WO2003082969A1 - Anti-glare polymer nanocomposites - Google Patents

Abstract

An anti-glare nanocomposite material that includes a polymer host and a plurality of nanoparticles dispersed within the polymer host is disclosed. The nanoparticles include at least one rare earth ion selected from the group consisting of neodymium (Nd), praseodymium (Pr) and holmium (Ho) rare earth ions.

Description

ANTI-GLARE POLYMER NANOCOMPOSITES

CROSS-REFERENCE TO RELATED APPLICATION

[001] This application claims priority from U.S. Provisional Patent Application

Serial No. 60/367,234 (Attorney Docket no. PHX-0071 ) filed March 25, 2002, which is herein incorporated by reference.

FIELD OF THE INVENTION

[002] The present invention generally relates to anti-glare materials. More particularly, the present invention relates to polymer composite anti-glare materials including nanoparticles.

BACKGROUND OF THE INVENTION

[003] The problem of glare typically occurs when light scattered from a surface shines on one's retina and reduces the contrast of an image being viewed. Glare can affect vision causing discomfort to an individual in many situations, such as, for example, when ambient light from the sun or overhead lighting reflects from a computer monitor or television being viewed by the individual.

[004] The retina is the eye's light sensing structure. It contains two types of cells, rods that handle vision in low light and cones that handle color vision and detail. Cone cells have three types of color sensitive pigments. A blue sensitive pigment responds to a wavelength range from about 400 to 530 nm with a peak response at about 450 nm. A green sensitive pigment responds to a wavelength range from about 460 nm to 620 nm with a peak response at about 525 nm. And, a red sensitive pigment responds to a wavelength range from about 450 to 700 nm with a peak response at about 575 nm.

[005] Glare can be reduced by an anti-glare material used as a coating that, for example, is suitably balanced in the degree of optical absorption over each of the three above described wavelength ranges. The anti-glare coating is particularly effective when at the degree of optical absorption at each of the three peak response wavelengths is balanced. One method for controlling the degree of optical absorption of the anti-glare materials is to include metal ions having specific absorption peaks in an optically transparent medium. For example, trivalent neodymium ions have an absorption peak at about 525 nm and 575 nm, trivalent praseodymium ions have an absorption peak at about 575 nm and 450 nm, and trivalent holmium ions have an absorption peak at about 525 nm and 450 nm.

[006] U.S. Patent No. 5,759,448, which is herein incorporated by reference, discloses an anti-glare optical material including a polymer containing a phosphate group and metal ions. In the polymer, the metal ions, such as trivalent neodymium ions, are in the form of a molecule of a metal compound, such as neodymium nitrate. The phosphate group serves to uniformly disperse the metal ions by chemically bonding the molecules of the metal compounds to the molecular structure of the polymer. Because the phosphate group must chemically bond to the polymer, the types of available polymers is limited. [007] A general solution to this limitation is provided by composite materials that are well known and that generally comprise two or more materials each offering its own set of properties or characteristics. The two or more materials may be joined together to form a system that exhibits properties derived from each of the materials. A common form of a composite is one with a body of a first material (a host matrix) with a second material distributed in the host matrix.

[008] One class of composite materials includes nanoparticles distributed within a host matrix material. Nanoparticles are particles of a material that have a size measured on a nanometer scale. Generally, nanoparticles are larger than a cluster (which might be only a few hundred atoms in some cases), but with a relatively large surface area-to-bulk volume ratio. While most nanoparticles have a size from about 10 nm to about 500 nm, the term nanoparticles can cover particles having sizes that fall outside of this range. For example, particles having a size as small as about 1 nm and as large as about 1x10³ nm could still be considered nanoparticles. Nanoparticles can be made from a wide array of materials. Among these materials examples include, transition metals, rare-earth metals, group VA elements, polymers, dyes, semiconductors, alkaline earth metals, alkali metals, group IIIA elements, and group IVA elements.

[009] Further, nanoparticles themselves may be considered a nanoparticle composite, which may comprise a wide array of materials, single elements, mixtures of elements, stoichiometric or non-stoichiometric compounds. The materials may be crystalline, amorphous, or mixtures, or combinations of such structures. [010] The host matrix may comprise a random glassy matrix such as an amorphous organic polymer. Organic polymers may include typical hydrocarbon polymers and halogenated polymers. It is generally desirable that in an optical component, such as a planar optical waveguide, an optical fiber, an optical film, or a bulk optical component, e.g., an optical lens or prism, the total optical loss be kept at a minimum. For example, in the case of a planar optical waveguide, the total loss should be approximately equal to, or less than, 0.5 dB/cm in magnitude, and such as less than 0.2 dB/cm. For a highly transparent optical medium to be used as the optical material, a fundamental requirement is that the medium exhibits little, or no, absorption and scattering losses.

[011] Intrinsic absorption losses commonly result from the presence of fundamental excitations that are electronic, vibrational, or coupled electronic-vibrational modes in origin. Further, the device operating wavelength of the optical component should remain largely different from the fundamental, or overtone, wavelengths for these excitations. Further, these absorptive overtones can cause the hydrocarbon polymers to physically or chemically degrade, thereby leading to additional and often times permanent increase in signal attenuation in the optical fibers or waveguides [012] Material scattering losses occur when the signal wave encounters abrupt changes in refractive index of the otherwise homogeneous uniform optical medium. These discontinuities can result from the presence of composition inhomogenieties, crystallites, nanoporous structures, voids, fractures, stresses, faults, or even foreign impurities such as dust or other particulates.

[013] Among the various mechanisms of optical scattering loss, an important factor is the porosity of the optical material. As a result of the interplay between various material characteristics, e.g., surface energy, solubility, glass transition temperature, entropy, etc., and processing conditions, e.g. temperature, pressure, atmosphere, etc., optical materials, such as amorphous perfluoropolymers can exhibit a large amount of nanoporous structures under normal processing conditions. Such nanoporous structures can cause optical scattering loss and should be eliminated, or converted to smaller sizes, in order to satisfy a certain low optical loss device performance requirement. The smaller sized pores are called nanopores. Nanopores are pores in a material that have a size measured on a nanometer scale. Generally, nanopores are larger than the size of an atom but smaller than 1000 nm. While most nanopores have a size from about 1 nm to about 500 nm, the term nanopores can cover pores having sizes that fall outside of this range. For example, pores having a size as small as about 0.5 nm and as large as about 1x10³ nm could still be considered nanopores By introducing nanoparticles into optically transparent host matrix, the absorption and scattering losses due to the nanoparticles may add to the optical loss. In order to keep the optical loss to a minimum, in addition to controlling the loss contribution from the host matrix, it is essential to control the absorption and scattering loss from the nanoparticles doped into the host matrix for optical applications. [014] For discrete nanoparticles that are approximately spherical in shape and

doped into the host matrix, the scattering loss , in dB per unit length, resulting from the

presence of the particles is dependent on the particle diameter d, the refractive index ratio of the nanoparticles and the waveguide core m=n_pa/n_core, and the volume fraction of the nanoparticles in the host waveguide core V_p. The nanoparticle induced scattering loss can be calculated by:

[016] where λ is the vacuum propagation wavelength of the light guided inside

the waveguide. As an example, when m=2, V_p=10%, λ=1550nm, d=10 nm, the

calculated scattering loss α is 0.07dB/cm. To fabricate a certain waveguide device with

a set loss specification, and therefore a nanoparticle induced waveguide loss budget of

α, the nanoparticle diameter d satisfies the following equation:

[018] where λ is the vacuum propagation wavelength of the light guided inside

the waveguide, m-n_parln_core the refractive index ratio of the nanoparticles and the core, and V_p the volume fraction of the nanoparticles in the host waveguide core. For

example, following Equation 2, with a nanoparticle loss budget of α = 0.5dB/cm, when

m=2, V_p=10%, λ=1550nm, the nanoparticle diameter d is generally smaller than 19 nm.

In general, the diameter of the nanoparticles is smaller than about 50nm, and advantageously, 20nm.

[019] The description for nanoparticle loss also can be applied to nanopore contributions to propagation loss by representing the nanopores as equivalent nanoparticles with refractive index of 1.

[020] Composite materials including nanoparticles distributed within a host matrix material have been used in optical applications. For example, U.S. Patent No. 5,777,433 (the '433 patent) discloses a light emitting diode (LED) that includes a packaging material including a plurality of nanoparticles distributed within a host matrix material. The nanoparticles increase the index of refraction of the host matrix material to create a packaging material that is more compatible with the relatively high refractive index of the LED chip disposed within the packaging material. Because the nanoparticles do not interact with light passing through the packaging material, the packaging material remains substantially transparent to the light emitted from the LED. [021] While the packaging material used in the '433 patent offers some advantages derived from the nanoparticles distributed within the host matrix material, the composite material of the '433 patent remains problematic. For example, the composite material of the '433 patent includes glass or ordinary hydrocarbon polymers, such as epoxy and plastics, as the host matrix material. While these materials may be suitable in certain applications, they limit the capabilities of the composite material in many other areas. For example, the host matrix materials of the '433 patent commonly exhibit high absorption losses.

[022] Moreover, the method of the '433 patent is problematic in not accounting for optical scattering loss from relatively large nanopores or nanoporous structures. In fact, among the various mechanisms of optical scattering loss, an important factor is the porosity of the optical material. As a result of the interplay between various material characteristics, e.g., surface energy, solubility, glass transition temperature, entropy, etc., and processing conditions, e.g. temperature, pressure, atmosphere, etc., optical materials, such as amorphous perfluoropolymers, can exhibit a large amount of nanoporous structures under normal processing conditions. Such nanoporous structures can cause optical scattering loss and should be eliminated, or converted to smaller sizes, in order to satisfy a certain low optical loss device performance requirement. By controlling the pore sizes and pore structures, optical scattering losses can be greatly reduced. The method of the '433 patent does not recognize the presence of discrete pores or porous structure nor teach control of their sizes and structures.

