Patent Application
20050019547
1. Field of the Invention
The present invention relates to a novel composite material utilizing a film of a porous material having ultra-minute pores (mesopores) formed in a self-organizing manner. More specifically, the present invention relates to a novel optical composite material, a polarized light-emitting film prepared utilizing a porous film material having a controlled mesopore structure, and a method for producing the same.
2. Related Background Art
Several attempts have been made to obtain polarized-light emission by controlling the orientation of polymer chains of a polymer. For example, a method where a polymer film is extended in one direction has been reported. One of the methods for controlling the orientation of polymer chains is utilization of nanospace of porous materials.
Generally, porous materials are classified into the following three classes by an IUPAC definition according to their pore sizes:
The mesoporous materials have a feature that they are formed into various macroscopic morphologies other than powders under peculiar synthetic conditions, Monolith, films, fibers, spheres, and hollow spheres have been obtained, and the respective applications are expected.
For example, Science, Vol. 288, pp. 652 (2000) reports that the mesoporous structure of a mesostructured silica was controlled to control the orientation of a polymer material held in the mesostructured silica. According to this report, the mesostructured silica was prepared in a strong magnetic field to control the orientation of the mesopores, and a conjugated polymer was introduced into the mesopores, whereby polarized light-emission was observed.
However, a large sized apparatus is required to generate the above-mentioned strong magnetic field for controlling the orientation of the mesopores of the mesostructured silica. Furthermore, the mesopore structure in the resultant mesostructured silica has a relatively wide distribution in the mesopore orientation. Finally, the mesostructured material obtained by this procedure is monolithic, with macroporous voids between domains that produce and opaque, low optical quality material.
The inventors of the present invention have succeeded to prepare a film having high polarization anisotropy by forming a mesostructured silica film having highly uniaxially oriented mesopores by a simple method, and introducing light-emitting conjugated polymer molecules into the mesopores to strictly control the orientation of the polymer chains.
Thus, according to one aspect of the present invention, there is provided a polarized light-emitting film comprising a porous silica film formed on a substrate and a conjugated polymer held in a plurality of uniaxially oriented, tubular mesopores in the porous silica film, wherein fluorescence emitted from the film is polarized in a direction parallel to the orientation direction of the mesopores.
According to the present invention, the film emits fluorescence of which the intensity measured through a polarizer with a polarization direction of the polarizer parallel to the orientation direction of the mesopores is three times or more of the fluorescence intensity measured through a polarizer with a polarization direction vertical to the orientation direction of the mesopores.
According to the present invention, the film is preferably a mesostructured silica film formed using assemblies of surfactant molecules as a template.
According to the present invention, the porous silica film may be patterned in a desired shape.
According to the present invention, the substrate is capable of controlling the orientation of the tubular mesopores in the mesostructured silica formed thereon to one direction.
According to the present invention, it is preferable that the substrate has a polymer film on a surface thereof, the polymer film is capable of controlling the direction of the tubular mesopores in the mesostructured silica formed thereon to one direction. Preferably, the polymer film has a structural anisotropy in a plane.
According to the present invention, the conjugated polymer is preferably poly[2-methoxy-5-(2′-ethyl-hexyloxy)-1,4-phenylene vinylene].
According to another aspect of the present invention, there is provided a method for producing a polarized light-emitting film comprising the steps of:
According to the present invention, a step of patterning the mesostructured silica film in a desired pattern is preferably carried out after the step of forming on a substrate a mesostructured silica film containing a plurality of tubular molecular assemblies of molecules of a surfactant arranged in one direction; and before the step of removing the surfactant from the mesostructured silica film to form hollow tubular mesopores.
According to the film forming method of the present invention, the substrate is capable of controlling the orientation of the tubular mesopores in the mesostructured silica formed thereon to one direction.
According to still another aspect of the present invention, there is provided a method for producing a polarized light-emitting film comprising the steps of:
According to the present invention, a step of patterning the film of the mesostructured silica in a desired pattern is preferably carried out after the step of forming on a substrate a mesostructured silica film containing a plurality of tubular molecular assemblies of molecules of a surfactant arranged in one direction; and before the step of removing the surfactant from the mesostructured silica film to form hollow tube-shaped mesopores.
