The present invention is directed to a color display device which can display high quality color states, and an electrophoretic fluid for such an electrophoretic display.
In order to achieve a color display, color filters are often used. The most common approach is to add color filters on top of black/white sub-pixels of a pixelated display to display the red, green and blue colors. When a red color is desired, the green and blue sub-pixels are turned to the black state so that the only color displayed is red. When the black state is desired, all three-sub-pixels are turned to the black state. When the white state is desired, the three sub-pixels are turned to red, green and blue, respectively, and as a result, a white state is seen by the viewer.
The biggest disadvantage of such a technique is that since each of the sub-pixels has a reflectance of about one third (⅓) of the desired white state, the white state is fairly dim. To compensate this, a fourth sub-pixel may be added which can display only the black and white states, so that the white level is doubled at the expense of the red, green or blue color level (where each sub-pixel is only one fourth of the area of the pixel). Brighter colors can be achieved by adding light from the white pixel, but this is achieved at the expense of color gamut to cause the colors to be very light and unsaturated. A similar result can also be achieved by reducing the color saturation of the three sub-pixels. Even with these approaches, the white level is normally substantially less than half of that of a black and white display, rendering it an unacceptable choice for display devices, such as e-readers or displays that need well readable black-white brightness and contrast.
The present invention not only provides a realistic solution for a color display device which can display highly saturated color states, but also eliminates the need of color filters.
More specifically, the present invention is directed to an electrophoretic fluid comprising a first type of pigment particles, a second type of pigment particles and a third type of pigment particles, all of which are dispersed in a solvent or solvent mixture, wherein:
In one embodiment, the first type of pigment particles and the second type of pigment particles are of the black and white colors, respectively.
In one embodiment, the third type of pigment particles is non-white and non-black.
In one embodiment, the third type of pigment particles is of a color selected from the group consisting red, green, blue, yellow, cyan and magenta.
In one embodiment, the three types of pigment particles have different levels of threshold voltage. One of the first type and second type of particles may have a threshold voltage. The third type of particles may be larger than the first or the second type of particles. The third type of particles may be about 2 to about 50 times larger than the first or second type of particles. The third type of particles may carry the same charge polarity as the type of particles which has a threshold voltage. The third type of particles may have a charge level less than about 50% of the charge intensity of the first type or second type of particles.
In one embodiment, the three types of pigment particles have different levels of mobility. The charge intensity of the first type of pigment particles may be at least about 2 times the charge intensity of the second type of pigment particles and the charge intensity of the third type of particles may be about 50% less than the charge intensity of the second type of particles. The third type of particles may be larger than the first or the second type of particles. The third type of particles may be about 2 to about 50 times larger than the first or second type of particles.
In one embodiment, the fluid of the present invention is filled in display cells, which are sandwiched between a common electrode layer and a layer of pixel electrodes. The display cells may be microcups or microcapsules.
In one embodiment, the display cells are aligned with the pixel electrodes. In another embodiment, the display cells are not aligned with the pixel electrodes.
In one embodiment, the third type of pigment particles is of the same color in all display cells. In another embodiment, the third type of pigment particles is of different colors in display cells.
In one embodiment, the fluid of the present invention is driven by a voltage potential difference (ΔV) between the common electrode and the pixel electrode (see
In one embodiment, a driving method for an electrophoretic display comprising display cells filled with an electrophoretic fluid, which fluid is sandwiched between a common electrode and a layer of pixel electrodes and comprises a first type of pigment particles, a second type of pigment particles and a third type of pigment particles, all of which are dispersed in a solvent or solvent mixture, wherein:
In one embodiment, the method further comprises applying a shaking waveform before an area corresponding to a pixel electrode is driven to the color state of the first type of pigment particles.
In one embodiment, when the color of the third type of particles is seen at a viewing side, the first and second types of particles gather at the side opposite of the viewing side, resulting in an intermediate color between colors of the first and second types of particles.
