US20060082627A9 - Formulation and method for depositing a material on a substrate - Google Patents
Formulation and method for depositing a material on a substrate Download PDFInfo
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- US20060082627A9 US20060082627A9 US10/469,443 US46944304A US2006082627A9 US 20060082627 A9 US20060082627 A9 US 20060082627A9 US 46944304 A US46944304 A US 46944304A US 2006082627 A9 US2006082627 A9 US 2006082627A9
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- 239000000463 material Substances 0.000 title claims abstract description 46
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 238000009472 formulation Methods 0.000 title claims abstract description 35
- 238000000151 deposition Methods 0.000 title claims abstract description 21
- 239000000758 substrate Substances 0.000 title claims abstract description 20
- 238000000034 method Methods 0.000 title claims description 28
- 239000002904 solvent Substances 0.000 claims abstract description 62
- 238000009835 boiling Methods 0.000 claims abstract description 19
- 229920000642 polymer Polymers 0.000 claims description 26
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 16
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 claims description 8
- 230000008021 deposition Effects 0.000 claims description 7
- XHLHPRDBBAGVEG-UHFFFAOYSA-N 1-tetralone Chemical compound C1=CC=C2C(=O)CCCC2=C1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 239000008096 xylene Substances 0.000 claims description 4
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical compound C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 claims description 3
- 239000002800 charge carrier Substances 0.000 claims description 3
- HHNHBFLGXIUXCM-GFCCVEGCSA-N cyclohexylbenzene Chemical compound [CH]1CCCC[C@@H]1C1=CC=CC=C1 HHNHBFLGXIUXCM-GFCCVEGCSA-N 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims 3
- 239000011877 solvent mixture Substances 0.000 claims 2
- HKTCLPBBJDIBGF-UHFFFAOYSA-N 1-phenyl-2-propan-2-ylbenzene Chemical group CC(C)C1=CC=CC=C1C1=CC=CC=C1 HKTCLPBBJDIBGF-UHFFFAOYSA-N 0.000 claims 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 12
- 238000005259 measurement Methods 0.000 description 7
- 239000004642 Polyimide Substances 0.000 description 3
- 229920001721 polyimide Polymers 0.000 description 3
- BFIMMTCNYPIMRN-UHFFFAOYSA-N 1,2,3,5-tetramethylbenzene Chemical compound CC1=CC(C)=C(C)C(C)=C1 BFIMMTCNYPIMRN-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 229920002959 polymer blend Polymers 0.000 description 2
- LIWRTHVZRZXVFX-UHFFFAOYSA-N 1-phenyl-3-propan-2-ylbenzene Chemical group CC(C)C1=CC=CC(C=2C=CC=CC=2)=C1 LIWRTHVZRZXVFX-UHFFFAOYSA-N 0.000 description 1
- RXACYPFGPNTUNV-UHFFFAOYSA-N 9,9-dioctylfluorene Chemical group C1=CC=C2C(CCCCCCCC)(CCCCCCCC)C3=CC=CC=C3C2=C1 RXACYPFGPNTUNV-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229920000547 conjugated polymer Polymers 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005525 hole transport Effects 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000001540 jet deposition Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/36—Inkjet printing inks based on non-aqueous solvents
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/10—Deposition of organic active material
- H10K71/12—Deposition of organic active material using liquid deposition, e.g. spin coating
- H10K71/13—Deposition of organic active material using liquid deposition, e.g. spin coating using printing techniques, e.g. ink-jet printing or screen printing
- H10K71/135—Deposition of organic active material using liquid deposition, e.g. spin coating using printing techniques, e.g. ink-jet printing or screen printing using ink-jet printing
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
- H10K85/151—Copolymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
Definitions
- the present invention relates to a formulation for depositing a material on a substrate, to a method of depositing a material on a substrate particularly by an ink-jet deposition technique, and to a method of producing a light-emitting device by such a deposition method.
