Selectively absorptive wire-grid polarizer

Information

  • Patent Grant
  • 7961393
  • Patent Number
    7,961,393
  • Date Filed
    Friday, June 22, 2007
    17 years ago
  • Date Issued
    Tuesday, June 14, 2011
    13 years ago
Abstract
A selectively absorptive, mulitlayer wire-grid polarizer for polarizing incident light includes a stack of thin film layers disposed over a substrate, including a wire-grid array of elongated metal elements having a period less than half the wavelength of the light. One of the layers can include a thin film layer with a refractive index greater than a refractive index of the substrate. One of the thin film layers can include a dielectric array of non-metal elements. One of the layers includes a material that is optically absorptive to the incident light.
Description
BACKGROUND

1. Field of the Invention


The present invention relates generally to wire-grid polarizers for the visible and near visible spectrum which are selectively absorptive.


2. Related Art


A wire grid polarizer (WGP) is an array of parallel wires disposed on the surface of a substrate, such as glass. Usually wire-grid polarizers are a single, periodic array of wires on the substrate. The grid acts as a diffraction grating when the period of the wires is greater than about half of the wavelength of light. The grid acts as a polarizer when the period of the wires is less than about half the wavelength of light.


While it is desirable for a WGP to transmit all of the light of one polarization and reflect all of the other polarization, no polarizer is perfect. Real WGPs will transmit some of the light of both polarizations and will reflect some of the light of both polarizations. When light is incident on the surface of a transparent material, such as a sheet of glass, a small amount of the light is reflected. For example, at normal incidence, about 4% of the incident light is reflected from each surface of the glass.


In some applications, it is also desirable for a WGP to transmit all of the light of one polarization while removing all, or most of, the light of the other polarization from the optical system.


It has been suggested to dispose a film under a WGP, or between the wires and the substrate, to move the first diffraction order to shorter wavelengths in order to improve performance in part of the visible spectrum, such as blue light. See U.S. Pat. No. 6,122,103. The film has an index of refraction less than that of the substrate. It has also been suggested to etch into either the substrate or underlying layer to further reduce the effective refractive index under the wire grid. See U.S. Pat. No. 6,122,103. It has been further suggested to form each wire as a composite with alternating metal and dielectric layers. See U.S. Pat. No. 6,532,111.


SUMMARY

It has been recognized that it would be advantageous to develop a wire-grid polarizer capable of selectively absorbing one polarization orientation of the light. In addition, it has been recognized that it would be advantageous to develop a polarizer that is easy to incorporate into many optical systems without significant changes to the optical design, and that is inorganic and durable. In addition, it has been recognized that a wire-grid polarizer can act as a metal for reflecting one polarization state and act as a thin film of lossy dielectric for the other polarization state. Thus, it has been recognized that form birefringence and effective index of refraction can be applied to a wire-grid polarizer. It has further been recognized that a thin film which acts as a lossy dielectric can be designed and configured to preferentially absorb energy in one polarization. In addition, it has been recognized that a wire-grid polarizer can be treated as a thin film layer, and incorporated into an optical stack. Briefly, and in general terms, the invention is directed to a selectively absorptive wire-grid polarizer device for polarizing incident light and selectively absorbing one polarization. A polarizing wire-grid layer is disposed over a substrate and has an array of parallel metal wires with a period less than half the wavelength of the incident light. A dielectric layer is disposed over the substrate and includes a dielectric material. An absorptive layer is disposed over the substrate and includes a material which is optically absorptive of the incident light such that one polarization is substantially absorbed. The absorptive layer also has a refractive index different than the refractive index of the dielectric layer.





BRIEF DESCRIPTION OF THE DRAWINGS

Additional features and advantages of the invention will be apparent from the detailed description which follows, taken in conjunction with the accompanying drawings, which together illustrate, by way of example, features of the invention; and, wherein:



FIG. 1
a is a cross-sectional side schematic view of a selectively absorptive, multilayer wire grid polarizer in accordance with an embodiment of the present invention (the figures are not to scale and features are shown greatly exaggerated for clarity);



FIG. 1
b is a cross-sectional side schematic view of another selectively absorptive, multilayer wire grid polarizer in accordance with another embodiment of the present invention (the figures are not to scale and features are shown greatly exaggerated for clarity);



FIG. 2 is a cross-sectional side schematic view of another selectively absorptive, multilayer wire grid polarizer in accordance with another embodiment of the present invention (the figures are not to scale and features are shown greatly exaggerated for clarity);



FIG. 3 is a cross-sectional side schematic view of another selectively absorptive, multilayer wire grid polarizer in accordance with another embodiment of the present invention (the figures are not to scale and features are shown greatly exaggerated for clarity);



FIG. 4 is a cross-sectional side schematic view of another selectively absorptive, multilayer wire grid polarizer in accordance with another embodiment of the present invention (the figures are not to scale and features are shown greatly exaggerated for clarity); and



FIG. 5 is a cross-sectional side schematic view of another selectively absorptive, multilayer wire grid polarizer in accordance with another embodiment of the present invention (the figures are not to scale and features are shown greatly exaggerated for clarity).





Reference will now be made to the exemplary embodiments illustrated, and specific language will be used herein to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended.


DETAILED DESCRIPTION OF EXAMPLE EMBODIMENT(S)

It has been recognized that, for one polarization of light, a wire-grid polarizer substantially acts as a metal that reflects the light (or one polarization thereof), while for the other polarization of the light, the wire-grid polarizer substantially acts as a thin film of lossy dielectric that transmits the light (or another polarization thereof). Thus, it has been recognized that two concepts, namely form birefringence and effective index of refraction, can be applied to improve the performance of the polarizer.


A wire-grid polarizer is not typically considered an example of form birefringence. Generally, birefringence means that a material has a different index of refraction for different polarizations. Birefringence is very common in crystalline materials, such as quartz, and in stretched polymers. Form birefringence refers to birefringence caused by the shape of a material.


When a material has variations in material properties, such as density, with the scale of the variation being smaller than the wavelength of light, the index of refraction is different from the index of uniform bulk material. There is an effective refractive index, which is the index that a uniform thin film would have that causes the same affect on light. The theoretical treatment of this effect is called effective medium theory. This phenomenon is used with dielectric materials to make such things as moth-eye antireflection coatings.


In addition, a wire-grid polarizer is not typically considered a thin film. In optics, both form birefringence and effective index are typically considered only for dielectric materials. It has been recognized, however, that treating a wire-grid polarizer as an equivalent birefringent thin film with effective indices of refraction allows one to consider it as an element in a thin film stack, and to use thin film design techniques with particular performance goals.


The present invention utilizes thin films in combination with a metallic wire grid polarizer to improve or, in other words, to engineer, the performance of the polarizer. Generally this may include films under and on top of the wire grid. Any one of these films may be uniform or a dielectric grid. The wire grid may be a composite grid, or have composite wires. Combining the wire grid with multiple layers of different material, and thus different refractive indices, can reduce reflection of the polarization that is desired to be transmitted. For example, a wire grid can be configured to transmit p polarized light. As discussed above, while it is desirable to transmit all the p polarized light, a typical wire grid will transmit some of both polarizations and reflect some of both polarizations. It has been found, however, that treating the wire grid as a birefringent thin film, and combining the wire grid with multiple thin films, reduces reflection of p polarized light.


In some applications, it is also desirable for a wire-grid polarizer to transmit all of the p polarized light while removing all, or most of, the s polarized light from an optical system, such as by absorbing the s polarized light as heat within the wire-grid polarizer. In this way, the wire-grid polarizer would behave substantially like the common polymer-based polarizers that have a wide variety of uses. This would make it easier to incorporate wire-grid polarizers into many optical systems without significant changes to the optical design. At the same time, many optical systems would benefit from the increase durability of an inorganic polarizer such as a wire-grid polarizer. Thus, a wire grid can be configured to poorly reflect s polarized light, or, in other words, to largely absorb the s polarized light rather than reflect it. This can be accomplished by combining the wire grid with multiple layers of different materials, certain of which have optical absorption characteristics. Therefore, whether the wire-grid is an efficient reflector of the s polarization, or is an absorber of s polarization, is a design choice. Either result can be affected by proper choice of dielectric films or grids either under or on top of the wire grid.


