An electrophoretic display (EPD) changes color by modifying the position of a charged colored particle with respect to a light-transmissive viewing surface. Such electrophoretic displays are typically referred to as “electronic paper” or “ePaper” because the resulting display has high contrast and is sunlight-readable, much like ink on paper. Electrophoretic displays have enjoyed widespread adoption in eReaders, such as the AMAZON KINDLE® because the electrophoretic displays provide a book-like reading experience, use little power, and allow a user to carry a library of hundreds of books in a lightweight handheld device.
For many years, electrophoretic displays included only two types of charged color particles, black and white. (To be sure, “color” as used herein includes black and white.) The white particles are often of the light scattering type, and comprise, e.g., titanium dioxide, while the black particle are absorptive across the visible spectrum, and may comprise carbon black, or an absorptive metal oxide, such as copper chromite. In the simplest sense, a black and white electrophoretic display only requires a light-transmissive electrode at the viewing surface, a back electrode, and an electrophoretic medium including oppositely charged white and black particles. When a voltage of one polarity is provided, the white particles move to the viewing surface, and when a voltage of the opposite polarity is provided the black particles move to the viewing surface. If the back electrode includes controllable regions (pixels)—either segmented electrodes or an active matrix of pixel electrodes controlled by transistors—a pattern can be made to appear electronically at the viewing surface. The pattern can be, for example, the text to a book.
More recently, a variety of color options have become commercially-available for electrophoretic displays, including three-color displays (black, white, red; black white, yellow), and four color displays (black, white, red, yellow). Similar to the operation of black and white electrophoretic displays, electrophoretic displays with three or four reflective pigments operate similar to the simple black and white displays because the desired color particle is driven to the viewing surface. The driving schemes are far more complicated than only black and white, but in the end, the optical function of the particles is the same.
Advanced Color electronic Paper (ACeP®) also included four particles, but the cyan, yellow, and magenta particles are subtractive rather than reflective, thereby allowing thousands of colors to be produced at each pixel. The color process is functionally equivalent to the printing methods that have long been used in offset printing and ink-jet printers. A given color is produced by using the correct ratio of cyan, yellow, and magenta on a bright white paper background. In the instance of ACeP, the relative positions of the cyan, yellow, magenta and white particles with respect to the viewing surface will determine the color at each pixel. While this type of electrophoretic display allows for thousands of colors at each pixel, it is critical to carefully control the position of each of the (50 to 500 nanometer-sized) pigments within a working space of about 10 to 20 micrometers in thickness. Obviously, variations in the position of the pigments will result in incorrect colors being displayed at a given pixel. Accordingly, exquisite voltage control is required for such a system. More details of this system are available in the following U.S. Patents, all of which are incorporated by reference in their entireties: U.S. Pat. Nos. 9,361,836, 9,921,451, 10,276,109, 10,353,266, 10,467,984, and 10,593,272.
This invention relates to color electrophoretic displays, especially, but not exclusively, to electrophoretic displays capable of rendering more than two colors using a single layer of electrophoretic material comprising a plurality of colored particles, for example white, cyan, yellow, and magenta particles. In some instances two of the particles will be positively-charged, and two particles will be negatively-charged. In some instances, one positively-charged particle will have a thick polymer shell and one negatively-charged particle has a thick polymer shell.
As described in U.S. Pat. No. 9,921,451, especially with respect to Table 3 of the '451 patent, improved color discrimination can be achieved with a “standard” active matrix backplane (i.e., including an array of thin-film transistors (TFT) that use amorphous silicon) by using so-called “top plane switching” in which the bias on the top electrode is altered during driving to achieve a larger voltage drop between the top electrode and the backplane. For example, to achieve a good magenta state it may be necessary to apply a voltage of +15V to the top electrode and −15V to the pixel electrode of the desired active matrix pixel so that the electrophoretic medium experiences an overall voltage drop of +30V (See FIG. 6A of the '451 patent). Later, when it is desired to, for example, produce a good yellow state, it may be necessary to apply a voltage of −15V to the top electrode and +15V to the pixel electrode of the desired active matrix pixel so that the electrophoretic medium experiences an overall voltage drop of −30V. (See FIG. 6C of the '451 patent). As described in more detail in the '451 patent, top plane switching can be used to address the electrophoretic medium as well as to clear prior optical states and to DC balance waveforms.
TFT-based thin film electronics may be used to control the addressing of pixel electrode for high-resolution displays such as LCD and EPD. Driver circuits can be integrated directly into the AM-TFT substrate, and TFT-based electronics are well suited to control pixel electrode voltages for EPD applications. TFTs can be made using a wide variety of semiconductor materials. A common material is silicon. The characteristics of a silicon-based TFT depend on the silicon's crystalline state, that is, the semiconductor layer can be either amorphous silicon (a-Si), microcrystalline silicon, or it can be annealed into low-temperature polysilicon (LTPS). TFTs based on a-Si are cheap to produce so that relatively large substrate areas can be manufactured at relatively low cost. One downside of TFTs based upon a-Si is that the bias across the TFT is typically limited to no more than 45V. Beyond 45V, the transistor can fail or have “breakthrough” during which excess current moves through the transistor and charges, e.g., a pixel electrode beyond the desired level. More exotic materials, such as metal oxides may also be used to fabricate thin film transistor arrays, and achieve higher voltages, but the fabrication costs of such devices is typically high because of the specialized equipment needed to handle/deposit the metal oxides.
For active matrix devices, the drive signals are often output from a controller to gate and scan drivers that, in turn, provide the required current-voltage inputs to active the various TFT in the active matrix. However, controller-drivers capable of receiving, e.g., image data, and outputting the necessary current-voltage inputs to active the TFTs are commercially available. Most active matrices of thin-film-transistors are drive with line-at-a-time (a.k.a., line-by-line) addressing, which is used in the vast majority of LCD and EPD displays. In such systems, one or more controllers are used to deliver a voltage to a series of scan lines and a series of gate lines, which are often arranged perpendicularly in a grid across the backplane. Other controllers, or the same controller, will also provide voltages to the top electrode as well as a common voltage (Vcom) provided to a storage capacitor that is typically associated with a given pixel electrode.
