POSITIVE PHOTORESIST COMPOSITION AND METHOD OF FORMING PATTERNED POLYIMIDE LAYER

Abstract

The present invention provides a positive photoresist composition comprising a cresol-type novolac resin, a diazonaphthoquinone-based sensitizer and an organic solvent; based on the cresol-type novolac resin with a total amount of 100 parts by weight, the amount of the diazonaphthoquinone-based sensitizer ranges from 40 parts to 60 parts by weight, the amount of the free cresol in the cresol-type novolac resin is lower than 2 parts by weight, and the alkaline dissolution rate (ADR) of the cresol-type novolac resin in an aqueous solution of 3.5 wt % to 7 wt % tetramethylammonium hydroxide is lower than 285 /s. The positive photoresist composition has excellent chemical resistance to the polyimide stripper, and can specifically improve the protective ability of the photoresist layer to the low-dielectric polyimide layer, thereby optimizing the manufacturing process and quality of the patterned polyimide layer.

Claims

1. A positive photoresist composition comprising: a cresol-type novolac resin, one of a diazonaphthoquinone-based sensitizer and an organic solvent; based on the cresol-type novolac resin with a total amount of 100 parts by weight, the amount of the diazonaphthoquinone-based sensitizer ranging from 40 parts to 60 parts by weight, the content of the free cresol in the cresol-type novolac resin being lower than 2 wt %, and the alkaline dissolution rate (ADR) of the cresol-type novolac resin in an aqueous solution of 3.5 wt % to 7 wt % tetramethylammonium hydroxide being lower than 285 /s.

2. The positive photoresist composition as claimed in claim 1, wherein the cresol-type novolac resin has a weight average molecular weight of 10,000 to 40,000.

3. The positive photoresist composition as claimed in claim 1, wherein the amount of the diazonaphthoquinone-based sensitizer ranges from 45 parts to 55 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

4. The positive photoresist composition as claimed in claim 1, wherein the positive photoresist composition comprises a fluorosurfactant.

5. The positive photoresist composition as claimed in claim 1, wherein the amount of the organic solvent is 100 parts by weight to 500 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

6. The positive photoresist composition as claimed in claim 2, wherein the amount of the organic solvent is 100 parts by weight to 500 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

7. The positive photoresist composition as claimed in claim 3, wherein the amount of the organic solvent is 100 parts by weight to 500 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

8. The positive photoresist composition as claimed in claim 4, wherein the amount of the organic solvent is 100 parts by weight to 500 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

9. The positive photoresist composition as claimed in claim 1, wherein the organic solvent contains 2-heptanone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, ethyl lactate, methyl ethyl ketone or any combinations thereof.

10. The positive photoresist composition as claimed in claim 5, wherein the organic solvent contains 2-heptanone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, ethyl lactate, methyl ethyl ketone or any combinations thereof.

11. A method for forming a patterned polyimide layer, comprising the following steps: coating the positive photoresist composition as claimed in claim 1 on a polyimide layer, so as to form a photoresist layer; exposing and developing the photoresist layer with a developer to obtain a patterned photoresist layer, the patterned photoresist layer covering a portion of the polyimide layer; stripping another portion of the polyimide layer that is not covered with the patterned photoresist layer by using a polyimide stripper; and removing the patterned photoresist layer by using a photoresist remover, so as to form a patterned polyimide layer.

12. The method as claimed in claim 11, wherein the developer is an aqueous solution of tetramethylammonium hydroxide with a concentration of 3.5 wt % to 7 wt %.

13. The method as claimed in claim 11, wherein the method includes a step of baking the patterned photoresist layer and the polyimide layer at a temperature ranging from 80 C. to 120 C. between the developing step and the stripping step.

14. The method as claimed in claim 11, wherein the photoresist remover contains acetone, methyl ethyl ketone, 2-pentanone, 3-pentanone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, ethyl lactate or any combination thereof.

15. The method as claimed in claim 11, wherein the polyimide stripper contains 1 wt % to 20 wt % of an organic amine compound, 5 wt % to 30 wt % of an organic nitrogen-containing compound and 50 wt % to 90 wt % of an aqueous ethylene glycol solution.

16. The method as claimed in claim 11, wherein the cresol-type novolac resin of the positive photoresist composition has a weight average molecular weight of 10,000 to 40,000.

17. The method as claimed in claim 11, wherein the amount of the diazonaphthoquinone-based sensitizer of the positive photoresist composition ranges from 45 parts to 55 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

18. The method as claimed in claim 11, wherein the positive photoresist composition comprises a fluorosurfactant.

19. The method as claimed in claim 11, wherein the amount of the organic solvent of the positive photoresist composition is 100 parts by weight to 500 parts by weight based on the cresol-type novolac resin with the total amount of 100 parts by weight.

20. The method as claimed in claim 11, wherein the organic solvent of the positive photoresist composition contains 2-heptanone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, ethyl lactate, methyl ethyl ketone or any combinations thereof.

