JP2018109141A - Ink composition, light conversion layer, and color filter - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an ink composition that is characterized by excellent dispersion stability of light-scattering particles, inhibited sedimentation, and excellent discharge stability.SOLUTION: An ink composition contains a luminescent nanocrystal particle, a light-scattering particle, the surface of which is at least partially coated with alumina, and a macromolecular dispersion.SELECTED DRAWING: None

Description

  The present invention relates to an ink composition, a light conversion layer, and a color filter.

  Conventionally, a color filter pixel portion in a display such as a liquid crystal display device uses, for example, a curable resist material containing red organic pigment particles or green organic pigment particles and an alkali-soluble resin and / or an acrylic monomer. Have been manufactured by photolithography.

  In recent years, there has been a strong demand for lower power consumption of displays, and instead of the red organic pigment particles or green organic pigment particles, for example, luminescent nanocrystal particles such as quantum dots, quantum rods, and other inorganic phosphor particles A method of forming a color filter pixel portion such as a red pixel and a green pixel by using the above has been actively studied.

  By the way, in the manufacturing method of the color filter by the said photolithography method, there existed a fault that resist materials other than the pixel part containing the comparatively expensive luminescent nanocrystal particle | grains were wasted from the characteristic of the manufacturing method. Under such circumstances, in order to eliminate the waste of the resist material as described above, it has been considered to form a light conversion substrate pixel portion by an ink jet method (Patent Document 1).

International Publication 2008/001693

  In the case where a color filter pixel portion (hereinafter also simply referred to as “pixel portion”) is formed from an ink composition using luminescent nanocrystal particles, the ink composition is used to scatter light from a light source irradiated to the pixel portion. The product may contain light-scattering particles together with the light-emitting nanocrystal particles. When the light scattering particles are contained, the dispersion stability (ink stability) of the light scattering particles in the ink composition is ensured, and the precipitation of the light scattering particles is suppressed. Is desirable. Furthermore, it is desirable that the ink composition is excellent in ejection stability from the viewpoint of reducing variation in film thickness for each pixel portion.

  Accordingly, the present invention provides an ink composition that is excellent in dispersion stability of the light-scattering particles, suppresses sedimentation separation, and provides excellent discharge stability, a light conversion layer using the ink composition, and An object is to provide a color filter.

  One aspect of the present invention relates to an ink composition comprising luminescent nanocrystal particles, light-scattering particles having at least a part of the surface covered with alumina, and a polymer dispersant. This ink composition is excellent in dispersion stability of light scattering particles.

  The light scattering particles may contain titanium oxide.

  The average particle diameter of the light scattering particles may be 0.05 to 1.0 μm.

  The weight average molecular weight of the polymer dispersant may be 1000 or more.

  The ink composition may further contain a thermosetting resin.

  The thermosetting resin may be alkali-insoluble.

  The ink composition may be an ink composition capable of forming an alkali-insoluble coating film.

  The ink composition may further contain a photopolymerizable compound.

  The photopolymerizable compound may be alkali-insoluble.

  The surface tension of the ink composition may be 20 to 40 mN / m.

  The viscosity of the ink composition may be 2 to 20 mPa · s.

  The ink composition may further contain a solvent having a boiling point of 180 ° C. or higher.

  The ink composition may be for a color filter.

  The ink composition may be an ink composition (inkjet ink) used in an inkjet method.

  One aspect of the present invention relates to a light conversion layer that includes a plurality of pixel portions, and each of the plurality of pixel portions includes a pixel portion that includes a cured product of the ink composition described above. This light conversion layer can be obtained by an ink jet method using the ink composition described above. Therefore, according to this light conversion layer, leakage light in the pixel portion hardly occurs, and excellent optical characteristics are easily obtained.

  The light conversion layer may further include a light-shielding portion provided between the plurality of pixel portions, and the plurality of pixel portions include the cured product and have a wavelength in the range of 420 to 480 nm as the luminescent nanocrystal particles. As a luminescent nanocrystal particle, the first pixel portion containing luminescent nanocrystal particles that absorb light of the above and emit light having an emission peak wavelength in the range of 605 to 665 nm, the cured product, and And a second pixel portion containing luminescent nanocrystal particles that absorb light having a wavelength in the range of 420 to 480 nm and emit light having an emission peak wavelength in the range of 500 to 560 nm.

  The plurality of pixel units may further include a third pixel unit having a transmittance of 30% or more for light having a wavelength in the range of 420 to 480 nm.

  One aspect of the present invention relates to a color filter including the above-described light conversion layer. According to this color filter, it is easy to obtain excellent optical characteristics.

  According to the present invention, an ink composition that has excellent dispersion stability of light scattering particles, suppresses sedimentation separation, and provides excellent ejection stability, and a light conversion layer using the ink composition and A color filter can be provided.

FIG. 1 is a schematic cross-sectional view of a color filter according to an embodiment of the present invention.

  Hereinafter, embodiments of the present invention will be described in detail.

<Ink composition>
An ink composition according to an embodiment includes a light-emitting nanocrystal particle, a light-scattering particle whose surface is covered with alumina (hereinafter also simply referred to as “light-scattering particle”), a polymer dispersant And containing. The ink composition of one embodiment is a color filter ink composition used for forming a pixel portion of a color filter by a method such as a photolithography method or an ink jet method. The ink composition having the above-described configuration contains light scattering particles having at least a part of the surface covered with alumina, and thus has excellent dispersion stability (ink stability) of the light scattering particles. Therefore, by using the ink composition, excellent optical characteristics can be easily obtained. That is, this ink composition is suitably used for the purpose of forming a color filter pixel portion by an inkjet method.

  By the way, when forming a color filter pixel part by the inkjet system using the conventional ink composition, the discharge stability from an inkjet nozzle may fall by aggregation of light-scattering particles, etc. However, when ejection cannot be stably performed by the ink jet method, composition variation or the like may occur in the formed pixel portion. As a result, for example, leakage light (light from the light source emits luminescent nanocrystals in the pixel portion). The occurrence of light that leaks out of the pixel portion without being absorbed by the particles) causes problems such as deterioration in color reproducibility of the pixel portion. Therefore, when the color filter pixel portion is formed by the ink jet method, the ink composition is required to have excellent ejection stability. On the other hand, since the ink composition having the above configuration has good dispersion stability of the light scattering particles, it is easy to obtain excellent ejection stability. Therefore, according to the ink composition, excellent optical characteristics are easily obtained even when the pixel portion is formed by an ink jet method. In other words, the ink composition is suitably used for forming a color filter pixel portion by an ink jet method.

  Hereinafter, an ink composition for color filter (ink-jet ink for color filter) used for an ink-jet method containing luminescent nanocrystal particles, light-scattering particles, and a polymer dispersant will be described as an example. .