According to the film production method of the present invention, the surfactant is preferably removed by calcination.
A polarized light-emitting film of the present invention has a structure schematically shown in
A porous silica film 12, in which tubular mesopores 13 are uniaxially oriented, is formed on a substrate 11, and a conjugated polymer 14 is held in the mesopores.
First, a method for producing a porous silica film with tubular mesopores uniaxially orientated on a substrate will be described. The porous silica used in the present invention is formed using micelles (assemblies) of molecules of a surfactant as a template, and is called mesoporous silica. Various methods for producing a mesoporous silica film have been reported. These methods are roughly classified into a method called solvent evaporation method and a method based on heterogeneous nucleation and growth occurring at the solid-liquid interface. The mesoporous silica film used in the present invention may be produced by either method, as long as the orientation of the mesopores on a substrate is controlled in one direction. Generally, it is difficult to control the orientation of the mesopores on a substrate by a solvent evaporation method. On the other hand, according to the method based on the heterogeneous nucleation and growth at the solid-liquid interface, the mesostructure formed on a substrate may reflect the surface anisotropy of the substrate. For example, control of the orientation of mesopores by using a crystalline substrate having surface anisotropy is reported in Journal of the American Chemical Society, Vol. 121, pp. 7618 (1999), and control of the orientation of mesopores using a polymer film formed on a substrate is reported in Chemistry of Materials, Vol. 11, pp. 1609 (1999).
In the present invention, a mesoporous silica film is preferably used, which is produced by a method based on heterogeneous nucleation and growth of mesostructured silica. This production method will be described below.
First, the substrate preparation process is described.
Here described is a method using a substrate provided with a polymer film having surface anisotropy. However, substrates applicable to the present invention are not limited thereto. For example, as described above, crystalline substrates having surface anisotropy, such as the (110) plane of silicon single crystal, can also be used. Needless to say, in this case, the process of forming a polymer film described below is not required.
A polymer film having surface anisotropy can be produced, for example, by a rubbing method or the Langmuir-Blodgett method. However, the method for forming a polymer film having surface anisotropy used in the present invention is not limited to these two methods. Any method is applicable as long as anisotropy can be induced. For example, anisotropy may be endowed by irradiating with polarized light.
The rubbing method is as follows: First, a polymer film is formed on the substrate surface by spin coating, dip coating, or the like, and then a rotary roller wrapped around with a cloth is pressed against the film to rub the film in one direction. There is no particular limitation to the polymer material to be used, as long as the material can withstand the mesostructured silica film production process described later. For example, polyimide, polyamide, polystyrene, or the like can be used. A polyimide film can be prepared by coating a substrate with the corresponding precursor polyamic acid followed by the imidization by heat treatment. The substrate on which the polymer film is formed can be of any material, as long as it can withstand the mesostructured silica film preparation process described later, including quartz, glass, silicon substrate, or the like. There is no particular limitation to the thickness of the polymer film. The thickness is preferably in the range of several nm to hundreds of nm. Also there is no particular limitation to the material of the cloth to be wrapped around the rubbing roller. For example, cotton, nylon, or the like can be used. Anisotropy resulting from the rubbing treatment varies depending upon the structure of the polymer used; it may be mainly shape anisotropy, or it may be anisotropy both in shape and the polymer structure. According to the present invention, either may be adopted as long as the orientation of mesopores formed on the polymer can be controlled in one direction.
