Patent Grant
10802373
This invention relates to electrophoretic displays. More specifically, in one aspect this invention relates to improved microcells containing electrophoretic fluid for electrophoretic displays. In another aspect, this invention relates to methods of making improved microcells for electrophoretic displays.
The term “electro-optic”, as applied to a material or a display, is used herein in its conventional meaning in the imaging 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. Although the optical property is typically color perceptible to the human eye, it 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.
The term “gray state” is used herein in its conventional meaning in the imaging art to refer to a state intermediate two extreme optical states of a pixel, and does not necessarily imply a black-white transition between these two extreme states. For example, several of the E Ink patents and published applications referred to below describe electrophoretic displays in which the extreme states are white and deep blue, so that an intermediate “gray state” would actually be pale blue. Indeed, as already mentioned, the change in optical state may not be a color change at all. The terms “black” and “white” may be used hereinafter to refer to the two extreme optical states of a display, and should be understood as normally including extreme optical states which are not strictly black and white, for example the aforementioned white and dark blue states. The term “monochrome” may be used hereinafter to denote a drive scheme which only drives pixels to their two extreme optical states with no intervening gray states.
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 U.S. Pat. No. 7,170,670 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.
One 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 move through a 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.
As noted above, electrophoretic media require the presence of a fluid. In most prior art electrophoretic media, this fluid is a liquid, but electrophoretic media can be produced using gaseous fluids; see, for example, Kitamura, T., et al., “Electrical toner movement for electronic paper-like display”, IDW Japan, 2001, Paper HCS1-1, and Yamaguchi, Y., et al., “Toner display using insulative particles charged triboelectrically”, IDW Japan, 2001, Paper AMD4-4). See also U.S. Pat. Nos. 7,321,459 and 7,236,291. Such gas-based electrophoretic media appear to be susceptible to the same types of problems due to particle settling as liquid-based electrophoretic media, when the media are used in an orientation which permits such settling, for example in a sign where the medium is disposed in a vertical plane. Indeed, particle settling appears to be a more serious problem in gas-based electrophoretic media than in liquid-based ones, since the lower viscosity of gaseous suspending fluids as compared with liquid ones allows more rapid settling of the electrophoretic particles.
Numerous patents and applications assigned to or in the names of the Massachusetts Institute of Technology (MIT), E Ink Corporation, E Ink California, LLC. and related companies describe various technologies used in encapsulated and microcell electrophoretic and other electro-optic media. Encapsulated electrophoretic media comprise numerous small capsules, each of which itself comprises an internal phase containing electrophoretically-mobile particles in a fluid medium, and a capsule wall surrounding the internal phase. In a microcell electrophoretic display, the charged particles and the fluid are not encapsulated within microcapsules 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 published US Application No. 2002/0075556. The technologies described above may be found, for example, in these patents and applications:
(a) Electrophoretic particles, fluids and fluid additives; see for example U.S. Pat. Nos. 7,002,728 and 7,679,814;
(b) Capsules, binders and encapsulation processes; see for example U.S. Pat. Nos. 6,922,276 and 7,411,719;
(c) Microcell structures, wall materials, and methods of forming microcells; see for example U.S. Pat. Nos. 6,672,921; 6,751,007; 6,753,067; 6,781,745; 6,788,452; 6,795,229; 6,806,995; 6,829,078; 6,833,177; 6,850,355; 6,865,012; 6,870,662; 6,885,495; 6,906,779; 6,930,818; 6,933,098; 6,947,202; 6,987,605; 7,046,228; 7,072,095; 7,079,303; 7,141,279; 7,156,945; 7,205,355; 7,233,429; 7,261,920; 7,271,947; 7,304,780; 7,307,778; 7,327,346; 7,347,957; 7,470,386; 7,504,050; 7,580,180; 7,715,087; 7,767,126; 7,880,958; 8,002,948; 8,154,790; 8,169,690; 8,441,432; 8,582,197; 8,891,156; 9,279,906; 9,291,872; and 9,388,307; and U.S. Patent Applications Publication Nos. 2003/0175480; 2003/0175481; 2003/0179437; 2003/0203101; 2013/0321744; 2014/0050814; 2015/0085345; 2016/0059442; 2016/0004136; and 2016/0059617;
(d) Methods for filling and sealing microcells; see for example U.S. Pat. Nos. 7,144,942 and 7,715,088;