In one embodiment, a display layer comprises an electrophoretic fluid sandwiched between a common electrode and a layer of pixel electrodes and having first and second surfaces on opposed sides thereof, the electrophoretic fluid comprising a first type of particles, a second type of particles and a third type of particles, all dispersed in a solvent or solvent mixture, the first, second and third types of particles having respectively first, second and third optical characteristics differing from one another, the first type of particles having a charge of one polarity and the second and third types of particles having charges of the opposite polarity, and the second type of particles having an electric field threshold, such that:
In one embodiment, a driving method for a display layer comprising an electrophoretic fluid sandwiched between a common electrode and a layer of pixel electrodes and having first and second surfaces on opposed sides thereof, the electrophoretic fluid comprising a first type of particles, a second type of particles and a third type of particles, all dispersed in a solvent or solvent mixture, the first, second and third types of particles having respectively first, second and third optical characteristics differing from one another, the first type of particles having a charge of one polarity and the second and third types of particles having charges of the opposite polarity, and the second type of particles having an electric field threshold, which method comprises:
In one embodiment, a driving method for a display layer comprising an electrophoretic fluid sandwiched between a common electrode and a layer of pixel electrodes and having first and second surfaces on opposed sides thereof, the electrophoretic fluid comprising a first type of particles, a second type of particles and a third type of particles, all dispersed in a solvent or solvent mixture, the first, second and third types of particles having respectively first, second and third optical characteristics differing from one another, the first type of particles having a charge of one polarity and the second and third types of particles having charges of the opposite polarity, and the second type of particles having an electric field threshold, which method comprises driving an area corresponding to a pixel electrode from a color state of the first type of particles to a color state of the third type of particles by applying an electric field between the common electrode and the pixel electrode, which electric field is the same as, or weaker than, the electric field threshold of the second type of particles.
The electrophoretic fluid (10) of present invention comprises three types of pigment particles dispersed in a dielectric solvent or solvent mixture (10a). For ease of illustration, the three types of pigment particles may be referred to as white particles (11), black particles (12) and colored particles (13), as shown in
A display layer utilizing the display fluid of the present invention has two surfaces, a first surface (16) on the viewing side and a second surface (17) on the opposite side of the first surface (16). The display fluid is sandwiched between the two surfaces. On the side of the first surface (16), there is a common electrode (14) which is a transparent electrode layer (e.g., ITO), spreading over the entire top of the display layer. On the side of the second surface (17), there is an electrode layer (15) which comprises a plurality of pixel electrodes (15a). The display fluid is filled in display cells. The display cells may be aligned with or not aligned with the pixel electrodes, as explained below. An area corresponding to a pixel electrode may be referred to as a pixel or a sub-pixel. The driving of an area corresponding to a pixel electrode is effected by applying a voltage potential difference (or known as an electric field) between the common electrode and the pixel electrode.
The pixel electrodes are described in U.S. Pat. No. 7,046,228, the content of which is incorporated herein by reference in its entirety. It is noted that while active matrix driving with a thin film transistor (TFT) backplane is mentioned for the layer of pixel electrodes, the scope of the present invention encompasses other types of electrode addressing as long as the electrodes serve the desired functions.
For the white particles (11), they may be formed from an inorganic pigment, such as TiO2, ZrO2, ZnO, Al2O3, Sb2O3, BaSO4, PbSO4 or the like.
For the black particles (12), they may be formed from CI pigment black 26 or 28 or the like (e.g., manganese ferrite black spinel or copper chromite black spinel) or carbon black.
