US2012178267A1PendingUtilityA1
Composition and method for low temperature deposition of silicon-containing films such as films including silicon, silicon nitride, silicon dioxide and/or silicon-oxynitride
Est. expiryNov 14, 2022(expired)· nominal 20-yr term from priority
H10P 14/6687H10P 14/6682H10P 14/6339H10P 14/6334H10P 14/6689H10P 14/69433C23C 16/308C07F 7/10C23C 16/345C23C 16/402C30B 25/02C30B 29/06C07F 7/12C07F 7/025
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Abstract
Silicon precursors for forming silicon-containing films in the manufacture of semiconductor devices, such as low dielectric constant (k) thin films, high k gate silicates, low temperature silicon epitaxial films, and films containing silicon nitride (Si 3 N 4 ), siliconoxynitride (SiO x N y ) and/or silicon dioxide (SiO 2 ). The precursors of the invention are amenable to use in low temperature (e.g., <500° C.) chemical vapor deposition processes, for fabrication of ULSI devices and device structures.
Claims
exact text as granted — not AI-modified1 . A disilicon cycloamide precursor comprising:
wherein:
each of R 8 can be the same as or different from the others and each is independently selected from the group consisting of H, C 1 -C 4 alkyl, and C 3 -C 6 cycloalkyl; and
each of R 9 can be the same as or different from the others and each is independently selected from the group consisting of H and NR 8 H.
2 . A method of forming a silicon-containing film on a substrate, comprising contacting a substrate under vapor deposition conditions with a vapor of a disilicon cycloamide precursor as claimed in claim 1 .
3 . The method of claim 2 , wherein said contacting is carried out at temperature below 600° C.
4 . The method of claim 2 , wherein said contacting is carried out at temperature below 550° C.
5 . The method of claim 2 , wherein said contacting is carried out at temperature in a range of from 350° C. to 550° C.
6 . The method of claim 2 , wherein the contacting is carried out in a low pressure chemical vapor deposition process wherein said vapor deposition conditions comprise pressure in a range of from 100 millitorr to 1000 torr.
7 . The method of claim 2 , wherein the substrate is contacted in said contacting with a co-reactant selected from the group consisting of:
oxygen; ozone; CO 2 ; nitrogen; ammonia; compounds of the formula R 3 Si—N 3 wherein each R is independently selected from C 1 -C 3 alkyl; compounds of the formula R—N═NR′ wherein each R is independently selected from C 1 -C 3 alkyl and R′ is R or H; compounds of the formula R—N═N + ═NR′ wherein each R is independently selected from C 1 -C 3 alkyl and R′ is R or H; dinitrogen oxide; hydrogen; silane; disilane; hafnium sources; and zirconium sources.
8 . The method of claim 2 , wherein the substrate is contacted in said contacting with an excess of a reducing agent to form a silicon epitaxial layer.
9 . The method of claim 7 , wherein the silicon-containing film comprises a low k dielectric film.
10 . The method of claim 7 , wherein the silicon-containing film comprises a high k gate silicate film.
11 . The method of claim 7 , wherein the silicon-containing film comprises a silicon nitride film.
12 . The method of claim 7 , wherein the silicon-containing film comprises a silicon oxynitride film.
13 . The method of claim 2 , wherein said contacting is carried out in an atomic layer deposition process.
14 . The method of claim 2 , wherein the disilicon cycloamide precursor is reacted with a co-reactant in a reaction scheme selected from the group consisting of those of reaction scheme (C) below:
wherein A is selected from the group consisting of R 3 Si—N 3 , R—N═NR′ and R—N═N + ═NR′, wherein each R is independently selected from the group consisting of C 1 -C 3 alkyl and R′ is R or H.
15 . A method of forming silicon nitride (Si 3 N 4 ) on a substrate, comprising contacting the substrate with
(i) a precursor of the formula
wherein:
each of R 8 can be the same as or different from the others and each is independently selected from the group consisting of H, C 1 -C 4 alkyl, and C 3 -C 6 cycloalkyl; and
each of R 9 can be the same as or different from the others and each is independently selected from the group consisting of H and NR 8 H; and
(ii) a nitrogen source compound.
16 . The method of claim 15 , wherein said nitrogen source compound comprises ammonia.
17 . The method of claim 15 , wherein said nitrogen source compound is selected from the group consisting of R 3 Si—N 3 , R—N═NR′ and R—N═N + ═NR′, wherein each R is independently selected from the group consisting of C 1 -C 3 alkyl substituents, and R′ is R or H.
18 . The method of claim 15 , wherein said nitrogen source compound is selected from the group consisting of (i) R-diazo compounds, wherein R is H, C 1 -C 4 alkyl or C 3 -C 6 cycloalkyl, (ii) triazoles, (iii) tetrazoles, (iv) amadines, (v) silylazides, (vi) aziridines, and (vii) molecules including organic acyclic or cyclic moieties that contain one or more —N—N bonds.
19 . The method of claim 15 , wherein said contacting is carried out at temperature below 600° C.
20 . The method of claim 15 , wherein said contacting is carried out at temperature below 550° C.Cited by (0)
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