(e) Films and sub-assemblies containing electro-optic materials; see for example U.S. Pat. Nos. 6,982,178 and 7,839,564;
(f) Backplanes, adhesive layers and other auxiliary layers and methods used in displays; see for example U.S. Pat. Nos. 7,116,318 and 7,535,624;
(g) Color formation and color adjustment; see for example U.S. Pat. Nos. 7,075,502 and 7,839,564;
(h) Methods for driving displays; see for example U.S. Pat. Nos. 7,012,600 and 7,453,445;
(i) Applications of displays; see for example U.S. Pat. Nos. 7,312,784 and 8,009,348; and
(j) Non-electrophoretic displays, as described in U.S. Pat. No. 6,241,921 and U.S. Patent Applications Publication No. 2015/0277160; and applications of encapsulation and microcell technology other than displays; see for example U.S. Patent Application Publications Nos. 2015/0005720 and 2016/0012710.
A microcell 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.
An electrophoretic display normally comprises a layer of electrophoretic material and at least two other layers disposed on opposed sides of the electrophoretic 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 electrophoretic 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 electrophoretic layer comprises an electrode, the layer on the opposed side of the electrophoretic layer typically being a protective layer intended to prevent the movable electrode damaging the electrophoretic layer.
Electro-optic displays, including electrophoretic displays, can be costly; for example, the cost of the color LCD found in a portable computer is typically a substantial fraction of the entire cost of the computer. As the use of such displays spreads to devices, such as cellular telephones and personal digital assistants (PDA's), much less costly than portable computers, there is great pressure to reduce the costs of such displays. The ability to form layers of electrophoretic media by printing techniques on flexible substrates, as discussed above, opens up the possibility of reducing the cost of electrophoretic components of displays by using mass production techniques such as roll-to-roll coating using commercial equipment used for the production of coated papers, polymeric films and similar media.
Current electrophoretic displays may also suffer from inefficient reflectance in a white optical state. For example, referring to
Thus, there is a need for microcell designs for electrophoretic displays with improved reflectance during certain optical states, such as a white optical state.
It is one aspect of the present invention to provide a polymeric film comprising a plurality of tapered microcells containing a dispersion of a first group and a second group of charged particles. The first group of charged particles may have a charge polarity opposite to a charge polarity of the second group of charged particles. The tapered microcells include a wall and at least a portion of the wall is configured to repel the first group of charged particles.
It is another aspect of the present invention to provide a method of making a laminate for an electrophoretic display comprising embossing a plurality of microcells having a tapered geometry through a layer of polymeric film and into a release sheet to form an embossed film; laminating the embossed film to a layer of conductive material on a protective sheet to form a laminated film; removing the release sheet from the polymeric film to form an opening to an interior of each microcell of the laminated film; filling the microcells with a dispersion fluid; and sealing the microcells.
These and other aspects of the present invention will be apparent in view of the following description.
The drawing Figures depict one or more implementations in accord with the present concepts, by way of example only, not by way of limitations. In the figures, like reference numerals refer to the same or similar elements.
In the following detailed description, numerous specific details are set forth by way of examples in order to provide a thorough understanding of the relevant teachings. However, it should be apparent to those skilled in the art that the present teachings may be practiced without such details.
The present invention seeks to provide a microcell design that improves light reflectance and minimizes light loss. The microcell design according to various embodiments of the present invention may include a tapered geometry to provide angled reflective walls that repel black or dark pigment. The various embodiments of the present invention may substantially improve the reflectivity when the microcell is displaying an extreme optical state, such as a white state. Increasing the white state may improve display visibility in low light conditions and may improve the color gamut of an electrophoretic display when a film comprising the microcells according to the present invention are combined with a color filter array (CFA).
