U.S. patent application number 12/923614 was filed with the patent office on 2011-02-03 for retardation plate, method for manufacturing the retardation plate, and liquid crystal display.
This patent application is currently assigned to TOPPAN PRINTING CO., LTD.. Invention is credited to Sosuke Akao, Godai Fukunaga, Takao Taguchi.
Application Number | 20110025952 12/923614 |
Document ID | / |
Family ID | 41135033 |
Filed Date | 2011-02-03 |
United States Patent
Application |
20110025952 |
Kind Code |
A1 |
Akao; Sosuke ; et
al. |
February 3, 2011 |
Retardation plate, method for manufacturing the retardation plate,
and liquid crystal display
Abstract
A retardation plate includes a light transmissive planar body
and a solidified liquid crystal layer which is a continuous film
made from the same material supported by the planar body. The
solidified liquid crystal layer comprises a plurality of regions in
which a thickness direction refractive indices are lowest. The
plurality of regions are arranged on the planar body, each region
has a different in-plane retardation and different thickness
direction retardation caused by the degree of orientational
disorder of mesogens and anisotropy of orientational disorder of
mesogens.
Inventors: |
Akao; Sosuke; (Tokyo,
JP) ; Fukunaga; Godai; (Tokyo, JP) ; Taguchi;
Takao; (Tokyo, JP) |
Correspondence
Address: |
STAAS & HALSEY LLP
SUITE 700, 1201 NEW YORK AVENUE, N.W.
WASHINGTON
DC
20005
US
|
Assignee: |
TOPPAN PRINTING CO., LTD.
Tokyo
JP
|
Family ID: |
41135033 |
Appl. No.: |
12/923614 |
Filed: |
September 29, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
PCT/JP2009/056174 |
Mar 26, 2009 |
|
|
|
12923614 |
|
|
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|
Current U.S.
Class: |
349/74 ; 349/194;
430/20 |
Current CPC
Class: |
G02F 1/133633 20210101;
G02B 5/3083 20130101; G02F 1/133636 20130101; G02F 1/133631
20210101; G02F 1/133634 20130101 |
Class at
Publication: |
349/74 ; 349/194;
430/20 |
International
Class: |
G02F 1/1347 20060101
G02F001/1347; G02F 1/13 20060101 G02F001/13; G03F 7/20 20060101
G03F007/20 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 31, 2008 |
JP |
2008-093498 |
Jun 24, 2008 |
JP |
2008-164894 |
Claims
1. A retardation plate comprising: a light transmissive planar
body; and a solidified liquid crystal layer which is a continuous
film made from the same material supported by the planar body, the
solidified liquid crystal layer comprising a plurality of regions
in each of which a thickness direction refractive index is the
lowest, the plurality of regions being arranged on the planar body,
the regions being different in in-plane retardation and thickness
direction retardation caused by degree of orientational disorder of
mesogens and anisotropy of orientational disorder of the
mesogens.
2. The retardation plate according to claim 1, wherein a number of
the regions in the solidified liquid crystal layer is 3 or
more.
3. The retardation plate according to claim 1, wherein in at least
one region of the solidified liquid crystal layer, an N.sub.z
coefficient represented by the formula (1) is different from that
of another region: Nz=(n.sub.x-n.sub.z)/(n.sub.x-n.sub.y) formula
(1) where n.sub.x is a maximum refractive index in the plane,
n.sub.y is a minimum refractive index in the plane, and n.sub.z is
a refractive index in a normal direction.
4. The retardation plate according to claim 2, wherein any one of
the first to third regions substantially has no in-plane
retardation.
5. The retardation plate according to claim 2, wherein at least one
of the first to third regions is different from other regions in an
axial direction in which a refractive index in the plane is the
highest.
6. The retardation plate according to claim 2, further comprising a
region having substantially no refractive index anisotropy.
7. The retardation plate according to claim 1, wherein the
solidified liquid crystal layer has a uniform thickness.
8. The retardation plate according to claim 1, wherein the
solidified liquid crystal layer is formed by polymerizing and/or
crosslinking a thermotropic liquid crystal compound or composition
in a state of an anisotropically disordered cholesteric
alignment.
9. The retardation plate according to claim 2, further comprising a
color filter layer which is interposed between the planar body and
the solidified liquid crystal layer, or faces the planar body with
the solidified liquid crystal layer interposed therebetween, the
color filter layer comprising first to third coloring layers having
different absorption spectra and facing the first to third regions,
respectively.
10. The retardation plate according to claim 9, wherein the
in-plane retardation of the solidified liquid crystal layer is the
smallest in the first region and the greatest in the third region,
and the Nz coefficient of the solidified liquid crystal layer is
the greatest in the first region and the smallest in the third
region, and a wavelength of light transmissible through the color
filter layer is the shortest in the first coloring layer, and the
longest in the third coloring layer.
11. A liquid crystal display comprising the retardation plate
according to claim 1.
12. A method of manufacturing a retardation plate, comprising
forming a solidified liquid crystal layer on a light-transmissive
planar body, the formation of the solidified liquid crystal layer
comprising: a film-forming step of forming a liquid crystal
material layer on the planar body, the liquid crystal material
layer comprising a photo-polymerizing or photo-crosslinking
thermotropic liquid crystal compound and a chiral agent, and
mesogens of the thermotropic liquid crystal compound forming a
cholesteric alignment structure; an exposure step of irradiating at
least two regions of the liquid crystal material layer with
polarized light under different conditions and with unpolarized
parallel light under different conditions, thereby polymerizing or
crosslinking at least a portion of the thermotropic liquid crystal
compound with different proportions and different degrees of
anisotropy to produce a polymerized or crosslinked product; a
developing step of heating thereafter the liquid crystal material
layer to a temperature equal to or higher than a phase transition
temperature at which the thermotropic liquid crystal compound is
changed from a liquid crystal phase to an isotropic phase, thereby
changing an orientation state of the mesogens of the unreacted
thermotropic liquid crystal compound in the at least two regions;
and a fixing step of polymerizing and/or crosslinking the unreacted
compound with the orientation state of the mesogens kept
changed.
13. The manufacturing method according to claim 12, wherein the
irradiation of unpolarized parallel light is performed before the
irradiation of polarized light in the exposure step.
14. The manufacturing method according to claim 12, wherein the
irradiation of polarized light is performed by irradiating with
linearly polarized light in the exposure step.
15. The manufacturing method according to claim 12, wherein the
irradiation of polarized light is performed by irradiating with
elliptically polarized light in the exposure step.
16. A method of manufacturing a retardation plate, comprising
forming a solidified liquid crystal layer on a light-transmissive
planar body, the formation of the solidified liquid crystal layer
comprising: a film-forming step of forming a liquid crystal
material layer on the planar body, the liquid crystal material
layer comprising a photo-polymerizing or photo-crosslinking
thermotropic liquid crystal compound and a chiral agent, and
mesogens of the thermotropic liquid crystal compound forming a
cholesteric alignment structure; an exposure step of irradiating at
least two regions of the liquid crystal material layer with
linearly polarized light with at least extinction ratios thereof
different from each other, thereby polymerizing or crosslinking at
least a portion of the thermotropic liquid crystal compound with
different proportions and different degrees of anisotropy to
produce a polymerized or crosslinked product; a developing step of
heating thereafter the liquid crystal material layer to a
temperature equal to or higher than a phase transition temperature
at which the thermotropic liquid crystal compound is changed from a
liquid crystal phase to an isotropic phase, thereby changing an
orientation state of the mesogens of the unreacted thermotropic
liquid crystal compound in the at least two regions; and a fixing
step of polymerizing and/or crosslinking the unreacted compound
with the orientation state of the mesogens kept changed.
17. A method of manufacturing a retardation plate, comprising
forming a solidified liquid crystal layer on a light-transmissive
planar body, the formation of the solidified liquid crystal layer
comprising: a film-forming step of forming a liquid crystal
material layer on the planar body, the liquid crystal material
layer containing a photo-polymerizing or photo-crosslinking
thermotropic liquid crystal compound and a chiral agent, and
mesogens of the thermotropic liquid crystal compound forming a
cholesteric alignment structure; an exposure step of irradiating at
least two regions of the liquid crystal material layer with
elliptically polarized light with at least ellipticities thereof
different from each other, thereby polymerizing or crosslinking at
least a portion of the thermotropic liquid crystal compound with
different proportions and different degrees of anisotropy to
produce a polymerized or crosslinked product; a developing step of
heating thereafter the liquid crystal material layer to a
temperature equal to or higher than a phase transition temperature
at which the thermotropic liquid crystal compound is changed from a
liquid crystal phase to an isotropic phase, thereby changing an
orientation state of the mesogens of the unreacted thermotropic
liquid crystal compound in the at least two regions; and a fixing
step of polymerizing and/or crosslinking the unreacted compound
with the orientation state of the mesogens kept changed.
18. The manufacturing method according to claim 12, wherein in the
exposure step, irradiating with linearly polarized light or
elliptically polarized light is performed such that an azimuth of
polarization axis in at least one of the regions is different from
that in the another region.
19. The manufacturing method according to claim 12, wherein in the
exposure step, a region which comprises the thermotropic liquid
crystal compound or composition as an unreacted compound and does
not comprise the polymerized or crosslinked product is formed by
irradiating neither with the polarized light nor with the
unpolarized parallel light, in this region, the orientation of the
mesogens of the unreacted thermotropic liquid crystal compound
disappears in the developing step, by heating the liquid crystal
material layer to the temperature equal to or higher than the phase
transition temperature at which the thermotropic liquid crystal
compound is changed from the liquid crystal phase to the isotropic
phase, and the unreacted compound is polymerized and/or crosslinked
in the fixing step maintaining the disappearance of the orientation
of the mesogens.
20. The manufacturing method according to claim 12, wherein in the
film-forming step, the liquid crystal material layer is formed as a
continuous film having a uniform thickness.
21. The manufacturing method according to claim 12, wherein in the
fixing step, the polymerizing and/or crosslinking the unreacted
compound reaction is induced by light irradiation.
22. The manufacturing method according to claim 12, wherein the
thermotropic liquid crystal compound is a material which is
polymerized and/or crosslinked by heating to a polymerizing and/or
crosslinking temperature higher than the phase transition
temperature, in the developing step, the orientation state of the
mesogen groups is changed by heating the liquid crystal material
layer at a temperature lower than the polymerization and/or
crosslinking temperature, and in the fixing step, the unpolymerized
and uncrosslinked thermotropic liquid crystal compound is
polymerized and/or crosslinked by heating the liquid crystal
material layer to a temperature equal to or higher than the
polymerization and/or crosslinking temperature.
23. The manufacturing method according to claim 22, wherein the
heating in the developing step is performed by raising a
temperature of the planar body continuously from a temperature in
the exposure step to a temperature in the fixing step.
24. The manufacturing method according to claim 12, further
comprising forming a color filter layer on the planar body before
the solidified liquid crystal layer is formed, wherein that the
solidified liquid crystal layer is formed on the color filter
directly or with another layer interposed therebetween.
25. The manufacturing method according to claim 12, further
comprising forming a color filter layer on the solidified liquid
crystal layer after the solidified liquid crystal layer is formed,
wherein that the color filter layer is formed on the solidified
liquid crystal layer directly or with another layer interposed
therebetween.
26. A retardation plate comprising: a light-transmissive planar
body; and a solidified liquid crystal layer which is a continuous
film made from the same material supported by the planar body, the
solidified liquid crystal layer comprising a plurality of regions
in each of which a thickness direction refractive index is the
lowest, the plurality of regions being arranged on the planar body,
the regions being different in in-plane birefringence and thickness
direction birefringence caused by degree of orientational disorder
of mesogens and anisotropy of orientational disorder of the
mesogens.
27. The retardation plate according to claim 26, wherein that a
number of the regions in the solidified liquid crystal layer is 3
or more.
28. The retardation plate according to claim 26, wherein in at
least one region of the solidified liquid crystal layer, an N.sub.z
coefficient represented by the formula (1) is different from that
of another region: Nz=(n.sub.x-n.sub.z)/(n.sub.x-n.sub.y) formula
(1) where n.sub.x is a maximum refractive index in the plane,
n.sub.y is a minimum refractive index in the plane, and n.sub.z is
a refractive index in a normal direction.
29. The retardation plate according to claim 27, wherein any one of
the first to third regions substantially has no in-plane
retardation.
30. The retardation plate according to claim 27, wherein at least
one of the first to third regions is different from other regions
in an axial direction in which a refractive index in the plane is
the highest.
31. The retardation plate according to claim 26, further comprising
a region having substantially no refractive index anisotropy.
