IP Library Granted Patent US 8,497,233
Granted Patent B2
US 8,497,233 · App. 13/138,468 · Granted Jul 30, 2013

Stripping compositions for cleaning ion implanted photoresist from semiconductor device wafers

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Quick Facts
Patent No.
US 8,497,233
App. No.
13/138,468
Granted
Jul 30, 2013
Kind
B2
Abstract

A composition for removal of high dosage ion implanted photoresist from the surface of a semiconductor device, the composition having at least one solvent having a flash point >65° C., at least one component providing a nitronium ion, and at least one phosphonic acid corrosion inhibitor compound, and use of such a composition to remove high dosage ion implanted photoresist from the surface of a semiconductor device.

Claims (27)

1. A composition for removal of high dosage ion implanted photoresist from the surface of a semiconductor device, the composition comprising:

at least one solvent having a flash point of >65° C.,

at least one component providing a nitronium ion, and

at least one phosphonic acid corrosion inhibitor compound.

2. A composition according to claim 1 wherein the at least one solvent is sulfolane.

3. A composition of claim 1 wherein the at least one component providing a nitronium ion is a nitronium compound selected from the group consisting of nitronium tetrafluoroborate (NO 2 BF 4 ), nitronium perchlorate (NO 2 ClO 4 ), nitronium fluorosulfate (NO 2 SO 3 F), and nitronium triflate (NO 2 SO 2 CF 3 ).

4. A composition according to claim 1 wherein the phosphonic acid corrosion inhibitor compound is selected from the group consisting of aminotrimethylenephosphonic acid, diethylenetriaminepenta(methylenephosphonic acid) (DETPA), N,N,N′,N′-ethylenediaminetetra(methylenephosphonic) 1,5,9-triazacyclododecane-N,N′,N″-tris(methylenephosphonic acid) (DOTRP), 1,4,7,10-tetrazacyclododecane-N,N′,N″,N′″-tetrakis(methylenephosphonic acid) (DOTP), nitrilotris(methylene) triphosphonic acid, diethylenetriaminepenta(methylenephosphonic acid) (DETAP), aminotri(methylenephosphonic acid), 1-hydroxyethylene-1,1-diphosphonic acid, bis(hexamethylene)triamine phosphonic acid, and 1,4,7-triazacyclononane-N,N′,N″-tris(methylenephosphonic acid) (NOTP).

5. A composition according to claim 1 wherein the at least one solvent is sulfolane, the nitronium compound is nitronium tetrafluoroborate, and the phosphonic acid corrosion inhibitor compound is aminotrimethylenephosphonic acid.

6. A composition according to claim 1 wherein the solvent is sulfolane and is present in an amount of from about 10 wt. % to about 94.99 wt. %, the at least one component providing a nitronium ion is present in an amount of from about 5 wt. % to about 90 wt. %, and the at least one phosphonic acid corrosion inhibitor is present in an amount of from about 0.01 wt. % to about 5.0 wt. % wherein the wt. percents are based on the total combined weight of the sulfolane, nitronium ion providing component, and phosphonic acid corrosion inhibitor compound.

7. A composition according to claim 1 comprising:

at least one solvent having a flash point >65° C.,

at least one component providing a nitronium ion and selected from the group consisting of nitric acid and a nitrate,

at least one phosphonic acid corrosion inhibitor, and

an acid stronger than nitric acid.

8. A composition according to claim 7 wherein the solvent is sulfolane.

9. A composition according to claim 7 wherein the acid stronger than nitric acid is selected from the group consisting of sulfuric acid, triflic acid, and tetrafluoroboric acid.

10. A composition according to claim 7 wherein the at least one component providing a nitronium ion is nitric acid.

11. A composition according to claim 7 wherein the phosphonic acid corrosion inhibitor compound is selected from the group consisting of aminotrimethylenephosphonic acid, diethylenetriaminepenta(methylenephosphonic acid) (DETPA), N,N,N′,N′-ethylenediaminetetra(methylenephosphonic) 1,5,9-triazacyclododecane-N,N′,N″-tris(methylenephosphonic acid) (DOTRP), 1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetrakis(methylenephosphonic acid) (DOTP), nitrilotris(methylene) triphosphonic acid, diethylenetriaminepenta(methylenephosphonic acid) (DETAP), aminotri(methylenephosphonic acid), 1-hydroxyethylene-1,1-diphosphonic acid, bis(hexamethylene)triamine phosphonic acid, and 1,4,7-triazacyclononane-N,N′,N″-tris(methylenephosphonic acid) (NOTP).

12. A composition according to claim 7 wherein the at least one solvent is sulfolane, the acid stronger than nitric acid is sulfuric acid, the phosphonic acid corrosion inhibitor compound is aminotrimethylenephosphonic acid, and the at least one component providing a nitronium ion is nitric acid.

13. A composition according to claim 7 wherein the weight ratio of the acid stronger than nitric acid to the remaining components of the composition is from about 20:1 to 1:10.

14. A composition according to claim 13 wherein the acid stronger than nitric acid is sulfuric acid and the weight ratio of sulfuric acid/remaining components of the composition is from about 9:2.

15. A composition according to claim 7 comprising:

about 49.75 wt % sulfolane, about 49.75 wt. % nitric acid (70%), and about 0.50 wt. % aminotrimethylenephosphonic acid,

said components being mixed with sulfuric acid in a weight ratio of sulfuric acid to said components of about 9:2.