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 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.
The term impulse, when used to refer to driving an electrophoretic display, is used herein to refer to the integral of the applied voltage with respect to time during the period in which the display is driven.
“Gate driver” is a power amplifier that accepts a low-power input from a controller, for instance a microcontroller integrated circuit (IC), and produces a high-current drive input for the gate of a high-power transistor such as a TFT coupled to a pixel electrode. “Source driver” is a power amplifier producing a high-current drive input for the source of a high-power transistor. “Top plane common electrode driver” or “top plane driver” or “top electrode driver” is a power amplifier producing a high-current drive input for the top plane electrode of a display.
“Waveform” denotes the entire voltage against time curve used to actuate a pixel in a microfluidic device. Typically, such a waveform will comprise a plurality of waveform elements, where these elements are essentially rectangular (i.e., where a given element comprises application of a constant voltage for a period of time). The elements may be called “voltage pulses” or “drive pulses”. The term “drive scheme” denotes a set of waveforms sufficient to effect a manipulation of one or more droplets in the course of a specific droplet operation. The term “frame” denotes a single update of all the pixel rows in a microfluidic device.
A particle that absorbs, scatters, or reflects light, either in a broad band or at selected wavelengths, is referred to herein as a colored or pigment particle. Various materials other than pigments (in the strict sense of that term as meaning insoluble colored materials) that absorb or reflect light, such as dyes or photonic crystals, etc., may also be used in the electrophoretic media and displays of the present invention.
Particle-based electrophoretic displays have been the subject of intense research and development for a number of years. In such displays, a plurality of charged particles (sometimes referred to as pigment 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) and E Ink Corporation describe various technologies used in encapsulated electrophoretic and other electro-optic media. Such encapsulated 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. Typically, the capsules are themselves held within a polymeric binder to form a coherent layer positioned between two electrodes. The technologies described in these patents and applications include:
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, U.S. Pat. No. 6,866,760. Accordingly, for purposes of the present application, such polymer-dispersed electrophoretic media are regarded as sub-species of encapsulated electrophoretic media.
A related type of electrophoretic display is a so-called microcell electrophoretic display. 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, U.S. Pat. Nos. 6,672,921 and 6,788,449.
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, U.S. Pat. Nos. 5,872,552; 6,130,774; 6,144,361; 6,172,798; 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. Other types of electro-optic displays may also be capable of operating in shutter mode. Electro-optic media operating in shutter mode can be used in multi-layer structures for full color displays; in such structures, at least one layer adjacent the viewing surface of the display operates in shutter mode to expose or conceal a second layer more distant from the viewing surface.
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; electrophoretic deposition (See U.S. Pat. No. 7,339,715); 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.
As indicated above most simple prior art electrophoretic media essentially display only two colors. Such electrophoretic media either use a single type of electrophoretic particle having a first color in a colored fluid having a second, different color (in which case, the first color is displayed when the particles lie adjacent the viewing surface of the display and the second color is displayed when the particles are spaced from the viewing surface), or first and second types of electrophoretic particles having differing first and second colors in an uncolored fluid (in which case, the first color is displayed when the first type of particles lie adjacent the viewing surface of the display and the second color is displayed when the second type of particles lie adjacent the viewing surface). Typically the two colors are black and white. If a full color display is desired, a color filter array may be deposited over the viewing surface of the monochrome (black and white) display. Displays with color filter arrays rely on area sharing and color blending to create color stimuli. The available display area is shared between three or four primary colors such as red/green/blue (RGB) or red/green/blue/white (RGBW), and the filters can be arranged in one-dimensional (stripe) or two-dimensional (2×2) repeat patterns. Other choices of primary colors or more than three primaries are also known in the art. The three (in the case of RGB displays) or four (in the case of RGBW displays) sub-pixels are chosen small enough so that at the intended viewing distance they visually blend together to a single pixel with a uniform color stimulus (‘color blending’). The inherent disadvantage of area sharing is that the colorants are always present, and colors can only be modulated by switching the corresponding pixels of the underlying monochrome display to white or black (switching the corresponding primary colors on or off). For example, in an ideal RGBW display, each of the red, green, blue and white primaries occupy one fourth of the display area (one sub-pixel out of four), with the white sub-pixel being as bright as the underlying monochrome display white, and each of the colored sub-pixels being no lighter than one third of the monochrome display white. The brightness of the white color shown by the display as a whole cannot be more than one half of the brightness of the white sub-pixel (white areas of the display are produced by displaying the one white sub-pixel out of each four, plus each colored sub-pixel in its colored form being equivalent to one third of a white sub-pixel, so the three colored sub-pixels combined contribute no more than the one white sub-pixel). The brightness and saturation of colors is lowered by area-sharing with color pixels switched to black. Area sharing is especially problematic when mixing yellow because it is lighter than any other color of equal brightness, and saturated yellow is almost as bright as white. Switching the blue pixels (one fourth of the display area) to black makes the yellow too dark.
Disclosed herein are improved methods of driving full color electrophoretic displays and full color electrophoretic displays using these drive methods. In one aspect, a method of driving an electro-optic display comprising a layer of electro-optic material disposed between a top electrode and a backplane. In the display, the backplane includes an array of pixel electrodes, wherein each pixel electrode is coupled to a thin film transistor (TFT) and a storage capacitor. The TFT includes a source, a gate, and a drain, wherein the gate is coupled to a gate line, the source is coupled to a scan line, and the drain is coupled to the pixel electrode, wherein a controller provides time-dependent voltages to the gate line, the scan line, the top electrode, and the storage capacitor. A first side of the storage capacitor is coupled to the pixel electrode and a second side of the storage capacitor is coupled to the controller. The method of driving includes a) providing a first high voltage to the scan line and a first low voltage to the top electrode and the second side of the storage capacitor, b) providing a first gate pulse sufficient to open the TFT, c) after the first gate pulse, providing a zero voltage to the scan line, the top electrode and the second side of the storage capacitor, d) providing a second gate pulse sufficient to open the TFT, e) after the second gate pulse, providing a second low voltage to the scan line and a second high voltage to the top electrode and the storage capacitor, and f) providing a third gate pulse sufficient to open the TFT.
