IP Library › Granted Patent US 12,517,432
Granted Patent B2
US 12,517,432 · App. 17/453,249 · Granted Jan 6, 2026

Substrate treating composition and method for fabricating a semiconductor device using the same

Inventors: Ju-Young Kim (Hwaseong-si, KR); Hyunwoo Kim (Hanam-si, KR); Makoto Nakajima (Toyama, JP); Satoshi Takeda (Toyama, JP); Shuhei Shigaki (Toyama, JP); Wataru Shibayama (Toyama, JP)
Assignees: SAMSUNG ELECTRONICS CO., LTD.; NISSAN CHEMICAL CORPORATION
G03F7/11C09D183/08G03F7/038G03F7/039G03F7/0757G03F7/2004G03F7/162G03F7/168
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 12,517,432
App. No.
17/453,249
Granted
Jan 6, 2026
Kind
B2
Abstract

Provided is a substrate treating composition. The substrate treating composition includes a first monomer, a second monomer and an acid. The first monomer is represented by Formula 1 and the second monomer is represented by Formula 7. The molecular weight of the solid content of the substrate treating composition including the first monomer, the second monomer and the acid is from about 1,000 g/mol to about 50,000 g/mol. X—Si(R1) 2 (R2)  [Formula 1] Y—Si(R3) 3   [Formula 7]

Claims (21)

1 . A substrate treating composition, consisting essentially of a solid content and a solvent, the solid content consisting a first monomer, a second monomer, a dehydration-condensation product of the first monomer and the second monomer, and an acid, wherein

the first monomer is represented by Formula 1:

X—Si(R1) 2 (R2)  [Formula 1]

wherein each of R1 and R2 is an alkyl group of 1 to 20 carbon atoms or an alkoxy group of 1 to 20 carbon atoms, and X is represented by Formula 2 or Formula 4:

the second monomer is represented by Formula 7:

Y—Si(R3) 3   [Formula 7]

wherein R3 is an alkoxy group of 1 to 20 carbon atoms, and Y is represented by Formula 8, Formula 9, Formula 10, Formula 11, Formula 12:

in which Ts is a p-toluenesulfonyl group,

in which Ms is a methanesulfonyl group,

in which Ms is a methanesulfonyl group,

wherein a molecular weight of the dehydration-condensation product of the first monomer and the second monomer is from 1,000 g/mol to 100,000 g/mol.

2 . The substrate treating composition of claim 1 , wherein X is bonded to a Si atom via a Si—C bond, and Y is bonded to a Si atom via a Si—C bond.

3 . The substrate treating composition of claim 1 , wherein the solvent comprises at least one of propylene glycol ethyl ether (PGEE), propylene glycol methyl ether acetate (PGMEA), propylene glycol methyl ether (PGME), or de-ionized water.

4 . The substrate treating composition of claim 3 , wherein the acid is a carboxylic acid.

5 . The substrate treating composition of claim 1 , wherein the first monomer is an organic silane represented by Formula 1-1 or Formula 1-3:

6 . The substrate treating composition of claim 1 , wherein the second monomer is an organic silane represented by Formula 7-1, Formula 7-2, Formula 7-3, Formula 7-4, or Formula 7-5:

in which Ts is a p-toluenesulfonyl group,

in which Ms is a methanesulfonyl group,

in which Ms is a methanesulfonyl group,

7 . The substrate treating composition of claim 1 , wherein a ratio of a content by wt % of the first monomer to a content by wt % of the solvent is 0.1:100.

8 . The substrate treating composition of claim 1 , wherein a ratio of a content by wt % of the second monomer to a content by wt % of a solution including the first monomer and the solvent is 0.0005:100.

Priority Claims (1)
KR 10-2018-0043246 · Apr 13, 2018 · national
Continuity (2)
Division 16243548 · Jan 9, 2019
Related Publication 20220057715A1 · Feb 24, 2022
References Cited (52)
US 3437517A · Eilerman · 1969 [cited by examiner]
US 4933381A · Hager · 1990 [cited by examiner]
US 4950583A · Brewer et al. · 1990 [cited by applicant]
US 5907015A · Sexsmith · 1999 [cited by examiner]
US 7679133B2 · Son et al. · 2010 [cited by applicant]
US 8553466B2 · Han et al. · 2013 [cited by applicant]
US 8559235B2 · Yoon et al. · 2013 [cited by applicant]
US 8654587B2 · Yoon et al. · 2014 [cited by applicant]
US 8835093B2 · Shibayama et al. · 2014 [cited by applicant]
US 8864894B2 · Shibayama et al. · 2014 [cited by applicant]
US 8968458B2 · Konno et al. · 2015 [cited by applicant]
US 8999630B2 · Hatakeyama et al. · 2015 [cited by applicant]
US 9005873B2 · Sakamoto et al. · 2015 [cited by applicant]
US 9023583B2 · Kishioka et al. · 2015 [cited by applicant]
US 9023588B2 · Nakajima et al. · 2015 [cited by applicant]
US 9170492B2 · Kawazu et al. · 2015 [cited by applicant]
US 9760006B2 · Nakajima et al. · 2017 [cited by applicant]
US 10133179B2 · Sung et al. · 2018 [cited by applicant]
US 20050277058A1 · Iwabuchi · 2005 [cited by examiner]
US 20110233648A1 · Seol et al. · 2011 [cited by applicant]
US 20120315765A1 · Nakajima · 2012 [cited by examiner]
US 20130216956A1 · Kishioka · 2013 [cited by examiner]
US 20140170855A1 · Nakajima · 2014 [cited by examiner]
US 20160222262A1 · Tamura et al. · 2016 [cited by applicant]
US 20180149977A1 · Shibayama · 2018 [cited by examiner]
US 20180186820A1 · Katsukawa et al. · 2018 [cited by applicant]
US 20190317406A1 · Kim et al. · 2019 [cited by applicant]
US 20210198496A1 · Pathak et al. · 2021 [cited by applicant]
CN 101910949 · 2010 [cited by applicant]
CN 102124064 · 2011 [cited by applicant]
CN 102754034 · 2012 [cited by applicant]
CN 102850549A · 2013 [cited by applicant]
CN 104449543A · 2015 [cited by applicant]
CN 107429114A · 2017 [cited by applicant]
EP 2538276 · 2012 [cited by applicant]
JP 06267892 · 1994 [cited by applicant]
JP H093432A · 1997 [cited by examiner]
JP 09054440 · 1997 [cited by applicant]
JP 2017151389 · 2017 [cited by applicant]
KR 1020070103085 · 2007 [cited by applicant]
KR 2008110537A · 2008 [cited by examiner]
KR 1020130009695 · 2013 [cited by applicant]
KR 20140045962A · 2014 [cited by examiner]
KR 1020170113390 · 2017 [cited by applicant]
KR 1020180013729 · 2018 [cited by applicant]
WO 2012050065 · 2012 [cited by applicant]
WO WO2016009939A1 · 2016 [cited by examiner]
WO WO2017119680A1 · 2017 [cited by examiner]
WO WO2017142153A1 · 2017 [cited by examiner]
WO WO2018079599A1 · 2018 [cited by examiner]
WO WO2019082934A1 · 2019 [cited by examiner]
Dufaud, et al., “Design of Heterogeneous Catalysts via Multiple Active Site Positioning in Organic-Inorganic Hybrid Materials”, J. Am. Chem. Soc. 2003, 125, pp. 9403-9413. [cited by applicant]