32. The retardation plate according to claim 26, wherein the
solidified liquid crystal layer has a uniform thickness.
33. The retardation plate according to claim 26, wherein the
solidified liquid crystal layer is formed by polymerizing and/or
crosslinking a thermotropic liquid crystal compound or composition
in a state of an anisotropically disordered cholesteric
alignment.
34. The retardation plate according to claim 27, further comprising
a color filter layer which is interposed between the planar body
and the solidified liquid crystal layer, or faces the planar body
with the solidified liquid crystal layer interposed therebetween,
the color filter layer comprising first to third coloring layers
having different absorption spectra and facing the first to third
regions, respectively.
35. The retardation plate according to claim 34, wherein the
in-plane retardation of the solidified liquid crystal layer is the
smallest in the first region and the greatest in the third region,
and the Nz coefficient of the solidified liquid crystal layer is
the greatest in the first region and the smallest in the third
region, and a wavelength of light transmissible through the color
filter layer is the shortest in the first coloring layer, and the
longest in the third coloring layer.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This is a Continuation Application of PCT Application No.
PCT/JP2009/056174, filed Mar. 26, 2009, which was published under
PCT Article 21(2) in Japanese.
[0002] This application is based upon and claims the benefit of
priority from prior Japanese Patent Applications No. 2008-093498,
filed Mar. 31, 2008; and No. 2008-164894, filed Jun. 24, 2008, the
entire contents of both of which are incorporated herein by
reference.
BACKGROUND OF THE INVENTION
[0003] 1. Field of the Invention
[0004] The present invention relates to an optical technique that
can be applied, for example, to a display such as liquid crystal
display.
[0005] 2. Description of the Related Art
[0006] Liquid crystal displays have characteristics of thin-shaped,
lightweight and low power consumption. Thus, in recent years, their
application to mobile devices and stationary equipments such as
television receivers increases rapidly.
[0007] In order to make it possible for a liquid crystal display to
display a multi-colored image, a color filter is utilized. For
example, in a transmissive or reflective liquid crystal display
that can display a multi-colored image, a color filter including
red, green and blue coloring layers is utilized in most cases. On
the other hand, in a semi-transparent liquid crystal display that
can display a multi-colored image, a color filter including red,
green and blue coloring layers for transmissive display and red,
green and blue coloring layers for reflective display is utilized
in most cases.
[0008] Many liquid crystal displays include a retardation layers.
For example, in a liquid crystal display of a television receiver,
a retardation layer is utilized in combination with a linearly
polarizing film in order to display an image that can be easily
recognized regardless of the viewing direction. On the other hand,
in a reflective or semi-transparent liquid crystal display, an
absorption-type circularly polarizing plate including a
quarter-wave plate or a combination of a quarter-wave plate and a
half-wave plate as a retardation layer is utilized in order to
achieve an excellent visibility under a high-luminance light source
such as sun.
[0009] However, in spite of the fact that the red, green and blue
pixels are different in wavelength range of display color from one
another, the retardation of a retardation layer is usually even
throughout its surface. For this reason, it is difficult to adopt
optimal designs into all the pixels different in display color.
[0010] In addition, each of the retardation of a liquid crystal
layer and the retardation of a retardation layer has wavelength
dispersion. For this reason, when employing a design for
sufficiently compensating the retardation of a liquid crystal cell
using a retardation layer at pixels that display a certain color,
the retardation layer may insufficiently compensate the retardation
of a liquid crystal cell at pixels that display other colors.
[0011] Furthermore, in the case where a quarter-wave plate, which
causes a retardation by a quarter of a wavelength (.lamda./4) at a
center wavelength of green wavelength range, for example, about 550
nm, is combined with a linearly polarizing plate to be used as a
circularly polarizing plate, even when the refractive index
anisotropy, i.e., birefringence .DELTA.n of the quarter-wave plate
is almost uniform throughout the wavelength range of visible rays,
a retardation greater than .lamda./4 will be caused within a blue
wavelength range having a center wavelength of, for example, about
450 nm. Also, a retardation smaller than .lamda./4 will be caused
within a red wavelength range having a center wavelength of, for
example, about 630 nm. Thus, when the circularly polarizing plate
is irradiated with blue and red lights as natural lights, the
transmitted light will be not a circularly polarized light but an
elliptically polarized light. In fact, since the birefringence is
greater on the short-wavelength's side of the visible range, i.e.,
within the blue wavelength range and is smaller on the
long-wavelength's side of the visible range, i.e., within the red
wavelength range, this problem is often more serious.
[0012] In view of this problem, a solidified liquid crystal layer
containing a plurality of regions differing in thickness, that is,
in retardation is proposed in, for example, JP-A 2005-24919 and
JP-A 2006-85130.
[0013] Specifically, JP-A 2005-24919 describes that a color filter
layer composed of red, green and blue coloring layers different in
thickness is formed, and a solidified liquid crystal layer is
formed on the color filter layer. The solidified liquid crystal
layer is obtained by coating an alignment layer with a coating
solution containing photo-polymerizing liquid crystal compound and
irradiating the coated film with ultraviolet rays.
[0014] According to this method, due to the relief structure that
the coloring layers produces on the surface of the color filter
layer, a solidified liquid crystal layer thicker at a position of
the thinner coloring layer and thinner at a position of the thicker
coloring layer can be obtained. That is, a solidified liquid
crystal layer different in thickness among pixels that displays
different colors can be obtained. In other words, a solidified
liquid crystal layer including regions that cause different
retardations can be obtained.
[0015] JP-A 2006-85130 describes a semi-transparent liquid crystal
display that includes a color filter layer and a solidified liquid
crystal layer. In this liquid crystal display, each coloring layer
of the color filter layer is thicker at the transmissive portions
of pixels and thinner at the reflective portion of the pixels. That
is, the surface of the color filter layer is provided with a relief
structure. The solidified liquid crystal layer is obtained by
forming a polyimide layer on the surface of the color filter layer
provided with the relief structure, performing a rubbing process on
the whole surface of the polyimide layer, coating the polyimide
layer with ultraviolet-curing liquid crystal monomer, and
irradiating the coated layer with ultraviolet rays. Alternatively,
coating the surface of the color filter layer with a liquid crystal
polymer and subjecting the whole of the coated film to a
photo-alignment process obtain the solidified liquid crystal layer.
The solidified liquid crystal layer thus obtained is thinner at the
transmissive portions of pixels and thicker at the reflective
portions of the pixels. That is, according to the method, a
solidified liquid crystal layer that includes regions causing
different retardations can be obtained.
[0016] However, according to the technique described in JP-A
2005-24919, it is necessary to accurately adjust the differences in
thickness among the coloring layers. Similarly, according to the
technique described in JP-A 2006-85130, it is necessary to
accurately adjust the difference between the thickness of the
coloring layer at the reflective portion and the thickness of the
coloring layer at the transmissive portion. For this reason, when
the above-described techniques are employed, the design for the
color filter layer is limited or the degree of difficulty in
manufacturing the color filter layer increases. Therefore, in order
to achieve the design thickness at each region of the solidified
liquid crystal layer, it is necessary to consider various factors
such as flowability of a coating solution and a shrinkage ratio of
the coated film.
[0017] JP-A 2008-505369 (KOHYO) proposes a biaxial oriented film
having periodically varying local birefringence. The film described
therein is a short pitch cholesteric film, and develops additional
in-plane anisotropy (.DELTA.n.sub.x-y) in the negative C-type
structure, due to the helical strain. More specifically, a drawing
indicates the development of an index ellipsoid which satisfies
n.sub.x.noteq.n.sub.y.noteq.n.sub.z, wherein n.sub.x and n.sub.y
are greater than n.sub.z, and has biaxial negative C-type
symmetry.
[0018] According to the description, the film is produced by, for
example, irradiating the material with linearly polarized light,
preferably linearly polarized UV light to induce the photoreaction
of a photosensitive compound in a selected region of the material.
In the film, the helical structure is uniform, but the
birefringence varies locally throughout the helix.
BRIEF SUMMARY OF THE INVENTION
[0019] An object of the present invention is to make it possible to
easily manufacture a retardation layer that includes a plurality of
regions which are different in in-plane retardation and thickness
direction retardation, and a retardation plate having this
retardation layer.
[0020] According to a first aspect of the present invention, there
is provided a retardation plate comprising a light transmissive
planar body; and a solidified liquid crystal layer which is a
continuous film made from the same material supported by the planar
body, the solidified liquid crystal layer comprising a plurality of
regions in each of which a thickness direction refractive index is
the lowest, the plurality of regions being arranged on the planar
body, the regions being different in in-plane retardation and
thickness direction retardation caused by degree of orientational
disorder of mesogens and anisotropy of orientational disorder of
the mesogens.
[0021] According to a second aspect of the present invention, there
is provided a liquid crystal display comprising the aforementioned
retardation plate.
[0022] According to a third aspect of the present invention, there
is provided a method of manufacturing a retardation plate,
comprising forming a solidified liquid crystal layer on a
light-transmissive planar body, the formation of the solidified
liquid crystal layer comprising a film-forming step of forming a
liquid crystal material layer on the planar body, the liquid
crystal material layer comprising a photo-polymerizing or
photo-crosslinking thermotropic liquid crystal compound and a
chiral agent, and mesogens of the thermotropic liquid crystal
compound forming a cholesteric alignment structure; an exposure
step of irradiating at least two regions of the liquid crystal
material layer with polarized light under different conditions and
with unpolarized parallel light under different conditions, thereby
polymerizing or crosslinking at least a portion of the thermotropic
liquid crystal compound with different proportions and different
degrees of anisotropy to produce a polymerized or crosslinked
product; a developing step of heating thereafter the liquid crystal
material layer to a temperature equal to or higher than a phase
transition temperature at which the thermotropic liquid crystal
compound is changed from a liquid crystal phase to an isotropic
phase, thereby changing an orientation state of the mesogens of the
unreacted thermotropic liquid crystal compound in the at least two
regions; and a fixing step of polymerizing and/or crosslinking the
unreacted compound with the orientation state of the mesogens kept
changed.
[0023] According to a fourth aspect of the present invention, there
is provided a method of manufacturing a retardation plate,
comprising forming a solidified liquid crystal layer on a
light-transmissive planar body, the formation of the solidified
liquid crystal layer comprising a film-forming step of forming a
liquid crystal material layer on the planar body, the liquid
crystal material layer comprising a photo-polymerizing or
photo-crosslinking thermotropic liquid crystal compound and a
chiral agent, and mesogens of the thermotropic liquid crystal
compound forming a cholesteric alignment structure; an exposure
step of irradiating at least two regions of the liquid crystal
material layer with linearly polarized light with at least
extinction ratios thereof different from each other, thereby
polymerizing or crosslinking at least a portion of the thermotropic
liquid crystal compound with different proportions and different
degrees of anisotropy to produce a polymerized or crosslinked
product; a developing step of heating thereafter the liquid crystal
material layer to a temperature equal to or higher than a phase
transition temperature at which the thermotropic liquid crystal
compound is changed from a liquid crystal phase to an isotropic
phase, thereby changing an orientation state of the mesogens of the
unreacted thermotropic liquid crystal compound in the at least two
regions; and a fixing step of polymerizing and/or crosslinking the
unreacted compound with the orientation state of the mesogens kept
changed.
[0024] According to a fifth aspect of the present invention, there
is provided a method of manufacturing a retardation plate,
comprising forming a solidified liquid crystal layer on a
light-transmissive planar body, the formation of the solidified
liquid crystal layer comprising a film-forming step of forming a
liquid crystal material layer on the planar body, the liquid
crystal material layer containing a photo-polymerizing or
photo-crosslinking thermotropic liquid crystal compound and a
chiral agent, and mesogens of the thermotropic liquid crystal
compound forming a cholesteric alignment structure; an exposure
step of irradiating at least two regions of the liquid crystal
material layer with elliptically polarized light with at least
ellipticities thereof different from each other, thereby
polymerizing or crosslinking at least a portion of the thermotropic
liquid crystal compound with different proportions and different
degrees of anisotropy to produce a polymerized or crosslinked
product; a developing step of heating thereafter the liquid crystal
material layer to a temperature equal to or higher than a phase
transition temperature at which the thermotropic liquid crystal
compound is changed from a liquid crystal phase to an isotropic
phase, thereby changing an orientation state of the mesogens of the
unreacted thermotropic liquid crystal compound in the at least two
regions; and a fixing step of polymerizing and/or crosslinking the
unreacted compound with the orientation state of the mesogens kept
changed.