The third type of particles may be of a color such as red, green, blue, magenta, cyan or yellow. The pigments for this type of particles may include, but are not limited to, CI pigment PR 254, PR122, PR149, PG36, PG58, PG7, PB28, PB15:3, PY138, PY150, PY155 or PY20. Those are commonly used organic pigments described in color index handbook “New Pigment Application Technology” (CMC Publishing Co, Ltd, 1986) and “Printing Ink Technology” (CMC Publishing Co, Ltd, 1984). Specific examples include Clariant Hostaperm Red D3G 70-EDS, Hostaperm Pink E-EDS, PV fast red D3G, Hostaperm red D3G 70, Hostaperm Blue B2G-EDS, Hostaperm Yellow H4G-EDS, Hostaperm Green GNX, BASF Irgazine red L 3630, Cinquasia Red L 4100 HD, and Irgazin Red L 3660 HD; Sun Chemical phthalocyanine blue, phthalocyanine green, diarylide yellow or diarylide AAOT yellow.
In addition to the colors, the first, second and third types of particles may have other distinct optical characteristics, 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 percentages of the three types of pigment particles in the fluid may vary. For example, the black particle may take up about 0.1% to 10%, preferably 0.5% to 5% by volume of the electrophoretic fluid; the white particle may take up about 1% to 50%, preferably 5% to 15% by volume of the fluid; and the colored particle may take up about 2% to 20%, preferably 4% to 10% by volume of the fluid.
There may be other particulate matters in the fluid which are included as additives to enhance performance of the display device, such as switching speed, imaging bistability and reliability.
The solvent in which the three types of pigment particles are dispersed is clear and colorless. It preferably has a low viscosity and a dielectric constant in the range of about 2 to about 30, preferably about 2 to about 15 for high particle mobility. Examples of suitable dielectric solvent include hydrocarbons such as isopar, decahydronaphthalene (DECALIN), 5-ethylidene-2-norbornene, fatty oils, paraffin oil, silicon fluids, aromatic hydrocarbons such as toluene, xylene, phenylxylylethane, dodecylbenzene or alkylnaphthalene, halogenated solvents such as perfluorodecalin, perfluorotoluene, perfluoroxylene, dichlorobenzotrifluoride, 3,4,5-trichlorobenzotrifluoride, chloropentafluoro-benzene, dichlorononane or pentachlorobenzene, and perfluorinated solvents such as FC-43, FC-70 or FC-5060 from 3M Company, St. Paul, Minn., low molecular weight halogen containing polymers such as poly(perfluoropropylene oxide) from TCI America, Portland, Oreg., poly(chlorotrifluoro-ethylene) such as Halocarbon Oils from Halocarbon Product Corp., River Edge, N.J., perfluoropolyalkylether such as Galden from Ausimont or Krytox Oils and Greases K-Fluid Series from DuPont, Del., polydimethylsiloxane based silicone oil from Dow-corning (DC-200).
Two of the three types of pigment particles carry opposite charge polarities and the third type of pigment particles is slightly charged. The term “slightly charged” is intended to refer to the charge level of the particles less than about 50%, preferably about 5% to about 30%, of the charge intensity of the stronger charged particles. In one embodiment, the charge intensity may be measured in terms of zeta potential. In one embodiment, the zeta potential is determined by Colloidal Dynamics AcoustoSizer IIM with a CSPU-100 signal processing unit, ESA EN #Attn flow through cell (K:127). The instrument constants, such as density of the solvent used in the sample, dielectric constant of the solvent, speed of sound in the solvent, viscosity of the solvent, all of which at the testing temperature (25° C.) are entered before testing. Pigment samples are dispersed in the solvent (which is usually a hydrocarbon fluid having less than 12 carbon atoms), and diluted to between 5-10% by weight. The sample also contains a charge control agent (Solsperse 17000®, available from Lubrizol Corporation, a Berkshire Hathaway company; “Solsperse” is a Registered Trade Mark), with a weight ratio of 1:10 of the charge control agent to the particles. The mass of the diluted sample is determined and the sample is then loaded into the flow through cell for determination of the zeta potential.
If the black particles are positively charged and the white particles are negatively charged, then the colored pigment particles may be slightly charged. In other words, in this example, the charges carried by the black and the white particles are much more intense than the charge carried by the colored particles.