Next, the Langmuir-Blodgett method is described. According to the Langmuir-Blodgett method, a single molecular film of an amphiphile formed at a gas-liquid interface is transferred onto a substrate, and a desired film thickness can be obtained by lamination. The Langmuir-Blodgett film used herein includes not only a film which is formed on a gas-liquid interface and transferred to a substrate, but also a film modified after being transferred to the substrate. The Langmuir-Blodgett film can also be made from a polymer. For example, a polyimide Langmuir-Blodgett film can be prepared as follows: An alkylamine salt of polyamic acid, a precursor of polyimide, is synthesized and dissolved in an appropriate solvent, and the resultant solution is dropped onto a water surface. Then a substrate is immersed in and is withdrew from water repeatedly to form a Langmuir-Blodgett film of a desired film thickness on the substrate. After the film formation, the film is heat-treated in a nitrogen atmosphere for the dehydration-imidization and deamination, whereby a polyimide Langmuir-Blodgett film is produced. In the polyimide Langmuir-Blodgett film thus produced, polymer chains are oriented in the moving direction of the substrate during the film formation, which is confirmed by polarized infrared absorption spectroscopy or the like.
Then, a mesostructured silica film is formed on the substrate having an anisotropic polymer film prepared as described above.
A mesostructured silica film can be formed by holding the above-mentioned substrate in an aqueous solution containing a surfactant, silicon alkoxide (a silica source), and an acid that works as a hydrolysis catalyst. The substrate is held in the solution with the surface having the polymer film downward in order to prevent the deposition of the precipitation on the surface.
Various surfactants can be used as the surfactant, such as cationic surfactants (e.g., alkylammonium) and non-ionic surfactants having ethylene oxide as a hydrophilic group. For example, cetyl trimethyl ammonium chloride or polyoxyethylene cetyl ether can be used.
As the alkoxide that can be used as a silica source, tetraethoxysilane, tetramethoxysilane, tetrapropoxysilane, and the like are preferably used.
Examples of the acid that works as a hydrolysis catalyst are hydrochloric acid, nitric acid, and sulfuric acid. Hydrochloric acid is most generally used.
According to the present invention, the above-mentioned mesostructured silica film may be patterned to a desired shape, if required. For patterning, a general patterning technique can be used, such as ordinary photolithography and micromachining with a focused ion beam. These patterning processes are preferably performed before the removing process of the surfactant.
The surfactant is removed from the mesostructured silica film containing the tubular assemblies of the surfactant oriented in one direction on the substrate, whereby a mesoporous silica film having uniaxially oriented tubular mesopores is obtained. There are various methods for removing the surfactant. Any method can be used as long as it can remove the surfactant without damaging the mesoporous structure.
Calcination in an atmosphere containing oxygen is most generally used. For example, the film thus formed is calcined in air at 550° C. for 10 hours, whereby an organic component can be removed completely while the mesopore structure is maintained. In this case, the polymer film formed on the surface of the substrate is also removed. Therefore, finally, a mesoporous silica film having a uniaxially oriented mesoporous structure is directly formed on a substrate.
In addition to the above-mentioned calcination method, the surfactant may be removed by solvent extraction or with a supercritical fluid. Although it is difficult to remove organic components completely by these methods, a silica film having uniaxially oriented tube-shaped mesopores can be formed on a substrate made of a material that cannot withstand a high temperature during calcination.
Furthermore, other than by calcination or extraction, the surfactant can be removed by ozone oxidation. According to this method, the surfactant can be removed at a low temperature compared with calcination.
In the procedure as described above, a mesoporous silica film having uniaxially oriented tubular mesopores can be formed on a substrate. Depending upon the substrate to be used and the method for removing the surfactant, a polymer film may or may not be formed on the surface of the substrate. Both are applicable to the present invention.
Next, a conjugated polymer is introduced into the mesopores of the silica film having uniaxially oriented tubular mesopores. A conjugated conductive polymer that emits strong fluorescence is particularly preferably used, but not specifically limited. For example, poly[2-methoxy-5-(2′-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH—PPV) can be used or any other soluble semiconducting polymer can be used.
