Bottom-up conformal coating and photopatterning on PAG-immobilized surfaces

US11768435B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11768435-B2
Application numberUS-201916671426-A
CountryUS
Kind codeB2
Filing dateNov 1, 2019
Priority dateNov 2, 2018
Publication dateSep 26, 2023
Grant dateSep 26, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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Materials and methods to immobilize photoacid generators on semiconducting substrates are provided. PAG-containing monomers are copolymerized with monomers to allow the polymer to bind to a surface, and optionally copolymerized with monomers to enhance solubility to generate PAG-containing polymers. The PAG-containing monomers can be coated onto a surface, where the immobilized PAGs can then be used to pattern materials coated on top of the immobilized PAGs, allowing direct patterning without the use of a photoresist, thereby reducing process steps and cost. The disclosed materials and processes can be used to produce conformal coatings of controlled thicknesses.

First claim

Opening claim text (preview).

We claim: 1. A method of forming a structure, said method comprising: applying an acid-generating composition on a substrate surface, or on one or more intermediate layers optionally present on said substrate surface, said acid-generating composition comprising a polymer including recurring monomers comprising an acid-generating group; heating said acid-generating composition to form an acid-generating layer having an average thickness of between 2 nm and 5 nm; applying an acid-sensitive composition on said acid-generating layer, said acid-sensitive composition comprising less than about 0.5% by weight total of acids, photoacid generators, and thermal acid generators, based upon the total weight of the composition taken as 100% by weight; heating said acid-sensitive composition to form an acid-sensitive layer; and exposing at least a portion of said acid-sensitive layer to radiation. 2. The method of claim 1 , said polymer further comprising recurring monomers comprising a surface adhesion group. 3. The method of claim 2 , wherein said surface adhesion group is selected from the group consisting of hydroxys, epoxies, carboxylic acids, thiols, silanes, aldehydes, acetylacetonates, and combinations of the foregoing. 4. The method of claim 2 , wherein said recurring monomers comprising the surface adhesion group are selected from the group consisting of 2-hydroxyethyl methacrylate, hydroxypropyl methacrylate, glycidyl methacrylate, methacrylic acid, acrylic acid, mono-2-(methacryloyloxy)ethyl succinate, 2-(methylthio)ethyl methacrylate, 3-(trimethoxy silyl)propyl methacrylate, 3-[(4-ethenylphenyl)methoxy]-benzaldehyde, 2-(methacryloyloxy)ethyl acetoacetate, and combinations of the foregoing. 5. The method of claim 1 , wherein said acid-generating group is selected from the group consisting of onium salts, substituted forms of onium salts, triazines, and combinations thereof. 6. The method of claim 1 , wherein said acid-generating group is selected from the group consisting of triphenyl sulfonium perfluorosulfonates, alkyl-substituted triphenyl sulfonium perfluorosulfonates nonaflates, tris(4-tert-butylphenyl)sulfonium perfluoro-1-butanesulfonate, N-hydroxynaphthalimide triflate, N-hydroxy-5-norbornene-2,3-dicarboximide perfluoro-1-butanesulfonate), 2-methyl-2-(2 ‘-furylethylidene)-4,6-bis(trichloromethyl)-1,3,5-triazine, 24(4’-methoxy)styryl]-4,6-bis(trichloromethyl)-1,3,5-triazine, and combinations thereof. 7. The method of claim 1 , wherein said acid-generating group is bonded to a monomer selected from the group consisting of acrylates, acrylamides, acrylonitriles, esters, amides, aromatic amines and diamines, dianhydrides, and combinations thereof. 8. The method of claim 1 , wherein said recurring monomers comprising an acid-generating group include at least one of triphenylsulfonium 3-sulfopropyl methacrylate or triphenyl sulfonium 4-(methacryloxy)-2,3,5,6-tetrafluoro benzenesulfonate. 9. The method of claim 8 , wherein said polymer further comprises recurring monomers of at least one of hydroxyethylmethacrylate and styrene. 10. The method of claim 1 , said polymer further comprising recurring monomers comprising a solubility enhancing monomer selected from the group consisting of styrene, methyl methacrylate, methylstyrene, 4-tert-butylstyrene, n-butyl methacrylate, benzyl methacrylate, and combinations thereof. 11. The method of claim 1 , wherein said acid-generating composition comprises from about 0.5% to about 5% by weight of said polymer and about 95% to about 99.5% by weight of one or more solvents. 