[023] Additionally, the method of the '433 patent for dealing with agglomeration of the nanoparticles within the host matrix material is inadequate for many composite material systems. Agglomeration is a significant problem when making composite materials that include nanoparticles distributed within a host matrix material. Because of the small size and great numbers of nanoparticles that may be distributed within a host matrix material, there is a large amount of interfacial surface area between the surfaces of the nanoparticles and the surrounding host matrix material. As a result, the nanoparticle/host-matrix material system operates to minimize this interfacial surface area, and corresponding surface energy, by combining the nanoparticles together to form larger particles. This process is known as agglomeration. Once the nanoparticles have agglomerated within a host matrix material, it is extremely difficult to separate the agglomerated particles back into individual nanoparticles.

[024] i Agglomeration of the nanoparticles within the host matrix material may result in a composite material that lacks a desired characteristic. Specifically, when nanoparticles agglomerate, the larger particles formed may not behave in a similar way to the smaller nanoparticles. For example, while nanoparticles may be small enough to avoid scattering light within the composite material, agglomerated particles may be sufficiently large to cause scattering. As a result, a host matrix material may become substantially less transparent in the presence of such agglomerated particles. [025] To combat agglomeration, the composite material of the '433 patent includes an anti-flocculant coating disposed on the nanoparticles intended to inhibit agglomeration. Specifically, the '433 patent suggests using surfactant organic coatings to suppress agglomeration. These types of coatings, however, may be inadequate or ineffective especially when used with host matrix materials other than typical hydrocarbon polymers.

[026] The present invention is directed to overcoming one or more of the problems or disadvantages associated with the prior art by providing composite materials exhibiting improved optical properties, including improved anti-glare properties.

SUMMARY OF THE INVENTION

The present invention relates to composite materials for use in anti-glare materials. The present invention further relates to be bare, coated, bare core-shell, and coated core-shell nanoparticles dispersed in a host matrix. In one embodiment, the resulting composite exhibits a balanced degree of optical absorption over a three-color wavelength range of blue, green, and red. A balanced degree of optical absorption means that light is approximately equally absorbed for each of the three color wavelength range. Advantageously, the host matrix has a transparency of at least 90%.

Nanoparticles that can be used in the inventive composite comprises at least one earth ion chosen from holium (Ho), terbium (Tb), samarium (Sm), neodymium (Nd), europium (Eu), dysprosium (Dy), erbium (Er), and praseodymium (Pr), generally in amounts ranging from 1 % to 13% by weight.

The present invention also relates to an optical anti-glare device comprising: a host matrix and a plurality of nanoparticles within the host matrix. In one embodiment, the plurality of nanoparticles comprises at least one rare earth ion that optically absorbs light having a wavelength ranging from 400 to 700 nanometers.

BRIEF DESCRIPTION OF THE DRAWINGS

[027] The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate exemplary embodiments of the invention and, together with the written description, serve to explain the principles of the invention.

[028] In the drawings:

[029] Fig. 1 is a diagrammatic representation of a nanocomposite material according to an exemplary embodiment of the invention.

[030] Figs. 2A and 2B are diagrammatic representations of a nanocomposite material according to exemplary embodiments of the present invention.

[031] Fig. 3 is a diagrammatic representation of a nanocomposite material, including more than one different type of nanoparticle, according to an exemplary embodiment of the invention.

[032] Fig. 4A is a diagrammatic representation of a coated nanoparticle according to an exemplary embodiment of the present invention.

[033] Fig. 4B is a diagrammatic representation of yet another coated nanoparticle according to an exemplary embodiment of the present invention. [034] Fig. 5 is a flowchart diagram representing the process for forming a nanocomposite material according to an exemplary embodiment of the present invention.

[035] FIG. 6A and 6B depict absorption spectra for samarium.

[036] FIG. 7A and 7B depict absorption spectra for erbium.

[037] FIG. 8 depicts an Atomic Force Microscope (AFM) image of nanoparticles.

[038] FIG. 9 depicts the optical loss as a function of the nanoparticles size at two different wavelengths.

[039] FIG. 10 depicts the optical loss as a function of the nanoparticles size at two different wavelengths.

[040] FIG. 11 depicts the optical loss as a function of the nanoparticles sizes at two different wavelengths.

[041] FIG. 12 depicts the scattering loss with pore diameter for a fluoropolymer, with different fractions of residual porosity.

[042] FIG. 13 depicts the optical articles comprising the polymer nanocomposite according to one embodiment of the invention.

[043] FIG. 14A and 14B depict absorption spectra for holium.

[044] FIG. 15A and 15B depict absorption spectra for terbium.

[045] FIG. 16A and B depict absorption spectra for neodymium.

[046] FIG. 17A and B depict absorption spectra for europium.

[047] FIG. 18A and B depict absorption spectra for dysprosium. [048] FIG. 19A and B depict absorption spectra for praseodymium.

DETAILED DESCRIPTION OF THE INVENTION

[049] In the following description, reference is made to the accompanying drawings that form a part thereof, and in which is shown by way of illustration specific exemplary embodiments in which the invention can be practiced. These embodiments are described in sufficient detail to enable those skilled in the art to practice the invention, and it is to be understood that other embodiments can be utilized and that changes can be made without departing from the scope of the present invention. [050] For the purpose of this disclosure the distribution of nanoparticles in a matrix is termed a composite material. Composite materials comprising nanoparticles distributed within a polymer matrix material may offer desirable properties. They may for example, improve the thermal stability, chemical resistance, biocompatibility of components and materials comprising them. In one embodiment, the small size of the nanoparticles may impart the composite material with properties derived from the nanoparticles without significantly affecting other properties of the matrix material. For example, nanoparticles may be smaller than the wavelength of incident light, typically ranging from about 1200 nm to about 1700 nm, such that incident light does not interact with the nanoparticles. In other words, the incident light does not scatter from , interactions with the nanoparticles. Therefore, when appropriately sized nanoparticles are distributed within a transparent host matrix, the host matrix material may remain optically transparent because scattering of the light incident upon the nanoparticles within the host matrix material is insignificant or absent.

[051] FIG. 1 provides a diagrammatic representation of a composite material according to an embodiment of the invention. In one embodiment, the composite material includes random glassy polymer host matrix 10 and plurality of nanoparticles 11 dispersed either uniformly or non-uniformly within the host matrix 10. Suitable host matrix may comprise an amorphous organic polymer. Organic polymers may include typical hydrocarbon polymers and halogenated polymers. It is generally desirable that in an optical component, such as an optical film, or a bulk optical component, e.g., an optical lens, filter, prism, plate, or canopy enclosure, the total optical loss, consisting of both absorption and the scattering loss, be kept at a minimum. [052] Among the various mechanisms of optical scattering loss, an important factor is the porosity of the optical material. As a result of the interplay between various material characteristics, e.g., surface energy, solubility, glass transition temperature, entropy, etc., and processing conditions, e.g. temperature, pressure, atmosphere, etc., optical materials, such as amorphous perfluoropolymers can exhibit a large amount of nanoporous structures under normal processing conditions. Such nanoporous structures can cause optical scattering loss and should be eliminated, or converted to smaller sizes, in order to satisfy a certain low optical loss device performance requirement. By controlling the pore sizes and pore structures, optical scattering losses can be greatly reduced. For discrete nanopores that are approximately spherical in shape and are evenly distributed into a host matrix, the scattering loss α, in dB per unit

length, resulting from the presence of the nanopores, is dependent on the pore diameter of, the refractive index ratio of the pores and the surrounding host material m=n_po n_sur, and the volume fraction of the nanopores in the host V_p. The nanopore induced scattering loss can be calculated by:

[054] wherein λ is the vacuum propagation wavelength of the light inside the

compositematerial. As an example, when m=1.3, V_p=10%, λ=1550 nm, d=10 nm, the

calculated scattering loss α is 0.001 dB/cm. To fabricate a certain optical component

with a set loss specification, and therefore a nanopore induced scattering loss budget of

α, the nanopore diameter d should satisfy the following relationship:

[056] wherein λ is the vacuum propagation wavelength of the light inside the

composite, m=n_Po n_sur the refractive index ratio of the nanopores and the host material, and V_p the volume fraction of the nanopores in the host material. For example,

following Equation 2, with a nanopore loss budget of = 0.5 dB/cm, when m=1.3,

V_p=10%, λ=1550 nm, the nanopore diameter d must be smaller than 37 nm. In certain embodiments, the diameter of the nanopores should be smaller than 100 nm, and further smaller than 50 nm.

[057] By treating the pores as spherical particles of refractive index equal to 1 ,

the expected scattering loss as function of pore diameter, for wavelength (λ) equals

1310 nm, as shown in FIG. 12. For the case of nanopores in a fluoropolymer film (n = 1.34), a residual porosity of 5 vol% with an average diameter of 20 nm, would lead

to a scattering loss of 1.4 x 10^"4 dB/cm at λ = 1310 nm. Such residual nanoporosity

does not lead to any significant scattering loss. However, for film which was highly porous, with a porosity volume fraction as high as 25%, scattering losses will remain below 7 x 10^"4 dB/cm as long as the pore diameter does not exceed 20 nm. [058] Nanoporous materials comprising nanopores distributed within a host matrix material may be used in optical applications. For example, in an optical article, the composite material should exhibit little, or no, optical attenuation, or loss, in signal propagation through the material. A potential source for loss dependent behavior are material scattering centers such as relatively extensive pore or void structures present in the composite material.

