Imprint lithography techniques have been widely investigated as alternatives to conventional photolithography for high-resolution patterning. Imprint lithography techniques generally use a template containing topography to replicate a surface relief on a substrate.
Briefly, in one aspect, the present disclosure describes a method of making a patterned surface structure on a substrate. The method includes providing one or more patterned templates each including a relief structure; coating the relief structure of each patterned templates with a replication medium in the form of a liquid; solidifying the replication medium to replicate a pattern of the relief structure on a first side of the replication medium and form a planar surface on a second side thereof opposite the first side; transferring the one or more patterned templates with the respective replication media to an array of sub-regions of a tiling region on a major surface of a substrate, the planar surface of each replication medium being in contact to the respective sub-regions of the substrate; and removing the one or more patterned templates from the substrate to form a patterned surface structure on the substrate.
Various unexpected results and advantages are obtained in exemplary embodiments of the disclosure. One such advantage of exemplary embodiments of the present disclosure is that a substantially solid replication medium at room temperature can be formed from a liquid form on a patterned template, which eases handling and storage during intermediate processing steps such as, for example, while coating or transferring replication medium on other patterned templates for other sub-regions on the same substrate.
Various aspects and advantages of exemplary embodiments of the disclosure have been summarized. The above Summary is not intended to describe each illustrated embodiment or every implementation of the present certain exemplary embodiments of the present disclosure. The Drawings and the Detailed Description that follow more particularly exemplify certain preferred embodiments using the principles disclosed herein.
The disclosure may be more completely understood in consideration of the following detailed description of various embodiments of the disclosure in connection with the accompanying figures, in which:
In the drawings, like reference numerals indicate like elements. While the above-identified drawing, which may not be drawn to scale, sets forth various embodiments of the present disclosure, other embodiments are also contemplated, as noted in the Detailed Description. In all cases, this disclosure describes the presently disclosed disclosure by way of representation of exemplary embodiments and not by express limitations. It should be understood that numerous other modifications and embodiments can be devised by those skilled in the art, which fall within the scope and spirit of this disclosure.
For the following Glossary of defined terms, these definitions shall be applied for the entire application, unless a different definition is provided in the claims or elsewhere in the specification.
Certain terms are used throughout the description and the claims that, while for the most part are well known, may require some explanation. It should be understood that:
The terms “(co)polymer” or “(co)polymers” includes homopolymers and copolymers, as well as homopolymers or copolymers that may be formed in a miscible blend, e.g., by coextrusion or by reaction, including, e.g., transesterification. The term “copolymer” includes random, block and star (e.g. dendritic) copolymers.
The term “protectant resin” refers to a film or a film forming composition of monomer, polymer, solvent, and/or other additives composed so as to substantially protect a surface from damage or contamination when disposed on the surface.
The term “protective tile” refers to a film of protectant resin, substantially solid, disposed on a surface such that at least a portion of the surface is covered by said film of protectant resin and thereby protected from damage or contamination.
The term “imprint lithography” refers to a method of replicating a pre-defined relief structure of a patterned template by imprinting or embossing the patterned template into a replication medium. The imprinting or embossing step includes mechanical deformation of a replication medium that results in replication of the relief structure. A pattern transfer process can optionally be used to transfer the pattern of the replication medium into the underlying substrate by, e.g., wet etching, reactive ion etching, etc. Embodiments of this disclosure is different from conventional imprint lithography processes in that, for example, embodiments of this disclosure provide methods which do not include imprinting or embossing steps for mechanical deformation of a replication medium.
The term “structured transfer film” refers to an article including a patterned template having a relief structure and a backfill layer applied to the relief structure, where the structured transfer film is configured and arranged for transfer of at least a portion of the backfill layer to a substrate while substantially preserving the backfill layer relief structures of that portion. Embodiments of this disclosure are different from conventional structured transfer film processes in that, for example, i) embodiments of this disclosure provide methods for tiling one or more structured transfer films; ii) embodiments of this disclosure provide a replication medium that is applied as a liquid and then solidified to form a structured transfer film article that is solid at room temperature, and thereby easier to handle and/or transport; iii) embodiments of this disclosure provide a replication medium including a curable polymeric resin which is solid at room temperature and can be hardened or toughened through curing before removing the one or more patterned templates; and iv) embodiments of this disclosure provide a tiled patterned surface structure that can be used to generate a tool for further replication processing such as electroplating, polymer replication, etching, etc.