- a light-emitting device typically comprises a layer of an electroluminescent polymer 3 sandwiched between a cathode 2 and an anode 1 such that charge carriers can move between the electrodes and the layer of electroluminescent polymer. It is typically produced by depositing a layer of electroluminescent polymer 3 on a glass substrate 5 coated with an anode layer 1 such as a layer of indium-tin oxide (ITO) and depositing a cathode layer 2 such as a calcium layer over the layer of electroluminescent polymer 3 .
- anode layer 1 such as a layer of indium-tin oxide (ITO)
- ITO indium-tin oxide
- the device may comprise further layers, such as a hole transport layer 4 (such as a layer of doped polyethylene dioxythiophene as described in EP0686662) provided between the anode 1 and the electroluminescent polymer layer 3 and an electron transport layer provided between the cathode and the electroluminescent layer (not provided in the device shown in FIG. 1 ).
- a hole transport layer 4 such as a layer of doped polyethylene dioxythiophene as described in EP0686662
- an electron transport layer provided between the cathode and the electroluminescent layer (not provided in the device shown in FIG. 1 ).
- An ink-jet technique may be used for depositing the layer of electroluminescent polymer.
- Such a technique is described in EP0880303A1, whose content is incorporated herein by reference.
- This technique basically involves the controlled deposition of drops of a solution of the electroluminescent polymer through a nozzle followed by evaporation of the solvent.
- This technique is particularly suited to the deposition of patterned layers of the electroluminescent polymer. For example, in some applications, it may be required to have a layer of electroluminescent polymer comprising an ordered array of pixels, wherein each pixel is produced by the deposition of a single drop of solution of the electroluminescent polymer. It is desirable in such cases that the polymer is distributed uniformly in the spot remaining after evaporation of the solvent.
- a formulation for depositing a material on a substrate comprising the material to be deposited on the substrate dissolved in a solvent system comprising a first solvent component having a relatively high boiling point and which exhibits a relatively low solubility with respect to the material to be deposited, and a second solvent component having a relatively low boiling point and which exhibits a relatively high solubility with respect to the material to be deposited.
- references to the solubility of each solvent component with respect to the material are references to the solubility of the material in each solvent component.
- Ink-jet techniques typically, require formulations having a viscosity of up to about 20 cps.
- a typical viscosity for an ink-jet formulation is about 10 cps.
- the first solvent component may comprise one or more solvents that have a relatively high boiling point and exhibit a relatively low solubility with respect to the material to be deposited (in relation to the second solvent component), and the second solvent component may likewise comprise one or more solvents that have a relatively low boiling point and exhibit a relatively high solubility with respect to the material to be deposited (in relation to the first solvent component).
- the second solvent component has a boiling point in the range of 100 to 200° C. and the first solvent component has a boiling point in the range of 130 to 300° C.
- the difference in boiling point between the first and second solvent components is preferably in the range of 30 to 250° C., further preferably in the range of 70 to 150° C.
- the solubility of the material to be deposited in the first solvent component is preferably up to 0.5% weight per volume, further preferably in the range of 0.03 to 0.3% weight per volume, and the solubility of the material to be deposited in the second solvent is preferably greater than 0.5% weight per volume, further preferably greater than 1.5% weight per volume.
- the proportion of the first solvent component should preferably be selected such that upon removal of the second solvent component the remaining solution of the material in the first solvent component would be substantially at or above saturation.
- the proportion of the first solvent component is in the range of 10 to 60 volume percent, further preferably 20 to 50 volume percent.
- the proportion of the second solvent component is in the range of 40 to 90 volume percent, preferably 50 to 80 volume percent.
- a method of depositing a material on a substrate comprising depositing one or more drops of a solution of the material onto the substrate through a nozzle according to an ink-jet technique and drying each deposited drop, wherein the solution of the material comprises a formulation as described above.
- the solvent system is selected such that the material begins to precipitate at a relatively early stage in the drying of the drop, i.e. such that precipitation occurs whilst a substantial amount of solvent remains unevaporated.
- the solvent system is selected such that the variation in thickness of the dried drop of material on the substrate is less than 80% of the maximum thickness, preferably less than 50%, and further preferably less than 30%. It is most preferred that the thickness variation is less than 15%.