[059] Thus, nanopores can be distributed in the host matrix in great numbers as separate individual pores, or as joined clusters, some even extending as a continuous interconnected network-like structure over the entire material sample, thereby forming a nanoporous structure. [060] Clustering of the nanopores within the host matrix material may result in a porous material that lacks a desired characteristic. Specifically, when nanopores fuse together, the larger nanoporous structures formed may not behave in a similar way to the smaller nanopores. For example, while nanopores may be small enough to avoid scattering light within the matrix material, fused pores may be sufficiently large to cause scattering. As a result, a host matrix material may become substantially less transparent in the presence of such nanoporous structures. [061] Thus, for example, of many potential host matrix polymer materials, halogenated polymers have been shown to have potential to be used in the optical field. Halogenated polymers, such as fluoropolymers, are well known to be problematic toward pore-like structures. However, in the optical field, the presence of such porous structures, especially on nanometer length scales, in optical articles made of halogenated polymers can ultimately cause light to scatter, especially, for example, in optical thin films, sheets, or bulk articles, thereby resulting in significant optical signal attenuation. To achieve lower optical loss, it is, therefore, important to control the size and distribution of the nanopores and associated nanoporous structures. [062] In one embodiment, the host matrix 10 may comprise a polymer, a copolymer, a terpolymer, either by itself or in a blend with other matrix material. [063] In another embodiment, the host matrix 10 can comprise a halogenated elastomer, a perhalogenated elastomer, a halogenated plastic, or a perhalogenated plastic, either by itself or in a blend with other matrix material listed herein. [064] In yet another embodiment, the host matrix 10 may comprise a polymer, a copolymer, or a terpolymer, having at least one halogenated monomer represented by one of the following formulas:

[066] wherein R¹, R², R³, R⁴, and R⁵, which may be identical or different, are each chosen from linear or branched hydrocarbon-based chains, possibly forming at least one carbon-based ring, being saturated or unsaturated, wherein at least one hydrogen atom of the hydrocarbon-based chains may be halogenated; a halogenated alkyl, a halogenated aryl, a halogenated cyclic alky, a halogenated alkenyl, a halogenated alkylene ether, a halogenated siloxane, a halogenated ether, a halogenated polyether, a halogenated thioether, a halogenated silylene, and a halogenated silazane. Yi and Y₂, which may be identical or different, are each chosen from H, F, CI, and Br atoms. Y₃ is chosen from H, F, CI, and Br atoms, CF₃, and CH₃. [067] Alternatively, the polymer may comprise a condensation product made from the monomers listed below:

[068] HO-R-OH + NCO-R'-NCO; or [069] HO-R-OH + Ary¹ -Ary²,

[070] wherein R, R', which may be identical or different, are each chosen from halogenated alkylene, halogenated siloxane, halogenated ether, halogenated silylene, halogenated arylene, halogenated polyether, and halogenated cyclic alkylene. Ary¹,

Ary², which may be identical or different, are each chosen from halogenated aryls and halogenated alkyl aryls.

[071] Ary as used herein, is defined as being a saturated, or unsaturated, halogenated aryl, or a halogenated alkyl aryl group.

[072] Alternatively, the host matrix 10 can comprise a halogenated cyclic olefin polymer, a halogenated cyclic olefin copolymer, a halogenated polycyclic polymer, a halogenated polyimide, a halogenated polyether ether ketone, a halogenated epoxy resin, a halogenated polysulfone, or halogenated polycarbonate.

[073] In certain embodiments, the host matrix 10, for example, a fluorinated polymer host matrix 10, may exhibit very little absorption loss over a wide wavelength range. Therefore, such fluorinated polymer materials may be suitable for optical applications.

[074] In one embodiment, the halogenated aryl, alkyl, alkylene, alkylene ether, alkoxy, siloxane, ether, polyether, thioether, silylene, and silazane groups are at least partially halogenated, meaning that at least one hydrogen in the group has been replaced by a halogen. In another embodiment, at least one hydrogen in the group may be replaced by fluorine. Alternatively, these aryl, alkyl, alkylene, alkylene ether, alkoxy, siloxane, ether, polyether, thioether, silylene, and silazane groups may be completely halogenated, meaning that each hydrogen of the group has been replaced by a halogen. In an exemplary embodiment, the aryl, alkyl, alkylene, alkylene ether, alkoxy, siloxane, ether, polyether, thioether, silylene, and silazane groups may be completely fluorinated, meaning that each hydrogen has been replaced by fluorine. Furthermore, the alkyl and alkylene groups may include between 1 and 12 carbon atoms. [075] Additionally, host matrix 10 may comprise a combination of one or more different halogenated polymers, such as fluoropolymers, blended together. Further, host matrix 10 may also include other polymers, such as halogenated polymers containing functional groups such as phosphinates, phosphates, carboxylates, silanes, siloxanes, sulfides, including POOH, POSH, PSSH, OH, S0₃H, S0₃R, S0₄R, COOH, NH₂, NHR, NR₂, CONH₂, NH-NH₂, and others, where R may comprise any of aryl, alkyl, alkylene, siloxane, silane, ether, polyether, thioether, silylene, and silazane. Further, host matrix 10 may also include homopolymers or copolymers of vinyl, acrylate, methacrylate, vinyl aromatic, vinyl esters, alpha beta unsaturated acid esters, unsaturated carboxylic acid esters, vinyl chloride, vinylidene chloride, and diene monomers. Further, the host matrix may also include a hydrogen-containing fluoroelastomer, a hydrogen-containing perfluoroelastomer, a hydrogen containing fluoroplastic, a perfluorothermoplastic, at least two different fluoropolymers, or a cross- linked halogenated polymer. [076] Examples of the host matrix 10 include: poIy[2,2-bistrifluoromethyl-4,5- difluoro-1 ,3-dioxole-co-tetrafluoroethylene], poly[2,2-bisperfluoroalkyl-4,5-difluoro-1 ,3- dioxole-co-tetrafluoroethylene], poly[2,3-(perfluoroalkenyl) perfluorotetrahydrofuran], poly[2,2,4-trifluoro-5-trifluoromethoxy-1 ,3-dioxole-co-tetrafluoroethylene], poly(pentafluorostyrene), fluorinated polyimide, fluorinated polymethylmethacrylate, polyfluoroacrylates, polyfluorostyrene, fluorinated polycarbonates, fluorinated poly (N- vinylcarbazole), fluorinated acrylonitrile-styrene copolymer, fluorinated Nafion®, fluorinated poly(phenylenevinylene), perfluoro-polycyclic polymers, polymers of fluorinated cyclic olefins, or copolymers of fluorinated cyclic olefins. [077] Additionally, the host matrix may comprise any polymer sufficiently clear for optical applications. Examples of such polymers include polymethylmethacrylates, polystyrenes, polycarbonates, polyimides, epoxy resins, cyclic olefin copolymers, cyclic olefin polymers, acrylate polymers, PET, polyphenylene vinylene, polyether ether ketone, poly (N-vinylcarbazole), acrylonitrile-styrene copolymer, or poly(phenylenevinylene).

[078] By including halogens, such as fluorine, into host matrix 10, the optical properties of host matrix 10 and the resulting composite material are improved over conventional composite materials. Unlike the C-H bonds of hydrocarbon polymers, carbon-to-halogen bonds (such as C-F) shift the vibrational overtones toward longer wavelengths out of the ranges used in telecommunication applications. As hydrogen is removed through partial to total halogenation, the absorption of light by vibrational overtones is reduced. One parameter that quantifies the amount of hydrogen in a polymer is the molecular weight per hydrogen for a particular monomeric unit. For highly halogenated polymers useful in optical applications, this ratio may be 100 or greater. This ratio approaches infinity for perhalogenated materials. [079] One class of composite materials includes nanoparticles distributed within a host matrix material. Nanoparticles are particles of a material that have a size measured on a nanometer scale. Generally, nanoparticles are larger than a cluster (which might be only a few hundred atoms in some cases), but with a relatively large surface area-to-bulk volume ratio. While most nanoparticles have a size from about 10 nm to about 500 nm, the term nanoparticles can cover particles having sizes that fall outside of this range.

[080] For example, particles having a size as small as about 1 nm and as large as about 1x10³ nm could still be considered nanoparticles. By introducing nanoparticles into optically transparent host matrix, the absorption and scattering losses due to the nanoparticles may add to the optical loss. In order to keep the optical loss to a minimum, in addition to controlling the loss contribution from the host matrix, it is essential to control the absorption and scattering loss from the nanoparticles doped into the host matrix for optical applications.

[081] FIGs. 9, 10, and 11 provide examples of scattering loss due to the presence of nanoparticles. Nanocomposite containing nanoparticles with a refractive index of about 1.6725 and a host material with a refractive index of about 1.6483 at 988 nm exhibit a loss of about 0.6 dB/cm. On the other hand, when the index mismatch between the host and the nanoparticles is large, high scattering loss is expected when the particle size exceeds 50 nm as shown in FIG. 10 and 11. The presence of small nanoparticles with particle diameter less than 20 nm even at high nanoparticles loading (4 vol%) does not lead to any significant scattering loss. Therefore, it is necessary to keep the nanoparticles size below 20 nm in order to maintain the low optical loss caused by the presence of nanoparticles.

[082] Nanoparticles can be made from a wide array of materials. Among these materials examples include, transition metals, rare-earth metals, group VA elements, polymers, dyes, semiconductors, alkaline earth metals, alkali metals, group IIIA elements, and group IVA elements. Nanoparticles can be made from a wide array of materials. Among these materials examples include metal, glass, ceramics, refractory materials, dielectric materials, carbon or graphite, natural and synthetic polymers including plastics and elastomers, dyes, ion, alloy, compound, composite, or complex of transition metal elements, rare-earth metal elements, group VA elements, semiconductors, alkaline earth metal elements, alkali metal elements, group IIIA elements, and group IVA elements or polymers and dyes.