As illustrated in FIGS. 1a-4, selectively absorptive, multilayer wire-grid polarizer devices, indicated generally at 10a-e, respectively, are shown as exemplary implementations in accordance with the invention for polarizing incident light 12, or substantially separating one polarization state from an orthogonal polarization state, while absorbing one polarization state. Such devices are believed to have substantial utility in visible light applications, or for use with visible light in the range of approximately 400-700 nm (nanometers), or 0.4-0.7 μm (micrometers or microns). Such visible light applications can include projection display devices such as projectors. The multilayer wire-grid polarizer devices described herein can be utilized in various different capacities, such as polarizers, beam splitters, analyzers, etc. It is also believed that the devices herein have utility in near-visible applications, such as ultraviolet and/or infrared applications, or for use with light in the range of approximately 250-400 nm or 700-10,000 nm. Thus, the term “light” is used broadly herein to refer to visible light, ultraviolet light and infrared light, or electromagnetic waves in the range of 250-10,000 nm.


The polarizers 10a-e include a substrate 14 carrying or supporting a plurality or stack of film layers 18, including a wire grid or a wire grid layer 22. The substrate 14 can be transparent to the light being treated. For example, the substrate can be glass (Bk7). Other substrates can be quartz or plastic or fused silica. In addition, the substrate 14 can have a substantial thickness ts with respect to the remaining thin film layers. Furthermore, the substrate can have a refractive index (or index of refraction) ns. For example, a glass substrate (Bk7) has a refractive index ns of 1.52 (at 550 nm). (It will be appreciated that the refractive index varies slightly with wavelength.)


The wire grid or wire grid layer 22 includes a wire-grid array of elongated metal elements or wires 26. The elements 26 have lengths longer than a wavelength of the light, and are located in a generally parallel arrangement with a period P less than half the wavelength of the light. Thus, for use with visible light, the elements 26 have a length larger than the wavelength of visible light, or greater than 700 nm (0.7 μm). The length, however, can be much longer. The elements 26 can have a center-to-center spacing, pitch or period P less than half the wavelength of visible light, or less than 350 nm (0.36 μm). In one aspect, the period P can be less than 200 nm for visible light applications. In another aspect, the period P can be less than 120 nm for visible light applications. The elements 26 can also have a width w in the range of 10 to 90% of the pitch or period. The elements 26 can also have a thickness or a height t less than the wavelength of the light, or less than 400 nm (0.4 μm) for visible light applications. In one aspect, the thickness can be less than 0.2 μm for visible light applications.


For ultra violet applications, the period P can be less than 200 nm. In one aspect, the period P can be less than 125 nm for ultra violet applications. For infrared applications, the period P can be less than 500 nm (but greater than 350 nm). In another aspect, the period P can be less than 5,000 nm for infrared applications. The elements 26, or the array, generally interact with the incident light to generally transmit a transmitted beam 30 having a substantially uniform and constant linear polarization state (such as p polarization). The s polarization which would normally reflect as reflected beam 34 is generally absorbed, as described in greater detail below. The elements generally transmit light with a first polarization state (p polarization), oriented locally orthogonal or transverse to the elements. It will be appreciated that the wire-grid polarizer will separate the polarization states of the light with a certain degree of efficiency, or some of both polarization states may be transmitted and/or absorbed. The remaining reflected beam can be reduced to 10% or less of the original amount of energy in that polarization.


The elements 26 or array can be formed on or over the substrate by photo-lithography. The elements 26 can be conductive, and can be formed of aluminum, silver, gold or copper. In addition, the elements are inorganic, and thus robust.


The plurality of film layers 18 can include layers under and/or over the wire grid layer 22. Thus, one or more layers can be disposed between the substrate 14 and the wire grid layer 22, as shown in FIGS. 2, 3 and 4. In addition, one or more layers can be disposed over the wire grid layer 22, as shown in FIGs. 1a, 1b, 3 and 4. The layers 18 can be formed of different materials, or materials different than the substrate 14, and even from each other. Thus, the layers 18 can have refractive indices n different than the refractive index ns of the substrate 14. Furthermore, it has been found that at least one of the layers having a refractive index n1-3 greater than the refractive index ns of the substrate 14 decreases reflection of the p polarized light. Thus, in accordance with one aspect of the invention, the polarizer 10d or 10e has at least one film layer disposed between the substrate 14 and the wire grid layer 22, and the film layer has a refractive index n1 greater than the refractive index ns of the substrate 14. In accordance with another aspect of the invention, the polarizer can have at least two film layers, or at least three thin film layers.


One or more of the layers can be a dielectric layer 30a-c. In one aspect, the dielectric layer 30a and 30b can be disposed over the wire grid layer 22, as shown in FIGS. 1a and 1b. In another aspect, the dielectric layer 30c can be disposed under the wire-grid layer 22, or between the wire-grid layer 22 and the substrate, as shown in FIG. 2. The dielectric layer can be optically transmissive to the incident light.


In addition, one of the layers can be an absorptive layer 34a and 34b. In one aspect, the absorptive layer 34a can be disposed over the wire-grid layer 22, as shown in FIGS. 1a and 1b. In another aspect, the absorptive layer 34b can be disposed under the wire-grid layer 22, or between the wire-grid layer 22 and the substrate 14, as shown in FIG. 2. The absorptive layer can be optically absorptive to the incident light. The wire-grid layer and the absorptive layer can be separated by the dielectric layer. Both the absorptive layer and the dielectric layer(s) can be formed of or can include a dielectric material. In addition, both the absorptive layer and the dielectric layer(s) can have different refractive indices. One of the refractive indices can be greater than the refractive index of the substrate. As described above, the different refractive indices of the layers coupled with the significantly different absorption characteristics of the different dielectric layers is believed to cause the energy in the s-polarized light to be preferentially absorbed in the absorbing dielectric layer and thus to decrease reflection of the s polarized light.


It will be appreciated that different materials are optically transmissive or optically absorptive for different wavelengths of incident light. For visible light applications, the dielectric layer includes a dielectric material that is optically transmissive to visible light, while the absorptive layer includes a material that is optically absorptive to visible light. Similarly, for ultra violet applications, the dielectric layer includes a dielectric material that is optically transmissive to ultra violet light, while the absorptive layer includes a material that is optically absorptive to ultra violet light. Similarly, for infrared applications, the dielectric layer includes a material that is optically transmissive to infrared light, while the absorptive layer includes a material that is optically absorptive to infrared light.


The dielectric layer and the absorptive layer can be formed of or can include a dielectric material. For example, the layers can be formed of: aluminum oxide; antimony trioxide; antimony sulphide; beryllium oxide; bismuth oxide; bismuth triflouride; cadmium sulphide; cadmium telluride; calcium fluoride; ceric oxide; chiolite; cryolite; germanium; hafnium dioxide; lanthanum fluoride; lanthanum oxide; lead chloride; lead fluoride; lead telluride; lithium fluoride; magnesium fluoride; magnesium oxide; neogymium fluoride; neodymium oxide; praseodymium oxide; scandium oxide; silicon; silicon oxide; disilicon trioxide; silicon dioxide; sodium fluoride; tantalum pentoxide; tellurium; titanium dioxide; thallous chloride; yttrium oxide; zinc selenide; zinc sulphide; and zirconium dioxide, and combinations thereof. The film layers can be deposited on the substrate. In the case of metal oxides, they can be deposited by starting with an oxide evaporant material (with additional oxygen backfill as needed). The material, however, can also be deposited by evaporating a base metal, then oxidizing the deposited material with O2 in the background.