When the surface of the mesopores is modified with an organic substance beforehand to provide the hydrophobic surface, introduction of the polymer into the mesopores tends to be remarkably enhanced. For example, treatment with phenyldimethylchlorosilane can make the mesopores hydrophobic efficiently by bonding organic groups to siranol groups in the mesopores. However, the agent usable for hydrophobic treatment of the mesopores is not limited to the above, and agents other than silane coupling agents can be used as long as the same effect can be obtained. Specifically, modification of the mesopore surface is carried out by soaking the mesoporous silica film in a solution of a desired silane coupling agent. However, the modification method is not limited thereto. For example, a reaction in the gas phase is also applicable. For the improvement of the coupling reaction, a material that works as a catalyst of the reaction may be added. As a catalyst, a non-protic amine, such as triethylamine or the like, can be used.
When a mesoporous silica film on a substrate is soaked in and then taken out from a solution of a conjugated polymer, some conjugated polymer can adhere to the outer surface of the film in addition to the inner surface of the mesopores. Therefore, the removed film is washed with a solvent capable of dissolving the conjugated polymer to remove the compound attached to the outer surface of the film.
As described above, a composite comprising a mesoporous silica film having uniaxially oriented tubular mesopores and a conjugated polymer introduced into the mesopores can be prepared.
Next, the characterization of the composite will be described. Characterization must be carried out both on the structure and on the optical properties.
First, the characterization of the structure will be described.
The structure of a mesoporous silica film formed on a substrate can be evaluated in detail by X-ray diffraction analysis. For analysis of a local structure, measurement in the θ-2θ scanning geometry is used. When the produced film is measured by this method, diffraction peaks of (h00) lattice planes corresponding to a honeycomb mesopore structure are observed, whereby the formation of the regular mesostructure can be confirmed.
In order to confirm the orientation of the mesopores over the entire substrate surface, X-ray diffraction analysis is useful. However, in the above-mentioned θ-2θ scanning geometry, the information on the orientation of the mesopores cannot be obtained. For this purpose, the in-plane X-ray diffraction analysis described below is effective.
According to the in-plane X-ray diffraction analysis, X-rays are impinged on the film on the substrate at a very small angle in the vicinity of the critical angle for total reflection, and the X-ray diffracted to the in-plane direction is detected. This analysis gives the structural information on lattice planes perpendicular to the substrate surface. By measuring an in-plane rocking curve of a certain lattice plane using the in-plane X-ray diffraction analysis, the information on the orientation direction of the mesopores in the mesoporous silica film can be obtained. This technique is described in, for example, Chemistry of Materials, Vol. 12, pp. 49 (2000).
Regarding the mesoporous silica film having a uniaxially oriented mesopore structure used in the present invention, diffraction peaks assigned to (100) and (200) are observed in the θ-2θ scanning geometry, and two diffraction peaks are observed with a 180° interval in the in-plane rocking curve. From these measurements, the uniaxial orientation of the regular tubular mesopores in the film was confirmed.
Introduction of a conjugated polymer into the mesopores is often confirmed by the change in color. For example, the film to which the above-mentioned MEH—PPV has introduced becomes uniformly red, confirming the introduction of the polymer into mesopores. Needless to say, corresponding visible absorption spectrum can be used for the confirmation of the introduction of a conjugated polymer. As a comparison experiment, when a glass substrate without a mesoporous silica film formed thereon is soaked in the polymer solution, essentially all of the polymer adhering to the surface is removed in the subsequent washing process, and color change cannot be observed. In addition to these methods, introduction of the polymer can be confirmed by IR. However, in this case, contrivance may be needed for the measurement, such as the use of the attenuated total reflecance (ATR) method and the use of a substrate that is transparent in the infrared region.
Next, characterization of the optical properties will be described. For the fluorescence from the film, the polarization dependency of both excitation light and fluorescence must be determined. In this case, the film is irradiated with excitation light with the electric field parallel or perpendicular to the orientation of the mesopores in the mesoporous silica film determined by the X-ray diffraction analysis, and the fluorescence emitted from the film is measured through a second emission polarizer. The intensities of the fluorescence are measured for the component with the electric field parallel and perpendicular to the orientation of the mesopores.