[083] Further, the materials may be crystalline, amorphous, or mixtures, or combinations of such structures. Nanoparticles 11 may be bare, coated, bare core- shell, coated core-shell. Further, nanoparticles themselves may considered a nanoparticle matrix, which may comprise a wide array of materials, single elements, mixtures of elements, stoichiometric or non-stoichiometric compounds. The materials may be crystalline, amorphous, or mixtures, or combinations of such structures. [084] Moreover, nanoparticles themselves may be considered a nanoparticle matrix, which may comprise a wide array of materials, single elements, mixtures of elements, stoichiometric or non-stoichiometric compounds [085] A plurality of nanoparticles 11 may include an outer coating layer 12, which at least partially coats nanoparticles 11 and inhibits their agglomeration. Suitable coating materials may have a tail group, which is compatible with the host matrix, and a head group, that could attach to the surface of the particles either through physical adsorption or chemical reaction. The nanoparticles 11 according to the present invention may be doped with an effective amount of dopant material. An effective amount is that amount necessary to achieve the desired result, for example, in the present invention. The nanoparticles of doped glassy media, single crystal, or polymer are embedded in the host matrix core material 10. The active nanoparticles may be randomly and uniformly distributed. The nano-particles of rare-earth doped, or co- doped, glasses, single crystals, organic dyes, or polymers are embedded in the polymer core material. In cases where there is interface delamination due to mismatches of mechanical, chemical, or thermal properties between the nanoparticles and the surrounding polymer core host matrix, a compliance layer may be coated on the nanoparticles to enhance the interface properties between the nanoparticles and the host matrix polymer core material. [086] As shown in FIG. 1 , the nanoparticles may include an outer layer 12. As used herein, the term layer is a relatively thin coating on the outer surface of an inner core (or another inner layer) that is sufficient to impart different characteristics to the outer surface. The layer need not be continuous or thick to be an effective layer, although it may be both continuous and thick in certain embodiments. [087] Nanoparticles 11 may comprise various different materials, and they may be fabricated using several different methods. In one embodiment of the invention, the nanoparticles are produced using an electro-spray process. In this process, very small droplets of a solution including the nanoparticle precursor material emerge from the end of a capillary tube, the end of which is maintained at a high positive or negative potential. The large potential and small radius of curvature at the end of the capillary tube creates a strong electric field causing the emerging liquid to leave the end of the capillary as a mist of fine droplets. A carrier gas captures the fine droplets, which are then passed into an evaporation chamber. In this chamber, the liquid in the droplets evaporates and the droplets rapidly decrease in size. When the liquid is entirely evaporated, an aerosol of nanoparticles is formed. These particles may be collected to form a powder or they may be dispersed into a solution. The size of the nanoparticles is variable and depends on processing parameters.

[088] In an exemplary embodiment of the present invention, nanoparticles 11 have a major dimension of less than about 50 nm. That is, the largest dimension of the nanoparticle (for example the diameter in the case of a spherically shaped particle) is less than about 50 nm and in further embodiments about 20 nm. [089] Other processes are also useful for making the nanoparticles 11 of the present invention. For example, the nanoparticles may be fabricated by laser ablation, laser-driven reactions, flame and plasma processing, solution-phase synthesis, sol-gel processing, spray pyrolysis, flame pyrolysis, laser pyrolysis, flame hydrolysis, mechanochemical processing, sono-electro chemistry, physical vapor deposition, chemical vapor deposition, mix-alloy processing, decomposition-precipitation, liquid phase precipitation, high-energy ball milling, hydrothermal methods, glycothermal methods, vacuum deposition, polymer template processes, micro emulsion processes or any other suitable method for obtaining particles having appropriate dimensions and characteristics. The sol-gel process is based on the sequential hydrolysis and condensation of alkoxides, such as metal alkoxides, initiated by an acidic or a basic aqueous solution in the presence of a cosolvent. Controlling the extent of hydrolysis and condensation reactions with water, surfactants, or coating agents can lead to final products with particle diameters in the nanometer range. The sol-gel process can be used to produce nanoscale metal, ceramic, glass and semiconductor particles. The size of nanoparticles made from varieties of methods can be determined using Transmission Electron Microscope (TEM), Atomic Force Microscope (AFM), or surface area analysis. For crystalline materials, X-ray powder diffraction pattern can also be used to calculate the crystallite size based on line broadening according to a procedure described in Chapter 9 of "X-Ray Diffraction Procedure", published by Wiley in 1954. [090] The presence of the nanoparticles can affect other properties of the composite material. For example, for optical applications, the nanoparticle material may be selected according to a particular, desired index of refraction. For certain structural applications, the type of material used to form the nanoparticles 11 may be selected according to its thermal properties, or coefficient of thermal expansion. Still other applications may depend on the mechanical, magnetic and electrical properties of the material used to form nanoparticles 11.

[091] Several classes of materials may be used to form nanoparticles 11 depending upon the effect the nanoparticles are to have on the properties of the composite containing them. In one embodiment, nanoparticles 11 may include one or more active materials, which allow the composite to be an anti-glare media. Active materials act as anti-glare media toward a light signal as the light signal encounters the active material. Active materials may include transition metal elements, rare-earth metal elements, the actinide element uranium, group VA elements, semiconductors, and group IVA elements in the forms of ions, alloys, compounds, composites, complexes, chromophores, dyes or polymers. Examples of such active materials include but are not limited to Ce³⁺, Pr³⁺, Nd³⁺, Pm³⁺, Sm³⁺, Eu³⁺, Gd³⁺, Tb³⁺, Dy³⁺, Ho³⁺, Er³⁺, Tm³⁺, Yb³⁺, V²⁺, V³⁺, Cr²*, Cr³⁺, Cr⁴⁺, Mn⁵⁺, Co²⁺, Fe²⁺, Ni²⁺, Ti³⁺, U³⁺, and Bi³⁺, as well as the semiconductors such as Si, Ge, SiGe, GaP, GaAs, InP, InAs, InSb, PbSe, PbTe. Active materials can also comprise combinations of the above mentioned materials, with rare earth ions, such as Pr³⁺, Nd³⁺ and Ho³⁺, for example, as nanoparticles in an appropriate matrix for anti-glare media.

[092] In certain embodiments, the semiconductor materials, for example, Si, Ge, SiGe,

GaP, GaAs, GaN, InP, InAs, InSb, PbSe, PbTe, InGaAs, and other stoichiometries as well as compositions, alone, or together, or doped with an appropriate ion may be incorporated in a nanoparticle for anti-glare media.

Metal containing materials such as metal chalocogenides, metal salts, transition metals, transition metal complexes, transition metal containing compounds, transition metal oxides, and organic dyes, such as, for example, Rodamin-B, DCM, Nile red, DR-19, and

DR-1 , and polymers may be used. ZnS, or PbS doped with a rare-earth or transition metal for gain media can also be used to form nanoparticles.

[093] In another embodiment, nanopores with index of refraction equal to 1 , for example, may be incorporated in a host matrix for tuning and control of the index of refraction of the composite material.

[094] Because many semiconductor materials have refractive index values between about 2 and about 5, these materials can be used to tune the refractive index of the nanocomposite materials for optical applications, such as anti-glare media. Thus, semiconductor materials may also be used to form nanoparticles 11. These materials include, for example, Si, Ge, SiGe, GaP, GaAs, InP, InAs, InSb, ZnS, PbS, PbSe, PbTe, and other semiconductor materials, as well as their counterparts doped with a rare-earth or transition metal ions.

[095] Still other materials such as inorganic salts, oxides or compounds can be used to tune the refractive index of the nanocomposite materials for optical applications, such as anti-glare media. For example lithium niobate, barium titinate, proustite, yttrium aluminate, rutile, and ziroconate and other related materials, as well as their counterparts doped with a rare-earth or transition metal ions. [096] In a further embodiment, the inorganic materials having the index of refraction values between about 1 and 4, for example, may be incorporated in a nanoparticle for tuning and control of the index of refraction of the composite material. These materials include, for example, NaCl, Ti0₂, Si0₂, B₂0₃, P₂0₅, Ge₂0₃, Zn0₂, LiNb0₃, BaTi0₃, YAIO₃, Proustite, Zirconate, and other related materials as well as their counterparts doped with appropriate ions.

Inclusion of nanoparticles, or nanopores, 11 into host matrix material 10, in certain applications according to the present invention, may provide a composite material useful in optical waveguide applications. For example, nanoparticles 11 provide the capability of fabricating an anti-glare material having a particular index of refraction. By controlling the index of refraction in this way, transmission losses in optical path resulting from index of refraction mismatches in adjacent materials could be minimized. Additionally, because of the small size of nanoparticles 11 , the composite material may retain all of the desirable transmission properties of the host matrix material 10. Using the nanoparticles disclosed herein, the index of refraction is tuned to from about 1 to about 5.

[097] One method to manufacture the waveguide assemblies according to the present invention, begin by first preparing the substrate. The surface of the substrate is cleaned to remove any adhesive residue that may be present on the surface of the substrate. Typically, a substrate is cast or injection molded, providing a relatively smooth surface on which it can be difficult to deposit a perfluoropolymer, owing to the non-adhesive characteristics of perfluoropolymers in general. After cleaning, the substrate is prepared to provide better adhesion of the lower layer to the surface of the substrate. The substrate can be prepared by roughening the surface or by changing the chemical properties of the surface to better retain the perfluoropolymer comprising the lower layer. One example of the roughening method is to perform reactive ion etching (RIE) using argon. The argon physically deforms the surface of the substrate, generating a desired roughness of approximately 50 to 100 nanometers in depth. One example of the method that can change the chemical properties of the surface of the substrate is to perform RIE using oxygen. The oxygen combines with the polymer comprising the surface of the substrate, causing a chemical reaction on the surface of the substrate and oxygenating the surface of the substrate. The oxygenation of the substrate can allow the molecules of the perfluoropolymer comprising the lower layer to bond with the substrate. Those skilled in the art will recognize that other methods can also be used to prepare the substrate. [098] The lower layer is then deposited onto the substrate. For a lower layer constructed from poly[2,2,4-trifluoro-5-trifluoromethoxy-1 ,3-dioxole-co- tetrafluoroethylene], solid poly[2,2,4-trifluoro-5-trifluoromethoxy-1 ,3-dioxole-co- tetrafluoroethylene] is dissolved in a solvent, perfluoro (2-butyltetrahydrofuran), which is sold under the trademark FC-75, as well as perfluoroalkylamine, which is sold under the trademark FC-40. Other potential solvents are a perfluorinated polyether, such as that

sold under the trademark H GALDEN^® series HT170, or a hydrofluoropolyether, such as

that sold under the trademarks H GALDEN^® series ZT180 and ZT130. For a lower

layer constructed from other polymers, each polymer is dissolved in a suitable solvent to form a polymer solution. The polymer solution is then spin-coated onto the substrate using known spin-coating techniques. The substrate and the lower layer are then heated to evaporate the solvent from the solution.

