U.S. patent application number 10/984251 was filed with the patent office on 2005-06-09 for electro-optic assemblies and materials for use therein.
Invention is credited to Fazel, Shafiq Nisarali, Honeyman, Charles H., Klingenberg, Eric Howard.
Application Number | 20050124751 10/984251 |
Document ID | / |
Family ID | 33130237 |
Filed Date | 2005-06-09 |
United States Patent
Application |
20050124751 |
Kind Code |
A1 |
Klingenberg, Eric Howard ;
et al. |
June 9, 2005 |
Electro-optic assemblies and materials for use therein
Abstract
An electro-optic display comprises first and second substrates,
and an adhesive layer and a layer of electro-optic material
disposed between these substrates, the adhesive layer comprising a
mixture of a polymeric adhesive material and an additive selected
from a salt, a polyelectrolyte, a polymer electrolyte, a solid
electrolyte, a conductive metal powder, a ferrofluid, a
non-reactive solvent, a conductive organic compound, and
combinations thereof. In one aspect, there is provided an adhesive
comprising a mixture of a polymeric adhesive material and an
additive selected from a salt, a polyelectrolyte, a polymer
electrolyte, a solid electrolyte, and combinations thereof.
Inventors: |
Klingenberg, Eric Howard;
(Emmaus, PA) ; Fazel, Shafiq Nisarali; (Allentown,
PA) ; Honeyman, Charles H.; (Roslindale, MA) |
Correspondence
Address: |
AIR PRODUCTS AND CHEMICALS, INC.
PATENT DEPARTMENT
7201 HAMILTON BOULEVARD
ALLENTOWN
PA
181951501
|
Family ID: |
33130237 |
Appl. No.: |
10/984251 |
Filed: |
November 9, 2004 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10984251 |
Nov 9, 2004 |
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10810761 |
Mar 26, 2004 |
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60320059 |
Mar 27, 2003 |
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Current U.S.
Class: |
524/502 ;
524/366; 524/507 |
Current CPC
Class: |
G02F 1/167 20130101;
G02F 1/1675 20190101; G02F 2202/28 20130101; B32B 7/12 20130101;
B32B 7/06 20130101; C09J 11/02 20130101; C09J 9/02 20130101 |
Class at
Publication: |
524/502 ;
524/507; 524/366 |
International
Class: |
C08L 001/00 |
Claims
1. An adhesive comprising a mixture of a polymeric adhesive
material and an additive selected from a salt, a polyelectrolyte, a
polymer electrolyte, a solid electrolyte, and combinations
thereof.
2. The adhesive of claim 1 wherein the polymeric adhesive material
is selected from a polyurethane, vinyl acetate, vinyl acetate
ethylene, an epoxy, a polyacrylic-based adhesive, and combinations
thereof.
3. An adhesive comprising a mixture of a polymeric adhesive
material and an additive selected from a conductive metal powder, a
ferrofluid, a non-reactive solvent, a conductive organic compound,
and combinations thereof.
4. The adhesive of claim 3 wherein the polymeric adhesive material
is selected from a polyurethane, vinyl acetate, vinyl acetate
ethylene, an epoxy, a polyacrylic-based adhesive, and combinations
thereof.
5. An adhesive comprising a polymeric adhesive material and an
additive comprising a salt.
6. The adhesive of claim 5 wherein the salt is at least one
selected from potassium acetate, tetraalkylammonium salts,
LiCF.sub.3SOF.sub.3, LiClO.sub.4, LiPF.sub.6, LiBF.sub.4,
LiAsF.sub.6, and LiN(CF.sub.3SO.sub.2).sub.3.
7. An adhesive comprising a polymeric adhesive material and an
additive comprising a polyelectrolyte.
8. The adhesive of claim 7 wherein the polyelectrolyte is at least
one selected from polyacrylic acid, polystyrene sulfonate,
poly(2-vinylpyridine), poly(4-vinylpyridine), poly(dimethylammonium
chloride, poly(dimethylaminoethyl methacrylate), and
poly(diethylaminoethyl methacrylate).
9. An adhesive comprising a polymeric adhesive material and an
additive comprising a polymer electrolyte.
10. The adhesive of claim 9 wherein the polymer electrolyte is at
least one selected from polyether compounds, polyamines, and
polymers which contain quaternary ammonium groups.
11. An adhesive comprising a polymeric adhesive material and an
additive comprising a solid electrolyte.
12. An adhesive comprising a polymeric adhesive material and an
additive comprising a conductive metal powder.
13. The adhesive of claim 12 wherein the conductive metal powder
comprises nickel.
14. An adhesive comprising a polymeric adhesive material and an
additive comprising a ferrofluid.
15. An adhesive comprising a polymeric adhesive material and an
additive comprising a non-reactive solvent.
16. The adhesive of claim 15 wherein the non-reactive solvent is at
least one selected from water, diethyl ether, dipropyl ether,
diethyleneglycol, glyme, diglyme, and N-methylpyrrolidone.
17. An adhesive comprising a polymeric adhesive material and an
additive comprising a conductive organic compound.
18. The adhesive of claim 17 wherein the conductive organic
compound is at least one selected from polyaniline, polythiophene,
polypyrrole, poly-3,4-dioxyethylene thiophene, and derivatives
thereof.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional of application Ser. No.
10/810,761, filed 26 Mar. 2004, which claims the benefit of
Provisional Application Ser. No. 60/320,059, filed Mar. 27, 2003,
both of which are incorporated herein by reference in their
entirity.
[0002] This application is also related to (a) copending
application Ser. No. 10/064,389, filed Jul. 9, 2002 (Publication
No.2003/0025855), which itself claims benefit of Provisional
Application Ser. No. 60/304,117, filed Jul. 9, 2001; (b) copending
application Ser. No. 10/249,957, filed May 22, 2003 (Publication
No. 2004/0027326), which itself claims benefit of Provisional
Application Ser. No. 60/319,300, filed Jun. 10, 2002, and
Provisional Application Ser. No. 60/320,186, filed May 12, 2003;
and (c) copending application Ser. No. 10/605,024, filed Sep. 2,
2003, which itself claims benefit of Provisional Application Ser.
No. 60/319,516, filed Sep. 2, 2002.
[0003] The entire contents of these copending applications, and of
all other U.S. patents and published and copending applications
mentioned below, are herein incorporated by reference.
BACKGROUND OF THE INVENTION
[0004] Electro-optic assemblies useful in the production of
electro-optic displays, and to materials for use in such assemblies
are disclosed. More specifically, binders and adhesive compositions
having controlled volume resistivity, and electro-optic assemblies
incorporating such materials, are disclosed. The materials
disclosed herein may be useful in applications other than
electro-optic displays.
[0005] Electro-optic displays comprise a layer of electro-optic
material, a term which is used herein in its conventional meaning
in the art to refer to a material having first and second display
states differing in at least one optical property, the material
being changed from its first to its second display state by
application of an electric field to the material. The optical
property is typically color perceptible to the human eye, but may
be another optical property, such as optical transmission,
reflectance, luminescence or, in the case of displays intended for
machine reading, pseudo-color in the sense of a change in
reflectance of electromagnetic wavelengths outside the visible
range.