[Luminescent nanocrystal particles]
The luminescent nanocrystal particle is a nano-sized crystal that absorbs excitation light and emits fluorescence or phosphorescence. For example, the maximum particle diameter measured by a transmission electron microscope or a scanning electron microscope is 100 nm or less. It is a crystal.

  The luminescent nanocrystal particles can emit light (fluorescence or phosphorescence) having a wavelength different from the absorbed wavelength, for example, by absorbing light having a predetermined wavelength. The luminescent nanocrystal particles may be red luminescent nanocrystal particles that emit light (red light) having an emission peak wavelength in the range of 605 to 665 nm, and light having an emission peak wavelength in the range of 500 to 560 nm. It may be a green-emitting nanocrystal particle that emits (green light), or a blue-emitting nanocrystal particle that emits light (blue light) having an emission peak wavelength in the range of 420 to 480 nm. . In the present embodiment, it is preferable that the ink composition includes at least one of these luminescent nanocrystal particles. The light absorbed by the luminescent nanocrystal particles may be, for example, light having a wavelength in the range of 400 nm to less than 500 nm (blue light), or light having a wavelength in the range of 200 nm to 400 nm (ultraviolet light). The emission peak wavelength of the luminescent nanocrystal particles can be confirmed in, for example, a fluorescence spectrum or a phosphorescence spectrum measured using an ultraviolet-visible spectrophotometer.

  The red-emitting nanocrystal particles are 665 nm or less, 663 nm or less, 660 nm or less, 658 nm or less, 655 nm or less, 653 nm or less, 651 nm or less, 650 nm or less, 647 nm or less, 645 nm or less, 643 nm or less, 640 nm or less, 637 nm or less, 635 nm or less The emission peak wavelength is preferably 632 nm or less or 630 nm or less, and the emission peak wavelength is preferably 628 nm or more, 625 nm or more, 623 nm or more, 620 nm or more, 615 nm or more, 610 nm or more, 607 nm or more, or 605 nm or more. These upper limit value and lower limit value can be arbitrarily combined. In addition, also in the following similar description, the individually described upper limit value and lower limit value can be arbitrarily combined.

  The green light-emitting nanocrystal particles have emission peak wavelengths at 560 nm or less, 557 nm or less, 555 nm or less, 547 nm or less, 545 nm or less, 543 nm or less, 540 nm or less, 537 nm or less, 535 nm or less, 532 nm or less, or 530 nm or less. It is preferable to have an emission peak wavelength at 528 nm or more, 525 nm or more, 523 nm or more, 520 nm or more, 515 nm or more, 510 nm or more, 507 nm or more, 505 nm or more, 503 nm or more, or 500 nm or more.

  Blue-emitting nanocrystalline particles have a peak emission wavelength at 480 nm or less, 477 nm or less, 475 nm or less, 467 nm or less, 465 nm or less, 463 nm or less, 460 nm or less, 457 nm or less, 452 nm or less, or 450 nm or less. The emission peak wavelength is preferably 450 nm or more, 445 nm or more, 440 nm or more, 435 nm or more, 430 nm or more, 428 nm or more, 425 nm or more, 422 nm or more, or 420 nm or more.

  According to the solution of the Schrodinger wave equation of the well-type potential model, the wavelength of light emitted from the luminescent nanocrystal particles depends on the size (for example, particle diameter) of the luminescent nanocrystal particles. It also depends on the energy gap of the crystal grains. Therefore, the luminescent color can be selected by changing the constituent material and size of the luminescent nanocrystal particles to be used.

  The luminescent nanocrystal particles may be luminescent nanocrystal particles (luminescent semiconductor nanocrystal particles) containing a semiconductor material. Examples of the luminescent semiconductor nanocrystal particles include quantum dots (hereinafter also referred to as “QD”), quantum rods, and the like. Among these, quantum dots are preferable from the viewpoints that the emission spectrum can be easily controlled and the reliability can be ensured, the production cost can be reduced, and the mass productivity can be improved.

  The luminescent semiconductor nanocrystal particle may be composed of only a core including a first semiconductor material, and includes a core including the first semiconductor material and a second semiconductor material different from the first semiconductor material, And a shell covering at least a part of the core. In other words, the structure of the luminescent semiconductor nanocrystal particles may be a structure consisting only of the core (core structure) or a structure consisting of the core and the shell (core / shell structure). The luminescent semiconductor nanocrystal particle includes a third semiconductor material different from the first and second semiconductor materials in addition to the shell including the second semiconductor material (first shell), You may have further the shell (2nd shell) which coat | covers at least one part. In other words, the structure of the luminescent semiconductor nanocrystal particles may be a structure (core / shell / shell structure) including a core, a first shell, and a second shell. Each of the core and the shell may be a mixed crystal including two or more kinds of semiconductor materials (for example, CdSe + CdS, CIS + ZnS, etc.).

  The luminescent nanocrystal particles are selected from the group consisting of II-VI semiconductors, III-V semiconductors, I-III-VI semiconductors, IV semiconductors and I-II-IV-VI semiconductors as semiconductor materials. Preferably, at least one semiconductor material is included.

Specific semiconductor materials include CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, ZnO, HgS, HgSe, HgTe, CdSeS, CdSeTe, CdSTe, ZnSeS, ZnSeTe, ZnSTe, HgSeTe, HgSeTe, HgSTe, Se. CdZnTe, CdHgS, CdHgSe, CdHgTe, HgZnS, HgZnSe, CdHgZnTe, CdZnSeS, CdZnSeTe, CdZnSTe, CdHgSeS, CdHgSeTe, CdHgSTe, HgZnSeS InP, InAs, InSb, GaNP, GANAS, GaNSb, GaPAs, Ga Sb, AlNP, AlNAs, AlNSb, AlPAs, AlPSb, InNP, InNAs, InNSb, InPAs, InPSb, GaAlNP, GaAlNAs, GaAlNSb, GaAlPAs, GaAlPSb, GaInNP, GaInNAsIn, GaInNSB, GaInPAsInGa InAlPSb; SnS, SnSe, SnTe, PbS, PbSe, PbTe, SnSeS, SnSeTe, SnSTe, PbSeS, PbSeTe, PbSTe, SnPbS, SnPbSe, SnPbTe, SnPbSSe, SnPbSeTe, SnPbSTe; Si, Ge, SiC, SiGe, AgInSe 2, CuGaSe _2, CuInS _2, CuG _{S 2, CuInSe 2, AgInS 2} , AgGaSe 2, AgGaS 2, C, include Si and Ge. The luminescent semiconductor nanocrystal particles are easy to control the emission spectrum, and from the viewpoint of reducing production costs and improving mass productivity while ensuring reliability, CdS, CdSe, CdTe, ZnS, _{ZnSe, ZnTe, ZnO, HgS,} HgSe, HgTe, InP, InAs, InSb, GaP, GaAs, GaSb, AgInS 2, AgInSe 2, AgInTe 2, AgGaS 2, AgGaSe 2, AgGaTe 2, CuInS 2, CuInSe 2, CuInTe 2 It is preferable to contain at least one selected from the group consisting of CuGaS ₂ , CuGaSe ₂ , CuGaTe ₂ , Si, C, Ge, and Cu ₂ ZnSnS ₄ .