In one embodiment, steps a)-f) are completed in three subsequent frames. In one embodiment, the top electrode is light-transmissive. In one embodiment, the top electrode and the second side of the storage capacitor are electrically coupled to a common node. In one embodiment, the TFT is fabricated from amorphous silicon. In one embodiment, the first and second high voltages are +15V. In one embodiment, the first and second low voltages are −15V. In one embodiment, the layer of electro-optic material includes an encapsulated electrophoretic medium comprising a plurality of types of charged particles that move between the top electrode and the backplane in response to an applied electric field. In one embodiment, the electrophoretic medium is encapsulated in a plurality of microcapsules or encapsulated in a plurality of sealed microcells. In one embodiment, the encapsulated electrophoretic medium comprises four different types of charged particles.
In another aspect, a method of driving an electro-optic display comprising a layer of electro-optic material disposed between a top electrode and a backplane. In the display, the backplane includes an array of pixel electrodes, wherein each pixel electrode is coupled to a thin film transistor (TFT) and a storage capacitor. The TFT includes a source, a gate, and a drain, wherein the gate is coupled to a gate line, the source is coupled to a scan line, and the drain is coupled to the pixel electrode, wherein a controller provides time-dependent voltages to the gate line, the scan line, the top electrode, and the storage capacitor. A first side of the storage capacitor is coupled to the pixel electrode and a second side of the storage capacitor is coupled to the controller. The method of driving comprises a) providing a first high voltage to the scan line and a first low voltage to the top electrode and the second side of the storage capacitor, b) providing a first gate pulse sufficient to open the TFT, c) after the first gate pulse, providing a second low voltage to the scan line, d) providing a second gate pulse sufficient to open the TFT, e) after the second gate pulse, providing a second high voltage to the top electrode and the second side of the storage capacitor, and f) providing a third gate pulse sufficient to open the TFT.
In one embodiment, steps a)-f) are completed in three subsequent frames. In one embodiment, the top electrode is light-transmissive. In one embodiment, the top electrode and the second side of the storage capacitor are electrically coupled to a common node. In one embodiment, the TFT is fabricated from amorphous silicon. In one embodiment, the first and second high voltages are +15V. In one embodiment, the first and second low voltages are −15V. In one embodiment, the layer of electro-optic material includes an encapsulated electrophoretic medium comprising a plurality of types of charged particles that move between the top electrode and the backplane in response to an applied electric field. In one embodiment, the electrophoretic medium is encapsulated in a plurality of microcapsules or encapsulated in a plurality of sealed microcells. In one embodiment, the encapsulated electrophoretic medium comprises four different types of charged particles.
In another aspect, a method of driving an electro-optic display comprising a layer of electro-optic material disposed between a top electrode and a backplane. In the display, the backplane includes an array of pixel electrodes, wherein each pixel electrode is coupled to a thin film transistor (TFT) and a storage capacitor. The TFT includes a source, a gate, and a drain, wherein the gate is coupled to a gate line, the source is coupled to a scan line, and the drain is coupled to the pixel electrode, wherein a controller provides time-dependent voltages to the gate line, the scan line, the top electrode, and the storage capacitor. A first side of the storage capacitor is coupled to the pixel electrode and a second side of the storage capacitor is coupled to the controller. The method of driving comprises a) providing a first high voltage to the scan line and a first low voltage to the top electrode and the second side of the storage capacitor, b) providing a first gate pulse sufficient to open the TFT, c) after the first gate pulse, providing a second high voltage to the top electrode and the second side of the storage capacitor, d) providing a second gate pulse sufficient to open the TFT, e) after the second gate pulse, providing a second low voltage to the scan line, and f) providing a third gate pulse sufficient to open the TFT.
In one embodiment, steps a)-f) are completed in three subsequent frames. In one embodiment, the top electrode is light-transmissive. In one embodiment, the top electrode and the second side of the storage capacitor are electrically coupled to a common node. In one embodiment, the TFT is fabricated from amorphous silicon. In one embodiment, the first and second high voltages are +15V. In one embodiment, the first and second low voltages are −15V. In one embodiment, the layer of electro-optic material includes an encapsulated electrophoretic medium comprising a plurality of types of charged particles that move between the top electrode and the backplane in response to an applied electric field. In one embodiment, the electrophoretic medium is encapsulated in a plurality of microcapsules or encapsulated in a plurality of sealed microcells. In one embodiment, the encapsulated electrophoretic medium comprises four different types of charged particles.
In another aspect, a method of driving an electro-optic display. The display includes a layer of electro-optic material disposed between a top electrode and a backplane, the backplane including an array of pixel electrodes, wherein each pixel electrode is coupled to a thin film transistor (TFT) and a storage capacitor, the TFT including a source, a gate, and a drain, wherein the gate is coupled to a gate line, the source is coupled to a scan line, and the drain is coupled to the pixel electrode, wherein the controller provides time-dependent voltages to the gate line, the scan line, and the top electrode. The electro-optic display is configured to execute the following steps (in order): (a) provide a first voltage to the top electrode, (b) provide a specific voltage to each electrode of the array of pixel electrodes in a first sequential order, wherein at least 10 pixels of the array have specific voltages different from the majority of the pixel electrodes, (c) provide a specific voltage to each electrode of the array of pixel electrodes in a second sequential order, wherein the order of providing specific voltages to pixel electrodes in the second sequential order is a reverse order of the first sequential order, and wherein each pixel receives the same specific voltage in both the first sequential order and the second sequential order, and (d) provide a second voltage different from the first voltage to the top electrode. The pixel electrodes do not receive another voltage from the controller between steps (b) and (c). In one embodiment, the TFT is fabricated from amorphous silicon. In one embodiment, the top electrode is light-transmissive. In one embodiment, the first voltage is +15V and the second voltage is −15V. In one embodiment, the first voltage is −15V and the second voltage is +15V. In one embodiment, at least 100 pixels of the array have specific voltages different from the majority of the pixel electrodes. In one embodiment, the layer of electro-optic material includes an encapsulated electrophoretic medium comprising a plurality of types of charged particles that move between the top electrode and the backplane in response to an applied electric field. In one embodiment, the electrophoretic medium is encapsulated in a plurality of microcapsules or encapsulated in a plurality of sealed microcells. In one embodiment, the encapsulated electrophoretic medium comprises four different types of charged particles.