For the polarized light-emitting film of the present invention, four measurements are carried out: (excitation lights with the electric field component parallel and perpendicular to the orientation of the mesopores)×(fluorescence with the electric field component parallel and perpendicular to the orientation of the mesopores). As a result, the strong fluorescence is observed only in the optical geometry where the electric field of the excitation light and the electric field of the fluorescence are both parallel to the orientation of the mesopores. This is attributed to the high-degree uniaxial orientation of the polymer chains in the mesopores.
As described above, according to the present invention, by highly controlling the orientation of nano-scaled spaces of a porous material in macroscopic scales by a simple method based on self-organization, conjugated polymer chains can be aligned in the spaces, and whereby, the polarization of the light emitted from the polymer can be controlled.
Hereinafter, the present invention will be described in more detail by way of Examples. However, the present invention is not limited to Examples.
In this example, a mesostructured silica film having a uniaxially oriented tubular micelle assembly was produced on a substrate provided with a polyimide alignment film subjected to rubbing treatment thereon. The resultant silica film on the substrate was calcined in air to form a mesoporous silica film. (Do we need to include surface passivation here?) Thereafter, poly[2-methoxy-5-(2′-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH—PPV) was introduced into the mesopores, thereby producing a composite film that can emits highly polarized fluorescence. The structure of the film produced in this Example 1 is schematically shown in
After a silica glass substrate was washed with acetone, isopropyl alcohol, and pure water, its surface was cleaned in an ozone generation apparatus. Then the substrate was coated with a solution of polyamic acid A in NMP by spin coating. The polyamic acid on the silica glass substrate was baked at 200° C. for one hour to convert to polyimide A having the following structure.
The film of polyimide A thus obtained was subject to rubbing treatment under the conditions shown in Table 1, and the obtained polyimide A film on the silica glass substrate was used as the substrate for the mesostructured silica film formation.
A mesostructured silica film was formed on the substrate with the rubbing-treated polyimide film. In this Example 1, a nonionic surfactant polyethylene oxide 10 cetyl ether (C16H33(OCH2CH2)10OH, C16EO10) having polyethylene oxide as a hydrophilic group was used.
5.52 g of C16EO10 was dissolved in 129 ml of pure water, and 20.6 ml of concentrated hydrochloric acid (36%) was added to the mixture, and stirred thoroughly. Then 2.20 ml of tetraethoxysilane (TEOS) was added to the solution, and stirred for 3 minutes. The molar ratio of the each component in the final solution was TEOS:H2O:HCl:C16EO10=0.1:100 3:0.11.
The above-mentioned substrate with the rubbed polyimide A film was held in the reactant solution with the polymer-coated surface downward, in a Teflon vessel 21 having a structure shown in
The substrate placed in the reactant solution for a predetermined period of time was taken out from the vessel, and thoroughly washed with pure water and was dried at room temperature in an ambient atmosphere. It was confirmed that a continuous mesostructured silica film was formed on the substrate. The thickness of the mesostructured silica film was determined to be 200 nm by a profilometer.
This film was analyzed by X-ray diffraction analysis. As a result, a strong diffraction peak corresponding to a plane interval of 5.02 nm, assigned to the (100) plane of a mesostructured silica of hexagonal porous structure, was confirmed. Thus, the film was confirmed to have a mesoporous structure in which tubular mesopores are hexagonally packed.
In order to quantitatively evaluate the uniaxial orientation of a mesopores in the mesostructured silica film, the film was analyzed by in-plane X-ray diffraction. The in-plane rotation angle dependency on the (110) plane diffraction intensity(in-plane rocking curve) measured in this Example 1 showed that, the mesopores in this mesostructured silica film was uniaxially oriented in a direction perpendicular to the rubbing direction of the polyimide film. The distribution of the orientation direction was estimated to be about 19° from the full width of the half maximum of the diffraction peak in the in-plane rocking curve.