The terms “about” or “approximately” with reference to a numerical value or a shape means+/−five percent of the numerical value or property or characteristic, but expressly includes the exact numerical value. For example, a viscosity of “about” 1 Pa-sec refers to a viscosity from 0.95 to 1.05 Pa-sec, but also expressly includes a viscosity of exactly 1 Pa-sec. Similarly, a perimeter that is “substantially square” is intended to describe a geometric shape having four lateral edges in which each lateral edge has a length which is from 95% to 105% of the length of any other lateral edge, but which also includes a geometric shape in which each lateral edge has exactly the same length.
The term “substantially” with reference to a property or characteristic means that the property or characteristic is exhibited to a greater extent than the opposite of that property or characteristic is exhibited. For example, a substrate that is “substantially” transparent refers to a substrate that transmits more radiation (e.g. visible light) than it fails to transmit (e.g. absorbs and reflects). Thus, a substrate that transmits more than 50% of the visible light incident upon its surface is substantially transparent, but a substrate that transmits 50% or less of the visible light incident upon its surface is not substantially transparent.
As used in this specification and the appended embodiments, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to fine fibers containing “a compound” includes a mixture of two or more compounds. As used in this specification and the appended embodiments, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
As used in this specification, the recitation of numerical ranges by endpoints includes all numbers subsumed within that range (e.g. 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.8, 4, and 5).
Exemplary embodiments of the present disclosure may take on various modifications and alterations without departing from the spirit and scope of the present disclosure. Accordingly, it is to be understood that the embodiments of the present disclosure are not to be limited to the following described exemplary embodiments, but is to be controlled by the limitations set forth in the claims and any equivalents thereof. Various exemplary embodiments of the disclosure will now be described with particular reference to the Drawings.
At 110, protective tiles (10a, 10b, 10c, etc.) are provided to cover each of the sub-regions 5a, 5b, 5c, etc. In the depicted embodiment, each tile of the array of patterns has a rectangular shape. A layer of protectant resin is deposited onto each sub-region. The protectant resin is solidified to form an array of the protective tiles (e.g., 10a, 10b, 10c, etc.) corresponding to the array of sub-regions (e.g., 10a, 10b, 10c, etc.).
In many applications, the first major surface 21 of the substrate 2 may be contaminated thereon with an unacceptable number and size of particles. When coated on the first major surface 21 of the substrate 2, the protectant resin may be flowable and then solidified into a protective tile so as to capture all or a substantial amount of the particles contaminating the sub-regions on the substrate surface. The flowable protectant resin can capture the particles on the surface typically by physically surrounding at least a portion of each of the captured particles. The particles are captured when the coated material solidifies into the layer. Depending on the exact composition of the flowable protectant resin, the solidification of material may be accomplished through drying, cooling, heat curing, radiation curing, polymerization from reactive precursors, or the like. In a roll-to-roll process, it is usually convenient to perform the solidifying while the substrate (e.g., a web) is being conveyed in a continuous motion in the machine direction.
Suitable protectant resin compositions for the substrate 2 may include acrylates such as, for example, radiation curing acrylates, monomeric acrylates, oligomeric acrylates, urethane acrylates, silicone acrylates, fluorinated acrylates, ethoxylated acrylates including, for example, ethoxylated trimethylolpropane triacrylate and preferably six-mole ethoxylated trimethylolpropane triacrylate. In some embodiments, suitable protectant resin compositions for the substrate may also include thermoplastic polymers including polyvinyl alcohol, polyvinyl butyral, polymethyl methacrylate, polystyrene, reactive polymers including, for example, acrylate or vinyl functionalized polystyrene or polymethyl methacrylate, polyolefins including, for example cyclic polyolefin copolymers. In some embodiments, suitable protectant resin compositions for the substrate may further include epoxies including, for example, silicone epoxies, fluorinated epoxies, and radiation curing epoxies. In some embodiments, suitable protectant resin compositions for the substrate may further include polymers formed by ring opening metathesis polymerization.