  Examples of the red light emitting semiconductor nanocrystal particles include CdSe nanocrystal particles and nanocrystal particles having a core / shell structure, where the shell portion is CdS and the inner core portion is CdSe. Nanocrystal particles having a core / shell structure, wherein the shell portion is CdS and the inner core portion is ZnSe, mixed crystal nanocrystal particles of CdSe and ZnS, InP nanocrystals A crystal particle, a nanocrystal particle having a core / shell structure, wherein the shell portion is ZnS and an inner core portion is InP, a nanocrystal particle having a core / shell structure, The shell portion is a mixed crystal of ZnS and ZnSeS and the inner core portion is InP, the mixed crystal nanocrystal particles of CdSe and CdS, ZnSe and CdS Nanocrystalline particles having a core / shell / shell structure, wherein the first shell portion is ZnSe, the second shell portion is ZnS, and the inner core portion is InP Nanocrystal particles, nanocrystal particles having a core / shell / shell structure, wherein the first shell portion is a mixed crystal of ZnS and ZnSe, the second shell portion is ZnS, and the inner core portion Nanocrystal particles in which is InP.

  Examples of the green light emitting semiconductor nanocrystal particles include CdSe nanocrystal particles, mixed crystal nanocrystal particles of CdSe and ZnS, and nanocrystal particles having a core / shell structure, where the shell portion is ZnS. A nanocrystal particle having an inner core portion of InP and a nanocrystal particle having a core / shell structure, wherein the shell portion is a mixed crystal of ZnS and ZnSeS and the inner core portion is InP. A nanocrystalline particle having a crystalline particle, a core / shell / shell structure, wherein the first shell portion is ZnSe, the second shell portion is ZnS, and the inner core portion is InP. , A nanocrystal particle having a core / shell / shell structure, wherein the first shell portion is a mixed crystal of ZnS and ZnSe, the second shell portion is ZnS, and the inner core portion is Nanocrystalline particles or the like is nP and the like.

  Examples of blue-emitting semiconductor nanocrystal particles include ZnSe nanocrystal particles, ZnS nanocrystal particles, and nanocrystal particles having a core / shell structure, where the shell portion is ZnSe and the inner core portion. , ZnS nanocrystal particles, CdS nanocrystal particles, nanocrystal particles having a core / shell structure, wherein the shell portion is ZnS and the inner core portion is InP, the core / shell A nanocrystalline particle having a structure, wherein the shell portion is a mixed crystal of ZnS and ZnSeS and the inner core portion is InP, and the nanocrystalline particle having a core / shell / shell structure. The first shell portion is ZnSe, the second shell portion is ZnS, and the inner core portion is InP. A Roh crystal grains, the first shell portion is a mixed crystal of ZnS and ZnSe, a second shell portion is ZnS, include nanocrystalline like core portion of the inner is InP. By changing the average particle diameter of the semiconductor nanocrystal particles with the same chemical composition, the color to be emitted from the particles can be changed to red or green. Further, as the semiconductor nanocrystal particles, it is preferable to use particles having the least adverse effect on the human body or the like. When semiconductor nanocrystal particles containing cadmium, selenium, etc. are used as luminescent nanocrystal particles, the semiconductor nanocrystal particles that do not contain the above elements (cadmium, selenium, etc.) as much as possible are selected and used alone, or the above elements It is preferable to use in combination with other luminescent nanocrystal particles so as to reduce as much as possible.

  The shape of the luminescent nanocrystal particles is not particularly limited, and may be any geometric shape or any irregular shape. The shape of the luminescent nanocrystal particles may be, for example, spherical, ellipsoidal, pyramidal, disc-shaped, branched, net-shaped, rod-shaped, or the like. However, as the luminescent nanocrystal particles, it is possible to further improve the uniformity and fluidity of the ink composition by using particles having less directionality (for example, spherical, tetrahedral, etc.). Is preferable.

  The average particle diameter (volume average diameter) of the luminescent nanocrystal particles may be 1 nm or more from the viewpoint that light emission at a desired wavelength is easily obtained and from the viewpoint of excellent dispersibility and storage stability. The above may be sufficient and 2 nm or more may be sufficient. From the viewpoint of easily obtaining a desired emission wavelength, it may be 40 nm or less, 30 nm or less, or 20 nm or less. The average particle diameter (volume average diameter) of the luminescent nanocrystal particles is obtained by measuring with a transmission electron microscope or a scanning electron microscope and calculating the volume average diameter.

  The luminescent nanocrystal particles preferably have an organic ligand on the surface thereof from the viewpoint of dispersion stability. The organic ligand may be coordinated to the surface of the luminescent nanocrystal particle, for example. In other words, the surface of the luminescent nanocrystal particle may be passivated by the organic ligand. Further, when the ink composition contains a polymer dispersant described later, the luminescent nanocrystal particles may have a polymer dispersant on the surface thereof. In the present embodiment, for example, the organic ligand is removed from the luminescent nanocrystal particles having the organic ligand, and the polymer dispersant is exchanged between the organic ligand and the polymer dispersant, thereby replacing the polymer dispersant on the surface of the luminescent nanocrystal particles. May be combined. However, from the viewpoint of dispersion stability when an inkjet ink is used, it is preferable that a polymer dispersant is added to the luminescent nanocrystal particles in which the organic ligand is coordinated.

  As an organic ligand, a functional group for ensuring affinity with a resin and a solvent (hereinafter, also simply referred to as “affinity group”) and a functional group for ensuring adsorbability to a luminescent nanocrystal ( Hereinafter, it is preferably a compound having simply “adsorbing group”. As the affinity group, an aliphatic hydrocarbon group is preferable. The aliphatic hydrocarbon group may be linear or have a branched structure. The aliphatic hydrocarbon group may have an unsaturated bond or may not have an unsaturated bond. Examples of the adsorbing group include a hydrogen group, amino group, carboxyl group, thiol group, phosphoric acid group, phosphonic acid group, phosphine group, phosphine oxide group, and alkoxysilyl. Examples of the organic ligand include TOP (trioctylphosphine), TOPO (trioctylphosphine oxide), oleic acid, oleylamine, octylamine, trioctylamine, hexadecylamine, octanethiol, dodecanethiol, hexylphosphonic acid ( HPA), tetradecylphosphonic acid (TDPA), and octylphosphinic acid (OPA).