[0006] The electro-optic displays of the present invention
typically contain an electro-optic material, which is a solid in
the sense that the electro-optic material has solid external
surfaces, although the material may, and often does, have internal
liquid- or gas-filled spaces, and to methods for assembling
displays using such an electro-optic material. Such displays using
solid electro-optic materials may hereinafter for convenience be
referred to as "solid electro-optic displays". Thus, the term
"solid electro-optic displays" includes rotating bichromal member
displays (see below), encapsulated electrophoretic displays,
microcell electrophoretic displays and encapsulated liquid crystal
displays.
[0007] The terms "bistable" and "bistability" are used herein in
their conventional meaning in the art to refer to displays
comprising display elements having first and second display states
differing in at least one optical property, and such that after any
given element has been driven, by means of an addressing pulse of
finite duration, to assume either its first or second display
state, after the addressing pulse has terminated, that state will
persist for at least several times, for example at least four
times, the minimum duration of the addressing pulse required to
change the state of the display element. It is shown in published
U.S. Patent Application No. 2002/0180687 that some particle-based
electrophoretic displays capable of gray scale are stable not only
in their extreme black and white states but also in their
intermediate gray states, and the same is true of some other types
of electro-optic displays. This type of display is properly called
"multi-stable" rather than bistable, although for convenience the
term "bistable" may be used herein to cover both bistable and
multi-stable displays.
[0008] Several types of electro-optic displays are known. One type
of electro-optic display is a rotating bichromal member type as
described, for example, in U.S. Pat. Nos. 5,808,783; 5,777,782;
5,760,761; 6,054,071 6,055,091; 6,097,531; 6,128,124; 6,137,467;
and 6,147,791 (although this type of display is often referred to
as a "rotating bichromal ball" display, the term "rotating
bichromal member" is preferred as more accurate since in some of
the patents mentioned above the rotating members are not
spherical). Such a display uses a large number of small bodies
(typically spherical or cylindrical), which have two or more
sections with differing optical characteristics, and an internal
dipole. These bodies are suspended within liquid-filled vacuoles
within a matrix, the vacuoles being filled with liquid so that the
bodies are free to rotate. The appearance of the display is changed
to applying an electric field thereto, thus rotating the bodies to
various positions and varying which of the sections of the bodies
is seen through a viewing surface. This type of electro-optic
medium is typically bistable.
[0009] Another type of electro-optic display uses an electrochromic
medium, for example an electrochromic medium in the form of a
nanochromic film comprising an electrode formed at least in part
from a semi-conducting metal oxide and a plurality of dye molecules
capable of reversible color change attached to the electrode; see,
for example O'Regan, B., et al., Nature 1991, 353, 737; and Wood,
D., Information Display, 18(3), 24 (March 2002). See also Bach, U.,
et al., Adv. Mater., 2002, 14(11), 845. Nanochromic films of this
type are also described, for example, in U.S. Pat. No. 6,301,038,
International Application Publication No. WO 01/27690, and in U.S.
Patent Application 2003/0214695. This type of medium is also
typically bistable.
[0010] Another type of electro-optic display, which has been the
subject of intense research and development for a number of years,
is the particle-based electrophoretic display, in which a plurality
of charged particles moves through a suspending fluid under the
influence of an electric field. Electrophoretic displays can have
attributes of good brightness and contrast, wide viewing angles,
state bistability, and low power consumption when compared with
liquid crystal displays. Nevertheless, problems with the long-term
image quality of these displays have prevented their widespread
usage. For example, particles that make up electrophoretic displays
tend to settle, resulting in inadequate service-life for these
displays.
[0011] Numerous patents and applications assigned to or in the
names of the Massachusetts Institute of Technology (MIT) and E Ink
Corporation have recently been published describing encapsulated
electrophoretic media. Such encapsulated media comprise numerous
small capsules, each of which itself comprises an internal phase
containing electrophoretically-mobile particles suspended in a
liquid suspending medium, and a capsule wall surrounding the
internal phase. Typically, the capsules are themselves held within
a polymeric binder to form a coherent layer positioned between two
electrodes. Encapsulated media of this type are described, for
example, in U.S. Pat. Nos. 5,930,026; 5,961,804; 6,017,584;
6,067,185; 6,118,426; 6,120,588; 6,120,839; 6,124,851; 6,130,773;
6,130,774; 6,172,798; 6,177,921; 6,232,950; 6,249,721; 6,252,564;
6,262,706; 6,262,833; 6,300,932; 6,312,304; 6,312,971; 6,323,989;
6,327,072; 6,376,828; 6,377,387; 6,392,785; 6,392,786; 6,413,790;
6,422,687; 6,445,374; 6,445,489; 6,459,418; 6,473,072; 6,480,182;
6,498,114; 6,504,524; 6,506,438; 6,512,354; 6,515,649; 6,518,949;
6,521,489; 6,531,997; 6,535,197; 6,538,801; 6,545,291; 6,580,545;
6,639,578; 6,652,075; 6,657,772; 6,664,944; 6,680,725; 6,683,333;
and 6,704,133; and U.S. Patent Applications Publication Nos.
2002/0019081; 2002/0021270; 2002/0053900; 2002/0060321;
2002/0063661; 2002/0063677; 2002/0090980; 2002/0106847;
2002/0113770; 2002/0130832; 2002/0131147; 2002/0145792;
2002/0171910; 2002/0180687; 2002/0180688; 2002/0185378;
2003/0011560; 2003/0011868; 2003/0020844; 2003/0025855;
2003/0034949; 2003/0038755; 2003/0053189; 2003/0096113;
2003/0102858; 2003/0132908; 2003/0137521; 2003/0137717;
2003/0151702; 2003/0189749; 2003/0214695; 2003/0214697;
2003/0222315; 2004/0008398; 2004/0012839; 2004/0014265; and
2004/0027327; and International Applications Publication Nos. WO
99/67678; WO 00/05704; WO 00/38000; WO 00/38001; WO00/36560; WO
00/67110; WO 00/67327; WO 01/07961; WO 01/08241; WO 03/092077; and
WO 03/107,315.
[0012] Many of the aforementioned patents and applications
recognize that the walls surrounding the discrete microcapsules in
an encapsulated electrophoretic medium could be replaced by a
continuous phase, thus producing a so-called "polymer-dispersed
electrophoretic display" in which the electrophoretic medium
comprises a plurality of discrete droplets of an electrophoretic
fluid and a continuous phase of a polymeric material, and that the
discrete droplets of electrophoretic fluid within such a
polymer-dispersed electrophoretic display may be regarded as
capsules or microcapsules even though no discrete capsule membrane
is associated with each individual droplet; see for example, the
aforementioned 2002/0131147. Accordingly, for purposes of the
present application, such polymer-dispersed electrophoretic media
are regarded as sub-species of encapsulated electrophoretic
media.
