IP Library Granted Patent US 7,198,815
Granted Patent B2
US 7,198,815 · App. 11/224,588 · Granted Apr 3, 2007

Tantalum amide complexes for depositing tantalum-containing films, and method of making same

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Quick Facts
Patent No.
US 7,198,815
App. No.
11/224,588
Granted
Apr 3, 2007
Kind
B2
Abstract

Tantalum precursors useful in depositing tantalum nitride or tantalum oxides materials on substrates, by processes such as chemical vapor deposition and atomic layer deposition. The precursors are useful in forming tantalum-based diffusion barrier layers on microelectronic device structures featuring copper metallization and/or ferroelectric thin films.

Claims (27)

1. A method of making a microelectronic device, comprising vaporizing a precursor to form a precursor vapor, and contacting the precursor vapor with a substrate to form said Ta material thereon, wherein said microelectronic device comprises said substrate, and wherein the precursor comprises at least one tantalum species selected from the group consisting of:

(i) tethered amine tantalum complexes of the formula (I):

wherein:

each of R 1 , R 2 , R 3 and R 5 is independently selected from the group consisting of H, C 1 –C 4 alkyl, silyl, C 3 –C 8 cycloalkyl, C 1 –C 4 alkylsilyl, C 6 –C 10 aryl and nitrogen-containing groups such as NR 6 R 7 , wherein R 6 and R 7 are the same as or different from one another and each is independently selected from the group consisting of H, C 1 –C 4 alkyl, and C 3 –C 8 cycloalkyl, or alternatively NR 1 R 2 may be represented by the molecular moiety

wherein m=1, 2, 3, 4, 5 or 6;

R 4 is selected from the group consisting of C 1 –C 4 alkylene, silylene (—SiH 2 —), C 1 –C 4 dialkylsilylene and NR 8 , wherein R 8 is selected from the group consisting of H, C 3 –C 8 cycloalkyl and C 1 –C 4 alkyl; and

n is 1, 2, 3, or 4, but where R 4 is silylene, C 1 –C 4 dialkylsilylene or NR 8 , n must be 1;

(ii) tethered amine tantalum complexes of the formula (II):

wherein:

each of R 1 , R 2 , R 3 and R 5 is independently selected from the group consisting of H, C 1 –C 4 alkyl, silyl, C 3 –C 8 cycloalkyl, C 1 –C 4 alkylsilyl, C 6 –C 10 aryl and nitrogen-containing groups such as NR 6 R 7 , wherein R 6 and R 7 are the same as or different from one another and each is independently selected from the group consisting of H, C 1 –C 4 alkyl, and C 3 –C 8 cycloalkyl, or alternatively NR 1 R 2 may be represented by the molecular moiety

wherein m=1, 2, 3, 4, 5 or 6;

R 4 is selected from the group consisting of C 1 –C 4 alkylene, silylene (—SiH 2 —), C 1 –C 4 dialkylsilylene and NR 8 , wherein R 8 is selected from the group consisting of H, C 3 –C 8 cycloalkyl and C 1 –C 4 alkyl; and

n is 1, 2, 3, or 4, but where R 4 is silylene, C 1 –C 4 dialkylsilylene or NR 8 , n must be 1; and

(iii) tantalum amide compounds of the formula (III):

(R 1 R 2 N) 5−n Ta(NR 3 R 4 ) n   (III)

wherein:

at least one of NR 1 R 2 and NR 3 R 4 may be represented by the molecular moiety

wherein m=1, 2, 3, 4, 5 or 6, and wherein when only one of NR 1 R 2 and NR 3 R 4 is said molecular moiety

the other of NR 1 R 2 and NR 3 R 4 has substituents R 1 and R 2 in the case of NR 1 R 2 and R 3 and R 4 in the case of NR 3 R 4 which are the same as or different from one another and each is independently selected from the group consisting of C 1 –C 4 alkyl, silyl, C 3 –C 8 cycloalkyl, C 1 –C 4 alkylsilyl, and C 6 –C 10 aryl, and

n is 1, 2, 3, or 4.

2. The method of claim 1 , wherein said precursor comprises at least one tantalum species selected from tethered amine tantalum complexes of formula (I).

3. The method of claim 1 , wherein said precursor comprises at least one tantalum species selected from tethered amine tantalum complexes of formula (II).

4. The method of claim 1 , wherein said precursor comprises at least one tantalum species selected from tantalum amide compound of formula (III).

5. The method of claim 1 , wherein said microelectronic device comprises copper metallization.

6. The method of claim 1 , wherein said microelectronic device comprises a ferroelectric film.

7. The method of claim 1 , wherein said contacting comprises chemical vapor deposition.

8. The method of claim 1 , wherein said contacting comprises atomic layer deposition.

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 →