JP4888049B2 - Liquid crystal display element - Google Patents

Description

  The present invention relates to a liquid crystal display element using monostable ferroelectric liquid crystal having spontaneous polarization.

  Liquid crystal display elements have been widely used from large displays to portable information terminals because of their thinness and low power consumption, and their development is actively underway. So far, liquid crystal display elements have been developed and put to practical use, such as TN mode, STN multiplex drive, and active matrix drive using thin layer transistors (TFTs) for TN, but these use nematic liquid crystals. In addition, the response speed of the liquid crystal material is as slow as several ms to several tens of ms, and it cannot be said that it is sufficiently compatible with moving image display.

  Ferroelectric liquid crystal (FLC) is a liquid crystal suitable for high-speed devices because its response speed is as short as μs order. Ferroelectric liquid crystals proposed by Clark and Lagerwol are widely known as bistable ones having two stable states when no voltage is applied (FIG. 14 top), but for switching in two states of light and dark. Although it has limited memory characteristics, it has a problem that gradation display cannot be performed.

In recent years, the state of the liquid crystal layer when no voltage is applied is stabilized in a single state (hereinafter referred to as “monostable”). ) Is continuously changed, and the transmitted light intensity is analog-modulated so that gradation display is possible (see Non-Patent Document 1, lower part of FIG. 14). As the liquid crystal exhibiting monostability, generally, a ferroelectric liquid crystal that changes phase with the cholesteric phase (Ch) -chiral smectic C (SmC ^* ) phase in the temperature lowering process and does not pass through the smectic A (SmA) phase is used ( FIG. 13 top).

On the other hand, the ferroelectric liquid crystal is a material that changes in phase with a cholesteric phase (Ch) -smectic A (SmA) phase-chiral smectic C (SmC ^* ) phase in the temperature lowering process and exhibits an SmC ^* phase via the SmA phase. There is. Most of the ferroelectric liquid crystal materials currently reported have a phase series that passes through the latter SmA phase compared to the former material that does not pass through the SmA phase. It is known that a ferroelectric liquid crystal having a phase sequence passing through the latter SmA phase usually has two stable states with respect to a single-layer normal (lower stage in FIG. 13) and exhibits bistability. .

  In recent years, color liquid crystal display elements have been actively developed. As a method for realizing color display, there are generally a color filter method and a field sequential color method. In the color filter system, a white light source is used as a backlight, and color display is realized by attaching R, G, B micro color filters to each pixel. On the other hand, the field sequential color system switches the backlight to R, G, B, R, G, B ... in time, and opens and closes the black and white shutter of the ferroelectric liquid crystal to synchronize with it, and the afterimage effect of the retina Thus, the colors are mixed temporally to realize color display. In this field sequential color system, color display is possible with one pixel, and it is not necessary to use a color filter with low transmittance. Therefore, bright and high-definition color display is possible, and low power consumption and low cost can be realized. Useful in terms.

  In the field sequential color system, one pixel is time-divided, so that a liquid crystal as a black and white shutter needs to have high-speed response in order to obtain good moving image display characteristics. If a ferroelectric liquid crystal is used, this problem can be solved. As the ferroelectric liquid crystal used in this case, it is particularly desirable that the ferroelectric liquid crystal exhibits monostability in order to enable gradation display by analog modulation as described above and to realize high-definition color display. In addition, there are two types of ferroelectric liquid crystal exhibiting monostability: one that responds to both positive and negative voltages (lower right in FIG. 14) and one that responds only to positive and negative voltages (lower left in FIG. 14). is there. In particular, when a ferroelectric liquid crystal is driven using a thin film transistor (TFT) element, it is particularly preferable to respond to a voltage of either positive or negative polarity because the influence of reversal current due to spontaneous polarization is small.

  Here, FIG. 15 shows an example of a driving sequence of a liquid crystal display element by a field sequential color system using TFT elements. In FIG. 15, it is assumed that the voltage applied to the liquid crystal display element is 0 to ± V (V), data write scan is performed with a positive polarity voltage, and data erase scan is performed with a negative polarity voltage. It is assumed that a ferroelectric liquid crystal that exhibits monostability and responds only to a positive or negative voltage is used.

  As a response of the ferroelectric liquid crystal which shows monostability and responds only to a voltage of either positive or negative polarity, as illustrated in FIG. 12 (a)) and a case where a bright state is obtained in response to a negative polarity voltage (FIG. 12 (b)). Therefore, as shown in FIG. 15, when the ferroelectric liquid crystal showing the response (liquid crystal response 1) of FIG. 12A is used, a bright state is obtained when a positive polarity voltage is applied, and FIG. When a ferroelectric liquid crystal exhibiting a response (liquid crystal response 2) is used, a bright state is obtained when a negative polarity voltage is applied.

The ferroelectric liquid crystal using the TFT element is driven by applying a constant voltage to the common electrode of the common electrode substrate facing the TFT substrate and applying a voltage to the pixel electrode of each pixel of the TFT substrate. Here, when the pixel electrode voltage is relatively high with respect to the common electrode, a positive polarity voltage application is applied, and when the pixel electrode voltage is relatively low, a negative polarity voltage application is applied.
When using a ferroelectric liquid crystal that responds only to positive polarity voltage, positive polarity voltage application (writing) and negative polarity voltage application (erasing) are alternated to balance the charge. To do. When a TFT element is used, voltage cannot be written to all pixels at the same time, so scanning is performed for each line. Therefore, the writing of the first line and the writing of the L line are out of timing. The same applies to erasing. In the example shown in FIG. 15, erasing is performed from the first line after writing of all lines is completed.
Further, in the field sequential color method, writing and erasing are performed in synchronization with the flashing of the backlight. In FIG. 15, + (R) indicates that the address scanning is performed in synchronization with the R (red) backlight, and − (R) indicates that the R backlight is synchronized. This indicates that erase scanning (application of a negative polarity voltage) was performed. Similarly, + (G), − (G), + (B), and − (B) indicate that scanning is performed in synchronization with the backlights of G (green) and B (blue), respectively.

As described above, in the field sequential color system, the ferroelectric liquid crystal is made to respond by performing the write scan and the erase scan in synchronization with the temporal switching of the backlight R, G, B. When scanning in synchronism, if a ferroelectric liquid crystal showing a liquid crystal response 1 is used, the writing scan of the first line (+ (R)) and the writing scan of the L line (+ (R)) are performed. In any case, a bright state is obtained while the R backlight is lit. On the other hand, when the ferroelectric liquid crystal showing the liquid crystal response 2 is used, the write scan (+ (R)) and the erase scan (− (R)) are shifted in time between the first line and the L line. The erasing scan (-(R)) on the Lth line synchronized with the R backlight results in a bright state when the G backlight is turned on (thick frame in FIG. 15). Further, when scanning in synchronization with the G backlight, the L-line erasing scan (-(G)) synchronized with the G backlight results in a bright state when the B backlight is turned on. (Thick frame in FIG. 15).
In FIG. 15, bright (R) indicates that a bright state is obtained by scanning synchronized with an R (red) backlight, and dark indicates R (red), G (green), and B (blue). ) Indicates a dark state by scanning synchronized with each backlight. Similarly, bright (G) and bright (B) are also shown to be in a bright state by scanning synchronized with G (green) and B (blue) backlights, respectively.

  In a normal liquid crystal display device, it is determined which of the positive polarity voltage and the negative polarity voltage is used for writing scanning or erasing scanning and cannot be easily changed. In order to avoid this, it is necessary to match the polarity of the voltage to which the ferroelectric liquid crystal exhibiting monostability responds to the polarity of the applied voltage. Since the response of the ferroelectric liquid crystal is determined by the direction of spontaneous polarization of the ferroelectric liquid crystal, the polarity of the voltage to which the ferroelectric liquid crystal responds can be controlled if the direction of spontaneous polarization can be controlled. .

  Ferroelectric liquid crystals are difficult to align because they have higher molecular ordering than nematic liquid crystals. In particular, in a ferroelectric liquid crystal that does not pass through the SmA phase, two regions having different layer normal directions (hereinafter referred to as “double domain”) are generated (the upper part of FIG. 13). Such a double domain becomes a serious problem because black-and-white inversion is displayed during driving. For this reason, various alignment processing methods have been studied.

  For example, as a method for improving the double domain, an electric field applied slow cooling method is known in which a liquid crystal cell is heated to a temperature equal to or higher than the cholesteric phase and gradually cooled while a DC voltage is applied (see Non-Patent Document 2). When this electric field application annealing method is used, the direction of spontaneous polarization can be controlled by the direction of the applied electric field. However, in this method, if the temperature rises again above the phase transition point, alignment disturbance occurs, and the manufacturing process becomes complicated, and alignment disturbance occurs in a portion where the electric field between the pixel electrodes does not act. There's a problem.

  Further, as a method for monostabilizing the ferroelectric liquid crystal, a method is proposed in which photo-alignment films are used as upper and lower alignment films, and materials having different compositions are used for these photo-alignment films (Patent Document 1, Patent). Reference 2 and Patent Document 3). In this method, the reason why a good alignment state can be obtained by using materials having different compositions for the upper and lower photo-alignment films is not clear, but the interaction between the upper and lower photo-alignment films and the ferroelectric liquid crystal is different. It is thought to be due to. However, in the liquid crystal display element obtained by this method, the direction of spontaneous polarization of the ferroelectric liquid crystal cannot be known unless it is actually driven.

  Furthermore, as another method for monostabilizing the ferroelectric liquid crystal, a reactive liquid crystal layer is formed on one of the upper and lower alignment films by applying and aligning the reactive liquid crystal, and this reaction is performed. Has been proposed (see Patent Document 4). In this method, the reactive liquid crystal is relatively similar in structure to the ferroelectric liquid crystal, so that the interaction with the ferroelectric liquid crystal becomes stronger, so that the alignment is more effective than when only the alignment film is used. By forming the reactive liquid crystal layer on one of the upper and lower alignment films, the ferroelectric liquid crystal can be aligned without causing alignment defects such as double domains. However, even in the liquid crystal display element obtained by this method, the direction of spontaneous polarization of the ferroelectric liquid crystal cannot be known unless it is actually driven.

JP 2005-208353 A JP 2005-234549 A JP 2005-234550 A JP 2005-258428 A NONAKA, T., LI, J., OGAWA, A., HORNUNG, B., SCHMIDT, W., WINGEN, R., and DUBAL, H., 1999, Liq. Cryst., 26, 1599. PATEL, J., and GOODBY, J. W., 1986, J. Appl. Phys., 59, 2355.

  The present invention has been made in view of the above problems, and in a liquid crystal display element using a ferroelectric liquid crystal exhibiting monostability, a liquid crystal capable of controlling the direction of spontaneous polarization of the ferroelectric liquid crystal. The main object is to provide a display element.

  To achieve the above object, the present invention provides a first substrate, a first electrode layer formed on the first substrate, and a photoisomerization reaction formed on the first electrode layer. A first alignment treatment substrate having a first alignment film, which is a photo-alignment film containing a photoisomerizable material that imparts anisotropy to the alignment film, and a second substrate, and the second substrate A second electrode layer formed thereon and a photo-alignment film or rubbing formed on the second electrode layer and containing a photo-dimerization-type material that imparts anisotropy to the alignment film by causing a photo-dimerization reaction A second alignment processing substrate having a second alignment film as a film is disposed so that the first alignment film and the second alignment film face each other, and the first alignment film and the second alignment film A liquid crystal display element having a ferroelectric liquid crystal sandwiched between, wherein the ferroelectric liquid crystal exhibits monostability, and When a voltage is applied so that the second electrode layer is a negative electrode, the ferroelectric liquid crystal has a molecular direction parallel to the first alignment substrate surface and a tilt angle of about 2 of the ferroelectric liquid crystal. Provided is a liquid crystal display element characterized in that it is doubled.

  According to the present invention, the first alignment film, which is a photo-alignment film containing a photoisomerization-type material, and the photo-alignment film containing a photo-dimerization-type material, or the second alignment film, which is a rubbing film, By utilizing the tendency of the spontaneous polarization of the ferroelectric liquid crystal toward the first alignment film side, which is a photo-alignment film containing a control type material, the direction of the spontaneous polarization of the ferroelectric liquid crystal is controlled, It is possible to mono-stabilize the alignment of the dielectric liquid crystal. Accordingly, it is possible to avoid problems as described in the background art section above.

  In the above invention, the first alignment processing substrate is a TFT substrate having a thin film transistor (TFT) formed on the first base material, and the second alignment processing substrate is configured such that the second electrode layer is a common electrode. A common electrode substrate is preferable. This is because such a configuration can prevent light leakage near the gate electrode when the TFT element is switched off.

  Further, the liquid crystal display element of the present invention is preferably driven by an active matrix system using a thin film transistor. This is because by adopting an active matrix system using a TFT element, a target pixel can be reliably turned on and off, so that a high-quality display is possible.

  Furthermore, the liquid crystal display element of the present invention is preferably driven by a field sequential color system. The above ferroelectric liquid crystal is monostable, so it can display gray scales, and it can be driven by the field sequential color method to display a bright and high-definition color video with low power consumption, low cost, wide viewing angle, and wide viewing angle. It is because it is realizable.

  In the present invention, a photo-alignment film containing a photoisomerizable material is used for the first alignment film, and a photo-alignment film or rubbing film containing a photo-dimerization material is used for the second alignment film. Controlling the direction of spontaneous polarization of ferroelectric liquid crystal by utilizing the tendency of spontaneous polarization of ferroelectric liquid crystal toward the first alignment film, which is a photo-alignment film containing an isomerized material. There is an effect that can be.

  In order to investigate the direction of spontaneous polarization of the ferroelectric liquid crystal, the inventors conducted the following experiment.

First, a liquid crystal display element in which a ferroelectric liquid crystal was sandwiched between a photo-alignment film containing a photoisomerizable material and a photo-alignment film containing a photodimerization material was produced.
A glass substrate on which an ITO electrode is formed is spin-coated with a photoisomerizable material (trade name: LIA01, manufactured by Dainippon Ink Co., Ltd.), dried at 100 ° C. for 3 minutes, and then subjected to linearly polarized ultraviolet rays of about 1000 mJ / cm. ^Two irradiations were performed for the alignment treatment. Further, a 2% by mass cyclopentanone solution of a photodimerization type material (Rolic technologies, trade name: ROP103) was spin-coated on a glass substrate on which an ITO electrode was formed, and dried at 130 ° C. for 15 minutes. Then, an alignment treatment was performed by irradiating with linearly polarized ultraviolet rays of about 100 mJ / cm ² .

