CN101311224A - Hybrid material composition, flexible transparent film comprising the same and photoelectric device - Google Patents

Hybrid material composition, flexible transparent film comprising the same and photoelectric device Download PDF

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CN101311224A
CN101311224A CNA2007101092439A CN200710109243A CN101311224A CN 101311224 A CN101311224 A CN 101311224A CN A2007101092439 A CNA2007101092439 A CN A2007101092439A CN 200710109243 A CN200710109243 A CN 200710109243A CN 101311224 A CN101311224 A CN 101311224A
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dioxide
silicon
alkane
transparent film
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CN101311224B (en
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吕奇明
张含章
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Industrial Technology Research Institute ITRI
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Abstract

The invention relates to a hybrid material composite with high transparency, high heat resistance and low thermal expansion coefficient, a flexible transparent film and photoconducting devices containing the composite. The composite comprises: a. silicon dioxide(SiO2) and b. polyamide, which is characterized in that the weight ratio of the silicon dioxide(SiO2) and the polyamide is between 1:9 and 9:1.

Description

Hybrid material composition, the flexible transparent film that comprises it and photoelectric device
Technical field
The present invention relates to a kind of hybrid material composition, the hybrid material composition of particularly a kind of high-transmittance, high heat-resisting, low thermal coefficient of expansion, and the film and the photoelectric device that utilize its gained.
Background technology
In recent years, along with the fast development of plane technique of display, in the improvement of indicating meter, also be focussed in particular on little, the lightweight demand of volume.In order to obtain slimming, lightweight, the method that present industry is adopted has two kinds: one is to use thinner glass, and two are to use plastic material to make substrate.Yet, if use the following glass of 0.5 millimeter thickness as substrate, the caused buckling phenomenon of the meeting own weight of Yi Fashengyin glass in manufacturing processed, and cause breaking.In addition, glass has fragile, not shock-resistant and congenital shortcoming such as thickness and weight is bigger.Therefore, this type of substrate will can't satisfy demands such as light weight, slimming and the deflection of new generation product application, folding use gradually.
Utilize plastic base (also being called flexibility (flexible) substrate) to form flat-panel screens, except the indicating meter that uses glass substrate than tradition have lighter, thinner, shock-resistant, be difficult for that but broken curved surface shows and advantage such as can reel, and also can utilize continuous mode (roll-to-roll) production, so can significantly reduce production costs, therefore become the development trend of following indicating meter of new generation.Yet, there are many process conditions restrictions still need overcome at present, and plastic material character still need be improved, just can make the comprehensive importing flat-panel screens of plastic base processing procedure and replace glass substrate, for example: 1. have high-clarity, high thermal stability, low thermal coefficient of expansion, and the exploitation of the plastic base material of high resistant manner simultaneously.2. the exploitation that has the nesa coating of deflection character.3. make the device process technique exploitation of thin film transistor (thin filmtransistor) on the plastic base.The relevant panel processing procedure of 4 back segments and developing material and collocation etc.Wherein, the flexible flat indicating meter develops successful important key factor no more than the development progress of flexible transparent plastic baseplate material, its development trend with about the developing direction and the utilization of following whole flexible display panel.
Be applicable to the employed plastic base of flat-panel screens in order to provide, Japanese Patent JP2005-187768 has disclosed the method that inorganic materials is imported pi, with the further properties of materials (thermal stability, thermal expansivity) that improves.This method comprises utilizes organic solvent with aliphatics or the dissolving of half aliphatics pi, then adds the reaction of coupler and pi functional end-group, then adds silane oxide and water again and participates in reaction.Yet, owing to use silane oxide and water as reactant, at most can only blending small amounts of inorganic silica gel material (mostly being 20% most) in the disclosed matrix material of this patent, therefore make the effect of modification be restricted.
For increasing the blending ratio of inorganic materials, reach the purpose of modification, another prior art has disclosed mixes polyamic acid PAA (polyamic acid) with silicic acid oligomer (silicic acid oligomer).Though this method can be increased to 40% with the doping ratio of inorganics, however the material of gained must be through high temperature endless loop reaction so have yellow color, make substrate after its transparency obviously reduce.