- the solvent system is selected such that in a formulation having 0.5% w/v of the material to be deposited, the dried drop has a thickness at its centre (i.e. the region enclosed by the ring of increased thickness, if present) of 60 to 140 nm, preferably about 70 nm to 100 nm, which is desirable for EL efficiency and lifetime of an organic light-emitting device.
- the material for deposition on the substrate may, for example, be an organic material such as a polymer or a blend of polymers. In one application, it comprises one or more semiconducting conjugated polymers such as a charge transport polymer or a light-emissive polymer, or a blend of the two.
- a method of producing a light-emitting device comprising a layer of an electroluminescent material sandwiched between two electrodes such that charge carriers can move between the electrodes and the layer of electroluminescent material, wherein the layer of electroluminescent material is produced by a method as described above.
- FIG. 1 is a schematic view of a light-emissive device
- FIGS. 2 and 3 are graphs showing the thickness profile for a spot obtained by an ink-jet technique using a formulation according to embodiments of the present invention
- FIG. 4 is a graph showing the thickness profile for a spot of an electroluminescent polymer deposited using a solvent consisting entirely of 1,2-dimethylbenzene;
- FIG. 5 is a graph showing the thickness profile, for a spot obtained by an ink-jet technique using a formulation according to another embodiment of the present invention.
- FIG. 6 illustrates some recurring units and polymers.
- a solvent blend was prepared from 60 vol. % 1,2-dimethylbenzene (b.p.: 144.4° C.) and 40 vol. % ⁇ -tetralone (b.p.: 255° C.).
- a 0.5% w/v solution of an alternating polymer of 9,9-dioctylfluorene units and benzothiadiazole units (F8BT) having a peak molecular weight of about 266,000 was prepared using this solvent blend. Drops of this solution were deposited by an ink-jet method on the surface of a polyimide substrate that had been modified to lower its surface energy. The drops were allowed to dry at room temperature and humidity (20° C. ⁇ 1.0° C. and 30-40% R.H.), and Dektak measurements of the profile of the dried drops were taken. The results of the measurements are shown in FIG. 2 .
- a solvent blend was prepared from 60 vol. % 1,2-dimethylbenzene and 40 vol. % cyclohexylbenzene. Drops of a 0.5% w/v solution of the same F8BT polymer as Example 1 were deposited on a surface-modified polyimide substrate by an ink-jet method. Dektak measurements of the profile of the dried drops were taken. The results of the measurements are shown in FIG. 3 .
- the use of the formulations according to the present invention produced dried drops that were significantly improved in terms of uniformity of thickness compared to the comparative example. It is thought that the improved thickness uniformity is a result of the following mechanism. During drying of the drop, the volatile low boiling point solvent evaporates quickly leaving behind a saturated solution in the high boiling point solvent; this in turn causes the polymer to be precipitated rapidly preventing radial flow within the drop and thus creating a relatively uniform distribution of the polymer in the drop.
- the improved uniformity of thickness results in an increased thickness at the centre of the drop for the same concentration of material in the formulation. Being able to control the thickness at the centre of the drop is considered to be an important factor in improving the efficiency of a light-emitting device produced by an ink-jet technique.
- the present invention thus allows an increase in centre thickness without increasing the concentration in the formulation of the material to be deposited. This can have advantages in producing a device having pixels of the desired size at the desired resolution.
- FIG. 5 shows a Dektak measurement profile of a dried drop deposited by an ink-jet technique using a 0.5% w/v solution of a polymer blend in this three component solvent system.
- the polymer blend is relatively highly soluble in the first two, low boiling point solvents relative to the third high boiling point solvent.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Electroluminescent Light Sources (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
- The present invention relates to a formulation for depositing a material on a substrate, to a method of depositing a material on a substrate particularly by an ink-jet deposition technique, and to a method of producing a light-emitting device by such a deposition method.