  Next, a ferroelectric liquid crystal (manufactured by AZ Electronic Materials, trade name: on a substrate on which a photo-alignment film containing a photodimerization-type material is formed (in this experiment, a second alignment treatment substrate). R2301) was applied by an inkjet method in the isotropic phase. Next, an ultraviolet heat curable sealant (manufactured by Kyoritsu Chemical Industry Co., Ltd., trade name: WORLD ROCK 718) was applied to the peripheral edge of the second alignment treatment substrate using a seal dispenser.

Next, the hot plate disposed in the vacuum chamber was heated to 110 ° C., and the second alignment processing substrate coated with the ferroelectric liquid crystal was placed on the hot plate. Next, the substrate on which the photo-alignment film containing the photoisomerizable material is formed (in this experiment, the first alignment treatment substrate) is adsorbed by an adsorption plate heated to 110 ° C., and the second alignment treatment substrate is obtained. And the 1st orientation processing board | substrate was made to oppose so that the orientation processing direction of each orientation film might become parallel. Subsequently, both substrates were brought into close contact with each other in a state where the vacuum chamber was evacuated so that the pressure between the substrates was sufficiently reduced, and then the inside of the vacuum chamber was returned to normal pressure. Next, ultraviolet rays were irradiated at 1 J / cm ² to cure the ultraviolet heat curable sealant, and both substrates were adhered. Next, the liquid crystal cell was gradually cooled to room temperature to align the ferroelectric liquid crystal, thereby producing a liquid crystal display element.

  When a voltage was applied so that the electrode of the second alignment substrate was a negative electrode, the molecular direction of the ferroelectric liquid crystal changed about twice the tilt angle. About 75% of the ferroelectric liquid crystal molecules were changed in molecular direction by about twice the tilt angle.

  In addition, by changing the types and combinations of the photoisomerization material and the photodimerization material, the photoalignment film containing the photoisomerization material and the photoalignment film containing the photodimerization material are changed in the same manner as described above. When a liquid crystal display element in which a ferroelectric liquid crystal was sandwiched between the two was produced, the same result as above was obtained.

Next, a liquid crystal display element in which a ferroelectric liquid crystal was sandwiched between a photo-alignment film containing a photoisomerizable material and a rubbing film was produced.
A glass substrate on which an ITO electrode is formed is spin-coated with a photoisomerizable material (trade name: LIA01, manufactured by Dainippon Ink Co., Ltd.), dried at 100 ° C. for 3 minutes, and then subjected to linearly polarized ultraviolet rays of about 1000 mJ / cm. ^Two irradiations were performed for the alignment treatment. Further, a polyimide (manufactured by Nissan Chemical Co., Ltd., trade name: SE-7962) was printed on the glass substrate on which the ITO electrode was formed, and a rubbing treatment was performed to form a rubbing film.

  Next, the ferroelectric liquid crystal (product name: R2301 manufactured by AZ Electronic Materials Co., Ltd.) is in an isotropic state on the substrate on which the rubbing film is formed (in this experiment, the second alignment processing substrate). And it apply | coated by the inkjet method. Next, an ultraviolet heat curable sealant (manufactured by Kyoritsu Chemical Industry Co., Ltd., trade name: WORLD ROCK 718) was applied to the peripheral edge of the second alignment treatment substrate using a seal dispenser.

Next, the hot plate disposed in the vacuum chamber was heated to 110 ° C., and the second alignment processing substrate coated with the ferroelectric liquid crystal was placed on the hot plate. Next, the substrate on which the photo-alignment film containing the photoisomerizable material is formed (in this experiment, the first alignment treatment substrate) is adsorbed by an adsorption plate heated to 110 ° C., and the second alignment treatment substrate is obtained. And the 1st orientation processing board | substrate was made to oppose so that the orientation processing direction of each orientation film might become parallel. Subsequently, both substrates were brought into close contact with each other in a state where the vacuum chamber was evacuated so that the pressure between the substrates was sufficiently reduced, and then the inside of the vacuum chamber was returned to normal pressure. Next, ultraviolet rays were irradiated at 1 J / cm ² to cure the ultraviolet heat curable sealant, and both substrates were adhered. Next, the liquid crystal cell was gradually cooled to room temperature to align the ferroelectric liquid crystal, thereby producing a liquid crystal display element.

  When a voltage was applied so that the electrode of the second alignment substrate was a negative electrode, the molecular direction of the ferroelectric liquid crystal changed about twice the tilt angle. About 70% of the ferroelectric liquid crystal molecules changed in molecular direction about twice the tilt angle.

  In addition, the ferroelectric liquid crystal is sandwiched between the photo-alignment film containing the photoisomerization material and the rubbing film in the same manner as described above by changing the type and combination of the materials of the photoisomerization type material and the rubbing film. When a liquid crystal display device was manufactured, the same result as above was obtained.

Next, a liquid crystal display element in which a ferroelectric liquid crystal was sandwiched between a photo-alignment film containing a pair of photoisomerizable materials was produced.
Two glass substrates on which ITO electrodes are formed are each spin-coated with a photoisomerizable material (trade name: LIA01, manufactured by Dainippon Ink Co., Ltd.), dried at 100 ° C. for 3 minutes, and then subjected to linearly polarized ultraviolet light. About 1000 mJ / cm ^{2 was} irradiated to perform alignment treatment.

  Next, a ferroelectric liquid crystal (manufactured by AZ Electronic Materials, trade name: R2301) was applied on one substrate in an isotropic phase by an inkjet method. Next, an ultraviolet heat curable sealant (manufactured by Kyoritsu Chemical Industry Co., Ltd., trade name: WORLD ROCK 718) was applied to the peripheral edge of the substrate using a seal dispenser.

Next, the hot plate disposed in the vacuum chamber was heated to 110 ° C., and the substrate coated with the ferroelectric liquid crystal was placed on the hot plate. Next, the other substrate was adsorbed by an adsorption plate heated to 110 ° C., and both substrates were opposed so that the alignment treatment directions of the respective alignment films were parallel. Subsequently, both substrates were brought into close contact with each other in a state where the vacuum chamber was evacuated so that the pressure between the substrates was sufficiently reduced, and then the inside of the vacuum chamber was returned to normal pressure. Next, ultraviolet rays were irradiated at 1 J / cm ² to cure the ultraviolet heat curable sealant, and both substrates were adhered. Next, the liquid crystal cell was gradually cooled to room temperature to align the ferroelectric liquid crystal, thereby producing a liquid crystal display element.

  When a voltage is applied so that the electrode of one substrate is a negative electrode, the molecular direction of some ferroelectric liquid crystals changes about twice the tilt angle, but the molecular direction of some ferroelectric liquid crystals changes. There wasn't. About 50% of the ferroelectric liquid crystal molecules were changed in molecular direction by about twice the tilt angle.

  Similarly to the above, a liquid crystal display element in which a ferroelectric liquid crystal is sandwiched between a photo-alignment film containing a pair of photodimerization type materials, and a ferroelectric liquid crystal is sandwiched between a pair of rubbing films. When a liquid crystal display device was produced, the same result as above was obtained.

  From the results of the above experiments, the present inventors used a photo-alignment film containing a photoisomerizable material in one alignment film and a photo-alignment film containing a photodimerization-type material in the other alignment film, or rubbing. It was found that when the film is used, the spontaneous polarization of the ferroelectric liquid crystal tends to be directed toward the photo-alignment film containing the photoisomerizable material.

Hereinafter, the liquid crystal display element of the present invention will be described in detail.
The liquid crystal display element of the present invention includes a first base material, a first electrode layer formed on the first base material, and an alignment film formed on the first electrode layer and causing a photoisomerization reaction. Formed on the second base material and the second base material, the first base material having a first orientation film that is a photo-alignment film containing a photoisomerizable material that imparts anisotropy to the first base material. The second electrode layer is a photo-alignment film or rubbing film formed on the second electrode layer and containing a photo-dimerization-type material that imparts anisotropy to the alignment film by causing a photo-dimerization reaction. A second alignment treatment substrate having two alignment films is disposed so that the first alignment film and the second alignment film face each other, and a ferroelectric is provided between the first alignment film and the second alignment film. A liquid crystal display element sandwiching a conductive liquid crystal, wherein the ferroelectric liquid crystal exhibits monostability and has the second power supply. When a voltage is applied so that the layer becomes a negative electrode, the molecular direction of the ferroelectric liquid crystal changes approximately twice the tilt angle of the ferroelectric liquid crystal in parallel with the first alignment treatment substrate surface. It is characterized by being.

  As described above, the ferroelectric liquid crystal used in the present invention exhibits monostability, and when a voltage is applied so that the second electrode layer is a negative electrode, the molecular direction of the ferroelectric liquid crystal is It changes approximately twice as much as the tilt angle of the ferroelectric liquid crystal in parallel to the first alignment processing substrate surface.

  As illustrated in FIG. 1, the ferroelectric liquid crystal rotates along a cone ridge line in which the liquid crystal molecules 1 are inclined from the layer normal z and have a bottom surface perpendicular to the layer normal z. In such a cone, the tilt angle of the liquid crystal molecules 1 with respect to the layer normal z is referred to as a tilt angle θ.

  “Showing monostability” means a state in which the state of the ferroelectric liquid crystal when no voltage is applied is stabilized in one state. More specifically, as shown in FIG. 1, the liquid crystal molecule 1 can operate on a cone between two states inclined by a tilt angle ± θ with respect to the layer normal z, but the liquid crystal molecule can be operated when no voltage is applied. 1 is the state stabilized in any one state on the cone.

The liquid crystal display element of the present invention will be described with reference to the drawings.
FIG. 2 is a schematic cross-sectional view showing an example of the liquid crystal display element of the present invention. In the liquid crystal display element 2 illustrated in FIG. 2, the first alignment treatment substrate 6 in which the first electrode layer 4 and the first alignment film 5 are sequentially formed on the first base material 3, and the second base material 13. The second alignment processing substrate 16 on which the second electrode layer 14 and the second alignment film 15 are sequentially formed is opposed to the first alignment film 5 of the first alignment processing substrate 6 and the second alignment processing substrate 16. A ferroelectric liquid crystal is sandwiched between the two alignment films 15 to form a liquid crystal layer 10. The first alignment film 5 is a photo-alignment film containing a photoisomerizable material, and the second alignment film 15 is a photo-alignment film or a rubbing film containing a photodimerization-type material. Further, the first alignment film 5 and the second alignment film 15 are arranged so that their alignment processing directions are parallel to each other.

  From the above experimental results, when a photo-alignment film containing a photoisomerizable material is used for the first alignment film and a photo-alignment film containing a photodimerization-type material or a rubbing film is used for the second alignment film, photoisomerization is achieved. It was found that the spontaneous polarization of the ferroelectric liquid crystal tends to be directed to the first alignment film side that is the photo-alignment film containing the mold material. This is considered to be due to the polar surface interaction, which is the interaction between the ferroelectric liquid crystal and the first alignment film surface and the second alignment film surface.

  An example of the alignment state of the ferroelectric liquid crystal used in the present invention is shown in FIG. From the above experimental results, the first alignment film, which is a photo-alignment film containing a photoisomerizable material, and the second alignment film, which is a photo-alignment film containing a photodimerization-type material, or a rubbing film, Since the alignment film tends to have a relatively positive polarity, the spontaneous polarization Ps of the liquid crystal molecules 1 is caused by the polar surface interaction in the state where no voltage is applied, as illustrated in FIG. It tends to face the 5th side. In FIG. 3, the first base material and the second base material are omitted, and liquid crystal molecules are shown for the ferroelectric liquid crystal.

Further, as illustrated in FIG. 4, when a voltage is applied so that the first electrode layer 4 is a positive electrode (+) and the second electrode layer 14 is a negative electrode (−), the liquid crystal molecules are affected by the polarity of the applied voltage. 1 spontaneous polarization Ps is directed to the second alignment film 15 side. In FIG. 4, the first base material and the second base material are omitted.
Further, when a voltage is applied so that the first electrode layer is a negative electrode (−) and the second electrode layer is a positive electrode (+), the liquid crystal molecules 1 of the liquid crystal molecules 1 are affected by the polarity of the applied voltage as illustrated in FIG. Spontaneous polarization Ps comes to face the second alignment film 14 side. In this case, the direction of spontaneous polarization is the same as that in the state where no voltage is applied.
The direction of spontaneous polarization is such a direction because the direction of spontaneous polarization is the direction in which the polarization of the ferroelectric liquid crystal and the polarization of the alignment film or the polarity of the voltage are electrically balanced. This is because the state becomes stable.

  When no voltage is applied or a voltage application state having a positive polarity to the second electrode layer (FIG. 3) is changed to a voltage application state having a negative polarity to the second electrode layer (FIG. 4), the negative voltage of this applied voltage is set. And the negative polarity of the spontaneous polarization of the liquid crystal molecules cause the liquid crystal molecules 1 to rotate about an angle of 2θ as illustrated in FIG. That is, when a voltage is applied so that the second electrode layer is a negative electrode, the molecular direction of the ferroelectric liquid crystal is approximately parallel to the first alignment processing substrate surface and is approximately equal to the tilt angle θ of the ferroelectric liquid crystal. It changes twice.

  As described above, in the present invention, it is possible to control the direction of the spontaneous polarization of the liquid crystal molecules by utilizing the tendency of the spontaneous polarization of the ferroelectric liquid crystal toward the first alignment film side.