[0013] An encapsulated electrophoretic display typically does not
suffer from the clustering and settling failure mode of traditional
electrophoretic devices and provides further advantages, such as
the ability to print or coat the display on a wide variety of
flexible and rigid substrates. (Use of the word "printing" is
intended to include all forms of printing and coating, including,
but without limitation: pre-metered coatings such as patch die
coating, slot or extrusion coating, slide or cascade coating,
curtain coating; roll coating such as knife over roll coating,
forward and reverse roll coating; gravure coating; dip coating;
spray coating; meniscus coating; spin coating; brush coating; air
knife coating; silk screen printing processes; electrostatic
printing processes; thermal printing processes; ink jet printing
processes; and other similar techniques.) Thus, the resulting
display can be flexible. Further, because the display medium can be
printed (using a variety of methods), the display itself can be
made inexpensively.
[0014] A related type of electrophoretic display is a so-called
"microcell electrophoretic display". In a microcell electrophoretic
display, the charged particles and the suspending fluid are not
encapsulated within capsules but instead are retained within a
plurality of cavities formed within a carrier medium, typically a
polymeric film. See, for example, International Application
Publication No. WO 02/01281, and U.S. Patent Application
Publication No. 2002/0075556, both assigned to Sipix Imaging,
Inc.
[0015] Other types of electro-optic materials, for example,
polymer-dispersed liquid crystal, may also be used in the displays
of the present invention.
[0016] Although electrophoretic media are often opaque (since, for
example, in many electrophoretic media, the particles substantially
block transmission of visible light through the display) and
operate in a reflective mode, many electrophoretic displays can be
made to operate in a so-called "shutter mode" in which one display
state is substantially opaque and one is light-transmissive. See,
for example, the aforementioned U.S. Pat. Nos. 6,130,774 and
6,172,798, and U.S. Pat. Nos. 5,872,552; 6,144,361; 6,271,823;
6,225,971; and 6,184,856. Dielectrophoretic displays, which are
similar to electrophoretic displays but rely upon variations in
electric field strength, can operate in a similar mode; see U.S.
Pat. No. 4,418,346.
[0017] In addition to the layer of electro-optic material, an
electro-optic display normally comprises at least two other layers
disposed on opposed sides of the electro-optic material, one of
these two layers being an electrode layer. In most such displays
both the layers are electrode layers, and one or both of the
electrode layers are patterned to define the pixels of the display.
For example, one electrode layer may be patterned into elongate row
electrodes and the other into elongate column electrodes running at
right angles to the row electrodes, the pixels being defined by the
intersections of the row and column electrodes. Alternatively, and
more commonly, one electrode layer has the form of a single
continuous electrode and the other electrode layer is patterned
into a matrix of pixel electrodes, each of which defines one pixel
of the display. In another type of electro-optic display, which is
intended for use with a stylus, print head or similar movable
electrode separate from the display, only one of the layers
adjacent the electro-optic layer comprises an electrode, the layer
on the opposed side of the electro-optic layer typically being a
protective layer intended to prevent the movable electrode damaging
the electro-optic layer.
[0018] The manufacture of a three-layer electro-optic display
normally involves at least one lamination operation. For example,
in several of the aforementioned MIT and E Ink patents and
applications, there is described a process for manufacturing an
encapsulated electrophoretic display in which an encapsulated
electrophoretic medium comprising capsules in a binder is coated on
to a flexible substrate comprising indium-tin-oxide (ITO) or a
similar conductive coating (which acts as an one electrode of the
final display) on a plastic film, the capsules/binder coating being
dried to form a coherent layer of the electrophoretic medium firmly
adhered to the substrate. Separately, a backplane, containing an
array of pixel electrodes and an appropriate arrangement of
conductors to connect the pixel electrodes to drive circuitry, is
prepared. To form the final display, the substrate having the
capsule/binder layer thereon is laminated to the backplane using a
lamination adhesive. (A very similar process can be used to prepare
an electrophoretic display useable with a stylus or similar movable
electrode by replacing the backplane with a simple protective
layer, such as a plastic film, over which the stylus or other
movable electrode can slide.) In one preferred form of such a
process, the backplane is itself flexible and is prepared by
printing the pixel electrodes and conductors on a plastic film or
other flexible substrate. The obvious lamination technique for mass
production of displays by this process is roll lamination using a
lamination adhesive. Similar manufacturing techniques can be used
with other types of electro-optic displays. For example, a
microcell electrophoretic medium or a rotating bichromal member
medium may be laminated to a backplane in substantially the same
manner as an encapsulated electrophoretic medium.
[0019] In the processes described above, the lamination of the
substrate carrying the electro-optic layer to the backplane may
advantageously be carried out by vacuum lamination. Vacuum
lamination is effective in expelling air from between the two
materials being laminated, thus avoiding unwanted air bubbles in
the final display; such air bubbles may introduce undesirable
artifacts in the images produced on the display. However, vacuum
lamination of the two parts of an electro-optic display in this
manner imposes stringent requirements upon the lamination adhesive
used, especially in the case of a display using an encapsulated
electrophoretic medium. The lamination adhesive should have
sufficient adhesive strength to bind the electro-optic layer to the
layer (typically an electrode layer) to which it is to be
laminated, and in the case of an encapsulated electrophoretic
medium, the adhesive should also have sufficient adhesive strength
to mechanically hold the capsules together. If the electro-optic
display is to be of a flexible type (and one of the important
advantages of rotating bichromal member and encapsulated
electrophoretic displays is that they can be made flexible), the
adhesive should have sufficient flexibility not to introduce
defects into the display when the display is flexed. The lamination
adhesive should have adequate flow properties at the lamination
temperature to ensure high quality lamination, and in this regard,
the demands of laminating encapsulated electrophoretic and some
other types of electro-optic media are unusually difficult; the
lamination has be conducted at a temperature of not more than about
130.degree. C. since the medium cannot be exposed to substantially
higher temperatures without damage, but the flow of the adhesive
must cope with the relatively uneven surface of the
capsule-containing layer, the surface of which is rendered
irregular by the underlying capsules. The lamination temperature
should indeed be kept as low as possible, and room temperature
lamination would be ideal, but no commercial adhesive has been
found which permits such room temperature lamination. The
lamination adhesive should be chemically compatible with all the
other materials in the display.
[0020] As discussed in detail in the aforementioned copending
application Ser. No. 10/064,389, a lamination adhesive used in an
electro-optic display should meet certain electrical criteria, and
this introduces considerable problems in the selection of the
lamination adhesive. Commercial manufacturers of lamination
adhesives naturally devote considerable effort to ensuring that
properties, such as strength of adhesion and lamination
temperatures, of such adhesives are adjusted so that the adhesives
perform well in their major applications, which typically involve
laminating polymeric and similar films. However, in such
applications, the electrical properties of the lamination adhesive
are not relevant, and consequently the commercial manufacturers pay
no heed to such electrical properties. Indeed, substantial
variations (of up to several fold) in certain electrical properties
may exist between different batches of the same commercial
lamination adhesive, presumably because the manufacturer was
attempting to optimize non-electrical properties of the lamination
adhesive (for example, resistance to bacterial growth) and was not
at all concerned about resulting changes in electrical
properties.