[099] In one embodiment, the lower layer is spin-coated as several thinner layers, such that a first thin layer is applied to the substrate, baked to evaporate the solvent, and annealed to density the polymer, a second thin layer is applied to the first layer and densified, and a third thin layer is applied to the second layer and densified . For example, after all of the layers are applied, the lower layer achieves a height ranging from 8 to 12 micrometers. Although the application of three layers is described, those skilled in the art will recognize that more or less than three layers can be used. [0100] After the lower layer has dried and densified, the polymer core is deposited onto the lower layer, for example, using the same technique as described above to deposit the lower layer onto the substrate. Instead of depositing several sublayers of the core onto the lower layer, however, only one layer of the core is deposited, for example, deposited onto the lower layer. In one embodiment, the core is soluble in a solvent in which the lower layer is not soluble so that the solvent does not penetrate the lower layer and disturb the lower layer. For a core constructed from poly[2,3- (perfluoroalkenyl) perfluorotetrahydrofuran], solid poly[2,3-(perfluoroalkenyl) perfluorotetrahydrofuran] is dissolved in a solvent, such as perfluorotrialkylamine, which is sold under the trademark CT-SOLV 180™, or any other solvent that readily dissolves polymer, forming a polymer solution. Alternatively, poly[2,3-(perfluoroalkenyl) perfluorotetrahydrofuran] can be commercially obtained already in solution. After the core material is applied and dried, the core film is densified using a low temperature baking process. After the core is dried, a thickness of the core and lower layer is, for example, ranging approximately from 12 to 16 microns.

[0101] Next, the upper layer is deposited onto the core, the core layer, and any remaining portion of the lower layer not covered by the core or the core layer. For example, similar to the lower layer, the upper layer is spincoated in layers, such that a first layer is applied to the core and a remaining portion of the lower layer not covered by the core, baked to evaporate the solvent, and annealed to density the polymer, a second layer is applied to the first layer, baked and densified, and a third layer is applied to the second layer, baked, and densified. In one embodiment, the upper layer is soluble in a solvent in which the core and core layer are not soluble so that the solvent does not penetrate the core and the core layer and disturb the core or the core layer. For example, after all of the layers are applied, the entire waveguide achieves a height ranging approximately from 15 to 50 micrometers. Although the application of three layers is described, those skilled in the art will recognize that more or less than three layers can be used. Alternatively, the upper layer can be a different material from the lower layer, but with approximately the same refractive index as the lower layer, for example, a photocuring fluorinated acrylate or a thermoset. [0102] The layers are not necessarily flat, but contour around the core with decreasing curvature for each successive layer. Although the last layer is shown with a generally flat top surface, those skilled in the art will recognize that the top surface of the last layer need not necessarily be flat. Those skilled in the art will also recognize that single layer layers with high degrees of flatness or planarization can be achieved by either spincoating or casting processes.

[0103] After forming the multi-layer structure, the assembly is cut to a desired size and shape, for example, by dicing. A desired shape is generally rectangular, although those skilled in the art will recognize that the assembly can be cut to other shapes as well.

[0104] Other examples of optical components that can be made with the disclosed nanoporous materials processing method include, but are not limited to: optical bulk articles, such as prisms, lenses, filters, plates, and canopy enclosures, optical anti-reflection coatings, and optical band-pass thin film filters, as illustrated in the Figures 13(a) through 13(c).

[0105] In certain embodiments, anti-glare components according to the present invention can be fabricated from nanoporous materials by extrusion methods. Bulk optical components, as illustrated in Figures 13(b) and 13(c), such as optical prisms, optical lenses, optical storage diskettes, etc., can be made with nanoporous materials by injection molding, casting, extrusion, etc. Optical thin film band-pass filters and anti- reflection coatings can be fabricated from nanoporous materials by extrusion, casting, dipping, spin-coating, etc.

[0106] In one embodiment, the metal Ag, for example, may be incorporated in a nanoparticle for tuning and control of the electrical conductivity of the composite material so as to provide wavelength tunability to the anti-glare material. [0107] In another embodiment, the semiconductor Si, for example, may be incorporated in a nanoparticle for tuning and control of the electrical conductivity of the composite material so as to provide wavelength tunability to the anti-glare material. [0108] In a further embodiment, the dielectric insulator Si0₂, for example, may be incorporated in a nanoparticle for tuning and control of the electrical conductivity of the composite material so as to provide wavelength tunability to the anti-glare material. [0109] In addition to anti-glare, at least one active material may be incorporated as nanoparticles in the matrix to change other properties of the composite material, as exemplified below: dielectric constant - dielectric insulators, such as NaCl, Ti0₂, Si0₂, B2O₃, Ge₂0₃, Zn0₂, LiNb0₃, and BaTi0₃, and various forms and combinations of ions, alloys, compounds, composites, complexes, chromophores, dyes or polymers, such as PVDF; magnetic susceptibility - paramagnetic, ferromagnetic, antiferromagnetic, ferrimagnetic, and diamagnetic materials; and mechanical properties - combinations of alloys, compounds, crystals, composites, complexes, chromophores, dyes or polymers;

electro-optic properties - LiNb0₃, KNb0₃, KTiOP0₄, β-BaB₂0₄, KTiOAs0₄,

KH₂P0₄, KD₂P0₄, NH₄H₂P0₄, and 2-methyl-4-nitroaniline (MNA); magneto-optic properties - YV0₄, TbP0 , HoYbBilG, (Cd,Mn,Hg)Te, MnAs, Y₂.₈₂ Ceo.i8Fe₅0 ₂, Bi-substituted iron garnet, Yttrium Iron Garnet, Terbium Gallium Garnet, Lithium Niobate, and paramagnetic rare-earth ions containing at least on nanoparticles chosen from Tb⁺³, Y⁺³, and Ce⁺³; and thermo-optic properties - inorganic optical media such as the glass Si0₂, and organic optical media, such as the polymer polymethylmethacrylate (PMMA).

[0111] In one embodiment, the nanoparticles are coated with a long chain alkyl group, long chain ether group, or polymer, such as a halogenated long chain alkyl group, halogenated long chain ether group, or halogenated polymer. Examples of other halogenated coatings include fluorinated polymers, such as fluorinated phosphates, polyphosphates, phosphinates, dithiophosphinates, pyrophosphates, fluoroalkyl titanates, fluoroalkyl zirconates, fluorinated silanes, alcohols, amines, carboxylates, amides, sulfates, esters, acid chloride, acetylacetonates, thiols, blends or mixtures of the above coatings.

[0112] Metal containing materials such as metal chalocogenides (e.g., Bi₂Te₃,

Bi Te₃), metal salts, transition metals, transition metal complexes, transition metal containing compounds, transition metal oxides, and organic dyes, such as, for example,

Rodamin-B, DCM, Nile red, DR-19, and DR-1 , and polymers may be used. ZnS, or PbS doped with a rare-earth or transition metal for anti-glare media can also be used to form nanoparticles.

[0113] In optical waveguide applications, the major dimension of the nanoparticles described herein is smaller than the wavelength of light used. Therefore, light impinging upon nanoparticles 11 will not interact with, or scatter from, the nanoparticles. As a result, the presence of nanoparticles 11 dispersed within the host matrix material 10 has little or no effect on light transmitted through the host matrix.

Even in the presence of nanoparticles 11 , the low absorption loss of host matrix 10 may be maintained.

[0114] Another embodiment according to the present invention comprises an optical anti-glare device.

[0115] When the nanoparticles in the anti-glare media comprise at least one material chosen from Pr, Nd, and Ho. In a further embodiment, the nanoparticles in the anti-glare media may comprise one or more active materials. The index of refraction of the anti-glare media and/or adjacent material layers may be adjusted to a desired value with the inclusion of nanoparticles.

[0116] Generally, the index of refraction of a composite that includes nanoparticles of appropriate compositions can be adjusted to different selected values. For example, adding nanoparticles disclosed herein to the host matrix will tune the refractive index of the composite to be from 1 to about 5. As a result, the nanocomposite material is suitable for use in various optical applications such as waveguides according to the present invention. The index of refraction for the nanoparticles may be determined using techniques known to one of ordinary skill in the art. For example, one can use a refractometer, elipsometer, or index matching fluid to determine the refractive index of the particles either as a film or as powders. For the measurement of nanoparticles powder samples, one can use the index matching fluid to determine the refractive index of the material. Typically, a drop of index matching fluid or immersion oil is placed onto a glass slide. A small amount of powder sample can then be mixed into the fluid droplet. The slide can then be viewed using a transmission optical microscope. The microscope is equipped with a sodium D line filter to ensure that the refractive index is being measured at a wavelength of 588 nm. The boundary between the index matching fluid and the powder can be seen when the index of the fluid and the sample is not matched. The same procedure should be repeated, using immersion oils with successively higher indices of refraction, until the boundary line can no longer be seen. At this point, the index of the immersion oil matches that of the powder.