In general, in a liquid crystal display element using ferroelectric liquid crystal, two opposing alignment films are arranged so that their alignment treatment directions are parallel to each other. For example, in the liquid crystal display element shown in FIG. 2, when no voltage is applied, the liquid crystal molecules 1 are aligned along the alignment treatment direction d of the first alignment film and the second alignment film as illustrated in FIG. A uniform orientation state is obtained. When a voltage is applied so that the first electrode layer is a positive electrode (+) and the second electrode layer is a negative electrode (−), the spontaneous polarization Ps is caused by the influence of the polarity of the applied voltage as illustrated in FIG. 6B. The direction of is reversed. Also in this case, the liquid crystal molecules 1 are in a uniform alignment state. Further, when a voltage is applied so that the first electrode layer is a negative electrode (−) and the second electrode layer is a positive electrode (+), the spontaneous polarization Ps is caused by the influence of the polarity of the applied voltage as illustrated in FIG. The direction of is reversed. In this case, the liquid crystal molecules 1 are in the same alignment state as in the voltage-free state.
FIG. 6A is a schematic diagram showing the alignment state of the liquid crystal molecules from the upper surface of FIG. 3, and the spontaneous polarization Ps is directed from the front side to the back side of the drawing (the mark “X” in FIG. 6A). ). FIG. 6B is a schematic diagram showing the alignment state of the liquid crystal molecules from the upper surface of FIG. 4, and the spontaneous polarization Ps is directed from the back of the page to the near side (the mark ● in FIG. 6B). ).

  In the present invention, since the direction of spontaneous polarization can be controlled as described above, the alignment of the ferroelectric liquid crystal can be mono-stabilized without causing alignment defects. That is, the ferroelectric liquid crystal exhibits monostability. In addition, since the ferroelectric liquid crystal is aligned without using the method of slow cooling by applying an electric field, there is an advantage that the alignment can be maintained even when the temperature is raised above the phase transition temperature and the occurrence of alignment defects can be suppressed.

  When a voltage is applied so that the second electrode layer is a negative electrode, the ferroelectric liquid crystal whose molecular direction changes about twice the tilt angle is preferably 70% or more, more preferably 80% or more, Preferably it is 90% or more, Most preferably, it is 95% or more. This is because a favorable contrast ratio can be obtained within the above range.

In addition, said ratio can be measured as follows.
For example, as shown in FIG. 7, the first alignment treatment substrate 6 in which the first electrode layer 4 and the first alignment film 5 are laminated on the first base material 3, and the second electrode layer 14 on the second base material 13. In the liquid crystal display element in which the liquid crystal layer 10 including the ferroelectric liquid crystal is formed between the first alignment processing substrate 16 and the second alignment processing substrate 16 on which the second alignment film 15 is laminated, the first alignment processing substrate 6 and the second alignment processing It is assumed that polarizing plates 17a and 17b are provided on the outside of the substrate 16 so that light is incident from the polarizing plate 17a side and light is emitted from the polarizing plate 17b side. The two polarizing plates 17a and 17b have their polarization axes substantially perpendicular to each other, and the polarization axis of the polarizing plate 17a and the alignment treatment direction (the alignment direction of the liquid crystal molecules) of the first alignment film 4 are substantially parallel. Are arranged as follows.

  When no voltage is applied, the linearly polarized light transmitted through the polarizing plate 17a and the alignment direction of the liquid crystal molecules coincide with each other. Therefore, the refractive index anisotropy of the liquid crystal molecules does not appear, and the linearly polarized light transmitted through the polarizing plate 17a remains as it is. It passes through the molecules, is blocked by the polarizing plate 17b, and enters a dark state. On the other hand, in the voltage application state, the liquid crystal molecules move on the cone, and the linearly polarized light transmitted through the polarizing plate 17a and the alignment direction of the liquid crystal molecules have a predetermined angle. Therefore, the linearly polarized light transmitted through the polarizing plate 17a. Becomes elliptically polarized light due to the birefringence of the liquid crystal molecules. Of the elliptically polarized light, only linearly polarized light that coincides with the polarization axis of the polarizing plate 17b is transmitted through the polarizing plate 17b and becomes bright.

  Therefore, when a voltage is applied so that the second electrode layer is a negative electrode, a bright state is obtained when the molecular direction of the ferroelectric liquid crystal changes approximately twice the tilt angle. On the other hand, when a voltage is applied so that the second electrode layer is a negative electrode, for example, when a portion of the ferroelectric liquid crystal whose molecular direction does not change partially exists, a dark state is partially obtained. Therefore, from the white / black area ratio of black and white (bright / dark) display obtained when the voltage is applied, the molecular direction of the ferroelectric liquid crystal is about 2 of the tilt angle when the voltage is applied so that the first electrode layer is a negative electrode. The ratio of what doubles can be calculated.

Further, in the liquid crystal display element provided with the polarizing plate as described above, when the voltage is not applied and when the negative polarity voltage is applied to the first electrode layer, the dark state is positive and the first electrode layer is positive. The light state is obtained when the polarity voltage is applied. Therefore, when the liquid crystal display element is driven by the field sequential color method, as illustrated in FIG. 8, for example, when the G (green) backlight is turned on, the liquid crystal display element is brightened by scanning synchronized with the R (red) backlight. It is possible to avoid the state.
The symbols and the like in FIG. 8 are the same as the symbols and the like shown in FIG.

  The liquid crystal display element of the present invention can be driven by an active matrix system using a thin film transistor (TFT). In this case, the first alignment processing substrate is a TFT substrate having TFTs formed on the first base material, and the second alignment processing substrate is a common electrode substrate in which the second electrode layer is a common electrode. preferable. FIG. 9 is a schematic perspective view showing an example of an active matrix liquid crystal display element using TFTs.

  The liquid crystal display element 2 illustrated in FIG. 9 includes a TFT substrate (first alignment treatment substrate) 6 in which TFT elements 25 are arranged in a matrix on the first base material 3, and a common electrode (on the second base material 13). And a common electrode substrate (second alignment processing substrate) 16 on which a second electrode layer) 14 is formed. On the TFT substrate (first alignment processing substrate) 6, a gate electrode 24x, a source electrode 24y, and a pixel electrode (first electrode layer) 4 are formed. The gate electrode 24x and the source electrode 24y are arranged vertically and horizontally, respectively, and by applying a signal to the gate electrode 24x and the source electrode 24y, the TFT element 25 can be operated to drive the ferroelectric liquid crystal. A portion where the gate electrode 24x and the source electrode 24y intersect with each other is insulated by an insulating layer (not shown), and the signal of the gate electrode 24x and the signal of the source electrode 24y can operate independently. A portion surrounded by the gate electrode 24x and the source electrode 24y is a pixel which is a minimum unit for driving the liquid crystal display element of the present invention. Each pixel includes at least one TFT element 25 and a pixel electrode (first electrode). Layer) 4 is formed. Then, by sequentially applying a signal voltage to the gate electrode and the source electrode, the TFT element of each pixel can be operated. In FIG. 9, the liquid crystal layer and the first alignment film are omitted.

In the above liquid crystal display element, for example, when the gate electrode is set to a high potential of about 30 V, the TFT element is switched on, a signal voltage is applied to the ferroelectric liquid crystal by the source electrode, and the gate electrode is set to a low level of about −10 V. When the potential is set, the TFT element is turned off. In the switch-off state, as illustrated in FIG. 10, a voltage is applied between the common electrode (second electrode layer) 14 and the gate electrode 24x so that the common electrode (second electrode layer) 14 side is positive. . Since the ferroelectric liquid crystal does not operate in this switch-off state, the pixel is in a dark state.
In the present invention, as described above, when no voltage is applied, the spontaneous polarization of liquid crystal molecules tends to be directed toward the first alignment substrate due to the polar surface interaction. That is, in the switch-off state, as illustrated in FIG. 10, the spontaneous polarization Ps of the liquid crystal molecules 1 faces the TFT substrate (first alignment processing substrate) 6 side. Therefore, the direction of spontaneous polarization is not affected by the voltage applied between the common electrode (second electrode layer) 14 and the gate electrode 24x.
On the other hand, for example, when the spontaneous polarization is directed to the common electrode substrate (second alignment processing substrate) side in the state where no voltage is applied, due to the influence of the voltage applied between the common electrode and the gate electrode in the switch-off state, The direction of spontaneous polarization is reversed near the region where the gate electrode is provided. Then, in the vicinity of the region where the gate electrode is provided, the ferroelectric liquid crystal operates and light leakage occurs even though the switch is off.
On the other hand, as described above, in the present invention, the direction of spontaneous polarization is not affected by the voltage applied between the common electrode and the gate electrode, so that no light leakage occurs. Therefore, in the present invention, light leakage near the gate electrode can be prevented by controlling the direction of spontaneous polarization and using the second alignment substrate as a common electrode substrate.

  Hereinafter, each structure in the liquid crystal display element of this invention is demonstrated.

1. Ferroelectric liquid crystal The ferroelectric liquid crystal used in the present invention exhibits monostability, and when a voltage is applied so that the second electrode layer is a negative electrode, the molecular direction of the ferroelectric liquid crystal is the first. It changes approximately twice the tilt angle of the ferroelectric liquid crystal in parallel with the alignment substrate surface.

  “When the voltage is applied so that the second electrode layer is a negative electrode, the molecular direction of the ferroelectric liquid crystal changes about twice the tilt angle θ of the ferroelectric liquid crystal with respect to the first alignment substrate surface. “To” means that the liquid crystal molecules are stabilized in one state on the cone when no voltage is applied, and the liquid crystal molecules are changed from the mono-stabilized state to the cone when the voltage is applied so that the second electrode layer becomes the negative electrode. When a voltage is applied so that the second electrode layer is positive, the liquid crystal molecules maintain a mono-stabilized state or the second electrode layer is negative from the mono-stabilized state. The inclination angle from the mono-stabilized state of the liquid crystal molecules when the voltage is applied so that the second electrode layer is negative and the second electrode layer is inclined to the opposite side of the voltage applied to the second electrode layer. Tilt angle from mono-stabilized state of liquid crystal molecules when voltage is applied so that becomes positive Means that even large Ri.

  FIG. 11 is a schematic diagram illustrating an example of the alignment state of a ferroelectric liquid crystal exhibiting monostability. 11A shows a case where no voltage is applied, FIG. 11B shows a case where a voltage is applied so that the second electrode layer becomes a negative electrode, and FIG. 11C shows a case where the second electrode layer becomes a positive electrode. A case where a voltage is applied is shown. When no voltage is applied, the liquid crystal molecules 1 are stabilized in one state on the cone (FIG. 11A). When a voltage is applied so that the second electrode layer is a negative electrode, the liquid crystal molecules 1 are tilted from the stabilized state (broken line) to one side (FIG. 11B). In addition, when a voltage is applied so that the second electrode layer becomes a positive electrode, the liquid crystal molecules 1 are applied when a voltage is applied so that the second electrode layer becomes a negative electrode from a stabilized state (broken line). It tilts to the opposite side (FIG. 11 (c)). At this time, the inclination angle δ when the voltage is applied so that the second electrode layer becomes the negative electrode is larger than the inclination angle ω when the voltage is applied so that the second electrode layer becomes the positive electrode. In addition, in FIG. 11, d shows an orientation process direction and z shows a layer normal line.

  When a voltage is applied so that the second electrode layer is a negative electrode, the liquid crystal molecules are tilted from the mono-stabilized state to one side on the cone at an angle corresponding to the magnitude of the applied voltage. Further, in the ferroelectric liquid crystal, as illustrated in FIG. 11A, the position A (the direction of the liquid crystal molecules 1), the position B (the alignment treatment direction d), and the position C do not necessarily match. Absent. Therefore, as illustrated in FIG. 11B, the maximum tilt angle δ when a voltage is applied so that the second electrode layer is a negative electrode is approximately twice the tilt angle θ (angle 2θ).

  For example, as shown in FIG. 5, the direction of the liquid crystal molecules 1 changes approximately twice the tilt angle θ (angle 2θ) in parallel to the first alignment processing substrate surface. About 2 times change means the case of 2θ-2θ-5 ° change.

  The angle at which the molecular direction of the ferroelectric liquid crystal changes in parallel to the first alignment processing substrate surface can be measured as follows. First, a polarizing microscope and a liquid crystal display element in which polarizing plates are arranged in crossed Nicols are arranged so that the polarization axis of one polarizing plate and the alignment direction of liquid crystal molecules in the liquid crystal layer are parallel, and this position is used as a reference. . When a voltage is applied, the liquid crystal molecules come to have a predetermined angle with the polarization axis, so that the polarized light transmitted through one polarizing plate is transmitted through the other polarizing plate to be in a bright state. With this voltage applied, the liquid crystal display element is rotated to a dark state. And the angle which rotated the liquid crystal display element at this time is measured. The angle by which the liquid crystal display element is rotated is an angle at which the molecular direction of the ferroelectric liquid crystal changes in parallel to the first alignment processing substrate surface.

  As described above, when a voltage is applied so that the second electrode layer is a negative electrode, the liquid crystal molecules are inclined from the mono-stabilized state to one side on the cone at an angle corresponding to the magnitude of the applied voltage. When the liquid crystal display element is actually driven, the direction of the liquid crystal molecules does not change approximately twice the tilt angle when a voltage is applied so that the second electrode layer is a negative electrode.

Specifically, as such a ferroelectric liquid crystal, for example, half-V shaped switching (hereinafter referred to as HV-shaped switching) in which liquid crystal molecules operate only when a positive or negative voltage as shown in FIG. 12 is applied. A ferroelectric liquid crystal exhibiting characteristics is used. When the ferroelectric liquid crystal exhibiting such HV-shaped switching characteristics is used, the opening time as a black and white shutter can be made sufficiently long, whereby each color that can be temporally switched can be displayed brighter. A bright color liquid crystal display element can be realized.
The “HV-shaped switching characteristic” refers to an electro-optical characteristic in which the light transmittance with respect to an applied voltage is asymmetric.

The phase series of the ferroelectric liquid crystal is not particularly limited as long as it exhibits a chiral smectic C phase (SmC ^* ). For example, the phase sequence changes in phase with the nematic phase (N) -cholesteric phase (Ch) -chiral smectic C phase (SmC ^* ) in the temperature lowering process, the nematic phase (N) -chiral smectic C phase (SmC ^* ) , Nematic phase (N) -smectic A phase (SmA) -chiral smectic C phase (SmC ^* ), phase change, nematic phase (N) -cholesteric phase (Ch) -smectic A phase (SmA ) -Chiral smectic C phase (SmC ^* ) and the like.