In addition, the third type of particles which carries a slight charge has a charge polarity which is the same as the charge polarity carried by either one of the other two types of the stronger charged particles.
The three types of particles may have varying sizes. In one embodiment, one of the three types of particles is larger than the other two types. It is noted that among the three types of particles, the one type of particles which is slightly charged preferably has the larger size. For example, both the black and the white particles are relatively small and their sizes (tested through dynamic light scattering) may range from about 50 nm to about 800 nm and more preferably from about 200 nm to about 700 nm, and in this example, the colored particles which are slightly charged, preferably are about 2 to about 50 times and more preferably about 2 to about 10 times larger than the black particles and the white particles.
The term “threshold voltage” or “electric field threshold”, in the context of the present invention, is defined as the maximum electric field that may be applied for a period of time (typically not longer than 30 seconds, preferably not longer than 15 seconds), to a group of particles, without causing the particles to appear at the viewing side of a pixel, when the pixel is driven from a color state different from the color state of the group of particles. The term “viewing side”, in the present application, refers to the first surface in a display layer where images are seen by the viewers.
The threshold voltage or electric field threshold is either an inherent characteristic of the charged particles or an additive-induced property.
In the former case, the threshold voltage or electric field threshold is generated, relying on certain attraction force between oppositely charged particles or between particles and certain substrate surfaces.
In the case of additive-induced threshold voltage or electric field threshold, a threshold agent which induces or enhances the threshold characteristics of an electrophoretic fluid may be added. The threshold agent may be any material which is soluble or dispersible in the solvent or solvent mixture of the electrophoretic fluid and carries or induces a charge opposite to that of the charged particles. The threshold agent may be sensitive or insensitive to the change of applied voltage. The term “threshold agent” may broadly include dyes or pigments, electrolytes or polyelectrolytes, polymers, oligomers, surfactants, charge controlling agents and the like.
Additional information relating to the threshold agent may be found in U.S. Pat. No. 8,115,729, the content of which is incorporated herein by reference in its entirety.
The following are a few examples illustrating the present invention.
This example is demonstrated in
The white particles (21) are negatively charged while the black particles (22) are positively charged, and both types of the particles are smaller than the colored particles (23).
The colored particles (23) carry the same charge polarity as the black particles which have the threshold voltage, but are slightly charged. As a result, the black particles move faster than the colored particles (23), when an applied voltage potential is higher than the threshold voltage of the black particles because of the stronger charge intensity they carry.
In
In
The colored particles (23) move towards the pixel electrode because they are also positively charged. However, because of their lower charge intensity and larger size, they move slower than the black particles.
In
The driving from the white color state in
A driving method for an electrophoretic display comprising display cells filled with an electrophoretic fluid sandwiched between a common electrode and a layer of pixel electrodes, which fluid comprises a first type of pigment particles, a second type of pigment particles and a third type of pigment particles, all of which are dispersed in a solvent or solvent mixture, wherein:
In this method, the first type of pigment particles (21) is of the white color; the second type of pigment particles (22) is of the black color; and the third type of pigment particles (23) is of the red color, as shown in
In order to drive the display to the color state of the third type of pigment particles, i.e., red (see
In
In this scenario, when the color of the third type of particles is seen at the viewing side, the other two types of the particles may be mixed at the non-viewing side (side opposite of the viewing side), resulting in an intermediate color state between colors of the first and second types of particles. If the first and second types of particles are black and white and the third type of particles is red, then in
The driving method ideally would ensure both color brightness (i.e., preventing the black particles from being seen) and color purity (i.e., preventing the white particles from being seen) in the scenario of
One solution to this is the use of a shaking waveform prior to driving from the color state of the first type of pigment particles (i.e., white) to the color state of the third type of pigment particles (i.e., red). The shaking waveform consists of repeating a pair of opposite driving pulses for many cycles. For example, the shaking waveform may consist of a +15V pulse for 20 msec and a −15V pulse for 20 msec and such a pair of pulses is repeated for 50 times. The total time of such a shaking waveform would be 2000 msec (see
The shaking waveform may be applied to an area corresponding to a pixel electrode regardless of its optical state (black, white or red) prior to a driving voltage is applied. After the shaking waveform is applied, the optical state would not be a pure white, pure black or pure red. Instead, the color state would be from a mixture of the three types of particles.