［式（１）中、ｐは０〜５０の整数を示し、ｑは０〜５０の整数を示す。］ The organic ligand preferably has an aliphatic hydrocarbon having an ethylene oxide chain and / or a propylene oxide chain as an affinity group from the viewpoint that the dispersibility and luminescence intensity of the luminescent nanocrystal particles are further improved. The organic ligand may be, for example, an organic ligand represented by the following formula (1).

[In Formula (1), p shows the integer of 0-50, q shows the integer of 0-50. ]

  In the organic ligand represented by the formula (1), at least one of p and q is preferably 1 or more, and both p and q are more preferably 1 or more.

  As the luminescent nanocrystal particles, those dispersed in a colloidal form in an organic solvent or the like can be used. It is preferable that the surface of the luminescent nanocrystal particles dispersed in the organic solvent is passivated by the above-described organic ligand. Examples of the organic solvent include cyclohexane, hexane, heptane, chloroform, toluene, octane, chlorobenzene, tetralin, diphenyl ether, propylene glycol monomethyl ether acetate, butyl carbitol acetate, or a mixture thereof.

  A commercial item can be used as a luminescent nanocrystal particle. Examples of commercially available luminescent nanocrystal particles include indium phosphine / zinc sulfide, D-dot, CuInS / ZnS, and InP / ZnS from Aldrich, manufactured by NN-Labs.

  The content of the luminescent nanocrystal particles may be 5% by mass or more, or 10% by mass or more based on the mass of the nonvolatile content of the ink composition, from the viewpoint of excellent leakage light reduction effect. 15 mass% or more, 20 mass% or more, 30 mass% or more, or 40 mass% or more. The content of the luminescent nanocrystal particles may be 70% by mass or less, or 60% by mass or less, based on the mass of the non-volatile content of the ink composition, from the viewpoint of being superior in ejection stability. It may be less than or equal to 50% by weight or less than or equal to 50% by weight. When the luminescent nanocrystal particles are modified with an organic ligand, the total amount of the luminescent nanocrystal particles and the organic ligand that modifies the luminescent nanocrystal particles may be in the above range. In this specification, “the mass of the non-volatile content of the ink composition” refers to the mass obtained by subtracting the mass of the solvent from the total mass of the ink composition when the ink composition contains a solvent. When a solvent is not included, the total mass of the ink composition is indicated.

[Light scattering particles]
The light scattering particles are, for example, optically inactive inorganic fine particles. The light scattering particles can scatter light from the light source irradiated to the color filter pixel portion. The light scattering particles of this embodiment are those in which at least a part of the surface of the particles is covered with alumina. Of the surface of the light scattering particles, for example, 50 area% or more may be covered with alumina, and the entire surface of the light scattering particles may be covered with alumina. The light scattering particles can also be referred to as light scattering particles surface-treated with alumina.

  As a method of covering at least a part of the surface of the light scattering particles with alumina (surface treatment with alumina), for example, a wet processing method (adding an aluminum salt aqueous solution to the light scattering particle slurry and neutralizing the solution) And a method of adsorbing on the surface of the light scattering particles). Examples of the light scattering particles include “MPT-141”, “CR-50”, “CR-50-2”, “CR-58”, “CR-58-2”, “CR” manufactured by Ishihara Sangyo Co., Ltd. Commercial products such as “−60”, “CR-60-2”, “JR405”, “JR603”, “JR605”, “JR701”, and “JR806” manufactured by Teika Co., Ltd. can also be used. The surface of the light scattering particles may be covered with alumina and other components such as silica, zinc oxide, titanium oxide, zirconium oxide, and organic substances such as stearic acid and polysiloxane.

  The shape of the light scattering particles may be spherical, filamentous, indeterminate. However, as the light scattering particles, it is possible to use particles having less directivity as the particle shape (for example, spherical, tetrahedral, etc. particles), thereby improving the uniformity, fluidity and light scattering of the ink composition. It is preferable in that it can be increased and more excellent dispersion stability of the light scattering particles can be obtained.

  The average particle diameter (volume average diameter) of the light-scattering particles in the ink composition is 0.05 μm or more from the viewpoint of being excellent in the dispersion stability of the light-scattering particles and the effect of reducing leakage light. It may be 0.1 μm or more, or 0.2 μm or more. The average particle diameter (volume average diameter) of the light-scattering particles in the ink composition may be 1.0 μm or less and 0.6 μm or less from the viewpoint of better dispersion stability of the light-scattering particles. It may be 0.4 μm or less. The average particle diameter (volume average diameter) of the light-scattering particles in the ink composition is 0.05 to 1.0 μm, 0.05 to 0.6 μm, 0.05 to 0.4 μm, and 0.2 to 1. It may be 0.0 μm, 0.2 to 0.6 μm, 0.2 to 0.4 μm, 0.3 to 1.0 μm, 0.3 to 0.6 μm, or 0.3 to 0.4 μm. From the viewpoint of easily obtaining such an average particle diameter (volume average diameter), the average particle diameter (volume average diameter) of the light-scattering particles used may be 50 nm or more and 1000 nm or less. The average particle diameter (volume average diameter) of the light scattering particles in the ink composition is obtained by measuring with a dynamic light scattering nanotrack particle size distribution meter and calculating the volume average diameter. The average particle diameter (volume average diameter) of the light-scattering particles used is obtained by measuring the particle diameter of each particle with, for example, a transmission electron microscope or a scanning electron microscope and calculating the volume average diameter.

  The content of the light-scattering particles may be 0.1% by mass or more and 1% by mass or more based on the mass of the nonvolatile content of the ink composition from the viewpoint of excellent leakage light reduction effect. Alternatively, it may be 5% by mass or more, 7% by mass or more, 10% by mass or more, or 12% by mass or more. The content of the light-scattering particles may be 60% by mass or less, and 50% by mass based on the mass of the non-volatile content of the ink composition, from the viewpoint of superior discharge stability and the effect of reducing leakage light. Or 40% by mass or less, 30% by mass or less, 25% by mass or less, 20% by mass or less, or 15% by mass. It may be the following. In this embodiment, since the ink composition contains a polymer dispersant, the light scattering particles can be favorably dispersed even when the content of the light scattering particles is in the above range.

  The mass ratio of the content of the light-scattering particles to the content of the light-emitting nanocrystal particles (light-scattering particles / light-emitting nanocrystal particles) is 0.1 or more from the viewpoint of excellent leakage light reduction effect. It may be 0.2 or more, or 0.5 or more. The mass ratio (light scattering particles / luminescent nanocrystal particles) is 5.0 or less from the viewpoint of excellent leakage light reduction effect and excellent continuous discharge properties (discharge stability) during ink jet printing. It may be 2.0 or less and may be 1.5 or less. In addition, it is thought that leakage light reduction by light-scattering particles is based on the following mechanism. That is, when no light-scattering particles are present, it is considered that the backlight light only passes almost straight through the pixel portion and is less likely to be absorbed by the light-emitting nanocrystal particles. On the other hand, if the light-scattering particles are present in the same pixel portion as the light-emitting nanocrystal particles, the backlight light is scattered in all directions in the pixel portion, and the light-emitting nanocrystal particles can receive it. Even if the same backlight is used, it is considered that the light absorption amount in the pixel portion increases. As a result, it is considered that leakage light can be prevented by such a mechanism.

