liquid crystal 6CHBT dispersed in polyvinyl alcohol. Morphology of these films was analyzed using an electron microscope. When using selected technologyof homogenizing the mixture components, there takes place formation of liquid crystals dispersed in the polymer matrix with the average sizes of liquid-crystal droplets close to 500 nm (nanoPDLC). It has been found that simultaneous introduction of magnetite and nanotubes results in lowering the conductivity of nano-PDLC as compared to the total conductivity of nano-PDLC with each kind of nanoparticles separately. It has been suggested that the main mechanism of this effect lies in formation of deep centers for electron capture by complexes with different types of nanoparticles, which leads to a decrease in electronic conductivity through the polymer matrix. 2014 Article Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes / P. Kopcansky, M. Timko,Z. Mitrova, N. Tomasovicova, L. Tomco, O.V. Kovalchuk, T.M. Kovalchuk, I.V. Oleinikova, A.I. Lad, I.P. Studenyak // Semiconductor Physics Quantum Electronics & Optoelectronics. — 2014. — Т. 17, № 4. — С. 384-388. — Бібліогр.: 8 назв. — англ. 1560-8034 PACS 61.30.Pq, 61.48.De, 75.30.Hx, 77.22.Cx, 77.84.Nh https://nasplib.isofts.kiev.ua/handle/123456789/118423 en Semiconductor Physics Quantum Electronics & Optoelectronics application/pdf Інститут фізики напівпровідників імені В.Є. Лашкарьова НАН України |
| institution |
Digital Library of Periodicals of National Academy of Sciences of Ukraine |
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DSpace DC |
| language |
English |
| description |
Studied in this work has been the effect of nanoparticles – magnetite and
single-wall carbon nanotubes – separately and together on the conductivity of nematic
liquid crystal 6CHBT dispersed in polyvinyl alcohol. Morphology of these films was
analyzed using an electron microscope. When using selected technologyof homogenizing
the mixture components, there takes place formation of liquid crystals dispersed in the
polymer matrix with the average sizes of liquid-crystal droplets close to 500 nm (nanoPDLC).
It has been found that simultaneous introduction of magnetite and nanotubes
results in lowering the conductivity of nano-PDLC as compared to the total conductivity
of nano-PDLC with each kind of nanoparticles separately. It has been suggested that the
main mechanism of this effect lies in formation of deep centers for electron capture by
complexes with different types of nanoparticles, which leads to a decrease in electronic
conductivity through the polymer matrix. |
| format |
Article |
| author |
Kopčanský, P. Timko, M. Mitrova, Z. Tomašovičová, N. Tomčo, L. Kovalchuk, O.V. Kovalchuk, T.M. Oleinikova, I.V. Lad, A.I. Studenyak, I.P. |
| spellingShingle |
Kopčanský, P. Timko, M. Mitrova, Z. Tomašovičová, N. Tomčo, L. Kovalchuk, O.V. Kovalchuk, T.M. Oleinikova, I.V. Lad, A.I. Studenyak, I.P. Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes Semiconductor Physics Quantum Electronics & Optoelectronics |
| author_facet |
Kopčanský, P. Timko, M. Mitrova, Z. Tomašovičová, N. Tomčo, L. Kovalchuk, O.V. Kovalchuk, T.M. Oleinikova, I.V. Lad, A.I. Studenyak, I.P. |
| author_sort |
Kopčanský, P. |
| title |
Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes |
| title_short |
Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes |
| title_full |
Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes |
| title_fullStr |
Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes |
| title_full_unstemmed |
Peculiarities of nonadditive changes in conductivity of nano-PDLC under influence of magnetite and single-wall carbon nanotubes |
| title_sort |
peculiarities of nonadditive changes in conductivity of nano-pdlc under influence of magnetite and single-wall carbon nanotubes |
| publisher |
Інститут фізики напівпровідників імені В.Є. Лашкарьова НАН України |
| publishDate |
2014 |
| url |
https://nasplib.isofts.kiev.ua/handle/123456789/118423 |
| citation_txt |
Peculiarities of nonadditive changes in conductivity
of nano-PDLC under influence of magnetite
and single-wall carbon nanotubes / P. Kopcansky, M. Timko,Z. Mitrova, N. Tomasovicova, L. Tomco, O.V. Kovalchuk, T.M. Kovalchuk, I.V. Oleinikova, A.I. Lad, I.P. Studenyak // Semiconductor Physics Quantum Electronics & Optoelectronics. — 2014. — Т. 17, № 4. — С. 384-388. — Бібліогр.: 8 назв. — англ. |
| series |
Semiconductor Physics Quantum Electronics & Optoelectronics |
| work_keys_str_mv |
AT kopcanskyp peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT timkom peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT mitrovaz peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT tomasovicovan peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT tomcol peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT kovalchukov peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT kovalchuktm peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT oleinikovaiv peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT ladai peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes AT studenyakip peculiaritiesofnonadditivechangesinconductivityofnanopdlcunderinfluenceofmagnetiteandsinglewallcarbonnanotubes |
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2025-12-02T10:26:19Z |
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2025-12-02T10:26:19Z |
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| fulltext |
Semiconductor Physics, Quantum Electronics & Optoelectronics, 2014. V. 17, N 4. P. 384-388.