The invention provides improved methods of driving electro-optic media devices with so-called top-plane switching, i.e., where the voltage on the top electrode is varied during the course of a device update. In some embodiments, the invention is used with an electrophoretic medium including four particles wherein two of the particles are colored and subtractive and at least one of the particles is scattering. Typically, such a system includes a white particle and cyan, yellow, and magenta subtractive primary colored particles. Such a system is shown schematically in
A display device may be constructed using an electrophoretic fluid of the invention in several ways that are known in the prior art. The electrophoretic fluid may be encapsulated in microcapsules or incorporated into microcell structures that are thereafter sealed with a polymeric layer. The microcapsule or microcell layers may be coated or embossed onto a plastic substrate or film bearing a transparent coating of an electrically conductive material. This assembly may be laminated to a backplane bearing pixel electrodes using an electrically conductive adhesive. Alternatively, the electrophoretic fluid may be dispensed directly on a thin open-cell grid that has been arranged on a backplane including an active matrix of pixel electrodes. The filled grid can then be top-sealed with an integrated protective sheet/light-transmissive electrode.
Regarding
The electrophoretic medium 120 is typically compartmentalized such by a microcapsule 126 or the walls of a microcell 127. The entire display stack is typically disposed on a substrate 150, which may be rigid or flexible. The display (101, 102) typically also includes a protective layer 160, which may simply protect the top electrode 110 from damage, or it may envelop the entire display (101, 102) to prevent ingress of water, etc. Electrophoretic displays (101, 102) may also include one or more adhesive layers 140, 170, and/or sealing layers 180 as needed. In some embodiments an adhesive layer may include a primer component to improve adhesion to the electrode layer 110, or a separate primer layer (not shown in FIG. 1 or 2) may be used. (The structures of electrophoretic displays and the component parts, pigments, adhesives, electrode materials, etc., are described in many patents and patent applications published by E Ink Corporation, such as U.S. Pat. Nos. 6,922,276; 7,002,728; 7,072,095; 7,116,318; 7,715,088, and 7,839,564, all of which are incorporated by reference herein in their entireties.
Amorphous silicon TFT backplanes usually have only one transistor per pixel electrode or propulsion electrode. As illustrated in in
Increasing the capacitance of the storage capacitor Cs reduces cross-talk, but at the cost of rendering the pixels harder to charge, and increasing the charge time. As shown in
Most commercial electrophoretic displays use amorphous silicon based thin-film transistors (TFTs) in the construction of active matrix backplanes (See
To obtain a high-resolution display, individual pixels of a display must be addressable without interference from adjacent pixels. One way to achieve this objective is to provide an array of non-linear elements, such as transistors or diodes, with at least one non-linear element associated with each pixel, to produce an active matrix display 400, shown in
Conventionally, in high resolution arrays, the pixels are arranged in a two-dimensional array of rows and columns, such that any specific pixel is uniquely defined by the intersection of one specified row and one specified column. The sources of all the transistors in each column are connected to a single column (scan) line 406, while the gates of all the transistors in each row are connected to a single row (gate) line 408; again the assignment of sources to rows and gates to columns is conventional but essentially arbitrary, and could be reversed if desired. The gate lines 408 are connected to a gate line driver 412, which essentially ensures that at any given moment only one row is selected, i.e., that there is applied to the selected row electrode a select voltage such as to ensure that all the transistors in the selected row are conductive, while there is applied to all other rows a non-select voltage such as to ensure that all the transistors in these non-selected rows remain non-conductive. The column scan lines 406 are connected to scan line drivers 410, which place upon the various scan lines 406 voltages selected to drive the pixels in the selected row to their desired optical states. (The aforementioned voltages are relative to a common top electrode, and is not shown in
Thus, as described above, it is possible to increase the active field above a pixel electrode using top plane switching. In the instance of ACeP®, each of the eight principal colors (red, green, blue, cyan magenta, yellow, black and white) corresponds to a different arrangement of the four pigments, such that the viewer only sees those colored pigments that are on the viewing side of the white pigment (i.e., the only pigment that scatters light). This is shown in
For example, in U.S. Pat. No. 9,921,451, seven different voltages are applied to each pixel electrode to facilitate a full palette of colors at each individual pixel electrodes: three positive, three negative, and zero. Typically, the maximum voltages used in these waveforms are higher than that can be handled by amorphous silicon thin-film transistors, without top plane switching however.
An obvious issue with top plane switching is that when the top plane is switched from a first state, e.g., −15V to a second state +15V the electro-optic medium or droplets between the top plane and the pixel electrode (i.e., VFPL) will experience a huge swing in electric field, which may result in the pixel not achieving the correct impulse during that frame. Thus, if VTOP is changed and VCOM is not compensated, a pixel may not achieve the correct color, or a droplet may not move as quickly as is anticipated. To overcome this dramatic shift, the VCOM and VTOP lines are typically tied together, e.g., through a common node, as shown in
Nonetheless, as explained in
As shown in
The location-dependent effects of top plane switching are further detailed in
A second problem that is observed with top plane switching for larger area active matrix switching is that, even though the voltage between the pixel electrode and the top electrode is “correct” for much of the frame, the total impulse (voltage×time), which ultimately determines the response of e.g., the electro-optic medium or the droplet is not the same between the pixels in the first row of the array and the pixels in the last row of the array. This phenomenon is illustrated in
In a typical system, as illustrated in
One straightforward solution to this shortcoming is to change the pattern of addressing the gate lines to help alleviate this non-uniformity, thereby creating a “superframe” of driving that involves more than one scan of each gate lines for each voltage and more than one pattern of addressing the lines to aid uniformity. Of course, adding additional update pathing between top plane updates increases the length of each frame. Nonetheless, in many applications, the extra time is acceptable to avoid under-switching some of the pixels, as described above.