[Polymer dispersant]
In the present invention, the polymer dispersant is a polymer compound having a weight average molecular weight of 750 or more and having a functional group having an affinity for the light scattering particles, and the function of dispersing the light scattering particles. Have The polymer dispersing agent is adsorbed to the light scattering particle via a functional group having affinity for the light scattering particle, and the light scattering particle is formed by electrostatic repulsion and / or steric repulsion between the polymer dispersing agents. Disperse in the ink composition. The polymer dispersant is preferably bonded to the surface of the light-scattering particle and adsorbed to the light-scattering particle, but is bonded to the surface of the light-emitting nanocrystal particle and adsorbed to the light-emitting nanoparticle. It may be free in the ink composition.

  By the way, when forming the color filter pixel portion by the ink jet method using the conventional ink composition, one of the causes of the decrease in the ejection stability is considered to be aggregation of the luminescent nanocrystal particles and the light scattering particles. . Therefore, it is conceivable to improve the ejection stability by miniaturizing the luminescent nanocrystal particles and the light-scattering particles and reducing the content of the luminescent nanocrystal particles and the light-scattering particles. In this case, the effect of reducing the leakage light is likely to be reduced, and it is difficult to achieve both the discharge stability and the reduction of the leakage light at a high level. On the other hand, according to the ink composition further containing the polymer dispersant, it is possible to achieve both excellent ejection stability and reduction of leakage light at a high level. The reason why such an effect is obtained is not clear, but the polymer dispersant significantly suppresses aggregation of the light-emitting nanocrystal particles and the light-scattering particles (particularly, the light-scattering particles). It is guessed.

  Examples of the functional group having an affinity for the light-scattering particles include an acidic functional group, a basic functional group, and a nonionic functional group. The acidic functional group has a dissociable proton and may be neutralized with a base such as amine or hydroxide ion, and the basic functional group is neutralized with an acid such as organic acid or inorganic acid. May be.

Examples of the acidic functional group include a carboxyl group (—COOH), a sulfo group (—SO ₃ H), a sulfuric acid group (—OSO ₃ H), a phosphonic acid group (—PO (OH) ₃ ), and a phosphoric acid group (—OPO ( OH) ₃ ), a phosphinic acid group (—PO (OH) —), and a mercapto group (—SH).

  Examples of basic functional groups include primary, secondary and tertiary amino groups, ammonium groups, imino groups, and nitrogen-containing heterocyclic groups such as pyridine, pyrimidine, pyrazine, imidazole and triazole.

Nonionic functional groups include hydroxy group, ether group, thioether group, sulfinyl group (—SO—), sulfonyl group (—SO ₂ —), carbonyl group, formyl group, ester group, carbonate group, amide group, Examples include carbamoyl group, ureido group, thioamide group, thioureido group, sulfamoyl group, cyano group, alkenyl group, alkynyl group, phosphine oxide group, and phosphine sulfide group.

  From the viewpoint of dispersion stability of light-scattering particles, from the viewpoint of hardly causing the side effect that the luminescent nanocrystal particles settle, from the viewpoint of ease of synthesis of the polymer dispersant, and from the viewpoint of stability of the functional group, acidic functional As the group, a carboxyl group, a sulfo group, a phosphonic acid group, and a phosphoric acid group are preferably used, and as the basic functional group, an amino group is preferably used. Among these, a carboxyl group, a phosphonic acid group, and an amino group are more preferably used, and most preferably an amino group is used.

  The polymer dispersant having an acidic functional group has an acid value. The acid value of the polymer dispersant having an acidic functional group is preferably 1 to 150 mgKOH / g. When the acid value is 1 mgKOH / g or more, sufficient dispersibility of the light-scattering particles can be easily obtained, and when the acid value is 150 mgKOH / g or less, the storage stability of the pixel portion (cured product of the ink composition). Is difficult to decrease.

The acid value of the polymer dispersant can be measured as follows. A sample solution prepared by dissolving 1 ml of the polymer dispersant pg and phenolphthalein test solution in 50 ml of a mixed solution of toluene and ethanol mixed at a volume ratio of 1: 1 was prepared, and a 0.1 mol / L ethanol potassium hydroxide solution was prepared. Titrate until the sample solution turns pale red (dissolved in 7.0 ml of potassium hydroxide in 5.0 ml of distilled water and adjusted to 1000 ml by adding 95 vol% ethanol). It can be calculated.
Acid value = q × r × 5.661 / p
In the formula, q represents the titration (ml) of 0.1 mol / L ethanol potassium hydroxide solution required for titration, and r represents the titer of 0.1 mol / L ethanol potassium hydroxide solution required for titration. P represents the mass (g) of the polymer dispersant.

  In addition, the polymer dispersant having a basic functional group has an amine value. The amine value of the polymer dispersant having a basic functional group is preferably 1 to 200 mgKOH / g. When the amine value is 1 mgKOH / g or more, sufficient dispersibility of the light-scattering particles can be easily obtained, and when the amine value is 200 mgKOH / g or less, the storage stability of the pixel portion (cured product of the ink composition). Is difficult to decrease.

The amine value of the polymer dispersant can be measured as follows. A sample solution prepared by dissolving a polymer dispersant xg and 1 ml of bromophenol blue sample solution in 50 ml of a mixed solution in which toluene and ethanol were mixed at a volume ratio of 1: 1 was prepared, and the sample solution was prepared with 0.5 mol / L hydrochloric acid. Titration is performed until a green color is exhibited, and the amine value can be calculated by the following formula.
Amine number = y / x × 28.05
In the formula, y represents the titration amount (ml) of 0.5 mol / L hydrochloric acid required for titration, and x represents the mass (g) of the polymer dispersant.

  The polymer dispersant may be a polymer (homopolymer) of a single monomer, or may be a copolymer (copolymer) of a plurality of types of monomers. The polymer dispersant may be any of a random copolymer, a block copolymer, or a graft copolymer. When the polymer dispersant is a graft copolymer, it may be a comb-shaped graft copolymer or a star-shaped graft copolymer. Polymer dispersants include, for example, acrylic resins, polyester resins, polyurethane resins, polyamide resins, polyethers, phenol resins, silicone resins, polyurea resins, amino resins, polyethylamines and other polyamines, epoxy resins, polyimides, etc. It may be.

  Commercially available products can also be used as the polymer dispersant, and examples of commercially available products include Ajinomoto Fine Techno Co., Ltd. Ajisper PB series, BYK's DISPERBYK series and BYK- series, BASF's Efka series. Etc. can be used.