In some embodiments, suitable protectant resin composition for the substrate may also include various blends of above listed materials additionally including solvents and functional additives such as, for example, surfactants plasticizers, and photoinitiators including diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide.
For example, a suitable protectant resin composition for the substrate may include a blend of multiple commercial grades of polyvinyl alcohol in an aqueous solution, preferably commercial grades of polyvinyl alcohol between 80 and 95% hydrolyzed, preferably with average molecular weight between 9,000 and 124,000, preferably a blend of polyvinyl alcohol with average molecular weight between 31,000-50,000, and polyvinyl alcohol with average molecular weight between 85,000-124,000, and more preferably a blend comprising 50:50 ratio by weight of polyvinyl alcohol with average molecular weight between 31,000-50,000 and polyvinyl alcohol with average molecular weight between 85,000-124,000 in an aqueous solution with concentration in the range from 5-50%, preferably with concentration in the range from 10-25%. For example, a suitable protectant resin composition for the substrate may include a colloidal dispersion of polyurethane in water.
Suitable protectant resin compositions can be unreactive with various adhesion promoters which may be disposed on the first major surface 21 of the substrate 2. Suitable protectant resin compositions can have high enough strength and low enough adhesion to the first major surface 21 of the substrate 2 in order to be peeled from said surface without breakage. Suitable protectant resin compositions can be homogenous and solid at a temperature of at least about 25 degrees Celsius with no constitutive components having melting temperature or glass transition temperature below this threshold so that no residual film is left on the first major surface 21 of the substrate 2 upon peeling said resin from said surface.
In some embodiments, secondary carrier films can be laminated on the protective tiles after the protective tiles are attached to the sub-regions. The lamination of the secondary carrier film can make it easier to remove the protective tiles from the sub-regions. In some embodiments, the secondary carrier films can be applied via a roller. Exemplary secondary carrier films may include polycarbonate, polyethylene terephthalate, polyethylene terephthalate glycol, or polyvinyl alcohol.
At 120, at least one of the protective tiles (e.g., at least one of 10a, 10b, 10c, etc.) is removed from one of the sub-regions (e.g., 5a, 5b, 5c, etc.) to expose the first major surface of the substrate directly beneath. In some embodiments, the protective tile can be removed from the sub-region by peeling the protective tile from the substrate. After removing the protective tile, the sub-regions can be substantially free of ultra-fine particles having a diameter of at least about 0.1 micrometers and larger particles.
At 130, a patterned template 30 having a relief structure 31 is provided to receive a replication medium 20 to in the form of a flowable fluid (e.g., liquid). An optional supporting film 32 can be provided to support the relief structure 31. The relief structure 31 of the patterned template 30 is a structured surface including an arrangement of pattern elements 312 extending away from a base surface thereof and voids 314 formed between the pattern elements 312. The pattern elements 312 can contain microscale and/or nanoscale feature(s) in a regular or random arrangement.
At 135, the replication medium 20 in the form of a flowable fluid (e.g., liquid) is provided onto the relief structure 31 of the patterned template 30, filling voids on the relief structure 31 and conforming to the patterned surface of the relief structure 31. The replication medium 20 is then solidified thereon.
In some preferred embodiments, the replication medium 20 includes a reactive thermoplastic polymer, plasticized with a reactive crosslinker. The plasticizer serves to control the glass transition temperature to allow for low temperature lamination. The plasticizer also reacts to further harden the resin before removal of the patterned template. In some embodiments, suitable replication medium compositions may include blends of reactive polymers and reactive monomers, preferably including reactive thermoplastic polymers. Exemplary thermoplastic polymers can include a (meth)acrylate-functional polymer, a vinyl functional polymer, an epoxy-functional polymer, etc. Exemplary plasticizers can include mono-functional (meth)acrylates, multi-functional (meth)acrylates, multi-functional thiols, epoxide monomers, etc.
Suitable replication medium may include resins having a glass transition temperature greater than 25 degrees Celsius when the resins are solidified by drying or curing. Suitable replication medium may include resins having an elastic modulus greater than 300 MPa when the resins are solidified by drying or curing.
