IP Library Granted Patent US 11,384,268
Granted Patent B2
US 11,384,268 · App. 16/619,343 · Granted Jul 12, 2022

Curable silicone composition for die bonding use

Inventors: Ryosuke Yamazaki (Chiba, JP); Shinichi Yamamoto (Chiba, JP)
Assignee: DuPont Toray Specialty Materials Kabushiki Kaisha
C09J183/04C08G77/08C08G77/12C08K3/36C08K5/5435C08K2201/006C09J2203/326
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Quick Facts
Patent No.
US 11,384,268
App. No.
16/619,343
Granted
Jul 12, 2022
Kind
B2
Abstract

A curable silicone composition for die bonding use contains at least (A) an organopolysiloxane having at least two alkenyl groups per molecule, (B) an organopolysiloxane having at least two siloxane units each represented by the formula: RHSiO (wherein R represents a monovalent hydrocarbon group having 1 to 12 carbon atoms and having no aliphatic unsaturated bond) per molecule, (C) a platinum-group metal-based catalyst for hydrosilylation reactions, (D) a hydrosilylation reaction inhibitor and (E) an adhesiveness-imparting agent, wherein the scorch time (ts1), which is defined in JIS K 6300-2, at a die bonding temperature is 20 to 60 seconds, and the 90% vulcanization time [tc(90)] with respect to the maximum torque value during the vulcanization time of 600 seconds is 300 to 500 seconds. The curable silicone composition for die bonding use according to the present invention can adhere a semiconductor chip to a support strongly.

Claims (34)

1. A curable silicone composition for die bonding use, comprising at least

(A) 100 parts by mass of organopolysiloxane having at least 2 alkenyl groups per molecule,

(B) organopolysiloxane having, per molecule, at least 2 siloxane units represented by the formula RHSiO (in the formula, R is a monovalent C1-12 hydrocarbon group having no aliphatic unsaturated bonds) {in an amount such that the molar ratio of the silicon atom-bonded hydrogen atoms in this component with respect to the alkenyl groups in component (A) is 0.1-10},

(C) platinum-group metal hydrosilylation reaction catalyst in an amount such that the amount, in mass units, of platinum-group metal in this component is 10 ppm with respect to the total amount of components (A) and (B),

(D) 0.001-5 parts by mass of hydrosilylation reaction inhibitor per 100 parts by mass of the total amount of components (A) and (B), and

(E) 0.01-10 parts by mass of adhesiveness-bestowing agent per 100 parts by mass of the total amount of components (A) and (B),

wherein the scorch time (ts1) is 20-60 seconds at the die bonding temperature, specified in JIS K 6300-2, and, with respect to the maximum torque value up to a vulcanization time of 600 seconds, the 90% vulcanization time [tc(90)] is 300-500 seconds.

2. The curable silicone composition for die bonding use as claimed in claim 1 , where component (A) contains an organopolysiloxane resin comprising at least

a siloxane unit represented by the formula R 1 3 SiO 1/2 (in the formula, R 1 is an identical or different monovalent C1-12 hydrocarbon group having no aliphatic unsaturated bonds), a siloxane unit represented by the formula R 1 2 R 2 SiO 1/2 (in the formula, R 1 is as described above, and R 2 is a C2-12 alkenyl group), and

a siloxane unit represented by the formula SiO 4/2 , wherein the molar ratio of the total amount of siloxane units represented by formula R 1 3 SiO 1/2 and siloxane units represented by formula R 1 2 R 2 SiO 1/2 , with respect to the siloxane unit represented by formula SiO 4/2 , is 0.5-1.6.