Therefore, how improving the mutual solubility of pi and silicon-dioxide and mixing proportion to obtain high-clarity, high thermal stability, low thermal coefficient of expansion, and the plastic base of high resistant manner, is the problem that the plane shows the process technique important research.
Summary of the invention
The object of the present invention is to provide the hybrid material composition of a kind of high-transmittance, high heat-resisting, low thermal coefficient of expansion, can be used to further form and be applicable to optoelectronic equipment () flexible transparent film for example: display unit or solar cell.
For reaching above-mentioned purpose, high-transmittance of the present invention, high hybrid material composition heat-resisting, low thermal coefficient of expansion can comprise a. silicon-dioxide (SiO 2) and the b. pi, it is characterized in that this silicon-dioxide (SiO 2) and the weight ratio of pi between 1: 9 to 9: 1, preferred weight ratio is between 2: 8 to 9: 1.It can comprise following fabrication steps: with silicon-dioxide (SiO 2) be dissolved in the organic solvent and uniform mixing, wherein this silicon-dioxide (SiO with pi 2) and the weight ratio of pi system between 2: 8 to 9: 1; And, add silicone surfactant and participate in reaction with polar functional group.
In addition, one embodiment of the present invention provides flexible transparent film, and this film can comprise a. silicon-dioxide (SiO 2) and the b. pi, it is characterized in that this silicon-dioxide (SiO 2) and the weight ratio of pi between 1: 9 to 9: 1.It can comprise following fabrication steps: with silicon-dioxide (SiO 2) be dissolved in the organic solvent and uniform mixing obtains solution this silicon-dioxide (SiO wherein with pi 2) and the weight ratio of pi between 2: 8 to 9: 1; In above-mentioned solution, add silicone surfactant, obtain coating composition with polar functional group; And, utilize this coating composition to form rete, and this rete is heat-treated.Wherein this heat treated temperature is between 100~300 degree.
Below by several embodiment and comparing embodiment and conjunction with figs., illustrating further method of the present invention, feature and advantage, but be not to be used for limiting the scope of the invention, scope of the present invention should be as the criterion with appended claims.
Description of drawings
Fig. 1 shows the analytical results of the thermogravimetric analysis of the embodiment of the invention 5 and comparing embodiment 1 gained substrate.
Fig. 2-4 shows that the silicon-dioxide/pi of the embodiment of the invention 5 gained blendes together film (numbering: SiO2/BB64) the surface scan formula electron microscope spectrogram under different enlargement ratios.
Embodiment
The invention provides silicon-dioxide/pi hybrid material composition, it has high-transmittance, high heat-resisting, low thermal coefficient of expansion, the upper and lower plate that can be applicable to bendable flat-panel screens supports, and said composition is mainly formed according to the different ratios hybrid reaction by silicon-dioxide and pi.
Silicon-dioxide is except having high transparent, high heat-stable characteristic, also has the ultra low heat expansion coefficient, and pi has high transparent, high heat-resisting and good flexibility, forms so the present invention mainly utilizes silicon-dioxide to mix according to different ratios with pi to have that height is transparent, height is heat-resisting and silicon-dioxide/pi low thermal coefficient of expansion blendes together the composition of thin-film material.In addition, the present invention utilizes organic solution to dissolve this silicon-dioxide in advance, forming the silicon-dioxide of microstructure, and further mixes with pi, and the addition of silicon-dioxide is improved, and obtains characteristics such as high transparent, high heat-resisting and low thermal coefficient of expansion.
A series of preferred embodiments are described according to the present invention comprises the film that silicon-dioxide/pi blendes together material, and its penetration coefficient can be higher than 90%, glass transition temp can be higher than 350 degree, thermal expansivity can be less than 30ppm/ ℃.