In some embodiments, the replication medium may further include radiation curing monomers, polymers, oligomers, solvents, functional additives such as surfactants or others, a combination thereof, etc.
Suitable compositions for the replication medium 20 may further include acrylates including radiation curing acrylates, monomeric acrylates, oligomeric acrylates, urethane acrylates, silicone acrylates, fluorinated acrylates, ethoxylated acrylates. Suitable replication medium compositions may also include thermoplastic polymers including polyvinyl alcohol, polyvinyl butyral, polymethyl methacrylate, polystyrene, reactive polymers including, for example, acrylate or vinyl functionalized polystyrene or polymethyl methacrylate, polyolefins including, for example cyclic polyolefin copolymers. Suitable replication medium compositions may also include epoxies including, for example, silicone epoxies, fluorinated epoxies, and radiation curing epoxies. Suitable replication medium compositions may also include polymers formed by ring opening metathesis polymerization.
Suitable replication medium compositions may also include various blends of above listed materials additionally including solvents and functional additives such as, for example, surfactants plasticizers, and photoinitiators including diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide.
In some embodiments, an adhesion promoter may be included as an additive in the replication medium or may be provided on the planar surface of the replication medium prior to contacting to the substrate 2. The adhesion promoter layer may also be provided on the exposed sub-region of the substrate 2 to promote the adhesion of the replication medium 20 to the sub-region of the substrate. Exemplary silane coupling agents include 3-(trimethoxysilyl)propyl methacrylate. Another exemplary silane coupling agent is (3-trimethoxysilylpropylcarbamoyloxy)ethyl prop-2-enoate, described in Example 7 of U.S. Pat. No. 9,790,396, which is incorporated herein by reference.
In some embodiments, a patterned template, such as the patterned template 30 in
In some embodiments, the patterned template may include a release layer or release-treated with materials such as, for example, an organosilicon compound (e.g., hexamethyldisiloxane or HMDSO), a fluorinated coating, fluorinated monolayers, silicone coatings, or silicone monolayers. In one example, which is not intended to be limiting, the release layer can be formed through plasma enhanced chemical vapor deposition (PECVD) of hexamethyldisiloxane, which forms a thin surface having a thickness of about 1 nm to about 10 nm, or about 2 nm to about 8 nm. A protective layer can then be applied to the treated relief structure. Application methods may include, for example, overcoating, printing, lamination, or a combination of these processes. Exemplary overcoating methods may include die coating, spray coating, vapor coating, dip coating, spin coating, etc. Exemplary printing methods include digital printing (inkjet, valve jet etc.), flexo-printing, stencil printing etc. Laminated protective layers include single or multilayer films with or without adhesive. Overcoated and printed protective layers include polymer-solvent dispersions, polymer solvent solutions, reactive polymer solutions, ionic networking acrylate, radiation curing monomers, oligomers, thermoplastics, etc. Overcoated and printed protective layers can be set or solidified by a number of methods including radiation curing, thermal curing, drying, etc.
The relief structure of the patterned template can be cleaned by removing a protective layer therefrom before applying a replication medium thereon. In some embodiments, the patterned template 30 can be cleaned by peeling a layer of protectant resin from the relief structure. The relief structure can be substantially free of ultra-fine particles having a diameter of at least about 0.1 micrometers and larger particles after peeling off the protectant resin.
Suitable protectant resin compositions for protecting and cleaning the patterned template 30 may include acrylates including radiation curing acrylates, monomeric acrylates, oligomeric acrylates, urethane acrylates, silicone acrylates, fluorinated acrylates, ethoxylated acrylates including, for example, ethoxylated trimethylolpropane triacrylate and preferably six-mole ethoxylated trimethylolpropane triacrylate. Suitable protectant resin compositions for the template may also include thermoplastic polymers including polyvinyl alcohol, polyvinyl butyral, polymethyl methacrylate, polystyrene, reactive polymers including, for example, acrylate or vinyl functionalized polystyrene or polymethyl methacrylate, polyolefins including, for example cyclic polyolefin copolymers. Suitable protectant resin compositions for the template may also include epoxies including, for example, silicone epoxies, fluorinated epoxies, and radiation curing epoxies. Suitable protectant resin compositions for the substrate may also include polymers formed by ring opening metathesis polymerization.