[0021] However, in electro-optic displays, in which the lamination
adhesive is normally located between the electrodes, which apply
the electric field needed to change the electrical state of the
electro-optic medium, the electrical properties of the adhesive may
become crucial. As will be apparent to electrical engineers, the
volume resistivity of the lamination adhesive becomes important,
since the voltage drop across the electro-optic medium is
essentially equal to the voltage drop across the electrodes, minus
the voltage drop across the lamination adhesive. If the resistivity
of the adhesive layer is too high, a substantial voltage drop will
occur within the adhesive layer, requiring an increase in voltage
across the electrodes. Increasing the voltage across the electrodes
in this manner is undesirable, since it increases the power
consumption of the display, and may require the use of more complex
and expensive control circuitry to handle the increased voltage
involved. On the other hand, if the adhesive layer, which extends
continuously across the display, is in contact with a matrix of
electrodes, as in an active matrix display, the volume resistivity
of the adhesive layer should not be too low, or lateral conduction
of electric current through the continuous adhesive layer may cause
undesirable cross-talk between adjacent electrodes. Also, since the
volume resistivity of most materials decreases rapidly with
increasing temperature, if the volume resistivity of the adhesive
is too low, the performance of the display at temperatures
substantially above room temperature is adversely affected. For
these reasons, there is an optimum range of lamination adhesive
resistivity values for use with any given electro-optic medium,
this range varying with the resistivity of the electro-optic
medium. The volume resistivities of encapsulated electrophoretic
media are typically around 10.sup.10 ohm cm, and the resistivities
of other electro-optic media are usually of the same order of
magnitude. Accordingly, the volume resistivity of the lamination
adhesive should normally be around 10.sup.8 to 10.sup.12 ohm cm, or
about 10.sup.9 to 10.sup.11 ohm cm, at the operating temperature of
the display, typically around 20.degree. C. The lamination adhesive
should also have a variation of volume resistivity with temperature
which is similar to that of the electro-optic medium itself.
[0022] The number of commercial materials which can meet most of
the previously discussed, rather disparate requirements for a
lamination adhesive for use in an electro-optic display is small,
and in practice a small number of water-dispersed urethane
emulsions have been used for this purpose. A similar group of
materials have been used as the binder for an encapsulated
electrophoretic medium.
[0023] However, the use of such polyester-based urethane emulsions
as lamination adhesives is still a not entirely satisfactory
compromise between the desired mechanical and electrical
properties. Lamination adhesives such as acrylic polymers and
pressure sensitive adhesives are available with much better
mechanical properties, but the electrical properties of these
materials are unsuitable for use in electro-optic displays.
Moreover, hitherto there has been no satisfactory way of varying
the electrical properties of the urethane emulsions to "fine tune"
them to match the electrical properties of a specific electro-optic
medium. Accordingly, it would be highly advantageous if some way
could be found to "decouple" the mechanical and electrical
properties of a lamination adhesive so that each set of properties
could be optimized separately.
[0024] Furthermore, in considering the choice of a lamination
adhesive for use in an electro-optic display, attention must be
paid to the process by which the display is to be assembled. Most
prior art methods for final lamination of electrophoretic displays
are essentially batch methods in which the electro-optic medium,
the lamination adhesive and the backplane are only brought together
immediately prior to final assembly, and it is desirable to provide
methods better adapted for mass production. However, the
aforementioned copending application Ser. No. 10/249,957 describes
a method of assembling a solid electro-optic display (including a
particle-based electrophoretic display), which is well adapted for
mass production. Essentially, this copending application describes
a so-called "front plane laminate" ("FPL") which comprises, in
order, a light-transmissive electrically-conductive layer; a layer
of a solid electro-optic medium in electrical contact with the
electrically-conductive layer; an adhesive layer; and a release
sheet. Typically, the light-transmissive electrically-conductive
layer will be carried on a light-transmissive substrate, which is
preferably flexible, in the sense that the substrate can be
manually wrapped around a drum (say) 10 inches (254 mm) in diameter
without permanent deformation. The term "light-transmissive" is
used in this copending application and herein to mean that the
layer thus designated transmits sufficient light to enable an
observer, looking through that layer, to observe the change in
display states of the electro-optic medium, which will be normally
be viewed through the electrically-conductive layer and adjacent
substrate (if present). The substrate will be typically be a
polymeric film, and will normally have a thickness in the range of
about 1 to about 25 mil (25 to 634 .mu.m), preferably about 2 to
about 10 mil (51 to 254 .mu.m). The electrically-conductive layer
is conveniently a thin metal layer of, for example, aluminum or
indium-tin-oxide, or may be a conductive polymer. Polyethylene
terephthalate (PET) films coated with aluminum or ITO are available
commercially, for example as "aluminized Mylar" ("Mylar" is a
Registered Trade Mark) from E.I. du Pont de Nemours & Company,
Wilmington Del., and such commercial materials may be used with
good results in the front plane laminate.
[0025] Assembly of an electro-optic display using such a front
plane laminate may be effected by removing the release sheet from
the front plane laminate and contacting the adhesive layer with the
backplane under conditions effective to cause the adhesive layer to
adhere to the backplane, thereby securing the adhesive layer,
electro-optic medium layer and electrically-conductive layer to the
backplane. This process is well-adapted to mass production since
the front plane laminate may be mass produced, typically using
roll-to-roll coating techniques, and then cut into pieces of any
size needed for use with specific backplanes.
[0026] The aforementioned copending application Ser. No. 10/249,957
also describes a method for testing the electro-optic medium in a
front plane laminate prior to incorporation of the front plane
laminate into a display. In this testing method, the release sheet
is provided with an electrically conductive layer, and a voltage
sufficient to change the optical state of the electro-optic medium
is applied between this electrically conductive layer and the
electrically conductive layer on the opposed side of the
electro-optic medium. Observation of the electro-optic medium will
then reveal any faults in the medium, thus avoiding laminating
faulty electro-optic medium into a display, with the resultant cost
of scrapping the entire display, not merely the faulty front plane
laminate.
[0027] The aforementioned copending application Ser. No. 10/249,957
also describes a second method for testing the electro-optic medium
in a front plane laminate by placing an electrostatic charge on the
release sheet, thus forming an image on the electro-optic medium.
This image is then observed in the same way as before to detect any
faults in the electro-optic medium.
[0028] The aforementioned copending application Ser. No. 10/605,024
describes a so-called "double release film" which is essentially a
simplified version of the front plane laminate previously
described. One form of the double release sheet comprises a layer
of a solid electro-optic medium sandwiched between two adhesive
layers, one or both of the adhesive layers being covered by a
release sheet. Another form of the double release sheet comprises a
layer of a solid electro-optic medium sandwiched between two
release sheets. Both forms of the double release film are intended
for use in a process generally similar to the process for
assembling an electro-optic display from a front plane laminate
already described, but involving two separate laminations;
typically, in a first lamination the double release sheet is
laminated to a front electrode to form a front sub-assembly, and
then in a second lamination the front sub-assembly is laminated to
a backplane to form the final display.
[0029] In view of the advantages of the assembly method using a
front plane laminate described in the aforementioned copending
application Ser. No. 10/249,957, it is desirable that a lamination
adhesive be capable of being incorporated into such a front plane
laminate. It is also desirable that a lamination adhesive be
capable of being incorporated into a double release film as
previously described.