Next, the mesostructured silica film formed on the substrate was calcined to remove the surfactant from the mesopores, whereby a mesoporous silica film was obtained. Calcination was carried out by increasing the temperature up to 550° C. by 2° C./minute and the subsequent keeping at 550° C. for 10 hours. After cooling down to room temperature, the mesostructured silica film was observed with optical microscopy. Neither peeling off of the film from the substrate nor cracking in the film was observed after the calcination. This is attributed to the fact that the thinness of the polyimide film is thin enough to be removed without separating the mesoporous silica film and the substrate.
The film after the calcination was analyzed by X-ray diffraction analysis. A strong diffraction peak corresponding to the lattice plane with a distance of 4.37 nm, assigned to the (100) plane of a mesostructured silica with a hexagonal porous structure, was confirmed. This result confirms that the mesopore structure was held.
Furthermore, the film after the calcination was analyzed by in-plane X-ray diffraction analysis. As a result, the same diffraction profile as that before the calcination was obtained, and it was confirmed that the orientation distribution of the mesopores were completely held even after the calcination.
Then, the calcined mesoporous silica film was treated with a silane coupling agent to make the inner walls of the mesopores hydrophobic. In this Example 1, the film immediately after the calcination was soaked in phenyldimethylchlorosilane overnight, whereby silanol groups on the inner surface of the mesopores silica were modified. In this case, triethylamine was added as a catalyst for the coupling reaction. The mesoporous silica film after the reaction was washed with hexanes and dried at 110° C. The films were then washed a final time with methanol and dried again at 110° C.
Next, this film was soaked in an 1% chlorobenzene solution of MEH—PPV to introduce MEH—PPV into the mesopores. MEH—PPV used herein had a weight-average molecular weight of 100,000 or less. While the substrate was being soaked, the solution was heated to 80° C. After 48 hours, the substrate was taken out, and washed with chlorobenzene to remove excess MEH—PPV adhering to the outer surface.
Thus produced mesoporous silica film with MEH—PPV introduced thereto was dried in air, and thereafter, optical measurements described later were conducted. The dried film was uniformly red.
Thus, obtained was a mesostructured silica film formed on a substrate, containing MEH—PPV in the uniaxially oriented tubular mesopores thereof. The in-plane X-ray diffraction analysis confirmed that the mesoporous silica film after the MEH—PPV introduction have an intact uniaxially oriented hexagonal mesoporous structure.
Next, a method for measuring the fluorescent behavior of the film thus produced will be described.
As an excitation light source, the 532 nm line of a frequency doubled diode pumped solid state Nd:YAG laser was used. The light was then circularly polarized using a ¼ wave plate and a Glan-Thomson calcite polarizer was employed in order to obtain a high-degree of polarization. The sample was fixed so that the mesopores are arranged horizontally, and the direction of the electric field of the excitation light was changed so as to be parallel or perpendicular to the direction of the mesopores of the mesostructure film. The polarization direction was rotated using a half wave plate. The intensity of the fluorescence emitted from the sample was measured through a polarizer to obtain the information on the polarization condition in the fluorescence. The polarizer was set so that the polarization direction becomes parallel and perpendicular to the direction of the mesopores in the sample film. In the apparatus used in the present example, a spectrometer consisting of a linear CCD detector and a grating monochromator with no polarization dependence was used to measure the emission.
In the present example, in order to describe the anisotropy of the measured light emission intensity, a symbol “I” representing the intensity will be provided with abbreviations of H (Horizontal) and V (Vertical) representing the three directions: the polarization direction of the excitation light, the polarization direction of the fluorescence, and the orientation direction of the mesopores, in this order. For example, the intensity represented by IHVH refers to the following case: when the mesopores are horizontally arranged, the excitation light with the electric field parallel to the orientation direction of the mesopores is made incident, and the polarized light emission with the electric field perpendicular to the orientation direction of the mesopores is observed.
In the present example, a linear CCD detector was used.
Excitation light with the electric field parallel to the direction of the mesopores was made incident upon a sample film fixed so that the mesopores were arranged horizontally, and the fluorescence was observed in the two polarization directions, i.e., the geometry of HHH and the geometry of HVH.