Being prepared as follows of this silicon-dioxide/pi matrix material: with silicon-dioxide (SiO 2) be dissolved in the organic solvent, wherein be dissolved in the silicon-dioxide (SiO in this organic solvent 2) solid content less than 40%.Then, add pi solution, wherein the weight ratio of this silicon-dioxide and pi is between 2: 8 to 9: 1.Behind the uniform mixing, add silicone surfactant again and participate in reaction with polar functional group.
According to the present invention, this organic solvent can be N,N-dimethylacetamide (DMAC), dimethyl formamide (DMF), dimethyl sulfoxide (DMSO) (DMSO), gamma-butyrolactone (γ-butyrolactone).This silicone surfactant with polar functional group can be aminosiloxane (aminosiloxane), isocyanic acid siloxanes (isocynate siloxane).This pi has suc as formula the structure shown in (I):
Figure A20071010924300091
Formula (I)
Wherein, n is greater than 1; G is one or more polycyclic cycloalkyl, heterocyclic radical, cycloalkyl and heterocyclic radical with one or more unsaturated link(age)s, aryl, heteroaryl, aliphatic group, the ring grease dialkylene, aralkyl or heteroaralkyl, and each ring has 3 to 8 annular atomses, and the hydrogen on each annular atoms, optionally can be by halogen, alkyl, the sulfane base, alkoxyl group, the alkane thiazolinyl, the alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base replace, alkyl wherein, the sulfane base, alkoxyl group, the alkane thiazolinyl, the alkane alkynyl, alkene oxygen base or alkynyloxy group contain the 1-12 carbon atom, and it is a straight or branched; And, A is polycyclic cycloalkyl, heterocyclic radical, the cycloalkyl with one or more unsaturated link(age)s and heterocyclic radical, aryl, heteroaryl, aliphatic group, ring grease dialkylene, aralkyl or heteroaralkyl, and each ring has 3 to 8 annular atomses, and the hydrogen on each annular atoms, optionally can be replaced by halogen, alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base, wherein alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base or alkynyloxy group contain the 1-12 carbon atom, and it is a straight or branched.
In addition, according to one preferred embodiment of the present invention, the described G of its Chinese style (I) can be
Figure A20071010924300092
,
Figure A20071010924300093
Or
Figure A20071010924300094
This Z be oxygen ,-CH 2-,-C (CH 3) 2-,-Ar-O-Ar-, Ar-CH 2-Ar-,-Ar-C (CH 3) 2-Ar-or-Ar-SO 2-Ar-, this Ar represents phenyl ring, and the hydrogen of each annular atoms of G, optionally can be replaced by halogen, alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base.The described A of formula (I) is
Figure A20071010924300095
Or
Figure A20071010924300101
This Z be oxygen ,-CH 2-,-C (CH 3) 2-,-Ar-O-Ar-, Ar-CH 2-Ar-,-Ar-C (CH 3) 2-Ar-or-Ar-SO 2-Ar-, this Ar represents phenyl ring, and the hydrogen on each annular atoms of A, optionally can be replaced by halogen, alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base.
It is synthetic that pi of the present invention can utilize typical polycondensation (polycondensation), its synthetic method has two kinds, first method divides two stages to carry out, at first diamines (diamine) and dicarboxylic anhydride (dianhydride) monomer are reacted in polar solvent, form precursor (precursor) polyamic acid of pi, and then carry out inferior amidation (imidization) with pyroprocess (300~400 ℃) or chemical method and react, make its dehydration endless loop transform into pi.Second method is that diamines and dicarboxylic anhydride monomer are reacted in phenol solvent (meta-cresol (m-creso1), chlorophenol (C1-phenol)), is warming up to the reflux temperature reaction, forms pi.
