IP Library Granted Patent US 7,888,301
Granted Patent B2
US 7,888,301 · App. 10/581,475 · Granted Feb 15, 2011

Resist, barc and gap fill material stripping chemical and method

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,888,301
App. No.
10/581,475
Granted
Feb 15, 2011
Kind
B2
Abstract

An aqueous-based composition and process for removing photoresist, bottom anti-reflective coating (BARC) material, and/or gap fill material from a substrate having such material(s) thereon. The aqueous-based composition includes a fluoride source, at least one organic amine, at least one organic solvent, water, and optionally chelating agent and/or surfactant. The composition achieves high-efficiency removal of such material(s) in the manufacture of integrated circuitry without adverse effect on metal species on the substrate, such as copper, and without damage to SiOC-based dielectric materials employed in the semiconductor architecture.

Claims (131)

1. An aqueous-based removal composition comprising a fluoride source, at least one organic amine, at least one organic solvent, water, optionally at least one chelating agent, and optionally at least one surfactant, wherein the at least one organic amine comprises a species selected from the group consisting of N-(2-cyanoethyl) ethylenediamine, hydroxypropylpiperazine, aminopropylpiperazine, hydroxypropylmorpholine, aminoethylmorpholine, ethylene urea, trimethylaminoethylethanolamine, trimethylaminopropylethanolamine, and N-(2-cyanopropyl) ethylenediamine, and wherein said composition is useful for removing photoresist, bottom anti-reflective coating (BARC) materials, and/or gap fill materials from a substrate having such material(s) thereon.

2. The composition of claim 1 , wherein the at least one organic amine comprises N-(2-cyanoethyl)ethylenediamine.

3. The composition of claim 1 , wherein the fluoride source comprises a fluoride-containing compound selected from the group consisting of ammonium fluoride, hydrogen fluoride, ammonium bifluoride, tetraalkylammonium difluoride, alkyl phosphonium difluoride, and triethylamine trihydrofluoride.

4. The composition of claim 1 , wherein the fluoride source comprises ammonium fluoride.

5. The composition of claim 1 , further comprising at least one additional organic amine.

6. The composition of claim 5 , wherein the at least one additional organic amine comprises an amine-containing compound selected from the group consisting of hydroxyethylpiperazine, hydroxypropylpiperazine, amino ethylpip erazine, aminopropylpiperazine, hydroxyethylmorpholine, hydroxypropylmorpholine, aminoethylmorpholine, aminopropylmorpholine, triethanolamine, pentamethyldiethylenetriamine, dimethylaminoethoxyethanol, aminoethoxyethanol, ethylene urea, trimethylaminoethylethanolamine, trimethylaminopropylethanolamine, and N-(2-cyanopropyl) ethylenediamine.

7. The composition of claim 1 , wherein the at least one organic solvent comprises a compound selected from the group consisting of 1,4-butanediol, 1,3-butanediol, ethylene glycol, propylene glycol, N-methyl-2-pyrrolidone, DMSO, r-butyrolactone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, diethyleneglycol monobenzylether, ethyl lactate, ammonium lactate, and dimethyl acetamide.

8. The composition of claim 1 , wherein the at least one organic solvent comprises propylene glycol monomethyl ether.

9. The composition of claim 1 , comprising chelating agent.

10. The composition of claim 9 , wherein the chelating agent comprises a compound selected from the group consisting of iminodiacetic acid, boric acid, ammonium borate, ammonium tetraborate, gluconic acid, mannitol, and sorbitol.

11. The composition of claim 1 , comprising surfactant.

12. The composition of claim 11 , wherein the surfactant comprises a compound selected from the group consisting of: (C 1 -C 15 ) alkyl glucosides; (C 1 -C 15 ) alkyl ethylene oxide/propylene oxide;

(C 1 -C 10 ) alkyl phenoxy ethylene oxide/propylene oxide; and oxirane, methyl-, polymer with oxirane, ether with 2, 2′-(oxidoimino)bis(ethanol) (2:1) and N(-3-(C(-11-isoalkyloxy)propyl) derivatives.

13. The composition of claim 11 , wherein the surfactant comprises a compound selected from the group consisting of decyl glucoside, alkyl EOPO amine oxide, EO octylphenol, and EO nonylphenol.

14. The composition of claim 1 , selected from the group consisting of Formulations A-F, wherein all percentages are by weight, based on total weight of the formulation:

Formulation A

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.05% decyl glucoside;

Formulation B

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 25% propylene glycol monomethyl ether; and

about 30% de-ionized water;

Formulation C

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 24% propylene glycol monomethyl ether;

about 30% de-ionized water; and

about 1% ammonium tetraborate;

Formulation D

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.10% alkyl EOPO amine oxide surfactant;

Formulation E

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.10% EO octylphenol surfactant; and

Formulation F

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.10% EO nonylphenol surfactant;

wherein the total of the weight percentages of such components of the composition does not exceed 100% by weight.

15. The composition of claim 1 , comprising the following components, based on total weight of the composition:

0.1% wt.-15.0% wt. fluoride source;

20.0% wt.-60.0% wt. total organic amine;

1.0% wt.-60.0% wt. total organic solvent;

20.0% wt.-70.0% wt. water;

0.000% wt.-20.0% wt. chelating agent; and

0.000% wt.-5.0% wt. surfactant,

wherein the total of the weight percentages of such components of the composition does not exceed 100% by weight.