[0117] In one embodiment, there is a halogenated polymer host matrix having a refractive index, t7_matrix and a plurality of nanoparticles dispersed within the halogenated polymer host matrix having a refractive index t7_particie- In this embodiment, the halogenated polymer host matrix and the plurality of nanoparticles form a composite having a refractive index, η_COmp, where η_matm is not equal to η_pari\_c\e- Further, the nanoparticles within the halogenated polymer host matrix are in such an amount sufficient to result in a value for η_comp which is different from /^matrix- [0118] In another embodiment, a nanocomposite material can be fabricated that has a high index of refraction and low absorption loss, for example less than approximately 2.5 x 10^"4 dB/cm in the range from about 1.2 μm to about 1.7 μm. As previously stated, halogenated polymers, including fluorinated polymers, exhibit very little absorption loss (see Table 1 ).

TABLE 1. WAVELENGTHS AND INTENSITIES OF SOME IMPORTANT VIBRATIONAL OVERTONES

[0119] Therefore, these halogenated polymers may be particularly suitable for transmitting light in optical waveguides and other applications according to the present invention. In such applications, nanoparticles 11 are smaller than the wavelength of incident light. Therefore, light impinging upon nanoparticles 11 will not interact with, or scatter from, the nanoparticles. As a result, the presence of nanoparticles 11 dispersed within the host matrix material 10 has little or no effect on the optical clarity of the composite, even if the nanoparticles themselves comprise material, which in bulk form would not be optically clear, or even translucent. Thus, even in the presence of nanoparticles 11 , the low absorption loss of host matrix 10 may be maintained. [0120] By contrast, the presence of nanoparticles 11 within the host matrix material 10 may contribute to significantly different properties as compared to the host matrix material alone. For example, as already noted, nanoparticles 11 may be made from various semiconductor materials, which may have index of refraction values ranging from about 1 to about 5. Upon dispersion of nanoparticles 11 into the host matrix material 10, the resulting composite material will have an index of refraction value somewhere between the index of refraction of the host matrix material 10 (usually less than about 2) and the index of refraction of the nanoparticle material. The resulting, overall index of refraction of the composite material will depend on the concentration and make-up of nanoparticles 11 within the host matrix material 10. For example, as the concentration of nanoparticles 11 in the host matrix material 10 increases, the overall index of refraction may shift closer to the index of refraction of the nanoparticles 11. The value of t?_Comp can differ from the value of ^m_atrix by a range of about 0.2% to about 330%. In an exemplary embodiment, the ratio

is at least 3:2. In another exemplary embodiment, the ratio of

is at least 2:1. [0121] The nanoparticle containing composites as described herein, may be employed, for example, in various applications including, but not limited to, optical devices, windowpanes, mirrors, mirror panels, optical lenses, optical lens arrays, optical displays, liquid crystal displays, cathode ray tubes, optical filters, optical components, all these more generally referred to as components.

[0122] FIG. 4A schematically illustrates an optical waveguide 50 according to one embodiment of the present invention. Optical waveguide 50 includes a generally planar substrate 51 , a core material 54 for transmitting incident light and a layer material 52 disposed on the substrate 51 , which surrounds the core 54 and promotes total internal reflection of the incident light within the core material 54. The core 54 of the optical waveguide may be formed of a nanocomposite as illustrated, for example, in FIG. 1. [0123] The layer 51 and 52 may be each independently composed of an optical polymer, such as a perfluorinated polymer. The waveguide core 54 may be composed of a nanocomposite material for example doped glass, single crystal, or polymer particles with dimensions ranging from about 1 nm to about 100 nm are embedded in a polymer waveguide core.

[0124] In such an embodiment, the core 54 may include a host matrix and a plurality of nanoparticles dispersed within the host matrix. A majority of the plurality of nanoparticles present in core 54 may further include a halogenated outer coating layer. The layer material in certain embodiments may comprise a halogenated polymer host matrix. In certain embodiments, the layer material may further include nanoparticles dispersed in a host matrix in such a way that the relative properties of the core and layer can be adjusted to predetermined values.

[0125] Further, in one embodiment of the present invention, the host matrix material of the core 54 and/or layer 52 includes fluorine. The nanoparticles in the optical waveguide 50 may have an index of refraction of ranging from about 1 to about 5. By selecting a particular material having a particular index of refraction value, the index of refraction of the core 54 and/or layer 52 of the optical waveguide 50 may be adjusted to a predetermined desired value or to different predetermined values. [0126] The thermo-optic properties of the host matrix may be improved by including an effective amount of nanoparticles comprising different coefficient of thermal expansion. Many materials expand when heated, and contract when cooled. The coefficient of thermal expansion (CTE) is the ratio of the change in length (due to expansion or contraction) per unit temperature. For example, materials that expand when heated are said to have a positive CTE. Conversely, materials that contract when heated exhibit a negative CTE.

[0127] A mismatch between the CTE's of the materials comprising the composite can have a degrading effect on the composite materials. Both nanoparticles and polymer matrices have a CTE. Thermal expansion and contraction can lead to degradation of the mismatched CTE's composite materials comprising the nanoparticles. For example, when two materials, such as two different polymer matrices, each having different positive CTE's are adjacent to each other, stress can occur between the materials due to the differing expansion rates. [0128] Nanoparticles comprising materials having different CTE's can be used to adjust the CTE of a composite comprising the nanoparticles. In certain embodiments, nanoparticles comprised of materials having a negative CTE can be used in combination with nanoparticles comprised of materials having a positive CTE to adjust the CTE of the composite containing the nanoparticles.

[0129] The nanoparticles 11 may comprise materials having positive or negative thermal expansion coefficients. When nanoparticles having negative CTE's are combined with a matrix material and/or nanoparticles having positive CTE's, the resulting composite material will have a CTE between that of the negative CTE material and that of the positive CTE material. The negative CTE material need not be sized with the scale of nanoparticles. It may be sized larger than the scale of nanoparticles. In one embodiment, the CTE of the composite may therefore be controlled by choosing materials for the host matrix and/or nanoparticles having different relative CTE, and by varying the amounts of these materials within the host matrix.

[0130] The amount and type of materials comprising the nanocomposite may be chosen so that the nanocomposite exhibits little or no expansion or contraction (in other words, a CTE that is substantially zero) when cycled through various thermal environments. Alternatively, the host matrix material and the nanoparticles may be chosen to provide a composite having a specific positive or negative CTE. [0131] Among materials having negative CTE's, examples include Ni-Ti alloys,

ZrW₂0₈, ZrMo₂0₈, Y₂(W0₄)₃, V doped ZrP₂0₇, ZrV₂0₇, (Zr₂0)(P0₄)₂, Th₄(P0₄)₄P₂0₇, and AOM0₄, where A=Nb or Ta, and M = P, As, or V. Nanoparticles 11 formed from these materials exhibit a negative CTE, and therefore their dimensions shrink as temperature increases. One exemplary embodiment of materials exhibiting a negative CTE are the materials corresponding to formula (I) below:

A₁._y ⁴⁺A_y ¹⁺A_y ³⁺V₂-χPχ0₇ (I) where:

- A⁴⁺ is chosen form Hf, Zr, Zr_aMb, or Hf_aMb and mixtures thereof,

- a + b = 1.

- A¹⁺ is chosen form alkali earth metals,

- A³⁺ is chosen form rare-earth metals,

- M is chosen form Ti, Ce, Th, U, Mo, Pt, Pb, Sn, Ge or Si

- y ranges from about 0 to about 0.4,

- x ranges from about 0.6 to about 1.4,

[0132] Among the materials falling within formula (I), examples include

(ZrO)₂VP₂0₇, ZrVP0₇, Zr_0.8Lio_.2Yo.₂VP0₇, Zr₀.₈Ceo.₂VP0₇, and HfVP0₇. [0133] In one embodiment for controlling the CTE of the composite material, the amount of nanoparticles may range from approximately 10% to about 95% by volume of the composite material. These particles may comprise particles chosen to have a negative CTE. In another embodiment, one or more of the particles are chosen to have a negative CTE, and the remaining particles have a positive CTE. In yet another embodiment, the negative CTE material comprises particles that are larger than nanoparticle-sized, and ranging from about 5% to about 99% by volume of the composite material.

[0134] FIG. 4 illustrates an optical anti-glare device 60 according to another embodiment of the present invention. Optical anti-glare device 60 comprises an optical fiber with a core 64 surrounded by a layer 62. The core includes a host matrix and a plurality of nanoparticles dispersed within the host matrix. In one embodiment, core 64 comprises nanoparticles. The layer material in this embodiment comprises a host matrix. In certain embodiments, the layer material may also comprise nanoparticles dispersed in a host matrix. Further, in one embodiment of the present invention, the host matrix material of the core 64 and/or layer 62 includes fluorine. The plurality of nanoparticles in the optical anti-glare device 60 may have an index of refraction ranging from about 1 to about 5. By selecting a particular material having a particular index of refraction value, the overall index of refraction of the core 64 of the optical anti-glare device 60 may be adjusted to a predetermined desired value or to different predetermined values.

[0135] In addition to the materials mentioned, still other materials are useful as nanoparticles 11. For example, the nanoparticles, themselves, may comprise a polymer. In an exemplary embodiment of the invention, the polymer nanoparticles comprise polymers that contain functional groups that can bind ions, such as rare-earth ions. Such polymers include homopolymers or copolymers of vinyl, acrylic, vinyl aromatic, vinyl esters, alpha beta unsaturated acid esters, unsaturated carboxylic acid esters, vinyl chloride, vinylidene chloride, and diene monomers. The reactive groups of these polymers may comprise any of the following: POOH, POSH, PSSH, OH, S0₃H, S0₃R, S0₄R, COOH, NH₂, NHR, NR₂, CONH₂, NH-NH₂, and others, where R may be chosen from linear or branched hydrocarbon-based chains, possibly forming at least one carbon-based ring, being saturated and unsaturated, aryl, alkyl, alkylene, siloxane, silane, ether, polyether, thioeter, silylene, and silazane.