[0025] According to a sixth aspect of the present invention, there
is provided a retardation plate comprising a light-transmissive
planar body; and a solidified liquid crystal layer which is a
continuous film made from the same material supported by the planar
body, the solidified liquid crystal layer comprising a plurality of
regions in each of which a thickness direction refractive index is
the lowest, the plurality of regions being arranged on the planar
body, the regions being different in in-plane birefringence and
thickness direction birefringence caused by degree of orientational
disorder of mesogens and anisotropy of orientational disorder of
the mesogens.
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING
[0026] FIG. 1 is a perspective view schematically showing a
retardation plate according to an embodiment of the present
invention;
[0027] FIG. 2 is a sectional view taken along the line II-II of the
retardation plate shown in FIG. 1;
[0028] FIG. 3 is a sectional view schematically showing one example
of a method of forming a solidified liquid crystal layer;
[0029] FIG. 4 is a sectional view schematically showing one example
of a method of forming a solidified liquid crystal layer;
[0030] FIG. 5 is a sectional view schematically showing another
example of a method of forming a solidified liquid crystal
layer;
[0031] FIG. 6 is a sectional view schematically showing another
example of a method of forming a solidified liquid crystal
layer;
[0032] FIG. 7 is a sectional view schematically showing a process
following the process shown in FIG. 4;
[0033] FIG. 8 is a sectional view schematically showing a
retardation plate according to a modified example; and
[0034] FIG. 9 is an example of a liquid crystal display that can be
manufactured using the retardation plate shown in FIGS. 1 and
2.
DETAILED DESCRIPTION OF THE INVENTION
[0035] An embodiment of the present invention will be described
below with reference to the accompanying drawings. Note that the
same reference numerals in the drawings denote components that
achieve the same or similar functions, and a repetitive explanation
thereof will be omitted.
[0036] FIG. 1 is a perspective view schematically showing a
retardation plate according to an embodiment of the present
invention. FIG. 2 is a sectional view taken along the line II-II of
the retardation plate shown in FIG. 1.
[0037] The retardation plate 10 shown in FIGS. 1 and 2 includes a
planar body 110, a color filter layer 120 and a solidified liquid
crystal layer 130.
[0038] The planar body 110 has a light-transmitting property. The
planar body 110 is, for example, a transparent substrate.
[0039] The color filter layer 120 is formed on the planar body 110.
The color filter layer 120 includes coloring layers 120a to 120c
different in absorption spectrum from one another and adjacent to
one another on the planar body 110. For example, the light
transmitted by the coloring layer 120a is shorter in wavelength
than the light transmitted by the coloring layer 120b, and the
light transmitted by the coloring layer 120b is shorter in
wavelength than the light transmitted by the coloring layer
120c.
[0040] The color filter layer 120 may further include one or more
coloring layer different in absorption spectrum from the coloring
layer 120a to 120c. Here, as an example, it is supposed that the
first coloring layer 120a is a blue coloring layer, the second
coloring layer 120b is a green coloring layer, and the third
coloring layer 120c is a red coloring layer.
[0041] Each of the coloring layers 120a to 120c has a band-like
shape extending in the Y direction. The coloring layers 120a to
120c are alternately arranged in the X direction crossing the Y
direction to form a stripe arrangement. Note that the X direction
and the Y direction are directions parallel with the surface of the
planar body 110 that face the color filter layer 120. Note also
that the Z direction to be referred later is a direction
perpendicular to the X direction and the Y direction.
[0042] The coloring layers 120a to 120c may have other shapes. For
example, each of the coloring layers 120a to 120c has a rectangular
shape. In this case, the coloring layers 120a to 120c may form a
square arrangement of a delta arrangement.
[0043] Each of the coloring layers 120a to 120c is made of, for
example, a mixture containing a transparent resin and a pigment
dispersed therein. Forming a patterned layer of a coloring
composition that contains a pigment and a pigment carrier and
curing the patterned layer can obtain each of the coloring layers
120a to 120c. The coloring composition will be described later.
[0044] The solidified liquid crystal layer 130 is a retardation
layer, and is formed on the color filter layer 120. The solidified
liquid crystal layer 130 is a continuous film, and entirely covers
one main surface of the color filter layer 120.
[0045] The solidified liquid crystal layer 130 and the color filter
layer 120 may be in contact with each other or not. In the latter
case, an alignment layer may be interposed between the solidified
liquid crystal layer 130 and the color filter layer 120.
[0046] The solidified liquid crystal layer 130 includes a plurality
of regions arranged in the direction parallel with the main
surface. The plurality of regions each have birefringent anisotropy
and the refractive index in the direction of the thickness (Z) is
the lowest as compared with the refractive indices in the X- and
Y-directions.
[0047] For example, the solidified liquid crystal layer 130
includes regions 130a to 130c. The regions 130a to 130c are
adjacent to one another in a direction perpendicular to the Z
direction.
[0048] Specifically, regions 130a to 130c face the coloring layer
120a to 120c, respectively. The regions 130a to 130c have almost
the same shape.
[0049] The regions 130a to 130c are formed by polymerizing and/or
crosslinking a thermotropic liquid crystal compound or composition.
The regions 130a to 130c are equal in composition.
[0050] The regions 130a, 130b, and 130c are different in the
in-plane retardation and the thickness direction retardation. The
thickness direction retardation R.sub.th [nm] is expressed by the
following formula, wherein n.sub.x is the maximum refractive index
in the plane, n.sub.y is the minimum refractive index in the plane,
n.sub.z is the refractive index in the normal direction, and d
(.mu.m) is the film thickness:
R.sub.th=[(n.sub.x-n.sub.y)/2-n.sub.z].times.d.times.1000
[0051] One of the reasons of the differences in in-plane
retardation and in thickness direction retardation is that the
thermotropic liquid crystal compound is polymerized or crosslinked
in the state that these regions are different from one another in
the degree of orientational disorder of mesogens. For example, in a
region having a lower degree of orientational disorder of mesogens,
the in-plane retardation and thickness direction retardation are
increased. In a region having a higher degree of orientational
disorder of mesogens, on the other hand, the in-plane retardation
and thickness direction retardation are decreased.
[0052] Moreover, the differences in in-plane retardation and in
thickness direction retardation are caused by the polymerizing or
crosslinking the thermotropic liquid crystal compound in the state
that the degree of orientational disorder of mesogens is different
depending on the in-plane azimuth, that is, in the state that the
orientational disorder is anisotropic. In this case, the Nz factor
of a certain region is different from those of other regions. In,
for example, a region having a higher anisotropy of orientational
disorder, the Nz factor of this region is less. On the other hand,
in a region having a lower anisotropy of orientational disorder,
the Nz factor of this region is greater.
[0053] Incidentally, the Nz constant a value obtained from
Nz=(n.sub.x-n.sub.z)/(n.sub.x-n.sub.y). n.sub.x is a maximum
refractive index in a plane, n.sub.y is a minimum refractive index
in the plane, and n.sub.z is a refractive index in a normal
direction.
[0054] Here, the expression "degree of orientational disorder"
means the orientation state of mesogens MS in each of the regions
adjacent in-plane direction. The orientation state of the mesogens
MS may be uniform in the entire region or varied along the Z
direction. For example, in one region, the orientation may be
uniform near the upper surface, and disturbed near the lower
surface. In this case, the "degree of orientational disorder"
refers to an average of the degree of orientation in the direction
of thickness. Similarly, with regard to the expression
"orientational disorder anisotropy", the orientation state of the
mesogens MS may be varied along the Z-direction and, in this case,
"the degree of orientational disorder" also refers an average of
the degrees of orientation in the direction of the thickness.
[0055] More specifically, the region 130a has the highest in-plane
birefringence, while the smallest Nz coefficient. The region 130c
has the smallest in-plane birefringence, while the highest Nz
coefficient. The region 130b has the second highest in-plane
birefringence and Nz coefficient.
[0056] At least one of the regions may be an optically uniaxial
negative C-plate wherein the in-plane retardation is substantially
zero.
[0057] In at least one of the regions, the axial direction giving
the highest refractive index in the plane may be different from
those in the other regions. For example, in the region 130a, the
axis giving the highest refractive index in the plane is set in the
X direction, while in the region 130b, the axis giving the highest
refractive index in the plane is set in the direction forming an
angle of 45 degrees with the X- and Y-directions.
[0058] As described above, the regions 130a to 130c are different
in the degree of orientational disorder and/or in its anisotropy.
In other words, the difference in the retardation of the regions in
the retardation plate 10 of the present invention is mainly
attributed to the difference in the birefringence. Therefore, it is
not necessary to vary the thickness of the regions 130a to 130c
with the intention of varying the retardation of the regions 130a
to 130c. Depending on circumstances, the thicknesses of the regions
130a to 130c may be different from each other, but the formation of
the solidified liquid crystal layer 130 is easier when the
thicknesses of the regions 130a to 130c are equal.
[0059] As described above, the thicknesses of the regions 130a to
130c may be equal, thereby forming the solidified liquid crystal
layer 130 as a continuous film. As a result, the solidified liquid
crystal layer 130 is formed by a simplified process.
[0060] Further, the solidified liquid crystal layer 130 as a
continuous film makes the mass transfer from the color filter layer
120 to the outside of the retardation plate 10 more difficult than
the other patterned solidified liquid crystal layer 130 as a
discontinuous film. Therefore, in the case where the retardation
plate 10 that includes the solidified liquid crystal layer 130 as a
continuous layer is used, for example, in a liquid crystal layer,
it is possible to suppress the inclusion of impurities from the
color filter layer 120 into the liquid crystal layer.
[0061] As described above, the in-plane retardation and the
thickness direction retardation of the solidified liquid crystal
layer 130 are varied among the regions by varying the degree of the
orientational disorder and its anisotropy of the mesogen MS using,
for example, the following method: the orientation of a liquid
crystal including a rod-like shape mesogen is disordered so as to
give a cholesteric orientation (anisotropically disordered
cholesteric orientation) wherein the length direction of the
mesogen is perpendicular to the Z direction, and the orientation in
one direction is more disordered than in the other direction. In
this case, each of the regions 130a to 130c is a complex of a
positive A-plate and a negative C-plate which develop differences
in the in-plane retardation and the thickness direction retardation
corresponding to the degree of the orientational disorder and its
anisotropy.
[0062] Next, materials and manufacturing methods of the retardation
plate 10 will be described.
[0063] First, a light-transmissive planar body 110 is prepared. The
planar body 110 is, typically, a light-transmitting substrate such
as glass plate or resin plate. As a material of the glass plate,
soda-lime glass, low-alkali borosilicate glass or non-alkali
alumino borosilicate glass can be used, for example. As a material
of the resin plate, polycarbonate, polymethyl methacrylate or
polyethylene terephthalate may be used, for example. Also, the
planar body 110 is not always hard but may be, for example, a
light-transmissive film or sheet.
[0064] The planar body 110 may have a monolayer structure or a
multi-layered structure. For example, in the case where the
retardation plate 10 is a component of a liquid crystal display, a
light-transmitting substrate on which a transparent electrode made
of transparent conductor such as indium tin oxide or tin oxide may
be used as the planar body 110. Alternatively, as the planar body
110, a light-transmitting substrate on which a circuit such as
pixel circuit is formed may be used.
[0065] A color filter layer 120 is formed on the light-transmissive
planar body 110 by, for example, the method shown below.
[0066] The color filter layer 120 is obtained, for example, by
applying a coloring composition containing a pigment carrier and a
pigment dispersed in the pigment carrier to form a given pattern,
which is then cured, and these processes are repeated to form
coloring layers 120a to 120c respectively.
[0067] As the pigment of the coloring composition, organic pigment
and/or inorganic pigment can be used. The coloring composition may
contain a single organic or inorganic pigment, or a plurality of
organic pigments and/or inorganic pigments.
[0068] A pigment excellent in coloring property and heat-resisting
property, in particular, thermal decomposition-resisting property
is preferable, and normally, organic pigments are utilized. The
following color index numbers are examples of the organic pigments
that can be used in the coloring composition.
[0069] As an organic pigment of a red coloring composition, a red
pigment such as C. I. Pigment Red 7, 14, 41, 48:2, 48:3, 48:4,
81:1, 81:2, 81:3, 81:4, 146, 168, 177, 178, 179, 184, 185, 187,
200, 202, 208, 210, 246, 254, 255, 264, 270, 272 or 279 can be
used, for example. As an organic pigment of a red coloring
composition, a mixture of a red pigment and a yellow pigment may be
used. As the yellow pigment, C. I. Pigment Yellow 1, 2, 3, 4, 5, 6,
10, 12, 13, 14, 15, 16, 17, 18, 24, 31, 32, 34, 35, 35:1, 36, 36:1,
37, 37:1, 40, 42, 43, 53, 55, 60, 61, 62, 63, 65, 73, 74, 77, 81,
83, 93, 94, 95, 97, 98, 100, 101, 104, 106, 108, 109, 110, 113,
114, 115, 116, 117, 118, 119, 120, 123, 126, 127, 128, 129, 138,
147, 150, 151, 152, 153, 154, 155, 156, 161, 162, 164, 166, 167,
168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 179, 180, 181,
182, 185, 187, 188, 193, 194, 199, 198, 213 or 214 can be used, for
example.