© 2014, V. Lashkaryov Institute of Semiconductor Physics, National Academy of Sciences of Ukraine
384
PACS 61.30.Pq, 61.48.De, 75.30.Hx, 77.22.Cx, 77.84.Nh
Peculiarities of nonadditive changes in conductivity
of nano-PDLC under influence of magnetite
and single-wall carbon nanotubes
P. Kopčanský1, M. Timko1, Z. Mitrova1, N. Tomašovičová1, L. Tomčo1, O.V. Kovalchuk2,3,
T.M. Kovalchuk4, I.V. Oleinikova2, A.I. Lad2, I.P. Studenyak5
1Institute of Experimental Physics, Slovak Academy of Sciences,
47, Watsonova str., 04001 Košice, Slovak Republic
2Kyiv National University of Technologies and Design,
2, Nemirovich-Danchenko str., 01011 Kyiv, Ukraine
E-mail: akoval@knutd.com.ua
3Institute of Physics, National Academy of Sciences of Ukraine,
46, prospect Nauky, 03028 Kyiv, Ukraine
4V. Lashkaryov Institute of Semiconductor Physics, NAS of Ukraine,
41, prospect Nauky, 03028 Kyiv, Ukraine
5Uzhgorod National University, 46, Pidhirna str., 88000 Uzhgorod, Ukraine
Abstract. Studied in this work has been the effect of nanoparticles – magnetite and
single-wall carbon nanotubes – separately and together on the conductivity of nematic
liquid crystal 6CHBT dispersed in polyvinyl alcohol. Morphology of these films was
analyzed using an electron microscope. When using selected technologyof homogenizing
the mixture components, there takes place formation of liquid crystals dispersed in the
polymer matrix with the average sizes of liquid-crystal droplets close to 500 nm (nano-
PDLC). It has been found that simultaneous introduction of magnetite and nanotubes
results in lowering the conductivity of nano-PDLC as compared to the total conductivity
of nano-PDLC with each kind of nanoparticles separately. It has been suggested that the
main mechanism of this effect lies in formation of deep centers for electron capture by
complexes with different types of nanoparticles, which leads to a decrease in electronic
conductivity through the polymer matrix.
Keywords: magnetic nanoparticle, single-wall carbon nanotube, permittivity, ion
component of conductivity, electron component of conductivity, polymer matrix.
Manuscript received 11.02.14; revised version received 14.05.14; accepted for
publication 29.10.14; published online 10.11.14.
1. Introduction
An important place in up-to-date scientific works
belongs to studies of the effect of nanoparticles on
properties of various materials, including liquid crystals,
in order to obtain compositions with new functional
properties. In the most works, one type of nanoparticles
is used. But not always, using only one type of
nanoparticles as additives provides preparation of
material with desired properties.
When introducing nanoparticles of several different
types into a matrix even at low concentrations, it is not
always possible to predict the effect of nanoparticles
together, if being based on data about the impact of each
type of nanoparticles separately. In the work [1], we
studied the additive action of nanoparticles – magnetic
nanoparticles (MN) and single-wall carbon nanotubes
(SWNT) – on properties of homogeneous liquid crystal.
It was shown that introducing MN and SWNT with the
concentration 0.02 wt.% for each nanoparticle type into
Semiconductor Physics, Quantum Electronics & Optoelectronics, 2014. V. 17, N 4. P. 384-388.
© 2014, V. Lashkaryov Institute of Semiconductor Physics, National Academy of Sciences of Ukraine
385
liquid crystal leads approximately to the 20-fold increase
in conductivity, while each individual component
separately increases the LC conductivity no more than
doubly. One of the mechanisms of this effect may be
formation of complexes of nanoparticles that contribute
to formation of additional charge carriers. The efficiency
of this process can be essentially influenced by the size
effect (the value of LC volume), which can be achieved
by dispersing the LC molecules in the polymer matrix
(PDLC cell).
Partly, we solved the problem of the influence of
size effect on nonadditivity of action of magnetite and
nanotubes on the LC conductivity in the work [2] where
PDLC cells with the sizes of nematic droplets 8…10 μm
were studied. It was found that for these sizes the effect
of nonadditive action of carbon nanotubes and magnetite
on the composite conductivity is lower, but still quite
significant. That’s why, the purpose of this work was to
investigate the possibility of nonadditive action of
nanoparticles on the LC conductivity for smaller LC
droplet sizes than in [2].
2. Materials and methods of research
The samples of PDLCs were prepared using the
following method. Liquid crystal 6CHBT of amount
0.05 ml was added to 5 ml of 10% polyvinyl alcohol
(PVA). The samples was sonicated with an ultrasonic
oscillator (Branson model 450, 20 kHz, 280 W) for
1 min. A creamy white emulsion was obtained. A thin
bead was placed on a slide. After water evaporation, we
got a thin film. The sample thickness was 50 μm. This
technique was also used for preparation of the PDLC
films doped with various types of magnetic particles.
Into PDLC, we entered MN of spherical shape with the
average diameter 5 nm and SWNT with the length
1000 nm and the diameter 2 nm. Samples with the
nanoparticle concentrations 0.01, 0.1 and 0.2 wt.% were
prepared. Where we injected MN and SWNT, the
concentration of each type nanoparticles was the same.
As in [2], morphology of the obtained films was
studied using a scanning electron microscope JSM-35
(Japan) at the voltage 35 keV that accelerates the
electron beam. Before performing the study, we
deposited a thin layer of graphite on the film surface. So,
there were minimized effects that were caused by
charging the surface. All the obtained images were
recorded using a digital camera and then analyzed.
PDLC were deposited on glass plates coated with
ITO conductive layer. After drying the solvent, another
glass plate covered with a ITO layer was pressed to the
free surface of PDLC. To maintain good electrical
contact, we deposited a thin LC layer on the electrode
before pressing. The sandwich cell required for dielectric
measurements was formed in this manner. Since the
PDLC film took only the central part of the sample,
using the interference method at the edges of the
electrodes we measured the distance between the
electrodes and consequently the cell thickness.
Measurements of the thickness were performed in
different places of the sample. It made it possible to
check the uniformity of pressing the top electrode.