In one embodiment of the invention, the “superframe” involves a first frame where the gate lines start at the first line n and proceeds in the normal mode of operation iterating one at a time n+1, n+2 etc to the last line n=m where m is the number of gate lines. In the second frame of the superframe, the mth gate line is the first line addressed and the gate driver iterates in reverse starting at m, to m−1, m−2, and ending with n, the first line. In other words, the update involves two steps. A first step is to scan in the traditional “left to right, top to bottom” scan pathway. The second step is to scan in reverse, i.e., “right to left, bottom to top.” By having this arrangement where the iteration goes through the gate lines forward and then backwards before the top plane voltage is changed the uniformity of top plane switching of the panel is dramatically increased. An exemplary two step pathway is illustrated in
The invention exemplified in
In advanced embodiments, the performance shortcomings and risks to damage can be alleviated by inserting “rest” or “zero” frames between top plane switches. The zero frames may actually take VCOM and VS to 0V, or some nominal voltage value, or VCOM can be matched to VS for one frame or VS can be matched to VCOM for one frame. The idea is that as the top plane voltage changes, it is possible to prevent large voltage spikes on as yet un-scanned pixels, which could cause those pixels to leak and/or lose their charge and/or fail. In some embodiments, the best results are found when a single frame is inserted where all of the scan lines are fed the identical voltage as the last top electrode voltage and all of the TFTs are gated once. In some embodiments, all of the gates may be opened simultaneously or nearly simultaneously. Of course, adding additional frames to an optical waveform or an electrowetting drive protocol increase the time to complete the task.
It is understood that, even though the corresponding −30V to +30V pulse sequences are not shown in the figures, the driving polarity is arbitrary. Thus, the polarity of the pulse sequences can be flipped in order to achieve the same electrical performance, but with the opposite polarity. Of course, flipped polarities may have a real effect on the display medium or the electrophoretic propulsion, i.e., switching from white to black instead of from black to white, or causing a droplet to stay on a pixel electrode rather than move to an adjacent pixel electrode. Nonetheless, the driving waveforms and the methods of driving are identical except for the polarity of the voltage. Additionally, the pulse sequences described may be spaced apart with intervening frames of no voltage, for example, to stretch out the waveform. The sequences can also be repeated any number of times for the sake of repetitive driving, or to improve an ultimate optical state. The sequences described herein may also be combined as desired.
An alternative method of decreasing the strain on the TFT circuit and improving driving consistency is to take VS to VCOM between top plane switches. This method is illustrated in
Thus, the invention provides for improved top plane switching for driving electro-optic displays. Having thus described several aspects and embodiments of the technology of this application, it is to be appreciated that various alterations, modifications, and improvements will readily occur to those of ordinary skill in the art. Such alterations, modifications, and improvements are intended to be within the spirit and scope of the technology described in the application. For example, those of ordinary skill in the art will readily envision a variety of other means and/or structures for performing the function and/or obtaining the results and/or one or more of the advantages described herein, and each of such variations and/or modifications is deemed to be within the scope of the embodiments described herein. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments described herein. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, inventive embodiments may be practiced otherwise than as specifically described. In addition, any combination of two or more features, systems, articles, materials, kits, and/or methods described herein, if such features, systems, articles, materials, kits, and/or methods are not mutually inconsistent, is included within the scope of the present disclosure.
This application claims priority to U.S. Provisional Patent Application No. 63/292,440, filed Dec. 22, 2021 and to U.S. Provisional Patent Application No. 63/422,884, filed Nov. 4, 2022. All patents and publications disclosed herein are incorporated by reference in their entireties.