[0070] As an organic pigment of a green coloring composition, a
green pigment such as C. I. Pigment Green 7, 10, 36 or 37 can be
used, for example. As an organic pigment of a green coloring
composition, a mixture of a green pigment and a yellow pigment may
be used. As the yellow pigment, the same pigments as that described
for the red coloring composition can be used, for example.
[0071] As an organic pigment of a blue coloring composition, a blue
pigment such as C. I. Pigment Blue 15, 15:1, 15:2, 15:3, 15:4,
15:6, 16, 22, 60 or 64 can be used, for example. As an organic
pigment of a blue coloring composition, a mixture of a blue pigment
and a purple pigment may be used. As the purple pigment, C. I.
Pigment Violet 1, 19, 23, 27, 29, 30, 32, 37, 40, 42 or 50 can be
used, for example.
[0072] As the inorganic pigment, metal oxide powders, metal sulfide
powders, or metal powders such as yellow lead ore, zinc yellow,
iron red (red oxide of iron (III)), cadmium red, ultramarine blue,
chromic oxide green and cobalt green can be used, for example. The
inorganic pigment can be used, for example, in combination with the
organic pigment in order to achieve excellent application property,
sensitivity and developing property while balancing chroma and
lightness.
[0073] The coloring composition may further contain coloring
components other than the pigment. For example, the coloring
composition may contain dye if a sufficient thermal resistance can
be achieved. In this case, the dye can be used for color
matching.
[0074] Also, the pigment carrier contained in the above coloring
composition is constituted of a transparent resin, its precursor or
a mixture thereof. Examples of the transparent resin include
thermoplastic resins, thermosetting resins and photosensitive
resins, and examples of its precursor include polyfunctional
monomers or oligomers which are cured by irradiating with rays to
produce a resin. These compounds may be used either singly or in
combinations of two or more. In this case, the transparent resins
are those having a transmittance of 80% or higher and preferably
95% or higher throughout the entire wavelength range of 400 to 700
nm, which is the visible range.
[0075] In the coloring composition, the transparent resin is use at
an amount of, for example, 30 to 700 parts by mass, preferably 60
to 450 parts by mass with respect to 100 parts by mass of the
pigment. In the case where a mixture of the transparent resin and
the precursor thereof is used as the pigment carrier, the
transparent resin is used in the coloring composition at an amount
of, for example, 20 to 400 parts by mass, preferably 50 to 250
parts by mass with respect to 100 parts by mass of the pigment. In
this case, the precursor of the transparent resin is used in the
coloring composition at an amount of, for example, 10 to 300 parts
by mass, preferably 10 to 200 parts by mass with respect to 100
parts by mass of the pigment.
[0076] As the thermoplastic resin, butyral resins, styrene-maleic
acid copolymers, chlorinated polyethylenes, polyvinyl chlorides,
vinyl chloride-vinyl acetate copolymers, polyvinyl acetates,
polyurethane resins, polyester resins, acrylic resins, alkyd
resins, polystyrene resins, polyamide resins, rubber-based resins,
cyclized rubber resins, celluloses, polybutadiens, polyethylenes,
polypropylenes or polyimide resins can be used, for example.
[0077] As the thermosetting resin, epoxy resins, benzoguanamine
resins, rosin-modified maleic resins, rosin-modified fumaric
resins, melamine resins, urea resins or phenol resins can be used,
for example.
[0078] As the photosensitive resin, resins obtained by causing the
reaction of an acrylic compound, a methacrylic compound or cinnamic
acid having a reactive substituent such as isocyanate group,
aldehyde group and epoxy group with a linear polymer having a
reactive substituent such as hydroxyl group, carboxyl group and
amino group to introduce photo-crosslinking groups such as acryloyl
groups, methacryloyl groups and stylyl groups into the linear
polymer can be used, for example. Alternatively, resins obtained by
half-esterifying a linear polymer including acid anhydride such as
styrene-maleic anhydride copolymer and .alpha.-olefin-maleic
anhydride copolymer using acrylic compounds or methacrylic
compounds having hydroxyl group such as hydroxyalkyl acrylates and
hydroxyalkyl methacrylates may be used.
[0079] As the monomers and/or oligomers, which are the precursor of
the transparent resin, acrylic esters and methacrylic esters such
as 2-hydroxyethyl acrylate, 2-hydroxyetyl methacrylate,
2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, cycrohexyl
acrylate, cycrohexyl methacrylate, polyethylene glycol diacrylate,
polyethylene glycol dimethacrylate, pentaerythritol triacrylate,
pentaerythritol trimethacrylate, trimethylolpropane triacrylate,
trimethylolpropane trimethacrylate, dipentaerythritol hexaacrylate,
dipentaerythritol hexamethacrylate, tricyclodecanyl acrylate,
tricyclodecanyl methacrylate, melamine acrylate, melamine
methacrylate, epoxy acrylate and epoxy methacrylate; acrylic acid,
methacrylic acid, styrene, vinyl acetate, acrylamide,
methacrylamide, N-hydroxymethyl acrylamide, N-hydroxymethyl
methacrylamide or a mixture containing two or more of them can be
used, for example.
[0080] In the case where the coloring composition is cured using
light such as ultraviolet rays, for example, a photo-polymerization
initiator is added to the coloring composition.
[0081] As the photo-polymerization initiator, acetophenone-based
photo-polymerization initiator such as
4-phenoxydichloroacetophenone, 4-t-butyl-dichloroacetophenone,
diethoxyacetophenone,
1-(4-isopropylphenyl)-2-hydroxy-2-methylpropane-1-one,
1-hydroxycyclohexylphenylketone,
2-methyl-1[4-(methylthio)phenyl]-2-morpholinopropane-1-one and
2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butane-1-one;
benzoin-based photo-polymerization initiator such benzoin,
benzoylbenzoate, methylbenzoylbenzoate, 4-phenylbenzophenone,
hydroxybenzophenone, acrylated benzophenone and
4-benzoyl-4'-methyldiphenyl sulfide; thioxanthone-based
photo-polymerization initiator such as thioxanthone,
2-chlorothioxanthone, 2-methyltioxanthone, isopropylthioxanthone
and 2,4-diisopropylthioxanthone; triazine-based
photo-polymerization initiator such as 2,4,6-trichloro-s-triazine,
2-phenyl-4,6-bis(trichloromethyl)-s-triazine,
2-(p-methoxyphenyl)-4,6-bis(trichloromethyl)-s-triazine,
2-(p-tolyl)-4,6-bis(trichloromethyl)-s-triazine,
2-piperonyl-4,6-bis(trichloromethyl)-s-triazine,
2,4-bis(trichloromethyl)-6-styryl-s-triaine,
2-(naphto-1-yl)-4,6-bis(trichloromethyl)-s-triazine,
2-(4-methoxy-naphto-1-yl)-4,6-bis(trichloromethyl)-s-triazine,
2,4-trichloromethyl-(piperonyl)-6-triazine and
2,4-trichloromethyl(4'-methoxystyryl)-6-triazine; borate-based
photo-polymerization initiator; carbazole-based
photo-polymerization initiator; imidazole-based
photo-polymerization initiator; or a mixture containing two or more
of them can be used, for example.
[0082] The photo-polymerization initiator is used in the coloring
composition at an amount of, for example, 5 to 200 parts by mass,
preferably 10 to 150 parts by mass with respect to 100 parts by
mass of the pigment.
[0083] A sensitizer may be used together with the
photo-polymerization initiator.
[0084] As the sensitizer, a compound such as .alpha.-acyloxy ester,
acylphosphine oxide, methylphenyl glyoxylate, benzil,
9,10-phenanthrenequinone, camphor quinone, ethyl anthraquinone,
4,4'-diethyl isophthaloquinone,
3,3',4,4'-tetra(t-butylperoxycarbonyl)benzophenone and
4,4'-diehylamino benzophenone can be used.
[0085] The sensitizer is used at an amount of, for example, 0.1 to
60 parts by mass with respect to 100 parts by mass of the
photo-polymerization initiator.
[0086] The coloring composition may further contain a chain
transfer agent such as multi-functional thiol.
[0087] A multi-functional thiol is a compound having two or more
thiol groups. As the multi-functional thiol, hexanedithiol,
decanedithiol, 1,4-butanediol bisthiopropionate, 1,4-butanediol
bisthioglycolate, ethylene glycol bisthioglycolate, ethylene glycol
bisthiopropionate, trimethylolpropane tristhioglycolate,
trimethylolpropane tristhiopropionate, trimethylolpropane
tris(3-mercaptobutyrate), pentaerythritol tetrakisthioglycolate,
pentaerythritol tetrakisthiopropionate, trimercaptopropionic
tris(2-hydroxyethyl)isocyanurate, 1,4-dimethylmercaptobenzene,
2,4,6-trimercapto-s-triazine,
2-(N,N-dibutylamino)-4,6-dimercapto-s-triazine or a mixture
containing two or more of them can be used, for example.
[0088] The multi-functional thiol is used in the coloring
composition at an amount of, for example, 0.2 to 150 parts by mass,
preferably 0.2 to 100 parts by mass with respect to 100 parts by
mass of the pigment.
[0089] The coloring composition may further contain a solvent. When
the solvent is used, the dispersibility of the pigment increases.
As a result, the coloring composition can be easily applied to the
planar body 110 at a dried thickness of, for example, 0.2 to 5
.mu.m.
[0090] As the solvent, ketones such as methyl ethyl ketone, methyl
amyl ketone, diethyl ketone, acetone, methyl isopropyl ketone,
methyl isobutyl ketone and cyclohexanone; ether type solvents such
as ethyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane,
1,2-diethoxyethane and dipropylene glycol dimethyl ether; ester
type solvents such as methyl acetate, ethyl acetate, n-propyl
acetate, isopropyl acetate and n-butyl acetate; cellosolve type
solvents such as ethylene glycol monomethyl ether, ethylene glycol
monoethyl ether and propylene glycol monomethyl ether acetate;
alcohol type solvents such as methanol, ethanol, isopropanol,
n-propanol, isobutanol, n-butanol and amyl alcohol; BTX type
solvents such as benzene, toluene and xylene; and aliphatic
hydrocarbon type solvents such as hexane, heptanes, octane and
cyclohexane can be used, for example.
[0091] Further examples of the solvent further include terpene type
hydrocarbon oils such as turpentine oil, D-limonene and pinene;
paraffin type solvents such as mineral spirit, Swasol #310
(manufactured by Cosmo Matsuyama Oil Co. Ltd.), Solvesso #100
(Exxon Chemical Co., Ltd.); halogenated aliphatic hydrocarbon
solvents such as carbon tetrachloride, chloroform,
trichloroethylene and dichloromethane; halogenated aromatic
hydrocarbon solvents such as chlorobenzene; and carbitol type
solvents.
[0092] Also, a solvent such as aniline, triethylamine, pyridine,
acetic acid, acetonitrile, carbon disulfide, tetrahydrofuran,
N,N-dimethylformamide and N-methylpyrrolidone may be used. Among
these compounds, ketones and cellosolve type solvents are
preferable. These solvents may be used either singly or in
combinations of two or more.
[0093] The solvent is used in the coloring composition at an amount
of, for example, 800 to 4,000 parts by mass, preferably 1,000 to
2,500 parts by mass with respect to 100 parts by mass of the
pigment.
[0094] The coloring composition can be manufactured, for example,
by finely dispersing one or more pigment into the pigment carrier
and the organic solvent together with the above-described
photo-polymerization initiator as needed using a dispersing device
such as three-roll mill, two-roll mill, sand mill, kneader and
attritor. A coloring composition containing two or more pigments
may be manufactured by preparing dispersions containing different
pigments and mixing the dispersions together.
[0095] When dispersing the pigment into the pigment carrier and the
solvent, a dispersion aid such as resin-type pigment-dispersing
agent, surfactant and pigment derivative may be used. The
dispersion aid increases the dispersibility of the pigment and
suppresses the reaggregation of the dispersed pigment. Therefore,
in the case of using a coloring composition prepared by dispersing
a pigment into a pigment carrier and a solvent using a dispersion
aid, a color filter excellent in transparency can be obtained.
