Compositions for extreme ultraviolet lithography and related methods
US-2024092810-A1 · Mar 21, 2024 · US
US9857684B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9857684-B2 |
| Application number | US-201615072635-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 17, 2016 |
| Priority date | Mar 17, 2016 |
| Publication date | Jan 2, 2018 |
| Grant date | Jan 2, 2018 |
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A photoresist composition and methods of using the same are disclosed. The photoresist includes a polymer backbone, an acid labile group (ALG) chemically bonded to the polymer backbone, a photo-acid generator (PAG), a solvent, and a silicon-containing unit that is chemically bonded to one of: the ALG and a crosslinker. A method of using the photoresist composition includes forming a layer of the photoresist over a substrate, performing an exposing process to the photoresist layer; and developing the photoresist layer, thereby forming a patterned photoresist layer. The patterned photoresist layer includes the silicon-containing unit.
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What is claimed is: 1. A method for lithography patterning, comprising: forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer backbone, an acid labile group (ALG) chemically bonded to the polymer backbone, a photo-acid generator (PAG), a solvent, and a silicon-containing unit chemically bonded to a crosslinker; performing an exposing process to the photoresist layer; and developing the photoresist layer to remove portions of the photoresist layer that are not exposed by the exposing process, thereby forming a patterned photoresist layer. 2. The method of claim 1 , further comprising: baking the photoresist layer before the developing of the photoresist layer. 3. The method of claim 1 , wherein the silicon-containing unit is chemically bonded to the crosslinker through an intermediate bonding unit. 4. The method of claim 3 , wherein the intermediate bonding unit is an aromatic ring or a chain with 1 to 6 carbon atoms. 5. The method of claim 4 , wherein the chain comprises an alkyl group, an alkoxy group, a fluoro alkyl group, or a fluoroalkoxy group. 6. The method of claim 1 , wherein the crosslinker comprises amine, aziridine, hydroxyl, aliphatic epoxy, cycloaliphatic epoxy, oxetane, or maleic anhydride. 7. The method of claim 1 , wherein the silicon-containing unit comprises a silsesquioxane. 8. The method of claim 7 , wherein the silsesquioxane is a cage silsesquioxane, an incomplete cage silsesquioxane, a ladder silsesquioxane, or a random silsesquioxane. 9. The method of claim 1 , wherein the silicon-containing unit is also chemically bonded to another crosslinker. 10. The method of claim 1 , wherein the photoresist layer further includes another silicon-containing unit that is chemically bonded to the polymer backbone. 11. The method of claim 1 , wherein the photoresist layer further includes a polar unit that is chemically bonded to the polymer backbone, the polar unit comprising hydroxyl adamantine, norbornane lactone, γ-butyrolactone, or derivatives thereof. 12. A method for lithography patterning, comprising: forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer backbone, a first silicon-containing unit chemically bonded to the polymer backbone, an acid labile group (ALG) chemically bonded to the polymer backbone, a photo-acid generator (PAG), a solvent, and a second silicon-containing unit chemically bonded to a crosslinker, wherein the crosslinker is bondable to the polymer backbone if the ALG is cleaved off thereof; performing an exposing process to the photoresist layer, resulting in the ALG being cleaved off of the polymer backbone and the crosslinker bonding to the polymer backbone; and developing the photoresist layer to remove portions of the photoresist layer that are not exposed by the exposing process, thereby forming a patterned photoresist layer. 13. The method of claim 12 , wherein the crosslinker comprises amine, aziridine, hydroxyl, aliphatic epoxy, cycloaliphatic epoxy, oxetane, or maleic anhydride. 14. The method of claim 12 , wherein the second silicon-containing unit comprises a cage silsesquioxane, an incomplete cage silsesquioxane, a ladder silsesquioxane, or a random silsesquioxane. 15. The method of claim 12 , wherein the second silicon-containing unit is also chemically bonded to another crosslinker that is bondable to the polymer backbone after the ALG is cleaved off therefrom. 16. The method of claim 12 , wherein the photoresist layer further includes a polar unit that is chemically bonded to the polymer backbone, the polar unit comprising hydroxyl adamantine, norbornane lactone, γ-butyrolactone, or derivatives thereof. 17. The method of claim 12 , wherein the second silicon-containing unit is chemically bonded to the crosslinker through an intermediate bonding unit, the intermediate bonding unit is a chain comprising a fluoro alkyl group, or a fluoroalkoxy group. 18. A method for lithography patterning, comprising: forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer backbone, a first silicon-containing unit chemically bonded to the polymer backbone, a polar unit chemically bonded to the polymer backbone, an acid labile group (ALG) chemically bonded to the polymer backbone, a photo-acid generator (PAG), a solvent, and a second silicon-containing unit chemically bonded to a crosslinker; performing an exposing process to the photoresist layer; and developing the photoresist layer, thereby forming a patterned photoresist layer, wherein the polar unit comprises hydroxyl adamantine, norbornane lactone, γ-butyrolactone, or derivatives thereof. 19. The method of claim 18 , wherein the ALG is cyclopentane, cyclohexane, adamantane, norbornane, or a derivative thereof. 20. The method of claim 18 , wherein the photoresist layer becomes more hydrophilic if the ALG is cleaved off of the polymer backbone.
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Exposure; Apparatus therefor (photographic printing apparatus for making copies G03B27/00) · CPC title
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