Number | Name | Date | Kind |
---|---|---|---|
4418346 | Batchelder | Nov 1983 | A |
5872552 | Gordon, II et al. | Feb 1999 | A |
5930026 | Jacobson et al. | Jul 1999 | A |
6017584 | Albert et al. | Jan 2000 | A |
6130774 | Albert et al. | Oct 2000 | A |
6144361 | Gordon, II et al. | Nov 2000 | A |
6172798 | Albert et al. | Jan 2001 | B1 |
6184856 | Gordon, II et al. | Feb 2001 | B1 |
6225971 | Gordon, II et al. | May 2001 | B1 |
6241921 | Jacobson et al. | Jun 2001 | B1 |
6271823 | Gordon, II et al. | Aug 2001 | B1 |
6445489 | Jacobson et al. | Sep 2002 | B1 |
6504524 | Gates et al. | Jan 2003 | B1 |
6512354 | Jacobson et al. | Jan 2003 | B2 |
6531997 | Gates et al. | Mar 2003 | B1 |
6545797 | Chen et al. | Apr 2003 | B2 |
6664944 | Albert et al. | Dec 2003 | B1 |
6672921 | Liang et al. | Jan 2004 | B1 |
6753999 | Zehner et al. | Jun 2004 | B2 |
6788449 | Liang et al. | Sep 2004 | B2 |
6788452 | Liang et al. | Sep 2004 | B2 |
6825970 | Goenaga et al. | Nov 2004 | B2 |
6864875 | Drzaic et al. | Mar 2005 | B2 |
6866760 | Paolini, Jr. et al. | Mar 2005 | B2 |
6900851 | Morrison et al. | May 2005 | B2 |
6914714 | Chen et al. | Jul 2005 | B2 |
6922276 | Zhang et al. | Jul 2005 | B2 |
6972893 | Chen et al. | Dec 2005 | B2 |
6982178 | LeCain et al. | Jan 2006 | B2 |
6995550 | Jacobson et al. | Feb 2006 | B2 |
7002728 | Pullen et al. | Feb 2006 | B2 |
7012600 | Zehner et al. | Mar 2006 | B2 |
7023420 | Comiskey et al. | Apr 2006 | B2 |
7034783 | Gates et al. | Apr 2006 | B2 |
7038656 | Liang et al. | May 2006 | B2 |
7038670 | Liang et al. | May 2006 | B2 |
7046228 | Liang et al. | May 2006 | B2 |
7052571 | Wang et al. | May 2006 | B2 |
7061166 | Kuniyasu | Jun 2006 | B2 |
7061662 | Chung et al. | Jun 2006 | B2 |
7072095 | Liang et al. | Jul 2006 | B2 |
7075502 | Drzaic et al. | Jul 2006 | B1 |
7116318 | Amundson et al. | Oct 2006 | B2 |
7116466 | Whitesides et al. | Oct 2006 | B2 |
7119772 | Amundson et al. | Oct 2006 | B2 |
7144942 | Zang et al. | Dec 2006 | B2 |
7167155 | Albert et al. | Jan 2007 | B1 |
7170670 | Webber | Jan 2007 | B2 |
7176880 | Amundson et al. | Feb 2007 | B2 |
7177066 | Chung et al. | Feb 2007 | B2 |
7193625 | Danner et al. | Mar 2007 | B2 |
7202847 | Gates | Apr 2007 | B2 |
7236291 | Kaga et al. | Jun 2007 | B2 |
7242514 | Chung et al. | Jul 2007 | B2 |
7259744 | Arango et al. | Aug 2007 | B2 |
7304787 | Whitesides et al. | Dec 2007 | B2 |
7312784 | Baucom et al. | Dec 2007 | B2 |
7312794 | Zehner et al. | Dec 2007 | B2 |
7321459 | Masuda et al. | Jan 2008 | B2 |
7327511 | Whitesides et al. | Feb 2008 | B2 |
7339715 | Webber et al. | Mar 2008 | B2 |
7385751 | Chen et al. | Jun 2008 | B2 |
7408699 | Wang et al. | Aug 2008 | B2 |
7411719 | Paolini, Jr. et al. | Aug 2008 | B2 |
7453445 | Amundson | Nov 2008 | B2 |
7492339 | Amundson | Feb 2009 | B2 |
7492505 | Liang et al. | Feb 2009 | B2 |
7528822 | Amundson et al. | May 2009 | B2 |
7535624 | Amundson et al. | May 2009 | B2 |
7545358 | Gates et al. | Jun 2009 | B2 |
7583251 | Arango et al. | Sep 2009 | B2 |
7602374 | Zehner et al. | Oct 2009 | B2 |
7612760 | Kawai | Nov 2009 | B2 |
7667684 | Jacobson et al. | Feb 2010 | B2 |
7679599 | Kawai | Mar 2010 | B2 |
7679813 | Liang et al. | Mar 2010 | B2 |
7679814 | Paolini, Jr. et al. | Mar 2010 | B2 |
7683606 | Kang et al. | Mar 2010 | B2 |
7684108 | Wang et al. | Mar 2010 | B2 |
7688297 | Zehner et al. | Mar 2010 | B2 |
7715088 | Liang et al. | May 2010 | B2 |
7729039 | LeCain et al. | Jun 2010 | B2 |
7733311 | Amundson et al. | Jun 2010 | B2 |
7733335 | Zehner et al. | Jun 2010 | B2 |
7787169 | Abramson et al. | Aug 2010 | B2 |
7791789 | Albert et al. | Sep 2010 | B2 |
7800813 | Wu et al. | Sep 2010 | B2 |
7821702 | Liang et al. | Oct 2010 | B2 |
7839564 | Whitesides et al. | Nov 2010 | B2 |
7859742 | Chiu et al. | Dec 2010 | B1 |
7910175 | Webber | Mar 2011 | B2 |
7952557 | Amundson | May 2011 | B2 |
7952790 | Honeyman et al. | May 2011 | B2 |
7956841 | Albert et al. | Jun 2011 | B2 |
7982479 | Wang et al. | Jul 2011 | B2 |
7982941 | Lin et al. | Jul 2011 | B2 |
7999787 | Amundson et al. | Aug 2011 | B2 |
8009348 | Zehner et al. | Aug 2011 | B2 |
8040594 | Paolini, Jr. et al. | Oct 2011 | B2 |
8054526 | Bouchard | Nov 2011 | B2 |
8077141 | Duthaler et al. | Dec 2011 | B2 |
8098418 | Paolini, Jr. et al. | Jan 2012 | B2 |