Dielectric properties of the samples were studied
within the frequency range 10–1…106 Hz at the
temperature 293 K by using the oscilloscopic method
[3]. The amplitude of the measuring signal with the
triangular shape was 0.25 V.
3. Results and analysis
3.1. Morphology of films
Analysis of morphology of PDLC films showed that,
when selected technology of homogenization was used,
the sizes of LC impurities in the studied PDLC did not
exceed 1 mm and the average one was 500 nm.
Therefore, the obtained dispersions of liquid crystal were
called nano-PDLC. The small sizes of LC droplets were
confirmed studying the transmission of nano-PDLC in
the visible spectral range.
Being based on the analysis of the images of nano-
PDLC, we ascertained that morphology of nano-PDLC
does not substantially change in dependence on the type
and concentration of nanoparticles. Quantitative
estimations of the nanoparticle diameter could not be
performed because the edges of LC nano-impurities are
blurred. It is known from [4] that after the phase
separation, when preparing PDLC, clear boundaries
between the LC droplets and polymer matrix are not
observed. There is always an intermediate layer
consisting of a mixture of monomers of polymer and LC
molecules (at the molecular level). The thickness of this
layer is about 1 mm, which is comparable with the sizes
of LC droplets in the case of nano-PDLC.
3.2. Frequency dependence of the permittivity and
conductivity of nano-PDLC with nanoparticles
Since we have analyzed the frequency dependence of the
permittivity and conductivity σ of nano-PDLC with
MN in detail in the work [5], let us consider in detail the
similar properties of nano-PDLC with SWNT and nano-
PDLC with SWNT and MN together.
Fig. 1 shows spectra of permittivity : nano-
PDLC (1), nano-PDLC + 0.01 wt.% SWNT (2), nano-
PDLC + 0.1 wt.% SWNT (3) and nano-PDLC +
0.2 wt.% SWNT (4).
As it was shown in [6], significant values of
(especially at low frequencies) are caused by effect of
the near-electrode processes. As seen from Fig. 1, the
greatest impact of SWNT on the value is observed in
the range of frequencies 1 to 103 Hz. At the lowest
frequencies f as well as for f >103 Hz, SWNT impact on
the value is much lower. The part of the dielectric
spectrum for f >103 Hz displays bulk properties of the
samples. Therefore, we can conclude that at the
indicated concentrations, SWNT does not significantly
change the value of the nano-PDLC bulk.
Semiconductor Physics, Quantum Electronics & Optoelectronics, 2014. V. 17, N 4. P. 384-388.
© 2014, V. Lashkaryov Institute of Semiconductor Physics, National Academy of Sciences of Ukraine
386
10-1 100 101 102 103 104 105
101
102
103
104
105
1
2
3
4
'
f, Hz
Fig. 1. Frequency dependences of permittivity : nano-
PDLC (1), nano-PDLC + 0.01 wt.% SWNT (2), nano-PDLC +
0.1 wt.% SWNT (3), and nano-PDLC + 0.2 wt.% SWNT (4).
The sample thickness is 50±5 μm. The temperature 273 K.
The decrease of the influence of SWNT on the
value of nano-PDLC at the frequencies f <1 Hz can be
explained by taking into account the structure of near-
electrode layer. As it is known, this layer consists of
ordered (closest to the electrode) and diffuse parts. It
was shown in [6] that the lower the frequency, the
thinner is the part of near-electrode layer, to which the
electric field is applied. From this it follows that
reducing the impact of SWNT on the value of nano-
PDLC at the frequencies f <1 Hz corresponds to
processes in the ordered part of the near-electrode layer,
the thickness of which is smaller than that of SWNT.
Fig. 2 shows the spectra of permittivity : nano-
PDLC (1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.%
MN (2), nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN
(3), and nano-PDLC + 0.2 wt.% SWNT + 0.2 wt.%
MN (4).
10-1 100 101 102 103 104 105
101
102
103
104
105
1
2
3
4
'
f, Hz
Fig. 2. Frequency dependences of permittivity : nano-PDLC
(1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.% MN (2),
nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN (3), and nano-
PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (4). The sample
thickness is 50±5 μm. The temperature 273 K.
From the comparison of Figs 1 and 2, it can be
concluded that the above mentioned regularities of
influence of SWNT on the value of nano-PDLC are
also kept when adding MN. However, the effect of
SWNT separately on the value of nano-PDLC is
greater than that of SWNT and MN together. This fact is
very important to explain the impact of nanoparticles on
the conductivity of nano-PDLC.
Fig. 3 shows the frequency dependence of the
conductivity σ: nano-PDLC (1), nano-PDLC +
0.01 wt.% SWNT (2), nano-PDLC + 0.1 wt.% SWNT
(3), and nano-PDLC + 0.2 wt.% SWNT (4).
As it follows from the analysis of the data, with
few exception of nano-PDLC without nanoparticles,
there are no parts on the frequency dependences of
conductivity, where the σ value does not depend on
frequency. In all the samples of micro-PDLC, we
observed spectral regions where the conductivity is
independent of frequency, and we explained this effect
by ionic conductivity through the LC drops [2]. Due to
large sizes, these drops either “locked” electrodes in
their location (it was clearly visible in the photos) or the
distance between the drops was sufficient for the passage
of ions.
It follows from the analysis of Fig. 1 (curve 1)
that for the frequencies from 1 to 103 Hz, the
conductivity is a power function of the frequency with
a small exponent.
Summarizing, we can conclude that unlike micro-
PDLC, in nano-PDLC the purely ionic conductivity is
not observed. From this conclusion does not follow that
the ionic conductivity is excluded from the process of
charge transfer through the sample. However,
contribution of the ionic conductivity is not essential,
because it is limited by the conductivity of the polymer
parts between LC drops.