Following spy enumerates embodiment 1~8, in order to explanation the present invention, so that make the present invention can be more clear:
The preparation of pi
Embodiment 1: pi B1317-BAPPm's (BB) is synthetic
At room temperature, use three-necked bottle also to pass to nitrogen, with 0.0147 mole BAPPm pentanoic ( ) dissolve in the meta-cresol (m-cresol) of 32.94g.Treat the BAPPm pentanoic dissolve fully after again with 0.015 mole B1317 dicarboxylic anhydride (
Figure A20071010924300103
) add, after B1317 dissolves fully, continue stirring 1 hour, and form the polyamic acid solution of sticky shape.Then, be heated to 220 ℃, continue 3 hours, in this reaction process, with de-watering apparatus water is got rid of simultaneously.Reaction solution is splashed in the methyl alcohol, make the pi precipitation, and in vacuum drying oven, dried 12 hours, obtain pi B1317-BAPPm (BB).
Reaction formula is as follows:
Figure A20071010924300111
The preparation of silicon-dioxide/pi laminated film
Embodiment 2:
At room temperature, 3g silicon-dioxide is dissolved among the DMAc with solid content 20%, then 7gB1317-BAPPm (BB) is dissolved among the DMAc with solid content 20%, and both are put into the 20g sample bottle.Then, add the 0.3g aminosiloxane in sample bottle, after at room temperature stirring 30 minutes, coat on glass in the scraper mode it, and put into baking oven and under 80 ℃ and 150 ℃, respectively toasted 1 hour, and take off from glass, the silicon-dioxide/pi that just can obtain thickness and be 537 μ m blendes together film (SiO2/BB37).At last, measure this silicon-dioxide/pi blend together film (numbering: coefficient of expansion SiO2/BB37) and penetration coefficient, the result sees also table 1.
Embodiment 3:
At room temperature, 4g silicon-dioxide is dissolved among the DMAc with solid content 20%, then 6gB1317-BAPPm (BB) is dissolved among the DMAc with solid content 20%, and both are put into the 20g sample bottle.Then, add the 0.2g aminosiloxane in sample bottle, after at room temperature stirring 30 minutes, coat on glass in the scraper mode it, and put into baking oven and under 80 ℃ and 150 ℃, respectively toasted 1 hour, and take off from glass, the silicon-dioxide/pi that just can obtain thickness and be 55 μ m blendes together film (SiO2/BB46).At last, measure this silicon-dioxide/pi blend together film (numbering: coefficient of expansion SiO2/BB46) and penetration coefficient, the result sees also table 1.
Embodiment 4:
At room temperature, 5g silicon-dioxide is dissolved among the DMAc with solid content 20%, then 5gB1317-BAPPm (BB) is dissolved among the DMAc with solid content 20%, and both are put into the 20g sample bottle.Then, add the 0.2g aminosiloxane in sample bottle, after at room temperature stirring 30 minutes, coat on glass in the scraper mode it, and put into baking oven and under 80 ℃ and 150 ℃, respectively toasted 1 hour, and take off from glass, the silicon-dioxide/pi that just can obtain thickness and be 52 μ m blendes together film (SiO2/BB55).At last, measure this silicon-dioxide/pi blend together film (numbering: coefficient of expansion SiO2/BB55) and penetration coefficient, the result sees also table 1.
Embodiment 5:
At room temperature, 6g silicon-dioxide is dissolved among the DMAc with solid content 20%, then 4gB1317-BAPPm (BB) is dissolved among the DMAc with solid content 20%, and both are put into the 20g sample bottle.Then, add the 0.2g aminosiloxane in sample bottle, after at room temperature stirring 30 minutes, coat on glass in the scraper mode it, and put into baking oven and under 80 ℃ and 150 ℃, respectively toasted 1 hour, and take off from glass, the silicon-dioxide/pi that just can obtain thickness and be 53 μ m blendes together film (SiO2/BB64).At last, measure this silicon-dioxide/pi blend together film (numbering: coefficient of expansion SiO2/BB64) and penetration coefficient, the result sees also table 1.