[0096] The dispersion aid is used in the coloring composition at an
amount of, for example, 0.1 to 40 parts by mass, preferably 0.1 to
30 parts by mass with respect to 100 parts by mass of the
pigment.
[0097] The resin-type pigment-dispersing agent includes a
pigment-affinitive moiety having a property of undergoing
adsorption by the pigment and a moiety having a compatibility with
the pigment carrier. The resin-type pigment-dispersing agent is
adsorbed by the pigment so as to stabilize the dispersibility of
the pigment in the pigment carrier.
[0098] As the resin-type pigment-dispersing agent, an oil-based
dispersing agent such as polyurethane, polycarboxylate, e.g.
polyacrylate, unsaturated polyamide, polycarboxylic acid, partial
amine salt of polycarboxylic acid, ammonium polycarboxylate,
alkylamine polycarboxylate, polysiloxane, long-chain polyaminoamide
phosphate and hydroxyl group-containing polycarboxylate, modified
compounds thereof, amide produced through a reaction of poly(lower
alkylene imine) with polyester having a free carboxyl group and a
salt thereof; water-soluble resin or water-soluble macromolecular
compound such as acrylic acid-styrene copolymer, methacrylic
acid-styrene copolymer, acrylic acid-acrylate copolymer, acrylic
acid-methacrylate copolymer, methacrylic acid-acrylate copolymer,
methacrylic acid-methacrylate copolymer, styrene-maleic acid
copolymer, polyvinyl alcohol and polyvinyl pyrrolidone; polyester;
modified polyacrylate; ethylene oxide/propylene oxide adduct;
phosphate; or a compound containing two or more of them can be
used, for example.
[0099] As the surfactant, an anionic surfactant such as
polyoxyethylene alkylether sulfate, dodecylbenzene sodium
sulfonate, alkali salt of styrene-acrylic acid copolymer,
alkylnaphthaline sodium sulfonate, alkyldiphenyl ether sodium
disulfonate, monoethanol amine lauryl sulfate, triethanol amine
lauryl sulfate, ammonium lauryl sulfate, monoethanol amine
stearate, sodium stearate, sodium lauryl sulfate, monoethanol amine
of styrene-acrylic acid copolymer and polyoxyethylene alkylether
phosphate; a nonionic surfactant such as polyoxyethylene oleyl
ether, polyoxyethylene lauryl ether, polyoxyethylene nonylphenyl
ether, polyoxyethylene alkylether phosphate, polyoxyethylene
sorbitan monostearate and polyethyleneglycol monolaurate; a
cationic surfactant such as alkyl quaternary ammonium salt and an
ethylene oxide adduct thereof; an amphoteric surfactant such as
alkyl betaine, e.g. betaine alkyldimethyl aminoacetate and
alkylimidazoline; and a mixture containing two or more of them can
be used, for example.
[0100] The dye derivative is a compound produced by introducing a
substituent into an organic dye. Although the dye derivative is
similar in hue to the pigment used, the hue of the former may be
different from that of the latter if the loading thereof is small.
Note that the term "organic dye" includes aromatic polycyclic
compounds exhibiting a light yellow color such as naphthalene-based
compounds and anthraquinone-based compounds, which are generally
not referred to as "dye", in addition to compounds generally
referred to as "dye". As the dye derivative, those described in
JP-A 63-305173, JP-B 57-15620, JP-B 59-40172, JP-B 63-17102 or JP-B
5-9469 can be used, for example. Especially, the dye derivatives
having a basic group are highly effective in the dispersion of
pigment. The coloring composition may contain a single dye
derivative or a plurality of dye derivatives.
[0101] A storage-stability improver may be added to the coloring
composition in order to improve the temporal stability of its
viscosity. As the storage-stability improver, benzyltrimethyl
chloride; quaternary ammonium chloride such as diethylhydroxy
amine; organic acid such as lactic acid and oxalic acid; methyl
ether of the organic acid; t-butyl pyrocatechol; organic phosphine
such as tetraethyl phosphine and tetraphenyl phosphine; phosphite;
or a mixture containing two or more of them can be used, for
example.
[0102] The storage-stability improver is contained in the coloring
composition at an amount of, for example, 0.1 to 10 parts by mass
with respect to 100 parts by mass of the pigment.
[0103] To the coloring composition, an adhesion improver such as
silane coupling agent may be added in order to improve the adhesion
to the substrate.
[0104] As the silane coupling agent, vinyl silane such as vinyl
tris(.beta.-methoxyethoxy)silane, vinylethoxy silane and
vinyltrimethoxy silane; acrylsilane and metacrylsilane such as
.gamma.-methacryloxypropyl trimethoxy silane; epoxy silane such as
.beta.-(3,4-epoxycyclohexyl)ethyltrimethoxy silane,
.beta.-(3,4-epoxycyclohexyl)methyltrimethoxy silane,
.beta.-(3,4-epoxycyclohexyl)ethyltriethoxy silane,
.beta.-(3,4-epoxycyclohexyl)methyltriethoxy silane,
.gamma.-glycidoxypropyl trimethoxy silane and
.gamma.-glycidoxypropyl triethoxy silane; amino silane such as
N-.beta.(aminoethyl) .gamma.-aminopropyl trimethoxy silane,
N-.beta.(aminoethyl) .gamma.-aminopropyl triethoxy silane,
N-.beta.(aminoethyl) .gamma.-aminopropyl methyldiethoxy silane,
.gamma.-aminopropyl triethoxy silane, .gamma.-aminopropyl
trimethoxy silane, N-phenyl-.gamma.-aminopropyl trimethoxy silane
and N-phenyl-.gamma.-aminopropyl triethoxy silane; thiosilane such
as .gamma.-mercaptopropyl trimethoxy silane and
.gamma.-mercaptopropyl triethoxy silane; or a mixture containing
two or more of them can be used, for example.
[0105] The silane coupling agent is contained in the coloring
composition at an amount of, for example, 0.01 to 100 parts by mass
with respect to 100 parts by mass of the pigment.
[0106] The coloring composition can be prepared in the form of a
gravure offset printing ink, a waterless offset printing ink, a
silk screen printing ink, or a solvent developer-type or alkaline
developer-type colored resist. The colored resist is the one that
is obtained by dispersing dye in a composition containing a
thermoplastic resin, thermosetting resin or photosensitive resin, a
monomer, a photo-polymerization initiator and an organic
solvent.
[0107] The pigment is used at an amount of, for example, 5 to 70
parts by mass, preferably 20 to 50 parts by mass with respect to
100 parts by mass of the total solid contents in the coloring
composition. Note that a large part of the remainder of the solid
contents in the coloring layer is the resin binder included in the
pigment carrier.
[0108] Prior to using the coloring composition for forming a film,
particles having a size of 5 .mu.m or more, preferably 1 .mu.m or
more, more preferably 0.5 .mu.m or more may be removed from the
coloring composition using a refiner such as centrifugal separator,
sintered filter and membrane filter.
[0109] Each of the coloring layers 120a to 120c can by formed, for
example, by printing. According to printing, printing using the
coloring composition and drying it thereafter can form each of the
coloring layers 120a to 120c. Therefore, the printing method is low
cost and excellent in mass productivity. Further, since the
printing technique is improved in recent years, printing can form
fine patterns having high dimension accuracy and high
smoothness.
[0110] In the case where printing is used, the coloring composition
should be designed to have a composition that would not cause the
coloring composition to be dried and solidified on the printing
plate or the blanket. Also, in the printing, it is important to
optimize the flowability of the coloring composition in the
printer. Therefore, a dispersing agent or an extender may be added
to the coloring composition so as to adjust the viscosity
thereof.
[0111] Each of the coloring layers 120a to 120c may be formed using
photolithography. According to photolithography, the color filter
layer 120 can be formed with higher accuracy as compared with the
case where printing is utilized.
[0112] In this case, the coloring composition prepared as a solvent
developer-type or alkaline developer-type colored resist is applied
first to the planar body 110. For this application, an application
method such as spray coating, spin coating, slit coating and roll
coating is utilized. The coated film is formed to have a dried
thickness of, for example, 0.2 to 10 .mu.m.
[0113] Next, the coated film is dried. For example a vacuum drier,
a convection oven, an IR oven or a hot plate is used for drying the
coated film. Drying the coated film can be omitted.
[0114] Subsequently, the coated film is irradiated with ultraviolet
rays via a photomask. That is, the coated film is subjected to a
pattern exposure.
[0115] Then, the coated film is immersed in a solvent developer or
an alkaline developer. Alternatively, the coated film is sprayed
with the developer. Thus, soluble portions are removed from the
coated film to obtain the coloring layer 120a as a resist
pattern.
[0116] Further, by the same method as described above, the coloring
layers 120b and 120c are formed in this order. Thus, the color
filter layer 120 is obtained. Note that in this method, a heat
treatment may be executed in order to promote the polymerization of
the colored resists.
[0117] In the photolithography process, for example, an aqueous
solution of sodium carbonate or sodium hydroxide can be used as the
alkaline developer. Alternatively, a liquid containing an organic
alkali such as dimethylbenzyl amine and triethanol amine may be
used as the alkaline developer.
[0118] An additive such as defoaming agent or surfactant may be
added to the developer. A shower developing method, a spray
developing method, a dip developing method or a paddle developing
method may be utilized for developing, for example.
[0119] In order to enhance the sensitivity to light exposure, the
following process may be further executed. That is, after drying
the first coated film of the colored resist, an alkaline-soluble
resin, for example, polyvinyl alcohol or water-soluble acrylic
resin is applied to the first coated film. After drying the second
coated film, the above-described pattern exposure is performed. The
second coated film prevents the polymerization in the first coated
film from being inhibited by oxygen. Therefore, a higher
sensitivity to light exposure can be achieved.
[0120] The color filter layer 120 may be formed by other methods.
For example, it may be formed using an inkjet method, an
electrodeposition method or a transfer method. In the case where
the color filter layer 120 is formed using the inkjet method, each
coloring layer is obtained, for example, by forming a
light-shielding partition wall on the planar body 110 in advance
and injecting an ink from a nozzle toward regions separated by the
light-shielding partition wall. In the case where the color filter
layer 120 is formed using the electrodeposition method, each
coloring layer is obtained, for example, by forming a transparent
conductive layer on the planar body 110 in advance and depositing
the coloring composition on the transparent conductive film
utilizing an electrophoresis of colloidal particles made of the
coloring composition. In the case where the transfer method is
used, the color filter layer 120 is formed on a surface of a
releasable transfer base sheet in advance, and then the color
filter layer 120 is transferred from the base sheet onto the planar
body 110.
[0121] Next, a method for manufacturing the solidified liquid
crystal layer 130 will be described.
[0122] FIGS. 3 and 4 are sectional views schematically showing an
example of a method of forming a solidified liquid crystal
layer.
[0123] The solidified liquid crystal layer 130 is obtained, for
example, by forming a liquid crystal material layer 130' containing
a photo-polymerizing or photo-crosslinking thermotropic liquid
crystal material on the color filter layer 120 and subjecting the
liquid crystal material layer 130' to a pattern exposure and a heat
treatment.
[0124] The liquid crystal material layer 130' can be obtained, for
example, by applying a coating solution, containing a thermotropic
liquid crystal compound and a chiral agent, on the color filter
layer 120 and drying the coated film, if necessary. In the liquid
crystal material layer 130', the mesogens of the thermotropic
liquid crystal compound form a cholesteric alignment structure.
[0125] As the thermotropic liquid crystal compound, alkyl
cyanobiphenyl, alkoxy biphenyl, alkyl terphenyl, phenyl
cyclohexane, biphenyl cyclohexane, phenyl bicyclohexane,
pyrimidine, cyclohexane carboxylic acid ester, halogenated
cyanophenol ester, alkyl benzoic acid ester, alkyl cyanotolane,
dialkoxy tolane, alkyl alkoxy tolane, alkyl cyclohexyl tolane,
alkyl bicyclohexane, cyclohexyl phenyl ethylene, alkyl cyclohexyl
cyclohexene, alkyl benzaldehyde azine, alkenyl benzaldehyde azine,
phenyl naphthalene, phenyl tetrahydronaphtalene, phenyl
decahydronaphthalene, derivatives thereof, acrylates of the
compounds, or methacrylates of the compounds can be used, for
example.
[0126] The chiral agent is a low molecular weight compound having
an optically active moiety, and typical examples thereof have a
molecular weight of 1500 or less. The chiral agent is used for the
purpose of inducing a helical structure in the positive uniaxial
nematic regularity developed by a polymerizable liquid crystal
material exhibiting nematic regularity. As long as the object is
achieved, the type of the chiral agent is not particularly limited.