  Commercially available products include, for example, “DISPERBYK-130”, “DISPERBYK-161”, “DISPERBYK-162”, “DISPERBYK-163”, “DISPERBYK-164”, “DISPERBYK-166”, “DISPERBYK-” manufactured by Big Chemie. 167 "," DISPERBYK-168 "," DISPERBYK-170 "," DISPERBYK-171 "," DISPERBYK-174 "," DISPERBYK-180 "," DISPERBYK-182 "," DISPERBYK-183 "," DISPERBYK-184 " , “DISPERBYK-185”, “DISPERBYK-2000”, “DISPERBYK-2001”, “DISPERBYK-2008”, “DISP” RBYK-2009 "," DISPERBYK-2020 "," DISPERBYK-2022 "," DISPERBYK-2025 "," DISPERBYK-2050 "," DISPERBYK-2070 "," DISPERBYK-2096 "," DISPERBYK-2150 "," DISPERBY " 2155 "," DISPERBYK-2163 "," DISPERBYK-2164 "," BYK-LPN21116 "and" BYK-LPN6919 ";" EFKA4010 "," EFKA4015 "," EFKA4046 "," EFKA4047 "," EFK "manufactured by BASF , “EFKA4080”, “EFKA4300”, “EFKA4310”, “EFKA4320”, “EFKA4330”, “EFK” "4340", "EFKA4560", "EFKA4585", "EFKA5207", "EFKA1501", "EFKA1502", "EFKA1503" and "EFKA PX-4701"; "Solsparse 3000", "Solsparse 9000", "Lubrisol" "Sol Sparse 13240", "Sol Sparse 13650", "Sol Sparse 13940", "Sol Sparse 11200", "Sol Sparse 13940", "Sol Sparse 16000", "Sol Sparse 17000", "Sol Sparse 18000", "Sol Sparse 20000", "Sol Sparse 21000", " "Sol Sparse 24000", "Sol Sparse 26000", "Sol Sparse 27000", "Sol Sparse 28000", "Sol Sparse 32000" “Sol Sparse 32500”, “Sol Sparse 32550”, “Sol Sparse 32600”, “Sol Sparse 33000”, “Sol Sparse 34750”, “Sol Sparse 35100”, “Sol Sparse 35200”, “Sol Sparse 36000”, “Sol Sparse 37500”, “Sol Sparse 38500”, "Solsparth 39000", "Solsparth 41000", "Solsperse 54000", "Solsperse 71000" and "Solsperse 76500"; "Ajisper PB821", "Azisper PB882", "Azisper PB881", "PN411" manufactured by Ajinomoto Fine Techno Co., Ltd. And “PA111”; “TEGO Dispers 650”, “TEGO Dispers 660C”, “TEGO” manufactured by Evonik "Dispers 662C", "TEGO Dispers 670", "TEGO Dispers 685", "TEGO Dispers 700", "TEGO Dispers 710" and "TEGO Dispers 760W"; "Disparon DA" 703-50 "manufactured by Enomoto Kasei 725 "or the like can be used.

  As the polymer dispersant, in addition to the above-mentioned commercially available products, a cationic monomer containing a basic group and / or an anionic monomer having an acidic group, a monomer having a hydrophobic group, and other monomers if necessary Those synthesized by copolymerizing (nonionic monomers, monomers having a hydrophilic group, etc.) can be used. As for details of the cationic monomer, the anionic monomer, the monomer having a hydrophobic group, and other monomers, there can be mentioned monomers described in paragraphs 0034 to 0036 of JP-A No. 2004-250502.

  Further, for example, a compound obtained by reacting a polyalkyleneimine and a polyester compound described in JP-A-54-37082, JP-A-61-174939, or the like, or a polyallylamine described in JP-A-9-169821 A compound in which the amino group of the side chain is modified with polyester, a graft polymer having a polyester type macromonomer described in JP-A-9-171253 as a copolymerization component, and a polyester polyol addition described in JP-A-60-166318 Preferred examples include polyurethane.

  The weight average molecular weight of the polymer dispersant may be 750 or more from the viewpoint that the light scattering particles can be favorably dispersed and the effect of reducing leakage light can be improved. It may be 2000 or more, or 3000 or more. The weight average molecular weight of the polymer dispersant can disperse the light-scattering particles well, improve the leakage light reduction effect, and can discharge the viscosity of the inkjet ink and is suitable for stable discharge. From this viewpoint, it may be 100,000 or less, 50000 or less, or 30000 or less.

  From the viewpoint of dispersibility of the light-scattering particles, the content of the polymer dispersant may be 0.5 parts by mass or more with respect to 100 parts by mass of the light-scattering particles, It may be 5 parts by mass or more. The content of the polymer dispersion may be 50 parts by mass or less and 30 parts by mass or less with respect to 100 parts by mass of the light-scattering particles from the viewpoint of wet heat stability of the pixel part (cured product of the ink composition). It may be 10 parts by mass or less.

[Thermosetting resin]
The ink composition may further contain a thermosetting resin. A thermosetting resin is a resin that functions as a binder in a cured product and is crosslinked and cured by heat. The thermosetting resin has a curable group. Examples of the curable group include an epoxy group, an oxetane group, an isocyanate group, an amino group, a carboxyl group, a methylol group, and the like, from the viewpoint of excellent heat resistance and storage stability of a cured product of the ink composition, and a light shielding part ( For example, an epoxy group is preferable from the viewpoint of excellent adhesion to a black matrix and a substrate. The thermosetting resin may have one type of curable group or may have two or more types of curable groups.

  The thermosetting resin may be a polymer (homopolymer) of a single monomer, or may be a copolymer (copolymer) of a plurality of types of monomers. Further, the thermosetting resin may be any of a random copolymer, a block copolymer, or a graft copolymer.

  As the thermosetting resin, a compound having two or more thermosetting functional groups in one molecule is used, and it is usually used in combination with a curing agent. When using a thermosetting resin, you may further add the catalyst (curing catalyst) which can accelerate | stimulate a thermosetting reaction. In other words, the ink composition may contain a thermosetting resin, and a thermosetting component including a curing agent and a curing catalyst used as necessary. In addition to these, a polymer having no polymerization reactivity per se may be further used.

  As a compound having two or more thermosetting functional groups in one molecule, for example, an epoxy resin having two or more epoxy groups in one molecule (hereinafter also referred to as “polyfunctional epoxy resin”) may be used. “Epoxy resin” includes both monomeric epoxy resins and polymeric epoxy resins. The number of epoxy groups contained in one molecule of the polyfunctional epoxy resin is preferably 2 to 50, and more preferably 2 to 20. The epoxy group may be a structure having an oxirane ring structure, and may be a glycidyl group, an oxyethylene group, an epoxycyclohexyl group, or the like. As an epoxy resin, the well-known polyvalent epoxy resin which can be hardened | cured with carboxylic acid can be mentioned. Such epoxy resins are widely disclosed in, for example, published by Masaki Shinbo, “Epoxy Resin Handbook” published by Nikkan Kogyo Shimbun (1987), and these can be used.