According to one embodiment of the present invention illustrated in
The geometry of the microcells according to the various embodiments of the present invention also facilitates reflectance. For example, in
The geometry of the microcells may be provided in a variety of shapes. For example, referring to the plan views of the various embodiments illustrated in
Providing a wall angle for the microcell geometry that is steep, i.e. a more acute angle at the apex, may inhibit the black pigment from adhering to the wall and minimize the exposed area of the pigment packed into the apex. Furthermore, it is likely that steeper walls would result in more uniform coating of the viewing surface with pigment. For example, when switching from a black optical state to a white optical state, the white pigment is initially packed in the apex of the microcell and must then migrate from the apex to the viewing surface of the microcell. If the microcell is too shallow, the vertical distance traveled by the white pigment is short relative to the lateral dimension of the viewing area. For relatively steeper walls, the ratio of lateral to vertical distance traveled by the pigment is lower. A high ratio is likely to result in a thicker pigment coating in the center of the viewing area and a thinner, more transmissive coating about the perimeter of the viewing area upon switching the optical state. The ratio of lateral to vertical movement of the pigment should be selected to promote substantially uniform coverage of the pigment across the entire viewing area of each microcell. Other factors may also be considered when selecting the geometry of the microcell. For example, a shallow geometry will promote reflectivity by providing a shorter path for the light to be reflected. The dimensions of the microcell geometry may also be selected based on the desired display resolution, contrast, and switching speed of the electrophoretic display. In a preferred embodiment, the depth of the microcells is 20 to 50 microns.
Providing the microcells with a tapered geometry may also result in an increase of optically active surface area of the electrophoretic display. Referring again to
Referring to
In an alternative embodiment of an electrophoretic display, the location of the single continuous electrode layer and the pixel electrodes may be reversed, such that the single continuous electrode layer is located on the backplane and the pixel electrodes are located on the viewing side of the microcells. In this embodiment, it is not necessary for the single continuous electrode layer to be light-transmissive; however, the pixel electrodes must be light-transmissive. In this arrangement, it may be possible to provide colored pixel electrodes, so that the pixel electrodes may simultaneously serve as the CFA.
In another embodiment of the present invention, a method of making the tapered microcells is provided. As is known by those of skill in the art of microcell formation, embossing techniques are typically used wherein a tool, such as an embossing cylinder having a pattern in the shape of the microcells on its surface, is rolled onto a polymeric film. After embossing, the microcells are filled with a dispersion containing the charged pigment. To seal the microcells, a crosslinkable oligomeric or monomeric fluid may be coated over the filled microcells. An alternative sealing step may include laminating a sealant layer over the cups.
Referring to
The embossing step of the preferred method may comprise embossing an array of microcells 10 having a tapered geometry into a polymeric film 32, such as polyester, that is laminated to a release sheet 34. The film should be highly reflective by metallizing or incorporating reflective additives in the polymeric film, for example. If the polymeric film is metallized prior to embossing, the metal layer would most likely become discontinuous at all the edges of the microcell thereby avoiding electrical shorts between the front and rear electrodes of the display. A non-conductive reflective coating designed for constructive interference may also be applied to the film, such as the commercially available films used to improve emissive display backlight efficiency known to those of skill in the art, for example. The non-conductive reflective coating is preferably applied after embossing because the coatings are typically composed of oxides that may not survive embossing.
In a preferred embodiment of the present invention, the reflective coating on the embossed polymeric film may be a dielectric mirror. As known to those of skill in the art, a dielectric mirror comprises a plurality of thin layers of dielectric material deposited on a substrate. The reflectivity properties of the dielectric mirror depend on the type of dielectric material and the thickness of the coating. Various thin-film deposition methods may be employed to manufacture the dielectric mirror, such as physical vapor deposition (e.g. evaporative deposition and ion beam assisted deposition), chemical vapor deposition, ion beam deposition, molecular beam epitaxy, and sputter deposition. Dielectric materials used to form the dielectric mirror include, but are not limited to, aluminum, magnesium fluoride, silicon dioxide, tantalum pentoxide, zinc sulfide (n=2.32), and titanium dioxide (n=2.4).
