The present disclosure generally relates to fabricating a nano-sized structure in a resin element by using nanoimprint lithography (NIL), and specifically relates to reducing adhesive failure during ML demolding by forming a layer of polymerization inhibiting compound at the interface between the molded resin element and the template.
NIL is widely used to fabricate nanometer scale patterns. Nanoimprint lithography is a method of fabricating nanostructure by using a mold having a nano-sized pattern to mold an imprint resist. The imprint resist can be a resin element. Demolding, the process to separate the template from the molded resin element, is one of the processed performed in NIL. Adhesive failure during demolding can destroy the nano-sized structure formed in the molded resin element.
Embodiments relate to fabricating a nano-sized structure in a resin element by nanoimprint lithography (NIL), where adhesive failure during NIL demolding is reduced by inhibiting polymerization at the interface of the template and the molded resin element. The resin element includes a polymerization inhibiting compound, which migrates to a surface of the resin element so that a layer of the polymerization inhibiting compound is formed at the interface of the template and the resin element.
In one or more embodiments, the resin element is made with a mixture of the polymerization inhibiting compound and a resin at a ratio in a range from 1:99 to 1:9. The polymerization inhibiting compound includes at least one of the following functional groups: amine, phenol, quinone, nitroso, persistent free radical, or any combination thereof. The resin is a fluorine resin. A surface of the resin element is exposed to air and another surface of the resin element is attached onto a substrate.
The resin element is aged to promote migration of the polymerization inhibiting compound to the interface of the resin element with air. The aging includes heating the resin element. Thus, a layer of the polymerization inhibiting compound is formed at the interface of the resin element and air. The layer of the polymerization inhibiting compound has a thickness no more than 38 nanometers. The polymerization inhibiting compound inhibits polymerization at the interface.
The template is pressed onto the surface of the resin element that is exposed to air (or the surface of the resin element to the template) to form the nano-sized structure in the NIL resin. The resin element is cured, e.g., by exposing the resin element to ultraviolet light, after the nano-sized structure is formed in the resin element. Then the template is removed from the resin element after the resin element is cured. Because there is no polymerization at the interface of the template and the resin element, the template is not adhered to the resin element. And, there is no adhesive failure while the template is being removed.
Figure (
The figures depict embodiments of the present disclosure for purposes of illustration only.
A nanostructure is fabricated in a resin element by pressing a template onto the resin element. A surface of the template has a nano-sized pattern and contacts with the resin element during the pressing. A layer of polymerization inhibiting compound is formed at the interface of the template and the resin element before or during the pressing. The polymerization inhibiting compound includes one or more functional groups that inhibit polymerization at the interface so that the interface is not adhesive. Therefore, adhesive failure during demolding is inhibited.
Figure (
The template 110 can be a hard template. The hard template has a rigid structure (i.e., including a rigid nano-sized pattern). It can be made from polymer microspheres, porous membrane, plastic foam, ion exchange resin, carbon fiber, porous anodic aluminum oxide, or other types of rigid materials. Because the nano-sized pattern is rigid, the dimensions and configuration of the nano-sized structure in the resin element 120 can be precisely controlled. The template 110 can also be a soft template. Different from the hard template, the soft template has a flexible structure. The soft template can be made from surfactant, polymer, biopolymer, or other types of non-rigid materials. Compared with the hard template, the soft template is easier to build and remove. Also, it does not require complex equipment and strict production conditions.
The resin element 120 includes a resin having low surface energy, such as a fluorine resin. In one example, the resin element 120 comprises a fluorinated phenolic resin. Because the surface energy is low, the resin element is not sticky, which facilitates demolding (i.e., removing the template 110 from the resin element 120 after the nano-sized structure is formed). In the embodiment of
The layer of the polymerization inhibiting compound 130 is at the interface of the template 110 and the resin element 120. In some embodiments, the thickness of the layer is no more than 10 nm to avoid destroying the nano-sized pattern 215. In one embodiment, the thickness of the layer is in the range from 5 nm to 10 nm. The polymerization inhibiting compound 130 is a polymer that includes at least one of the following functional groups: amine, phenol, quinone, nitroso, persistent free radical, or some combination thereof. Examples of persistent free radicals include nitroxide, alkoxyamine, etc. The functional groups inhibit polymerization at the interface so that the interface is not adhesive. Therefore, it is easy to remove the template 110 from the resin element 120. And, adhesive failure during demolding is prevented. The layer of the polymerization inhibiting compound 130 can be formed by different process, including depositing the polymerization inhibiting compound 130 onto the template 110, diffusing the polymerization inhibiting compound 130 from the template 110 to the interface, or promoting migration of the polymerization inhibiting compound 130 from the resin element 120 to the interface. These processes are described below in detail.