12. The method of claim 1 , said acid-sensitive composition further comprising a polymer chosen from: a polymer that crosslinks upon exposure to an acid so that the portion exposed to radiation becomes insoluble in photoresist developers; (ii) a polymer comprising recurring monomers having a protecting group that is removable upon exposure to an acid so as to change the solubility of the portion exposed to radiation; and (iii) a polymer that crosslinks upon exposure to heat and that decrosslinks upon exposure to an acid. 13. The method of claim 1 , wherein said acid-sensitive layer is chosen from: a layer comprising from about 50% to about 90% by weight carbon, based on the total solids in the layer taken as 100% by weight; or a layer comprising from about 10% to about 50% by weight silicon, based on the total solids in the layer taken as 100% by weight. 14. The method of claim 1 , wherein said substrate surface is on a semiconductor substrate selected from the group consisting of silicon, SiGe, SiO 2 , Si 3 N 4 , SiON, aluminum, tungsten, tungsten silicide, gallium arsenide, germanium, tantalum, tantalum nitride, Ti 3 N 4 , hafnium, HfO 2 , ruthenium, indium phosphide, coral, black diamond, glass, or mixtures of the foregoing. 15. The method of claim 1 , further comprising, after said exposing, selectively removing portions of said acid-sensitive layer to form a pattern. 16. The method of claim 15 , further comprising transferring said pattern into said one or more intermediate layers, if present, and into said substrate surface. 17. The method of claim 1 , wherein said substrate surface comprises topography formed therein. 18. The method of claim 1 , wherein: said substrate surface includes at least one of: a trench having sidewalls, there being an initial trench width between said sidewalls; and raised features having respective sidewalls that are spaced an initial width apart; and said applying an acid-generating composition comprises applying said acid-generating composition on said trench sidewalls, said raised feature sidewalls, or both said trench sidewalls and said raised feature sidewalls, said method further comprising removing at least some of said acid-sensitive layer so as to create one or both of the following: a second width between trench sidewalls that is smaller than said initial trench width; and a second width between said sidewalls that is smaller than said initial width between said respective sidewalls. 19. The method of claim 1 , wherein said acid-generating composition is selectively applied to areas on said substrate surface. 20. The method of claim 19 , wherein said selectively applied is accomplished by including one or both of the following on said substrate surface: one or more areas to which said acid-generating composition has an affinity; and one or more areas to which said acid-generating composition lacks an affinity. 21. The method of claim 20 , wherein said substrate surface includes raised features having respective sidewalls and said one or more areas to which said acid-generating composition has an affinity are on said respective sidewalls, wherein said applying said acid-generating composition comprises applying said acid-generating composition to said sidewalls, and further comprising removing at least some of said raised features to leave spacers formed of said acid-generating composition. 22. The method of claim 21 , wherein said spacers are used as a pattern that is transferred to said one or more intermediate layers, if present, and to said substrate surface. 23. A microelectronic structure comprising: a substrate having a surface; one or more optional intermediate layers on said substrate surface; an acid-generating layer on said one or more optional intermediate layers, if present, or on said substrate surface, if no intermediate layers are present, said acid-generating layer having

Assignees

Inventors

Classifications

  • Manufacture or treatment of masks on semiconductor bodies, e.g. by lithography or photolithography · CPC title

  • G03F7/0955Primary

    one of the photosensitive systems comprising a non-macromolecular photopolymerisable compound having carbon-to-carbon double bonds, e.g. ethylenic compounds · CPC title

  • Styrene · CPC title

  • and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate · CPC title

  • and containing oxygen, e.g. 2-sulfoethyl (meth)acrylate · CPC title

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What does patent US11768435B2 cover?
Materials and methods to immobilize photoacid generators on semiconducting substrates are provided. PAG-containing monomers are copolymerized with monomers to allow the polymer to bind to a surface, and optionally copolymerized with monomers to enhance solubility to generate PAG-containing polymers. The PAG-containing monomers can be coated onto a surface, where the immobilized PAGs can then be…
Who is the assignee on this patent?
Brewer Science Inc
What technology area does this patent fall under?
Primary CPC classification G03F7/0955. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Sep 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 9 related publications on this page (citations in our corpus or others sharing the same primary CPC).