Suitable protectant resin composition for the template may also include various blends of above listed materials additionally including solvents and functional additives such as, for example, surfactants plasticizers, and photoinitiators including diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide.
For example, a suitable protectant resin composition for the template may include a blend of multiple commercial grades of polyvinyl alcohol in an aqueous solution, preferably commercial grades of polyvinyl alcohol between 80 and 95% hydrolyzed, preferably with average molecular weight between 9,000 and 124,000, preferably a blend of polyvinyl alcohol with average molecular weight between 31,000-50,000, polyvinyl alcohol with average molecular weight between 85,000-124,000, and glycerol, and more preferably a blend comprising 45:45:10 ratio by weight of polyvinyl alcohol with average molecular weight between 31,000-50,000, polyvinyl alcohol with average molecular weight between 85,000-124,000, and glycerol in an aqueous solution with concentration in the range from 5-50%, preferably with concentration in the range from 10-25%. For example, a suitable protectant resin composition for the template may include a colloidal dispersion of polyurethane in water.
The relief structure 31 of the patterned template 30 can be cleaned by any suitable cleaning methods. Typical cleaning methods may include encapsulant stripping, solvent rinse, sonication, CO2 snow cleaning etc. Solvent rinsing includes sequential rinses with solvents such as isopropanol, acetone, de-ionized water etc. Encapsulant stripping describes the removal of overcoated, printed, or adhesive protective layers where particles are encapsulated by or adhered to the protective lay in the application process and stripped from the patterned templates when the protective layer is removed. Removal of a protective layer may be done with the aid of static neutralization including static string, nuclear type static bars, active static bars etc.
Referring again to
Patterned templates can be converted by removing at least some non-structured margins thereof before transferring to a flat or curved substrate. Converting methods may include, for example, press punch converting, rotary die cutting, laser cutting, scissor cutting, etc. Converting may include lamination of a carrier layer to allow for roll to roll handling of patterned templates after converting. Patterned templates may be kiss-cut to a carrier layer and left in a continuous roll or sheeted and packaged in-line as individual parts.
In some embodiments, the coated patterned templates can be transferred for tiling a flat substrate through a serial or parallel approach (e.g., as illustrated in the embodiments of
In some embodiments, the coated patterned templates can be transferred for tiling a curved substrate (e.g., a cylindrical sleeve) through a serial or parallel approach (e.g., as illustrated in the embodiments of
Optionally, heat can be applied to the coated replication medium 20 such that the solid layer of the replication medium 20 is sufficiently flowable to make conformal contact with the substrate. The composition of the replication medium can be designed to lower the processing temperatures so that thermal expansion mismatch between the replication medium, the substrate, and the patterned template can be minimized.
Further, optionally, the replication medium can be hardened through curing. For example, curing can be carried out by exposing the replication medium 20 to actinic radiation to crosslink the polymer. For example, in the embodiments depicted in
At 160, after the replication medium 20 is hardened, the patterned template 30 is removed from the sub-region to expose the formed replication pattern on the hardened or toughened replication medium 20′. In some embodiments, the patterned template can be left on and act as a protectant layer for the structure on some sub-regions while the other sub-regions are being laminated sequentially.
At 170, a protective layer 40 is provided to cover the formed replication pattern on the hardened or toughened replication medium 20′ within the sub-region. The protective layer 40 may be a washable or strippable protective layer. The protective layer 40 may include a protectant resin such as, for example, polymer-solvent dispersions, polymer solvent solutions, reactive polymer solutions, ionic networking acrylate, radiation curing monomers, oligomers, thermoplastics, etc. It is to be understood that in some embodiments, the preferred protection may be provided by leaving the patterned template in place rather than doing an additional coating step for protection.