For the method as described above, a shaking waveform is applied to an area corresponding to a pixel electrode prior to the area being driven to the color state (i.e., white) of the first type of pigment particles. With this added shaking waveform, even though the white state is measurably the same as that without the shaking waveform, the color state (i.e., red) of the third type of pigment particles would be significantly better than that without the shaking waveform, on both color brightness and color purity. This is an indication of better separation of the white particles from the red particles as well as the black particles from the red particles.
Each of the driving pulse in the shaking waveform is applied for not exceeding half of the driving time required from the full black state to the full white state. For example, if it takes 300 msec to drive an area corresponding to a pixel electrode from a full black state to a full white state or vice versa, the shaking waveform may consist of positive and negative pulses, each applied for not more than 150 msec. In practice, it is preferred that the pulses are shorter.
In an alternative design as demonstrated in
The white pigment particles (31) are negatively charged while the black pigment particles (32) are positively charged, and both types of the pigment particles are smaller than the colored particles (33).
The colored particles (33) carry the same charge polarity as the white particles which have the threshold voltage, but are slightly charged. As a result, the white particles move faster than the colored particles (33), when an applied voltage potential is higher than the threshold voltage of the white particles because of the stronger charge intensity they carry.
In
In
The colored particles (33) move towards the pixel electrode as they are also negatively charged. However, because of their lower charge intensity and larger size, they move slower than the white particles.
In
The driving of
It is also possible to have the colored particles to have a threshold voltage, as shown in
The black pigment particles (42) are negatively charged while the colored pigment particles (43) are positively charged, and both types of the pigment particles are smaller than the white particles (41).
The white particles (41) carry the same charge polarity as the colored particles which have the threshold voltage, but are slightly charged. As a result, the colored particles move faster than the white particles (41), when an applied voltage potential difference is higher than the threshold voltage of the colored particles because of the stronger charge intensity they carry.
In
In
The white particles (41) move towards the pixel electrode as they are also positively charged. However, because of their lower charge intensity and larger size, they move slower than the colored particles.
In
The driving of
In an alternative embodiment of the present invention, all three types of pigment particles have different levels of charge intensity, thus different levels of mobility.
For example, the first and second types of particles carry opposite charge polarities and the charge intensity of first type of particles is at least about 2 times, preferably about 3 to about 15 times, the charge intensity of the second type of particles, or vice versa. The charge intensity of the third type of particles is less than about 50%, preferably about 5% to about 30%, the charge intensity of the first or second type of particles, whichever has a lower charge intensity. In a specific example, if black particles have twice the charge intensity of the white particles, then the colored particles may have less than 50% the charge intensity of the white particles.
The particles that carry the least charge intensity are preferably larger than the other two types of particles.
Due to different levels of charge intensity, the three types of pigment particles would have different levels of mobility. The higher the charge intensity, the faster the particles move. The following example demonstrates this embodiment of the invention.
This example is shown in
Therefore if it takes a driving time, t, for the black particles to travel the distance between the common electrode and a pixel electrode (“d”), it would then take 2t for the white particles and at least 4t for the colored particles, to travel the same distance, d.
In addition, the black particles are positively charged and the white particles are negatively charged. The colored particles carry the same charge polarity as the particles having the highest intensity, that is, the black particles in this case.
In
In
Because of their low charge intensity and low mobility, the colored particles barely move. While the black and colored particles carry the same charge polarity, the black particles would move to be closer to the common electrode because of their higher charge intensity and smaller size.