To further promote reflectivity of the microcell walls, the various embodiments of the present invention may include features to prevent the black pigment from adhering to the walls of the microcell. In order to limit the presence of the black pigment to either spreading across the front viewing surface or packing into the apex of the microcell, the walls may be surface treated to repel the black pigment. For example, the microcell walls may be coated with a fluorinated polymer or other low surface energy material. Alternatively, after metallizing the surface of the microcells, the walls of the microcells may be treated with the same chargeable groups used to form the electrophoretic black pigment. If the microcell walls have a charge polarity that is similar to the charge polarity of the black pigment, the microcell walls will repel the black pigment.
In one embodiment, the metallized surface of the embossed polymeric film may include reactive sites that may be reacted with a reagent having a silane moiety bonded to one or more polar groups and/or one or more polymeric/polymerizable groups. The reactive sites may be hydroxyl groups, amine groups, carboxylic acid groups or derivatives thereof (e.g., amides or esters), alcohol or phenol groups or halogens, depending on the chemical functionality of the material used to provide the microcells walls with a reflective surface. The reactive sites may also be planted onto the surface of the microcell walls by conventional means or by special treatment such as hydration as described in U.S. Ser. No. 13/149,599 filed on May 31, 2011, the content of which is incorporated herein by reference in its entirety.
The polar group of the reagent may contribute charge to the microcell wall surface. For example, polar groups such as —NH— may contribute a positive charge and polar groups such as —OH or —COOH may contribute a negative charge. The polymeric/polymerizable group includes, but is not limited to, vinyl, acrylate, methacrylate groups or the like.
Reactive agents may include, but are not limited to N-(3-acryloxy-2-hydroxypropyl)-3-aminopropyltriethoxysilane (Gelest), 3-(N-allylamino)propyltrimethoxysilane (Gelest), 3-(N-styrylmethyl-2-aminoethylamino)-propyltrimethoxysilane (Gelest) or vinylbenzylaminoethylaminopropyl-trimethoxysilane (Z-6032, by Dow Corning).
The silane coupling reaction of the reagent to the microcell surface may be initiated by first hydrolyzing the silane moiety to form a reactive silanol group (Si—OH) which can subsequently bond with hydroxyl groups at the surface of the embossed film via a condensation reaction.
To prevent the white pigment having an opposite charge polarity from strongly adhering to the microcell walls, a steric stabilizing layer may be added to the walls in the same manner as is used on the black pigment. For example after the silane coupling reaction, the polymeric/polymerizable group may be polymerized if necessary with one or more types of monomers, oligomers or polymers, and combinations thereof, to form polymer stabilizers. The polymer stabilizers are desired to create a steric barrier of about 1 nm to about 50 nm, preferably about 5 nm to about 30 nm, and more preferably about 10 nm to about 20 nm, in thickness, on the microcell wall surface.
Suitable polymers, in the context of the present invention, may include, but are not limited to, polyethylene, polypropylene, polyacrylate, polyurethane, polyester or polysiloxane. Suitable monomers include, but are not limited to, lauryl acrylate, lauryl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, hexyl acrylate, hexyl methacrylate, n-octyl acrylate, n-octyl methacrylate, n-octadecyl acrylate and n-octadecyl methacrylate. Selection of the material for the polymer stabilizers would depend on the compatibility of the material with the solvent used in the electrophoretic fluid.