16. A composition according to claim 7 wherein at least one or more of the solvent, the acid stronger than nitric acid, and the phosphonic acid corrosion inhibitor components has been heated to a temperature above a temperature to be used for cleaning ion implanted photoresist, and the composition is formed by mixing the heated component(s) with the nitronium ion providing component that has been maintained at a temperature of about room temperature.

17. A composition according to claim 16 wherein the composition is formed by mixing all the components of the composition together at a time of about 5 minutes or less before the composition is to be used as a cleaner of high dosage ion implanted photoresist from the surface of a semiconductor device.

18. A process for the removal of high dosage ion implanted photoresist from the surface of a semiconductor device, the process comprising contacting the high dosage ion implanted photoresist with a composition of claim 1 for a time and temperature sufficient to remove the photoresist.

Assignments (17)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Nov 16, 2020
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
To: AVANTOR PERFORMANCE MATERIALS, LLC; NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC; RELIABLE BIOPHARMACEUTICAL, LLC; THERAPAK, LLC
Reel/Frame 054440/0877 →
SECURITY AGREEMENT (NOTES) Recorded Nov 6, 2020
From: AVANTOR FLUID HANDLING, LLC; AVANTOR PERFORMANCE MATERIALS, LLC; NUSIL TECHNOLOGY LLC; RELIABLE BIOPHARMACEUTICAL, LLC; THERAPAK, LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 054343/0414 →
SECURITY AGREEMENT Recorded Nov 29, 2017
From: AVANTOR PERFORMANCE MATERIALS, LLC; NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC; RELIABLE BIOPHARMACEUTICAL, LLC; THERAPAK, LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 044528/0960 →
SECURITY AGREEMENT Recorded Nov 28, 2017
From: AVANTOR PERFORMANCE MATERIALS, LLC; NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC; RELIABLE BIOPHARMACEUTICAL, LLC; THERAPAK, LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 044811/0400 →
RELEASE (REEL 041966 / FRAME 0247) Recorded Nov 27, 2017
From: JEFFERIES FINANCE LLC
To: NUSIL TECHNOLOGY, LLC; APPLIED SILICONE COMPANY LLC; AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY AVANTOR PERFORMANCE MATERIALS, INC.)
Reel/Frame 044810/0154 →
RELEASE (REEL 041966 / FRAME 0211) Recorded Nov 27, 2017
From: JEFFERIES FINANCE LLC
To: NUSIL TECHNOLOGY, LLC; APPLIED SILICONE COMPANY, LLC; AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY AVANTOR PERFORMANCE MATERIALS, INC.)
Reel/Frame 044810/0207 →
SECURITY INTEREST Recorded Mar 10, 2017
From: NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC; AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY KNOWN AS AVANTOR PERFORMANCE MATERIALS, INC.)
To: JEFFERIES FINANCE LLC
Reel/Frame 041966/0211 →
SECURITY INTEREST Recorded Mar 10, 2017
From: NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC; AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY KNOWN AS AVANTOR PERFORMANCE MATERIALS, INC.)
To: JEFFERIES FINANCE LLC
Reel/Frame 041966/0247 →
RELEASE OF SECURITY INTEREST Recorded Mar 10, 2017
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY KNOWN AS AVANTOR PERFORMANCE MATERIALS, INC.); NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC
Reel/Frame 041966/0313 →
CHANGE OF NAME Recorded Mar 2, 2017
From: AVANTOR PERFORMANCE MATERIALS, INC.
To: AVANTOR PERFORMANCE MATERIALS, LLC
Reel/Frame 041442/0976 →
MERGER Recorded Oct 3, 2016
From: AVANTOR PERFORMANCE MATERIALS, INC.
To: AVANTOR PERFORMANCE MATERIALS, LLC
Reel/Frame 039924/0311 →
SECURITY INTEREST Recorded Sep 30, 2016
From: NUSIL TECHNOLOGY LLC; APPLIED SILICONE COMPANY LLC; AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY KNOWN AS AVANTOR PERFORMANCE MATERIALS, INC.)
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
Reel/Frame 040192/0613 →
RELEASE OF SECURITY INTEREST Recorded Sep 30, 2016
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: AVANTOR PERFORMANCE MATERIALS, LLC (FORMERLY KNOWN AS AVANTOR PERFORMANCE MATERIALS, INC.)
Reel/Frame 039915/0035 →
SECURITY INTEREST Recorded Jun 21, 2016
From: AVANTOR PERFORMANCE MATERIALS, INC.
To: CREDIT SUISSE, AG, CAYMAN ISLANDS BRANCH
Reel/Frame 038976/0610 →
RELEASE OF SECURITY INTEREST Recorded Jun 21, 2016
From: CREDIT SUISSE, AG, CAYMAN ISLANDS BRANCH
To: AVANTOR PERFORMANCE MATERIALS, INC.
Reel/Frame 038976/0233 →
SECURITY INTEREST Recorded Jun 21, 2016
From: AVANTOR PERFORMANCE MATERIALS, INC.
To: CREDIT SUISSE, AG, CAYMAN ISLANDS BRANCH
Reel/Frame 038976/0478 →
SECURITY INTEREST Recorded Oct 3, 2014
From: AVANTOR PERFORMANCE MATERIALS, INC.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
Reel/Frame 033882/0488 →