Circuit build-up film for wafer-level packaging, and fabrication method and use thereof
11286386 · 2022-03-29
Assignee
Inventors
- De WU (Wuhan, CN)
- Shuhang LIAO (Wuhan, CN)
- Yi Wang (Wuhan, CN)
- Junxing SU (Wuhan, CN)
- Feifei LIANG (Wuhan, CN)
Cpc classification
C08L2205/035
CHEMISTRY; METALLURGY
C08L63/00
CHEMISTRY; METALLURGY
C08K5/0025
CHEMISTRY; METALLURGY
C08L2205/025
CHEMISTRY; METALLURGY
C08L2203/206
CHEMISTRY; METALLURGY
C08L63/00
CHEMISTRY; METALLURGY
International classification
C08L63/00
CHEMISTRY; METALLURGY
Abstract
A circuit build-up film for wafer-level packaging (WLP) includes 40 to 60 parts by mass of a first epoxy resin, 15 to 30 parts by mass of a second epoxy resin, 25 to 50 parts by mass of a curing agent, 0.1 to 5 parts by mass of a curing accelerator, 5 to 20 parts by mass of an additive, 320 to 650 parts by mass of an inorganic filler, and 0.01 to 5 parts by mass of a silane coupling agent (SCA), where the additive is obtained by subjecting an epoxy resin to a reaction with a polyhydroxyl-terminated dendritic crosslinking agent. The build-up film shows prominent fluidity during heating and curing, and can completely fill gaps among wafers. A packaging process using the build-up film is simple. Regardless of the number of wafers, packaging can be completed through one procedure with the build-up film.
Claims
1. A circuit build-up film for wafer-level packaging (WLP), comprising the following components: a first epoxy resin of 40 to 60 parts by mass, a second epoxy resin of 15 to 30 parts by mass, a curing agent of 25 to 50 parts by mass, a curing accelerator of 0.1 to 5 parts by mass, an additive of 5 to 20 parts by mass, an inorganic filler of 320 to 650 parts by mass, and a silane coupling agent (SCA) of 0.01 to 5 parts by mass, wherein the first epoxy resin is one or more from the group consisting of a bisphenol A epoxy resin, a bisphenol F epoxy resin, and a biphenyl epoxy resin; the second epoxy resin is one or two from the group consisting of a naphthalene epoxy resin and a dicyclopentadiene-phenol epoxy resin; and the additive is obtained by subjecting a bisphenol A epoxy resin or a bisphenol F epoxy resin to a reaction with a polyhydroxyl-terminated dendritic crosslinking agent at 100° C. to 160° C. for 2 h to 4 h, wherein an amount of the polyhydroxyl-terminated dendritic crosslinking agent is 1% to 5% by mass of an amount of the epoxy resin used in the reaction, the polyhydroxyl-terminated dendritic crosslinking agent is a hydroxyl-terminated polyamidoamine (PAMAM) dendrimer.
2. The circuit build-up film for the WLP according to claim 1, wherein when the second epoxy resin is two from the group consisting of the naphthalene epoxy resin and the dicyclopentadiene-phenol epoxy resin, the naphthalene epoxy resin accounts for 5 to 10 parts by mass and the dicyclopentadiene-phenol epoxy resin accounts for 15 to 25 parts by mass.
3. The circuit build-up film for the WLP according to claim 1, wherein the curing agent is one or more from the group consisting of an amine curing agent, a mercaptan curing agent, an anhydride curing agent, and a phenolic resin curing agent.
4. The circuit build-up film for the WLP according to claim 1, wherein the curing accelerator is an imidazole curing accelerator.
5. The circuit build-up film for the WLP according to claim 1, wherein the inorganic filler is silica.
6. The circuit build-up film for the WLP according to claim 1, wherein the SCA is γ-glycidoxypropyltrimethoxysilane.
7. The circuit build-up film for the WLP according to claim 1, further comprising: 0.1 to 5 parts by mass of a colorant.
8. A fabrication method of the circuit build-up film for the WLP according to claim 1, comprising: mixing the first epoxy resin, the second epoxy resin, the curing agent, the curing accelerator, the additive, the inorganic filler, and the SCA in a specified ratio; and coating a resulting mixture slurry on a base film, and drying the base film.
9. The fabrication method according to claim 8, wherein when the second epoxy resin is two from the group consisting of the naphthalene epoxy resin and the dicyclopentadiene-phenol epoxy resin, the naphthalene epoxy resin accounts for 5 to 10 parts by mass and the dicyclopentadiene-phenol epoxy resin accounts for 15 to 25 parts by mass.
10. The fabrication method according to claim 8, wherein the curing agent is one or more from the group consisting of an amine curing agent, a mercaptan curing agent, an anhydride curing agent, and a phenolic resin curing agent.