Before the step of
As shown in this example, the switching among three optical states therefore could be achieved by controlling the driving time frame, driving amplitude or both.
The larger and slower moving particles in this example are the colored particles. However, the designs may vary depending on the needs. It is also possible to make the black or white particles the larger and slower moving particles.
The electrophoretic fluid in an electrophoretic display device is filled in display cells. The display cells may be microcups as described in U.S. Pat. No. 6,930,818, the content of which is incorporated herein by reference in its entirety. The display cells may also be other types of micro-containers, such as microcapsules, microchannels or equivalents, regardless of their shapes or sizes. All of these are within the scope of the present application.
In one embodiment of the present invention, the display device utilizing the present electrophoretic fluid is a high-light display device and in this embodiment, the colored particles are of the same color in all display cells. Each display cell would be a pixel in such a highlight display device if the display cells are aligned with the pixel electrodes. However, as shown in
In another embodiment, the display device utilizing the present electrophoretic fluid may be a multi-color display device. In this embodiment, the colored particles are of different colors in the display cells. In this embodiment, the display cells and the pixel electrodes are aligned.
In
While the present invention has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications may be made to adapt a particular situation, materials, compositions, processes, process step or steps, to the objective and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto.
This application is a continuation of application Ser. No. 14/458,185, filed Apr. 12, 2014 (Publication No. 2014/0347407, now U.S. Pat. No. 9,360,733, issued Jun. 7, 2016), which is a continuation-in-part of application Ser. No. 13/875,145, filed May 1, 2013 (now U.S. Pat. No. 8,964,282, issued Feb. 24, 2015); which is a continuation-in-part of application Ser. No. 13/633,788, filed Oct. 2, 2012 (now U.S. Pat. No. 8,717,664, issued May 6, 2014); the above applications are incorporated herein by reference in their entirety.
Number | Name | Date | Kind |
---|---|---|---|
3756693 | Ota | Sep 1973 | A |
6600534 | Tanaka | Jul 2003 | B1 |
6680726 | Gordon, II | Jan 2004 | B2 |
6751007 | Liang | Jun 2004 | B2 |
6781745 | Chung | Aug 2004 | B2 |
6859302 | Liang | Feb 2005 | B2 |
6864875 | Drzaic | Mar 2005 | B2 |
6870661 | Pullen | Mar 2005 | B2 |
6930818 | Liang | Aug 2005 | B1 |
6967762 | Machida | Nov 2005 | B2 |
6987503 | Inoue | Jan 2006 | B2 |
7019889 | Katase | Mar 2006 | B2 |
7034987 | Schlangen | Apr 2006 | B2 |