Description

BRIEF DESCRIPTION OF THE DRAWING

[0033] FIG. 1 is a schematic view of a manufacturing process of a patterned polyimide layer in accordance with one or more embodiments.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0034] Hereinafter, several embodiments are described to illustrate the implementation of the present invention; one skilled in the art can easily realize the advantages and effects of the present invention from the following specifications. Various modifications and variations could be made in order to practice or apply the present invention without departing from the spirit and scope of the invention.

[0035] Preparing a Positive Photoresist Composition

[0036] Various cresol-type novolac resins, diazonaphthoquinone-based sensitizers (1-phenol-4-(1-(4-(2-(4-(phenol)methyl)phenyl)propyl-2)phenyl)-1-(4-phenolyl phenyl)ethyl)phenyl diazonaphthoquinone derivative), fluorine surfactant (MEGAFAC F-477, purchased from the DIC Corporation) and the organic solvent (2-heptanone) were mixed in the amounts as shown in Table 1 below to prepare the positive photoresist compositions of Examples 1 to 3 and Comparative Examples 1 to 4, respectively. The characteristics of the cresol-type novolac resin used in each example and each comparative example are shown in Table 1 below.

[0037] The difference between the positive photoresist compositions of the examples and comparative examples was that the amount of the cresol-type novolac resin, the amount of the diazonaphthoquinone-based sensitizer, and the molar ratio of meta-cresol to para-cresol in the cresol-type novolac resin (shown as the molar ratio of meta-cresol:para-cresol in Table 1 below), the content of the free cresol in cresol-type novolac resin, the alkaline dissolution rate of the cresol-type novolac resin in an aqueous solution of 3.5 wt % tetramethylammonium hydroxide, and the weight average molecular weight (Mw) of the cresol-type novolac resin.

TABLE-US-00001 TABLE 1 Amounts of each component, the molar ratio of the meta-cresol:para-cresol in cresol-type novolac resin, the content of free cresol, ADR and Mw in the positive photoresist compositions of Examples 1 to 3 (EX1 to EX3) and Comparative Examples 1 to 4 (C1 to C4) description EX1 EX2 EX3 C1 C2 C3 C4 the molar ratio of the 6:4 7:3 3:7 7:3 6:4 6:4 6:4 m-cresol:p-cresol the content of free 1.6 wt % 1.7 wt % 1.5 wt % 3.6 wt % 1.6 wt % 1.6 wt % 1.9 wt % cresol ADR (TMAH 3.5%) 64 /s 237 /s 213 /s 180 /s 64 /s 64 /s 720 /s Mw of cresol-type 12750 10576 11247 14886 12750 12750 5520 novolac resin Amount of cresol-type 100 100 100 100 100 100 100 novolac resin (part by weight, PBW) Amount of Sensitizer 55 45 55 55 35 65 55 (PBW) Amount of Additive 0.22 0.22 0.22 0.22 0.22 0.22 0.22 (PBW) Amount of Solvent 190 190 190 190 190 190 190 (PBW)

[0038] Method of Forming a Patterned Polyimide Layer

[0039] A positive photoresist composition prepared in Examples 1 to 3 and Comparative Examples 1 to 4 was used, and then sequentially underwent coating, exposing, developing, stripping, photoresist removing and other steps to form a patterned polyimide layer.

[0040] The method of forming a patterned polyimide layer in each of the examples and comparative examples was substantially the same, except that the positive photoresist compositions used were different, so as to compare the performance difference of the positive photoresist compositions of the different examples and comparative examples applied in the patterned polyimide layer. For the detailed method of forming the patterned polyimide layer, please refer to FIG. 1 and the description of the following steps.

[0041] As shown in FIG. 1, an 8-inch silicon wafer 10 was prepared, formed thereon with a low-dielectric polyimide layer 20 having a thickness of 100 nm. The positive photoresist composition was coated on the polyimide layer 20 by using a spin-coating machine, and then heated at 100 C. for 2.5 minutes by using a baking sheet to obtain a uniform photoresist layer 30 with a thickness of 15 m. Subsequently, the exposure step was performed by irradiating an appropriate energy on the photomask M by using an exposure machine, and then a development step was performed by using a 5% aqueous solution of tetramethylammonium hydroxide (developer) to obtain a patterned photoresist layer 30A. The patterned photoresist layer 30A was covered on a portion of the polyimide layer 20. Here, the total film thickness of the polyimide layer 20 and the patterned photoresist layer 30A was measured and recorded as T1. Then the silicon wafer 10 with the polyimide layer 20 and the patterned photoresist layer 30A was heated at 110 C. for 5 minutes by using a baking sheet, and then was immersed in a polyimide stripper preheated to 50 C. (PIC01 sold by EverDependUp Co., Ltd.) for about 3 minutes, until a portion of the polyimide layer 20 (that is, the polyimide layer not covered by the patterned photoresist layer 30A) was removed. Here, the total film thickness of the polyimide layer 20 and the patterned photoresist layer 30A was measured and recorded as T2. At last, the whole of the silicon wafer 10 after measuring the residual film percentage was immersed in acetone (photoresist remover) for 1 minute, and the process of forming the patterned polyimide layer was completed. A patterned polyimide layer 20A was formed on the silicon wafer 10.

