Holding device, method of determining attraction abnormality in holding device, lithography apparatus, and method of manufacturing article
US-2024393682-A1 · Nov 28, 2024 · US
US9417520B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9417520-B2 |
| Application number | US-201414171919-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 4, 2014 |
| Priority date | Feb 18, 2013 |
| Publication date | Aug 16, 2016 |
| Grant date | Aug 16, 2016 |
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A method of patterning a block copolymer layer, the method including: providing a substrate including a topographic pattern on a surface of the substrate, wherein the topographic pattern includes a trench and a mesa; forming, on the surface of the substrate, an underlayer including a polymer, wherein the polymer includes a repeating unit derived from a substituted or unsubstituted aromatic vinyl monomer and has an anchoring group; heat-treating the underlayer to anchor the underlayer to the surface of the substrate via the anchoring group; irradiating the heat-treated underlayer with light to form a crosslinked polymer with a crosslink between carbon atoms of main chains of the polymer; forming a block copolymer layer on the underlayer including the crosslinked polymer; and heat-treating the block copolymer layer to form a self-assembled structure of the block copolymer directed by the topographic pattern.
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What is claimed is: 1. A method of patterning a block copolymer layer, the method comprising: providing a substrate comprising a topographic pattern on a surface of the substrate, wherein the topographic pattern comprises a trench and a mesa; forming, on the surface of the substrate, an underlayer comprising a polymer, having an anchoring group, wherein the polymer consists of a first repeating unit derived from a substituted or unsubstituted aromatic vinyl monomer or a combination of the first repeating unit and a second repeating unit derived from at least one non-aromatic vinyl monomer selected from a substituted or unsubstituted C1 to C10 alkyl(meth)acrylate, and a substituted or unsubstituted C6 to C20 aryl(meth)acrylate; heat-treating the underlayer to anchor the underlayer to the surface of the substrate via the anchoring group; irradiating the heat-treated underlayer with light to form a crosslinked polymer with a crosslink between carbon atoms of main chains of the polymer, wherein an aromatic group of the first repeating unit is directly linked to a main chain carbon atom of the polymer; forming a block copolymer layer on the underlayer comprising the crosslinked polymer; and heat-treating the block copolymer layer to form a self-assembled structure of the block copolymer directed by the topographic pattern, wherein the light in the irradiating the heat-treated underlayer is a UV light having a wavelength of shorter than or equal to about 300 nanometers, wherein the anchoring group is selected from a hydroxyl group, a thiol group, an azide group, a carboxylic acid group, an amide group, an amine group, or a trichlorosilane group, and wherein the anchoring group is disposed at a main chain carbon atom of the terminal end of the polymer. 2. The method of claim 1 , wherein the polymer in the underlayer comprises a repeating unit derived from a vinyl monomer comprising a substituted or unsubstituted benzene moiety, a substituted or unsubstituted naphthalene moiety, a substituted or unsubstituted anthracene moiety, a substituted or unsubstituted pyridine moiety, a substituted or unsubstituted pyrrole moiety, a substituted or unsubstituted furan moiety, or a substituted or unsubstituted thiophene moiety. 3. The method of claim 1 , wherein the polymer in the underlayer comprises a repeating unit derived from a substituted or unsubstituted styrene, a substituted or unsubstituted vinyl naphthalene, a substituted or unsubstituted vinylanthracene, a substituted or unsubstituted vinylpyridine, a substituted or unsubstituted vinylpyrrole, a substituted or unsubstituted vinylfuran, a substituted or unsubstituted vinylthiophene, or a combination thereof. 4. The method of claim 1 , wherein the polymer in the underlayer comprises a repeating unit derived from styrene, a C1 to C10 alkyl substituted styrene, a halogen substituted styrene, 1-vinylpyrrole, 2-vinylpyrrole, 3-vinylpyrrole, 2-vinylpyridine, 4-vinylpyridine, 2-vinylfuran, 3-vinylfuran, 2-vinylthiophene, 3-vinylthiophene, or a combination thereof. 5. The method of claim 1 , wherein the polymer in the underlayer is a homopolymer, a random copolymer, or a block copolymer. 