- As shown schematically in
FIG. 1 , a light-emitting device typically comprises a layer of anelectroluminescent polymer 3 sandwiched between acathode 2 and ananode 1 such that charge carriers can move between the electrodes and the layer of electroluminescent polymer. It is typically produced by depositing a layer ofelectroluminescent polymer 3 on aglass substrate 5 coated with ananode layer 1 such as a layer of indium-tin oxide (ITO) and depositing acathode layer 2 such as a calcium layer over the layer ofelectroluminescent polymer 3. The device may comprise further layers, such as a hole transport layer 4 (such as a layer of doped polyethylene dioxythiophene as described in EP0686662) provided between theanode 1 and theelectroluminescent polymer layer 3 and an electron transport layer provided between the cathode and the electroluminescent layer (not provided in the device shown inFIG. 1 ). - An ink-jet technique may be used for depositing the layer of electroluminescent polymer. Such a technique is described in EP0880303A1, whose content is incorporated herein by reference. This technique basically involves the controlled deposition of drops of a solution of the electroluminescent polymer through a nozzle followed by evaporation of the solvent. This technique is particularly suited to the deposition of patterned layers of the electroluminescent polymer. For example, in some applications, it may be required to have a layer of electroluminescent polymer comprising an ordered array of pixels, wherein each pixel is produced by the deposition of a single drop of solution of the electroluminescent polymer. It is desirable in such cases that the polymer is distributed uniformly in the spot remaining after evaporation of the solvent.
- Solutions of the electroluminescent polymer in solvents such as isodurene have conventionally been used in this technique. However, there has been noticed the problem with conventional solvents that after a drop of the deposited solution has dried most of the electroluminescent polymer is deposited as a ring around the edge of the remaining spot leaving only a very thin film of the polymer at the centre of the spot. This can result in relatively poor device efficiency.
- It is an aim of the present invention to provide a formulation with which a film of the desired thickness profile can be deposited on a substrate according to a technique involving controlled drop deposition.
- According to a first aspect of the present invention, there is provided a formulation for depositing a material on a substrate, the formulation comprising the material to be deposited on the substrate dissolved in a solvent system comprising a first solvent component having a relatively high boiling point and which exhibits a relatively low solubility with respect to the material to be deposited, and a second solvent component having a relatively low boiling point and which exhibits a relatively high solubility with respect to the material to be deposited.
- References to the solubility of each solvent component with respect to the material are references to the solubility of the material in each solvent component.
- Ink-jet techniques typically, require formulations having a viscosity of up to about 20 cps. A typical viscosity for an ink-jet formulation is about 10 cps.
- The first solvent component may comprise one or more solvents that have a relatively high boiling point and exhibit a relatively low solubility with respect to the material to be deposited (in relation to the second solvent component), and the second solvent component may likewise comprise one or more solvents that have a relatively low boiling point and exhibit a relatively high solubility with respect to the material to be deposited (in relation to the first solvent component).
- In one embodiment, the second solvent component has a boiling point in the range of 100 to 200° C. and the first solvent component has a boiling point in the range of 130 to 300° C. The difference in boiling point between the first and second solvent components is preferably in the range of 30 to 250° C., further preferably in the range of 70 to 150° C. The solubility of the material to be deposited in the first solvent component is preferably up to 0.5% weight per volume, further preferably in the range of 0.03 to 0.3% weight per volume, and the solubility of the material to be deposited in the second solvent is preferably greater than 0.5% weight per volume, further preferably greater than 1.5% weight per volume.
- The proportion of the first solvent component should preferably be selected such that upon removal of the second solvent component the remaining solution of the material in the first solvent component would be substantially at or above saturation. In one embodiment, the proportion of the first solvent component is in the range of 10 to 60 volume percent, further preferably 20 to 50 volume percent.
- In one embodiment, the proportion of the second solvent component is in the range of 40 to 90 volume percent, preferably 50 to 80 volume percent.
- According to another aspect of the invention, there is provided a method of depositing a material on a substrate comprising depositing one or more drops of a solution of the material onto the substrate through a nozzle according to an ink-jet technique and drying each deposited drop, wherein the solution of the material comprises a formulation as described above.