Suitable protectant resin composition 40 for protecting and cleaning the replication pattern 20′ may include acrylates including radiation curing acrylates, monomeric acrylates, oligomeric acrylates, urethane acrylates, silicone acrylates, fluorinated acrylates, ethoxylated acrylates including, for example, ethoxylated trimethylolpropane triacrylate and preferably six-mole ethoxylated trimethylolpropane triacrylate. Suitable protectant resin compositions for the replication pattern may also include thermoplastic polymers including polyvinyl alcohol, polyvinyl butyral, polymethyl methacrylate, polystyrene, reactive polymers including, for example, acrylate or vinyl functionalized polystyrene or polymethyl methacrylate, polyolefins including, for example cyclic polyolefin copolymers. Suitable protectant resin compositions for the replication pattern may also include epoxies including, for example, silicone epoxies, fluorinated epoxies, and radiation curing epoxies. Suitable protectant resin compositions for the replication pattern may also include polymers formed by ring opening metathesis polymerization.
Suitable protectant resin composition for the replication pattern may also include various blends of above listed materials additionally including solvents and functional additives such as, for example, surfactants plasticizers, and photoinitiators including diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide.
For example, a suitable protectant resin composition for the replication pattern may include a blend of multiple commercial grades of polyvinyl alcohol in an aqueous solution, preferably commercial grades of polyvinyl alcohol between 80 and 95% hydrolyzed, preferably with average molecular weight between 9,000 and 124,000, preferably a blend of polyvinyl alcohol with average molecular weight between 31,000-50,000, polyvinyl alcohol with average molecular weight between 85,000-124,000, and glycerol, and more preferably a blend comprising 45:45:10 ratio by weight of polyvinyl alcohol with average molecular weight between 31,000-50,000, polyvinyl alcohol with average molecular weight between 85,000-124,000, and glycerol in an aqueous solution with concentration in the range from 5-50%, preferably with concentration in the range from 10-25%. For example, a suitable protectant resin composition for the replication pattern may include a colloidal dispersion of polyurethane in water.
At 180, the steps from 120 to 170 are repeated for each of the rest of the sub-regions to form a replication pattern within each sub-region. In some embodiments, some steps can be completed in the order listed for each subregion in order to benefit from the process design (e.g., to complete steps 120 through 170 for subregion 1, then complete steps 120 through 170 for subregion 2; don't do step 120 for subregions 1 and 2, then step 130 for subregions 1 and 2, etc.). In some embodiments, the steps can be repeated by using one or more patterned templates (e.g., from one up to the number of subregions). The steps can be repeated to pattern a large area with fine features as compared to conventional direct patterning methods. The protective layers used herein can eliminate opportunities for particulate contamination and damage in the step and repeat process.
It is to be understood that the steps in
Referring again to
Articles and methods described herein have various applications. For example, it can be used to develop a process technology for making large-area-coverage nano-structured tools for pattern replication. Replication tools can be made by using the patterned surface structure on the sub-regions of a substrate (e.g., the replication patterns of the hardened or toughened replication medium 20′ in
Structured patterns can be made on cylindrical tools with length scales on the order of microscale and nanoscale. This provides a robust way of producing cylindrical tools with smaller features (e.g., nanoscale) and/or with patterns that are not conducive to traditional micro-structured tooling manufacturing routes such as diamond turning machines (DTMs).
Exemplary embodiments of the present disclosure provide a substantially solid replication medium at room temperature which is formed on a patterned template. The processes described herein can ease handling and storage during intermediate processing steps such as, for example, while coating or transferring replication medium on other patterned templates for other subregions on the same substrate. Embodiments described herein are advantageous over conventional imprint lithography techniques which use a liquid replication medium where particles can become embed into the replication medium during storage and the coating can continue to flow during handling. In embodiments of the present disclosure, the planar surface of the solid replication medium can be inspected for contamination prior to transferring to the substrate which is advantageous for deducing overall defectivity on the patterned surface structure on the substrate as the defectivity in each subregion can be monitored and regulated during the process. Embodiments described herein are advantageous compared to conventional imprint techniques which coat a substrate with replication medium and the defectivity of one subregion can be substantially higher than the others and render the pattered substrate unusable for the desired applications.