The chiral agent may be any compound which mixes with the
polymerizable liquid crystal material showing nematic regularity in
a state of solution or melt, and induces a desired helical
structure in the polymerizable liquid crystal material without
impairing the liquid crystallinity of the material.
[0127] The chiral agent must have some chirality in its molecule,
because it is used for inducing a helical structure in the liquid
crystal. Accordingly, the chiral agent used herein is preferably,
for example, a compound having one or more asymmetric carbons, a
compound having an asymmetric point on the hetero atom such as a
chiral amine or sulfoxide, or a compound having an optically active
moiety with axial asymmetry, such as cumulene or binaphthol.
Specific examples include commercially available chiral nematic
liquid crystals such as Paliocolor LC 756 (manufactured by BASF),
or a chiral dopant liquid crystal S-811 (manufactured by Merck
Ltd.).
[0128] Since the solidified liquid crystal layer 130 of the present
invention is required to have high transparency in the visible
region, the chiral agent is added in an amount such that the
helical pitch of the liquid crystal material layer 130' is short
and the wavelength of the selective reflection is about 400 nm or
less. The specific content of the chiral agent may be 2 to 50 parts
by weight based on the thermotropic liquid crystal compound,
depending on the type of the thermotropic liquid crystal compound
or the distortion inducing force of the chiral agent.
[0129] The coating solution may contain a photo-polymerization
initiator.
[0130] As the photo-polymerization initiator, dichroic
photo-polymerization initiator may be used. Examples of the
photo-polymerization initiator include biphenylcyclohexane
derivatives represented by the following chemical formula. Such a
dichroic photo-polymerization initiator is desirable from the
viewpoint that it tends to induce the immobilization of a
thermotropic liquid crystal compound orientated in a specific
direction in the plane in the exposure process which will be
described later and a solidified liquid crystal layer 130 having
large in-plane anisotropy is easily obtained.
##STR00001##
[0131] The photo-polymerization initiator unnecessarily has
dichroism. For example, as the photo-polymerization initiator, the
same compounds (hereinafter referred to as "other
photo-polymerization initiators") as those used for the above
coloring composition may be used. Even if other
photo-polymerization initiators are used without adding the
dichroic photo-polymerization initiator to the coating solution, or
any photo-polymerization initiator is not used, a retardation plate
10 according to this embodiment can be obtained. This reason is
presumed that the photo-polymerizing or photo-crosslinking
thermotropic liquid crystal material itself has anisotropy to
photoreaction. The aforementioned other photo-polymerization
initiators are desirable from the viewpoint that it tends to induce
more exact immobilization in a small dose of light in the
developing process which will be described later because it has
high sensitivity and therefore, strong solidified liquid crystal
layer 130 is easily obtained.
[0132] As the photo-polymerization initiator, any one of the above
dichroic photo-polymerization initiators and the other
photo-polymerization initiators or a mixture of two or more of
these photo-polymerization initiators may be added. The content of
the photo-polymerization initiator is preferably 0.1 to 30 parts by
weight and more preferably 0.3 to 10 parts by weight based on 100
parts by weight of the liquid crystal compound in the coating
solution.
[0133] A sensitizer may be used in combination with the
photo-polymerization initiator. As the sensitizer, the same
compounds as those used for the above coloring composition may be
used. The sensitizer may be contained in an amount of 0.1 to 60
parts by weight based on 100 parts by weight of the
photo-polymerization initiator.
[0134] A solvent may be added to the coating solution.
[0135] As the solvent, the same compounds as those used for the
above coloring composition may be used. The solvent may be used in
an amount of 100 to 3000 parts by weight and preferably 200 to 1000
parts by weight based on 100 parts by weight of the liquid crystal
compound in the coating solution.
[0136] A thermal polymerization initiator, a polymerization
inhibitor, a surfactant, a resin, a polyfunctional monomer and/or
oligomer, a chain transfer agent and a storage-stability improver
and an adhesion improver may be added to the coating solution in
each appropriate amount.
[0137] As the thermal polymerization initiator, for example,
peroxide initiators such as benzoyl peroxide (BPO),
t-butylperoxy-2-ethylhexanate (PBO), di-t-butyl peroxide (PBD),
t-butyl-peroxyisopropyl carbonate (PBI) and
n-butyl-4,4'-bis(t-butylperoxy)varelate (PHV); and azo type
initiators such as 2,2'-azobisisobutyronitrile,
2,2'-azobis(2-methylbutyronitrile),
1,1'-azobis(cyclohexane-1-carbonitrile),
2,2'-azobis(2-methylpropane), 2,2'-azobis(2-methylbutane),
2,2'-azobis(2-methylpentane), 2,2'-azobis(2,3-dimethylbutane),
2,2'-azobis(2-methylhexane), 2,2'-azobis(2,4-dimethylpentane),
2,2'-azobis(2,3,3-trimethylbutane),
2,2'-azobis(2,4,4-trimethylpentane), 3,3-azobis(3-methylpentane),
3,3'-azobis(3-methylhexane), 3,3'-azobis(3,4-dimethylpentane),
3,3'-azobis(3-ethylpentane),
dimethyl-2,2'-azobis(2-methylpropionate),
diethyl-2,2'-azobis(2-methylpropionate) and
di-tert-butyl-2,2'-azobis(2-methylpropionate) may be used.
[0138] As the polymerization inhibitor, for example, phenol-based
inhibitors such as 2,6-di-t-butyl-p-cresol,
3-t-butyl-4-hydroxyanisole, 2-t-butyl-4-hydroxyanisole,
2,2'-methylenebis(4-methyl-6-t-butylphenol),
2,2'-methylenebis(4-ethyl-6-t-butylphenol),
4,4'-butylidenebis(3-methyl-6-t-butylphenol),
4,4'-thiobis(3-methyl-6-t-butylphenol), styrenated phenol,
styrenated p-cresol,
1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenyl)butane,
tetrakis[methylene-3-(3',5'-di-1-butyl-4'-hydroxyphenyl)propionate]methan-
e, octadecyl 3-(3,5-di-t-butyl-4-hydroxyphenylpropionate),
1,3,5-trimethyl-2,4,6-tris(3,5-di-t-butyl-4-hydroxybenzyl)benzene,
2,2'-dihydroxy-3,3'-di(.alpha.-methylcyclohexyl)-5,5'-dimethyldiphenylmet-
hane, 4,4'-methylenebis(2,6-di-t-butylphenol),
tris(3,5-di-t-butyl-4-hydroxyphenyl)isocyanurate,
1,3,5-tris(3',5'-di-t-butyl-4-hydroxybenzoyl)isocyanurate,
bis[2-methyl-4-(3-n-alkylthiopropionyloxy)-5-t-butylphenyl]sulfide,
1-oxy-3-methyl-isopropylbenzene, 2,5-di-t-butylhydroquinone,
2,2'-methylenebis(4-methyl-6-nonylphenol), alkylated bisphenol,
2,5-di-t-amylhydroquinone, polybutylated Bisphenol A, Bisphenol A,
2,6-di-t-butyl-p-ethylphenol,
2,6-bis(2'-hydroxy-3-t-butyl-5'-methyl-benzyl)-4-methylphenol,
1,3,5-tris(4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate,
terephthaloyl-di(2,6-dimethyl-4-t-butyl-3-hydroxybenzyl sulfide),
2,6-di-t-butylphenol,
2,6-di-t-butyl-.alpha.-dimethylamino-p-cresol,
2,2'-methylene-bis(4-methyl-6-cyclohexylphenol), triethylene
glycol-bis[3-(3-t-butyl-5-methyl-4-hydroxyphenyl)propionate],
hexamethylene glycol-bis(3,5-di-t-butyl-4-hydroxyphenyl)propionate,
3,5-di-t-butyl-4-hydroxytoluene,
6-(4-hydroxy-3,5-di-t-butylaniline)-2,4-bis(octylthio)-1,3,5-triazine,
N,N'-hexamethylenebis(3,5-di-t-butyl-4-hydroxy-hydrocyamide),
diethyl 3,5-di-t-butyl-4-hydroxybenzyl-phosphate,
2,4-dimethyl-6-t-butylphenol,
4,4'-methylenebis(2,6-di-t-butylphenol),
4,4'-thiobis(2-methyl-6-t-butylphenol),
tris[.beta.-(3,5-di-t-butyl-4-hydroxyphenyl)propionyl-oxyethyl]
isocyanurate, 2,4,6-tributylphenol, glycol
bis[3,3-bis(4'-hydroxy-3'-t-butylphenyl)-butylate],
4-hydroxymethyl-2,6-di-t-butylphenol and
bis(3-methyl-4-hydroxy-5-t-butylbenzyl)sulfide can be used.
[0139] Also, as the polymerization inhibitor, amine-based
inhibitors such as N-phenyl-N'-isopropyl-p-phenylenediamine,
N-phenyl-N'-(1,3-dimethylbutyl)-p-phenylenediamine,
N,N'-diphenyl-p-phenylenediamine,
2,2,4-trimethyl-1,2-dihydroquinoline polymer and
diaryl-p-phenylenediamine; sulfur-based inhibitors such as
dilauryl-thiodipropionate, distearyl-thiodipropionate and
2-mercaptobenzimidanol; and phosphorous-based inhibitors such as
distearylpentaerythritol diphosphite can be used.
[0140] As the surfactant, resin, polyfunctional monomer and/or
oligomer, chain transfer agent, storage-stability improver and
adhesion improver and the like, the same compounds as those used in
the above coloring composition can be used.
[0141] For applying the coating solution, a printing method such as
spin coating, slit coating, relief printing, screen printing,
planographic printing, reverse printing and gravure printing; the
printing method incorporated into an offset system; an inkjet
method; or bar coat method can be used, for example.
[0142] The liquid crystal material layer 130' is formed, for
example, as a continuous layer having a uniform thickness.
According to the method described above, the liquid crystal
material layer 130' can be formed as a continuous film having a
uniform thickness as long as the surface to be coated is
sufficiently flat.
[0143] Prior to the application of the coating solution, the
surface of the color filter layer 120 may be subjected to an
alignment process such as rubbing process. Alternatively, prior to
the application of the coating solution, an alignment layer for
regulating the orientation of the liquid crystal compound may be
formed on the color filter layer 120. Forming a transparent layer
of resin such as polyimide on the color filter layer 120 and
subjecting the transparent resin layer to an alignment process such
as rubbing process can obtain the alignment layer, for example. The
alignment layer may be formed using a photo-alignment
technique.
[0144] In the liquid crystal material layer 130', the mesogen of
the thermotropic liquid crystal compound is oriented to have a
cholesteric structure. Depending on the case, a dichroic
photo-polymerization initiator is orientated to exhibit a
cholesteric structure together with the mesogens. Therefore,
irradiation of the liquid crystal material layer 130' with
unpolarized light and polarized light achieves polymerization,
i.e., crosslinking, with desired proportions and desired degrees of
anisotropy. In other words, the thermotropic liquid crystal
compound is heterogeneously polymerized or crosslinked.
[0145] The liquid crystal material layer 130' obtained in the above
manner is subjected to an exposure process. That is, as shown in
FIG. 3, a plurality of regions of the liquid crystal material layer
130' are subjected to pattern exposure. Pattern exposure light L1
is composed of a combination of polarized light and unpolarized
parallel light, and the condition of the polarized light and the
condition of the unpolarized parallel light differ with regions.
Either of the polarized light and unpolarized parallel light may be
applied first. Also, the light L1 applied to some regions may be
one light, and some regions may not be irradiated with any type of
light.
[0146] The above description "difference in the condition of the
irradiation with unpolarized parallel light" means that there is a
difference in any one of exposure time, illuminance, emission line
and the like or in combinations of these conditions. Usually, light
is applied in such a manner that different irradiation energy, that
is, a different exposure value of light is applied to each region.
However, reciprocity natures are observed though depending on the
type of material. In this case, it is not always necessary to use a
different exposure value of light. For example, light may be
applied to one region at high luminance for a short time and to
another region at low luminance for a long time, with the result
that the exposure values of light (illuminance.times.exposure time)
of the both regions are equal to each other.
[0147] The condition of the polarized light irradiation includes
the ellipticity and extinction ratio of the polarized light. The
above description "difference in the irradiation with the polarized
light" means that there is a difference in any one of the
ellipticity and extinction of the polarized light or combinations
of these conditions in addition to the conditions changed in the
above irradiation with the unpolarized parallel light. Usually,
light is applied in such a manner that a different exposure value
of light is applied to each region. However, the condition of the
polarized light is the same as that of the unpolarized parallel
light in the point that it is not always necessary to use a
different exposure value of light. Examples of the light to be used
in the case of the irradiation with the polarized light include
linearly polarized light and elliptically polarized light. Although
the ellipticity and extinction ratio may be selected as the
conditions which are to be changed as described above, it is simple
to use linearly polarized light and to fix the extinction ratio,
while changing other conditions.