- The solvent system is selected such that the material begins to precipitate at a relatively early stage in the drying of the drop, i.e. such that precipitation occurs whilst a substantial amount of solvent remains unevaporated.
- The solvent system is selected such that the variation in thickness of the dried drop of material on the substrate is less than 80% of the maximum thickness, preferably less than 50%, and further preferably less than 30%. It is most preferred that the thickness variation is less than 15%.
- In one embodiment, the solvent system is selected such that in a formulation having 0.5% w/v of the material to be deposited, the dried drop has a thickness at its centre (i.e. the region enclosed by the ring of increased thickness, if present) of 60 to 140 nm, preferably about 70 nm to 100 nm, which is desirable for EL efficiency and lifetime of an organic light-emitting device.
- In the above, the material for deposition on the substrate may, for example, be an organic material such as a polymer or a blend of polymers. In one application, it comprises one or more semiconducting conjugated polymers such as a charge transport polymer or a light-emissive polymer, or a blend of the two.
- According to yet another aspect of the present invention, there is provided a method of producing a light-emitting device comprising a layer of an electroluminescent material sandwiched between two electrodes such that charge carriers can move between the electrodes and the layer of electroluminescent material, wherein the layer of electroluminescent material is produced by a method as described above.
- According to another aspect of the present invention, there is provided a use of a formulation as described above for reducing or avoiding a ring deposition effect.
-
FIG. 1 is a schematic view of a light-emissive device; -
FIGS. 2 and 3 are graphs showing the thickness profile for a spot obtained by an ink-jet technique using a formulation according to embodiments of the present invention; -
FIG. 4 is a graph showing the thickness profile for a spot of an electroluminescent polymer deposited using a solvent consisting entirely of 1,2-dimethylbenzene; -
FIG. 5 is a graph showing the thickness profile, for a spot obtained by an ink-jet technique using a formulation according to another embodiment of the present invention; and -
FIG. 6 illustrates some recurring units and polymers. - A solvent blend was prepared from 60 vol. % 1,2-dimethylbenzene (b.p.: 144.4° C.) and 40 vol. % α-tetralone (b.p.: 255° C.). A 0.5% w/v solution of an alternating polymer of 9,9-dioctylfluorene units and benzothiadiazole units (F8BT) having a peak molecular weight of about 266,000 was prepared using this solvent blend. Drops of this solution were deposited by an ink-jet method on the surface of a polyimide substrate that had been modified to lower its surface energy. The drops were allowed to dry at room temperature and humidity (20° C.±1.0° C. and 30-40% R.H.), and Dektak measurements of the profile of the dried drops were taken. The results of the measurements are shown in
FIG. 2 . - A solvent blend was prepared from 60 vol. % 1,2-dimethylbenzene and 40 vol. % cyclohexylbenzene. Drops of a 0.5% w/v solution of the same F8BT polymer as Example 1 were deposited on a surface-modified polyimide substrate by an ink-jet method. Dektak measurements of the profile of the dried drops were taken. The results of the measurements are shown in
FIG. 3 . - Drops of a 0.5% w/v solution of the same F8BT polymer as Examples 1 and 2 in 1,2-dimethylbenzene were deposited on a surface-modified polyimide substrate by an ink-jet method. Dektak measurements of the profile of the dried drops were taken. The results of the measurements are shown in
FIG. 4 . - As can be seen from a comparison of
FIGS. 2, 3 and 4, the use of the formulations according to the present invention produced dried drops that were significantly improved in terms of uniformity of thickness compared to the comparative example. It is thought that the improved thickness uniformity is a result of the following mechanism. During drying of the drop, the volatile low boiling point solvent evaporates quickly leaving behind a saturated solution in the high boiling point solvent; this in turn causes the polymer to be precipitated rapidly preventing radial flow within the drop and thus creating a relatively uniform distribution of the polymer in the drop. - Furthermore, the improved uniformity of thickness results in an increased thickness at the centre of the drop for the same concentration of material in the formulation. Being able to control the thickness at the centre of the drop is considered to be an important factor in improving the efficiency of a light-emitting device produced by an ink-jet technique. The present invention thus allows an increase in centre thickness without increasing the concentration in the formulation of the material to be deposited. This can have advantages in producing a device having pixels of the desired size at the desired resolution.