In one aspect, the dielectric layer and/or the absorptive layer can be formed of or can include a material selected from: cadmium telluride, germanium, lead telluride, silicon oxide, tellurium, titanium dioxide, silicon, cadmium sulifide, zinc selenide, zinc sulfide, cadmium telluride, germanium, lead telluride, silicon oxide, tellurium, titanium dioxide, silicon, magnesium fluoride, aluminum oxide, cadmium telluride, germanium, non-stoichiometric versions of these material, and combinations thereof. It is believed that cadmium telluride, germanium, lead telluride, silicon oxide, tellurium, titanium dioxide, silicon, cadmium sulifide, zinc selenide, zinc sulfide are appropriate for the ultra-violet range; cadmium telluride, germanium, lead telluride, silicon oxide, tellurium, titanium dioxide, silicon are appropriate for the visible range; and magnesium fluoride, aluminum oxide, cadmium telluride, germanium, and combinations thereof are appropriate for the infrared range.


In another aspect, the dielectric layer and/or the absorptive layer can be formed of or can include a material selected from: silicon nitride, titanium nitride, titanium carbide, silicon carbide, tantalum, cupric oxide, cuprous oxide, cupric chloride, cuprous chloride, cuprous sulfide, titanium, tungsten, niobium oxide, aluminum silicate, boron nitride, boron oxide, tantalum oxide, carbon and combinations thereof.


In addition to the material listed herein, ionic states of the material can also be included, particularly for transition metal oxides, hydrides, nitrides, salts, etc.


Many of the film dielectric materials mentioned above can be deposited using various deposition techniques such as sputtering, Chemical Vapor Deposition (CVD), or evaporation to produce films that are not stoichiometric. This can be used to produce dielectric thin films that have different optical properties than the common bulk stoichiometric material. For example, it is possible to produce a titanium oxide dielectric film by sputtering that is oxygen-starved, and therefore has much higher optical absorption than the standard film. Such a film can be used to produce a wire grid that strongly absorbs one polarization rather than strongly reflecting the same polarization using the present invention.


In a similar manner, it is possible to do the same thing with other metal oxides such as zirconium oxide, magnesium oxide, silicon oxide, etc. Similar effects can also be accomplished with metal fluorides such as magnesium fluoride, with metal nitrides such as silicon nitride, and with metal sulphides, silicides, or selenides.


The thicknesses and materials (or refractive indices) of the film layers can be manipulated to reduce reflection of p polarized light, or (either alternatively or simultaneously) to enhance the absorption of s polarized light, as described in greater detail below.


To amplify on the above discussion about materials, and the importance the particular molecular state, or the stoichiometry of the material, it is useful to recall that stoichiometric reactions are those that maintain an equilibrium with bonding conditions met. However there are additions to specific stoichiometric compounds that need to be considered. For example, ionic states of compounds exist that defy full enumeration. Consider the common compound rust, it can be either Ferric Oxide (Fe2O3-Iron III) or Ferrous Oxide (FeO-Iron II). Note that in some conditions, ferrous Oxide can be considered the non-stoichiometric compound. In our applications, there are various ionic states in which the chemical element can be stable but with different optical properties. Appropriate deposition techniques can therefore produce films of mixed compositions with a variety of optical properties. For example, in the literature there is documentation of TiO2, TiO3 and TiO4 (complexed with various ligands). Aluminum also has an amphoteric nature that is stabilized as an acid or base compound. Inclusion of all forms and applications of all the interesting materials is not practical because the potential list is endless. Generally, the invention can be practiced with a large variety of non-stoichiometric or mixed-state materials that are fabricated to produce the desired absorptive properties. This is a significant degree of freedom that is not typically available when a high-transmission, low-absorption film is desired, because the properties of low-absorption in an optical material are well-known to be coupled with pure, stoichiometric films that are not in a mixed state. Therefore, it is difficult to compile a simple list of materials, or to otherwise define a finite set of materials that work within the scope of the invention. As discussed, with proper fabrication conditions, a wide, almost infinite variety of materials could be defined that will work within the scope of the invention.


Returning now to the figures, one or more of the thin film layers, such as the dielectric layer 30a-c, can include a dielectric grid including an array of non-metal elements 38. The non-metal and metal elements 38 and 26 of the arrays can be oriented substantially parallel with one another. In addition, the arrays can have substantially equal periods and/or widths. In one aspect, the non-metal elements 38 of the dielectric grid and the metal elements 26 are aligned, or the non-metal elements 38 are aligned with the metal elements 26 of the wire grid layer, as shown in FIGS. 1a, 1b, 2 and 3. In another aspect, the non-metal elements 38 of the dielectric grid and the metal elements 26 are off-set, or the non-metal elements 38 are off-set with respect to the metal elements 26 of the wire grid layer, as shown in FIG. 4.


As discussed above, the number, thicknesses t, and materials (or refractive indices) of the thin film layers 18 can be varied to reduce reflection of p polarized light (increase transmission of p polarized light) and/or reduce transmission of s polarized light (increase reflection or absorption of s polarized light). Some of the layers can be uniform in structure and material, while other layers can include grids, such as metal elements 26 of the wire grid layer 22 or non-metal elements 38 of a dielectric grid. Examples of specific configurations and a method of selecting materials and corresponding thicknesses of the absorbing films or ribs are discussed below.


In general, optical material and optical film absorption characteristics can be determined by the optical indices n and k of the material, wherein n is the normal index of refraction, and k is the complex part which represents the absorption behavior of the material in question. When k is essentially zero, then the material is highly transparent or transmissive. In determining the desired absorption characteristics for a specific configuration of the invention, control of the film thickness of the specific material can compensate for various values of the optical parameter k value. Specifically if the k value is lower than desired, the film thickness can be increased to compensate or achieve the desired performance in the polarizer. In like manner, if the k value is higher than desired, the material can still be used with a compensating reduction in the film thickness. Since the exact thicknesses of films will depend on the wavelength range desired in the application, the trade-offs for transmission of the transmitted polarization and absorption of the reflected polarization that meet the need of the specific application, and other application-specific issues, it is impractical to define a simple rule relating the k value to a film thickness. In general, the range of interest for k is between 0.1 and 4.5.


Exemplary k values are shown in Table 1. The table demonstrates selectivity as a function of the k value. From the table, it can be seen that Cadmium Telluride is an example of a single compound that would act in all three band widths. Lead Telluride, Silicon Oxide, Tellurium, Titanium Dioxide and Silicon are compounds that would work in both the Ultra Violet (UV) band width and also the Visible bandwidth. Cadmium Sulfide, Zinc Selenide and Zinc Sulfide are compounds that have functional absorption in only the UV band but not in the visible or Infra Red (IR). Other compounds could be identified that absorb only in the visible band, only in the IR band, or only in the UV band, or various combinations of the 3 optical bands. It will be noted also, that the list presented includes many materials that are not considered as common or “standard” optical materials. This illustrates the new degrees of freedom introduced in the invention by noting that absorbing materials are desirable in practicing the invention. This list is presented to demonstrate possible compound dedication to specific wave bands but is not to be considered all inclusive. Thus, the absorptive material can have a k value between 0.1 to 4.5.












TABLE 1





Compound
UV (k values)
Visible (k values)
IR (k values)


















Cadmium Telluride
1.739
0.406
0.23


Germanium
3.96
2.165
0.123


Lead Telluride
1.22
5.9


Silicon Oxide
1.52
0.464


Tellurium
1.71
5.21


Titanium Dioxide
3.19
0.251


Cadmium Sulfide
1.64


Zinc Selenide
1.421


Zinc Sulfide
0.54









The film layers can extend continuously across the substrate 14, and can be homogeneous, consistent or constant layers in at least two directions, or both parallel to the wires and orthogonal to the wires.


Referring to FIG. 1a, a selectively absorptive, multilayer wire-grid polarizer 10a is shown. The polarizer 10a includes a wire-grid layer or wire-grid 22 disposed on a substrate 14, and three film layers 30a, 34a and 30b disposed over the wire-grid. The wire-grid 22 can include elements or wires 26 formed of aluminum. The substrate can be glass (BK7). The three film layers are disposed over or on the wire-grid layer 22. The three film layers can be discontinuous to form dielectric grids. One of the film layers 30a is disposed on the wire-grid layer 22 can be formed of an optically transmissive material with respect to the incident light, defining a dielectric layer. Another film layer 34a is disposed on the dielectric layer 30a and includes an optically absorptive material with respect to the incident light, defining an absorptive layer. Another film layer 30b is disposed on the absorptive layer 34a and includes an optically transmissive material with respect to the incident light, defining another dielectric layer.