11. The fabrication method according to claim 8, wherein the curing accelerator is an imidazole curing accelerator.
12. The fabrication method according to claim 8, wherein the inorganic filler is silica.
13. The fabrication method according to claim 8, wherein the SCA is γ-glycidoxypropyltrimethoxysilane.
14. Use of the circuit build-up film for the WLP according to claim 1, comprising: covering wafers of a semiconductor mounting structure with the circuit build-up film, and heating and curing the circuit build-up film to fill and package the semiconductor mounting structure, wherein the semiconductor mounting structure comprises a substrate and a plurality of wafers arranged on the substrate.
15. The use according to claim 14, wherein when the second epoxy resin is two from the group consisting of the naphthalene epoxy resin and the dicyclopentadiene-phenol epoxy resin, the naphthalene epoxy resin accounts for 5 to 10 parts by mass and the dicyclopentadiene-phenol epoxy resin accounts for 15 to 25 parts by mass.
16. The use according to claim 14, wherein the curing agent is one or more from the group consisting of an amine curing agent, a mercaptan curing agent, an anhydride curing agent, and a phenolic resin curing agent.
17. The use according to claim 14, wherein the curing accelerator is an imidazole curing accelerator.
18. The use according to claim 14, wherein the inorganic filler is silica.
19. The use according to claim 14, wherein the SCA is γ-glycidoxypropyltrimethoxysilane.
20. The use according to claim 14, wherein the circuit build-up film further comprises: 0.1 to 5 parts by mass of a colorant.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3) Reference numerals in the figures: 1: wafer, 2: substrate, and 3: circuit build-up film.
DETAILED DESCRIPTION OF THE EMBODIMENTS
(4) In order to make the objectives, technical solutions, and advantages of the present disclosure more comprehensible, specific implementations of the present disclosure are described in further detail below. It should be understood that the specific implementations described are merely intended to explain the present disclosure, rather than to limit the present disclosure.
(5) The circuit build-up film for WLP provided by the present disclosure includes an epoxy resin, 25 to 50 parts by mass of a curing agent, 0.1 to 5 parts by mass of a curing accelerator, 5 to 20 parts by mass of an additive, 320 to 650 parts by mass of an inorganic filler, and 0.01 to 5 parts by mass of an SCA, where the epoxy resin includes 40 to 60 parts by mass of a first epoxy resin and 15 to 30 parts by mass of a second epoxy resin; the first epoxy resin is one or more from the group consisting of a bisphenol A epoxy resin, a bisphenol F epoxy resin, and a biphenyl epoxy resin, and is preferably a bisphenol A epoxy resin; and the second epoxy resin is one or two from the group consisting of a naphthalene epoxy resin and a dicyclopentadiene-phenol epoxy resin.
(6) The additive is an epoxy-modified dendritic crosslinking agent and is obtained by subjecting an epoxy resin to a reaction with a polyhydroxyl-terminated dendritic crosslinking agent at 100° C. to 160° C. for 2 h to 4 h, during which hydroxyl in the dendritic crosslinking agent opens a ring of epoxy. The parts by mass of the dendritic crosslinking agent may be 1% to 5% of the parts by mass of the epoxy resin. In this specific implementation, 100 parts by mass of a bisphenol F epoxy resin are subjected to a reaction with 5 parts by mass of a polyhydroxyl-terminated dendritic crosslinking agent, and the polyhydroxyl-terminated dendritic crosslinking agent may be the T60 product purchased from Weihai Chenyuan Molecular New Material Co., Ltd.
(7) The curing agent may be any curing agent corresponding to an epoxy resin used, and is not particularly limited. As required, the curing agent may be one or more from the group consisting of an amine curing agent, a mercaptan curing agent, an anhydride curing agent, and a phenolic resin curing agent. In this specific implementation, a phenolic resin curing agent is adopted. The curing accelerator can be any conventional curing accelerator, and is also not particularly limited. In this specific implementation, an imidazole curing accelerator is adopted. The curing accelerator can be used at a conventional amount. The inorganic filler can be a conventional inorganic filler, such as silica, calcium silicate, and boron nitride. The SCA is located between an inorganic interface and an organic interface, and can form a bonding layer of organic matrix-SCA-inorganic matrix at an interface, which plays the role of connecting materials with many different properties. The SCA may preferably be γ-glycidoxypropyltrimethoxysilane. The circuit build-up film of the present disclosure may further include 0.1 to 5 parts by mass of a colorant, and the colorant is used to provide a color for the circuit build-up film. Specifically, a pigment such as carbon black can be used. The colorant is a non-essential component.
(8) The circuit build-up film of the present disclosure can be fabricated by a film coating process: mixing the mixed epoxy resin, the curing agent, the curing accelerator, the additive, the inorganic filler, and the SCA in a specified ratio; and coating a resulting mixture slurry on a base film with a film coating machine, and drying the film to obtain the circuit build-up film of the present disclosure. In a specific implementation, the base film is generally a PET film.
(9) As shown in
(10) In order to further prove the advantages of the circuit build-up film of the present disclosure, the following comparison test was conducted. In the following examples and comparative examples, a phenolic resin was used as a curing agent, 2-phenylimidazole was used as a curing accelerator, silica was used as an inorganic filler, carbon black was used as a colorant, and γ-glycidoxypropyltrimethoxysilane was used as an SCA.