10-1 100 101 102 103 104 105
10-6
10-5
10-4
10-3
1
2
3
4
O
hm
-1
m
-1
f, Hz
Fig. 3. Frequency dependences of conductivity σ: nano-PDLC
(1), nano-PDLC + 0.01 wt.% SWNT (2), nano-PDLC +
0.1 wt.% SWNT (3), and nano-PDLC + 0.2 wt.% SWNT (4).
The sample thickness is 50±5 μm. The temperature 273 K.
Semiconductor Physics, Quantum Electronics & Optoelectronics, 2014. V. 17, N 4. P. 384-388.
© 2014, V. Lashkaryov Institute of Semiconductor Physics, National Academy of Sciences of Ukraine
387
It is the significant influence of conductivity
electron components in nano-PDLC, as compared to
micro-PDLC, that can explain the sharp increase in
conductivity for the samples with the concentration
0.2 wt.% SWNT (Fig. 3, curve 4) almost over the whole
frequency range. This effect can be explained by
creation of a percolation lattice between SWNT [7, 8].
Intermediate links between SWNT is nano-PDLC with
electron type conductivity.
To determine features of this percolation, it is
reasonable to study how the conductivity of nano-PDLC
will change when MN and SWNT are added together to
nano-PDLC. Fig. 4 shows the frequency dependence of
σ conductivity: nano-PDLC (1), nano-PDLC +
0.01 wt.% SWNT + 0.01 wt.% MN (2), nano-PDLC +
0.1 wt.% SWNT + 0.1 wt.% MN (3) and nano-PDLC +
0.2 wt.% SWNT + 0.2 wt.% MN (4).
The most important conclusion to be drawn from
Fig. 4 is the lack of a sharp increase in the conductivity
for the sample nano-PDLC + 0.2 wt.% SWNT +
0.2 wt.% MN (curve 4). That is adding to the sample
nano-PDLC + 0.2 wt.% SWNT of small amount of
0.2 wt.% MN leads to the fact that in contrast to the data
shown in Fig. 3 there is no abrupt change in the
conductivity at the nanotube concentration 0.2 wt.%.
The reason for this effect may be creation of complexes
of nanoparticles with SWNT and MN. These complexes
may reduce the efficiency of formation of percolation
lattice and thus increase the concentration of
nanoparticles in the case of percolation transition.
3.3. Nonadditive effect of magnetic nanoparticles,
carbon nanotubes (separately and together) on the
conductivity of nano-PDLC
After analyzing the properties of the samples under
study, let us consider the main problem of this work – to
determine features of nonadditive action of MN and
SWNT on the conductivity of nano-PDLC. To
characterize the difference between the conductivity of
the samples with two types of nanoparticles and the
conductivity of samples with each particle type
separately, in the work [2] we proposed to use the
coefficient of nonadditivity. To calculate this coefficient,
we used the following relation
21
12
nonadk ,
where σ12 is the conductivity value when entering MN
and SWNT together into nano-PDLC, σ1 and σ2 are the
values of conductivity under the action of each type of
nanoparticles separately.
Fig. 5 shows the frequency dependence of knonad for
three different concentrations of nanoparticles:
0.01 wt.% (1), 0.1 wt.% (2), and 0.2 wt.% (3).
The main conclusion following from the analysis of
Fig. 5 can be summarized as follows: regardless of the
chosen concentrations of nanoparticles, the conductivity
of nano-PDLC with two types of nanoparticles is lower
than that with combined effect of each nanoparticle
separately (the value of knonad for all the selected
concentrations is less than unity). This property
fundamentally distinguishes the effect of nanoparticles
on the conductivity of nano-PDLC from the action of the
same type of nanoparticles on the conductivity of
homogeneous liquid crystal and micro-PDLC.
It is caused by the fact (as already noted above) that
the ionic conductivity is not revealed in a “pure” form in
nano-PDLC. Therefore, there is no appropriate
mechanisms that would lead to an increase in the knonad
value. In the case of electron transfer, morphology of
PDLC films will essentially influence on the presence of
deep levels for electron capture. Analysis of the
influence of type and concentration nanoparticles (within
the ranges that were taken for these researches) showed
that morphology of nano-PDLC is not significantly
changed under the influence of nanoparticles. Therefore,
we can predict that the main mechanism of small values
of knonad in the case of nano-PDLC is creation of deep
levels for capturing carriers by the above nanoparticles
of two types.
10-1 100 101 102 103 104 105
10-6
10-5
10-4
1
2
3
4
O
hm
-1
m
-1
f, Hz
Fig. 4. Frequency dependences of conductivity σ: nano-PDLC
(1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.% MN(2),
nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN (3), and nano-
PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (4). The sample
thickness is 50±5 μm. The temperature 273 K.
10-1 100 101 102 103 104 105
0.2
0.3
0.4
0.5
0.6
0.7
k no
na
d
f, Hz
1
2
3
Fig. 5. Frequency dependences of knonad of nano-PDLC for
three different concentrations of nanoparticles: 0.01 wt.% (1),
0.1 wt.% (2), and 0.2 wt.% (3). The sample thickness is
50±5 μm. The temperature 273 K.
Semiconductor Physics, Quantum Electronics & Optoelectronics, 2014. V. 17, N 4. P. 384-388.
© 2014, V. Lashkaryov Institute of Semiconductor Physics, National Academy of Sciences of Ukraine
388
In the framework of the proposed mechanism that
explains the reasons of small values of knonad in the case
of nano-PDLC, it is useful to analyze the frequency
dependence of nano-PDLC for different concentrations
of nanoparticles (Fig. 5). As follows from the analysis of
this figure, on average (within the frequency range) the
samples with the lowest concentrations of the studied
nanoparticles (0.01 wt.%) have the smallest knonad value.
