Low refractive index layer, laminated film, method for producing low refractive index layer, method for producing laminated film, optical element, and image display device
US-2018215124-A1 · Aug 2, 2018 · US
US12550643B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12550643-B2 |
| Application number | US-202117355154-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 22, 2021 |
| Priority date | Jun 22, 2021 |
| Publication date | Feb 10, 2026 |
| Grant date | Feb 10, 2026 |
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Novel cyclic silicon precursors and oxidants are described. Methods for depositing silicon-containing films on a substrate are described. The substrate is exposed to a silicon precursor and a reactant to form the silicon-containing film (e.g., elemental silicon, silicon oxide, silicon nitride). The exposures can be sequential or simultaneous.
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What is claimed is: 1 . A method of depositing a silicon-containing material on a semiconductor substrate, the method comprising exposing the semiconductor substrate to a cyclic silicon precursor and a reactant, the cyclic silicon precursor includes a 3- or 4-membered ring containing silicon, wherein the cyclic silicon precursor has a general formula of: where X and Y are independently selected from SiH2, NH, S, or Se, wherein at least one of X or Y is S, and R1, R2, R3, and R4 are independently selected from an alkyl group. 2 . The method of claim 1 , wherein the silicon-containing material comprises silicon nitride and the reactant is selected from the group consisting of hydrazine, alkyl hydrazine, allyl hydrazine, hydrogen (H2), ammonia (NH 3 ), R′NH 2 , R′ 2 NH, R′ 3 N, R′ 2 SINH 2 , (R′sSi) 2 NH, and (R′ 3 Si) 3 N, where each R′ is independently H or an alkyl group having 1-12 carbon atoms. 3 . The method of claim 1 , wherein the silicon-containing material comprises silicon nitride comprising a nitrogen containing content in a range of from 1% to 40% on an atomic basis. 4 . The method of claim 1 , wherein the cyclic silicon precursor comprises 5 . The method of claim 1 , wherein the silicon-containing material comprises silicon oxide, and the reactant is selected from the group consisting of an oxaziridine and a P/S/N oxide. 6 . The method of claim 5 , wherein the reactant is an oxaziridine. 7 . The method of claim 6 , wherein the silicon oxide film comprises greater than 98 atomic % of silicon and oxygen atoms. 8 . The method of claim 6 , wherein the oxaziridine comprises a compound with a general formula of: where R 1 , R 2 and R 3 are independently selected from H, SO 2 NO 2 , CN, C1-C8 alkyl, C1-C8 perfluoroalkyl, pyridine, aryl, substituted aryl, perfluoroaryl, SO 2 -NO 2 substituted aryl, or R 2 and R 3 are combined to form a carbonyl. 9 . The method of claim 6 , wherein the oxaziridine comprises one or more of: 10 . The method of claim 6 , wherein the oxaziridine is bicyclic. 11 . The method of claim 10 , wherein the oxaziridine comprises one or more of: 12 . The method of claim 5 , wherein the P/S/N oxide comprises a compound with a general formula of: where R 4 , R 5 and R 6 are independently selected from H, alkyl, or aryl, and R 4 and R 5 may join to form a three to six membered ring including at least one P, S or N heteroatom. 13 . The method of claim 12 , wherein comprises one or more of H 3 PO, (CH 3 ) 3 PO, (C 2 H 5 ) 3 PO, MPPO (3-methyl-1-phenyl-2-phospholene 1-oxide), 3-methyl-1-phenyl-2-phospholene 1-oxide, neopentylene phosphite (5,5-Dimethyl-1,3,2-dioxaphosphinane 2-oxide), HASPO-1 (4,4,5,5-Tetramethyl-1,3,2-dioxaphospholane 2-oxide), 2-Methyl-4,4,5,5-tetramethyl-1,3,2-dioxaphospholan-2-one, or diphenylphosphine oxide. 14 . The method of claim 12 , wherein comprises one or more of H 2 SO, or MPSO (methyl phenyl sulfoxide). 15 . The method of claim 12 , wherein comprises one or more of H 3 N→O, trimethylamine n-oxide, pyridine-n-oxide, TEMPO ((2,2,6,6-Tetramethylpiperidin-1-yl)oxyl), N-hydroxyphthalimide, or 4-methylmorpholine n-oxide. 16 . A method of depositing a silicon-containing material on a semiconductor substrate, the method comprising exposing the semiconductor substrate to a cyclic silicon precursor and a reactant, the cyclic silicon precursor includes a 3- or 4-membered ring containing silicon, wherein the cyclic silicon precursor has a general formula of: where X and Y are independently selected from SiH 2 , NH, S, or Se, and R 1 , R 2 , R 3 , and R 4 are independently selected from an alkyl group, and wherein the silicon-containing material comprises silicon oxide, and the reactant is a P/S/N oxide. 17 . The method of claim 16 , wherein X is S and Y is NH. 18 . The method of claim 17 , wherein the P/S/N oxide comprises a compound with a general formula of: where R 4 , R 5 and R 6 are independently selected from H, alkyl, or aryl, and R 4 and R 5 may join to form a three to six membered ring including at least one P, S or N heteroatom. 19 . The method of claim 18 , wherein comprises one or more of H 3 PO, (CH 3 ) 3 PO, (C 2 H 5 ) 3 PO, MPPO (3-methyl-1-phenyl-2-phospholene 1-oxide), 3-methyl-1-phenyl-2-phospholene 1-oxide, neopentylene phosphite (5,5-Dimethyl-1,3,2-dioxaphosphinane 2-oxide), HASPO-1 (4,4,5,5-Tetramethyl-1,3,2-dioxaphospholane 2-oxide), 2-Methyl-4,4,5,5-tetramethyl-1,3,2-dioxaphospholan-2-one, or diphenylphosphine oxide, wherein comprises one or more of H 2 SO, or MPSO (methyl phenyl sulfoxide), and wherein comprises one or more of H 3 N→O, trimethylamine n-oxide, pyridine-n-oxide, TEMPO ((2,2,6,6-Tetramethylpiperidin-1-yl)oxyl), N-hydroxyphthalimide, or 4-methylmorpholine n-oxide.
by exposure to a plasma · CPC title
the material being a silicon oxide, e.g. SiO2 · CPC title
the material being a silicon nitride not containing oxygen, e.g. SixNy or SixByNz · CPC title
the precursor containing a compound comprising Si · CPC title
deposition by cyclic CVD, e.g. ALD, ALE or pulsed CVD · CPC title
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