The polarizer 10a can be configured for use with visible incident light (400-700 nm). The thickness or height twg of the elements 26 of the wire-grid can be 160 nm. The first dielectric layer or grid 30a can have a thickness t1 of 100 nm, and can be formed of silicon oxide (SiO2), with an index of refraction ns of 1.45. The absorptive layer or grid 34a can also have a thickness t2 of 100 nm, and can be formed of an optically absorptive material with respect to visible light with an index of refraction n2 of 2.5. The period P of the grids can be 144 nm. The width of the elements can be 45% of the period P, or 57 nm. The light 12 can be incident at 45 degrees.


Such a polarizer 10a can be formed by depositing the layers of aluminum, silicon dioxide, absorptive material, and silicon dioxide, and then etching the layers to form the ribs and wires.


The performance of the polarizer 10a of FIG. 1a is compared to a similar polarizer without dielectric grids on top and the reflected s polarization is substantially less with the polarizer 10a and the transmitted p polarization is also greater with the polarizer 10a. Because the period P of the grids is less than the wavelength of visible light, they all essentially behave as thin films.


Referring to FIG. 1b, another selectively absorptive, multilayer wire-grid polarizer 10b is shown that is similar in most respects to the polarizer 10a of FIG. 1a. In addition, the polarizer 10b includes grooves 50 etched in the substrate 14b to form ribs 54 extending therefrom. The wires 26 of the wire-grid layer 22 can be supported on the ribs 54, and thus can have the same period. Such a polarizer can be formed by over etching the above layers to etch the grooves into the substrate.


Referring to FIG. 2, another selectively absorptive, multilayer wire-grid polarizer 10c is shown that is similar in most respects to those described above. In addition, the polarizer 10c has the absorptive layer 34b and the dielectric layer 30c disposed between the wire-grid layer 22 and the substrate 14.


Referring to FIGS. 3 and 4, other selectively absorptive, multilayer wire-grid polarizers 10d and 10e are shown that are similar in most respect to those described above. In addition, the polarizers 10d and 10e have other film layers disposed above and below the wire-grid layer 22.


Referring to FIG. 5, another selectively absorptive, multilayer wire-grid polarizer 10f is shown that is similar in many respects to the polarizer 10a shown in FIG. 1a. In addition, the polarizer includes at least three layers disposed between the substrate 14 and the wire-grid layer 22.


The examples presented here are but a few of the many possibilities that may be realized from this invention. In general, a combination of uniform layers and dielectric grids may be designed for specific applications such as optimizing transmittance or reflectance over a given range of incident angles for a given band of light. Also, a combination of uniform layers and dielectric grids may be designed for specific applications such as optimizing transmittance or one polarization and absorption of the orthogonal polarization over a given range of incident angles for a given band of light. Optimization may be made for transmittance or reflectance; for transmittance or absorption, or for some combination of the characteristics together. Optimization may be made for incidence from the air side on the polarizer or from the substrate side or both.


Various aspects of wire-grid polarizers, optical trains and/or projection/display systems are shown in U.S. Pat. Nos. 5,986,730; 6,081,376; 6,122,103; 6,208,463; 6,243,199; 6,288,840; 6,348,995; 6,108,131; 6,452,724; 6,710,921; 6,234,634; 6,447,120; and 6,666,556, which are herein incorporated by reference.


Although the wire-grid polarizers have been illustrated as facing the light source, or with the elongated elements facing towards the light source, it is understood that this is for illustrational purposes only. Those skilled in the art will appreciate that the wire-grid polarizers can be oriented to face towards imaging bearing beams, such as from a liquid crystal array, for the simple purpose of avoiding passing the image bearing beam through the substrate, and thus avoiding ghost images or multiple reflections associated with light passing through mediums, such as the substrate. Such configurations may result in the wire-grid polarizer facing away from the light source.


While the forgoing examples are illustrative of the principles of the present invention in one or more particular applications, it will be apparent to those of ordinary skill in the art that numerous modifications in form, usage and details of implementation can be made without the exercise of inventive faculty, and without departing from the principles and concepts of the invention. Accordingly, it is not intended that the invention be limited, except as by the claims set forth below.