[0136] The polymers for use as nanoparticles may alternatively comprise main chain polymers containing rare-earth ions in the polymer backbone, or side chain or cross-linked polymers containing the above-mentioned functional groups. The polymers may be highly halogenated yet immiscible with the host matrix polymer. For example, nanoparticles of inorganic polymer, prepared by reacting erbium chloride with perfluorodioctylphosphinic acid, exhibit high crystallinity and are immiscible with poly[2,3-(perfluoroalkenyl) perfluorotetrahydrofuran]. Blending these nanoparticles with the fluorinated polymer host will lead to a nanocomposite. Additionally, the nanoparticles may comprise organic dye molecules, ionic forms of these dye molecules, or polymers containing these dye molecules in the main chain or side chain, or cross- linked polymers. When the nanoparticles comprise polymers that are not halogenated, they may be optionally coated with a halogenated coating as described herein. [0137] Composite materials comprising the amplifiers of the present invention may contain different types of nanoparticles. For example, FIG. 5 illustrates an exemplary embodiment of the present invention in which several groups of nanoparticles 11 , 21 , and 71 are present within halogenated matrix 10. Each group of nanoparticles 11 , 21 , and 71 is comprised of a different material surrounded by an outer layer (for example, layer 12 on particle 21).

[0138] Nanocomposites fabricated from several different nanoparticles may offer properties derived from the different nanoparticles. For example, nanoparticles 11 , 21 , and 71 may provide a range of different optical, structural, or other properties. One skilled in the art will recognize that the present invention is not limited to a particular number of different types of nanoparticles dispersed within the host matrix material. Rather, any number of different types of nanoparticles may be useful in various applications. Depending on the end use, the nanoparticles according to the present invention may be bare, or contain at least one outer layer. As shown in FIG. 1 , the nanoparticles may include an outer layer 12. The layer 12 may serve several important functions. It may be used to protect nanoparticle 11 from moisture or other potentially detrimental substances. Additionally, layer 12 may also prevent agglomeration. Agglomeration is a problem when making composite materials that include nanoparticles distributed within a matrix material. [0139] In one embodiment, by selecting a layer 12 of a material that is compatible with a given host matrix material, layer 12 may eliminate the interfacial energy between the nanoparticle surfaces and host matrix 10. As a result, the nanoparticles in the composite material do not tend to agglomerate to minimize the interfacial surface area/surface energy that would exist between uncoated nanoparticles and host matrix material 10. Layer 12, therefore, enables dispersion of nanoparticles 11 into host matrix material 10 without agglomeration of the nanoparticles.

[0140] When the outer layer 12 is halogenated, it may comprise at least one halogen chosen from fluorine, chlorine, and bromine. In an exemplary embodiment of the present invention, the halogenated outer layer 12 may include, for example, halogenated polyphosphates, halogenated phosphates, halogenated phosphinates, halogenated thiophosphinates, halogenated dithiophosphinates, halogenated pyrophosphates, halogenated alkyl titanates, halogenated alkyl zirconates, halogenated silanes, halogenated alcohols, halogenated amines, halogenated carboxylates, halogenated amides, halogenated sulfates, halogenated esters, halogenated acid chloride, halogenated acetylacetonate, halogenated disulfide, halogenated thiols, and halogenated alkylcyanide. While fluorine analogs of these materials can be used, analogs of these materials incorporating halogens other than fluorine, as well as hydrogen, may also be employed in outer layer 12.

[0141] In addition to protecting the nanoparticles 11 and suppressing agglomeration, layer 12 may also be designed to interact with the surfaces of nanoparticles 11. For example, halogenated outer layer 12 may comprise a material, such as one of the above listed layers, which reacts with and neutralizes an undesirable radical group, for example OH or esters, that may be found on the surfaces of nanoparticles 11. In this way, layer 12 may prevent the undesirable radical from reacting with host matrix 10.

[0142] Coatings on nanoparticles 11 are not limited to a single layer, such as halogenated outer coating layer 12 shown in FIG. 1. Nanoparticles may be coated with a plurality of layers.

[0143] FIG. 6 schematically depicts one nanoparticle suspended within host matrix material 10. As shown, inner layer 84 is disposed between nanoparticle 80 and halogenated outer layer 82. In certain situations the interaction between a particular nanoparticle material 80 and a particular halogenated outer layer 84 may be unknown. In these situations, nanoparticles 80 may be coated with an inner coating layer 84 comprising a material that interacts with one or both of the nanoparticle material and the halogenated outer coating layer material in a known way to create a passivation layer. Such an inner coating layer may prevent, for example, delamination of the halogenated outer coating layer 82 from nanoparticle 80. While inner coating layer 84 is shown in FIG. 6 as a single layer, inner coating layer 84 may include multiple layers of similar or different materials.

[0144] FIG. 7 is a flowchart diagram representing process steps for forming a composite material according to an exemplary embodiment of the present invention. Nanoparticles 11 , as shown in FIG. 1 are formed during step 101. Once formed, nanoparticles 11 are coated with a outer coating layer 12 at step 103. Optionally, at step 102, an inner coating layer 84 (or passivation layer), as shown in FIG. 7, may be formed on the nanoparticles 80. Inner coating layer 84, which may include one or more passivation layers, may be formed prior to formation of outer coating layer 82 using methods similar to those for forming outer coating layer 82.

[0145] Nanoparticles may be coated in several ways. For example, nanoparticles may be coated in situ, or, in other words, during the formation process. The nanoparticles may be formed (for example by electro-spray) in the presence of a coating material. In this way, once nanoparticles 11 have dried to form an aerosol, they may already include layer 12 of the desired host material.

[0146] In one embodiment, layer 12 may be formed by placing the nanoparticles into direct contact with the coating material. For example, nanoparticles may be dispersed into a solution including a halogenated coating material. In some embodiments, nanoparticles may include a residual coating left over from the formation process. In these instances, nanoparticles may be placed into a solvent including constituents for forming the outer coating layer. Once in the solvent, a chemical replacement reaction may be performed to substitute outer coating layer 12 for the preexisting coating on the plurality of nanoparticles 11. In one embodiment, nanoparticles may be coated with a coating in a gas phase reaction, for example, in a gas phase reaction of hexamethyldisilazane. [0147] In another embodiment, the nanoparticles may be dispersed by co- dissolving them, and the host matrix, in a solvent (forming a solution), spin coating the solution onto a substrate, and evaporating the solvent from the solution. [0148] In another embodiment, the nanoparticles may be dispersed in a monomer matrix, which is polymerized after the dispersion. For example, metal oxide nanoparticles can be dispersed into a liquid monomer under sonication. The resulting mixture is then degassed and mixed with either a thermal initiator or a photo-initiator, such as azo, peracid, peroxide, or redox type intiators. The mixture is then heated to induce polymerization forming a polymer nanocomposite. Additionally, the pre- polymerized mixture can be spin-coated onto a substrate followed by thermally or photo-induced polymerization to form a nanocomposite thin film. [0149] In yet another embodiment, coatings may be in the form of a halogenated monomer. Once the monomers are absorbed on the surface of the particles, they can be polymerized or cross-linked. Additionally, coatings in the form of polymers can be made by subjecting the particles, under plasma, in the presence of halogenated monomers, to form coated nanoparticles with plasma induced polymerization of the particle surface. The coating techniques described are not intended to be an exhaustive list. Indeed, other coating techniques known to one of ordinary skill in the art may be used.

[0150] Once nanoparticles have been formed and optionally coated, they are dispersed into host matrix at step 104 to obtain a uniform distribution of nanoparticles within host matrix, a high shear mixer, or a sonicator may be used. Such high shear mixers may include, for example, a homogenizer or a jet mixer. [0151] Another method of dispersing nanoparticles throughout the host matrix is to co- dissolve the nanoparticles with a polymer in a suitable solvent, spin-coating the solution onto a substrate, and then evaporating the solvent to form a polymer nanocomposite film.

[0152] Yet another method of dispersing nanoparticles throughout the host matrix is to disperse nanoparticles into a monomer, and then polymerize the monomer to form a nanocomposite. The monomer can be chosen from the group comprising acrylate, methacrylate, styrene, vinyl carbozole, halogenated methacrylate, halogenated acrylate, halogenated styrene, halogenated substituted styrene, trifluorovinyl ether monomer, epoxy monomer with a cross-linking agent, and anhydride/diamine, although those skilled in the art will recognize that other monomers can be used as well. The dispersion techniques described are not intended to be an exhaustive list. Indeed, other dispersion techniques known to one of ordinary skill in the art can be used. [0153] In one embodiment of the present invention, the host matrix may comprise various types of nanoparticles. For example, in certain embodiments the host matrix may comprise particles and/or nanoparticles having positive and/or negative CTE. In other embodiments the index of refraction of the host matrix can be adjusted by including a single type, or various types, of nanoparticles where the nanoparticles comprise an index of refraction. The host matrix may also comprise nanoparticles comprising active materials. In addition, in certain embodiments, the host matrix may comprise nanoparticles comprising sulfides. Embodiments of the present invention also include matrices comprising particles and/or nanoparticles comprising positive and/or negative CTE, and/or various nanoparticles comprising various indexes of refraction, and/or active materials, and/or sulfides. In certain embodiments the nanoparticles comprise coatings, while in other embodiments, the nanoparticles have no coating. FIG.8 shows the AFM image of an exemplary nanoparticles with particle size of less then 50 nm. In addition, in certain embodiments, the matrices may be halogenated or non-halogenated. Thus, different combinations are explicitly considered. [0154] In another embodiment, the polymer nanocomposites comprising a host matrix and nanoparticles of various functionalities may further offer improvement in abrasion resistance properties. When fluoropolymers are doped with hard, inorganic materials such as Siθ₂, Tiθ₂, YAG, etc, the polymer abrasion properties are enhanced by the presence of the inorganic components. These types of polymer composites offer additional advantages such as thermal and chemical stability, improved weatherability, and low water absorption when compared with conventional hydrocarbon based composites. For a typical hydrocarbon polymer matrix, such as poly(methyl

methacrylate), the water absorption is 0.3% for 60°C water immersion test. On the

other hand, a perfluorinated polymer under the same test condition has less then 0.01 % water absorption. [0155] In yet another embodiment, the polymer nanocomposites comprising a host matrix and nanoparticles of various functionalities may further offer improvement in anti-glare materials. The inventive materials are designed optical polymer nanocomposites, generally comprised of an amorphous polymer material that exhibit high optical transparency over the three color fields and that acts at the same time as a host matrix for incorporating one, or more, coated inorganic, organic, or polymer nanoparticles with one, or more, particles incorporating a selected rare-earth ion in the wavelength regions of the three principal maxima of the optic cells, namely 450 nm, 525 nm, and 575 nm.