16. The composition of claim 1 , wherein the pH of the composition is in a range from about 5 to about 9.

17. A method of removing photoresist, BARC material, and/or gap fill material from a substrate having said material(s) thereon, said method comprising contacting the substrate with an aqueous-based removal composition for sufficient time to at least partially remove said material from the substrate, wherein the aqueous-based removal composition includes a fluoride source, at least one organic amine, at least one organic solvent, water, optionally at least one chelating agent, and optionally at least one surfactant, wherein the at least one organic amine comprises a species selected from the group consisting of N-(2-cyanoethyl) ethylenediamine, hydroxypropylpiperazine, aminopropylpiperazine, hydroxypropylmorpholine, aminoethylmorpholine, ethylene urea, trimethylaminoethylethanolamine, trimethylaminopropylethanolamine, and N-(2-cyanopropyl) ethylenediamine

18. The method of claim 17 , wherein the substrate comprises a semiconductor device structure.

19. The method of claim 17 , wherein said contacting is carried out for a time of from about 1 minute to about 5 minutes.

20. The method of claim 17 , wherein said contacting is carried out at temperature in a range of from about 20° C. to about 40° C.

21. The method of claim 17 , wherein the fluoride source comprises a fluoride-containing compound selected from the group consisting of ammonium fluoride, hydrogen fluoride, ammonium bifluoride, tetraalkylammonium difluoride, alkyl phosphonium difluoride, and triethylamine trihydrofluoride.

22. The method of claim 17 , wherein the at least one organic amine comprises N-(2-cyanoethyl)ethylenediamine.

23. The method of claim 17 , wherein the aqueous-based removal composition further comprises at least one additional organic amine.

24. The method of claim 23 , wherein the at least one additional organic amine comprises an amine-containing compound selected from the group consisting of hydroxyethylpiperazine, hydroxypropylpiperazine, amino ethylpip erazine, aminopropylpiperazine, hydroxyethylmorpho line, hydroxypropylmorpho line, amino ethylmorpho line, aminopropylmorpho line, triethanolamine, pentamethyldiethylenetriamine, dimethylaminoethoxyethanol, aminoethoxyethanol, ethylene urea, trimethylaminoethylethanolamine, trimethylaminopropylethanolamine, and N-(2-cyanopropyl) ethylenediamine.

25. The method of claim 17 , wherein the at least one organic solvent comprises a compound selected from the group consisting of 1,4-butanediol, 1,3-butanediol, ethylene glycol, propylene glycol, N-methyl-2-pyrrolidone, DMSO, r-butyrolactone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, diethyleneglycol monobenzylether, ethyl lactate, ammonium lactate, and dimethyl acetamide.

26. The method of claim 17 , comprising at least one chelating agent selected from the group consisting of iminodiacetic acid, boric acid, ammonium borate, ammonium tetraborate, gluconic acid, mannitol, and sorbitol.

27. The method of claim 17 , comprising at least one surfactant selected from the group consisting of: (C 1 -C 15 ) alkyl glucosides; (C 1 -C 15 ) alkyl ethylene oxide/propylene oxide; (C 1 -C 10 ) alkyl phenoxy ethylene oxide/propylene oxide; and oxirane, methyl-, polymer with oxirane, ether with 2,2′-(oxidoimino)bis(ethanol) (2:1) and N(-3-(C(-11-isoalkyloxy)propyl) derivatives.

28. The method of claim 17 , selected from the group consisting of Formulations A-F, wherein all percentages are by weight, based on total weight of the formulation:

Formulation A

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.05% decyl glucoside;

Formulation B

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 25% propylene glycol monomethyl ether; and

about 30% de-ionized water;

Formulation C

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 24% propylene glycol monomethyl ether;

about 30% de-ionized water; and

about 1% ammonium tetraborate;

Formulation D

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.10% alkyl EOPO amine oxide surfactant;

Formulation E

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.10% EO octylphenol surfactant; and

Formulation F

about 8% NH 4 F/HF;

about 30% hydroxyethylmorpholine;

about 7% N-(2-cyanoethyl) ethylenediamine;

about 15% propylene glycol monomethyl ether;

about 40% de-ionized water; and

about 0.10% EO nonylphenol surfactant;

wherein the total of the weight percentages of such components of the composition does not exceed 100% by weight.

29. The method of claim 17 , wherein the composition comprises the following components, based on total weight of the composition:

0.1% wt.-15.0% wt. fluoride source;

20.0% wt.-60.0% wt. total organic amine;

1.0% wt.-60.0% wt. total organic solvent;

20.0% wt.-70.0% wt. water;

0.000% wt.-20.0% wt. chelating agent; and

0.000% wt.-5.0% wt. surfactant,

wherein the total of the weight percentages of such components of the composition does not exceed 100% by weight.

30. The method of claim 17 , wherein the pH of the composition is in a range from about 5 to about 9.

31. The method of claim 17 , further comprising contacting the substrate with deionized water following contact with the aqueous-based removal composition.

32. The method of claim 17 , further comprising residue material selected from the group consisting of photoresist, BARC materials, gap fill materials, and combinations thereof.

Assignments (10)
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 Dec 19, 2016
From: ADVANCED TECHNOLOGY MATERIALS, INC.
To: ENTEGRIS, INC.
Reel/Frame 041029/0903 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2011
From: NISSAN CHEMICAL INDUSTRIES, LTD.
To: ADVANCED TECHNOLOGY MATERIALS, INC.
Reel/Frame 025650/0313 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2011
From: BERNHARD, DAVID D.
To: ADVANCED TECHNOLOGY MATERIALS, INC.
Reel/Frame 025617/0699 →