Claims
  • 1. A selectively absorptive wire-grid polarizer device for polarizing incident light and selectively absorbing one polarization, the device comprising: a) a substrate;b) at least two thin film layers, disposed over the substrate, the film layers having different refractive indices with respect to one another and each having a thickness less than 170 nm;c) the refractive index of at least one of the two film layers being greater than a refractive index of the substrate; andd) a wire-grid layer, disposed over the substrate, the wire-grid layer including an array of elongated metal elements having lengths longer than a wavelength of the incident light and a period less than half the wavelength of the incident light; ande) at least one of the film layers including a material which is optically absorptive of the incident light defining an absorptive layer such that one polarization is substantially absorbed.
  • 2. A device in accordance with claim 1, wherein the at least two film layers includes at least three continuous film layers disposed between the substrate and the wire-grid layer.
  • 3. A device in accordance with claim 1, wherein the at least two film layers includes a dielectric grid disposed between the substrate and the wire-grid layer with an array of dielectric ribs, the metal elements of the wire-grid layer and the dielectric ribs of the dielectric grid being oriented substantially parallel with one another and having substantially equal periods.
  • 4. A device in accordance with claim 1, wherein the at least two film layers includes a dielectric layer disposed over the wire-grid layer with an array of dielectric ribs, and a continuous film layer disposed between the wire-grid layer and the dielectric layer and being continuous in a direction orthogonal to the ribs.
  • 5. A device in accordance with claim 1, wherein the at least two film layers are discontinuous to form an array of parallel ribs oriented parallel with the elements of the wire-grid layer.
  • 6. A device in accordance with claim 1, wherein the at least two film layers include a material selected from the group consisting of: metal oxides, metal nitrides, metal fluorides, metal selenides, and metal sulphides that have been deposited to be non-stoichiometric, and combinations thereof.
  • 7. A device in accordance with claim 1, wherein the absorptive layer includes a dielectric grid including an array of non-metal elements, the non-metal and metal elements of the arrays being oriented substantially parallel with one another, and the arrays having substantially equal periods.
  • 8. A device in accordance with claim 7, wherein non-metal elements of the dielectric grid are aligned below the metal elements of the wire grid layer.
  • 9. A device in accordance with claim 7, wherein non-metal elements of the dielectric grid are off-set below the metal elements of the wire grid layer.
  • 10. A device in accordance with claim 7, wherein non-metal elements of the dielectric grid are aligned above the metal elements of the wire grid layer.
  • 11. A device in accordance with claim 7, wherein non-metal elements of the dielectric grid are off-set above the metal elements of the wire grid layer.
  • 12. A device in accordance with claim 7, wherein the material of the absorptive layer is selected from the group consisting of: silicon nitride, titanium nitride, titanium carbide, silicon carbide, tantalum, cupric oxide, cuprous oxide, cupric chloride, cuprous chloride, cuprous sulfide, titanium, tungsten, niobium oxide, aluminum silicate, boron nitride, boron oxide, tantalum oxide, carbon and combinations thereof.
  • 13. A device in accordance with claim 7, wherein the material of the absorptive layer has an optical parameter k value between 0.1 and 4.5.
  • 14. A device in accordance with claim 1, wherein absorptive thin film layer has a thickness less than 150 nm.
  • 15. A device in accordance with claim 1, wherein absorptive thin film layer has a thickness less than 100 nm.
  • 16. A device in accordance with claim 1, wherein the wire-grid layer and the at least two film layers in combination define an array of ribs, wherein a width of an individual rib is approximately the same at a base of the individual rib as at a top of the individual rib.
  • 17. A device in accordance with claim 1, wherein the wire grid layer and the at least two film layers in combination define an array of ribs with gaps therebetween, wherein a distance between ribs at a base of the ribs is approximately the same as a distance between the ribs at a top of the ribs.
  • 18. A divice in accordance with claim 1, wherein the elongated metal elements comprise aluminum; the at least two film layers comprises at least three film layers; at least one of the at least three film layers comprises silicon dioxide; another at least one of the least three film layers comprises silicon; and another at least one of the at least three film layers comprises tantlaum.
  • 19. A selectively absorptive wire-grid polarizer device for polarizing incident light and selectively absorbing one polarization, the device comprising: a) a substrate having a refractive index;b) a polarizing wire-grid layer disposed over the substrate having an array of parallel metal wires with a period less than half the wavelength of the incident light;c) a dielectric layer disposed over the substrate including a dielectric material; andd) an absorptive thin film layer disposed over the substrate including a material which is optically absorptive of the incident light such that one polarization is substantially absorbed and having a refractive index different than a refractive index of the dielectric layer and a thickness less than 170 nm.
  • 20. A device in accordance with claim 19, further comprising at least three continuous film layers disposed between the substrate and the wire-grid layer, the continuous film layers being continuous in a direction orthogonal to the wires.
  • 21. A device in accordance with claim 19, wherein the device selectively absorbs light within the visible spectrum; wherein the period of the array of elements of the wire-grid layer is less than 350 nm; and wherein the material of the absorptive layer includes a material that is optically absorptive of light in the visible spectrum.
  • 22. A device in accordance with claim 19, wherein the device selectively absorbs light within the ultra violet spectrum; wherein the period of the array of elements of the wire-grid layer is less than 200 nm; and wherein the material of the absorptive layer includes a material that is optically absorptive of light in the ultra violet spectrum.
  • 23. A device in accordance with claim 19, wherein the device selectively absorbs light within the infrared spectrum; wherein the period of the array of elements of the wire-grid layer is less than 500 nm; and wherein the material of the absorptive layer includes a material that is optically absorptive of light in the infrared spectrum.
  • 24. A device in accordance with claim 19, wherein the dielectric layer and the absorptive layer are each discontinuous to form an array of ribs with the ribs being parallel and aligned with the wires of the wire-grid layer.
  • 25. A device in accordance with claim 19, wherein the material of the absorptive layer is selected from the group consisting of: silicon nitride, titanium nitride, titanium carbide, silicon carbide, tantalum, cupric oxide, cuprous oxide, cupric chloride, cuprous chloride, cuprous sulfide, titanium, tungsten, niobium oxide, aluminum silicate, boron nitride, boron oxide, tantalum oxide, carbon and combinations thereof.
  • 26. A device in accordance with claim 19, wherein absorptive thin film layer has a thickness less than 100 nm.
  • 27. A device in accordance with claim 19, wherein absorptive thin film layer has a thickness less than 50 nm.
  • 28. A device in accordance with claim 19, wherein absorptive thin film layer has a thickness less than 10 nm.
  • 29. A selectively absorptive wire-grid polarizer device for polarizing incident light and selectively absorbing one polarization, the device comprising: a) a substrate having a refractive index;b) at least three different thin film layers each having a thickness less than 170 nm and disposed over the substrate, including: i) a polarizing layer including a conductive material;ii) an absorptive layer having a refractive index greater than a refractive index of the substrate and including a material that is optically absorptive to the incident light; andiii) a dielectric layer having a refractive index different than the refractive index of the absorptive layer; andc) the at least three layers being discontinuous to form an array of parallel ribs having a period less than a wavelength of the incident light.
  • 30. A selectively absorptive wire-grid polarizer device for polarizing incident light and selectively absorbing one polarization, the device comprising: a) a substrate;b) a wire-grid layer, disposed over the substrate, the wire-grid layer including an array of elongated metal elements having lengths longer than a wavelength of the incident light and a period less than half the wavelength of the incident light; andc) at least two thin film layers, disposed over the wire-grid layer, the film layers having different refractive indices with respect to one another and each having a thickness less than 170 nm, wherein the refractive index of at least one of the two film layers is greater than a refractive index of the substrate and at least one of the film layers includes a material which is optically absorptive of the incident light defining an absorptive layer such that one polarization is substantially absorbed.
  • 31. A device in accordance with claim 30, further comprising grooves etched in the substrate to from ribs extending therefrom, wherein the wire-grid layer is supported on the ribs.
  • 32. A device in accordance with claim 30, wherein: the elongated metal elements comprise aluminum;at least two of the at least two film layers comprises silicon.
  • 33. A device in accordance with claim 32, wherein at least one of the at least two film layers comprises silicon dioxide.
PRIORITY CLAIM

This is a continuation-in-part of U.S. patent application Ser. No. 11/005,927, filed on Dec. 6, 2004 now U.S. Pat. No. 7,570,424; which is herein incorporated by reference. This is related to U.S. patent application Ser. No. 11/767,336, filed Jun. 22, 2007, entitled “Reflection-Repressed Wire-grid Polarizer”; which is herein incorporated by reference.