  In general, a ferroelectric liquid crystal having a phase sequence passing through an SmA phase as illustrated in the lower part of FIG. 13 has a small distance between smectic layers in the process of phase change, and a smectic layer is used to compensate for the volume change. A domain having a bent chevron structure and different major axis directions of the liquid crystal molecules is formed depending on the bending direction, and alignment defects called zigzag defects and hairpin defects are likely to occur at the interface. In general, a ferroelectric liquid crystal having a phase sequence that does not pass through the SmA phase as illustrated in the upper part of FIG. 13 is likely to generate two regions (double domains) having different layer normal directions. In the present invention, the alignment of the ferroelectric liquid crystal can be mono-stabilized without causing such alignment defects.

  Such a ferroelectric liquid crystal can be variously selected from generally known liquid crystal materials according to required characteristics.

In particular, a liquid crystal material that exhibits an SmC ^* phase from the Ch phase without passing through the SmA phase is suitable as a material that exhibits HV-shaped switching characteristics. Specifically, “R2301” manufactured by AZ Electronic Materials may be mentioned.

In addition, as the liquid crystal material that passes through the SmA phase, a material that expresses the SmC ^* phase from the Ch phase through the SmA phase is preferable because of a wide range of material selection. In this case, a single liquid crystal material exhibiting an SmC ^* phase can be used, but a non-chiral liquid crystal (hereinafter sometimes referred to as a host liquid crystal) having a low viscosity and easily exhibiting an SmC phase is used. By adding a small amount of an optically active substance that does not show large spontaneous polarization and an appropriate helical pitch, the liquid crystal material showing the phase sequence as described above has low viscosity and can realize faster response. preferable.

The host liquid crystal is preferably a material exhibiting an SmC phase in a wide temperature range, and can be used without particular limitation as long as it is generally known as a host liquid crystal of a ferroelectric liquid crystal. For example, the general formula:
^{Ra-Q 1 -X 1 - (} Q 2 -Y 1) m -Q 3 -Rb
(In the formula, Ra and Rb are each a linear or branched alkyl group, alkoxy group, alkoxycarbonyl group, alkanoyloxy group or alkoxycarbonyloxy group, and Q ¹ , Q ² and Q ³ are each 1 , 4-phenylene group, 1,4-cyclohexylene group, pyridine-2,5-diyl group, pyrazine-2,5-diyl group, pyridazine-3,6-diyl group, 1,3-dioxane-2,5 -Diyl group, and these groups may have a substituent such as a halogen atom, a hydroxyl group, and a cyano group, and X ¹ and Y ¹ are each —COO—, —OCO—, —CH ₂ O— , —OCH ₂ —, —CH ₂ CH ₂ —, —C≡C—, or a single bond, and m is 0 or 1.). As the host liquid crystal, the above compounds can be used alone or in combination of two or more.

The optically active substance added to the host liquid crystal is not particularly limited as long as it is a material having a large spontaneous polarization and the ability to induce an appropriate helical pitch, and is generally added to a liquid crystal composition exhibiting an SmC phase. Any known material can be used. In particular, a material that can induce large spontaneous polarization with a small addition amount is preferable. Examples of such an optically active substance include the following general formula:
^{Rc-Q 1 -Za-Q 2} -Zb-Q 3 -Zc-Rd
(In the formula, Q ¹ , Q ² and Q ³ represent the same meaning as in the above general formula, and Za, Zb and Zc are —COO—, —OCO—, —CH ₂ O—, —OCH ₂ —, —CH _{2, respectively.} CH ₂ —, —C≡C—, —CH═N—, —N═N—, —N (→ O) ═N—, —C (═O) S— or a single bond, and Rc is asymmetric. A linear or branched alkyl group which may have a carbon atom, an alkoxy group, an alkoxycarbonyl group, an alkanoyloxy group or an alkoxycarbonyloxy group, wherein Rd is a linear or branched group having an asymmetric carbon atom; And an alkyl group, an alkoxy group, an alkoxycarbonyl group, an alkanoyloxy group or an alkoxycarbonyloxy group, and Rc and Rd may be substituted with a halogen atom, a cyano group or a hydroxyl group. Can be used. As the optically active substance, the above compounds may be used alone or in combination of two or more.

  Specific examples of the ferroelectric liquid crystal passing through the SmA phase include “FELIXM4851-100” manufactured by AZ Electronic Materials.

In a liquid crystal display element using a ferroelectric liquid crystal exhibiting monostability, the transmittance depends on the tilt angle of liquid crystal molecules when a voltage is applied. When either positive or negative voltage is applied, the liquid crystal molecules are tilted on the cone. Therefore, for example, as shown in FIG. 12, the tilt angle of the liquid crystal molecules changes according to the magnitude of the applied voltage, and the transmittance changes. At this time, the transmittance is maximized when the tilt angle of the liquid crystal molecules from the monostable state is 45 °.
Therefore, in order to realize high transmittance, when a voltage is applied so that the second electrode layer becomes a negative electrode during actual driving, the inclination angle of the liquid crystal molecules from a monostable state can be 45 °. It is preferable to use a dielectric liquid crystal.
For example, when a ferroelectric liquid crystal having a maximum tilt angle δ from a monostable state of liquid crystal molecules as shown in FIG. 11 is larger than 45 °, when the liquid crystal display element is actually driven, When a voltage is applied so that the second electrode layer becomes a negative electrode, the tilt angle of the liquid crystal molecules from the monostable state can be set to 45 °. As described above, when a voltage is applied so that the second electrode layer becomes a negative electrode during actual driving, the direction of the liquid crystal molecules does not change approximately twice the tilt angle.

In the present invention, the ferroelectric liquid crystal is sandwiched between the first alignment film and the second alignment film to constitute a liquid crystal layer.
In addition to the ferroelectric liquid crystal, the liquid crystal layer may contain a compound having any function depending on the function required for the liquid crystal display element. Examples of such a compound include a polymerized polymerizable monomer. By containing such a polymerizable monomer polymer in the liquid crystal layer, the alignment of the liquid crystal material is so-called “polymer stabilization”, and a liquid crystal display device excellent in alignment stability can be obtained.

  The polymerizable monomer used in the polymerized polymer of the polymerizable monomer is not particularly limited as long as it is a compound that generates a polymer by a polymerization reaction, and a thermosetting resin monomer that generates a polymerization reaction by heat treatment, and actinic radiation. An actinic radiation curable resin monomer that undergoes a polymerization reaction upon irradiation of can be exemplified. Among these, it is preferable to use an actinic radiation curable resin monomer. When a thermosetting resin monomer is used, it is necessary to perform a heating process in order to cause a polymerization reaction. Therefore, the regular arrangement of the ferroelectric liquid crystal is impaired by such a heating process, There is a risk of inducing a phase transition. On the other hand, when the actinic radiation curable resin monomer is used, there is no such fear, and the alignment of the ferroelectric liquid crystal is hardly harmed by the polymerization reaction.

  Examples of the actinic radiation curable resin monomer include an electron beam curable resin monomer that undergoes a polymerization reaction upon irradiation with an electron beam, and a photocurable resin monomer that undergoes a polymerization reaction upon irradiation with light. Among these, it is preferable to use a photocurable resin monomer. It is because a manufacturing process can be simplified by using a photocurable resin monomer.

  The photocurable resin monomer is not particularly limited as long as it causes a polymerization reaction when irradiated with light having a wavelength in the range of 150 nm to 500 nm. Among them, it is preferable to use an ultraviolet curable resin monomer that generates a polymerization reaction when irradiated with light having a wavelength in the range of 250 nm to 450 nm, particularly in the range of 300 nm to 400 nm. This is because it has advantages in terms of the ease of the irradiation apparatus.

  The polymerizable functional group possessed by the ultraviolet curable resin monomer is not particularly limited as long as it causes a polymerization reaction upon irradiation with ultraviolet rays in the above wavelength region. In particular, it is preferable to use an ultraviolet curable resin monomer having an acrylate group.

  Further, the UV curable resin monomer may be a monofunctional monomer having one polymerizable functional group in one molecule, or a polyfunctional having two or more polymerizable functional groups in one molecule. It may be a monomer. Among these, it is preferable to use a polyfunctional monomer. By using a polyfunctional monomer, a stronger polymer network can be formed, so that the intermolecular force and the polymer network at the alignment film interface can be strengthened. Thereby, the disorder of the alignment of the ferroelectric liquid crystal due to the temperature change can be suppressed.

  Among the polyfunctional monomers, bifunctional monomers having a polymerizable functional group at both ends of the molecule are preferably used. By having a polymerizable functional group at both ends of the molecule, it is possible to form a polymer network with a wide interval between polymers, and to prevent a decrease in driving voltage of the ferroelectric liquid crystal due to the inclusion of a polymer of a polymerizable monomer. Because.

  Of the ultraviolet curable resin monomers, it is preferable to use an ultraviolet curable liquid crystal monomer that exhibits liquid crystallinity. The reason why such an ultraviolet curable liquid crystal monomer is preferable is as follows. That is, since the ultraviolet curable liquid crystal monomer exhibits liquid crystallinity, it can be regularly arranged by the alignment regulating force of the alignment film. For this reason, the ultraviolet curable liquid crystal monomer can be fixed while maintaining the regular alignment state by causing a polymerization reaction after the ultraviolet light curable liquid crystal monomer is regularly arranged. By the presence of the polymer having such a regular alignment state, the alignment stability of the ferroelectric liquid crystal can be improved, and excellent heat resistance and impact resistance can be obtained.

  The liquid crystal phase exhibited by the ultraviolet curable liquid crystal monomer is not particularly limited, and examples thereof include an N phase, an SmA phase, and an SmC phase.

  Examples of the ultraviolet curable liquid crystal monomer used in the present invention include compounds represented by the following formulas (1) to (3).

In the above formulas (1) and (2), A, B, D, E and F represent benzene, cyclohexane or pyrimidine, and these may have a substituent such as halogen. A and B, or D and E may be bonded via a bonding group such as an acetylene group, a methylene group, or an ester group. M ¹ and M ² may be any of a hydrogen atom, an alkyl group having 3 to 9 carbon atoms, an alkoxycarbonyl group having 3 to 9 carbon atoms, or a cyano group. Further, the acryloyloxy group at the end of the molecular chain and A or D may be bonded via a bonding group such as an alkylene group having 3 to 6 carbon atoms.

  In the above formula (3), Y is hydrogen, alkyl having 1 to 20 carbons, alkenyl having 1 to 20 carbons, alkyloxy having 1 to 20 carbons, alkyloxycarbonyl having 1 to 20 carbons, It represents formyl, alkylcarbonyl having 1 to 20 carbons, alkylcarbonyloxy having 1 to 20 carbons, halogen, cyano or nitro.

  Among the above, the compounds represented by the following formulas can be exemplified as those suitably used.

  Moreover, the said polymerizable monomer may be used independently and may be used in combination of 2 or more type. When two or more different polymerizable monomers are used, for example, an ultraviolet curable liquid crystal monomer represented by the above formula and another ultraviolet curable resin monomer can be used.

  When an ultraviolet curable liquid crystal monomer is used as the polymerizable monomer, the polymer of the polymerizable monomer is a main chain liquid crystal type polymer in which the main chain exhibits liquid crystallinity by having an atomic group exhibiting liquid crystallinity in the main chain. It may be a side chain liquid crystal polymer in which the side chain exhibits liquid crystallinity by having an atomic group exhibiting liquid crystallinity in the side chain. Especially, it is preferable that the polymer of a polymerizable monomer is a side chain liquid crystal type polymer. This is because the presence of an atomic group exhibiting liquid crystallinity in the side chain increases the degree of freedom of the atomic group, so that the atomic group exhibiting liquid crystallinity is easily aligned. Further, as a result, the alignment stability of the ferroelectric liquid crystal can be improved.

The amount of the polymerized monomer in the liquid crystal layer is not particularly limited as long as the alignment stability of the ferroelectric liquid crystal is within a desired range, but usually 0.5% by mass in the liquid crystal layer. It is preferably within the range of ˜30% by mass, more preferably within the range of 1% by mass to 20% by mass, and even more preferably within the range of 1% by mass to 10% by mass. This is because if it exceeds the above range, the drive voltage may increase or the response speed may decrease. Further, if the amount is less than the above range, the alignment stability of the ferroelectric liquid crystal becomes insufficient, and the heat resistance and impact resistance of the liquid crystal display element may be impaired.
Here, the abundance of the polymerizable monomer polymer in the liquid crystal layer is determined by measuring the weight of the remaining polymerizable monomer polymer with an electronic balance after washing the monomolecular liquid crystal in the liquid crystal layer with a solvent. It can be calculated from the obtained remaining amount and the total mass of the liquid crystal layer.

  In the present invention, since the ferroelectric liquid crystal exhibits monostability, a liquid crystal display element that can be driven by an active matrix method using a thin film transistor (TFT) and can control gradation by voltage modulation is provided. Obtainable.

  The thickness of the liquid crystal layer is preferably in the range of 1.2 μm to 3.0 μm, more preferably 1.3 μm to 2.5 μm, and still more preferably in the range of 1.4 μm to 2.0 μm. This is because if the thickness of the liquid crystal layer is too thin, the contrast may be lowered. Conversely, if the thickness of the liquid crystal layer is too thick, the ferroelectric liquid crystal may be difficult to align. The thickness of the liquid crystal layer can be adjusted by bead spacers, columnar spacers, partition walls, or the like.

As a method for forming the liquid crystal layer, a method generally used as a method for manufacturing a liquid crystal cell can be used. For example, a vacuum injection method, a liquid crystal dropping method, or the like can be used.
In the vacuum injection method, for example, a ferroelectric liquid crystal that is made an isotropic liquid by heating is applied to a liquid crystal cell that has been prepared using a first alignment processing substrate and a second alignment processing substrate in advance by utilizing the capillary effect. The liquid crystal layer can be formed by pouring and sealing with an adhesive.
Further, in the liquid crystal dropping method, for example, a heated ferroelectric liquid crystal is dropped on the second alignment film of the second alignment processing substrate, a sealant is applied to the peripheral portion of the first alignment processing substrate, and the first is applied under reduced pressure. A liquid crystal layer can be formed by superimposing the first alignment treatment substrate and the second alignment treatment substrate and bonding them with a sealant.