One may assume that it is for this concentration of
nanoparticles, the deep levels of electron capture, which
are caused by complexes of two different types of
nanoparticles, most efficiently influence on the transport
of charge carriers.
In the case of increasing the nanoparticle
concentration, besides the centers of electron capture,
the additional channels of electron transfer through
polymer may also arise in nano-PDLC. The efficiency of
increasing the charge carrier concentration may be
higher than that of increasing the concentration of the
centres for electron capture. This may be the reason for
the increase of the knonad value with the concentration of
nanoparticles (curves 2 and 3 in Fig. 5).
4. Conclusions
Thus it is shown that, as in micro-PDLC, introduction of
magnetic nanoparticles and nanotubes with the
concentrations less than 0.2 wt.% separately and
together into nano-PDLC cannot significantly change
morphology of the films.
In contrast to the homogeneous liquid crystal and
micro-PDLC, the conductivity of nano-PDLC with MN
and SWNT is less than the total effect of each
nanoparticle separately. The main factors for this effect
are: (i) lack of ionic component of conductivity through
nano-PDLC; (ii) formation of deep centers for capture of
electrons by complexes with different types of
nanoparticles. It has been shown that the second factor
operates most efficiently, when the chosen concentration
of nanoparticles is the lowest one (0.01 wt.%).
Formation of complexes between MN and SWNT
is the reason for increasing the concentration of
nanoparticles in the case of percolation transition, when
MN and SWNT act jointly on the conductivity of nano-
PDLC with respect to the effect only of the nanotubes.
References
1. P. Kopčanský, O.V. Kovalchuk, N. Tomašovičová
et al., Nonadditive changes in the conductivity of
nematic liquid crystal when introducing single-
walled carbon nanotubes and magnetite // The 13th
Small Triangle Meeting on Theoretical Physics.
Institute of Experimental Physics, Kosice,
Slovakia, p. 72-79 (2012).
2. P. Kopčanský, M. Timko, Z. Mitrova, V. Zavisova,
M. Koneracká, N. Tomašovičová, L. Tomčo,
O.V. Kovalchuk, V.M. Bykov, T.M. Kovalchuk,
Nonadditive changes in conductivity of micro
PDLC under the influence of carbon nanotubes and
magnetic nanoparticles // Semiconductor Physics,
Quantum Electronics and Optoelectronics, 16(4),
p. 374-378 (2013).
3. A.J. Twarowski, A.C. Albrecht, Depletion layer in
organic films: Low frequency measurements in
polycrystalline tetracene // J. Chem. Phys. 20,
p. 2255 (1979).
4. H. Stark, Physics of colloidal dispersions in
nematic liquid crystals // Phys. Repts. 351(6),
p. 387-474 (2001).
5. P. Kopčanský, M. Timko, Z. Mitrova, V. Zavisova,
M. Koneracká, N. Tomašovičová, L. Tomčo,
O.V. Kovalchuk, V.M. Bykov, T.M. Kovalchuk,
A.I. Lad, Effect of magnetic nanoparticles with
various geometrical shapes on morphology and
dielectric properties of nanodispersions of nematic
liquid crystal in polymer matrix // Semiconductor
Physics, Quantum Electronics and Optoelectronics,
16(3), p. 253-258 (2013).
6. A.V. Koval’chuk, Relaxation processes and charge
transport across liquid crystal-electrode interface //
J. Phys.: Condens. Matter, 13, p. 10333 (2001).
7. A.I. Goncharuk, N.I. Lebovka, L.N. Lisetski, and
S.S. Minenko, Aggregation, percolation and phase
transitions in nematic liquid crystal EBBA doped
with carbon nanotubes // J. Phys. D: Appl. Phys.
42, 165411 (2009).
8. A. Koval’chuk, L. Dolgov, O. Yaroshchuk, Dielec-
tric studies of dispersions of carbon nanotubes in
liquid crystals 5CB // Semiconductor Physics,
Quantum Electronics & Optoelectronics, 11, p. 337
(2008).
Semiconductor Physics, Quantum Electronics & Optoelectronics, 2014. V. 17, N 4. P. 384-388.
PACS 61.30.Pq, 61.48.De, 75.30.Hx, 77.22.Cx, 77.84.Nh
Peculiarities of nonadditive changes in conductivity
of nano-PDLC under influence of magnetite
and single-wall carbon nanotubes
P. Kopčanský1, M. Timko1, Z. Mitrova1, N. Tomašovičová1, L. Tomčo1, O.V. Kovalchuk2,3,
T.M. Kovalchuk4, I.V. Oleinikova2, A.I. Lad2, I.P. Studenyak5
1Institute of Experimental Physics, Slovak Academy of Sciences,
47, Watsonova str., 04001 Košice, Slovak Republic
2Kyiv National University of Technologies and Design,
2, Nemirovich-Danchenko str., 01011 Kyiv, Ukraine
E-mail: akoval@knutd.com.ua
3Institute of Physics, National Academy of Sciences of Ukraine,
46, prospect Nauky, 03028 Kyiv, Ukraine
4V. Lashkaryov Institute of Semiconductor Physics, NAS of Ukraine,
41, prospect Nauky, 03028 Kyiv, Ukraine
5Uzhgorod National University, 46, Pidhirna str., 88000 Uzhgorod, Ukraine
Abstract. Studied in this work has been the effect of nanoparticles – magnetite and single-wall carbon nanotubes – separately and together on the conductivity of nematic liquid crystal 6CHBT dispersed in polyvinyl alcohol. Morphology of these films was analyzed using an electron microscope. When using selected technologyof homogenizing the mixture components, there takes place formation of liquid crystals dispersed in the polymer matrix with the average sizes of liquid-crystal droplets close to 500 nm (nano-PDLC). It has been found that simultaneous introduction of magnetite and nanotubes results in lowering the conductivity of nano-PDLC as compared to the total conductivity of nano-PDLC with each kind of nanoparticles separately. It has been suggested that the main mechanism of this effect lies in formation of deep centers for electron capture by complexes with different types of nanoparticles, which leads to a decrease in electronic conductivity through the polymer matrix.
