IP Library Granted Patent US 12,292,689
Granted Patent B2
US 12,292,689 · App. 17/561,603 · Granted May 6, 2025

Alkaline cleaning composition, cleaning method, and manufacturing method of semiconductor

Inventors: Hui-yi Tang (Taichung, TW); Tzu-chi Wang (Taichung, TW); Yu-nung Chen (Taichung, TW); Yi-cheng Chen (Taichung, TW)
Assignee: Daxin materials corporation
G03F7/322C11D3/2068C11D3/28C11D3/30C11D3/43C11D7/3209C11D7/3218C11D7/3281C11D7/50C11D2111/22
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 12,292,689
App. No.
17/561,603
Granted
May 6, 2025
Kind
B2
Abstract

An alkaline cleaning composition is provided. The alkaline cleaning composition includes an alkaline compound, 5% to 40% by weight of propylene glycol monomethyl ether, 10% to 30% by weight of water, and a polar solvent. Wherein, the polar solvent includes acetals, glycol ethers, pyrrolidones, or a combination thereof, and the alkaline cleaning composition is free of benzenesulfonic acid.

Claims (20)

1. An alkaline cleaning composition, comprising a quaternary ammonium hydroxide, 5% to 40% by weight of propylene glycol monomethyl ether, 10% to 30% by weight of water, and a polar solvent;

wherein the polar solvent comprises a solvent having a structure shown in a following formula (3), (4), or (5), or a combination thereof:

wherein R 1 and R 2 are independently hydrogen or a C 1 -C 6 alkyl group that is unsubstituted or at least one —CH 2 — is substituted with —O—; R 3 and R 4 are independently a C 1 -C 4 alkylene group; and R 5 and R 6 are independently a C 1 -C 3 alkyl group;

wherein R 1 is hydrogen or a C 1 -C 4 alkyl group that is unsubstituted or substituted with a hydroxyl group; R 2 and R 3 are independently hydrogen or a C 1 -C 2 alkyl group; and n is an integer ranging from 1 to 4; and

wherein R 1 is a C 1 -C 3 alkyl group; and the alkaline cleaning composition is free of benzenesulfonic acid.

2. The alkaline cleaning composition according to claim 1 , wherein the quaternary ammonium hydroxide has a structure shown in a following formula (1):

wherein R 1 to R 4 are each independently a C 1 -C 4 alkyl group that is unsubstituted or substituted with a hydroxyl group.

3. The alkaline cleaning composition according to claim 1 , wherein the quaternary ammonium hydroxide is at least one selected from the group consisting of tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide, ethyltrimethylammonium hydroxide, diethyldimethylammonium hydroxide, (2-hydroxyethyl)trimethylammonium hydroxide, bis(2-hydroxyethyl)dimethylammonium hydroxide, and tris(2-hydroxyethyl)methylammonium hydroxide.

4. The alkaline cleaning composition according to claim 1 , wherein an amount of the quaternary ammonium hydroxide in the alkaline cleaning composition ranges from 0.1% to 20% by weight.

5. The alkaline cleaning composition according to claim 1 , wherein the polar solvent is at least one selected from the group consisting of 4,8-dimethyl-2,5,7,10-tetraoxaundecane, 2,5,7,10-tetraoxaundecane, 6-(2-methoxyethoxy)-2,5,7,10-tetraoxaundecane, propylene glycol, propylene glycol monoethyl ether, ethylene glycol monomethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, dipropylene glycol monomethyl ether, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, and N-isopropyl-2-pyrrolidone.

6. The alkaline cleaning composition according to claim 1 , wherein an amount of the polar solvent in the alkaline cleaning composition ranges from 5% to 84.9% by weight.

7. An alkaline cleaning composition, comprising a quaternary ammonium hydroxide, 5% to 40% by weight of propylene glycol monomethyl ether, 10% to 30% by weight of water, and a polar solvent;

wherein the polar solvent is at least one selected from the group consisting of N-isopropyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, 2,5,7,10-tetraoxaundecane, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, and propylene glycol, and the alkaline cleaning composition is free of benzenesulfonic acid.

8. A cleaning method, comprising a step of using the alkaline cleaning composition according to claim 1 to clean and remove a residue or a residual film attached onto a device component, wherein the residue or the residual film comprises a resist or an inorganic substance comprising silicon atoms.

9. A manufacturing method of a semiconductor, comprising following steps:

providing a substrate;

coating a siloxane resin layer on the substrate;

coating a photoresist layer on the siloxane resin layer to form a multilayered substrate;

performing photolithography and etching processes on the multilayered substrate; and

using the alkaline cleaning composition according to claim 1 to clean and remove residues of the siloxane resin layer and the photoresist layer attached onto the substrate.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2022
From: TANG, HUI-YI; WANG, TZU-CHI; CHEN, YU-NUNG; CHEN, YI-CHENG
To: DAXIN MATERIALS CORPORATION
Reel/Frame 059803/0030 →
Priority Claims (1)
TW 109146082 · Dec 24, 2020 · national
Continuity (1)
Related Publication 20220206394A1 · Jun 30, 2022
References Cited (29)
US 7700533B2 · Egbe et al. · 2010 [cited by applicant]
US 7888301B2 · Bernhard et al. · 2011 [cited by applicant]
US 8440599B2 · Egbe et al. · 2013 [cited by applicant]
US 8617417B2 · Inaba et al. · 2013 [cited by applicant]
US 9217929B2 · Egbe et al. · 2015 [cited by applicant]
US 9570285B2 · Liu et al. · 2017 [cited by applicant]
US 10035978B2 · Oie et al. · 2018 [cited by applicant]
US 20070225188A1 · Wang · 2007 [cited by applicant]
US 20080096785A1 · Egbe et al. · 2008 [cited by applicant]
US 20100152086A1 · Wu · 2010 [cited by examiner]
US 20150133356A1 · Pollard · 2015 [cited by examiner]
CN 101794088A · 2010 [cited by applicant]
CN 102051283A · 2011 [cited by applicant]
EP 1612858A2 · 2006 [cited by applicant]
EP 2281867A1 · 2011 [cited by examiner]
EP 3553811A1 · 2019 [cited by examiner]
JP H09269601A · 1997 [cited by applicant]
JP 2008103730A · 2008 [cited by applicant]
JP 2008129571A · 2008 [cited by applicant]
JP 2009224782A · 2009 [cited by applicant]
JP 2018109154A · 2018 [cited by applicant]
TW 200700938A · 2007 [cited by applicant]
TW 201139659A · 2011 [cited by applicant]
TW 201638679A · 2016 [cited by applicant]
WO 2015166826A1 · 2015 [cited by applicant]
WO 2017150620A1 · 2017 [cited by applicant]
WO 2020235605A1 · 2020 [cited by applicant]
European Search Report in European application No. 21216531.0,mailed on Aug. 26, 2022. [cited by applicant]
Japanese Office Action issued in corresponding Japanese Patent Application No. 2021206025.A dated Feb. 14, 2023, pp. 1-3. [cited by applicant]