BRIEF SUMMARY OF THE INVENTION
[0030] Accordingly, in one aspect there is provided an
electro-optic assembly comprising first and second substrates, and
an adhesive layer and a layer of electro-optic material disposed
between the first and second substrates, the adhesive layer
comprising a mixture of a polymeric adhesive material and an
additive selected from a salt, a polyelectrolyte, a polymer
electrolyte, a solid electrolyte, and combinations thereof. The
adhesive layer containing the additive may comprise from about
10.sup.-6 to about 10.sup.-4 moles of additive per gram of the
polymeric adhesive material. Typically, the layer will comprise
from about 10.sup.-5 to about 10.sup.-4 moles of additive per gram
of polymeric adhesive material. The layer may comprise a
polyurethane, vinyl acetate, vinyl acetate ethylene, epoxy, or a
polyacrylic based adhesive.
[0031] In one embodiment, the adhesive layer used in this
electro-optic assembly may comprise a mixture of the polymeric
adhesive material and a salt. The salt may be, for example, an
inorganic salt, an organic salt, or a combination thereof. In one
particular embodiment, the salt comprises potassium acetate. In an
alternative embodiment, the salt may comprise a quaternary ammonium
salt, for example a tetraalkylammonium salt, such as
tetrabutylammonium chloride or hexafluorophosphate.
[0032] In embodiments wherein the additive is a polyelectrolyte,
the polyelectrolyte may comprise, for example, a salt of a polyacid
such as, but not limited to, an alkali metal salt of polyacrylic
acid.
[0033] The adhesive layer containing the additive may provide other
functions besides an adhesive function. For example, the layer may
be provided with regions of differing colors and serve as a color
filter. Alternatively, the layer may comprise an optical biasing
element.
[0034] In the electro-optic assembly, at least one of the first and
second substrates may comprise an electrode. In one particular
embodiment, each of the first and second substrates comprises at
least one electrode. In another particular embodiment, the first
substrate may comprise a light-transmissive electrically-conductive
layer (which can act as an electrode), the second substrate may
comprise a release sheet, and the electro-optic medium may be a
solid electro-optic medium; thus, the entire electro-optic assembly
will have the form of a front plane laminate as described in the
aforementioned copending application Ser. No. 10/249,957.
[0035] In a further aspect of the present invention, there is
provided an article of manufacture (a double release sheet)
comprising: a layer of a solid electro-optic medium having first
and second surfaces on opposed sides thereof; a first adhesive
layer on the first surface of the layer of solid electro-optic
medium; a release sheet disposed on the opposed side of the first
adhesive layer from the layer of solid electro-optic medium; and a
second adhesive layer on the second surface of the layer of solid
electro-optic medium, at least one of the first and second adhesive
layers comprising a mixture of a polymeric adhesive material and an
additive selected from a salt, a polyelectrolyte, a polymer
electrolyte, a solid electrolyte, and combinations thereof.
[0036] In another aspect of the present invention, there is
provided an electro-optic assembly comprising first and second
substrates, and an adhesive layer and a layer of electro-optic
material disposed between the first and second substrates, the
adhesive layer comprising a mixture of a polymeric adhesive
material and an additive selected from a conductive metal powder, a
ferrofluid, a non-reactive solvent, a conductive organic compound,
and combinations thereof. The conductive metal powder may be, for
example, nickel.
[0037] In a still further aspect of the present invention, there is
provided an article of manufacture (a double release sheet)
comprising: a layer of a solid electro-optic medium having first
and second surfaces on opposed sides thereof; a first adhesive
layer on the first surface of the layer of solid electro-optic
medium; a release sheet disposed on the opposed side of the first
adhesive layer from the layer of solid electro-optic medium; and a
second adhesive layer on the second surface of the layer of solid
electro-optic medium, at least one of the first and second adhesive
layers comprising a mixture of a polymeric adhesive material and an
additive selected from a conductive metal powder, a ferrofluid, a
non-reactive solvent, a conductive organic compound, and
combinations thereof.
[0038] In another aspect, there is provided an electrophoretic
medium comprising a plurality of capsules, each of the capsules
comprising a capsule wall, a suspending fluid encapsulated within
the capsule wall and a plurality of electrically charged particles
suspended in the suspending fluid and capable of moving
therethrough on application of an electric field to the medium, the
medium further comprising a binder surrounding the capsules, the
binder comprising a mixture of a polymeric adhesive material and an
additive selected from a salt, a polyelectrolyte, a polymer
electrolyte, a solid electrolyte, and combinations thereof. The
binder containing the additive may comprise from about 10.sup.-6 to
about 10.sup.-4 moles of additive per gram of binder. Typically,
the binder will comprise from about 10.sup.-5 to about 10.sup.-4
moles of salt per gram of binder. The binder may comprise a
polyurethane, vinyl acetate, vinyl acetate ethylene, epoxy, or a
polyacrylic based adhesive.
[0039] In one embodiment, the binder used in this electrophoretic
medium may comprise a mixture of the polymeric adhesive material
and a salt. The salt may be, for example, an inorganic salt,
organic salt, or combination thereof. In one particular embodiment,
the salt comprises potassium acetate. In an alternative embodiment,
the salt may comprise a quaternary ammonium salt, for example a
tetraalkylammonium salt, such as tetrabutyl ammonium chloride or
hexafluorophosphate.
[0040] In embodiments wherein the additive in the binder is a
polyelectrolyte, the polyelectrolyte may comprise a salt of a
polyacid, for example an alkali metal salt of polyacrylic acid.
[0041] The binder containing the additive may provide other
functions besides an adhesive function. For example, the binder may
comprise an optical biasing element.
[0042] In yet another aspect, there is provided an electrophoretic
medium comprising a plurality of capsules, each of the capsules
comprising a capsule wall, a suspending fluid encapsulated within
the capsule wall and a plurality of electrically charged particles
suspended in the suspending fluid and capable of moving
therethrough on application of an electric field to the medium, the
medium further comprising a binder surrounding the capsules, the
binder comprising a mixture of a polymeric adhesive material and an
additive selected from a conductive metal powder, a ferrofluid, a
non-reactive solvent, a conductive organic compound, and
combinations thereof.
[0043] In another aspect, there is provided an adhesive comprising
a mixture of a polymeric adhesive material and an additive selected
from a salt, a polyelectrolyte, a polymer electrolyte, a solid
electrolyte, and combinations thereof. In this adhesive, the
polymeric adhesive material may be selected from a polyurethane,
vinyl acetate, vinyl acetate ethylene, an epoxy, a
polyacrylic-based adhesive, and combinations thereof.
[0044] Finally, there is provided an adhesive comprising a mixture
of a polymeric adhesive material and an additive selected from a
conductive metal powder, a ferrofluid, a non-reactive solvent, a
conductive organic compound, and combinations thereof. In this
adhesive, the polymeric adhesive material may be selected from a
polyurethane, vinyl acetate, vinyl acetate ethylene, an epoxy, a
polyacrylic-based adhesive, and combinations thereof.
BRIEF DESCRIPTION OF SEVERAL VIEWS OF THE DRAWINGS
[0045] FIG. 1 is a schematic cross-section through an electro-optic
assembly of the present invention having the form of a front plane
laminate.
[0046] FIG. 2 is a graph showing the volume resistivity of various
polymeric adhesive/additive mixtures as determined in the
experiments reported in Example 1 below.