Embodiment 6:
At room temperature, 7g silicon-dioxide is dissolved among the DMAc with solid content 20%, then 3gB1317-BAPPm (BB) is dissolved among the DMAc with solid content 20%, and both are put into the 20g sample bottle.Then, add the 0.12g aminosiloxane in sample bottle, after at room temperature stirring 30 minutes, coat on glass in the scraper mode it, and put into baking oven and under 80 ℃ and 150 ℃, respectively toasted 1 hour, and take off from glass, the silicon-dioxide/pi that just can obtain thickness and be 51 μ m blendes together film (SiO2/BB73).At last, measure this silicon-dioxide/pi blend together film (numbering: coefficient of expansion SiO2/BB73) and penetration coefficient, the result sees also table 1.
Comparing embodiment 1:
At room temperature, 10g B1317-BAPPm (BB) is dissolved among the DMAc with solid content 20%.Then, it is coated on glass in the scraper mode, and put into baking oven and respectively toasted under 80 ℃ and 150 ℃ 1 hour, and take off from glass, just can obtain thickness is the pi film of 57 μ m.At last, measure the thermal expansivity and the penetration coefficient of this pi film, the result sees also table 1.
Table 1
Silicon-dioxide/pi Thickness (μ m) Thermal expansivity (ppm/ ℃) Penetration coefficient (%)
Comparing embodiment 1 0/100 57 75.4 89.3
Embodiment 2 30/70 53 56.6 89.5
Embodiment 3 40/60 55 52.3 89.3
Embodiment 4 50/50 52 48.6 89.6
Embodiment 5 60/40 53 42.6 89.3
Embodiment 6 70/30 51 28.3 90.1
As shown in table 1, along with the increase of dioxide-containing silica, the thermal expansivity of this film significantly reduces, and especially when the weight ratio of silicon-dioxide and pi reaches 7: 3 (when dioxide-containing silica accounts for 70%), thermal expansivity more can be lower than 30ppm/ ℃.In addition, even dioxide-containing silica reaches 70%, this film still has high penetration coefficient.
Thermotolerance, strength test and surface analysis
Silicon-dioxide/the pi of embodiment 5 gained is blended together film, and (numbering: SiO2/BB64) the pure pi film with comparing embodiment 1 gained carries out thermogravimetric analysis (Thermal GravimetricAnalysis), and its result asks for an interview Fig. 1.Learn that by knowing among the figure dioxide-containing silica accounts for 60% film, its heat-resisting character is obviously improved many than pure pi substrate.In addition, please refer to Fig. 2-4, silicon-dioxide/pi that they are respectively embodiment 5 gained blendes together film (numbering: SiO2/BB64) the surface scan formula electron microscope spectrogram under different enlargement ratios.
Then, silicon-dioxide/the pi of embodiment 5 gained is blended together film, and (numbering: SiO2/BB64) the pure pi film with comparing embodiment 1 gained carries out strength analysis, measure its Young's modulus (Young ' s modulus (Gpa)), maximum stress (stress), and maximum tension (strain), its result is as shown in table 2.
Table 2
Silicon-dioxide/pi Young's modulus (Gpa) Maximum stress (Mpa) Maximum tension (%)
Comparing embodiment 1 0/100 0.68 61 9.2
Embodiment 6 60/40 2.46 92 3.8
As shown in table 2, the silicon-dioxide/pi of embodiment 5 gained blendes together film (numbering: SiO2/BB64) have higher physical strength, be suitable as the employed supporting substrate of flat-panel screens and replace traditional glass substrate.
Though the present invention discloses as above with preferred embodiment, so it is not in order to limit the present invention.Any the technical staff in the technical field of the invention, without departing from the spirit and scope of the present invention, Ying Kezuo changes arbitrarily and retouching, and therefore, protection scope of the present invention should be as the criterion with appended claims institute restricted portion.

Claims (20)

1. the hybrid material composition of a high-transmittance, high heat-resisting, low thermal coefficient of expansion comprises a. silicon-dioxide (SiO 2) and the b. pi, it is characterized in that this silicon-dioxide (SiO 2) and the weight ratio of pi between 1: 9 to 9: 1.
