Surface Treatment Compositions and Methods
US-2024258111-A1 · Aug 1, 2024 · US
US2022139704A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022139704-A1 |
| Application number | US-202217572509-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jan 10, 2022 |
| Priority date | Mar 29, 2017 |
| Publication date | May 5, 2022 |
| Grant date | — |
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Provided are a composition for depositing a silicon-containing thin film containing a bis(aminosilyl)alkylamine compound and a method for manufacturing a silicon-containing thin film using the same, and more particularly, a composition for depositing a silicon-containing thin film, containing the bis(aminosilyl)alkylamine compound capable of being usefully used as a precursor of the silicon-containing thin film, and a method for manufacturing a silicon-containing thin film using the same.
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1 . A composition for depositing a silicon-containing thin film, the composition comprising a bis(aminosilyl)alkylamine compound represented by the following Chemical Formula 2 or 3: in Chemical Formula 2 or 3, R is C1-C7alkyl or C2-C7alkenyl; R 5 to R 7 are each independently hydrogen, halogen, C1-C7alkyl, or C2-C7alkenyl; R 11 to R 14 are each independently hydrogen, C1-C5alkyl, or C2-C5alkenyl; and n and m are each independently an integer of 1 to 7. 2 . The composition of claim 1 , wherein in Chemical Formula 2 or 3, R 5 to R 7 are each independently hydrogen or C1-C7alkyl: R 11 to R 14 are each independently hydrogen, C1-C5alkyl, or C2-C5alkenyl; and n and m are each independently an integer of 1 to 4. 3 . The composition of claim 1 , wherein the bis(aminosilyl)alkylamine compound represented by Chemical Formula 2 or 3 is represented by the following Chemical Formula 6 or 7: R is C1-C7alkyl or C2-C7alkenyl; R 11 to R 14 are each independently hydrogen, C1-C7alkyl, or C2-C7alkenyl; and n and m are each independently an integer of 1 to 7. 4 . The composition of claim 3 , wherein in Chemical Formulas 6 and 7, R is C1-C5alkyl; R 11 to R 14 are each independently hydrogen, C1-C5alkyl, or C2-C5alkenyl; and n and m are each independently an integer of 1 to 4. 5 . The composition of claim 1 , wherein the bis(aminosilyl)alkylamine compound is selected from the following compounds: 6 . A bis(aminosilyl)alkylamine compound represented by the following Chemical Formula 2 or 3: in Chemical Formula 2 or 3, R is C1-C7alkyl or C2-C7alkenyl; R 5 to R 7 are each independently hydrogen, halogen, C1-C7alkyl, or C2-C7alkenyl; R 11 to R 14 are each independently hydrogen, C1-C5alkyl, or C2-C5alkenyl; and n and m are each independently an integer of 1 to 7. 7 . The bis(aminosilyl)alkylamine compound of claim 6 , wherein the bis(aminosilyl)alkylamine compound represented by Chemical Formula 2 or 3 is represented by the following Chemical Formula 6 or 7: In Chemical Formulas 6 and 7, R is C1-C7alkyl or C2-C7alkenyl; R 11 to R 14 are each independently hydrogen, C1-C7alkyl, or C2-C7alkenyl; and n and m are each independently an integer of 1 to 7.
the material being a silicon nitride not containing oxygen, e.g. SixNy or SixByNz · CPC title
the material being a silicon oxide, e.g. SiO2 · CPC title
the material being a silicon oxynitride, e.g. SiON or SiON:H · CPC title
the material containing Si, O and at least one of H, N, C, F or other non-metal elements, e.g. SiOC, SiOC:H or SiONC · CPC title
being a silicon carbide or silicon carbonitride and not containing oxygen, e.g. SiC or SiC:H · CPC title
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