2. First Alignment Processed Substrate The first alignment process substrate used in the present invention includes a first base material, a first electrode layer formed on the first base material, and formed on the first electrode layer. And a first alignment film that is a photo-alignment film containing a photoisomerizable material that imparts anisotropy to the alignment film by causing an isomerization reaction. Hereinafter, each structure in a 1st orientation processing board | substrate is demonstrated.

(1) First Alignment Film The first alignment film used in the present invention is formed on the first electrode layer, and provides photoisomerism that imparts anisotropy to the alignment film by causing a photoisomerization reaction. It is a photo-alignment film containing a conversion type material.

  Here, the photoisomerization reaction refers to a phenomenon in which a single compound changes to another isomer by light irradiation. By using a photoisomerizable material for the first alignment film, a stable isomer among a plurality of isomers is increased by light irradiation, whereby anisotropy can be easily imparted to the alignment film. Further, since the photo-alignment process is a non-contact alignment process, it is useful in that there is no generation of static electricity and dust, and the quantitative alignment process can be controlled.

  The photoisomerization type material used in the present invention is not particularly limited as long as it imparts anisotropy to the alignment film by causing a photoisomerization reaction, but it causes a photoisomerization reaction. It is preferable that it contains a photoisomerization reactive compound that imparts anisotropy to the alignment film. By including such a photoisomerization-reactive compound, a stable isomer among a plurality of isomers is increased by light irradiation, whereby anisotropy can be easily imparted to the alignment film. is there.

  The photoisomerization reactive compound is not particularly limited as long as it is a material having the above-mentioned characteristics, but has a dichroism that makes absorption different depending on the polarization direction, and can be irradiated by light irradiation. It is preferable that it causes an isomerization reaction. This is because anisotropy can be easily imparted to the alignment film by causing isomerization of the reaction site oriented in the polarization direction of the photoisomerization reactive compound having such characteristics.

  Further, the photoisomerization reaction in which the photoisomerization reactive compound is generated is preferably a cis-trans isomerization reaction. This is because isomers of either the cis form or the trans form are increased by light irradiation, whereby anisotropy can be imparted to the alignment film.

  Examples of such photoisomerization-reactive compounds include monomolecular compounds and polymerizable monomers that are polymerized by light or heat. These may be selected as appropriate according to the type of ferroelectric liquid crystal used. However, it is possible to stabilize the anisotropy by polymerizing after imparting anisotropy to the alignment film by light irradiation. Since it can be performed, it is preferable to use a polymerizable monomer. Among such polymerizable monomers, an acrylate monomer and a methacrylate monomer are preferable because anisotropy is imparted to the alignment film and the polymer can be easily polymerized while maintaining the anisotropy in a good state.

  The polymerizable monomer may be a monofunctional monomer or a polyfunctional monomer. However, since the anisotropy of the alignment film due to polymerization becomes more stable, it is a bifunctional monomer. Preferably there is.

  Specific examples of such a photoisomerization-reactive compound include compounds having a cis-trans isomerization-reactive skeleton such as an azobenzene skeleton or a stilbene skeleton.

  In this case, the number of cis-trans isomerization reactive skeletons contained in the molecule may be one or two or more, but the alignment control of the ferroelectric liquid crystal becomes easy. Two are preferable.

  The cis-trans isomerization reactive skeleton may have a substituent in order to further enhance the interaction with the liquid crystal molecules. The substituent is not particularly limited as long as it can enhance the interaction with the liquid crystal molecules and does not interfere with the orientation of the cis-trans isomerization reactive skeleton, and examples thereof include a carboxyl group and a sulfonic acid. A sodium group, a hydroxyl group, etc. are mentioned. These structures can be appropriately selected depending on the type of ferroelectric liquid crystal used.

In addition to the cis-trans isomerization reactive skeleton, the photoisomerization reactive compound contains many π electrons such as aromatic hydrocarbon groups so that the interaction with the liquid crystal molecules can be further enhanced. It may have an included group, and the cis-trans isomerization reactive skeleton and the aromatic hydrocarbon group may be bonded via a bonding group. The bonding group is not particularly limited as long as it can enhance the interaction with the liquid crystal molecule. For example, —COO—, —OCO—, —O—, —C≡C—, —CH ₂ —CH _2- , —CH ₂ O—, —OCH ₂ — and the like can be mentioned.

  In addition, when using a polymerizable monomer as a photoisomerization reactive compound, it is preferable to have the said cis-trans isomerization reactive skeleton as a side chain. By having the cis-trans isomerization reactive skeleton as a side chain, the effect of anisotropy imparted to the alignment film becomes larger, and it is particularly suitable for controlling the alignment of ferroelectric liquid crystals. Because it becomes. In this case, the aromatic hydrocarbon group or bonding group contained in the molecule is contained in the side chain together with the cis-trans isomerization reactive skeleton so that the interaction with the liquid crystal molecule is enhanced. It is preferable.

  Further, the side chain of the polymerizable monomer may have an aliphatic hydrocarbon group such as an alkylene group as a spacer so that the cis-trans isomerization reactive skeleton can be easily oriented.

  Among the photoisomerization reactive compounds of the monomolecular compound or polymerizable monomer as described above, the photoisomerization reactive compound used in the present invention is preferably a compound having an azobenzene skeleton in the molecule. This is because the azobenzene skeleton contains a lot of π electrons, and thus has a high interaction with liquid crystal molecules and is particularly suitable for controlling the alignment of ferroelectric liquid crystals.

  Hereinafter, the reason why the azobenzene skeleton can impart anisotropy to the alignment film by causing a photoisomerization reaction will be described. First, when the azobenzene skeleton is irradiated with linearly polarized ultraviolet light, the trans azobenzene skeleton having the molecular long axis oriented in the polarization direction is changed to a cis isomer as shown in the following formula.

  Since the cis isomer of the azobenzene skeleton is chemically unstable compared to the trans isomer, it thermally or absorbs visible light and returns to the trans isomer. Whether to become the right transformer body occurs with the same probability. Therefore, if the ultraviolet light is continuously absorbed, the ratio of the right-side trans isomer increases, and the average orientation direction of the azobenzene skeleton becomes perpendicular to the polarization direction of the ultraviolet light. In the present invention, by utilizing this phenomenon, the alignment direction of the azobenzene skeleton can be aligned, anisotropy can be imparted to the alignment film, and the alignment of liquid crystal molecules on the film can be controlled.

  Among such compounds having an azobenzene skeleton in the molecule, examples of the monomolecular compound include a compound represented by the following formula (4).

In the above formula (4), R ⁴¹ each independently represents a hydroxy group. R ⁴² represents _{^{- (A 41 -B 41 -A 41}} ) m - (D 41) n - represents a linking group represented ^{by, R 43} is _{^{(D 41) n - (A}} 41 -B 41 -A 41) _m represents a linking group represented by-. Here, A ⁴¹ represents a divalent hydrocarbon group, B ⁴¹ represents —O—, —COO—, —OCO—, —CONH—, —NHCO—, —NHCOO— or —OCONH—, and m represents Represents an integer of 0 to 3; D ⁴¹ represents a divalent hydrocarbon group when m is 0, and —O—, —COO—, —OCO—, —CONH—, —NHCO—, —NHCOO— when m is an integer of 1 to 3. Alternatively, -OCONH- is represented, and n represents 0 or 1. R ⁴⁴ each independently represents a halogen atom, a carboxy group, a halogenated methyl group, a halogenated methoxy group, a cyano group, a nitro group, a methoxy group or a methoxycarbonyl group. However, the carboxy group may form a salt with an alkali metal. R ⁴⁵ each independently represents a carboxy group, a sulfo group, a nitro group, an amino group or a hydroxy group. However, the carboxy group or the sulfo group may form a salt with the alkali metal.

  Specific examples of the compound represented by the above formula (4) include compounds represented by the following formulas (5) to (8).

  Examples of the polymerizable monomer having the azobenzene skeleton as a side chain include compounds represented by the following formula (9).

In the above formula (9), each R ⁵¹ is independently (meth) acryloyloxy group, (meth) acrylamide group, vinyloxy group, vinyloxycarbonyl group, vinyliminocarbonyl group, vinyliminocarbonyloxy group, vinyl group, An isopropenyloxy group, an isopropenyloxycarbonyl group, an isopropenyliminocarbonyl group, an isopropenyliminocarbonyloxy group, an isopropenyl group, or an epoxy group is represented. R ⁵² is _{^{- (A 51 -B 51 -A 51}} ) m - (D 51) n - represents a linking group represented ^{by, R 53} is _{^{(D 51) n - (A}} 51 -B 51 -A 51) _m represents a linking group represented by-. Here, A ⁵¹ represents a divalent hydrocarbon group, B ⁵¹ represents —O—, —COO—, —OCO—, —CONH—, —NHCO—, —NHCOO— or —OCONH—, and m represents Represents an integer of 0 to 3; D ⁵¹ represents a divalent hydrocarbon group when m is 0, and when m is an integer of 1 to 3, —O—, —COO—, —OCO—, —CONH—, —NHCO—, —NHCOO— Alternatively, -OCONH- is represented, and n represents 0 or 1. R ⁵⁴ each independently represents a halogen atom, a carboxy group, a halogenated methyl group, a halogenated methoxy group, a cyano group, a nitro group, a methoxy group or a methoxycarbonyl group. However, the carboxy group may form a salt with an alkali metal. R ⁵⁵ each independently represents a carboxy group, a sulfo group, a nitro group, an amino group or a hydroxy group. However, the carboxy group or the sulfo group may form a salt with the alkali metal.

  Specific examples of the compound represented by the above formula (9) include compounds represented by the following formulas (10) to (13).

  In the present invention, various cis-trans isomerization reactive skeletons and substituents can be selected from such photoisomerization reactive compounds according to required characteristics. In addition, these photoisomerization reactive compounds can also be used individually by 1 type or in combination of 2 or more types.

  In addition to the photoisomerization reactive compound, the photoisomerization type material may contain an additive within a range that does not interfere with the photoalignment of the alignment film. When a polymerizable monomer is used as the photoisomerization reactive compound, examples of the additive include a polymerization initiator and a polymerization inhibitor.

  The polymerization initiator or polymerization inhibitor may be appropriately selected from generally known compounds according to the type of photoisomerization reactive compound. The addition amount of the polymerization initiator or polymerization inhibitor is preferably in the range of 0.001% by mass to 20% by mass, and in the range of 0.1% by mass to 5% by mass with respect to the photoisomerization reactive compound. More preferably, it is within. This is because if the addition amount of the polymerization initiator or polymerization inhibitor is too small, the polymerization may not be started (prohibited), whereas if too large, the reaction may be inhibited.

  The wavelength region of the light that causes the photoisomerization reaction of the photoisomerizable material is preferably in the ultraviolet light range, that is, in the range of 10 nm to 400 nm, and more preferably in the range of 250 nm to 380 nm. .

  Next, the photo-alignment processing method will be described. First, on the first electrode layer, a first alignment film forming coating solution obtained by diluting the above photoisomerizable material with an organic solvent is applied and dried.

  The content of the photoisomerization reactive compound in the first alignment film forming coating solution is preferably in the range of 0.05% by mass to 10% by mass, and is 0.2% by mass to 2% by mass. More preferably within the range. If the content is less than the above range, it will be difficult to impart appropriate anisotropy to the alignment film. Conversely, if the content is more than the above range, the viscosity of the coating liquid will increase, so a uniform coating film will be formed. It is because it becomes difficult to form.

  As a coating method of the first alignment film forming coating solution, for example, spin coating method, roll coating method, rod bar coating method, spray coating method, air knife coating method, slot die coating method, wire bar coating method, ink jet method, A flexographic printing method, a screen printing method, or the like can be used.

  The thickness of the film obtained by applying the first alignment film forming coating solution is preferably in the range of 1 nm to 1000 nm, more preferably in the range of 3 nm to 100 nm. This is because if the film thickness is thinner than the above range, sufficient optical alignment may not be obtained, and conversely if the film thickness is thicker than the above range, it may be disadvantageous in terms of cost.

  The obtained film can impart anisotropy by causing a photoisomerization reaction by irradiating light with controlled polarization. The wavelength region of the light to be irradiated may be appropriately selected according to the constituent material of the alignment film to be used, but is preferably in the ultraviolet light range, that is, in the range of 100 nm to 400 nm, more preferably 250 nm to It is in the range of 380 nm. The polarization direction is not particularly limited as long as it can cause a photoisomerization reaction.

  Further, when a polymerizable monomer is used as the photoisomerization type material among the above photoisomerization reactive compounds, it is polymerized by heating after photoalignment treatment and applied to the alignment film. Anisotropy can be stabilized.

(2) First electrode layer The first electrode layer used in the present invention is not particularly limited as long as it is generally used as an electrode of a liquid crystal display element. At least one of the electrode layer and the second electrode layer of the second alignment treatment substrate is preferably formed of a transparent conductor. Preferred examples of the transparent conductor material include indium oxide, tin oxide, indium tin oxide (ITO), and the like.

  When the liquid crystal display element obtained by the present invention is driven by an active matrix system using TFTs, one of the first alignment processing substrate and the second alignment processing substrate is formed on the entire surface formed of the transparent conductor. An electrode is provided, and on the other side, a gate electrode and a source electrode are arranged in a matrix, and a TFT element and a pixel electrode are provided in a portion surrounded by the gate electrode and the source electrode.

  Examples of the method for forming the first electrode layer include chemical vapor deposition (CVD), physical vapor deposition (PVD) such as sputtering, ion plating, and vacuum deposition.

(3) 1st base material The 1st base material used for this invention will not be specifically limited if generally used as a base material of a liquid crystal display element, For example, a glass plate, a plastic plate, etc. are preferable. Can be mentioned.

(4) Other Configurations In the first alignment treatment substrate in the present invention, a partition wall may be formed on the first base material. In the case where the partition walls are formed on the second base material in the second alignment processing substrate, the partition walls are not formed on the first base material in the first alignment processing substrate. That is, the partition wall may be formed on the first alignment treatment substrate, and the partition wall may be formed on the second alignment treatment substrate.

  As a material for the partition wall, a material generally used for a partition wall of a liquid crystal display element can be used. Specifically, examples of the material for the partition include a resin, and among them, a photosensitive resin is preferably used. This is because the photosensitive resin is easy to pattern.