[0047] FIG. 3 is a graph plotting the average volume resistivities
of the various mixtures shown in FIG. 2 with additive
concentration.
[0048] FIG. 4 is a graph similar to FIG. 3 but showing the
variation of the volume resistivities of polymeric
adhesive/tetrabutylammonium hexafluorophosphate mixtures with salt
concentration as determined in the experiments reported in Example
2 below.
DETAILED DESCRIPTION OF THE INVENTION
[0049] As already indicated, certain additives to control the
volume resistivity of adhesive materials used, for example, in
adhesive layers of electro-optic assemblies and displays, and in
binders surrounding the capsules of encapsulated electrophoretic
media, are disclosed herein. The adhesive layers and binders
disclosed herein enable the volume resistivity to be varied without
substantially varying the mechanical properties of the adhesive
layer or binder. The adhesive layers and binders, through the
addition of one or more additives, expand the selection of adhesive
materials which have desirable mechanical properties but which
could not otherwise be used because their volume resistivities are
unsuitable. Thus, one can "fine tune" the volume resistivity of an
adhesive layer or binder, i.e., to adjust the volume resistivity of
the material to an optimum value for a particular display or
electrophoretic medium.
[0050] The electro-optic assembly of the present invention may
constitute a complete electro-optic display or only a sub-assembly
of such a display. As already indicated, and as discussed at length
in the aforementioned E Ink and MIT patents and applications, a
complete electro-optic display requires the presence of at least
one, and normally two, electrodes to produce the electric field
necessary to vary the optical state of the electro-optic material,
although in some cases only one of the two electrodes may be a
permanent part of the display, with the other electrode being in
the form a movable stylus or similar instrument which can be moved
over the display to write on the display. When the electro-optic
assembly of the present invention is in the form of a complete
display with two or more permanent electrodes, each of the first
and second substrates will comprise at least one electrode. For
example, the assembly may have the form of an active matrix
display, with the first substrate comprising a single continuous
light-transmissive electrode extending across multiple pixels, and
typically the whole, of the display (in practice, the first
substrate normally also comprises a polymeric film or similar
supporting layer which supports the relatively thin
light-transmissive electrode and protects the relatively fragile
electrode from mechanical damage), while the second substrate has
the form of a backplane comprising a support portion and a
plurality of pixel electrodes, which define the individual pixels
of the display. Obviously, such a backplane may further comprise
non-linear devices (typically thin film transistors) and other
circuitry used to produce on the pixel electrodes the potentials
needed to drive the display (i.e., to switch the various pixels to
the optical states necessary to provide a desired image on the
display).
[0051] Alternatively, the electro-optic assembly of the present
invention may constitute a sub-assembly of such a complete display.
In particular, the electro-optic assembly may have the form of a
front plane laminate as described in the aforementioned copending
application Ser. No. 10/249,957. In such a front plane laminate,
one of the substrates (for convenience, say the first substrate)
comprises a light-transmissive electrically-conductive layer
intended to form the front electrode of a final display (again, the
first substrate will normally also comprise a polymeric film or
similar supporting layer which supports the relatively thin
electrically-conductive layer and protect it from mechanical
damage), while the second substrate comprises a release sheet,
which is removed before the front plane laminate is laminated to a
backplane to form the final display.
[0052] Indeed, many of the double release sheets of the present
invention can be regarded as special types of electro-optic
assemblies of the invention. In practice, such double release
sheets typically comprise a layer of electro-optic material having
adhesive layers on both sides thereof, both adhesive layers being
covered by release sheets. Such a double release sheet comprises an
electro-optic assembly of the present invention in which both
substrates are release sheets.
[0053] The adhesive layer or binder contains one or more additives
selected from (a) a salt, a polyelectrolyte, a polymer electrolyte,
a solid electrolyte, and combinations thereof; or (b) a conductive
metal powder, a ferrofluid, a non-reactive solvent, a conductive
organic compound, and combinations thereof.
[0054] In certain embodiments, the additive may be a salt such as
an inorganic salt, organic salt, or combination thereof. Exemplary
salts include potassium acetate, and tetraalkylammonium salts,
especially tetrabutylammonium salts such as the chloride. Further
examples of salts include lithium salts such as
LiCF.sub.3SOF.sub.3, LiClO.sub.4, LiPF.sub.6, LiBF.sub.4,
LiAsF.sub.6, and LiN(CF.sub.3SO.sub.2).sub.3. The presently
preferred salt is tetrabutylammonium hexafluorophosphate, largely
because of the stability and inertness of this salt.
[0055] In other embodiments, the polymer electrolyte is a
polyelectrolyte. Polyelectrolytes are typically polymers in which
about 10% or more of the molecule is composed of a functional group
capable of ionizing to form a charged species. Examples of certain
functional groups within a polyelectrolyte include, but are not
limited to, carboxylic acids, sulfonic acids, phosphoric acids, and
quaternary ammonium compounds. These polymers can be combined with
organic or inorganic salts or alternatively used alone. Examples of
polyelectrolyes, include but are not limited to, polyacrylic acid,
polystyrene sulfonate, poly(2-vinylpyridine),
poly(4-vinylpyridine), poly(dimethylammonium chloride,
poly(dimethylaminoethyl methacrylate), poly(diethylaminoethyl
methacrylate). A preferred polyelectrolyte is the sodium salt of
polyacrylic acid.
[0056] In a further embodiment of the present invention, the
additive is a polymer electrolyte. The term "polymer electrolyte"
as used herein describes a polymer that is capable of solubilizing
a salt. The solubility of the salt in these polymers can be
enhanced by the presence of oxygen and/or nitrogen atoms in the
polymer which form ether, carbonyl, carboxylic acids, primary
secondary, tertiary, and quaternary amino groups, sulphonic, acids
etc. Examples of polymer electrolytes include polyether compounds
such as polyethylene oxide, polypropylene oxide,
polytetramethyleneoxide, polyamines such as polyethyleinimine,
polyvinyl pyrrolidinone, polymers which contain quaternary ammonium
groups such as N.sup.+R1R2R3R4 wherein R1, R2, R3, and R4 are each
independently a H or a straight, branched, or cyclic alkyl group
having from 1 to 25 carbon atoms and where the counter ion can be
either selected from any organic or inorganic anion.
[0057] Still other additives can include a conductive metal powder,
a ferro fluid, and/or a non-reactive solvent that may improve or,
alternatively, hinder the mobility of the ions in the solution.
Examples of suitable non-reactive solvents include water, diethyl
ether, dipropyl ether, diethyleneglycol, glyme, diglyme,
N-methylpyrrolidone, etc. In still another embodiment, a conductive
organic compound can be used as the additive. Some non-limiting
examples of these compounds include polyaniline, polythiophene,
polypyrrole, poly-3,4-dioxyethylene thiophene, and derivatives of
these materials in their n- or p-doped states.
[0058] The polymeric adhesive material that is used in the adhesive
layer or binder can be any polymeric material that fulfills the
particular needs of the end-use application. Examples of suitable
polymeric adhesive materials include polyurethane, vinyl acetate,
vinyl acetate ethylene, epoxy, a polyacrylic-based adhesive, or
combinations thereof. These adhesive materials may be solvent based
or aqueous based. An example of a particular polyurethane that can
used is described in copending U.S. application Ser. No. 10/715,916
filed 18 Nov. 2003 which is incorporated herein by reference in its
entirety and assigned to Air Products and Chemicals, Inc.