Keywords: magnetic nanoparticle, single-wall carbon nanotube, permittivity, ion component of conductivity, electron component of conductivity, polymer matrix.
Manuscript received 11.02.14; revised version received 14.05.14; accepted for publication 29.10.14; published online 10.11.14.
1. Introduction
An important place in up-to-date scientific works belongs to studies of the effect of nanoparticles on properties of various materials, including liquid crystals, in order to obtain compositions with new functional properties. In the most works, one type of nanoparticles is used. But not always, using only one type of nanoparticles as additives provides preparation of material with desired properties.
When introducing nanoparticles of several different types into a matrix even at low concentrations, it is not always possible to predict the effect of nanoparticles together, if being based on data about the impact of each type of nanoparticles separately. In the work [1], we studied the additive action of nanoparticles – magnetic nanoparticles (MN) and single-wall carbon nanotubes (SWNT) – on properties of homogeneous liquid crystal. It was shown that introducing MN and SWNT with the concentration 0.02 wt.% for each nanoparticle type into liquid crystal leads approximately to the 20-fold increase in conductivity, while each individual component separately increases the LC conductivity no more than doubly. One of the mechanisms of this effect may be formation of complexes of nanoparticles that contribute to formation of additional charge carriers. The efficiency of this process can be essentially influenced by the size effect (the value of LC volume), which can be achieved by dispersing the LC molecules in the polymer matrix (PDLC cell).
Partly, we solved the problem of the influence of size effect on nonadditivity of action of magnetite and nanotubes on the LC conductivity in the work [2] where PDLC cells with the sizes of nematic droplets 8…10 μm were studied. It was found that for these sizes the effect of nonadditive action of carbon nanotubes and magnetite on the composite conductivity is lower, but still quite significant. That’s why, the purpose of this work was to investigate the possibility of nonadditive action of nanoparticles on the LC conductivity for smaller LC droplet sizes than in [2].
2. Materials and methods of research
The samples of PDLCs were prepared using the following method. Liquid crystal 6CHBT of amount 0.05 ml was added to 5 ml of 10% polyvinyl alcohol (PVA). The samples was sonicated with an ultrasonic oscillator (Branson model 450, 20 kHz, 280 W) for 1 min. A creamy white emulsion was obtained. A thin bead was placed on a slide. After water evaporation, we got a thin film. The sample thickness was 50 μm. This technique was also used for preparation of the PDLC films doped with various types of magnetic particles. Into PDLC, we entered MN of spherical shape with the average diameter 5 nm and SWNT with the length 1000 nm and the diameter 2 nm. Samples with the nanoparticle concentrations 0.01, 0.1 and 0.2 wt.% were prepared. Where we injected MN and SWNT, the concentration of each type nanoparticles was the same.
As in [2], morphology of the obtained films was studied using a scanning electron microscope JSM-35 (Japan) at the voltage 35 keV that accelerates the electron beam. Before performing the study, we deposited a thin layer of graphite on the film surface. So, there were minimized effects that were caused by charging the surface. All the obtained images were recorded using a digital camera and then analyzed.
PDLC were deposited on glass plates coated with ITO conductive layer. After drying the solvent, another glass plate covered with a ITO layer was pressed to the free surface of PDLC. To maintain good electrical contact, we deposited a thin LC layer on the electrode before pressing. The sandwich cell required for dielectric measurements was formed in this manner. Since the PDLC film took only the central part of the sample, using the interference method at the edges of the electrodes we measured the distance between the electrodes and consequently the cell thickness. Measurements of the thickness were performed in different places of the sample. It made it possible to check the uniformity of pressing the top electrode.
Dielectric properties of the samples were studied within the frequency range 10–1…106 Hz at the temperature 293 K by using the oscilloscopic method [3]. The amplitude of the measuring signal with the triangular shape was 0.25 V.
3. Results and analysis
3.1. Morphology of films
Analysis of morphology of PDLC films showed that, when selected technology of homogenization was used, the sizes of LC impurities in the studied PDLC did not exceed 1 mm and the average one was 500 nm. Therefore, the obtained dispersions of liquid crystal were called nano-PDLC. The small sizes of LC droplets were confirmed studying the transmission of nano-PDLC in the visible spectral range.
Being based on the analysis of the images of nano-PDLC, we ascertained that morphology of nano-PDLC does not substantially change in dependence on the type and concentration of nanoparticles. Quantitative estimations of the nanoparticle diameter could not be performed because the edges of LC nano-impurities are blurred. It is known from [4] that after the phase separation, when preparing PDLC, clear boundaries between the LC droplets and polymer matrix are not observed. There is always an intermediate layer consisting of a mixture of monomers of polymer and LC molecules (at the molecular level). The thickness of this layer is about 1 mm, which is comparable with the sizes of LC droplets in the case of nano-PDLC.
3.2. Frequency dependence of the permittivity and conductivity of nano-PDLC with nanoparticles
Since we have analyzed the frequency dependence of the permittivity (( and conductivity σ of nano-PDLC with MN in detail in the work [5], let us consider in detail the similar properties of nano-PDLC with SWNT and nano-PDLC with SWNT and MN together.
Fig. 1 shows spectra of permittivity ((: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT (2), nano-PDLC + 0.1 wt.% SWNT (3) and nano-PDLC + 0.2 wt.% SWNT (4).