  The method for forming the partition wall is not particularly limited as long as the partition wall can be formed at a predetermined position, and a general patterning method can be applied. For example, a photolithography method, an inkjet method Method, screen printing method and the like.

  A plurality of partition walls are formed, and it is preferable that the plurality of partition walls are regularly formed at predetermined positions, and it is particularly preferable that the partition walls are formed at substantially equal intervals. This is because, when a liquid crystal display element is manufactured by a liquid crystal dropping method, if the formation positions of the plurality of partition walls are disordered, it may be difficult to accurately control the application amount of the ferroelectric liquid crystal.

  Further, the arrangement of the partition walls is not particularly limited, but the partition walls are preferably formed in the non-pixel region. This is because the alignment defect of the ferroelectric liquid crystal tends to occur in the vicinity of the partition wall, and it is preferable that the partition wall is formed in a non-pixel region that does not affect image display. For example, when the first alignment processing substrate is a TFT substrate, partition walls can be arranged on the gate electrode and the source electrode formed in a matrix.

  The plurality of partition walls are formed in a pattern shape. For example, the partition walls may be formed in a stripe shape, may be formed in a matrix shape, or may be formed in a frame shape. When the partition walls are formed in a matrix shape, impact resistance can be improved. Further, in the case where the partition wall is formed in a frame shape and a liquid crystal display element is manufactured by a liquid crystal dropping method, a frame-shaped partition wall is formed on the peripheral portion of the first base material, By applying a sealant to the outer periphery of the partition wall, the ferroelectric liquid crystal is prevented from coming into contact with the uncured sealant, and the characteristics of the ferroelectric liquid crystal are deteriorated by mixing impurities in the sealant. Can be avoided.

  Further, in the case where the partition walls are formed in a stripe shape and a liquid crystal display element is manufactured by a liquid crystal dropping method, the longitudinal direction of the stripe partition walls is substantially the same as the alignment treatment direction of the first alignment film. It is preferable that the partition walls are formed to be vertical. By applying the ferroelectric liquid crystal along the stripe-shaped partition wall, the ferroelectric liquid crystal can be induced to flow substantially parallel to the alignment treatment direction of the first alignment film. This is because the orientation of the film can be improved and the occurrence of alignment defects can be suppressed.

  Note that “substantially perpendicular” means that the angle formed by the longitudinal direction of the stripe-shaped partition walls and the alignment treatment direction of the first alignment film is in the range of 90 ° ± 5 °, and this angle is 90 ° ± A range of 1 ° is preferred. The angle can be measured by observing the alignment direction of the liquid crystal molecules (the alignment treatment direction of the first alignment film) and the longitudinal direction of the striped partition using a polarizing microscope.

  The pitch of the partition walls is about 100 μm to 10 mm, preferably in the range of 200 μm to 1.5 mm, more preferably in the range of 1.0 mm to 5.0 mm. This is because if the partition pitch is narrower than the above range, the display quality may be deteriorated due to poor alignment of the ferroelectric liquid crystal near the partition. On the contrary, if the partition pitch is wider than the above range, it may vary depending on the size of the liquid crystal display element, but the desired impact resistance may not be obtained, or it may be difficult to keep the cell gap constant. Because. In addition, the pitch of a partition means the distance from the center part of an adjacent partition to a center part.

  Moreover, the width | variety of a partition shall be about 1 micrometer-20 micrometers, Preferably it exists in the range of 2 micrometers-10 micrometers, More preferably, it exists in the range of 5 micrometers-10 micrometers. When a frame-like partition is formed on the peripheral edge of the first substrate, the width of the frame-like partition can prevent the contact between the ferroelectric liquid crystal and the uncured sealant. The width may be any, specifically about 10 μm to 3 mm, preferably in the range of 10 μm to 1 mm, more preferably in the range of 10 μm to 500 μm. If the partition wall width is wider than the above range, the partition wall is also provided in the pixel region, the effective pixel area may become narrow, and a good image display may not be obtained, and the partition wall width is more than the above range. This is because if it is narrow, it may be difficult to form a partition wall.

  In addition, the height of the partition walls is usually about the same as the cell gap.

  Note that the pitch, width, and height of the partition walls can be measured by observing a cross section of the partition walls using a scanning electron microscope (SEM).

  The number of partition walls is not particularly limited as long as it is plural, and is appropriately selected depending on the size of the liquid crystal display element.

  If the partition wall is formed on the first substrate, the formation position is not particularly limited. For example, the partition wall may be formed on the first substrate, and the partition wall may be formed on the first electrode layer. Should just be formed.

  Moreover, in the 1st orientation processing board | substrate in this invention, the columnar spacer may be formed on the 1st base material. When the columnar spacer is formed on the second base material in the second alignment processing substrate, the columnar spacer is not formed on the first base material in the first alignment processing substrate. That is, columnar spacers may be formed on the first alignment processing substrate, and columnar spacers may be formed on the second alignment processing substrate.

  As a material for the columnar spacer, a material generally used for a columnar spacer of a liquid crystal display element can be used. Specifically, examples of the material for the columnar spacer include a resin, and among them, a photosensitive resin is preferably used. This is because the photosensitive resin is easy to pattern.

  The method for forming the columnar spacer is not particularly limited as long as the columnar spacer can be formed at a predetermined position, and a general patterning method can be applied, for example, a photolithography method. Ink jet method, screen printing method and the like.

  A plurality of columnar spacers are formed, and the plurality of columnar spacers are preferably formed regularly at predetermined positions, particularly preferably at equal intervals. This is because, when a liquid crystal display element is manufactured by a liquid crystal dropping method, if the formation positions of the plurality of columnar spacers are disordered, it may be difficult to accurately control the application amount of the ferroelectric liquid crystal. .

  The pitch of the columnar spacers can be about 100 μm to 3 mm, preferably in the range of 200 μm to 1.5 mm, more preferably in the range of 300 μm to 1.0 mm. This is because if the pitch of the columnar spacers is narrower than the above range, the display quality may deteriorate due to poor alignment of the ferroelectric liquid crystal near the columnar spacers. On the other hand, if the pitch of the columnar spacers is wider than the above range, it may vary depending on the size of the liquid crystal display element, but the desired impact resistance may not be obtained or it may be difficult to keep the cell gap constant. Because there is. Note that the pitch of the columnar spacers refers to the distance from the center to the center of adjacent columnar spacers.

  As the size of the columnar spacer, for example, when the columnar spacer has a cylindrical shape, the diameter of the bottom surface is about 1 μm to 100 μm, preferably within the range of 2 μm to 50 μm, more preferably within the range of 5 μm to 20 μm. is there. If the size of the columnar spacer is larger than the above range, the columnar spacer is also provided in the pixel region, and the effective pixel area may be narrowed and a good image display may not be obtained. If the thickness is smaller than the above range, it may be difficult to form columnar spacers.

  Furthermore, the height of the columnar spacer is normally set to the same level as the cell gap.

  In addition, the pitch, size, and height of the columnar spacer can be measured by observing a cross section of the partition wall using a scanning electron microscope (SEM).

  Examples of the shape of the columnar spacer include a columnar shape, a prismatic shape, and a truncated cone shape.

  The arrangement of the columnar spacers is not particularly limited, but it is preferable that the columnar spacers are formed in the non-pixel region. This is because the alignment defect of the ferroelectric liquid crystal tends to occur near the columnar spacers, and therefore it is preferable that the columnar spacers are formed in non-pixel regions that do not affect image display. For example, when the first alignment processing substrate is a TFT substrate, columnar spacers can be arranged on the gate electrode and the source electrode formed in a matrix.

  The number of columnar spacers is not particularly limited as long as it is plural, and is appropriately selected depending on the size of the liquid crystal display element.

  The columnar spacer is not particularly limited as long as it is formed on the first substrate. For example, the columnar spacer may be formed on the first substrate, and the columnar spacer may be formed on the first electrode layer. Columnar spacers may be formed on the substrate.

In the 1st orientation processing board | substrate in this invention, the colored layer may be formed on the 1st base material. When the colored layer is formed on the second base material in the second alignment processing substrate, the coloring layer is not formed on the first base material in the first alignment processing substrate. That is, a colored layer may be formed on the first alignment processing substrate, and a coloring layer may be formed on the second alignment processing substrate.
When the colored layer is formed, a color filter type liquid crystal display element capable of realizing color display by the colored layer can be obtained.

  As a method for forming the colored layer, a method for forming a colored layer in a general color filter can be used. For example, a pigment dispersion method (color resist method, etching method), a printing method, an inkjet method, or the like can be used. it can.

3. Second alignment processing substrate The second alignment processing substrate used in the present invention is formed on the second base material, the second electrode layer formed on the second base material, and on the second electrode layer. And a second alignment film containing a photodimerization-type material that imparts anisotropy to the alignment film by causing a quantification reaction.
The second base material, the second electrode layer, and other configurations are the same as the first base material, the first electrode layer, and other configurations in the first alignment processing substrate, respectively. Description is omitted. Hereinafter, the second alignment film in the second alignment processing substrate will be described.

(1) Second Alignment Film The second alignment film used in the present invention includes a photo-alignment material containing a photodimerization-type material in which the second alignment film imparts anisotropy to the alignment film by causing a photodimerization reaction. There are two modes, a first mode that is a film and a second mode in which the second alignment film is a rubbing film. Hereinafter, the description will be made separately for each aspect.

(I) 1st aspect The 2nd alignment film in this aspect is formed on a 2nd electrode layer, and contains the photodimerization-type material which provides anisotropy to an alignment film by producing a photodimerization reaction. It is a photo-alignment film.

  Here, the photodimerization reaction refers to a reaction in which reaction sites aligned in the polarization direction by light irradiation undergo radical polymerization and two molecules are polymerized. This reaction stabilizes the alignment in the polarization direction and is anisotropic to the alignment film. It is possible to impart sex. The photodimerization type material has the advantages of high exposure sensitivity and a wide range of material selection. Further, since the photo-alignment process is a non-contact alignment process, it is useful in that there is no generation of static electricity and dust, and the quantitative alignment process can be controlled.

  The photodimerization type material used in the present invention is not particularly limited as long as it can impart anisotropy to the alignment film by a photodimerization reaction, but has a radical polymerizable functional group. And it is preferable to contain the photodimerization reactive compound which has the dichroism which makes absorption differ with polarization directions. This is because by radical polymerization of the reaction site oriented in the polarization direction, the orientation of the photodimerization reactive compound is stabilized and anisotropy can be easily imparted to the orientation film.

  Examples of the photodimerization reactive compound having such characteristics include a dimerization reactive polymer having at least one reactive site selected from cinnamate ester, coumarin, quinoline, chalcone group and cinnamoyl group as a side chain. Can do.

  Among these, the photodimerization reactive compound is preferably a dimerization reactive polymer containing cinnamate, coumarin or quinoline as a side chain. This is because anisotropy can be easily imparted to the alignment film by radical polymerization of α and β unsaturated ketone double bonds aligned in the polarization direction as reaction sites.

  The main chain of the dimerization reactive polymer is not particularly limited as long as it is generally known as a polymer main chain, but the reaction sites of the side chains such as aromatic hydrocarbon groups are not limited. It is preferable that it does not have a substituent containing a lot of π electrons that hinders the interaction.

  The weight average molecular weight of the dimerization reactive polymer is not particularly limited, but is preferably in the range of 5,000 to 40,000, and is preferably in the range of 10,000 to 20,000. Is more preferable. The weight average molecular weight can be measured by a gel permeation chromatography (GPC) method. If the weight-average molecular weight of the dimerization reactive polymer is too small, it may not be possible to impart appropriate anisotropy to the alignment film. On the other hand, if it is too large, the viscosity of the coating solution at the time of forming the alignment film increases, and it may be difficult to form a uniform coating film.

  An example of the dimerization reactive polymer is a compound represented by the following formula (14).

In the above formula (14), M ¹¹ and M ¹² each independently represent a monomer unit of a homopolymer or a copolymer. Examples thereof include ethylene, acrylate, methacrylate, 2-chloroacrylate, acrylamide, methacrylamide, 2-chloroacrylamide, styrene derivatives, maleic acid derivatives, and siloxane. M ¹² may be acrylonitrile, methacrylonitrile, methacrylate, methyl methacrylate, hydroxyalkyl acrylate or hydroxyalkyl methacrylate. x and y represent the molar ratio of each monomer unit in the case of a copolymer, and are numbers satisfying 0 <x ≦ 1, 0 ≦ y <1 and satisfying x + y = 1, respectively. It is. n represents an integer of 4 to 30,000. D ¹ and D ² represent spacer units.

R ¹ is a group represented by -A ^1- (Z ¹ -B ¹ ) _z -Z ^2- , and R ² is represented by -A ^1- (Z ¹ -B ¹ ) _z -Z ^3-. It is a group. Here, A ¹ and B ¹ are each independently a covalent single bond, pyridine-2,5-diyl, pyrimidine-2,5-diyl, 1,4-cyclohexylene, 1,3-dioxane-2, It represents 5-diyl or 1,4-phenylene which may have a substituent. Z ¹ and Z ² are each independently a covalent single bond, —CH ₂ —CH ₂ —, —CH ₂ O—, —OCH ₂ —, —CONR—, —RNCO—, —COO— or — Represents OOC-. R is a hydrogen atom or a lower alkyl group, and Z ³ is a hydrogen atom or an alkyl or alkoxy having 1 to 12 carbon atoms, which may have a substituent, cyano, nitro, or halogen. z is an integer of 0-4. E ¹ represents a photodimerization reaction site, and examples thereof include cinnamic acid ester, coumarin, quinoline, chalcone group, cinnamoyl group and the like. j and k are each independently 0 or 1.

  Specific examples of such a dimerization reactive polymer include compounds represented by the following formulas (15) to (18).

  More specific examples of the dimerization reactive polymer include compounds represented by the following formulas (19) to (22).

  As the photodimerization reactive compound, various photodimerization reaction sites and substituents can be selected from the above-mentioned compounds according to the required characteristics. Moreover, the photodimerization reactive compound can also be used individually by 1 type or in combination of 2 or more types.

  Further, the photodimerization type material may contain an additive in addition to the photodimerization reactive compound as long as the photoalignment of the alignment film is not hindered. Examples of the additive include a polymerization initiator and a polymerization inhibitor.