[0042] The film thicknesses T1 and T2 of each of the examples and the comparative examples measured in the foresaid process were recorded in Table 2 below. The ratio of T2/T1 was defined as residual film percentage, and the results were also shown in Table 2 below. The higher residual film percentage indicates the better chemical resistance of the photoresist layer to the polyimide stripper, which can improve the protective ability of the photoresist layer to the polyimide layer below.

[0043] In addition, after the processes of forming the patterned polyimide layer of each of the examples and the comparative examples, the surfaces of the respective patterned polyimide layers were separately observed by using an optical microscope to confirm whether there was a defect of photoresist residue on the patterned polyimide layer of Examples 1 to 3 and Comparative Examples 1 to 4. The observation results were also shown in Table 2 below. The observation can determine whether the photoresist layer is completely removed by the commonly-used photoresist remover as expected, so as to confirm the film quality of the patterned polyimide layer.

TABLE-US-00002 TABLE 2 The film thicknesses T1, T2 and residual film percentages measured with the polyimide layers patterned by the positive photoresist compositions of Examples 1 to 3 (EX1 to EX3) and Comparative Examples 1 to 4 (C1 to C4). Observation of the T1 (m) T2 (m) T2/T1 (%) photoresist residues EX 1 15.0 13.9 93 None EX 2 15.2 13.1 86 None EX 3 15.2 13.3 88 None C1 15.0 9.9 66 None C2 15.1 9.1 60 None C3 None C4 15.0 5.7 38 None

[0044] According to the results shown in Tables 1 and 2 above, if the positive photoresist composition has the following characteristics: (1) the positive photoresist composition has 100 parts by weight of cresol-type novolac resin and 40 to 60 parts by weight of diazonaphthoquinone-based sensitizer, (2) the content of free cresol in the cresol-type novolac resin is less than 2 wt %, and (3) the ADR (TMAH 3.5%) of the cresol-type novolac resin is lower than 285 /s, then for example, the residual film percentage of the positive photoresist composition of the Examples 1 to 3 can be measured to be at least 80%, and the overall photoresist layer can be easily removed in the patterning process by the photoresist remover commonly-used in the market, without the phenomenon of photoresist residue. On the other hand, in the absence of at least one of the foresaid features, for example, the corresponding residual film percentage of the positive photoresist compositions of Comparative Examples 1 to 4 described above was remarkably decreased, indicating that the photoresist layers in the positive photoresist compositions of Comparative Examples 1 to 4 were insufficient in chemical resistance to the polyimide strippers and the polyimide layer underneath cannot be protected as expected, and thereby the polyimide stripper was able to etch the polyimide layer covered by the patterned photoresist layer and this resulted in a remarkably lower residual film percentage, even film breakage in Comparative Example 3.

[0045] Further investigating the positive photoresist composition of each comparative example, it is concluded that since the content of free cresol of the cresol-type novolac resin in the positive photoresist composition of Comparative Example 1 had exceeded 2 wt %, the residual film percentage was only 66%; the cresol-type novolac resin in the positive photoresist composition of Comparative Example 2 and Comparative Example 3 was the same as that of Example 1, but the amount of the naphthoquinone sensitizer in the positive photoresist composition of Comparative Example 2 had been lower than the limit value of 40 wt %, so the residual film percentage was only 60%; the amount of the naphthoquinone sensitizer in the positive photoresist composition of Comparative Example 3 had exceeded the limit value of 60 wt %, so that occurring sensitizer precipitation in the process for the positive photoresist composition of Comparative Example 3 and cannot be used; and the ADR of the cresol-type novolac resin in the positive type photoresist composition of Comparative Example 4 was too high, and the residual film percentage was only 38%.

[0046] It has been confirmed by experimental results that if the positive photoresist composition has the following characteristics: (1) the positive photoresist composition has 100 parts by weight of cresol-type novolac resin and 40 to 60 parts by weight of diazonaphthoquinone-based sensitizer, (2) the content of free cresol in the cresol-type novolac resin is less than 2 wt %, and (3) the ADR (TMAH 3.5%) of the cresol-type novolac resin is lower than 285 /s, then the formed photoresist layer not only has high peelability and avoids photoresist residues in the process, but also optimizes the chemical resistance of the photoresist layer to the polyimide strippers, and enables the photoresist layer to protect the polyimide layer underneath effectively in wet etching, and thereby achieving the purpose of patterning the low-dielectric polyimide layer.

[0047] Even though numerous characteristics and advantages of the present invention have been set forth in the foregoing description, together with details of the structure and features of the invention, the disclosure is illustrative only. Changes may be made in the details, especially in matters of characteristic, range, and species of parts within the principles of the invention to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.