  Examples of the thermosetting resin having an epoxy group (including a polyfunctional epoxy resin) include a polymer of a monomer having an oxirane ring structure, and a copolymer of a monomer having an oxirane ring structure and another monomer. Specific polyfunctional epoxy resins include polyglycidyl methacrylate, methyl methacrylate-glycidyl methacrylate copolymer, benzyl methacrylate-glycidyl methacrylate copolymer, n-butyl methacrylate-glycidyl methacrylate copolymer, 2-hydroxyethyl methacrylate-glycidyl. Examples thereof include a methacrylate copolymer, (3-ethyl-3-oxetanyl) methyl methacrylate-glycidyl methacrylate copolymer, and styrene-glycidyl methacrylate. In addition, as the thermosetting resin of the present embodiment, compounds described in paragraphs 0044 to 0066 of JP-A-2014-56248 can also be used.

  Examples of the polyfunctional epoxy resin include bisphenol A type epoxy resin, bisphenol F type epoxy resin, brominated bisphenol A type epoxy resin, bisphenol S type epoxy resin, diphenyl ether type epoxy resin, hydroquinone type epoxy resin, and naphthalene type epoxy. Resin, biphenyl type epoxy resin, fluorene type epoxy resin, phenol novolac type epoxy resin, orthocresol novolac type epoxy resin, trishydroxyphenylmethane type epoxy resin, trifunctional type epoxy resin, tetraphenylolethane type epoxy resin, dicyclopentadiene Phenol type epoxy resin, hydrogenated bisphenol A type epoxy resin, bisphenol A nucleated polyol type epoxy resin, polypropylene glycol type epoxy Fat, glycidyl ester type epoxy resin, glycidyl amine type epoxy resin, glyoxal type epoxy resins, alicyclic epoxy resins, and the like heterocyclic epoxy resin.

  More specifically, bisphenol A type epoxy resins such as trade name “Epicoat 828” (manufactured by Japan Epoxy Resin), bisphenol F type epoxy resins such as trade name “YDF-175S” (manufactured by Toto Kasei), Brominated bisphenol A type epoxy resin such as “YDB-715” (manufactured by Toto Kasei Co., Ltd.), bisphenol S type epoxy resin such as “EPICLON EXA1514” (manufactured by DIC Corporation), product name “YDC-1312” ( Hydroquinone type epoxy resins such as Toto Kasei Co., Ltd., and naphthalene type epoxy resins such as trade names “EPICLON EXA4032”, “HP-4770”, “HP-4700”, “HP-5000” (manufactured by DIC Corporation), Product name "Epicoat YX4000H" (manufactured by Japan Epoxy Resin Co., Ltd.) Biphenyl type epoxy resin, bisphenol A type novolak epoxy resin such as trade name “Epicoat 157S70” (made by Japan Epoxy Resin), trade name “Epicoat 154” (made by Japan Epoxy Resin), trade name “YDPN-638” ( Phenol novolac type epoxy resins such as Toto Kasei Co., Ltd., cresol novolac type epoxy resins such as trade name “YDCN-701” (manufactured by Toto Kasei Co., Ltd.), trade names “EPICLON HP-7200”, “HP-7200H” (DIC) Dicyclopentadiene phenol type epoxy resin such as “Epicoat 1032H60” (manufactured by Japan Epoxy Resin Co., Ltd.), trade name “VG3101M80” (manufactured by Mitsui Chemicals), etc. Three officials Type epoxy resin, tetraphenylolethane type epoxy resin such as trade name “Epicoat 1031S” (manufactured by Japan Epoxy Resin Co., Ltd.), tetrafunctional type epoxy resin such as trade name “Denacol EX-411” (manufactured by Nagase Chemical Industries), Hydrogenated bisphenol A type epoxy resin such as trade name “ST-3000” (manufactured by Toto Kasei), glycidyl ester type epoxy resin such as trade name “Epicoat 190P” (made by Japan Epoxy Resin), trade name “YH-434” ”(Manufactured by Tohto Kasei Co., Ltd.), glycidyl amine type epoxy resin such as“ YDG-414 ”(manufactured by Tohto Kasei Co., Ltd.), and the product name“ Epolide GT-401 ”(manufactured by Daicel Chemical Industries). Alicyclic polyfunctional epoxy compounds, triglycidyl isocyanate (TGIC), etc. Heterocyclic epoxy resin and the like can be exemplified. Further, if necessary, a trade name “Neoto Tote E” (manufactured by Tohto Kasei Co., Ltd.) or the like can be mixed as an epoxy reactive diluent.

  In addition, as the polyfunctional epoxy resin, “Fine Dick A-247S”, “Fine Dick A-254”, “Fine Dick A-253”, “Fine Dick A-229-30A” manufactured by DIC Corporation, “ “Fine Dick A-261”, “Fine Dick A-249”, “Fine Dick A-266”, “Fine Dick A-241” “Fine Dick M-8020”, “Epicron N-740”, “Epicron N-770” "Epiclon N-865" (trade name) or the like can be used.

  When a polyfunctional epoxy resin having a relatively low molecular weight is used as the thermosetting resin, the epoxy group is replenished in the ink composition (inkjet ink) to increase the concentration of epoxy reactive sites and increase the crosslinking density. it can.

  Among the polyfunctional epoxy resins, from the viewpoint of increasing the crosslink density, it is preferable to use an epoxy resin having four or more epoxy groups in one molecule (polyfunctional epoxy resin having four or more functions). In particular, when a thermosetting resin having a weight average molecular weight of 10,000 or less is used in order to improve the ejection stability from the ejection head in the ink jet system, the strength and hardness of the pixel portion (cured product of the ink composition) is reduced. From the viewpoint of sufficiently increasing the crosslink density, it is preferable to blend a polyfunctional epoxy resin having 4 or more functionalities into the ink composition (inkjet ink).

  The thermosetting resin may be insoluble in alkali from the viewpoint of easily obtaining a color filter pixel portion having excellent reliability. The thermosetting resin is alkali-insoluble means that the amount of the thermosetting resin dissolved in a 1% by mass potassium hydroxide aqueous solution at 25 ° C. is 30% by mass or less based on the total mass of the thermosetting resin. Means that. The dissolution amount of the thermosetting resin is preferably 10% by mass or less, and more preferably 3% by mass or less.