2. the hybrid material composition of high-transmittance as claimed in claim 1, high heat-resisting, low thermal coefficient of expansion, wherein this silicon-dioxide (SiO 2) and the weight ratio of pi between 2: 8 to 9: 1.
3. the hybrid material composition of high-transmittance as claimed in claim 1, high heat-resisting, low thermal coefficient of expansion also comprises silicone surfactant.
4. the hybrid material composition of high-transmittance as claimed in claim 3, high heat-resisting, low thermal coefficient of expansion, wherein this silicone surfactant has polar functional group.
5. the hybrid material composition of high-transmittance as claimed in claim 4, high heat-resisting, low thermal coefficient of expansion, wherein this silicone surfactant with polar functional group is an aminosiloxane.
6. the hybrid material composition of high-transmittance as claimed in claim 1, high heat-resisting, low thermal coefficient of expansion, wherein this silicon-dioxide (SiO 2) be dissolved in the organic solvent, and solid content is less than 40%.
7. the hybrid material composition of high-transmittance as claimed in claim 1, high heat-resisting, low thermal coefficient of expansion, wherein this pi has suc as formula the structure shown in (I):
Formula (I)
Wherein, n is greater than 1;
G is one or more polycyclic cycloalkyl, heterocyclic radical, cycloalkyl and heterocyclic radical with one or more unsaturated link(age)s, aryl, heteroaryl, aliphatic group, the ring grease dialkylene, aralkyl or heteroaralkyl, and each ring has 3 to 8 annular atomses, and the hydrogen on each annular atoms, optionally can be by halogen, alkyl, the sulfane base, alkoxyl group, the alkane thiazolinyl, the alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base replace, alkyl wherein, the sulfane base, alkoxyl group, the alkane thiazolinyl, the alkane alkynyl, alkene oxygen base or alkynyloxy group contain 1-12 carbon atom, and it is a straight or branched; And
A is polycyclic cycloalkyl, heterocyclic radical, the cycloalkyl with one or more unsaturated link(age)s and heterocyclic radical, aryl, heteroaryl, aliphatic group, ring grease dialkylene, aralkyl or heteroaralkyl, and each ring has 3 to 8 annular atomses, and the hydrogen on each annular atoms, optionally can be replaced by halogen, alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base, wherein alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base or alkynyloxy group contain 1-12 carbon atom, and it is a straight or branched.
8. the hybrid material composition of high-transmittance as claimed in claim 7, high heat-resisting, low thermal coefficient of expansion, wherein G is
Figure A2007101092430003C1
Figure A2007101092430003C2
Or
Figure A2007101092430003C3
This Z be oxygen ,-CH 2-,-C (CH 3) 2-,-Ar-O-Ar-, Ar-CH 2-Ar-,-Ar-C (CH 3) 2-Ar-or-Ar-SO 2-Ar-, this Ar represents phenyl ring.
9. the hybrid material composition of high-transmittance as claimed in claim 7, high heat-resisting, low thermal coefficient of expansion, wherein A is
Figure A2007101092430003C4
Or
Figure A2007101092430003C5
This Z be oxygen ,-CH 2-,-C (CH3) 2-,-Ar-O-Ar-, Ar-CH2-Ar-,-Ar-C (CH3) 2-Ar-or-Ar-SO2-Ar-, this Ar represents phenyl ring.
10. flexible transparent film, this film comprises a. silicon-dioxide (SiO 2) and the b. pi, it is characterized in that this silicon-dioxide (SiO 2) and the weight ratio of pi between 1: 9 to 9: 1.
11. flexible transparent film as claimed in claim 10, wherein this silicon-dioxide (SiO 2) and the weight ratio of pi between 2: 8 to 9: 1.
12. flexible transparent film as claimed in claim 10 also comprises silicone surfactant.
13. flexible transparent film as claimed in claim 10, wherein this silicone surfactant has polar functional group.
14. flexible transparent film as claimed in claim 10, wherein this silicone surfactant with polar functional group is an aminosiloxane.
