IP Library Granted Patent US 8,541,318
Granted Patent B2
US 8,541,318 · App. 13/369,810 · Granted Sep 24, 2013

Monosilane or disilane derivatives and method for low temperature deposition of silicon-containing films using the same

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Quick Facts
Patent No.
US 8,541,318
App. No.
13/369,810
Granted
Sep 24, 2013
Kind
B2
Abstract

This invention relates to silicon precursor compositions for forming silicon-containing films by low temperature (e.g., <550° C.) chemical vapor deposition processes for fabrication of ULSI devices and device structures. Such silicon precursor compositions comprise at least a silane or disilane derivative that is substituted with at least one alkylhydrazine functional groups and is free of halogen substitutes.

Claims (28)

1. A method of forming a silicon-containing film on a substrate, comprising contacting a substrate under vapor deposition conditions with a vapor of a compound selected from the group consisting of:

(i) compounds of the formula:

wherein R 1 and R 2 may be the same as or different from each another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, aryl, and C 3 -C 6 cycloalkyl, or R 1 and R 2 together may form C 3 -C 6 heterocyclic functional group with N, and wherein X, Y, and Z may be the same as or different from one another and are independently selected from the group consisting of C 1 -C 7 alkyl, alkylamino, and dialkylamino; and

(ii) compounds of the formula:

wherein R 1 , R 2 , R 3 , and R 4 may be the same as or different from one another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, aryl, and C 3 -C 6 cycloalkyl, or R 1 and R 2 together may form a C 3 -C 6 heterocyclic functional group with N, or R 3 and R 4 together may form a C 3 -C 6 heterocyclic functional group with N, and wherein X 1 , X 2 , Y 1 , and Y 2 may be the same as or different from one another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, alkylamino, dialkylamino, and R 1 R 2 NNH—, wherein R 1 and R 2 are as described above, and wherein R 1 , R 2 , R 3 , R 4 , X 1 , X 2 , Y 1 , and Y 2 are not all methyl.

2. The method of claim 1 , wherein the vapor deposition conditions comprise temperature below 450° C.

3. The method of claim 1 , wherein the compound is selected from the group consisting of compounds of formula (I).

4. The method of claim 1 , wherein said film comprises silicon dioxide, silicon nitride or siliconoxynitride.

5. The method of claim 1 , wherein said film comprises a low dielectric constant silicon-containing film.

6. The method of claim 1 , wherein said film comprises a gate silicate film.

7. The method of claim 1 , wherein the substrate comprises a semiconductor device substrate.

8. The method of claim 1 , wherein said vapor deposition comprises chemical vapor deposition and said vapor is transported to said contacting at temperature below 300° C.

9. The method of claim 1 , conducted in an ULSI device fabrication process.

10. The method of claim 1 , wherein X, Y and Z are all C 1 -C 7 alkyl.

11. The method of claim 1 , wherein the compound is Me 3 Si(HNNMe 2 ).

12. The method of claim 11 , further comprising forming said vapor by volatilizing Me 3 Si(HNNMe 2 ) from a liquid phase.

13. A method of forming a silicon-containing film on a substrate, comprising contacting a substrate under vapor deposition conditions comprising a temperature below 450° C. with a vapor of a compound selected from the group consisting of:

(i) compounds of the formula:

wherein R 1 and R 2 may be the same as or different from each another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, aryl, and C 3 -C 6 cycloalkyl, or R 1 and R 2 together may form C 3 -C 6 heterocyclic functional group with N, and wherein X, Y, and Z are all the same as one another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, alkylamino, dialkylamino, and R 1 R 2 NNH—, wherein R 1 and R 2 are same as above and wherein R 1 R 2 , X, Y and Z are not all H; and

(ii) compounds of the formula:

wherein R 1 , R 2 , R 3 , and R 4 may be the same as or different from one another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, aryl, and C 3 -C 6 cycloalkyl, or R 1 and R 2 together may form a C 3 -C 6 heterocyclic functional group with N, or R 3 and R 4 together may form a C 3 -C 6 heterocyclic functional group with N, and wherein X 1 , X 2 , Y 1 , and Y 2 may be the same as or different from one another and are independently selected from the group consisting of H, C 1 -C 7 alkyl, alkylamino, dialkylamino, and R 1 R 2 NNH—, wherein R 1 and R 2 are as described above, and wherein R 1 , R 2 , R 3 , R 4 , X 1 , X 2 , Y 1 , and Y 2 are not all methyl.

14. The method of claim 13 , wherein X, Y and Z are all C 1 -C 7 alkyl.

15. The method of claim 13 , wherein said film comprises silicon dioxide, silicon nitride or siliconoxynitride.

16. The method of claim 13 , wherein said film comprises a low dielectric constant silicon-containing film.

17. The method of claim 13 , wherein said film comprises a gate silicate film.

18. The method of claim 13 , wherein the substrate comprises a semiconductor device substrate.

19. The method of claim 13 , wherein X, Y and Z are all alkylhydrazido.

20. The method of claim 19 , wherein the alkylhydrazido is methylhydrazido or ethylhydrazido.

Assignments (8)
SECURITY INTEREST Recorded Jul 8, 2022
From: ENTEGRIS, INC.; ENTEGRIS GP, INC.; POCO GRAPHITE, INC.; CMC MATERIALS, INC.; INTERNATIONAL TEST SOLUTIONS, LLC; QED TECHNOLOGIES INTERNATIONAL, INC.
To: TRUIST BANK, AS NOTES COLLATERAL AGENT
Reel/Frame 060613/0072 →
ASSIGNMENT OF PATENT SECURITY INTEREST RECORDED AT REEL/FRAME 048811/0679 Recorded Nov 5, 2019
From: GOLDMAN SACHS BANK USA
To: MORGAN STANLEY SENIOR FUNDING, INC.
Reel/Frame 050965/0035 →
SECURITY INTEREST Recorded Nov 13, 2018
From: ENTEGRIS, INC.; SAES PURE GAS, INC.
To: GOLDMAN SACHS BANK USA
Reel/Frame 048811/0679 →
RELEASE OF SECURITY INTEREST Recorded Nov 8, 2018
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: ENTEGRIS, INC.; POCO GRAPHITE, INC.; ATMI, INC.; ATMI PACKAGING, INC.; ADVANCED TECHNOLOGY MATERIALS, INC.
Reel/Frame 047477/0151 →
RELEASE OF SECURITY INTEREST Recorded Nov 8, 2018
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: ENTEGRIS, INC.; POCO GRAPHITE, INC.; ATMI, INC.; ATMI PACKAGING, INC.; ADVANCED TECHNOLOGY MATERIALS, INC.
Reel/Frame 047477/0032 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2015
From: ADVANCED TECHNOLOGY MATERIALS, INC.
To: ENTEGRIS, INC.
Reel/Frame 034894/0025 →
SECURITY INTEREST Recorded May 2, 2014
From: ENTEGRIS, INC.; POCO GRAPHITE, INC.; ATMI, INC.; ADVANCED TECHNOLOGY MATERIALS, INC.; ATMI PACKAGING, INC.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 032812/0192 →
SECURITY INTEREST Recorded May 1, 2014
From: ENTEGRIS, INC.; POCO GRAPHITE, INC.; ATMI, INC.; ADVANCED TECHNOLOGY MATERIALS, INC.; ATMI PACKAGING, INC.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 032815/0852 →