US2019287798A1PendingUtilityA1
Compositions and Processes for Depositing Carbon-Doped Silicon-Containing Films
Est. expiryJun 3, 2031(~4.8 yrs left)· nominal 20-yr term from priority
Inventors:Manchao XiaoXinjian LeiRonald Martin PearlsteinHaripin ChandraEugene Joseph Karwacki, Jr.Bing HanMark Leonard O'Neill
H10P 14/6922H10P 14/6682H10P 14/6339C23C 16/345C09D 5/00C23C 16/401C23C 16/30C07F 7/10C23C 16/45553C07F 7/0896H01L 21/0228H01L 21/02211C09D 7/63H01L 21/02126
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Claims
Abstract
Described herein are compositions for depositing a carbon-doped silicon containing film comprising: a precursor comprising at least one compound selected from the group consisting of: an organoaminosilane having a formula of R 8 N(SiR 9 LH) 2 , wherein R 8 , R 9 , and L are defined herein. Also described herein are methods for depositing a carbon-doped silicon-containing film using the composition wherein the method is one selected from the following: cyclic chemical vapor deposition (CCVD), atomic layer deposition (ALD), plasma enhanced ALD (PEALD) and plasma enhanced CCVD (PECCVD).
Claims
exact text as granted — not AI-modified1 . A composition for depositing a carbon-doped silicon containing film comprising:
a precursor comprising at least one compound selected from the group consisting of:
an organoaminosilane having a formula of R 8 N(SiR 9 LH) 2 , wherein
R 8 is selected from the group consisting of a C 1 to C 10 linear or branched alkyl group, a C 3 to C 10 cyclic alkyl group, a linear or branched C 2 to C 10 alkenyl group, a linear or branched C 2 to C 10 alkynyl group, a C 5 to C 10 aromatic group, and a C 3 to C 10 saturated or unsaturated heterocyclic group;
R 9 selected from the group consisting of hydrogen, C 1 to C 10 linear or branched alkyl, a C 3 to C 10 cyclic alkyl group, a linear or branched C 2 to C 10 alkenyl group, a linear or branched C 2 to C 10 alkynyl group, a C 5 to C 10 aromatic group, and a C 3 to C 10 saturated or unsaturated heterocyclic group; and
L is selected from the group consisting of Cl, Br, and I.
2 . The composition of claim 1 wherein R 8 is selected from the group consisting of Me, Et, n Pr, i Pr, n Bu, i Bu, s Bu, t Bu, isomers of pentyl, vinyl, phenyl, and alkyl substituted phenyl.
3 . The composition of claim 1 wherein R 9 is selected from the group consisting of hydrogen, Me, Et, n P, i Pr, n Bu, i Bu, s Bu, t Bu, isomers of pentyl, vinyl, phenyl, and alkyl substituted phenyl.
4 . A method of forming a carbon-doped silicon nitride film via an atomic layer deposition process, the method comprising the steps of:
a. providing a substrate in a reactor; b. introducing into the reactor a precursor comprising at least one organoaminosilane having a formula of R 8 N(SiR 9 LH) 2 , wherein R 8 is selected from the group consisting of a C 1 to C 10 linear or branched alkyl group, a C 3 to C 10 cyclic alkyl group, a linear or branched C 2 to C 10 alkenyl group, a linear or branched C 2 to C 10 alkynyl group, a C 5 to C 10 aromatic group, and a C 3 to C 10 saturated or unsaturated heterocyclic group; R 9 selected from the group consisting of hydrogen, C 1 to C 10 linear or branched alkyl, a C 3 to C 10 cyclic alkyl group, a linear or branched C 2 to C 10 alkenyl group, a linear or branched C 2 to C 10 alkynyl group, a C 5 to C 10 aromatic group, and a C 3 to C 10 saturated or unsaturated heterocyclic group; and
L is selected from the group consisting of Cl, Br, and I;
c. purging the reactor with a purge gas; d. introducing a nitrogen source into the reactor wherein the nitrogen source is selected from the group consisting of ammonia, hydrazine, monoalkylhydrazine, dialkylhydrazine, nitrogen, nitrogen/hydrogen, ammonia plasma, nitrogen plasma, nitrogen/hydrogen plasma, and mixture thereof; and e. purging the reactor with a purge gas, wherein steps b through e are repeated until a desired thickness of the film is obtained.
5 . A method of forming a carbon-doped silicon oxide film via an atomic layer deposition process, the method comprising the steps of:
a. providing a substrate in a reactor; b. introducing into the reactor at least one compound selected from the group consisting of: an organoaminosilane having a formula of R 9 N(SiR 9 LH) 2 , wherein R 9 is selected from the group consisting of a C 1 to C 10 linear or branched alkyl group, a C 3 to C 10 cyclic alkyl group, a linear or branched C 2 to C 10 alkenyl group, a linear or branched C 2 to C 10 alkynyl group, a C 5 to C 10 aromatic group, and a C 3 to C 10 saturated or unsaturated heterocyclic group; R 9 selected from the group consisting of hydrogen, C 1 to C 10 linear or branched alkyl, a C 3 to C 10 cyclic alkyl group, a linear or branched C 2 to C 10 alkenyl group, a linear or branched C 2 to C 10 alkynyl group, a C 5 to C 10 aromatic group, and a C 3 to C 10 saturated or unsaturated heterocyclic group; and
L is selected from the group consisting of Cl, Br, and I;
c. purging the reactor with a purge gas; d. introducing an oxygen source into the reactor wherein the oxygen source is selected from the group consisting of water, water plasma, oxygen, peroxide, oxygen plasma, ozone, NO, NO 2 , carbon monoxide, carbon dioxide, and combinations thereof; and e purging the reactor with a purge gas, wherein steps b through e are repeated until a desired thickness of the film is obtained.
6 . A film deposited by the method of claim 4 .
7 . A film deposited by the method of claim 5 .Join the waitlist — get patent alerts
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