[0148] The following descriptions will be furnished as to the case
of using a different exposure value in each area and using linearly
polarized light for the irradiation with the polarized light.
[0149] For example, on the liquid crystal material layer 130', the
region 130a' corresponding to the region 130a is irradiated with a
sufficient exposure value of unpolarized parallel light alone as
the light L1. On the liquid crystal material layer 130', the region
130b' corresponding to the region 130b is irradiated with a
sufficient exposure value of linearly polarized light as the light
L1. On the liquid crystal material layer 130', no light is applied
to the region 130c' corresponding to the region 130c.
[0150] In the liquid crystal material layer 130', the cholesteric
orientation state formed by the mesogen is immobilized according to
the type and exposure value of the irradiated light L1, whereby the
thermotropic liquid crystal compound is polymerized or crosslinked.
In the polymerized or crosslinked product of the thermotropic
liquid crystal compound, the mesogenic groups lose their
flowability, whereby the orientation variation in the subsequent
process is prevented.
[0151] For example, in the region 130a' irradiated with a
sufficient exposure value of unpolarized parallel light alone as
the light L1, the cholesteric orientation state of the mesogen is
immobilized with the state generally maintained. The content of the
polymerized or crosslinked product of the thermotropic liquid
crystal compound wherein the mesogenic groups are in the
cholesteric orientation state is the highest, and the content of
the unpolymerized and uncrosslinked thermotropic liquid crystal
compound is the smallest.
[0152] In region 130b' irradiated with a sufficient exposure value
of linearly polarized light alone as the light L1, mesogens
orientated in a specific azimuth in the plane corresponding to the
polarization axis among the mesogens forming a cholesteric
alignment structure are immobilized while the orientation state is
maintained. On the other hand, those orientated in other azimuths
are not immobilized and still has flowability, though the state of
the orientation is unchanged. In comparison with the region 130a',
the polymerized and/or crosslinked product of the thermotropic
liquid crystal compound having a immobilized orientation state is
present, but the proportion is tilted toward those having mesogenic
groups oriented in a specific direction. Therefore, as a whole, the
content of the unpolymerized or uncrosslinked thermotropic liquid
crystal compound is higher.
[0153] The light used in the exposure process is electromagnetic
waves such as ultraviolet rays, visible rays and infrared rays.
More specifically, ultraviolet rays including light having a
wavelength of 180 to 400 nm are typically used.
[0154] The exposure process may be performed by any method as long
as the above-described nonuniform polymerization or crosslinking
can be caused.
[0155] For example, the exposure process may include exposure
operations using photomasks having different patterns of the light
shielding layers. For example, the region 130a' is selectively
irradiated with a maximum exposure value of unpolarized parallel
light as the light L1 through a certain photomask, and the region
130b' is selectively irradiated with a maximum exposure value of
linearly polarized light as the light L1 through a photomask
different from the above one.
[0156] Alternatively, the exposure process may include exposure of
the region 130a' through a certain photomask, and exposure of the
region 130b' through the same photomask. In this case, for example,
the region 130a' is irradiated with a maximum exposure value of
unpolarized parallel light as the light L1 through a certain
photomask. Using the photomask, the region 130b is irradiated with
a maximum exposure value of linearly polarized light as the light
L1.
[0157] Alternatively, operations such as an operation of scanning
the liquid crystal material layer 130' by a luminous flux instead
of using a photomask may be performed.
[0158] Alternatively, the above-described methods may be combined.
Irrespective of which method is used for the first exposure
process, in the exposure process, the degree of polymerization or
the degree of polymerization anisotropy of the thermotropic liquid
crystal compound in the liquid crystal material layer 130' is
formed into a so-called "latent image".
[0159] After completing the exposure process, a developing process
is performed. That is, the liquid crystal material layer 130' is
heated to a temperature equal to or higher than the phase
transition temperature at which the thermotropic liquid crystal
compound changes from a liquid crystal phase to an isotropic phase.
As a result of the heating process, the "latent image" formed in
the above-described exposure process develops as a change of the
orientation state of the mesogen.
[0160] Details are as follows. The mesogen moiety of the
thermotropic liquid crystal compound as an unreacted compound is
not immobilized. Therefore, when the liquid crystal material layer
130' is heated to the phase transition temperature or higher, the
orientation of the mesogen of the unreacted compound is lowered.
For example, the mesogen of the unreacted compound changes from the
liquid crystal phase to the isotropic phase. On the other hand, the
mesogen of the polymerized or crosslinked product of the
thermotropic liquid crystal compound are immobilized.
[0161] Accordingly, as shown in FIG. 4, in the region 130a'
irradiated with a sufficient exposure value of unpolarized parallel
light alone as the light L1, the orientation state of the mesogen
MS is hardly changed by the heat treatment. The orientation state
is immobilized with the cholesteric orientation maintained. As a
result of this, a negative C-plate is obtained.
[0162] The orientation of the mesogen MS orientated in a specific
azimuth in the plane corresponding to the polarization axis in
region 130b' irradiated with a sufficient exposure value of
linearly polarized light as the light L1 is kept in a immobilized
state whereas the mesogen MS orientated in other azimuths are
disordered. That is, anisotropic orientational disorder arises. As
a result of this, the region 130b' develops a biaxiality composed
of a positive A-plate and a negative C-plate, and thus having both
of the in-plane retardation and the thickness direction
retardation. In the region 130c', to which no light is applied
before heating, the orientation structure of the mesogen MS
disappears upon heat treatment. As shown in the figure, in the
region 130c', the cholesteric orientation of the mesogen MS is
almost completely disordered to give an isotropic phase.
[0163] The exposure value of linearly polarized light, the exposure
value of unpolarized parallel light, the ratio of exposure values
of linearly polarized light and unpolarized parallel light and the
like are changed to perform the exposure process, and then, the
developing process is performed, thereby enabling optional control
of the orientation state of the mesogens MS in each of the
plurality of regions of the liquid crystal material layer 130'. One
example of these process will be described with reference to FIGS.
5 and 6.
[0164] FIG. 5 shows the liquid crystal material layer 130'
containing the regions 130a' to 130f'. As described above, the
regions 130a' to 130c' are irradiated with different types of the
light L1, and the regions 130d' to 130f' are also irradiated with
different types of the light L1.
[0165] The region 130c' is not irradiated with the light L1, and
the region 130a' is irradiated with a sufficient exposure value of
unpolarized parallel light as the light L1. The region 130d' is
irradiated with unpolarized parallel light as the light L1 with a
smaller exposure value than the region 130a'.
[0166] The region 130b' is irradiated with a sufficient exposure
value of linearly polarized light as the light L1, and the region
130e' is irradiated with linearly polarized light as the light L1
with a smaller exposure value than the region 130b'. Further, the
region 130f' is irradiated with unpolarized parallel light and
linearly polarized light as the light L1 with smaller exposure
values than the regions 130a' and 130b', respectively.
[0167] The sufficient exposure value of the unpolarized parallel
light refers to an exposure value by which the major portion of the
thermotropic liquid crystal compound is substantially polymerized
or crosslinked. Even if the light is applied with an exposure value
over the sufficient exposure value, no difference is found in the
orientation state in the subsequent first heat treatment process.
The sufficient exposure value of the linearly polarized light
refers to an exposure value by which the anisotropy of the
polymerizing or crosslinking the thermotropic liquid crystal
compound is maximized. In principle, when the quenching ratio of
the linearly polarized light is infinite, even if the light is
applied with an exposure value over the sufficient exposure value,
no difference is found in the orientation state in the subsequent
first heat treatment process.
[0168] In general cases, the quenching ratio of linearly polarized
light is finite, and the in-plane retardation gradually decreases
when the light is continuously applied with an exposure value over
the sufficient exposure value. When the exposure value is in such a
range, the thickness direction retardation cannot be controlled.
The present invention requires the differences in the in-plane
retardation and the thickness direction retardation, and thus does
not use the exposure value in the above range.
[0169] A specific value cannot be given for the sufficient exposure
value because it markedly varies depending on the type of the
thermotropic liquid crystal compound, the type and amount of the
photo-polymerization initiator, the presence or absence, type, and
amount of other additives, and the type and intensity of the
irradiated light. In typical cases, a sufficient exposure value is
about 200 mJ/cm.sup.2 to 1000 mJ/cm.sup.2. For example, when a
luminous flux of 20 mW/cm.sup.2 is used, sufficient exposure is
achieved with irradiation for about 10 to 100 seconds.
[0170] If the above-described sufficient exposure value is not
reached, the exposure value is insufficient, but the degree of
immobilization of the orientation by the light is not necessarily
proportional to the exposure value. The immobilization often
markedly proceeds with a small exposure value. For example, even if
the exposure value is half the sufficient exposure value, over half
of the orientation is immobilized. In order to achieve a
significant difference from the region irradiated with a sufficient
exposure value, the desirable exposure value may be markedly
smaller than the sufficient exposure value. More specifically, an
insufficient exposure value is about 2 mJ/cm.sup.2 to 180
mJ/cm.sup.2. For example, when a luminous flux of 20 mW/cm.sup.2 is
used, the exposure is insufficient when the irradiation time is
about 0.1 to 9 seconds.
[0171] FIG. 6 shows the result of the above-described heating
process performed after the completion of the exposure process
through the irradiation of the light L1.
[0172] In the region 130d' which has been irradiated with an
insufficient exposure value of unpolarized parallel light as the
light L1, the orientation of the uncured component, which remains
due to the insufficient exposure value, is disordered to give a
poorly orientated state. A negative C-plate is obtained owing to
the irradiation with the unpolarized parallel light, but the
thickness direction retardation is smaller than that in the region
130a.
[0173] In region 130e' irradiated with insufficient and linearly
polarized light as light L1, the in-plane retardation and thickness
direction retardation are both less than those of region 130b'.
However, biaxiality composed of a positive A-plate and a negative
C-plate is exhibited in the same manner as in the region 130b'.
[0174] In the region 130f' which has been irradiated with an
insufficient exposure value of linearly polarized light and an
insufficient exposure value of unpolarized parallel light as the
light L1, the nature of the orientation varies depending on the
exposure value ratio between the linearly polarized light and
unpolarized parallel light, and the total exposure value. More
specifically, the nature of the orientation obtained in the region
130a' and the nature of the orientation obtained in the region
130b' are developed, whereby biaxiality composed of an A-plate and
a negative C-plate is exhibited. However, the in-plane retardation
of this area 130f' is less than that of area 130b'. In other words,
The Nz coefficient is greater than in the region 130b'.
[0175] The exposure process may be performed by the above-described
method. When a halftone mask is used in the exposure process, the
exposure values of the linearly polarized light and unpolarized
parallel light applied to the respective regions may be controlled
as desired. The halftone mask has a light shielding layer at a
position corresponding to a specific region, and a
semi-transmissive layer at a position corresponding to another
region. Instead of the halftone mask, a gray-tone mask or a
wavelength-limiting mask may be used. The gray-tone mask has the
same structure as that of the halftone mask except that the
semitransparent layer is omitted, and it includes a plurality of
slits in the light-shielding layer in width equal to or smaller
than the resolution of the light-exposure apparatus. The
light-limiting mask includes portions different in wavelength range
of light allowed to pass through.
[0176] As explained about the region 130f', the desired biaxiality
is obtained through the appropriate selection of the exposure value
ratio between linearly polarized light and unpolarized parallel
light and their total exposure value. That is, the Nz coefficient
may be freely established.
[0177] The same effect is obtained not only in the case of using a
combination of the linearly polarized light and unpolarized
parallel light but also in the case of irradiating linearly
polarized lights differing in extinction ratio. When, for example,
linearly polarized light having an extinction ratio of 2:1 is
irradiated, this almost corresponds to the case where the
irradiation value of linearly polarized light (infinite extinction
ratio) is equal to the irradiation value of unpolarized parallel
light. When linearly polarized light having an extinction ratio
greater than 2:1 is irradiated, this corresponds to the case where
the irradiation value of linearly polarized light is greater than
the irradiation value of unpolarized parallel light.
[0178] The same effect is also obtained not only in the case of
using a combination of the linearly polarized light and unpolarized
parallel light, but also in the case of irradiating elliptically
polarized light differing in ellipticity. For example, when
elliptically polarized light having an ellipticity of 2 is
irradiated, this corresponds to the case where the irradiation
value of linearly polarized light having an infinite extinction
ratio is almost equal to the irradiation value of unpolarized
parallel light. Also, elliptically polarized light having an
ellipticity of greater than 2 is irradiated, this corresponds to
the case where the irradiation value of linearly polarized light is
greater than the irradiation value of unpolarized parallel
light.