The polymerization inhibiting compound 220 can be deposited physically or chemically. For example, the polymerization inhibiting compound 220 is deposited by using vapor deposition, initiated chemical vapor deposition (iCVD), atomic layer deposition (ALD), other types of deposition methods, or some combination thereof. The vapor deposition may be conducted under a reduced pressure. The iCVD may be conducted at a temperature no more than 100° C. so that chemistry of the polymerization inhibiting compound 220 and the template 210 are not affected during the deposition. In embodiments where the polymerization inhibiting compound is chemically deposited onto the surface of the template 210, the template 210 is prepared to be ready for the deposition beforehand. For example, before the chemical deposition, the template 210 is exposed to oxygen plasma to increase the concentration of hydroxyl groups at the surface having the nano-sized pattern 215. With the increased concentration of hydroxyl groups at the surface, the deposited polymerization inhibiting compound 220 can chemically bond to the surface. Alternatively or additionally, the polymerization inhibiting compound 220 can include a moiety that can chemically bond to the surface of the template 210 through coupling chemistry, such as alkoxysilane, chlorosilane, etc.
After the layer of the polymerization inhibiting compound 220 is deposited, the template 210 is pressed onto the resin element 230 attached on a substrate 240, as shown in
The pressing is completed in
After the resin element 230 is cured, the template 210 is removed from the resin element 230, as shown in
The NIL process also includes pressing 320 the surface of the template onto a resin element or the resin element onto the surface of the template to form the nano-sized structure in the resin element. The resin element is attached on a substrate.
The NIL process further includes curing 330 the resin element after forming the nano-sized structure in the resin element. The resin element can be cured by free radical curing or cationic curing.
Finally, the NIL process includes removing 340 the template from the resin element after curing the resin element. The functional groups of the polymerization inhibiting compound inhibit polymerization at the interface of the template and the resin element so that it is not adhesive at the interface. When the template is removed, the nano-sized structure formed in the resin element will be preserved.
The NIL process is advantageous for fabricating complicated nano-sized structures because the deposited layer of the polymerization inhibiting compound conforms to the nano-sized pattern of the template. And, the thickness of the layer is even across the whole deposited area. It is easy to control the thickness of the layer by conducting monolayer deposition.
In the embodiment of
As a result of the diffusion, a layer of the polymerization inhibiting compound 420 is formed at the interface of the template 410 and the resin element 430, as shown in
Next, the template 410 is removed from the molded resin element 430, as shown in
The NIL process also includes diffusing 520 the polymerization inhibiting compound from the template to the resin element to form a layer of the polymerization inhibiting compound at the interface of the template and the resin element. The diffusion is performed by holding the template together with the resin from five seconds to two minutes. In some embodiments, the diffusion is performed while the template and/or the resin are heated in order to increase the diffusion rate. The layer of the polymerization inhibiting compound formed by the diffusion has a thickness no more than 10 nm.
The NIL process further includes curing 530 the resin element after diffusing the polymerization inhibiting compound. The resin element is cured by being exposed to ultraviolet light. The ML process also includes removing 540 the template from the resin element after curing the resin element. The polymerization inhibiting compound at the interface of the resin element and template prevents adhesive failure during the removing.
Compared with the NIL process in
The NIL process also includes pressing 720 a surface of a template having a nano-sized pattern onto the surface of the resin element exposed to the air to form the nano-sized structure in the resin element. During and after the pressing, the polymerization inhibiting compound remains at the interface of the template and the resin element.
The NIL process further includes curing 730 the resin element after forming the nano-sized structure in the resin element and removing 740 the template from the resin element after curing the resin element. As discussed above, because the polymerization inhibiting compound inhibits polymerization at the interface of the molded resin element and the template, there is no adhesive failure during the removing.