[0156] Examples of the rare-earth metals include the lanthanide series, elements

Z=58 to Z=71 and their corresponding ions, Pr, Nd, and Ho. Thus, for example, it is found that suitable nanoparticles, with some or all possessing suitable optical absorption characteristics, can be introduced into the host matrix polymer composition ranging from about 0.1 to about 100 parts by weight of polymer. The light absorption performance of the optical polymer nanocomposite can be controlled by adjusting the concentrations and relative ratios of each of the rare-earth ions incorporated in the nanocomposite material. Consequently, the inventive materials have excellent anti-glare and transparency properties while appearing with little, or no, color due to the relatively low coloring coming from the adjusted rare-earth ions.

The composite materials of the present invention such as the fluoropolymers doped with nanoparticles and nanoparticles coated with fluorocarbon coatings offer advantages

Claims

such as improved thermal stability, chemical resistance, low water absorptivity, and biocompatibility.

WHAT IS CLAIMED IS:

1. An anti-glare composite material comprising:

- a host matrix and

- a plurality of nanoparticles within the host matrix, wherein the plurality of nanoparticles comprises at least one rare earth ion that optically absorbs light having a wavelength ranging from 400 to 700 nanometers.

2. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one material chosen from a halogenated elastomer, a perhalogenated elastomer, a halogenated plastic, and a perhalogenated plastic.

3. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one entity chosen from polymers, copolymers, and terpolymers comprising at least one halogenated monomer chosen from monomers of one of the following formulas:

wherein;

- R¹, R², R³, R⁴, and R⁵, which may be identical or different, are each chosen from linear and branched hydrocarbon-based chains, possibly forming at least one carbon-based ring, being saturated or unsaturated, wherein at least one hydrogen atom of the hydrocarbon-based chains may be halogenated; a halogenated alkyl, a halogenated aryl, a halogenated cyclic alky, a halogenated alkenyl, a halogenated alkylene ether, a halogenated siloxane, a halogenated ether, a halogenated polyether, a halogenated thioether, a halogenated silylene, and a halogenated silazane;

- Y-i and Y₂, which may be identical or different, are each chosen from H, F, CI, and Br atoms;

- Y₃ is chosen from H, F, CI, and Br atoms, CF₃, and CH₃.

4. The anti-glare composite material according to Claim 3, wherein at least one of R¹, R², R³, R⁴, and R⁵ is at least partially fluorinated.

5. The anti-glare composite material according to Claim 3, wherein at least one of R¹, R², R³, R⁴, and R⁵ is completely fluorinated.

6. The anti-glare composite material according to Claim 3, wherein at least one of R¹, R², R³, R⁴, and R⁵ is chosen from C₁-C₁₂, linear and branched, saturated and unsaturated hydrocarbon-based chains.

7. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one polymer condensation product of at least one of the following monomeric reactions: HO-R-OH + NCO-R'-NCO; and

HO-R-OH + Ary¹ -Ary²

wherein:

- R, R', which may be identical or different, are each chosen from halogenated alkylenes, halogenated siloxanes, halogenated ethers, halogenated silylenes, halogenated arylenes, halogenated polyethers, and halogenated cyclic alkylenes, and

- Ary¹, Ary², which may be identical or different, are each chosen from halogenated aryls and halogenated alkyl aryls.

8. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one material chosen from halogenated cyclic olefin polymers, halogenated cyclic olefin copolymers, halogenated polycyclic polymers, halogenated polyamides, halogenated polyether ether ketones, halogenated epoxy resins, halogenated polysulfones, and halogenated polycarbonates.

9. The anti-glare composite material according to Claim 8, wherein said host matrix comprises at least one material chosen from fluorinated polymers.

10. The anti-glare composite material according to Claim 1 , wherein said host matrix further comprises at least one halogenated polymer comprising at least one functional group chosen from phosphinates, phosphates, carboxylates, silanes, siloxanes, and sulfides.

11. The anti-glare composite material according to Claim 10, wherein said at least one functional group is chosen from POOH, POSH, PSSH, OH, S0₃H, S0₃R, S0₄R, COOH, NH₂, NHR, NR₂, CONH₂, and NH-NH₂, wherein R is chosen from linear and branched hydrocarbon-based chains, capable of forming at least one carbon-based ring, being saturated or unsaturated; alkylenes, siloxanes, silanes, ethers, polyethers, thioethers, silylenes, and silazanes.

13. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one material chosen from homopolymers and copolymers of vinyl, acrylate, methacrylate, vinyl aromatic, vinyl ester, alpha beta unsaturated acid ester, unsaturated carboxylic acid ester, vinyl chloride, vinylidene chloride, and diene monomers.

14. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one hydrogen-containing fluoro-elastomer.

15. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one cross-linked halogenated polymer.

16. The anti-glare composite material according to Claim 15, wherein said at least one cross-linked halogenated polymer comprises at least one fluorinated polymer.

17. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one perhalogenated polymer.

18. The anti-glare composite material according to Claim 17, wherein said at least one perhalogenated polymer is chosen from perfluorinated polymers.

19. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one perhalogenated elastomer.

20. The anti-glare composite material according to Claim 19, wherein said host matrix comprises at least one hydrogen-containing fluoroplastic.

21. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises a blend of at least one material chosen from halogenated, fluorinated, and perfluorinated polymers.

21. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one entity chosen from poly[2,2-bistrifluoromethyl-4,5-difluoro- 1 ,3-dioxole-co-tetrafluoroethylene], poly[2,2-bisperfluoroalkyl-4,5-difluoro-1 ,3-dioxole- co-tetrafluoroethylene], poly[2,3-(perfluoroalkenyl) perfluorotetrahydrofuran], and poly[2,2,4-trifluoro-5-trifluoromethoxy-1 ,3-dioxole-co-tetrafluoroethylene].

22. The anti-glare composite material according to Claim 1 , wherein said host matrix comprises at least one entity chosen from poly(pentafluorostyrene), fluorinated polyimide, fluorinated polymethylmethacrylate, polyfluoroacrylates, polyfluorostyene, fluorinated polycarbonates, fluorinated poly(phenylenevinylene), perfluoro-polycyclic polymers, fluorinated cyclic olefin polymers, and fluorinated cyclic olefin copolymers.

23. The anti-glare composite material according to Claim 1 , wherein the plurality of nanoparticles are distributed within said host matrix such that the composite exhibits anti-glare properties.

24. The anti-glare composite material according to Claim 1 , wherein said host matrix exhibits a balanced degree of optical absorption over a three-color wavelength range of blue, green, and red.

25. The anti-glare composite material according to Claim 1 , wherein said host matrix has a transparency of at least 90%

26. The anti-glare composite material according to Claim 1 , wherein said plurality of nanoparticles comprises at least one earth ion chosen from holium (Ho), terbium (Tb), samarium (Sm), neodymium (Nd), europium (Eu), dysprosium (Dy), erbium (Er), and praseodymium (Pr).

27. The anti-glare composite material according to Claim 1 , wherein said plurality of nanoparticles comprises at least one earth ion chosen from Nd, Pr, and Ho.

28. The anti-glare composite material according to Claim 27, wherein the Nd, Pr, and Ho are each present in an amount ranging from 1 % to 13% by weight.

29. The anti-glare composite material according to Claim 1 , wherein said plurality of nanoparticles further comprises at least one material chosen from transition metal elements, rare-earth metal elements, the actinide element uranium, group VA elements, semiconductor materials, and group IVA elements.

30. The anti-glare composite material according to Claim 29, wherein said at least one material is in a form chosen from ions, alloys, compounds, composites, complexes, chormophores, dyes, and polymers.

31. The anti-glare composite material according to Claim 30, wherein the ions are chosen from phosphate, halophosphate, arsenate, sulfate, borate, aliminate, gallate, silicate, germinate, oxide, vanadate, niobate, tantalate, molybdate, chromate, alkalihalogenate, halogenide, nitride, sulfide, selenide, sulfoselenide, and oxysulfide ions.

32. The anti-glare composite material according to Claim 29, wherein said semiconductor materials are chosen from at least one entity chosen from Si, Ge, SiGe, GaP, GaAs, GaN, InP, InAs, InSb, PbSe, PbTe, and InGaAs.

33. The anti-glare composite material according to Claim 1 , wherein a majority of said nanoparticles comprise at least one coating.

34. The anti-glare composite material according to Claim 33, wherein said nanoparticles comprise a halogen-containing layer.

35. The anti-glare composite material according to Claim 33, wherein said at least one coating is chosen from fluorinated polyphosphates, phosphates, dithiophosphates, pyrophosphates, flouroalkyltitanates, flouroalkyl zirconates, fluorinated silanes, alcohols, amines, carboxylates, amides, sulfates, esters, acid chlorides, acetylaceonate, and thiols.

36. An optical anti-glare device comprising:

- a host matrix and

- a plurality of nanoparticles within the host matrix, wherein the plurality of nanoparticles comprises at least one rare earth ion that optically absorbs light having a wavelength ranging from 400 to 700 nanometers.