(11) Formulas of the examples and comparative examples were shown in Table 1. Products obtained in the examples and comparative examples were tested for CTE1/2, storage modulus, and warpage, and test data were shown in Table 1.
(12) In this implementation, the CTE1/2 was tested as follows: the prepared circuit build-up films were stacked to a thickness of 1.2 mm, and then heated and cured at 180° C. for 1 h, and then the ASTME831-2019 standard method was used to test CTE;
(13) the storage modulus was tested as follows: the prepared circuit build-up films were stacked to a thickness of 1.2 mm, and then heated and cured at 180° C. for 1 h, and then the ASTME2254-2018 standard method was used to test the storage modulus;
(14) the warpage was tested as follows: the prepared circuit build-up film was applied on a 0.1 mm-thick round glass slide and then baked at 130° C. for 1 h, and after the round glass slide was cooled, an upturn height of the circuit build-up film on both sides of the round glass slide was tested, which was the warpage;
(15) the fluidity was tested as follows: a square circuit build-up film with a size of 5 mm×5 mm was taken and sandwiched with a copper sheet, and then baked at 120° C. for 5 min, and then a flow distance of the circuit build-up film on the copper sheet was observed, where if the flow distance is higher than 2 mm, it indicates that the fluidity is prominent, which is denoted as ⊚; and if the flow distance is less than 2 mm, it indicates that the fluidity is poor, which is denoted as x; and
(16) the tensile strength was tested as follows: a circuit build-up film with a size of 200 mm×10 mm was taken and tested with a universal tensile testing machine, a maximum load when the circuit build-up film broke was recorded, and then the tensile strength was calculated according to the formula: tensile strength=maximum load/breaking cross-sectional area.
(17) It can be seen from Table 1 that the circuit build-up film of the present disclosure has low CTE, high storage modulus, and small warpage, which will reduce or even avoid the cracking, warping, and other negative phenomena of wafers during the subsequent process and use. The circuit build-up film of the present disclosure has prominent fluidity, which helps to completely fill gaps among wafers.
(18) TABLE-US-00002 TABLE 1 Formulas and test results of the examples and comparative examples Example Example Example Example Comparative Comparative 1 2 3 4 Example 1 Example 2 Bisphenol A epoxy resin 50 parts 40 parts 50 parts 60 parts 75 parts 60 parts by mass by mass by mass by mass by mass by mass Naphthalene epoxy resin 20 parts — 10 parts 5 parts — 5 parts by mass by mass by mass by mass Dicyclopentadiene-phenol — 15 parts 15 parts 25 parts — 25 parts epoxy resin by mass by mass by mass by mass Phenolic resin 30 parts 25 parts 30 parts 50 parts 40 parts 50 parts by mass by mass by mass by mass by mass by mass 2-phenylimidazole 2 parts 2 parts 2 parts 2 parts 2 parts 2 parts by mass by mass by mass by mass by mass by mass Additive 15 parts 20 parts 5 parts 10 parts — — by mass by mass by mass by mass Silica 550 parts 320 parts 500 parts 650 parts 600 parts 650 parts by mass by mass by mass by mass by mass by mass Carbon black 1 parts 1 parts 1 parts 1 parts 1 parts 1 parts by mass by mass by mass by mass by mass by mass γ-glycidoxypropyl- 3 parts 3 parts 3 parts 3 parts 3 parts 3 parts trimethoxysilane by mass by mass by mass by mass by mass by mass CTE1/2 (unit: ppm/° C.) 10/25 11/30 10/27 9/25 28/77 25/70 Storage modulus (unit: GPa) 11 10 11 12 7 8 Warpage (unit: mm) 1.5 1.3 1.3 1.4 2.6 2.4 Fluidity ⊚ ⊚ ⊚ ⊚ x x Tensile strength (MPa) 2.3 1.9 1.8 2.1 1.1 1.2
(19) The addition of the additive with a dendritic main structure can improve a material system structure and make the circuit build-up film have more stable comprehensive mechanical properties. It can be seen from Table 1 that, compared with Comparative Examples 1 and 2, for the circuit build-up film of the present disclosure, the CTE is significantly reduced; the storage modulus is significantly improved, where the storage modulus of Example 4 is increased by about 50%; the warpage is reduced by nearly half at most; the tensile strength is also improved, where the tensile strength of Example 1 is increased by 90%, indicating a significant improvement effect; and the circuit build-up film of the present disclosure also has excellent fluidity. The CTE, storage modulus (to characterize the elasticity of a material), warpage, and fluidity all are external manifestations of an internal stress of a system material, and the tensile strength is the characterization of external mechanical properties of a material. Therefore, the test data in Table 1 prove that the comprehensive mechanical properties of the circuit build-up film of the present disclosure have been significantly improved.
(20) The above example is only one among various examples. Changes or modifications in different forms can be made by those skilled in the art on the basis of the above description, and these changes or modifications derived from the essential spirit of the present disclosure still belong to the protection scope of the present disclosure.