[0179] Furthermore, light L1 may be obtained by combining the above
approaches. For example, the linearly polarized light differing in
extinction ratio may be combined with the unpolarized parallel
light, or the elliptically polarized light differing in ellipticity
may be combined with the unpolarized parallel light to make each
combination light L1.
[0180] In the process of irradiation with linearly polarized light
or elliptically polarized light, the axial direction of the
polarized light applied to at least one region may be different
from that of the polarized light applied to other region. As a
result of this, in the subsequent developing process, the axial
direction in the plane in which the refractive index reaches peak
is different from that of the other region, corresponding to the
azimuth of polarization axis of the linearly or elliptically
polarized light.
[0181] As shown in FIG. 4, after different orientation states are
established in the respective regions, a fixing process is
performed to polymerize and/or crosslink unreacted compounds, with
the orientation state of the mesogen of the unreacted compound
maintained.
[0182] For example, as shown in FIG. 7, light L2 is applied over
the entire liquid crystal material layer 130', with the liquid
crystal material layer 130' kept at a temperature higher than the
phase transition temperature at which the thermotropic liquid
crystal compound changes from an isotropic phase to a liquid
crystal phase.
[0183] The liquid crystal material layer 130' is irradiated with
the light L2 with an exposure value sufficient for causing the
polymerization and/or crosslinking reaction of almost all of the
unreacted compound. As a result of this, the unreacted compound is
polymerized or crosslinked, and the mesogen having a changed
orientation state is immobilized. In this manner, the solidified
liquid crystal layer 130 is obtained.
[0184] In a liquid crystal compound, the first phase transition
temperature at which the compound changes from an isotropic phase
to a liquid crystal phase is lower than the second phase transition
temperature at which the compound changes from a liquid crystal
phase to an isotropic phase. Therefore, in a particular case, the
temperature of the liquid crystal material layer 130' in the fixing
process may be lower than the heating temperature in the developing
process. In normal cases, in consideration of convenience, the
temperature of the liquid crystal material layer 130' in the fixing
process is equal to or higher than the first phase transition
temperature.
[0185] The light L2 may be polarized light, but unpolarized light
is usually preferred from the viewpoint of convenience.
[0186] In the fixing process, the entire surface of the liquid
crystal material layer 130' may be irradiated with a uniform
exposure value. In this case, the use of a photomask having a fine
pattern is not necessary. As a result of this, the process is
simplified.
[0187] The fixing process may be performed by another methods.
[0188] For example, when the unreacted compound, or the
thermotropic liquid crystal compound is a material which is
polymerized and/or crosslinked by heating to a polymerization
and/or crosslinking temperature higher than the first phase
transition temperature, heating process may be performed in place
of applying light. More specifically, in place of applying light,
the liquid crystal material layer 130' is heated to a temperature
equal to or higher than the polymerization and/or crosslinking
temperature, thereby polymerizing and/or crosslinking the unreacted
compound. As a result of this, the solidified liquid crystal layer
130 is obtained. The heating temperature in the developing process
is, for example, equal to or higher than the first phase transition
temperature, and below the polymerization and/or crosslinking
temperature.
[0189] Alternatively, in the fixing process, the irradiation with
light and heating may be performed out sequentially. Such a
combination of light and heat can progress the polymerizing and/or
crosslinking the unreacted compound more exactly. As a result of
this, the solidified liquid crystal layer 130 has a greater
strength.
[0190] In the case where, for example, the unreacted compound is a
material which is polymerized and/or crosslinked by heating it to a
certain temperature, the heating temperature in the developing
process may be equal to or higher than the polymerization
temperature and/or crosslinking temperature of the compound. That
is, the developing process and the fixing process may be performed
simultaneously. However, in this case, the occurrence of
orientational disorder and the polymerization and/or crosslinking
progress at the same time. Therefore, the production conditions
affect the optical characteristics of the solidified liquid crystal
layer 130 relatively greatly.
[0191] As described with reference to FIGS. 3 and 4, a retardation
pattern is formed without a wet process in the retardation plate of
the present invention. In order to form the pattern by a wet
process, a liquid such as a solvent or an aqueous alkaline
solution, which has the capability to dissolve the liquid crystal
material layer is used. For example, the liquid crystal material
layer is dipped in this liquid or the liquid is sprayed on the
liquid crystal material layer by a spray or the like to remove an
uncured part, thereby forming a pattern. In such a wet process, the
conditions of the process have a significantly large influence on
the optical characteristics of a final product. For this reason,
according to the method including a wet process, deviations of the
optical properties from the target values prone to occur.
[0192] On the other hand, in the method of the present invention,
no wet process is performed in the first exposure process or later.
Therefore, it is possible to prevent the deviation of the
refractive index anisotropy from the target value due to the wet
process.
[0193] Note that the refractive index anisotropy and the exposure
value in the exposure process are not always in a proportional
relation. However, under the conditions in which materials and the
exposure values are unchanged, the reproducibility of the
refractive index anisotropy is high. Therefore, the conditions, for
example, an exposure value necessary for achieving certain
refractive index anisotropy can be found out easily, and a stable
manufacture can be done easily.
[0194] Various modifications can be made to the retardation plate
10 described with reference to FIGS. 1 to 4 and 7, i.e., a panel
substrate.
[0195] In the retardation plate 10, the solidified liquid crystal
layer 130 includes the regions 130a to 130c different in refractive
index anisotropy. The solidified liquid crystal layer 130 may
further include one or more regions different in refractive index
anisotropy from the regions 130a to 130c. For example, in a
semi-transparent liquid crystal display, each of the red, green and
blue pixels includes a transmissive portion and a reflective
portion. The transmissive portion and the reflective portion need
to be designed separately. Therefore, each of the portions of the
solidified liquid crystal layer 130 that correspond to the red,
green and blue pixels may include two or more regions different in
refractive index anisotropy from each other.
[0196] Also, the color filter layer 120 may include black partition
walls besides the aforementioned coloring layers. The black
partition walls are formed in such a manner as to divide coloring
layers 120a to 120c from one another.
[0197] The color filter layer 120 may be omitted from the
retardation plate 10. For example, in a liquid crystal display, one
of the substrates may include both a color filter layer and a
retardation layer. Alternatively, it is possible that one substrate
of a liquid crystal display includes a color filter layer and the
other substrate includes a retardation layer. In the latter case,
it is not necessary that the retardation plate 10 includes the
color filter layer 120. However, in the case where the retardation
plate 10 includes both the color filter layer 120 and the
solidified liquid crystal layer 130, an alignment between the color
filter layer 120 and the solidified is unnecessary when bonding
them together.
[0198] The solidified liquid crystal layer 130 may be interposed
between the planar body 110 and the color filter layer 120.
[0199] FIG. 8 is a sectional view schematically showing a
retardation plate according to a modified example. This retardation
plate 10 is the same as the retardation plate 10 described with
reference to FIGS. 1 to 4 except that the solidified liquid crystal
layer 130 is interposed between the planar body 110 and the color
filter layer 120.
[0200] In the case where such a structure is employed, for example,
in a liquid crystal display including the retardation plate 10, the
solidified liquid crystal layer 130 does not suppress the inclusion
of impurities from the color filter layer 120 into the liquid
crystal layer. However, in the case where this structure is
employed, there is no possibility that the color filter layer 120
is subjected to the exposure process and the heat treatment process
for forming the solidified liquid crystal layer 130. Therefore, in
the case where such a structure is employed, deteriorations of the
color filter layer 120 due to the light in the above exposure
process and by the heat in the above developing process and fixing
process are less prone to occur as compared with the case where the
structure shown in FIGS. 1 and 2 is employed.
[0201] Also, when this structure is adopted, the solidified liquid
crystal layer 130 can be formed on the planar body 110. Therefore,
the solidified liquid crystal layer 130 having performance
according to the design can be obtained more easily as compared
with the case of forming the solidified liquid crystal layer 130 on
the color filter layer 120 which is scarcely formed as a perfect
plane.
[0202] Typically, the solidified liquid crystal layer 130 has a
uniform thickness. However, in particular cases, the regions 130a
to 130c of the solidified liquid crystal layer 130 can be different
in thickness from one another.
[0203] Any of the aforementioned retardation plates 10 may be used
in various applications. For example, the retardation plate 10 may
be utilized for display technologies typified by liquid display
technologies.
[0204] FIG. 9 is a sectional view schematically showing an example
of a liquid crystal display that can be manufactured using the
retardation plate shown in FIGS. 1 and 2.
[0205] The liquid crystal display shown in FIG. 9 is a transmissive
liquid crystal display employing an active matrix driving method.
The liquid crystal display includes a color filter substrate 10',
an array substrate 20, a liquid crystal layer 30, a pair of
polarizing plates 40, and a backlight (not shown).
[0206] The color filter substrate 10' includes the retardation
plate 10 described above, a counter electrode 150, and an alignment
layer 160.
[0207] The counter electrode 150 is formed on the solidified liquid
crystal layer 130. It is a continuous film extending over the
display area. The counter electrode 150 is made of the
above-described transparent conductor, for example.
[0208] The alignment layer 160 covers the counter electrode 150.
Forming a transparent layer of resin such as polyimide on the
counter electrode 150 and subjecting the transparent resin layer to
an alignment process such as rubbing process can obtain the
alignment layer 160, for example. The alignment layer 160 may be
formed using a photo-alignment technique.
[0209] The array substrate 20 includes a substrate 210 facing the
alignment layer 160. The substrate 210 is a light-transmitting
substrate such as glass plate or resin plate.
[0210] On the surface of the substrate 210 facing the alignment
layer 160, pixel circuits (not shown), scanning lines (not shown),
signal lines (not shown), and pixel electrodes 250 are arranged.
The pixel circuits each includes a switching device such as
thin-film transistor and are arranged in a matrix on the substrate.
The scanning lines are arranged correspondingly with the rows of
the pixel circuits. The operation of each pixel circuit is
controlled by a scanning signal supplied via the scanning line. The
signal lines are arranged correspondingly with the columns of the
pixel circuits. Each pixel electrode 250 is connected to the signal
line via the pixel circuit. Each pixel electrode 250 faces one of
the coloring layers 120a to 120c.
[0211] The pixel electrodes 250 are covered with an alignment layer
260. Forming a transparent layer of resin such as polyimide on the
pixel electrode 250 and subjecting the transparent resin layer to
an alignment process such as rubbing process can obtain the
alignment layer 260, for example. The alignment layer 260 may be
formed using a photo-alignment technique.
[0212] The color filter substrate 10' and the array substrate 20
are bonded together via a frame-shaped adhesive layer (not shown).
The color filter substrate 10', the array substrate 20 and the
adhesive layer form a hollow structure.
[0213] The liquid crystal layer 30 is made of a liquid crystal
compound or a liquid crystal composition.
[0214] The liquid crystal compound or the liquid crystal
composition has flowability and fills the space enclosed with the
color filter substrate 10', the array substrate 20 and the adhesive
layer. The color filer substrate 10', the array substrate 20, the
adhesive layer and the liquid crystal layer 30 form a liquid
crystal cell.
[0215] The polarizing plates 40 are adhered to the main surfaces of
the liquid crystal cell. The polarizing plates 40 are arranged such
that their transmission axes intersect orthogonally, for
example.
[0216] In the liquid crystal display, the regions 130a to 130c of
the solidified liquid crystal layer 130 are almost equal in
thickness to one another and are different in refractive index
anisotropy from one another. Accordingly, it is possible to
optimize the refractive index anisotropy of each of the regions
130a to 130c so as to achieve an ideal optical compensation for
each of red, green and blue colors.
[0217] As described above, the retardation plate 10 can be used in
a transmissive liquid crystal display employing an active matrix
driving method. The retardation plate 10 can be used in other
displays.
[0218] For example, the retardation plate 10 may be used in a
semi-transparent liquid crystal display or a reflective liquid
crystal display. Also, driving methods other than an active matrix
driving method such as passive matrix driving method may be
employed in the liquid crystal display. Alternatively, the
retardation plate 10 may be used in displays other than liquid
crystal displays such as organic electroluminescent display.
[0219] Additional advantages and modifications will readily occur
to those skilled in the art. Therefore, the invention in its
broader aspects is not limited to the specific details and
representative embodiments shown and described herein. Accordingly,
various modifications may be made without departing from the spirit
or scope of the general inventive concept as defined by the
appended claims and their equivalents.
* * * * *