The NIL process has multiple advantages. One advantage is that there is no additional step to prepare the layer of the polymerization inhibiting compound since the layer is formed during the aging process. Another advantage is that the template and the polymerization inhibiting compound does not have to have orthogonal polymerization chemistries since the polymerization inhibiting compound is formed in the resin element. Thus, there are more materials that can be selected as the polymerization inhibiting compound.
| Number | Name | Date | Kind |
|---|---|---|---|
| 4090997 | Patel | May 1978 | A |
| 4535041 | Fielding et al. | Aug 1985 | A |
| 5079131 | Thackeray et al. | Jan 1992 | A |
| 5212028 | Fujino | May 1993 | A |
| 5278029 | Shirai et al. | Jan 1994 | A |
| 5407787 | McElhanon et al. | Apr 1995 | A |
| 5658711 | Matsuo et al. | Aug 1997 | A |
| 6358653 | Turberfield et al. | Mar 2002 | B1 |
| 6372406 | Brunsvold et al. | Apr 2002 | B1 |
| 6379869 | Schroeder et al. | Apr 2002 | B1 |
| 6673525 | Wheeler | Jan 2004 | B1 |
| 8198018 | Mennig et al. | Jun 2012 | B2 |
| 10857724 | Lane et al. | Dec 2020 | B1 |
| 11173649 | Austin et al. | Nov 2021 | B1 |
| 20040115566 | Reichmanis et al. | Jun 2004 | A1 |
| 20050271900 | Kobrin et al. | Dec 2005 | A1 |
| 20060281320 | Lin et al. | Dec 2006 | A1 |
| 20070282030 | Anderson et al. | Dec 2007 | A1 |
| 20080131791 | Cho | Jun 2008 | A1 |
| 20080254375 | Hayashida et al. | Oct 2008 | A1 |
| 20100038831 | Kawaguchi et al. | Feb 2010 | A1 |
| 20110008577 | Miyake et al. | Jan 2011 | A1 |
| 20110319516 | Xu | Dec 2011 | A1 |
| 20130108956 | Lu et al. | May 2013 | A1 |
| 20130281713 | Willson et al. | Oct 2013 | A1 |
| 20140030660 | Takanashi | Jan 2014 | A1 |
| 20140054822 | Ellison et al. | Feb 2014 | A1 |
| 20140209565 | Nakamura et al. | Jul 2014 | A1 |
| 20140235727 | Tufts | Aug 2014 | A1 |
| 20150079793 | Hattori | Mar 2015 | A1 |
| 20150099228 | Hatakeyama et al. | Apr 2015 | A1 |
| 20150301452 | Park et al. | Oct 2015 | A1 |
| 20170371240 | Liu | Dec 2017 | A1 |
| 20200090987 | Chandhok | Mar 2020 | A1 |
| 20200131337 | Matsumura | Apr 2020 | A1 |
| Number | Date | Country |
|---|---|---|
| H03146954 | Jun 1991 | JP |
| H1073713 | Mar 1998 | JP |
| Entry |
|---|
| United States Office Action, U.S. Appl. No. 16/216,809, filed Jun. 11, 2020, 10 pages. |
| Campbell et al., “Fabrication of Photonic Crystals for the Visible Spectrum by Holographic Lithography”, Nature, vol. 404, Mar. 2000, pp. 53-56. |
| ChemSpider, Royal Society of Chemisty, Boiling Point Data for 3, 6-Dihydro2H-Pyran, 2021, 3 Pages. |
| Ciapurin I.V., et al., “Modeling of Phase Volume Diffractive Gratings, Part 1: Transmitting Sinusoidal Uniform Gratings,” Optical Engineering, Jan. 2006, vol. 45 (1), pp. 1-9. |
| Miao Y, et al., “Vapor-Deposited Fluorinated Glycidyl Copolymer Thin Films with Low Surface Energy and Improved Mechanical Properties,” Macromolecules, vol. 39, No. 11, 2006, pp. 3895-3900. |
| Non-Final Office Action dated Sep. 13, 2021 U.S. Appl. No. 17/083,826, filed Oct. 29, 2020, 8 pages. |
| Non-Final Office Action dated Sep. 22, 2021 for U.S. Appl. No. 16/216,798, filed Dec. 11, 2018, 13 pages. |
| Pham V.Q., et al., “Positive Tone Photoresist Process for Supercritical Carbon Dioxide Development”, Chemistry of Materials, American Chemical Society, 2003, vol. 15 (26), pp. 4893-4895. |
| Stein A., et al., “Design and Functionality of Colloidal-Crystal-Templated Materials-Chemical Applications of Inverse Opals,” Chemical Society Reviews, 2013, vol. 42, pp. 2763-2803. |