US Referenced Citations (472)
Number Name Date Kind
2224214 Brown Dec 1940 A
2237567 Land Apr 1941 A
2287598 Brown Jun 1942 A
2391451 Fischer Dec 1945 A
2403731 MacNeille Jul 1946 A
2605352 Fishcer Jul 1952 A
2748659 Geffcken et al. Jun 1956 A
2813146 Glenn Nov 1957 A
2815452 Mertz Dec 1957 A
2887566 Marks May 1959 A
3046839 Bird et al. Jul 1962 A
3084590 Glenn, Jr. Apr 1963 A
3202039 Lang et al. Aug 1965 A
3235630 Doherty et al. Feb 1966 A
3291550 Bird et al. Dec 1966 A
3291871 Francis Dec 1966 A
3293331 Doherty Dec 1966 A
3436143 Garrett Apr 1969 A
3479168 Bird et al. Nov 1969 A
3536373 Bird et al. Oct 1970 A
3566099 Makas Feb 1971 A
3627431 Komarniski Dec 1971 A
3631288 Rogers Dec 1971 A
3653741 Marks Apr 1972 A
3731986 Fergason May 1973 A
3857627 Harsch Dec 1974 A
3857628 Strong Dec 1974 A
3876285 Schwarzmüller Apr 1975 A
3877789 Marie Apr 1975 A
3912369 Kashnow Oct 1975 A
3969545 Slocum Jul 1976 A
4009933 Firester Mar 1977 A
4025164 Doriguzzi et al. May 1977 A
4025688 Nagy et al. May 1977 A
4049944 Garvin et al. Sep 1977 A
4068260 Ohneda et al. Jan 1978 A
4073571 Grinberg et al. Feb 1978 A
4104598 Abrams Aug 1978 A
4181756 Fergason Jan 1980 A
4220705 Sugibuchi et al. Sep 1980 A
4221464 Pedinoff et al. Sep 1980 A
4268127 Oshima et al. May 1981 A
4289381 Garvin et al. Sep 1981 A
4294119 Soldner Oct 1981 A
4308079 Venables et al. Dec 1981 A
4441791 Hornbeck Apr 1984 A
4456515 Krueger et al. Jun 1984 A
4466704 Schuler et al. Aug 1984 A
4492432 Kaufmann et al. Jan 1985 A
4512638 Sriram et al. Apr 1985 A
4514479 Ferrante Apr 1985 A
4515441 Wentz May 1985 A
4515443 Bly May 1985 A
4532619 Sugiyama et al. Jul 1985 A
4560599 Regan Dec 1985 A
4679910 Efron et al. Jul 1987 A
4688897 Grinberg et al. Aug 1987 A
4701028 Clerc et al. Oct 1987 A
4711530 Nakanowatari et al. Dec 1987 A
4712881 Shurtz et al. Dec 1987 A
4724436 Johansen et al. Feb 1988 A
4743092 Pistor May 1988 A
4743093 Oinen May 1988 A
4759611 Downey, Jr. Jul 1988 A
4759612 Nakatsuka et al. Jul 1988 A
4763972 Papuchon et al. Aug 1988 A
4795233 Chang Jan 1989 A
4799776 Yamazaki et al. Jan 1989 A
4818076 Heppke et al. Apr 1989 A
4840757 Blenkhorn Jun 1989 A
4865670 Marks Sep 1989 A
4870649 Haven et al. Sep 1989 A
4893905 Efron Jan 1990 A
4895769 Land et al. Jan 1990 A
4904060 Grupp Feb 1990 A
4913529 Goldenberg et al. Apr 1990 A
4915463 Barbee, Jr. Apr 1990 A
4939526 Tsuda Jul 1990 A
4946231 Pistor Aug 1990 A
4966438 Mouchart et al. Oct 1990 A
4991937 Urino Feb 1991 A
5029988 Urino Jul 1991 A
5039185 Uchida et al. Aug 1991 A
5061050 Ogura Oct 1991 A
5087985 Kitaura et al. Feb 1992 A
5092774 Milan Mar 1992 A
5113285 Franklin et al. May 1992 A
5115305 Baur May 1992 A
5122887 Mathewson Jun 1992 A
5122907 Slocum Jun 1992 A
5139340 Okumura Aug 1992 A
5157526 Kondo et al. Oct 1992 A
5177635 Keilmann Jan 1993 A
5196926 Lee Mar 1993 A
5196953 Yeh et al. Mar 1993 A
5198921 Aoshima et al. Mar 1993 A
5204765 Mitsui et al. Apr 1993 A
5206674 Puech et al. Apr 1993 A
5216539 Boher et al. Jun 1993 A
5222907 Katabuchi et al. Jun 1993 A
5225920 Kasazumi et al. Jul 1993 A
5235443 Barnik et al. Aug 1993 A
5235449 Imazeki et al. Aug 1993 A
5239322 Takanashi et al. Aug 1993 A
5245471 Iwatsuka et al. Sep 1993 A
5267029 Kurematsu Nov 1993 A
5279689 Shvartsman Jan 1994 A
5295009 Barnik et al. Mar 1994 A
5298199 Hirose et al. Mar 1994 A
5305143 Taga et al. Apr 1994 A
5325218 Willett et al. Jun 1994 A
5333072 Willett Jul 1994 A
5349192 Mackay Sep 1994 A
5357370 Miyatake et al. Oct 1994 A
5383053 Hegg et al. Jan 1995 A
5387953 Minoura et al. Feb 1995 A
5391091 Nations Feb 1995 A
5401587 Montohiro et al. Mar 1995 A
5422756 Weber Jun 1995 A
5430573 Araujo et al. Jul 1995 A
5436761 Kamon Jul 1995 A
5455589 Huguenin et al. Oct 1995 A
5466319 Zager et al. Nov 1995 A
5477359 Okazaki Dec 1995 A
5485499 Pew et al. Jan 1996 A
5486935 Kalmanash Jan 1996 A
5486949 Schrenk et al. Jan 1996 A
5490003 Van Sprang Feb 1996 A
5499126 Abileah et al. Mar 1996 A
5504603 Winker et al. Apr 1996 A
5506704 Broer et al. Apr 1996 A
5508830 Imoto et al. Apr 1996 A
5510215 Prince et al. Apr 1996 A
5513023 Fritz et al. Apr 1996 A
5513035 Miyatake et al. Apr 1996 A
5517356 Araujo et al. May 1996 A
5535047 Hornbeck Jul 1996 A
5548427 May Aug 1996 A
5555186 Sjopua Sep 1996 A
5557343 Yamagishi Sep 1996 A
5559634 Weber Sep 1996 A
5570213 Ruiz et al. Oct 1996 A
5570215 Omae et al. Oct 1996 A
5574580 Ansley Nov 1996 A
5576854 Schmidt et al. Nov 1996 A
5579138 Sannohe et al. Nov 1996 A
5594561 Blanchard Jan 1997 A
5600383 Hornbeck Feb 1997 A
5609939 Petersen et al. Mar 1997 A
5612820 Schrenk et al. Mar 1997 A
5614035 Nadkarni Mar 1997 A
5619352 Koch et al. Apr 1997 A
5619356 Kozo et al. Apr 1997 A
5620755 Smith, Jr. et al. Apr 1997 A
5626408 Heynderickx et al. May 1997 A
5638197 Gunning, III et al. Jun 1997 A
5652667 Kurogane Jul 1997 A
5658060 Dove Aug 1997 A
5686979 Weber et al. Nov 1997 A
5706063 Hong Jan 1998 A
5706131 Ichimura et al. Jan 1998 A
5719695 Heimbuch Feb 1998 A
5731246 Bakeman et al. Mar 1998 A
5748368 Tamada et al. May 1998 A
5748369 Yokota May 1998 A
5751388 Larson May 1998 A
5751466 Dowling et al. May 1998 A
5767827 Kobayashi et al. Jun 1998 A
5798819 Hattori et al. Aug 1998 A
5808795 Shimomura et al. Sep 1998 A
5826959 Atsuchi Oct 1998 A
5826960 Gotoh et al. Oct 1998 A
5828489 Johnson et al. Oct 1998 A
5833360 Knox et al. Nov 1998 A
5838403 Jannson et al. Nov 1998 A
5841494 Hall Nov 1998 A
5844722 Stephens et al. Dec 1998 A
5886754 Kuo Mar 1999 A
5890095 Barbour et al. Mar 1999 A
5898521 Okada Apr 1999 A
5899551 Neijzen et al. May 1999 A
5900976 Handschy et al. May 1999 A
5907427 Scalora et al. May 1999 A
5912762 Li et al. Jun 1999 A
5914818 Tejada et al. Jun 1999 A
5917562 Woodgate et al. Jun 1999 A
5918961 Ueda Jul 1999 A
5930050 Dewald Jul 1999 A
5943171 Budd et al. Aug 1999 A
5958345 Turner et al. Sep 1999 A
5965247 Jonza et al. Oct 1999 A
5969861 Ueda et al. Oct 1999 A
5973833 Booth et al. Oct 1999 A
5978056 Shintani et al. Nov 1999 A
5982541 Li et al. Nov 1999 A
5986730 Hansen et al. Nov 1999 A