  The polymerization initiator or polymerization inhibitor may be appropriately selected from generally known compounds according to the type of the photodimerization reactive compound. The addition amount of the polymerization initiator or the polymerization inhibitor is preferably in the range of 0.001% by mass to 20% by mass, and in the range of 0.1% by mass to 5% by mass with respect to the photodimerization reactive compound. It is more preferable that This is because if the addition amount of the polymerization initiator or polymerization inhibitor is too small, the polymerization may not be started (prohibited), whereas if too large, the reaction may be inhibited.

  The wavelength region of light that causes the photodimerization reaction of the photodimerization material is preferably in the ultraviolet light range, that is, in the range of 10 nm to 400 nm, and more preferably in the range of 250 nm to 380 nm.

  Next, the photo-alignment processing method will be described. First, a second alignment film forming coating solution obtained by diluting the above-mentioned photodimerization-type material with an organic solvent is applied onto the second electrode layer and dried.

  The content of the photodimerization reactive compound in the second alignment film forming coating solution is preferably in the range of 0.05% by mass to 10% by mass, and in the range of 0.2% by mass to 2% by mass. More preferably, it is within. If the content is less than the above range, it will be difficult to impart appropriate anisotropy to the alignment film. Conversely, if the content is more than the above range, the viscosity of the coating liquid will increase, so a uniform coating film will be formed. It is because it becomes difficult to form.

  As a coating method of the second alignment film forming coating solution, for example, spin coating method, roll coating method, rod bar coating method, spray coating method, air knife coating method, slot die coating method, wire bar coating method, ink jet method, A flexographic printing method, a screen printing method, or the like can be used.

  The thickness of the film obtained by applying the second alignment film forming coating solution is preferably in the range of 1 nm to 1000 nm, more preferably in the range of 3 nm to 100 nm. This is because if the film thickness is thinner than the above range, sufficient optical alignment may not be obtained, and conversely if the film thickness is thicker than the above range, it may be disadvantageous in terms of cost.

  The obtained film can impart anisotropy by causing a photodimerization reaction by irradiating light with polarization controlled. The wavelength region of the light to be irradiated may be appropriately selected according to the constituent material of the alignment film to be used, but is preferably in the ultraviolet light range, that is, in the range of 100 nm to 400 nm, more preferably 250 nm to It is in the range of 380 nm. The polarization direction is not particularly limited as long as it can cause a photodimerization reaction.

(Ii) Second Aspect In the second aspect, the second alignment film is formed on the second electrode layer and is a rubbing film.

  The material used for the rubbing film is not particularly limited as long as it can impart anisotropy to the alignment film by rubbing treatment. For example, polyimide, polyamide, polyamideimide, polyetherimide, polyvinyl Examples thereof include alcohol and polyurethane. These may be used alone or in combination of two or more.

  As the rubbing treatment method, a method of applying anisotropy to the alignment film by applying the above-mentioned material on the second electrode layer and curing it, and rubbing the obtained film with a rubbing cloth in a certain direction is used. it can.

  Examples of the method for applying the material include a roll coating method, a rod bar coating method, a slot die coating method, a wire bar coating method, an ink jet method, a flexographic printing method, and a screen printing method.

  Further, the thickness of the rubbing film is set to about 1 nm to 1000 nm, and preferably in the range of 50 nm to 100 nm.

  As the rubbing cloth, for example, a cloth made of a fiber such as nylon resin, vinyl resin, rayon, or cotton can be used. For example, by rotating a drum wound with such a rubbing cloth and bringing it into contact with the surface of the film using the above material, fine grooves are formed in one direction on the film surface, and the alignment film has anisotropy. Is granted.

4). Other Configurations The liquid crystal display element of the present invention may have a polarizing plate as illustrated in FIG.
The polarizing plate used in the present invention is not particularly limited as long as it transmits only a specific direction among the wave of light, and a polarizing plate generally used as a polarizing plate of a liquid crystal display element should be used. Can do.

5. Method for Driving Liquid Crystal Display Element As a method for driving the liquid crystal display element of the present invention, the high-speed response of ferroelectric liquid crystal can be used. A field sequential color system that particularly requires high-speed response is suitable. According to the present invention, as described above, it is possible to avoid problems caused when driven by the field sequential color system.

  Further, the driving method of the liquid crystal display element of the present invention is not limited to the field sequential method, and may be a color filter method that performs color display using a colored layer.

  As a driving method of the liquid crystal display element of the present invention, an active matrix system using a thin film transistor (TFT) is preferable. This is because by adopting an active matrix system using TFTs, the target pixel can be reliably turned on and off, and a high-quality display becomes possible.

  In the present invention, the first alignment treatment substrate may be a TFT substrate, the second alignment treatment substrate may be a common electrode substrate, the first alignment treatment substrate may be a common electrode substrate, and the second alignment treatment substrate may be a TFT. Good. Among these, it is preferable that the first alignment processing substrate is a TFT substrate and the second alignment processing substrate is a common electrode substrate.

For example, in the liquid crystal display element shown in FIG. 9, when the gate electrode 24x is set to a high potential of about 30 V, the TFT element 25 is turned on, and a signal voltage is applied to the ferroelectric liquid crystal by the source electrode 24y. When the potential is lowered to about -10 V, the TFT element 25 is switched off. In the switch-off state, as illustrated in FIG. 10, a voltage is applied between the common electrode (second electrode layer) 14 and the gate electrode 24x so that the common electrode (second electrode layer) 14 side is positive. . Since the ferroelectric liquid crystal does not operate in this switch-off state, the pixel is in a dark state.
In the present invention, when no voltage is applied, the spontaneous polarization of the liquid crystal molecules tends to be directed toward the first alignment processing substrate due to the polar surface interaction. That is, in the switch-off state, as illustrated in FIG. 10, the spontaneous polarization Ps of the liquid crystal molecules 1 faces the TFT substrate (first alignment processing substrate) 6 side. Therefore, the direction of spontaneous polarization is not affected by the voltage applied between the common electrode (second electrode layer) 14 and the gate electrode 24x.
On the other hand, for example, when the spontaneous polarization is directed to the common electrode substrate (second alignment processing substrate) side in the state where no voltage is applied, due to the influence of the voltage applied between the common electrode and the gate electrode in the switch-off state, The direction of spontaneous polarization is reversed near the region where the gate electrode is provided. Then, in the vicinity of the region where the gate electrode is provided, the ferroelectric liquid crystal operates and light leakage occurs even though the switch is off.
On the other hand, as described above, in the present invention, the direction of spontaneous polarization is not affected by the voltage applied between the common electrode and the gate electrode, so that no light leakage occurs. Therefore, in the present invention, light leakage in the vicinity of the gate electrode can be prevented by controlling the direction of spontaneous polarization and using the first alignment substrate as the TFT substrate and the second alignment substrate as the common electrode substrate.

As described above, in the ferroelectric liquid crystal used in the present invention, when a voltage is applied so that the second electrode layer is a negative electrode, the molecular direction of the ferroelectric liquid crystal is relative to the first alignment treatment substrate surface. It changes approximately twice the tilt angle of the ferroelectric liquid crystal in parallel.
If the pixel electrode voltage is relatively high with respect to the common electrode, a positive polarity voltage application is assumed, and if the pixel electrode voltage is relatively low, a negative polarity voltage application is assumed. In this definition, when the first alignment processing substrate is a common electrode substrate and the second alignment processing substrate is a TFT substrate, the ferroelectric liquid crystal has a pixel electrode voltage relatively lower than the common electrode. That is, when a negative polarity voltage is applied, the molecular direction of the ferroelectric liquid crystal changes approximately twice the tilt angle of the ferroelectric liquid crystal in parallel with the first alignment processing substrate surface. Further, when the first alignment processing substrate is a TFT substrate and the second alignment processing substrate is a common electrode substrate, the ferroelectric liquid crystal has a pixel electrode voltage relatively higher than the common electrode, that is, a positive electrode. When a polarity voltage is applied, the molecular direction of the ferroelectric liquid crystal changes approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the first alignment substrate surface.

  Further, the driving method of the liquid crystal display element of the present invention may be a segment method.

6). Next, a method for manufacturing a liquid crystal display element of the present invention will be described. The liquid crystal display element of this invention can be manufactured by the method generally used as a manufacturing method of a liquid crystal display element. For example, a vacuum injection method, a liquid crystal dropping method, or the like can be used.
Hereinafter, as an example of a method for manufacturing a liquid crystal display element of the present invention, a method for manufacturing an active matrix liquid crystal display element using TFT elements will be described.

In the vacuum injection method, first, a transparent conductive film is formed on a second substrate by a vacuum vapor deposition method to form a common electrode on the entire surface. Further, a photo-dimerization type material is applied on the common electrode, and a second alignment film is formed by applying a photo-alignment process to obtain a second alignment process substrate. On the first substrate, a gate electrode and a source electrode are formed by patterning the conductive film in a matrix, and a pixel electrode is formed by patterning the transparent conductive film, and a TFT element is installed. Further, a photoisomerizable material is applied on the gate electrode, source electrode, TFT element, and pixel electrode, and a first alignment film is formed by applying a photo-alignment process to obtain a first alignment process substrate.
Next, beads are dispersed as spacers on the first alignment film of the first alignment processing substrate, and a sealant is applied to the periphery. The first alignment treatment substrate and the second alignment treatment substrate are opposed to each other so that the alignment treatment directions of the first alignment film and the second alignment film are substantially parallel, and are bonded and thermocompression bonded. Then, the ferroelectric liquid crystal is injected in an isotropic liquid state using the capillary effect from the injection port, and the injection port is sealed with an ultraviolet curable resin or the like. Thereafter, the ferroelectric liquid crystal can be aligned by slow cooling.

In the liquid crystal dropping method, first, a transparent conductive film is formed on the second base material by a vacuum deposition method to form a common electrode on the entire surface. Next, partition walls are formed in a pattern on the common electrode layer by photolithography. Next, a photodimerization-type material is applied on the common electrode and the partition, and a photo-alignment process is performed to form a second alignment film, thereby forming a second alignment-processed substrate. On the first substrate, a gate electrode and a source electrode are formed by patterning the conductive film in a matrix, and a pixel electrode is formed by patterning the transparent conductive film, and a TFT element is installed. Further, a photoisomerizable material is applied on the gate electrode, source electrode, TFT element, and pixel electrode, and a first alignment film is formed by applying a photo-alignment process to obtain a first alignment process substrate.
Next, a ferroelectric liquid crystal is discharged in an isotropic liquid state on the second alignment film of the second alignment processing substrate by an ink jet method. Further, a sealant is applied around the first alignment processing substrate. Next, the first alignment treatment substrate and the second alignment treatment substrate are heated to a temperature at which the ferroelectric liquid crystal exhibits a nematic phase or an isotropic phase, and the alignment treatment directions of the first alignment film and the second alignment film are substantially parallel. They are made to face each other, overlapped under reduced pressure, and bonded through a sealant. Thereafter, the encapsulated ferroelectric liquid crystal can be aligned by slowly cooling the liquid crystal cell to room temperature.

When aligning the ferroelectric liquid crystal, if a polymerizable monomer is added to the ferroelectric liquid crystal, the ferroelectric liquid crystal is aligned and then the polymerizable monomer is polymerized. The polymerization method of the polymerizable monomer is appropriately selected according to the type of the polymerizable monomer. For example, when an ultraviolet curable resin monomer is used as the polymerizable monomer, the polymerizable monomer can be polymerized by ultraviolet irradiation. .
Further, when polymerizing the polymerizable monomer, a voltage may or may not be applied to the liquid crystal layer composed of the ferroelectric liquid crystal, but no voltage is applied to the liquid crystal layer. It is preferable to polymerize a polymerizable monomer.

  Furthermore, polarizing plates may be attached to the top and bottom of the liquid crystal cell obtained as described above.

  The present invention is not limited to the above embodiment. The above-described embodiment is an exemplification, and the present invention has substantially the same configuration as the technical idea described in the claims of the present invention, and any device that exhibits the same function and effect is the present invention. It is included in the technical scope of the invention.

  Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples.

[Example 1]
(Production of first alignment processing substrate)
The glass substrate on which the ITO electrode is formed is thoroughly washed, and a photoisomerization type material (manufactured by Dainippon Ink Co., Ltd., trade name: LIA01) is spin-coated on the glass substrate at a rotation speed of 1500 rpm for 15 seconds, at 100 ° C. After drying for 3 minutes, alignment treatment was performed by irradiating with linearly polarized ultraviolet rays of about 1000 mJ / cm ² .

(Preparation of second alignment processing substrate)
The glass substrate on which the ITO electrode was formed was thoroughly washed, and a transparent resist (manufactured by JSR, trade name: NN780) was spin coated on the glass substrate, dried under reduced pressure, and prebaked at 90 ° C. for 3 minutes. Subsequently, it exposed to a mask with 100 mJ / cm ² ultraviolet rays, developed with an inorganic alkali solution, and post-baked at 230 ° C. for 30 minutes. Thereby, a columnar spacer having a height of 1.5 μm was formed.
Next, a 2% by mass cyclopentanone solution of a photodimerization type material (Rolic technologies, trade name: ROP103) is spin-coated at a rotation speed of 1500 rpm for 15 seconds on the substrate on which the columnar spacers are formed, and 130 ° C. And dried for 15 minutes, and then irradiated with about 100 mJ / cm ^{2 of} linearly polarized ultraviolet light for alignment treatment.

(Production of liquid crystal display element)
A ferroelectric liquid crystal (trade name: R2301, manufactured by AZ Electronic Materials) was applied onto the second alignment treatment substrate using an ink jet apparatus. At this time, the head of the ink jet device was heated to a temperature 20 ° C. higher than the N-phase-isotropic phase transition temperature of the ferroelectric liquid crystal, and the temperature of the second alignment processing substrate was set to room temperature.