- Good results have also been achieved using a solvent blend consisting of 40 vol. % mixed isomers of xylene (b.p.:138° C.); 40 vol. % 1,2,4-trimethylbenzene (b.p.:168° C.) and 20 vol. % 3-isopropylbiphenyl (b.p.:295° C.).
FIG. 5 shows a Dektak measurement profile of a dried drop deposited by an ink-jet technique using a 0.5% w/v solution of a polymer blend in this three component solvent system. The polymer blend is relatively highly soluble in the first two, low boiling point solvents relative to the third high boiling point solvent.
Claims (18)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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US10/469,443 US20060082627A9 (en) | 2001-02-27 | 2002-02-27 | Formulation and method for depositing a material on a substrate |
US12/248,858 US7807070B2 (en) | 2001-02-27 | 2008-10-09 | Formulation and method for depositing a material on a substrate |
Applications Claiming Priority (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW090104585A TW527432B (en) | 2001-02-28 | 2001-02-27 | A method and composition for depositing a polymer layer in the production of a light-emissive device, a method of forming a polymer layer on a substrate, and the use of a composition in an ink-jet method of depositing a polymer layer |
CN90104585 | 2001-02-27 | ||
GBGB0104875.0A GB0104875D0 (en) | 2001-02-28 | 2001-02-28 | A formulation for depositing a conjugated polymer layer |
GB0104875.0 | 2001-02-28 | ||
GB0107740.3 | 2001-03-28 | ||
GBGB0107740.3A GB0107740D0 (en) | 2001-03-28 | 2001-03-28 | Formulation and method for depositing a material on a substrate |
US29168401P | 2001-05-17 | 2001-05-17 | |
PCT/GB2002/000845 WO2002069119A1 (en) | 2001-02-27 | 2002-02-27 | Formulation for depositing a material on a substrate using ink jet printing |
US10/469,443 US20060082627A9 (en) | 2001-02-27 | 2002-02-27 | Formulation and method for depositing a material on a substrate |
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US12/248,858 Continuation US7807070B2 (en) | 2001-02-27 | 2008-10-09 | Formulation and method for depositing a material on a substrate |
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US20040109051A1 US20040109051A1 (en) | 2004-06-10 |
US20060082627A9 true US20060082627A9 (en) | 2006-04-20 |
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US10/469,443 Abandoned US20060082627A9 (en) | 2001-02-27 | 2002-02-27 | Formulation and method for depositing a material on a substrate |
US12/248,858 Expired - Fee Related US7807070B2 (en) | 2001-02-27 | 2008-10-09 | Formulation and method for depositing a material on a substrate |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US20040007706A1 (en) * | 2002-05-13 | 2004-01-15 | Shunpei Yamazaki | Semiconductor device and microprocessor |
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Cited By (8)
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US20060147615A1 (en) * | 2002-02-15 | 2006-07-06 | Byoung-Choo Park | Organic semiconductor devices and organic electroluminescent devices produced by using wet process |
US7666691B2 (en) * | 2002-02-15 | 2010-02-23 | Byoung-Choo Park | Organic semiconductor devices and organic electroluminescent devices produced by using wet process |
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US7385655B2 (en) | 2002-09-02 | 2008-06-10 | Semiconductor Energy Laboratory Co., Ltd. | Electronic circuit device with optical sensors and optical shutters at specific locations |
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Also Published As
Publication number | Publication date |
---|---|
US20090041928A1 (en) | 2009-02-12 |
CN1505846A (en) | 2004-06-16 |
JP2009266824A (en) | 2009-11-12 |
US20040109051A1 (en) | 2004-06-10 |
CN100377380C (en) | 2008-03-26 |
US7807070B2 (en) | 2010-10-05 |
JP5175799B2 (en) | 2013-04-03 |
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