5991075 Katsuragawa et al. Nov 1999 A
5991077 Carlson et al. Nov 1999 A
6005918 Harris et al. Dec 1999 A
6008871 Okumura Dec 1999 A
6008951 Anderson Dec 1999 A
6010121 Lee Jan 2000 A
6016173 Crandall Jan 2000 A
6018841 Kelsay et al. Feb 2000 A
6049428 Khan et al. Apr 2000 A
6053616 Fujimori et al. Apr 2000 A
6055103 Woodgate et al. Apr 2000 A
6056407 Iinuma et al. May 2000 A
6062694 Oikawa et al. May 2000 A
6075235 Chun Jun 2000 A
6081312 Aminaka et al. Jun 2000 A
6081376 Hansen et al. Jun 2000 A
6082861 Dove et al. Jul 2000 A
6089717 Iwai Jul 2000 A
6096155 Horden et al. Aug 2000 A
6096375 Ouderkirk et al. Aug 2000 A
6108131 Hansen et al. Aug 2000 A
6122103 Perkins et al. Sep 2000 A
6122403 Rhoads Sep 2000 A
6124971 Ouderkirk et al. Sep 2000 A
6141075 Ohmuro et al. Oct 2000 A
6147728 Okumura et al. Nov 2000 A
6172813 Tadic-Galeb et al. Jan 2001 B1
6172816 Tadic-Galeb et al. Jan 2001 B1
6181386 Knox Jan 2001 B1
6181458 Brazas, Jr. et al. Jan 2001 B1
6185041 TadicGaleb et al. Feb 2001 B1
6208463 Hansen et al. Mar 2001 B1
6215547 Ramanugan et al. Apr 2001 B1
6234634 Hansen et al. May 2001 B1
6243199 Hansen et al. Jun 2001 B1
6247816 Cipolla et al. Jun 2001 B1
6249378 Shimamura et al. Jun 2001 B1
6250762 Kuijper Jun 2001 B1
6251297 Komuro et al. Jun 2001 B1
6282025 Huang et al. Aug 2001 B1
6288840 Perkins et al. Sep 2001 B1
6291797 Koyama et al. Sep 2001 B1
6310345 Pittman et al. Oct 2001 B1
6339454 Knox Jan 2002 B1
6340230 Bryars et al. Jan 2002 B1
6345895 Maki et al. Feb 2002 B1
6348995 Hansen et al. Feb 2002 B1
6375330 Mihalakis Apr 2002 B1
6390626 Knox May 2002 B2
6398364 Bryars Jun 2002 B1
6406151 Fujimori Jun 2002 B1
6409525 Hoelscher et al. Jun 2002 B1
6411749 Teng et al. Jun 2002 B2
6424436 Yamanaka Jul 2002 B1
6426837 Clark et al. Jul 2002 B1
6447120 Hansen et al. Sep 2002 B1
6452724 Hansen et al. Sep 2002 B1
6460998 Watanabe Oct 2002 B1
6473236 Tadic-Galeb et al. Oct 2002 B2
6486997 Bruzzone et al. Nov 2002 B1
6490017 Huang et al. Dec 2002 B1
6496239 Seiberle Dec 2002 B2
6496287 Seiberle et al. Dec 2002 B1
6511183 Shimizu et al. Jan 2003 B2
6520645 Yamamoto et al. Feb 2003 B2
6532111 Kurtz et al. Mar 2003 B2
6547396 Svardal et al. Apr 2003 B1
6580471 Knox Jun 2003 B2
6583930 Schrenk et al. Jun 2003 B1
6585378 Kurtz et al. Jul 2003 B2
6624936 Kotchick et al. Sep 2003 B2
6643077 Magarill et al. Nov 2003 B2
6654168 Borrelli Nov 2003 B1
6661475 Stahl et al. Dec 2003 B1
6661484 Iwai et al. Dec 2003 B1
6665119 Kurtz et al. Dec 2003 B1
6666556 Hansen et al. Dec 2003 B2
6669343 Shahzad et al. Dec 2003 B2
6698891 Kato Mar 2004 B2
6704469 Xie et al. Mar 2004 B1
6710921 Hansen et al. Mar 2004 B2
6714350 Silverstein et al. Mar 2004 B2
6721096 Bruzzone et al. Apr 2004 B2
6746122 Knox Jun 2004 B2
6764181 Magarill et al. Jul 2004 B2
6769779 Ehrne et al. Aug 2004 B1
6781640 Hunag Aug 2004 B1
6785050 Lines et al. Aug 2004 B2
6788461 Kurtz et al. Sep 2004 B2
6805445 Silverstein et al. Oct 2004 B2
6809864 Martynov et al. Oct 2004 B2
6809873 Cobb Oct 2004 B2
6811274 Olczak Nov 2004 B2
6813077 Borrelli et al. Nov 2004 B2
6816290 Mukawa Nov 2004 B2
6821135 Martin Nov 2004 B1
6823093 Chang et al. Nov 2004 B2
6829090 Katsumata et al. Dec 2004 B2
6844971 Silverstein et al. Jan 2005 B2
6846089 Stevenson et al. Jan 2005 B2
6859303 Wang et al. Feb 2005 B2
6876784 Nikolov et al. Apr 2005 B2
6896371 Shimizu et al. May 2005 B2
6897926 Mi et al. May 2005 B2
6899440 Bierhuizen May 2005 B2
6900866 Kurtz et al. May 2005 B2
6909473 Mi et al. Jun 2005 B2
6920272 Wang Jul 2005 B2
6922287 Wiki et al. Jul 2005 B2
6926410 Weber et al. Aug 2005 B2
6927915 Nakai Aug 2005 B2
6934082 Allen et al. Aug 2005 B2
6943941 Flagello et al. Sep 2005 B2
6947215 Hoshi Sep 2005 B2
6954245 Mi et al. Oct 2005 B2
6972906 Hasman et al. Dec 2005 B2
6976759 Magarill et al. Dec 2005 B2
6981771 Arai et al. Jan 2006 B1
7009768 Sakamoto Mar 2006 B2
7013064 Wang Mar 2006 B2
7023512 Kurtz et al. Apr 2006 B2
7023602 Aastuen et al. Apr 2006 B2
7025464 Beeson et al. Apr 2006 B2
7046422 Kimura et al. May 2006 B2
7046441 Huang et al. May 2006 B2
7046442 Suganuma May 2006 B2
7050233 Nikolov et al. May 2006 B2
7050234 Gage et al. May 2006 B2
7075722 Nakai Jul 2006 B2
7085050 Florence Aug 2006 B2
7099068 Wang et al. Aug 2006 B2
7113335 Sales Sep 2006 B2
7116478 Momoki et al. Oct 2006 B2
7131737 Silverstein et al. Nov 2006 B2
7142363 Sato et al. Nov 2006 B2
7142374 Nikolov et al. Nov 2006 B2
7142375 Nikolov et al. Nov 2006 B2
7155073 Momoki et al. Dec 2006 B2
7158302 Chiu et al. Jan 2007 B2
7159987 Sakata Jan 2007 B2
7177259 Nishi et al. Feb 2007 B2
7184115 Mi et al. Feb 2007 B2
7185984 Akiyama Mar 2007 B2
7213920 Matsui et al. May 2007 B2
7220371 Suganuma May 2007 B2
7221420 Silverstein et al. May 2007 B2
7221501 Flagello et al. May 2007 B2
7227684 Wang et al. Jun 2007 B2
7230766 Rogers Jun 2007 B2
7234816 Bruzzone et al. Jun 2007 B2
7236655 Momoki et al. Jun 2007 B2
7255444 Nakashima et al. Aug 2007 B2
7256938 Barton et al. Aug 2007 B2
7268946 Wang Sep 2007 B2
7306338 Hansen et al. Dec 2007 B2
7375887 Hansen May 2008 B2
7414784 Mi et al. Aug 2008 B2
7561332 Little et al. Jul 2009 B2
7570424 Perkins et al. Aug 2009 B2
7619816 Deng et al. Nov 2009 B2
7630133 Perkins Dec 2009 B2
7670758 Wang et al. Mar 2010 B2
7692860 Sato et al. Apr 2010 B2
7722194 Amako et al. May 2010 B2
7789515 Hansen Sep 2010 B2
7813039 Perkins Oct 2010 B2
20010006421 Parriaux Jul 2001 A1
20010022687 Takahashi et al. Sep 2001 A1
20010053023 Kameno et al. Dec 2001 A1
20020001128 Moseley et al. Jan 2002 A1
20020003661 Nakai Jan 2002 A1
20020015135 Hanson Feb 2002 A1
20020040892 Koyama et al. Apr 2002 A1
20020122235 Kurtz et al. Sep 2002 A1
20020167727 Hansen et al. Nov 2002 A1
20020176166 Schuster Nov 2002 A1
20020181824 Huang et al. Dec 2002 A1
20020191286 Gale et al. Dec 2002 A1
20030058408 Magarill et al. Mar 2003 A1
20030072079 Silverstein et al. Apr 2003 A1
20030081178 Shimizu et al. May 2003 A1
20030081179 Pentico et al. May 2003 A1
20030117708 Kane Jun 2003 A1
20030156325 Hoshi Aug 2003 A1