8125501 | Amundson et al. | Feb 2012 | B2 |
8139050 | Jacobson et al. | Mar 2012 | B2 |
8159636 | Sun et al. | Apr 2012 | B2 |
8174490 | Whitesides et al. | May 2012 | B2 |
8213076 | Albert et al. | Jul 2012 | B2 |
8243013 | Sprague et al. | Aug 2012 | B1 |
8274472 | Wang et al. | Sep 2012 | B1 |
8289250 | Zehner et al. | Oct 2012 | B2 |
8300006 | Zhou et al. | Oct 2012 | B2 |
8305341 | Arango et al. | Nov 2012 | B2 |
8314784 | Ohkami et al. | Nov 2012 | B2 |
8325130 | Nam | Dec 2012 | B2 |
8363299 | Paolini, Jr. et al. | Jan 2013 | B2 |
8373649 | Low et al. | Feb 2013 | B2 |
8384658 | Albert et al. | Feb 2013 | B2 |
8422116 | Sprague et al. | Apr 2013 | B2 |
8441714 | Paolini, Jr. et al. | May 2013 | B2 |
8441716 | Paolini, Jr. et al. | May 2013 | B2 |
8456414 | Lin et al. | Jun 2013 | B2 |
8462102 | Wong et al. | Jun 2013 | B2 |
8466852 | Drzaic et al. | Jun 2013 | B2 |
8503063 | Sprague | Aug 2013 | B2 |
8514168 | Chung et al. | Aug 2013 | B2 |
8537105 | Chiu et al. | Sep 2013 | B2 |
8558783 | Wilcox et al. | Oct 2013 | B2 |
8558785 | Zehner et al. | Oct 2013 | B2 |
8558786 | Lin | Oct 2013 | B2 |
8558855 | Sprague et al. | Oct 2013 | B2 |
8576164 | Sprague et al. | Nov 2013 | B2 |
8576259 | Lin et al. | Nov 2013 | B2 |
8576470 | Paolini, Jr. et al. | Nov 2013 | B2 |
8576475 | Huang et al. | Nov 2013 | B2 |
8593396 | Amundson et al. | Nov 2013 | B2 |
8593721 | Albert et al. | Nov 2013 | B2 |
8605032 | Liu et al. | Dec 2013 | B2 |
8605354 | Zhang et al. | Dec 2013 | B2 |
8643595 | Chung et al. | Feb 2014 | B2 |
8649084 | Wang et al. | Feb 2014 | B2 |
8665206 | Lin et al. | Mar 2014 | B2 |
8670174 | Sprague et al. | Mar 2014 | B2 |
8681191 | Yang et al. | Mar 2014 | B2 |
8704756 | Lin | Apr 2014 | B2 |
8717664 | Wang et al. | May 2014 | B2 |
8730153 | Sprague et al. | May 2014 | B2 |
8786935 | Sprague | Jul 2014 | B2 |
8797634 | Paolini, Jr. et al. | Aug 2014 | B2 |
8810525 | Sprague | Aug 2014 | B2 |
8810899 | Sprague et al. | Aug 2014 | B2 |
8830559 | Honeyman et al. | Sep 2014 | B2 |
8873129 | Paolini, Jr. et al. | Oct 2014 | B2 |
8902153 | Bouchard et al. | Dec 2014 | B2 |
8902491 | Wang et al. | Dec 2014 | B2 |
8917439 | Wang et al. | Dec 2014 | B2 |
8928562 | Gates et al. | Jan 2015 | B2 |
8928641 | Chiu et al. | Jan 2015 | B2 |
8964282 | Wang et al. | Feb 2015 | B2 |
8976444 | Zhang et al. | Mar 2015 | B2 |
9013394 | Lin | Apr 2015 | B2 |
9013783 | Sprague | Apr 2015 | B2 |
9019197 | Lin | Apr 2015 | B2 |
9019198 | Lin et al. | Apr 2015 | B2 |
9019318 | Sprague et al. | Apr 2015 | B2 |
9082352 | Cheng et al. | Jul 2015 | B2 |
9116412 | Lin | Aug 2015 | B2 |
9146439 | Zhang | Sep 2015 | B2 |
9164207 | Honeyman et al. | Oct 2015 | B2 |
9170467 | Whitesides et al. | Oct 2015 | B2 |
9170468 | Lin et al. | Oct 2015 | B2 |
9171508 | Sprague et al. | Oct 2015 | B2 |
9182646 | Paolini, Jr. et al. | Nov 2015 | B2 |
9195111 | Anseth et al. | Nov 2015 | B2 |
9199441 | Danner | Dec 2015 | B2 |
9218773 | Sun et al. | Dec 2015 | B2 |
9224338 | Chan et al. | Dec 2015 | B2 |
9224342 | Sprague et al. | Dec 2015 | B2 |
9224344 | Chung et al. | Dec 2015 | B2 |
9230492 | Harrington et al. | Jan 2016 | B2 |
9251736 | Lin et al. | Feb 2016 | B2 |
9262973 | Wu et al. | Feb 2016 | B2 |
9268191 | Paolini, Jr. et al. | Feb 2016 | B2 |
9269311 | Amundson | Feb 2016 | B2 |
9279906 | Kang | Mar 2016 | B2 |
9285649 | Du et al. | Mar 2016 | B2 |
9293511 | Jacobson et al. | Mar 2016 | B2 |
9299294 | Lin et al. | Mar 2016 | B2 |
9341916 | Telfer et al. | May 2016 | B2 |
9360733 | Wang et al. | Jun 2016 | B2 |
9361836 | Telfer et al. | Jun 2016 | B1 |
9373289 | Sprague et al. | Jun 2016 | B2 |
9383623 | Lin et al. | Jul 2016 | B2 |
9390066 | Smith et al. | Jul 2016 | B2 |
9390661 | Chiu et al. | Jul 2016 | B2 |
9412314 | Amundson et al. | Aug 2016 | B2 |
9423666 | Wang et al. | Aug 2016 | B2 |
9459510 | Lin | Oct 2016 | B2 |
9460666 | Sprague et al. | Oct 2016 | B2 |
9495918 | Harrington et al. | Nov 2016 | B2 |
9501981 | Lin et al. | Nov 2016 | B2 |
9513527 | Chan et al. | Dec 2016 | B2 |
9513743 | Sjodin et al. | Dec 2016 | B2 |
9514667 | Lin | Dec 2016 | B2 |
9541814 | Lin et al. | Jan 2017 | B2 |
9542895 | Gates et al. | Jan 2017 | B2 |
9558696 | Son et al. | Jan 2017 | B2 |
9564088 | Wilcox et al. | Feb 2017 | B2 |
9612502 | Danner et al. | Apr 2017 | B2 |
9620048 | Sim et al. | Apr 2017 | B2 |