[0059] The additive incorporated into a polymeric adhesive material
may be formed in situ; in other words, one or more precursor
materials may be incorporated into the polymeric adhesive material
or binder where the precursor material(s) can react with one
another, or with the polymeric adhesive or binder, or be changed by
exposure of the adhesive material or binder to conditions (for
example, exposure to heat, light, or magnetic or electric fields)
which cause a change in the precursor materials to form the final
additive.
[0060] The adhesive material or binder may contain components other
than the additive (or other dopant) used to adjust its volume
resistivity; for example, the adhesive material or binder may also
contain a dye or other colorant. It is known to form full color
electro-optic displays by providing a color filter as a separate
layer on the viewing surface of the display (the surface through
which an observer views the display), this color filter containing
pixels of differing colors, for example red, green and blue.
However, when a color filter is spaced from the electro-optic
material in this manner, there is the possibility of image
distortion when the color image is viewed at a substantial angle to
the perpendicular to the viewing surface. To avoid such problems,
it is in principle desirable to place the color filter immediately
adjacent the electro-optic material itself. However, this requires
placing the color filter between the electrodes of the display, so
that the electrical properties of the color filter will affect the
performance of the display. This is a particular problem with a
color filter, since such filters are usually formed by dying a
polymeric base material with three differing dyes, or mixtures of
dyes, to form the red, green and blue or other colored portions,
and it is unlikely that the three differing dyes will affect the
electrical properties of the color filter in the same manner. The
adhesive layer and binders described herein may be used to
counteract the effects of the differing dyes and render the
electrical properties of the color filter substantially uniform,
thereby avoiding artifacts on the image due to non-uniform
electrical properties within the color filter.
[0061] It is also known (see the aforementioned 2003/0011560) that
an "optical biasing element" may be provided in the binder or
lamination adhesive of an encapsulated electrophoretic display to
adjust the appearance of the display. The provision of such an
optical biasing element may affect the electrical properties of the
adhesive or binder, and the electrical properties of an adhesive or
binder containing such an optical biasing element may be optimized
by used of the additives described herein.
[0062] The optimum amount of additive will of course vary widely
with the exact polymeric binder or adhesive material and the exact
additive used, and the desired volume resistivity of the final
mixture. However, by way of general guidance it may be indicated
that a concentration of from about 10.sup.-5 to about 10.sup.-4
moles of additive per gram of binder or adhesive has been found to
give useful results. When the additive is a salt, this range is for
1:1 salts such as tetrabutylammonium chloride, tetrabutylammonium
hexafluorophosphate and potassium acetate; if 1:2 salts such as
sodium carbonate or calcium chloride are used, lower
concentrations, of the order of 10.sup.-6 moles of salt per gram of
binder or adhesive may suffice. As shown in the Examples below, the
volume resistivity of adhesive materials typically varies in a
predictable manner with the concentration of the additive, and
hence the final choice of how much additive should be added to
achieve a desired volume resistivity may readily be determined
empirically.
[0063] Although small amounts of salts have been added to polymers
used as binders and lamination adhesives in prior art electro-optic
displays, for example as biocides to protect the polymers from
biological degradation during extended storage, such salts are
typically used up during storage as they perform their biocidal or
similar function. In contrast, the additives used in the present
invention are intended to be permanent constituents of the
polymeric binder or lamination adhesive since they are intended to
effect a permanent adjustment in the conductivity thereof. Also,
the optimum amounts of additives used are typically substantially
greater than the amounts of salts used as biocides etc.
[0064] Typically, no special procedures are required to incorporate
the additive into the adhesive material. If, as is typically the
case, the adhesive layer is formed by coating a film of a latex or
solution of the adhesive material on to a substrate, or on to the
electro-optic material, and drying to form the adhesive layer, the
additive will normally simply be dissolved or dispersed in the
latex or solution of the adhesive material before coating. The
additive may be added to the latex or solution neat or may be
dissolved in an aqueous solution, non-aqueous solution, or
combination thereof. Similarly if, as is typically the case, an
electrophoretic medium is formed by mixing a slurry in capsules in
a liquid with a latex or solution of polymeric binder and coating
the resultant mixture on to a substrate and drying to form the
electrophoretic medium, the additive will normally simply be
dissolved or dispersed in the latex or solution of the polymeric
binder before this latex or solution is mixed with the capsules. It
is of course necessary to ensure that the additive is uniformly
dispersed throughout the adhesive material in order to prevent
variations in conductivity within the final adhesive or binder
layer, but those skilled in coating technology will be familiar
with routine techniques, such as lengthy agitation on a roll mill,
for ensuring such uniform dispersion.
[0065] The choice of the specific additive to be used is governed
largely by considerations of compatibility with the other
components of the adhesive layer and solubility in the adhesive
material to which the additive is to be added. If, as is typically
the case, the additive is to be added to an aqueous latex of the
adhesive material, the additive should be chosen to have good water
solubility, so that among salts alkali metal and substituted
ammonium salts are generally preferred. Care should be taken to
ensure that the additive does not cause aggregation of the latex
particles. Also, the additive should desirably not cause major
changes in the pH of the adhesive material, and should not
chemically react with the adhesive material or other parts of the
final display with which it eventually comes into contact, for
example the backplane.
[0066] The addition of one or more additives greatly expands the
range of polymeric materials, which can be used as binders and
lamination adhesives in electro-optic displays. In particular, the
addition of one or more additives enables the use of polymeric
materials which have mechanical properties highly desirable in
electro-optic displays but which have volume resistivities in their
pure states too high to be useful. Also, since some electro-optic
displays, especially encapsulated electrophoretic displays and
electrochromic displays, are sensitive to moisture, the addition of
the one or more additive may be used to replace water-based
polyurethane dispersions hitherto used in such displays with
non-hygroscopic and/or hydrophobic polymeric materials.
[0067] It will be appreciated that the modified adhesives and
binders disclosed herein may be useful in applications other than
electro-optic displays.
[0068] A particularly preferred embodiment of the electro-optic
assembly of the present invention will now be described, though by
way of illustration only, with reference to FIG. 1 of the
accompanying drawings, which is a schematic section through one
such assembly having the form of a front plane laminate. This
electro-optic assembly comprises a substrate, a conductive layer,
an electro-optic layer, an adhesive layer, and a second substrate
in the form of a release sheet; the assembly is illustrated at an
intermediate stage of the manufacturing process for an
electro-optic display before the subassembly is laminated to a
second assembly, namely a backplane.
[0069] The front plane laminate (generally designated 100) shown in
FIG. 1 comprises a light-transmissive substrate 110, a
light-transmissive electrode layer 120, an electro-optic layer 130,
a lamination adhesive layer 180 and a release sheet 190; the
release sheet is illustrated in the process of being removed from
the lamination adhesive layer 180 preparatory to lamination of the
FPL 100 to a backplane.