20030161029 Kurtz et al. Aug 2003 A1
20030180024 Edlinger Sep 2003 A1
20030193652 Pentico et al. Oct 2003 A1
20030202157 Pentico et al. Oct 2003 A1
20030218722 Tsao et al. Nov 2003 A1
20030223118 Sakamoto Dec 2003 A1
20030223670 Nikolov et al. Dec 2003 A1
20040008416 Okuno Jan 2004 A1
20040042101 Wang Mar 2004 A1
20040047039 Wang et al. Mar 2004 A1
20040047388 Wang et al. Mar 2004 A1
20040051928 Mi Mar 2004 A1
20040070829 Kurtz et al. Apr 2004 A1
20040071425 Wang Apr 2004 A1
20040095637 Nikolov et al. May 2004 A1
20040120041 Silverstein et al. Jun 2004 A1
20040125449 Sales Jul 2004 A1
20040165126 Ooi et al. Aug 2004 A1
20040174596 Umeki Sep 2004 A1
20040201889 Wang et al. Oct 2004 A1
20040201890 Crosby Oct 2004 A1
20040218270 Wang Nov 2004 A1
20040227994 Ma et al. Nov 2004 A1
20040233362 Kashima Nov 2004 A1
20040258355 Wang et al. Dec 2004 A1
20042407777 Woodgate et al. Dec 2004
20050008839 Cramer et al. Jan 2005 A1
20050018308 Cassarley et al. Jan 2005 A1
20050045799 Deng et al. Mar 2005 A1
20050046941 Satoh et al. Mar 2005 A1
20050078374 Tairo et al. Apr 2005 A1
20050084613 Wang et al. Apr 2005 A1
20050088739 Chiu et al. Apr 2005 A1
20050122587 Ouderkirk et al. Jun 2005 A1
20050128567 Wang et al. Jun 2005 A1
20050128587 Suganuma Jun 2005 A1
20050152033 Kang et al. Jul 2005 A1
20050179995 Nikolov et al. Aug 2005 A1
20050180014 Nikolov et al. Aug 2005 A1
20050181128 Nikolov et al. Aug 2005 A1
20050190445 Fukuzaki Sep 2005 A1
20050195485 Hirai et al. Sep 2005 A1
20050201656 Nikolov et al. Sep 2005 A1
20050206847 Hansen et al. Sep 2005 A1
20050213043 Nakashima et al. Sep 2005 A1
20050259324 Flagello et al. Nov 2005 A1
20050271091 Wang Dec 2005 A1
20050275944 Wang et al. Dec 2005 A1
20050277063 Wang et al. Dec 2005 A1
20060001969 Wang et al. Jan 2006 A1
20060061862 Mi et al. Mar 2006 A1
20060072074 Matsui et al. Apr 2006 A1
20060072194 Lee Apr 2006 A1
20060087602 Kunisada et al. Apr 2006 A1
20060092513 Momoki May 2006 A1
20060103810 Ma et al. May 2006 A1
20060113279 Little Jun 2006 A1
20060118514 Little et al. Jun 2006 A1
20060119937 Perkins Jun 2006 A1
20060127829 Deng et al. Jun 2006 A1
20060187416 Ouchi et al. Aug 2006 A1
20060192960 Renes et al. Aug 2006 A1
20060215263 Mi et al. Sep 2006 A1
20060238715 Hirata et al. Oct 2006 A1
20060268207 Tan et al. Nov 2006 A1
20070146644 Mi et al. Jun 2007 A1
20070183035 Asakawa et al. Aug 2007 A1
20070195676 Hendriks et al. Aug 2007 A1
20070217008 Wang et al. Sep 2007 A1
20070223349 Shimada et al. Sep 2007 A1
20070242187 Yamaki et al. Oct 2007 A1
20070242228 Chen et al. Oct 2007 A1
20070242352 MacMaster Oct 2007 A1
20070297052 Wang et al. Dec 2007 A1
20080037101 Jagannathan et al. Feb 2008 A1
20080038467 Jagannathan et al. Feb 2008 A1
20080055549 Perkins Mar 2008 A1
20080055719 Perkins Mar 2008 A1
20080055720 Perkins Mar 2008 A1
20080055721 Perkins Mar 2008 A1
20080055723 Perkins Mar 2008 A1
20080266662 Perkins Oct 2008 A1
20080278811 Perkins Nov 2008 A1
20080316599 Wang et al. Dec 2008 A1
20090040607 Amako et al. Feb 2009 A1
20090053655 Deng et al. Feb 2009 A1
20090109377 Sawaki et al. Apr 2009 A1
20100103517 Davis et al. Apr 2010 A1
20100239828 Cornaby Sep 2010 A1
20100328768 Lines Dec 2010 A1
20100328769 Perkins Dec 2010 A1
20110080640 Kaida et al. Apr 2011 A1
Foreign Referenced Citations (117)
Number Date Country
2003267964 Dec 2003 AU
0296391 Feb 1954 CH
03815026.3 Aug 2005 CN
1692291 Nov 2005 CN
03814105.1 Nov 2005 CN
4164157 Jul 1925 DE
296391 Feb 1950 DE
3707984 Sep 1988 DE
103 27 963 Jan 2005 DE
10341596 Apr 2005 DE
102004041222 Mar 2006 DE
0317910 May 1989 EP
0336334 Oct 1989 EP
0349309 Jan 1990 EP
0357946 Mar 1990 EP
407830 Jan 1991 EP
416157 Mar 1991 EP
0488544 Jun 1992 EP
0507445 Oct 1992 EP
0518111 Dec 1992 EP
0543061 May 1993 EP
566 004 Oct 1993 EP
0588937 Mar 1994 EP
0606940 Jul 1994 EP
0349144 Sep 1994 EP
0634674 Jan 1995 EP
0670506 Sep 1995 EP
0521591 Oct 1995 EP
0731456 Sep 1996 EP
0744634 Nov 1996 EP
1239308 Nov 2002 EP
56156815 Dec 1981 JP
58-042003 Mar 1983 JP
61122626 Jun 1986 JP
10028675 Jan 1989 JP
02 -308106 Dec 1990 JP
2308106 Dec 1990 JP
3005706 Jan 1991 JP
403084502 Apr 1991 JP
3126910 May 1991 JP
04 366916 Jun 1991 JP
4-12241 Jan 1992 JP
4331913 Nov 1992 JP
06174907 Dec 1992 JP
5134115 May 1993 JP
5288910 Nov 1993 JP
5341234 Dec 1993 JP
6138413 May 1994 JP
6202042 Jul 1994 JP
7005316 Jan 1995 JP
7072428 Mar 1995 JP
7-146469 Jun 1995 JP
3501299 Aug 1995 JP
7202266 Aug 1995 JP
7294850 Nov 1995 JP
7294851 Nov 1995 JP
7318861 Dec 1995 JP
9015534 Jan 1997 JP
9090122 Apr 1997 JP
9090129 Apr 1997 JP
9178943 Jul 1997 JP
09-507926 Aug 1997 JP
9212896 Aug 1997 JP
9288211 Nov 1997 JP
10-003078 Jan 1998 JP
10073722 Mar 1998 JP
10084502 Mar 1998 JP
10-153706 Jun 1998 JP
10-260403 Sep 1998 JP
10- 268301 Oct 1998 JP
11-014814 Jan 1999 JP
1-164819 Mar 1999 JP
11064794 Mar 1999 JP
11142650 May 1999 JP
11-174396 Jul 1999 JP
11237507 Aug 1999 JP
11-258603 Sep 1999 JP
11-306581 Nov 1999 JP
2000-147487 May 2000 JP
2000284117 Oct 2000 JP
2001074935 Mar 2001 JP
2004157159 Jun 2004 JP
2004309903 Nov 2004 JP
20054513547 May 2005 JP
2005195824 Jul 2005 JP
2005534981 Nov 2005 JP
2006047813 Feb 2006 JP
2006133402 May 2006 JP
2006201540 Aug 2006 JP
2003-0079268 Oct 2003 KR
10-2003-0090021 Nov 2003 KR
10-2004-0046137 Jun 2004 KR
10-2005-0017871 Feb 2005 KR
10-0707083 Apr 2007 KR
1283685 Jan 1987 SU
1781659 Dec 1992 SU
WO9615474 May 1996 WO
WO9701788 Jan 1997 WO
WO0070386 Nov 2000 WO
WO 0189677 Apr 2001 WO
WO 0221205 Mar 2002 WO
WO 02077588 Oct 2002 WO
WO03054619 Jul 2003 WO
WO03069381 Aug 2003 WO
WO03102652 Dec 2003 WO
WO03107046 Dec 2003 WO
WO2004013684 Feb 2004 WO
WO 2004019020 Mar 2004 WO
WO2004019070 Mar 2004 WO
WO2004072692 Aug 2004 WO
WO2005019503 Mar 2005 WO
WO2005065182 Jul 2005 WO
WO2005079233 Sep 2005 WO
WO2005101112 Oct 2005 WO
WO2005123277 Dec 2005 WO
WO2006014408 Feb 2006 WO
WO2006036546 Apr 2006 WO
Related Publications (1)
Number Date Country
20080278811 A1 Nov 2008 US
Continuation in Parts (1)
Number Date Country
Parent 11005927 Dec 2004 US
Child 11767353 US