9620067 | Harrington et al. | Apr 2017 | B2 |
9671668 | Chan et al. | Jun 2017 | B2 |
9672766 | Sjodin | Jun 2017 | B2 |
9691333 | Cheng et al. | Jun 2017 | B2 |
9697778 | Telfer et al. | Jul 2017 | B2 |
9721495 | Harrington et al. | Aug 2017 | B2 |
9740076 | Paolini, Jr. et al. | Aug 2017 | B2 |
9759980 | Du et al. | Sep 2017 | B2 |
9792861 | Chang et al. | Oct 2017 | B2 |
9792862 | Hung et al. | Oct 2017 | B2 |
9812073 | Lin et al. | Nov 2017 | B2 |
9921451 | Telfer et al. | Mar 2018 | B2 |
9966018 | Gates et al. | May 2018 | B2 |
10037735 | Amundson | Jul 2018 | B2 |
10162242 | Wang et al. | Dec 2018 | B2 |
10209556 | Rosenfeld et al. | Feb 2019 | B2 |
10229641 | Yang et al. | Mar 2019 | B2 |
10276109 | Crounse et al. | Apr 2019 | B2 |
10319313 | Harris et al. | Jun 2019 | B2 |
10339876 | Lin et al. | Jul 2019 | B2 |
10353266 | Bouchard et al. | Jul 2019 | B2 |
10444553 | Laxton | Oct 2019 | B2 |
10467984 | Buckley et al. | Nov 2019 | B2 |
10514583 | Zhang | Dec 2019 | B2 |
10573257 | Emelie et al. | Feb 2020 | B2 |
10593272 | Telfer et al. | Mar 2020 | B2 |
10672350 | Amundson et al. | Jun 2020 | B2 |
20030102858 | Jacobson et al. | Jun 2003 | A1 |
20040246562 | Chung et al. | Dec 2004 | A1 |
20050253777 | Zehner et al. | Nov 2005 | A1 |
20070091418 | Danner et al. | Apr 2007 | A1 |
20070103427 | Zhou et al. | May 2007 | A1 |
20070176912 | Beames et al. | Aug 2007 | A1 |
20080024429 | Zehner | Jan 2008 | A1 |
20080024482 | Gates et al. | Jan 2008 | A1 |
20080043318 | Whitesides et al. | Feb 2008 | A1 |
20080048970 | Drzaic et al. | Feb 2008 | A1 |
20080136774 | Harris et al. | Jun 2008 | A1 |
20080303780 | Sprague et al. | Dec 2008 | A1 |
20090174651 | Jacobson et al. | Jul 2009 | A1 |
20090225398 | Duthaler et al. | Sep 2009 | A1 |
20090322721 | Zehner et al. | Dec 2009 | A1 |
20100156780 | Jacobson et al. | Jun 2010 | A1 |
20100194733 | Lin et al. | Aug 2010 | A1 |
20100194789 | Lin et al. | Aug 2010 | A1 |
20100220121 | Zehner et al. | Sep 2010 | A1 |
20100231580 | Miyasaka | Sep 2010 | A1 |
20100259524 | Markvoort | Oct 2010 | A1 |
20100265561 | Gates et al. | Oct 2010 | A1 |
20100289838 | Markvoort | Nov 2010 | A1 |
20110043543 | Chen et al. | Feb 2011 | A1 |
20110063314 | Chiu et al. | Mar 2011 | A1 |
20110175875 | Lin et al. | Jul 2011 | A1 |
20110193840 | Amundson et al. | Aug 2011 | A1 |
20110193841 | Amundson et al. | Aug 2011 | A1 |
20110199671 | Amundson et al. | Aug 2011 | A1 |
20110221740 | Yang et al. | Sep 2011 | A1 |
20120001957 | Liu et al. | Jan 2012 | A1 |
20120092319 | van Veenendaal | Apr 2012 | A1 |
20120098740 | Chiu et al. | Apr 2012 | A1 |
20120326957 | Drzaic et al. | Dec 2012 | A1 |
20130063333 | Arango et al. | Mar 2013 | A1 |
20130242378 | Paolini, Jr. et al. | Sep 2013 | A1 |
20130249782 | Wu et al. | Sep 2013 | A1 |
20130278995 | Drzaic et al. | Oct 2013 | A1 |
20140009817 | Wilcox et al. | Jan 2014 | A1 |
20140055840 | Zang et al. | Feb 2014 | A1 |
20140078576 | Sprague | Mar 2014 | A1 |
20140204012 | Wu et al. | Jul 2014 | A1 |
20140240210 | Wu et al. | Aug 2014 | A1 |
20140253425 | Zalesky et al. | Sep 2014 | A1 |
20140293398 | Wang et al. | Oct 2014 | A1 |
20140362213 | Tseng | Dec 2014 | A1 |
20150005720 | Zang et al. | Jan 2015 | A1 |
20150118390 | Rosenfeld et al. | Apr 2015 | A1 |
20150262255 | Khajehnouri et al. | Sep 2015 | A1 |
20150262551 | Zehner et al. | Sep 2015 | A1 |
20150268531 | Wang et al. | Sep 2015 | A1 |
20150301246 | Zang et al. | Oct 2015 | A1 |
20160012710 | Lu et al. | Jan 2016 | A1 |
20160048054 | Danner | Feb 2016 | A1 |
20160140910 | Amundson | May 2016 | A1 |
20160180777 | Lin et al. | Jun 2016 | A1 |
Number | Date | Country |
---|---|---|
20140015040 | Feb 2014 | KR |
Entry |
---|
Kitamura, T. et al., “Electrical toner movement for electronic paper-like display”, Asia Display/IDW '01, pp. 1517-1520, Paper HCS1-1 (2001). 2001. |
Yamaguchi, Y. et al., “Toner display using insulative particles charged triboelectrically”, Asia Display/IDW '01, pp. 1729-1730, Paper AMD4-4 (2001). 2001. |
Korean Intellectual Property Office, “International Search Report and Written Opinion”, PCT/US2022/052559, dated Apr. 21, 2023. |
Number | Date | Country | |
---|---|---|---|
20230197025 A1 | Jun 2023 | US |
Number | Date | Country | |
---|---|---|---|
63422884 | Nov 2022 | US | |
63292440 | Dec 2021 | US |