Embodiments of the present disclosure further provide a curable polymer resin replication medium having its planar surface in contact to a sub-region of a substrate. The curable polymer resin replication medium has a reduced temperature required to allow the material to become substantially flowable in order to conform the planar surface to the substrate. Embodiments described herein are advantageous over conventional imprint lithography as it reduces the process temperature and therefore reduces the potential for distortion of the relief structures of patterned templates due to mismatch of the thermal expansion coefficients of the patterned templates, replication medium, and substrate.
The operation of the present disclosure will be further described with regard to the following detailed examples. These examples are offered to further illustrate the various specific and preferred embodiments and techniques. It should be understood, however, that many variations and modifications may be made while remaining within the scope of the present disclosure.
These Examples are merely for illustrative purposes and are not meant to be overly limiting on the scope of the appended claims. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the present disclosure are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.
Unless otherwise noted, all parts, percentages, ratios, etc. in the Examples and the rest of the specification are by weight. Table 1 provides abbreviations and a source for all materials used in the Examples below:
Patterned template used in this example included a silicon containing release layer assembled according to the “method for release treatment” described in WO2020/095258 over a 5-micron thick structured layer composed of PHOTOMER 6210, SR238, SR351, and IRGACUR TPO in weight ratios of 60/20/20/0.5 on a polycarbonate backing film 4 thousandths of an inch in thickness (0.1 mm). The pattern of the patterned templates was an array of posts 150 nm in diameter and 450 nm in height. The pattern area size was 43 mm by 7 mm.
The substrate used in this example was Fischer 2 by 3 inch (5 cm by 7.6 cm) borosilicate microscope slide prepared by rinsing the with acetone and IPA wiping with a Vectra TX1010 clean room wipe. The substrate was treated with adhesion promoter. A 0.5 wt % solution of 2-(3-trimethoxysilylpropylcarbamoyloxy)ethyl prop-2-enoate; 3M Company (St. Paul), assembled as described in Example 7 of U.S. Pat. No. 9,790,396 in MEK was spin coated onto the substrate. The coating conditions were 1000 rpm for 60 seconds. The coated glass was exposed to a temperature of 140 degrees Celsius for 15 minutes before being cooled to room temperature.
The curable polymeric resin was prepared by combining and mixing DOWANOL PM, Lumicryl 2382, EB350, and TPO, in weight ratios of 796/182/21/1. The curable polymeric resin was spin coated onto the relief structured surface of the patterned template. The spin coating conditions were 500 rpm for 5 seconds and 1000 rpm for 30 seconds after statically applying a sufficient volume of curable polymeric resin to cover the relief structured region of the patterned template. The coated template was exposed to 60 degrees Celsius for 5 minutes to drive off any remaining solvent. The residual material was sufficiently solid at room temperature.
The planer surface of the curable polymeric replication medium was laminated to a treated glass with a hot roll laminator at the lowest speed setting at a temperature of 145° F. (62.8° C.). The nip was engaged with 60 psi (0.41 MPa). A 385 nm LED UV curing lamp was used to cure the replication medium. The sample was cured through the patterned template at 40V, 8A input for 90 seconds. The patterned template was subsequently peeled. By this process, the replication medium was transferred to the glass and the relief structure was exposed.
The substrate used in this example was Corning EAGLE XG 200.0×200.0×0.70 mm glass from Precision Glass & Optics, Santa Ana, CA prepared cleaning with a spin coater and solvent. The spin coater settings were an acetone dynamic dispense at 350 rpm for 10 seconds, IPA dynamic dispense at 350 rpm for 10 seconds, and drying at 1000 rpm for 15 seconds. The substrate was treated with adhesion promoter. A 0.5 wt % solution of 2-(3-trimethoxysilylpropylcarbamoyloxy)ethyl prop-2-enoate; 3M Company (St. Paul), assembled as described in Example 7 of U.S. Pat. No. 9,790,396 in MEK was spin coated onto the substrate. The coating conditions were 500 rpm for 5 seconds and 1000 rpm for 30 seconds. The coated glass was exposed to a temperature of 140 degrees Celsius for 60 minutes before being cooled to room temperature. The patterned template was prepared as in Example 1, except a 3 mil (0.08 mm) primed polyethylene terephthalate film was used as the backing film. The release treatment was preformed as in Example 1.