7038655 | Herb | May 2006 | B2 |
7038656 | Liang | May 2006 | B2 |
7038670 | Liang | May 2006 | B2 |
7046228 | Liang | May 2006 | B2 |
7075502 | Drzaic | Jul 2006 | B1 |
7259744 | Arango | Aug 2007 | B2 |
7271947 | Liang | Sep 2007 | B2 |
7292386 | Kanbe | Nov 2007 | B2 |
7312916 | Pullen | Dec 2007 | B2 |
7342556 | Oue | Mar 2008 | B2 |
7345810 | Chopra | Mar 2008 | B2 |
7352353 | Albert | Apr 2008 | B2 |
7382521 | Chopra | Jun 2008 | B2 |
7420549 | Jacobson | Sep 2008 | B2 |
7433113 | Chopra | Oct 2008 | B2 |
7474295 | Matsuda | Jan 2009 | B2 |
7492505 | Liang | Feb 2009 | B2 |
7557981 | Liang | Jul 2009 | B2 |
7572394 | Gu | Aug 2009 | B2 |
7636076 | Hung | Dec 2009 | B2 |
7652656 | Chopra | Jan 2010 | B2 |
7656576 | Suwabe | Feb 2010 | B2 |
7675502 | Chopra | Mar 2010 | B2 |
7679599 | Kawai | Mar 2010 | B2 |
7679813 | Liang | Mar 2010 | B2 |
7760419 | Lee | Jul 2010 | B2 |
7800813 | Wu | Sep 2010 | B2 |
7821702 | Liang | Oct 2010 | B2 |
7821792 | Belady | Oct 2010 | B2 |
7830592 | Sprague | Nov 2010 | B1 |
7848009 | Machida | Dec 2010 | B2 |
7852547 | Kim | Dec 2010 | B2 |
7852548 | Roh | Dec 2010 | B2 |
7875307 | Lin | Jan 2011 | B2 |
7952558 | Yang | May 2011 | B2 |
8040594 | Paolini, Jr. | Oct 2011 | B2 |
8054288 | Sugita | Nov 2011 | B2 |
8067305 | Zafiropoulo | Nov 2011 | B2 |
8072674 | Wang | Dec 2011 | B2 |
8077141 | Duthaler | Dec 2011 | B2 |
8081375 | Komatsu | Dec 2011 | B2 |
8115729 | Danner | Feb 2012 | B2 |
8120838 | Lin | Feb 2012 | B2 |
8237892 | Sprague | Aug 2012 | B1 |
8243013 | Sprague | Aug 2012 | B1 |
8395836 | Lin | Mar 2013 | B2 |
8422116 | Sprague | Apr 2013 | B2 |
8441714 | Paolini, Jr. | May 2013 | B2 |
8466852 | Drzaic | Jun 2013 | B2 |
8477404 | Moriyama | Jul 2013 | B2 |
8477405 | Ishii | Jul 2013 | B2 |
8520296 | Wang | Aug 2013 | B2 |
8558855 | Sprague | Oct 2013 | B2 |
8565522 | Swic | Oct 2013 | B2 |
8570272 | Hsieh | Oct 2013 | B2 |
8570639 | Masuzawa | Oct 2013 | B2 |
8574937 | Shi | Nov 2013 | B2 |
8576475 | Huang | Nov 2013 | B2 |
8605354 | Zhang | Dec 2013 | B2 |
8629832 | Tanabe | Jan 2014 | B2 |
8649084 | Wang | Feb 2014 | B2 |
8670174 | Sprague | Mar 2014 | B2 |
8674978 | Komatsu | Mar 2014 | B2 |
8687265 | Ahn | Apr 2014 | B2 |
8704754 | Machida | Apr 2014 | B2 |
8704756 | Lin | Apr 2014 | B2 |
8717661 | Kawai | May 2014 | B2 |
8717662 | Komatsu | May 2014 | B2 |
8717664 | Wang | May 2014 | B2 |
8786935 | Sprague | Jul 2014 | B2 |
8797636 | Yang | Aug 2014 | B2 |
8810899 | Sprague | Aug 2014 | B2 |
8902491 | Wang | Dec 2014 | B2 |
8917439 | Wang | Dec 2014 | B2 |
8963903 | Sakamoto | Feb 2015 | B2 |
8964282 | Wang | Feb 2015 | B2 |
9013516 | Sakamoto | Apr 2015 | B2 |
9013783 | Sprague | Apr 2015 | B2 |
9052564 | Sprague | Jun 2015 | B2 |
9170468 | Lin | Oct 2015 | B2 |
9176358 | Fujimori | Nov 2015 | B2 |
9251736 | Lin | Feb 2016 | B2 |
9285649 | Du | Mar 2016 | B2 |