As it was shown in [6], significant values of (( (especially at low frequencies) are caused by effect of the near-electrode processes. As seen from Fig. 1, the greatest impact of SWNT on the (( value is observed in the range of frequencies 1 to 103 Hz. At the lowest frequencies f as well as for f >103 Hz, SWNT impact on the (( value is much lower. The part of the dielectric spectrum for f >103 Hz displays bulk properties of the samples. Therefore, we can conclude that at the indicated concentrations, SWNT does not significantly change the (( value of the nano-PDLC bulk.
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Fig. 1. Frequency dependences of permittivity ((: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT (2), nano-PDLC + 0.1 wt.% SWNT (3), and nano-PDLC + 0.2 wt.% SWNT (4). The sample thickness is 50±5 μm. The temperature 273 K.
The decrease of the influence of SWNT on the (( value of nano-PDLC at the frequencies f <1 Hz can be explained by taking into account the structure of near-electrode layer. As it is known, this layer consists of ordered (closest to the electrode) and diffuse parts. It was shown in [6] that the lower the frequency, the thinner is the part of near-electrode layer, to which the electric field is applied. From this it follows that reducing the impact of SWNT on the (( value of nano-PDLC at the frequencies f <1 Hz corresponds to processes in the ordered part of the near-electrode layer, the thickness of which is smaller than that of SWNT.
Fig. 2 shows the spectra of permittivity ((: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.% MN (2), nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN (3), and nano-PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (4).
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'
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Fig. 2. Frequency dependences of permittivity ((: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.% MN (2), nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN (3), and nano-PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (4). The sample thickness is 50±5 μm. The temperature 273 K.
From the comparison of Figs 1 and 2, it can be concluded that the above mentioned regularities of influence of SWNT on the value (( of nano-PDLC are also kept when adding MN. However, the effect of SWNT separately on the (( value of nano-PDLC is greater than that of SWNT and MN together. This fact is very important to explain the impact of nanoparticles on the conductivity of nano-PDLC.
Fig. 3 shows the frequency dependence of the conductivity σ: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT (2), nano-PDLC + 0.1 wt.% SWNT (3), and nano-PDLC + 0.2 wt.% SWNT (4).
As it follows from the analysis of the data, with few exception of nano-PDLC without nanoparticles, there are no parts on the frequency dependences of conductivity, where the σ value does not depend on frequency. In all the samples of micro-PDLC, we observed spectral regions where the conductivity is independent of frequency, and we explained this effect by ionic conductivity through the LC drops [2]. Due to large sizes, these drops either “locked” electrodes in their location (it was clearly visible in the photos) or the distance between the drops was sufficient for the passage of ions.
It follows from the analysis of Fig. 1 (curve 1) that for the frequencies from 1 to 103 Hz, the conductivity is a power function of the frequency with a small exponent.
Summarizing, we can conclude that unlike micro-PDLC, in nano-PDLC the purely ionic conductivity is not observed. From this conclusion does not follow that the ionic conductivity is excluded from the process of charge transfer through the sample. However, contribution of the ionic conductivity is not essential, because it is limited by the conductivity of the polymer parts between LC drops.
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-1
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-1
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Fig. 3. Frequency dependences of conductivity σ: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT (2), nano-PDLC + 0.1 wt.% SWNT (3), and nano-PDLC + 0.2 wt.% SWNT (4). The sample thickness is 50±5 μm. The temperature 273 K.
It is the significant influence of conductivity electron components in nano-PDLC, as compared to micro-PDLC, that can explain the sharp increase in conductivity for the samples with the concentration 0.2 wt.% SWNT (Fig. 3, curve 4) almost over the whole frequency range. This effect can be explained by creation of a percolation lattice between SWNT [7, 8]. Intermediate links between SWNT is nano-PDLC with electron type conductivity.
To determine features of this percolation, it is reasonable to study how the conductivity of nano-PDLC will change when MN and SWNT are added together to nano-PDLC. Fig. 4 shows the frequency dependence of σ conductivity: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.% MN (2), nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN (3) and nano-PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (4).
The most important conclusion to be drawn from Fig. 4 is the lack of a sharp increase in the conductivity for the sample nano-PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (curve 4). That is adding to the sample nano-PDLC + 0.2 wt.% SWNT of small amount of 0.2 wt.% MN leads to the fact that in contrast to the data shown in Fig. 3 there is no abrupt change in the conductivity at the nanotube concentration 0.2 wt.%. The reason for this effect may be creation of complexes of nanoparticles with SWNT and MN. These complexes may reduce the efficiency of formation of percolation lattice and thus increase the concentration of nanoparticles in the case of percolation transition.
3.3. Nonadditive effect of magnetic nanoparticles, carbon nanotubes (separately and together) on the conductivity of nano-PDLC
After analyzing the properties of the samples under study, let us consider the main problem of this work – to determine features of nonadditive action of MN and SWNT on the conductivity of nano-PDLC. To characterize the difference between the conductivity of the samples with two types of nanoparticles and the conductivity of samples with each particle type separately, in the work [2] we proposed to use the coefficient of nonadditivity. To calculate this coefficient, we used the following relation
2
1
12
s
+
s
s
=
nonad
k
,
where σ12 is the conductivity value when entering MN and SWNT together into nano-PDLC, σ1 and σ2 are the values of conductivity under the action of each type of nanoparticles separately.
Fig. 5 shows the frequency dependence of knonad for three different concentrations of nanoparticles: 0.01 wt.% (1), 0.1 wt.% (2), and 0.2 wt.% (3).
The main conclusion following from the analysis of Fig. 5 can be summarized as follows: regardless of the chosen concentrations of nanoparticles, the conductivity of nano-PDLC with two types of nanoparticles is lower than that with combined effect of each nanoparticle separately (the value of knonad for all the selected concentrations is less than unity). This property fundamentally distinguishes the effect of nanoparticles on the conductivity of nano-PDLC from the action of the same type of nanoparticles on the conductivity of homogeneous liquid crystal and micro-PDLC.