6. The method of claim 1 , wherein the polymer in the underlayer is a hydroxy-terminated polystyrene, a hydroxy-terminated poly(methylstyrene), a hydroxy-terminated poly(ethylstyrene), a hydroxy-terminated poly(4-t-butylstyrene), a hydroxy-terminated poly(chlorostyrene), a hydroxy-terminated poly(2-vinylpyridine), a hydroxy-terminated poly(4-vinylpyridine), a hydroxy-terminated poly(1-vinylpyrrole), a hydroxy-terminated poly(2-vinylpyrrole), a hydroxy-terminated poly(vinylpyrrole), a hydroxy-terminated poly(methylmethacrylate-co-styrene) random copolymer, a hydroxy-terminated poly(styrene-co-vinylpyridine) random copolymer, a hydroxy-terminated poly(methylmethacrylate-co-vinylpyridine) random copolymer, or a combination thereof. 7. The method of claim 1 , wherein the heat-treating the underlayer is conducted at a temperature of greater than or equal to about 80° C. for about 30 minutes or longer. 8. The method of claim 1 , further comprising washing the heat-treated underlayer with an organic solvent prior to the irradiating the heat-treated underlayer with light. 9. The method of claim 8 , wherein the organic solvent is a C6 to C20 aromatic hydrocarbon, a C5 to C10 aliphatic hydrocarbon, a ketone, or a combination thereof. 10. The method of claim 1 , wherein the irradiating the heat-treated underlayer with light is conducted at a light intensity of greater than or equal to about 10 Joules/centimeter 2 . 11. The method of claim 1 , wherein the block copolymer comprises a block copolymer comprising a first repeating unit comprising styrene or a derivative thereof and a second repeating unit comprising (meth)acrylic acid ester, a block copolymer comprising a first repeating unit comprising styrene or a derivative thereof and a second repeating unit comprising siloxane or a derivative thereof, a block copolymer comprising a first repeating unit comprising styrene or a derivative thereof and a second repeating unit comprising an olefin, or a block copolymer comprising a first repeating unit comprising styrene or a derivative thereof and a second repeating unit comprising an alkylene oxide. 12. The method of claim 1 , wherein the block copolymer self-assembled by the heat-treating of the block copolymer layer comprises a cylinder structure parallel to the substrate or a lamella structure perpendicular to the substrate. 13. The method of claim 1 , wherein a thickness of the block copolymer layer is greater than or equal to 15 nanometers so that a self-assembled structure of the block copolymer is directed by the topographic pattern both in the trench and on the mesa. 14. The method of claim 1 , wherein a thickness of the underlayer is substantially equal to a depth of the trench so that a self-assembly of the block copolymer is directed in a direction orthogonal to the topographic pattern. 15. A patterned polymer structure including a substrate, an underlayer disposed on a surface of the substrate, and a block copolymer layer patterned on the underlayer, wherein the underlayer comprises a crosslinked polymer consisting of a first repeating unit derived from a substituted or unsubstituted aromatic vinyl monomer or a combination of the first repeating unit and a second repeating unit derived from at least one non-aromatic vinyl monomer selected from a substituted or unsubstituted C1 to C10 alkyl(meth)acrylate, and a substituted or unsubstituted C6 to C20 aryl(meth)acrylate, the crosslinked polymer is linked to the substrate via a moiety derived from an anchoring group, wherein the crosslinked polymer comprises a crosslink between carbon atoms of a main chain of the polymer, and an aromatic group of the first repeating unit is directly linked to a carbon atom of the main chain of the polymer, wherein the anchoring group is selected from a hydroxyl group, a thiol group, an azide group, a carboxylic acid group, an amide group, an amine group, or a trichlorosilane group, and wherein the anchoring group is disposed at a main chain carbon atom of the terminal end of the polymer.
Lithographic processes using patterning methods other than those involving the exposure to radiation, e.g. by stamping · CPC title
Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] · CPC title
of organic photoresist masks · CPC title
of masks comprising organic materials · CPC title
Exposure without an original mask, e.g. using a programmed deflection of a point source, by scanning, by drawing with a light beam, using an addressed light or corpuscular source (G03F7/70 takes precedence) · CPC title
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