The combined thickness of the polymeric film 32 and release sheet 34 should be greater than the desired final dimensions of the geometry of the microcells. The polymeric film 32 should have a depth that is less than the height of the corresponding pattern on the embossing tool to ensure that the embossing tool penetrates through the polymeric film 32 and into the release sheet 34 during embossing. The release sheet 34 should have approximately the same elastic modulus of the polymeric film 32 and a sufficient thickness, so that the embossing cylinder will not be damaged by the opposing cylinder tool surface. In a preferred embodiment, the release sheet may comprise silicone coated polyethylene terephthalate.
The laminating step of the preferred method may comprise laminating a protective PET layer, optional CFA and front plane electrode film (ITO), such as layers 24, 26, and 20 in
The forming of openings in each of the microcells may comprise separating the release sheet 34 from the polymeric film 32 to remove the bottom portion of the embossed microcells 10, thereby forming a small hole at the bottom of each of the microcells 10. The width of the holes should be large enough to allow easy access to the interior of the microcells for the dispersion fluid, but of minimal size to facilitate sealing after filling.
The filling step of the preferred method may be achieved by various techniques.
In one method, the microcells may be filled by first evacuating the interiors of the microcells, such as by placing the laminated polymeric film 32 and PET-ITO layer with the release sheet 34 removed in a vacuum chamber. After applying a vacuum to evacuate the microcells of gas, the dispersion fluid may be applied onto the surface of the polymeric film 32 containing the small holes immediately followed by release of the vacuum to draw the dispersion fluid into the microcells. To minimize the potential for solvent evaporation in the dispersion fluid, it is preferred to place the combined polymeric film 32 and PET-ITO layer in a vacuum chamber having as small a volume as possible, i.e. slightly larger than the volume of the combined polymeric film 32 and PET-ITO layer, and releasing the vacuum as soon as a sufficient volume of dispersion fluid for filling the microcells has been applied to the polymeric film 32.
Another method of filling the microcells may comprise immersing the laminated polyester film 32 and PET-ITO layer with the release sheet 34 removed in an ultrasonic bath filled with the dispersion fluid. The ultrasonic agitation would drive the gas out of the microcells to be replaced by the dispersion fluid. The bath may be held under slight vacuum to accelerate the process if necessary. Ultrasonic agitation is a preferred filling method because of the potential for being scalable to a continuous process.
Yet another filling method may comprise filling the microcells with a solvent vapor that has a boiling point below ambient temperature, for example, but above the pour point or freezing temperature of the dispersion fluid. The laminated polymeric film 32 and PET-ITO layer with the release sheet 34 removed may then be immersed in the dispersion fluid and subsequently cooled to a temperature below the boiling point of the solvent vapor in the microcells. This would cause the solvent vapor to condense and draw the dispersion fluid into the microcells. The solvent vapor is preferably miscible in the dispersion fluid.
When the microcells are filled with the dispersion fluid, a sealant that is preferably immiscible in the dispersion fluid may be used to seal the microcells. A lamination adhesive that simultaneously meets the electrical, optical, and mechanical requirements of the electrophoretic display and has low solvent permeability may be used to seal the microcells and form a front plane laminate (FPL) comprising the microcell design of the present invention. Alternatively, a separate sealant may be used to seal the microcells prior to applying a layer of lamination adhesive and optional releasable sheet for forming an FPL. Because the openings in the polymeric film 32 are small relative to the overall area of the polymeric film, the surface of the polymeric film 32 will provide an adequate area for wetting and adhesion with the sealant. Because the sealant is applied to the rear non-viewing surface of the electrophoretic display of this preferred method, the sealant is less likely to interfere with the optical properties of the display.
While preferred embodiments of the invention have been shown and described herein, it will be understood that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will occur to those skilled in the art without departing from the spirit of the invention. Accordingly, it is intended that the appended claims cover all such variations as fall within the spirit and scope of the invention.
This application claims the benefit of and priority to U.S. Provisional Application having Ser. No. 62/524,640, filed Jun. 26, 2017, the content of which is incorporated by reference herein in its entirety.
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| Number | Date | Country | |
|---|---|---|---|
| 62524640 | Jun 2017 | US |