9360733 | Wang | Jun 2016 | B2 |
9383623 | Lin | Jul 2016 | B2 |
9459510 | Lin | Oct 2016 | B2 |
20030002132 | Foucher | Jan 2003 | A1 |
20030095094 | Goden | May 2003 | A1 |
20030107631 | Goto | Jun 2003 | A1 |
20040190115 | Liang | Sep 2004 | A1 |
20070002008 | Tam | Jan 2007 | A1 |
20070080926 | Zhou | Apr 2007 | A1 |
20070080928 | Ishii | Apr 2007 | A1 |
20070126694 | Moriyama | Jun 2007 | A1 |
20070268556 | Chopra | Nov 2007 | A1 |
20070273637 | Zhou | Nov 2007 | A1 |
20080042928 | Schlangen | Feb 2008 | A1 |
20080062159 | Roh | Mar 2008 | A1 |
20080174531 | Sah | Jul 2008 | A1 |
20090034054 | Ikegami | Feb 2009 | A1 |
20100134407 | Wang | Jun 2010 | A1 |
20100165005 | Sprague | Jul 2010 | A1 |
20100165448 | Sprague | Jul 2010 | A1 |
20110043543 | Chen | Feb 2011 | A1 |
20110134508 | Kawashima | Jun 2011 | A1 |
20110175939 | Moriyama | Jul 2011 | A1 |
20110217639 | Sprague | Sep 2011 | A1 |
20120007897 | Yang | Jan 2012 | A1 |
20120194899 | Zhang | Aug 2012 | A1 |
20120299947 | Tsuda | Nov 2012 | A1 |
20130278995 | Drzaic | Oct 2013 | A1 |
20130300727 | Lin | Nov 2013 | A1 |
20140055840 | Zang | Feb 2014 | A1 |
20140340736 | Lin | Nov 2014 | A1 |
20140362213 | Tseng | Dec 2014 | A1 |
20150103394 | Wang | Apr 2015 | A1 |
20150198858 | Chan | Jul 2015 | A1 |
20150234250 | Lin | Aug 2015 | A1 |
20150268531 | Wang | Sep 2015 | A1 |
20150301246 | Zang | Oct 2015 | A1 |
20160011484 | Chan | Jan 2016 | A1 |
20160026062 | Zhang | Jan 2016 | A1 |
20160048054 | Danner | Feb 2016 | A1 |
20160116816 | Paolini | Apr 2016 | A1 |
20160116818 | Du | Apr 2016 | A1 |
20160140909 | Lin | May 2016 | A1 |
Number | Date | Country |
---|---|---|
1617033 | May 2005 | CN |
1089118 | Apr 2001 | EP |
2000322007 | Nov 2000 | JP |
2004020818 | Jan 2004 | JP |
2006343458 | Dec 2006 | JP |
2007140129 | Jun 2007 | JP |
2007322617 | Dec 2007 | JP |
2008033000 | Feb 2008 | JP |
2008033335 | Feb 2008 | JP |
2008209589 | Sep 2008 | JP |
2009116041 | May 2009 | JP |
2009192637 | Aug 2009 | JP |
2011158783 | Aug 2011 | JP |
1020070082680 | Aug 2007 | KR |
1020080023913 | Mar 2008 | KR |
20080034533 | Apr 2008 | KR |
1020110103765 | Sep 2011 | KR |
101232146 | Feb 2013 | KR |
201237529 | Sep 2012 | TW |
WO199953373 | Oct 1999 | WO |
WO2003016993 | Feb 2003 | WO |
WO2007013682 | Feb 2007 | WO |
WO2009105385 | Aug 2009 | WO |
WO2009124142 | Oct 2009 | WO |
WO2009134889 | Nov 2009 | WO |
WO2010027810 | Mar 2010 | WO |
Entry |
---|
European Patent Office, EP Appl. No. 18020193.1, European Search Report, dated Aug. 6, 2018. |
Number | Date | Country | |
---|---|---|---|
20160260372 A1 | Sep 2016 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 14458185 | Aug 2014 | US |
Child | 15153190 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 13875145 | May 2013 | US |
Child | 14458185 | US | |
Parent | 13633788 | Oct 2012 | US |
Child | 13875145 | US |