[0070] The substrate 110 is typically a transparent plastic film,
such as a 7 mil (177 .mu.m) polyethylene terephthalate sheet. The
lower surface (in FIG. 1) of substrate 110, which forms the viewing
surface of the final display, may have one or more additional
layers (not shown), for example a protective layer to absorb
ultra-violet radiation, barrier layers to prevent ingress of oxygen
or moisture into the final display, and anti-reflection coatings to
improve the optical properties of the display. Coated onto the
upper surface of substrate 110 is the thin light-transmissive
electrically conductive layer 120, preferably of ITO, which acts as
the common front electrode in the final display. PET films coated
with ITO are available commercially.
[0071] The electro-optic layer 130 may be deposited on the
conductive layer 120, typically by slot coating, the two layers
being in electrical contact. The electro-optic layer 130 shown in
FIG. 1 is an encapsulated electrophoretic medium and comprises
microcapsules 140, each of which comprises negatively charged white
particles 150 and positively charged black particles 160 suspended
in a hydrocarbon-based suspending fluid 165. The microcapsules 140
are held retained within a polymeric binder 170. Upon application
of an electrical field across electro-optic layer 130, white
particles 150 move to the positive electrode and black particles
160 move to the negative electrode, so that electro-optic layer 130
appears, to an observer viewing the display through substrate 110,
white or black depending on whether conductive layer 120 is
positive or negative relative to the adjacent pixel electrode in
the backplane.
[0072] The FPL 100 is desirably prepared by coating the lamination
adhesive 180, in liquid form, conveniently by slot coating, on to
release sheet 190, drying (or otherwise curing) the adhesive to
form a solid layer, and then laminating the adhesive and release
sheet to the electro-optic layer 130, which has previously been
coated on to the substrate 110 bearing the conductive layer 120;
this lamination may conveniently be effected using hot roll
lamination. (Alternatively, but less desirably, the lamination
adhesive may be applied over the electro-optic layer 130 and then
dried or otherwise cured before being covered with the release
sheet 190.) The release sheet 190 is conveniently a 7 mil (177
.mu.m) film; depending upon the nature of the electro-optic medium
used, it may be desirable to coat this film with a release agent,
for example a silicone. As illustrated in FIG. 1, the release sheet
190 is peeled or otherwise removed from the lamination adhesive 180
before the FPL 100 is laminated to a backplane (not shown) to form
the final display.
[0073] An additive, for example tetrabutylammonium
hexafluorophosphate, is included in the binder 170 and/or
lamination adhesive 180. If the additive is to be included in
binder 170, it is conveniently added to the capsule/binder slurry
which is coated on to a film comprising the substrate 110 and
conductive layer 120, as described in the aforementioned E Ink and
MIT patent and applications. Similarly, if the additive is to be
included in lamination adhesive 180, it is conveniently added to
the liquid form of the lamination adhesive before coating to form
the layer 180, as already described.
[0074] The following Examples are now given, though by way of
illustration only, to show details of preferred materials,
conditions and techniques used in the present invention.
EXAMPLE 1
[0075] A base adhesive material was prepared by blending NeoRez
(Registered Trade Mark) 9630 and NeoRez 9330, two polyurethane
dispersions available commercially from NeoResins, Inc., 730 Main
Street, Wilmington Mass. 01887. This material was divided into
eight samples of approximately 50 g each, each sample containing 40
percent by weight of solids, and varying amounts of potassium
acetate, tetrabutylammonium chloride, or poly(acrylic acid) aqueous
solution were added as indicated in the Table below; a control
sample was also provided with no additives.
1 TABLE Sample Weight of Mass (g) of No. sample (g) Additive
additive 0 50.12 N/A 0 1 50.00 Bu.sub.4NCl 0.012 2 50.06
Bu.sub.4NCl 0.051 3 50.30 Bu.sub.4NCl 0.099 4 50.10 KOAc 0.007 5
49.99 KOAc 0.040 6 50.00 KOAc 0.082 7 50.00 PAA, sodium salt 0.156
(40% wt aq.)
[0076] Each of the samples was mixed for a period of 7 to 10 days
to ensure a thoroughly homogeneous product and to re-disperse any
gel-like solids, which formed as a result of adding the additive as
a solid to the sample. At the end of each mixing period, visual
inspection confirmed that all the samples were free from any
significant amount of gel.
[0077] Each sample was then coated on to a release sheet and dried
to produce a layer of adhesive approximately 40 .mu.m thick. The
dried film was laminated to the conductive surface of a
poly(ethylene terephthalate) film provided with an indium tin oxide
coating, the release sheet was removed and the exposed surface of
the adhesive laminated to an experimental 2 inch by 2 inch (51 by
51 mm) backplane comprising a polymeric film coated with a layer of
graphite to produce a single-pixel test unit (essentially a
single-pixel display minus the layer of electro-optic medium). The
resultant test units were conditioned for 5 days at 25.degree. C.
and 30 percent relative humidity. The thickness of the adhesive was
measured and recorded, and the resistance of the adhesive layer was
determined. The volume resistivity of the adhesive was then
determined from these measurements and the results are shown in
FIG. 2 of the accompanying drawings. FIG. 3 shows the average
results from FIG. 2 against the additive concentration.
[0078] From the results in FIGS. 2 and 3 it will be seen that the
additives altered the volume resistivity of the adhesive by about
an order of magnitude, and that the variation in volume resistivity
was reasonably linear with additive concentration.
EXAMPLE 2
[0079] This Example illustrates the effect of tetrabutylammonium
hexafluorophosphate (NBU.sub.4PF.sub.6) in lowering the volume
resistivity of an adhesive material as described in the
aforementioned copending application Ser. No. 10/715,916.
[0080] Stock solutions of NBu.sub.4PF.sub.6 containing from 10 to
200 mg of the salt per gram of solution were prepared, and added to
various aliquots of a polyurethane dispersion to produce the
desired levels of the salt ranging from 10.sup.-7 to 10.sup.-4
moles of the salt per gram of adhesive solids (approximately 100 to
100,000 ppm of the salt on a weight/weight adhesive solids basis).
The resultant salt solution/dispersion mixtures were mixed on a
roller mill for at least three hours to ensure complete mixing.
[0081] The salt-containing dispersions thus prepared were coated in
the same way as in Example 1 above and dried at 60.degree. C. in
air for at least 10 minutes to produce dried adhesive layers having
thicknesses from 12 to 20 .mu.m. The resultant adhesive layers were
then converted to single pixel test units in the same way as in
Example 1 above; at least three test units were used for each salt
concentration. Control test units containing the same polyurethane
adhesive without any additive were also prepared. The completed
test units were conditioned at 30.degree. C. and 30 percent
relative humidity for one week prior to resistivity testing.
[0082] The volume resistivity of the test units was then measured
using driving pulses of 15V and 300 msec duration, and the
resultant data plotted in FIG. 4 of the accompanying drawings. From
this Figure it will be seen that the addition of the NBu.sub.4
PF.sub.6 resulted in a substantial decrease in the volume
resistivity of the adhesive material, by about two orders of
magnitude over the range of salt concentrations tested, and that
the volume resistivity varied linearly with salt concentration.
[0083] Numerous changes and modifications can be made in the
preferred embodiments of the present invention already described
without departing from the spirit and skill of the invention.
Accordingly, the foregoing description is to be construed in an
illustrative and not in a limitative sense
* * * * *