Next, an ultraviolet heat curable sealant (manufactured by Kyoritsu Chemical Industry Co., Ltd., trade name: WORLD ROCK 718) was applied onto the second alignment treatment substrate with a seal dispenser.
A hot plate placed in a vacuum chamber was heated to 110 ° C., and a second alignment processing substrate coated with a sealant was placed on the hot plate. Next, the first alignment treatment substrate was adsorbed by an adsorption plate, and the first alignment treatment substrate and the second alignment treatment substrate were opposed to each other so that their alignment treatment directions were parallel. Then, the substrates were brought into close contact with each other in a state where evacuation was performed so that the inside of the vacuum chamber became 10 Torr, and after applying a certain pressure, the inside of the vacuum chamber was returned to normal pressure. Next, ultraviolet rays were irradiated at 1 J / cm ² to cure the ultraviolet heat curable sealant, and both substrates were adhered.
Thereafter, the liquid crystal cell was gradually cooled to room temperature to align the ferroelectric liquid crystal, thereby producing a liquid crystal display element.

  In the obtained liquid crystal display element, the abundance ratio of the double domain in the panel is approximately 75:25, and when a voltage is applied so that the electrode of the second alignment treatment substrate becomes a negative electrode, the area is about 75%. Thus, the molecular direction of the ferroelectric liquid crystal changed approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the substrate surface.

[Example 2]
(Production of first alignment processing substrate)
The glass substrate on which the ITO electrode is formed is thoroughly washed, and a photoisomerization type material (manufactured by Dainippon Ink Co., Ltd., trade name: LIA01) is spin-coated on the glass substrate at a rotation speed of 1500 rpm for 15 seconds, at 100 ° C. After drying for 3 minutes, alignment treatment was performed by irradiating with linearly polarized ultraviolet rays of about 1000 mJ / cm ² .

(Preparation of second alignment processing substrate)
The glass substrate on which the ITO electrode is formed is thoroughly cleaned, and a 2% by mass cyclopentanone solution of photodimerization material (Rolic technologies, trade name: ROP103) is spun on the glass substrate for 15 seconds at a rotation speed of 1500 rpm. After coating and drying at 130 ° C. for 15 minutes, alignment treatment was performed by irradiation with about 100 mJ / cm ^{2 of} linearly polarized ultraviolet rays.

(Production of liquid crystal display element)
A 1.5 μm bead spacer was sprayed on the first alignment treatment substrate, and a sealant was applied to the second alignment treatment substrate with a seal dispenser. Next, both substrates were made to face each other so that their alignment treatment directions were parallel, and thermocompression bonding was performed to produce an empty liquid crystal cell.
Next, a ferroelectric liquid crystal (trade name: R2301, manufactured by AZ Electronic Materials) is used to attach a ferroelectric liquid crystal to the upper portion of the injection port, and an oven is used to obtain an N-phase-isotropic phase transition temperature of 10 Injection was performed at a temperature higher by 20 ° C to 20 ° C, and the temperature was slowly returned to room temperature.

  In the obtained liquid crystal display element, the abundance ratio of the double domain in the panel is 95: 5, and when the voltage is applied so that the electrode of the second alignment treatment substrate becomes a negative electrode, the strong ratio is obtained in a region of 95%. The molecular direction of the dielectric liquid crystal changed approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the substrate surface.

[Example 3]
(Production of first alignment processing substrate)
The glass substrate on which the ITO electrode is formed is thoroughly washed, and a photoisomerizable material (manufactured by Dainippon Ink Co., Ltd., trade name: LIA01) is spin-coated on the glass substrate for 30 seconds at a rotational speed of 4000 rpm, and at 100 ° C. After drying for 3 minutes, alignment treatment was performed by irradiating with linearly polarized ultraviolet rays of about 1000 mJ / cm ² .

(Preparation of second alignment processing substrate)
The glass substrate on which the ITO electrode was formed was thoroughly washed, a transparent resist (manufactured by JSR, trade name: NN780) was spin coated on the glass substrate, dried under reduced pressure, and prebaked at 90 ° C. for 3 minutes. Subsequently, it exposed to a mask with 100 mJ / cm ² ultraviolet rays, developed with an inorganic alkali solution, and post-baked at 230 ° C. for 30 minutes. Thereby, a columnar spacer having a height of 1.5 μm was formed.
Next, polyimide (manufactured by Nissan Chemical Industries, trade name: SE-7962) was printed on the substrate on which the columnar spacers were formed, and an alignment film was formed by rubbing.

(Production of liquid crystal display element)
A ferroelectric liquid crystal (trade name: R2301, manufactured by AZ Electronic Materials) was applied onto the second alignment treatment substrate using an ink jet apparatus. At this time, the head of the ink jet device was heated to a temperature 20 ° C. higher than the N-phase-isotropic phase transition temperature of the ferroelectric liquid crystal, and the temperature of the second alignment processing substrate was set to room temperature.

Next, an ultraviolet heat curable sealant (manufactured by Kyoritsu Chemical Industry Co., Ltd., trade name: WORLD ROCK 718) was applied onto the second alignment treatment substrate with a seal dispenser.
A hot plate placed in a vacuum chamber was heated to 110 ° C., and a second alignment processing substrate coated with a sealant was placed on the hot plate. Next, the first alignment treatment substrate was adsorbed by an adsorption plate, and the first alignment treatment substrate and the second alignment treatment substrate were opposed to each other so that their alignment treatment directions were parallel. Then, the substrates were brought into close contact with each other in a state where evacuation was performed so that the inside of the vacuum chamber became 10 Torr, and after applying a certain pressure, the inside of the vacuum chamber was returned to normal pressure. Next, ultraviolet rays were irradiated at 1 J / cm ² to cure the ultraviolet heat curable sealant, and both substrates were adhered.
Thereafter, the liquid crystal cell was gradually cooled to room temperature to align the ferroelectric liquid crystal, thereby producing a liquid crystal display element.

  In the obtained liquid crystal display element, the abundance ratio of double domains in the panel is approximately 70:30, and when a voltage is applied so that the electrode of the second alignment treatment substrate becomes a negative electrode, the area is about 70%. Thus, the molecular direction of the ferroelectric liquid crystal changed approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the substrate surface.

[Comparative Example 1]
Thoroughly clean the two glass substrates on which the ITO electrodes are formed, and each of these two glass substrates is coated with a photoisomerizable material (Dainippon Ink Co., Ltd., trade name: LIA01) at a rotational speed of 4000 rpm for 30 seconds. After spin coating and drying at 100 ° C. for 3 minutes, alignment treatment was performed by irradiation with about 1000 mJ / cm ^{2 of} linearly polarized ultraviolet rays.

One substrate was sprayed with 1.5 μm bead spacers, and a sealant was applied to the other substrate with a seal dispenser. Next, both substrates were made to face each other so that their alignment treatment directions were parallel, and thermocompression bonding was performed to produce an empty liquid crystal cell.
Next, a ferroelectric liquid crystal (trade name: R2301, manufactured by AZ Electronic Materials) is used to attach a ferroelectric liquid crystal to the upper portion of the injection port, and an oven is used to obtain an N-phase-isotropic phase transition temperature of 10 Injection was performed at a temperature higher by 20 ° C to 20 ° C, and the temperature was slowly returned to room temperature.

  In the obtained liquid crystal display element, the existence ratio of the double domain in the panel is approximately 50:50, and when a voltage is applied so that the electrode of one substrate becomes a negative electrode, it is strong in a region of about 50%. The molecular direction of the dielectric liquid crystal changed approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the substrate surface.

[Comparative Example 2]
The two glass substrates on which the ITO electrodes are formed are thoroughly washed, and a 2% by mass cyclopentanone solution of a photodimerization type material (Rolic technologies, trade name: ROP103) is applied to each of the two glass substrates. After spin coating at a rotation speed of 1500 rpm for 15 seconds and drying at 130 ° C. for 15 minutes, linearly polarized ultraviolet rays were irradiated at about 100 mJ / cm ² to perform alignment treatment.

One substrate was sprayed with 1.5 μm bead spacers, and a sealant was applied to the other substrate with a seal dispenser. Next, both substrates were made to face each other so that their alignment treatment directions were parallel, and thermocompression bonding was performed to produce an empty liquid crystal cell.
Next, a ferroelectric liquid crystal (trade name: R2301, manufactured by AZ Electronic Materials) is used to attach a ferroelectric liquid crystal to the upper portion of the injection port, and an oven is used to obtain an N-phase-isotropic phase transition temperature of 10 Injection was performed at a temperature higher by 20 ° C to 20 ° C, and the temperature was slowly returned to room temperature.

  In the obtained liquid crystal display element, the existence ratio of the double domain in the panel is approximately 50:50, and when a voltage is applied so that the electrode of one substrate becomes a negative electrode, it is strong in a region of about 50%. The molecular direction of the dielectric liquid crystal changed approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the substrate surface.

[Comparative Example 3]
The two glass substrates on which the ITO electrodes are formed are washed thoroughly, polyimide (Nissan Chemical Co., Ltd., trade name: SE-7962) is printed on the two glass substrates, and the alignment film is formed by rubbing. Formed.

One substrate was sprayed with 1.5 μm bead spacers, and a sealant was applied to the other substrate with a seal dispenser. Next, both substrates were made to face each other so that their alignment treatment directions were parallel, and thermocompression bonding was performed to produce an empty liquid crystal cell.
Next, a ferroelectric liquid crystal (trade name: R2301, manufactured by AZ Electronic Materials) is used to attach a ferroelectric liquid crystal to the upper portion of the injection port, and an oven is used to obtain an N-phase-isotropic phase transition temperature of 10 Injection was performed at a temperature higher by 20 ° C to 20 ° C, and the temperature was slowly returned to room temperature.

  In the obtained liquid crystal display element, the existence ratio of the double domain in the panel is approximately 50:50, and when a voltage is applied so that the electrode of one substrate becomes a negative electrode, it is strong in a region of about 50%. The molecular direction of the dielectric liquid crystal changed approximately twice the tilt angle of the ferroelectric liquid crystal parallel to the substrate surface.

It is a schematic diagram which shows the behavior of a liquid crystal molecule. It is a schematic sectional drawing which shows an example of the liquid crystal display element of this invention. It is a schematic diagram which shows an example of the orientation state of a ferroelectric liquid crystal. It is a schematic diagram which shows the other example of the orientation state of a ferroelectric liquid crystal. It is a schematic diagram which shows the spontaneous polarization of a ferroelectric liquid crystal. It is a schematic diagram which shows the other example of the orientation state of a ferroelectric liquid crystal. It is a schematic sectional drawing which shows the other example of the liquid crystal display element of this invention. It is a figure which shows the drive sequence of the liquid crystal display element by a field sequential color system. It is a schematic perspective view which shows the other example of the liquid crystal display element of this invention. It is a schematic diagram which shows the other example of the orientation state of a ferroelectric liquid crystal. It is a schematic diagram which shows the other example of the orientation state of a ferroelectric liquid crystal. It is the graph which showed the change of the transmittance | permeability with respect to the applied voltage of a ferroelectric liquid crystal. It is the figure which showed the difference in orientation by the difference in the phase sequence which a ferroelectric liquid crystal has. It is the graph which showed the change of the transmittance | permeability with respect to the applied voltage of a ferroelectric liquid crystal. It is a figure which shows the drive sequence of the liquid crystal display element by a field sequential color system.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 ... Liquid crystal molecule 2 ... Liquid crystal display element 3 ... 1st base material 4 ... 1st electrode layer 5 ... 1st alignment film 6 ... 1st orientation processing board | substrate 10 ... Liquid crystal layer 13 ... 2nd base material 14 ... 2nd electrode layer DESCRIPTION OF SYMBOLS 15 ... 2nd orientation film 16 ... 2nd orientation processing board | substrate z ... Layer normal line Ps ... Spontaneous polarization (theta) ... Tilt angle

Claims (4)

A first base material, a first electrode layer formed on the first base material, and light formed on the first electrode layer and imparting anisotropy to the alignment film by causing a photoisomerization reaction A first alignment treatment substrate having a first alignment film that is a photo-alignment film containing an isomerized material, a second substrate, a second electrode layer formed on the second substrate, and is formed on the second electrode layer, a second alignment treatment substrate having a second alignment film is La Bing film, and the first alignment film and the second alignment layer is arranged to face the first A liquid crystal display element comprising a ferroelectric liquid crystal sandwiched between a first alignment film and the second alignment film,
The ferroelectric liquid crystal has a phase sequence that does not pass through a smectic A phase, exhibits monostability, and exhibits HV-shaped switching (half-V shaped switching) characteristics,
When a voltage is applied to the ferroelectric liquid crystal so that the second electrode layer is a negative electrode, the ferroelectric liquid crystal has a molecular direction parallel to the first alignment substrate surface. all SANYO to about 2-fold changes in the tilt angle of the liquid crystal,
The first alignment processing substrate is a TFT substrate having a thin film transistor (TFT) formed on the first base material, and the second alignment processing substrate is a common electrode substrate in which the second electrode layer is a common electrode. the liquid crystal display element characterized by at.   A first base material, a first electrode layer formed on the first base material, and light formed on the first electrode layer and imparting anisotropy to the alignment film by causing a photoisomerization reaction A first alignment treatment substrate having a first alignment film that is a photo-alignment film containing an isomerized material, a second substrate, a second electrode layer formed on the second substrate, and A second alignment processing substrate formed on the second electrode layer and having a second alignment film that is a photo-alignment film containing a photodimerization-type material that imparts anisotropy to the alignment film by causing a photodimerization reaction; A liquid crystal display element in which the first alignment film and the second alignment film are disposed to face each other, and a ferroelectric liquid crystal is sandwiched between the first alignment film and the second alignment film. And
  The ferroelectric liquid crystal has a phase sequence that does not pass through a smectic A phase, exhibits monostability, and exhibits HV-shaped switching (half-V shaped switching) characteristics.
  When a voltage is applied to the ferroelectric liquid crystal so that the second electrode layer is a negative electrode, the ferroelectric liquid crystal has a molecular direction parallel to the first alignment substrate surface. It changes about twice the tilt angle of the liquid crystal,
  The first alignment processing substrate is a TFT substrate having a thin film transistor (TFT) formed on the first base material, and the second alignment processing substrate is a common electrode substrate in which the second electrode layer is a common electrode. A liquid crystal display element characterized by the above.   3. The liquid crystal display element according to claim 1, wherein the liquid crystal display element is driven by an active matrix system using a thin film transistor.   4. The liquid crystal display element according to claim 1, wherein the liquid crystal display element is driven by a field sequential color system.

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