It is caused by the fact (as already noted above) that the ionic conductivity is not revealed in a “pure” form in nano-PDLC. Therefore, there is no appropriate mechanisms that would lead to an increase in the knonad value. In the case of electron transfer, morphology of PDLC films will essentially influence on the presence of deep levels for electron capture. Analysis of the influence of type and concentration nanoparticles (within the ranges that were taken for these researches) showed that morphology of nano-PDLC is not significantly changed under the influence of nanoparticles. Therefore, we can predict that the main mechanism of small values of knonad in the case of nano-PDLC is creation of deep levels for capturing carriers by the above nanoparticles of two types.
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Fig. 4. Frequency dependences of conductivity σ: nano-PDLC (1), nano-PDLC + 0.01 wt.% SWNT + 0.01 wt.% MN(2), nano-PDLC + 0.1 wt.% SWNT + 0.1 wt.% MN (3), and nano-PDLC + 0.2 wt.% SWNT + 0.2 wt.% MN (4). The sample thickness is 50±5 μm. The temperature 273 K.
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1
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Fig. 5. Frequency dependences of knonad of nano-PDLC for three different concentrations of nanoparticles: 0.01 wt.% (1), 0.1 wt.% (2), and 0.2 wt.% (3). The sample thickness is 50±5 μm. The temperature 273 K.
In the framework of the proposed mechanism that explains the reasons of small values of knonad in the case of nano-PDLC, it is useful to analyze the frequency dependence of nano-PDLC for different concentrations of nanoparticles (Fig. 5). As follows from the analysis of this figure, on average (within the frequency range) the samples with the lowest concentrations of the studied nanoparticles (0.01 wt.%) have the smallest knonad value. One may assume that it is for this concentration of nanoparticles, the deep levels of electron capture, which are caused by complexes of two different types of nanoparticles, most efficiently influence on the transport of charge carriers.
In the case of increasing the nanoparticle concentration, besides the centers of electron capture, the additional channels of electron transfer through polymer may also arise in nano-PDLC. The efficiency of increasing the charge carrier concentration may be higher than that of increasing the concentration of the centres for electron capture. This may be the reason for the increase of the knonad value with the concentration of nanoparticles (curves 2 and 3 in Fig. 5).
4. Conclusions
Thus it is shown that, as in micro-PDLC, introduction of magnetic nanoparticles and nanotubes with the concentrations less than 0.2 wt.% separately and together into nano-PDLC cannot significantly change morphology of the films.
In contrast to the homogeneous liquid crystal and micro-PDLC, the conductivity of nano-PDLC with MN and SWNT is less than the total effect of each nanoparticle separately. The main factors for this effect are: (i) lack of ionic component of conductivity through nano-PDLC; (ii) formation of deep centers for capture of electrons by complexes with different types of nanoparticles. It has been shown that the second factor operates most efficiently, when the chosen concentration of nanoparticles is the lowest one (0.01 wt.%).
Formation of complexes between MN and SWNT is the reason for increasing the concentration of nanoparticles in the case of percolation transition, when MN and SWNT act jointly on the conductivity of nano-PDLC with respect to the effect only of the nanotubes.
References
1. P. Kopčanský, O.V. Kovalchuk, N. Tomašovičová et al., Nonadditive changes in the conductivity of nematic liquid crystal when introducing single-walled carbon nanotubes and magnetite // The 13th Small Triangle Meeting on Theoretical Physics. Institute of Experimental Physics, Kosice, Slovakia, p. 72-79 (2012).
2. P. Kopčanský, M. Timko, Z. Mitrova, V. Zavisova, M. Koneracká, N. Tomašovičová, L. Tomčo, O.V. Kovalchuk, V.M. Bykov, T.M. Kovalchuk, Nonadditive changes in conductivity of micro PDLC under the influence of carbon nanotubes and magnetic nanoparticles // Semiconductor Physics, Quantum Electronics and Optoelectronics, 16(4), p. 374-378 (2013).
3. A.J. Twarowski, A.C. Albrecht, Depletion layer in organic films: Low frequency measurements in polycrystalline tetracene // J. Chem. Phys. 20, p. 2255 (1979).
4. H. Stark, Physics of colloidal dispersions in nematic liquid crystals // Phys. Repts. 351(6), p. 387-474 (2001).
5. P. Kopčanský, M. Timko, Z. Mitrova, V. Zavisova, M. Koneracká, N. Tomašovičová, L. Tomčo, O.V. Kovalchuk, V.M. Bykov, T.M. Kovalchuk, A.I. Lad, Effect of magnetic nanoparticles with various geometrical shapes on morphology and dielectric properties of nanodispersions of nematic liquid crystal in polymer matrix // Semiconductor Physics, Quantum Electronics and Optoelectronics, 16(3), p. 253-258 (2013).
6. A.V. Koval’chuk, Relaxation processes and charge transport across liquid crystal-electrode interface // J. Phys.: Condens. Matter, 13, p. 10333 (2001).
7. A.I. Goncharuk, N.I. Lebovka, L.N. Lisetski, and S.S. Minenko, Aggregation, percolation and phase transitions in nematic liquid crystal EBBA doped with carbon nanotubes // J. Phys. D: Appl. Phys. 42, 165411 (2009).
8. A. Koval’chuk, L. Dolgov, O. Yaroshchuk, Dielec-tric studies of dispersions of carbon nanotubes in liquid crystals 5CB // Semiconductor Physics, Quantum Electronics & Optoelectronics, 11, p. 337 (2008).
© 2014, V. Lashkaryov Institute of Semiconductor Physics, National Academy of Sciences of Ukraine
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