Method of manufacturing semiconductor device and chemical liquid
US-10192733-B2 · Jan 29, 2019 · US
US11508569B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11508569-B2 |
| Application number | US-202016983119-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 3, 2020 |
| Priority date | Aug 21, 2019 |
| Publication date | Nov 22, 2022 |
| Grant date | Nov 22, 2022 |
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This disclosure relates to methods and compositions for treating a semiconductor substrate having a pattern disposed on a surface of the substrate. The methods can include a) supplying a sublimating material to a substrate having a pattern disposed on a surface thereof; b) maintaining the sublimating material on the surface for a time sufficient to modify the surface; c) solidifying the sublimating material on the surface; and d) removing by sublimation the sublimating material disposed on the surface.
Opening claim text (preview).
What is claimed is: 1. A method of treating a substrate, comprising: a) providing a sublimating material comprising a sublimating compound in an amount of from about 40% by weight to about 99.5% by weight of the sublimating material and a surface modification agent in an amount of from about 0.5% by weight to about 10% by weight of the sublimating material; b) supplying the sublimating material to a substrate having a pattern disposed on a surface thereof; c) maintaining the sublimating material on the surface for a time sufficient to modify the surface; d) solidifying the sublimating material on the surface; and e) removing by sublimation the sublimating material disposed on the surface; wherein the sublimating compound is selected from the group consisting of glacial acetic acid, octamethylcyclotetrasiloxane, pentafluorophenol, 2-acetyl-5-methyl furan, p-chlorotoluene, acrylic acid, pyrimidine, 4-methyl thiazole, p-xylene, ethylene dibromide, paraldehyde, ethylenediamine, 1,4-dioxane, formic acid, hexafluorobenzene, benzene, cyclohexane, 4-pyridinol, camphene, 2,2-dimethyl-1-propanol, cyanamide, dimethyl carbonate, trimethylsilanol, dimethyl sulfoxide, cyclohexanol, and trimethylacetonitrile. 2. The method of claim 1 , wherein the sublimating compound has a melting point of from about −20° C. to about 60° C. and a vapor pressure of at least about 1 mm Hg at 25° C. 3. The method of claim 1 , wherein the sublimating compound has a melting point of from about 0° C. to about 20° C. 4. The method of claim 1 , wherein the sublimating compound has a surface tension of at most about 65 mN/m at 25° C. 5. The method of claim 1 , wherein the sublimating compound has a viscosity of at most about 5 centistokes at 25° C. 6. The method of claim 1 , wherein the sublimating compound is selected from the group consisting of glacial acetic acid, octamethylcyclotetrasiloxane, pentafluorophenol, 2-acetyl-5-methyl furan, p-chlorotoluene, acrylic acid, pyrimidine, 4-methyl thiazole, p-xylene, ethylene dibromide, paraldehyde, ethylenediamine, 1,4-dioxane, hexafluorobenzene, benzene, cyclohexane, 4-pyridinol, camphene, 2,2-dimethyl-1-propanol, cyanamide, dimethyl carbonate, trimethylsilanol, cyclohexanol, and trimethylacetonitrile. 7. The method of claim 1 , wherein the sublimating compound is in an amount of from about 50% by weight to about 99.5% by weight of the sublimating material. 8. The method of claim 1 , wherein the surface modification agent is in an amount of from about 0.5% by weight to about 9% by weight of the sublimating material. 9. The method of claim 1 , wherein the surface comprises SiO 2 , SiN, TiN, SiOC, SiON, Si, SiGe, Ge, or W. 10. The method of claim 1 , wherein the sublimating material further comprises a catalyst. 11. The method of claim 10 , wherein the catalyst is triflic acid, triflic anhydride, methanesulfonic acid, acetic acid, or acetic anhydride. 12. The method of claim 10 , wherein the catalyst is in an amount of from about 0.1% by weight to about 10% by weight of the sublimating material. 13. The method of claim 1 , wherein the sublimating material further comprises a solvent. 14. The method of claim 13 , further comprising a solvent evaporation step. 15. The method of claim 13 , wherein the solvent is hexyl acetate, n-butyl acetate, t-butyl acetate, propylene glycol methyl ether acetate (PGMEA), or anisole. 16. The method of claim 1 , wherein the surface modification agent comprises a Si-containing compound. 17. The method of claim 16 , wherein the Si-containing compound is a disilazane. 18. The method of claim 17 , wherein the disilazane is hexamethyldisilazane, heptamethyldisilazane, N-methyl hexamethyldisilazane, 1,3-diphenyltetramethyldisilazane, or 1,1,3,3-tetraphenyl-1,3-dimethyldisilazane. 19. The method of claim 16 , wherein the Si-containing compound comprises a trimethylsilyl group. 20. The method of claim 19 , wherein the Si-containing compound is trimethylsilyltriflate, N-(trimethylsilyl)dimethylamine, N-(trimethylsilyl)diethylamine, 4-trimethylsilyloxy-3-penten-2-one, bis(trimethylsilyl)sulfate, methoxytrimethylsilane, ethoxytrimethylsilane, N-allyl-N,N-bis(trimethylsilyl)amine, N-(trimethylsilyl)diethylamine, N,N-bis-trimethylsilyl urea, trimethylsilanol, N-(trimethylsilyl)acetamide, or tris(trimethylsilyl)phosphate. 21. The method of claim 16 , wherein the Si-containing compound is an aminosilane. 22. The method of claim 21 , wherein the aminosilane is triisopropyl(dimethylamino)silane. 23. The method of claim 16 , wherein the Si-containing compound is a siloxane. 24. The method of claim 23 , wherein the siloxane is octamethylcyclotetrasiloxane or 1,3-bis(heptadecafluoro-1,2,2-tetrahydrodecyl)tetramethyldisiloxane.
Cleaning during device manufacture · CPC title
by incorporation in a layer which is removed with the contaminants · CPC title
Electricity · mapped topic
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