15. flexible transparent film as claimed in claim 10, wherein this silicon-dioxide (SiO 2) be dissolved in the organic solvent, and solid content system is less than 40%.
16. flexible transparent film as claimed in claim 10, wherein this pi has suc as formula the structure shown in (I):
Figure A2007101092430004C1
Formula (I)
Wherein, n is greater than 1;
G is one or more polycyclic cycloalkyl, heterocyclic radical, cycloalkyl and heterocyclic radical with one or more unsaturated link(age)s, aryl, heteroaryl, aliphatic group, the ring grease dialkylene, aralkyl or heteroaralkyl, and each ring has 3 to 8 annular atomses, and the hydrogen on each annular atoms, optionally can be by halogen, alkyl, the sulfane base, alkoxyl group, the alkane thiazolinyl, the alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base replace, alkyl wherein, the sulfane base, alkoxyl group, the alkane thiazolinyl, the alkane alkynyl, alkene oxygen base or alkynyloxy group contain the 1-12 carbon atom, and it is a straight or branched; And
A is polycyclic cycloalkyl, heterocyclic radical, the cycloalkyl with one or more unsaturated link(age)s and heterocyclic radical, aryl, heteroaryl, aliphatic group, ring grease dialkylene, aralkyl or heteroaralkyl, and each ring has 3 to 8 annular atomses, and the hydrogen on each annular atoms, optionally can be replaced by halogen, alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base, wherein alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base or alkynyloxy group contain 1-12 carbon atom, and it is a straight or branched.
17. flexible transparent film as claimed in claim 10, wherein G is
Figure A2007101092430004C2
Or
Figure A2007101092430004C3
This Z be oxygen ,-CH 2-,-C (CH3) 2-,-Ar-O-Ar-, Ar-CH2-Ar-,-Ar-C (CH3) 2-Ar-or-Ar-SO2-Ar-, this Ar represents phenyl ring.
18. flexible transparent film as claimed in claim 16, wherein A is
Figure A2007101092430004C4
Or
Figure A2007101092430005C1
This Z be oxygen ,-CH 2-,-C (CH3) 2-,-Ar-O-Ar-, Ar-CH2-Ar-,-Ar-C (CH3) 2-Ar-or-Ar-SO2-Ar-, this Ar represents phenyl ring.
19. flexible transparent film as claimed in claim 16, wherein the hydrogen on each annular atoms of A optionally can be replaced by halogen, alkyl, sulfane base, alkoxyl group, alkane thiazolinyl, alkane alkynyl, alkene oxygen base, alkynyloxy group or aromatic base.
20. a photoelectric device comprises flexible transparent film, wherein this flexible transparent film comprises a. silicon-dioxide (SiO 2) and the b. pi, it is characterized in that this silicon-dioxide (SiO 2) be not less than 2: 8 with the weight ratio of pi.
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Publication number Priority date Publication date Assignee Title
CN101787126B (en) * 2009-12-24 2013-06-12 广东生益科技股份有限公司 Polyamide acid composition, method for manufacturing two-layer process flexible copper-clad plates by use of same, and obtained two-layer process flexible copper-clad plate
CN103571189A (en) * 2012-07-18 2014-02-12 财团法人工业技术研究院 Polyimide-containing film and method for etching polyimide-containing film
CN103571189B (en) * 2012-07-18 2016-07-06 财团法人工业技术研究院 Method for etching polyimide-containing film
US9982108B2 (en) 2012-07-18 2018-05-29 Industrial Technology Research Institute Polyimide-containing layer and method for etching polyimide-containing layer
JP2015527422A (en) * 2013-05-20 2015-09-17 コーロン インダストリーズ インク Polyimide resin and polyimide film produced therefrom
CN113462157A (en) * 2021-07-21 2021-10-01 马鞍山东毅新材料科技有限公司 High-temperature-resistant polyimide display panel film and production process thereof
CN113462157B (en) * 2021-07-21 2023-09-26 马鞍山东毅新材料科技有限公司 High-temperature-resistant polyimide display panel film and production process thereof

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