Furthermore, in the case where the polarization direction of the incident light is perpendicular to the orientation direction of the mesopores, i.e., in VHH and VVH geometries, fluorescence was hardly observed in both geometries.
In this Example 2, a mesostructured silica film in which honeycomb packed tubular micelles were uniaxially aligned was formed on a substrate in the same manner as in Example 1, except that polyamide A was replaced with polyimide B, and the prepared silica film was subjected to patterning. Thereafter, the surfactant was removed, and MEH—PPV was introduced into the mesopores, whereby a patterned composite film exhibiting highlypolarized light emission was produced.
The structure of the film produced in the present example is as schematically shown in
A silica glass substrate was washed with acetone, isopropyl alcohol, and pure water and its surface was cleaned in an ozone generation apparatus. Then the substrate was coated with a solution of polyamic acid B in NMP by spin coating. The polyamic acid on the silica glass substrate was baked at 200° C. for one hour to convert to polyimide B having the following structure.
The polyimide B has substantially the same structure as that of the polyimide A, except that the length of the methylene group of the spacer is different.
The polyimide film was subject to rubbing treatment under the same conditions as in Example 1. Then, a mesostructured silica film was produced in the same manner as in Example 1. The film thus formed was a continuous transparent film and the appearance was the same as the one prepared in Example 1. The thickness was determined to be 200 nm by a profilometer.
The mesostructured silica film produced in this Example 2 was analyzed by X-ray diffraction analysis. As the results, it was clarified that the honeycomb-packed tubular micelles are uniaxially aligned in a direction perpendicular to the rubbing direction. The distribution of the orientation direction was estimated to be about 18° from the full width of the half maximum of the diffraction peak in the in-plane rocking curve.
Next, the film was patterned in a line shape by using a gallium focused ion beam. Patterning with the focused ion beam was performed by optimizing the conditions such as the accelerating voltage and the scanning speed to obtain a 2 μm-width/1 μm-space parallel lines pattern without the residues of the mesostructured silica between the lines. As schematically shown in
The calcined film was soaked in phenyldimethylchlorosilane under the same conditions as in Example 1 to make the inner surface of the mesopores silica hydrophobic. Thereafter, MEH—PPV having a weight-average molecular weight of 100,000 or less was introduced into the mesopores under the same conditions as in Example 1. The film after introduction of MEH—PPV was examined by X-ray diffraction analysis. As a result, it was confirmed that even if patterning was performed, the mesoporous structure did not change by calcination and the following introduction of MEH—PPV.
Fluorescent behavior of this film was observed in the same manner as in Example 1, using the same optical system. As a result, the intensity ratio of IHHH and IHVH was similar to that observed with non-patterned film, showing highly anisotropic fluorescence. As in Example 1, when the polarization direction of the incident light was perpendicular to the orientation direction of the mesopores, i.e., in VHH and VVH arrangements, fluorescence was hardly observed.
From these results, it was shown that the polymer chains 14 are aligned in the uniaxially oriented mesopores 13 as schematically shown in the enlarged figure in
When the fluorescent film in such a line-shaped pattern was prepared on a substrate surface with optimized refractive index and reflectivity, the direction of light emission from the film would be controlled.
When the fluorescent film is used as a polarized light source for a liquid crystal display, only when the intensity ratio of the polarized light of the two directions, i.e. the ratio of IHHH and IHVH, is 3 or more, satisfactory black can be displayed. The present invention can realized it.
As described above, according to the present invention, a mesoporous silica film having uniaxially oriented regular mesopores formed on a substrate is used as a host material, and a conjugated polymer is introduced into the mesopores, whereby a film material emitting highly polarized fluorescence can be produced by a simple method.
Various other modifications will be apparent too and can be readily made by those skilled in the art without departing from the scope and spirit of this invention. Accordingly, it is not intended that the scope of the claims appended hereto be limited to the description as set forth herein, but rather that the claims be broadly construed.
This work was supported by grant number N00014-99-1-0568, awarded by the Office of Naval Research. The United States Government has certain rights in this invention.