3. The curable silicone composition for die bonding use as claimed in claim 2 , where component (B) is an organopolysiloxane resin comprising at least

a siloxane unit represented by the formula R 4 3 SiO 1/2 (in the formula, R 4 is an identical or different monovalent C1-12 hydrocarbon group having no aliphatic unsaturated bonds),

a siloxane unit represented by the formula R 4 HSiO 2/2 (in the formula, R 4 is as described above), and

a siloxane unit represented by the formula SiO 4/2 ,

wherein the molar ratio of the siloxane unit represented by formula R 4 3 SiO 1/2 is 0.6-1.5 and the molar ratio of the siloxane unit represented by formula R 4 HSiO 2/2 is 1.5-3, with respect to the siloxane unit represented by formula SiO 4/2 .

4. The curable silicone composition for die bonding use as claimed in claim 2 , where component (B) is an organopolysiloxane comprising at least

a siloxane unit represented by the formula R 4 3 SiO 1/2 (in the formula, R 4 is an identical or different monovalent C1-12 hydrocarbon group having no aliphatic unsaturated bonds),

a siloxane unit represented by the formula R 4 HSiO 2/2 (in the formula, R 4 is as described above), and

having no siloxane units represented by the formula SiO 4/2 .

5. The curable silicone composition for die bonding use as claimed in claim 1 , where component (B) is an organopolysiloxane resin comprising at least

a siloxane unit represented by the formula R 4 3 SiO 1/2 (in the formula, R 4 is an identical or different monovalent C1-12 hydrocarbon group having no aliphatic unsaturated bonds),

a siloxane unit represented by the formula R 4 HSiO 2/2 (in the formula, R 4 is as described above), and

a siloxane unit represented by the formula SiO 4/2 ,

wherein the molar ratio of the siloxane unit represented by formula R 4 3 SiO 1/2 is 0.6-1.5 and the molar ratio of the siloxane unit represented by formula R 4 HSiO 2/2 is 1.5-3, with respect to the siloxane unit represented by formula SiO 4/2 .

6. The curable silicone composition for die bonding use as claimed in claim 1 , where component (B) is an organopolysiloxane comprising at least

a siloxane unit represented by the formula R 4 3 SiO 1/2 (in the formula, R 4 is an identical or different monovalent C1-12 hydrocarbon group having no aliphatic unsaturated bonds), and

a siloxane unit represented by the formula R 4 HSiO 2/2 (in the formula, R 4 is as described above), and

having no siloxane units represented by the formula SiO 4/2 .

7. The curable silicone composition for die bonding use as claimed in claim 1 , where component (D) is an alkyne alcohol and/or silylated alkyne alcohol.

8. The curable silicone composition for die bonding use as claimed in claim 1 , where component (E) is a reaction mixture comprising epoxy group-containing alkoxysilane and alkenyl group-containing diorganosiloxane oligomer having both molecular chain terminals silanol group-blocked.

9. The curable silicone composition for die bonding use as claimed in claim 1 , further comprising (F) fumed silica having a BET specific surface area of 20-200 m 2 / g at 1-20 parts by mass per 100 parts by mass of the total amount of components (A) and (B).

10. The curable silicone composition for die bonding use as claimed in claim 1 , which when cured forms a cured product having a type D durometer hardness, as defined in JIS K 6253-1997, of at least 50.

11. The curable silicone composition for die bonding use as claimed in claim 1 , which when cured forms a cured product having a flexural strain, as defined in JIS K 7171-1994, of at least 10%.

12. The curable silicone composition for die bonding use as claimed in claim 1 , for adhering LED elements to substrates.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2025
From: DUPONT TORAY SPECIALTY MATERIALS KABUSHIKI KAISHA
To: DUROPTIX MATERIALS KABUSHIKI KAISHA
Reel/Frame 073229/0238 →
CHANGE OF NAME Recorded Sep 3, 2020
From: DOW CORNING TORAY CO., LTD.
To: DUPONT TORAY SPECIALTY MATERIALS KABUSHIKI KAISHA
Reel/Frame 053681/0507 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2019
From: YAMAZAKI, RYOSUKE; YAMAMOTO, SHINICHI
To: DOW CORNING TORAY CO., LTD.
Reel/Frame 051178/0641 →