The curable polymeric resin was prepared by combining and mixing DOWANOL PM, Lumicryl 2382, EB350, and TPO, in weight ratios of 776/193/22/2. The curable polymeric resin was spin coated onto the relief structured surface of the patterned template. The spin coating conditions were 500 rpm for 5 seconds and 1000 rpm for 60 seconds and the coated template was let dry for 2 minutes at room temperature. The replication medium solution was filtered to 0.2 um. A protective layer of Hitachi Chemical Co. LD-K1010-75 (Lot #3926498408) was laminated with a hand roller to the planer surface of the replication medium. The coating was performed on four patterned templates.
The protective layer was removed from the planer surface of the curable polymeric replication medium on the first, second, third, and fourth patterned template. The planer surfaces of the replication medium on the first, second, third, and four patterned templates were simultaneously vacuum laminated (<26.7 Pa) to the first, second, third, and four subregions of the treated glass substrate with 60 psi (0.41 MPa) being applied to the surface of the patterned templates opposite the replication medium coating while being heated at 50 degrees Celsius for 45 minutes. The pressure was reduced from 60 psi (0.41 MPa) to atmospheric pressure (0.10 MPa). A 385 nm LED UV curing lamp was used to cure the replication medium. The sample was cured through the patterned template at 40V, 8A input for 5 minutes. The patterned templates were subsequently peeled. By this process, the replication medium was transferred to the glass and the relief structure was exposed in two subregions of the substrate.
Reference throughout this specification to “one embodiment,” “certain embodiments,” “one or more embodiments” or “an embodiment,” whether or not including the term “exemplary” preceding the term “embodiment,” means that a particular feature, structure, material, or characteristic described in connection with the embodiment is included in at least one embodiment of the certain exemplary embodiments of the present disclosure. Thus, the appearances of the phrases such as “in one or more embodiments,” “in certain embodiments,” “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily referring to the same embodiment of the certain exemplary embodiments of the present disclosure. Furthermore, the particular features, structures, materials, or characteristics may be combined in any suitable manner in one or more embodiments.
While the specification has described in detail certain exemplary embodiments, it will be appreciated that those skilled in the art, upon attaining an understanding of the foregoing, may readily conceive of alterations to, variations of, and equivalents to these embodiments. Accordingly, it should be understood that this disclosure is not to be unduly limited to the illustrative embodiments set forth hereinabove. In particular, as used herein, the recitation of numerical ranges by endpoints is intended to include all numbers subsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5). In addition, all numbers used herein are assumed to be modified by the term “about.”
Furthermore, all publications and patents referenced herein are incorporated by reference in their entirety to the same extent as if each individual publication or patent was specifically and individually indicated to be incorporated by reference. Various exemplary embodiments have been described. These and other embodiments are within the scope of the following claims.
Reference throughout this specification to “one embodiment,” “certain embodiments,” “one or more embodiments” or “an embodiment,” whether or not including the term “exemplary” preceding the term “embodiment,” means that a particular feature, structure, material, or characteristic described in connection with the embodiment is included in at least one embodiment of the certain exemplary embodiments of the present disclosure. Thus, the appearances of the phrases such as “in one or more embodiments,” “in certain embodiments,” “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily referring to the same embodiment of the certain exemplary embodiments of the present disclosure. Furthermore, the particular features, structures, materials, or characteristics may be combined in any suitable manner in one or more embodiments.
While the specification has described in detail certain exemplary embodiments, it will be appreciated that those skilled in the art, upon attaining an understanding of the foregoing, may readily conceive of alterations to, variations of, and equivalents to these embodiments. Accordingly, it should be understood that this disclosure is not to be unduly limited to the illustrative embodiments set forth hereinabove. In particular, as used herein, the recitation of numerical ranges by endpoints is intended to include all numbers subsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5). In addition, all numbers used herein are assumed to be modified by the term “about.”
Furthermore, all publications and patents referenced herein are incorporated by reference in their entirety to the same extent as if each individual publication or patent was specifically and individually indicated to be incorporated by reference. Various exemplary embodiments have been described. These and other embodiments are within the scope of the following claims.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2021/062391 | 12/28/2021 | WO |
Number | Date | Country | |
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63199477 | Dec 2020 | US |