  The weight-average molecular weight of the thermosetting resin is such that an appropriate viscosity is easily obtained as an ink-jet ink, the ink composition has good curability, and the solvent resistance of the pixel portion (cured product of the ink composition). From the viewpoint of improving wear resistance, it may be 750 or more, 1000 or more, or 2000 or more. From the viewpoint of obtaining an appropriate viscosity as an inkjet ink, it may be 500000 or less, 300000 or less, or 200000 or less. However, the molecular weight after crosslinking is not limited to this. In addition, in this specification, a weight average molecular weight is a weight average molecular weight of polystyrene conversion measured by GPC (gel permeation chromatography, Gel Permeation Chromatography).

  The content of the thermosetting resin is the viewpoint that an appropriate viscosity is easily obtained as an inkjet ink, the viewpoint that the curability of the ink composition is good, and the solvent resistance of the pixel portion (cured product of the ink composition). From the viewpoint of improving the wear resistance, it may be 10% by mass or more, 15% by mass or more, or 20% by mass or more, based on the mass of the nonvolatile content of the ink composition. From the viewpoint that the viscosity of the inkjet ink is not too high and the thickness of the pixel portion is not too thick for the light conversion function, the content of the thermosetting resin is based on the mass of the non-volatile content of the ink composition. It may be 90% by mass or less, 80% by mass or less, 70% by mass or less, 60% by mass or less, or 50% by mass or less.

[Curing agent and curing catalyst]
Examples of the curing agent and curing catalyst used for curing the thermosetting resin include 4-methylhexahydrophthalic anhydride, triethylenetetramine, diaminodiphenylmethane, phenol novolac resin, tris (dimethylaminomethyl) phenol, N, N-dimethylbenzylamine, 2-ethyl-4-methylimidazole, triphenylphosphine, 3-phenyl-1,1-dimethylurea and the like can be mentioned.

[Photopolymerizable compound]
The ink composition may further contain a polymerizable component that is polymerized by light irradiation instead of or in addition to the thermosetting component. The polymerizable component includes a polymerizable compound. The polymerizable compound is a radical photopolymerizable compound or a cationic photopolymerizable compound, and may be a photopolymerizable monomer or oligomer. These are used together with a photopolymerization initiator. The photoradical polymerizable compound is used with a photoradical polymerization initiator, and the photocationic polymerizable compound is used with a photocationic polymerization initiator. In other words, the ink composition may contain a photopolymerizable component containing a photopolymerizable compound and a photopolymerization initiator, and contains a photoradical polymerizable component containing a photoradical polymerizable compound and a photoradical polymerization initiator. The photocationic polymerizable component containing a photocationic polymerizable compound and a photocationic polymerization initiator may be contained. A photo radical polymerizable compound and a photo cationic polymerizable compound may be used in combination, or a compound having a photo radical polymerizable property and a photo cationic polymerizable property may be used. A photo radical polymerization initiator, a photo cationic polymerization initiator, May be used in combination. A photopolymerizable compound may be used individually by 1 type, and may use 2 or more types together.

  Examples of the radical photopolymerizable compound include (meth) acrylate compounds. The (meth) acrylate compound may be a monofunctional (meth) acrylate having one (meth) acryloyl group or a polyfunctional (meth) acrylate having a plurality of (meth) acryloyl groups. Monofunctional (meth) acrylate and polyfunctional (meta) from the viewpoint of excellent fluidity when used in ink, excellent viewpoint of ejection stability, and suppression of smoothness deterioration due to curing shrinkage during color filter production. ) Acrylate is preferably used in combination. In the present specification, (meth) acrylate means “acrylate” and “methacrylate” corresponding thereto. The same applies to the expression “(meth) acryloyl”.

  Examples of monofunctional (meth) acrylates include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, amyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, and octyl. (Meth) acrylate, nonyl (meth) acrylate, dodecyl (meth) acrylate, hexadecyl (meth) acrylate, octadecyl (meth) acrylate, cyclohexyl (meth) acrylate, methoxyethyl (meth) acrylate, butoxyethyl (meth) acrylate, phenoxy Ethyl (meth) acrylate, nonylphenoxyethyl (meth) acrylate, glycidyl (meth) acrylate, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (Meth) acrylate, isobornyl (meth) acrylate, dicyclopentanyl (meth) acrylate, dicyclopentenyl (meth) acrylate, dicyclopentenyloxyethyl (meth) acrylate, 2-hydroxy-3-phenoxypropyl (meth) acrylate , Tetrahydrofurfuryl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, benzyl (meth) acrylate, phenylbenzyl (meth) acrylate, succinic acid mono (2-acryloyloxyethyl), N- [2- (acryloyloxy) ) Ethyl] phthalimide, N- [2- (acryloyloxy) ethyl] tetrahydrophthalimide, and the like.

  The polyfunctional (meth) acrylate may be bifunctional (meth) acrylate, trifunctional (meth) acrylate, tetrafunctional (meth) acrylate, pentafunctional (meth) acrylate, hexafunctional (meth) acrylate, etc. Di (meth) acrylate in which two hydroxyl groups of diol compound are substituted by (meth) acryloyloxy group, di or tri (meth) acrylate in which two or three hydroxyl groups of triol compound are substituted by (meth) acryloyloxy group Etc.

  Specific examples of the bifunctional (meth) acrylate include 1,3-butylene glycol di (meth) acrylate, 1,4-butanediol di (meth) acrylate, 1,5-pentanediol di (meth) acrylate, 3- Methyl-1,5-pentanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, 1,8-octanediol di (meth) acrylate, 1,9 -Nonanediol di (meth) acrylate, tricyclodecane dimethanol di (meth) acrylate, ethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, dipropylene glycol di (meth) ) Acrylate, (Meth) acryloyl has two hydroxyl groups: propylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate, neopentyl glycol hydroxypivalate ester diacrylate, tris (2-hydroxyethyl) isocyanurate Di (meth) acrylate substituted with an oxy group, dipentaglycol in which two hydroxyl groups of a diol obtained by adding 4 mol or more of ethylene oxide or propylene oxide to 1 mol of neopentyl glycol are substituted with a (meth) acryloyloxy group Di (meth) in which two hydroxyl groups of diol obtained by adding 2 mol of ethylene oxide or propylene oxide to 1 mol of (meth) acrylate and bisphenol A are substituted by (meth) acryloyloxy groups Di (meth) acrylate in which two hydroxyl groups of triol obtained by adding 3 mol or more of ethylene oxide or propylene oxide to 1 mol of acrylate and trimethylolpropane are substituted by (meth) acryloyloxy group, 4 mol in 1 mol of bisphenol A Examples include di (meth) acrylates in which two hydroxyl groups of a diol obtained by adding at least a mole of ethylene oxide or propylene oxide are substituted with (meth) acryloyloxy groups.

  Specific examples of trifunctional (meth) acrylates include trimethylolpropane tri (meth) acrylate, glycerin triacrylate, pentaerythritol tri (meth) acrylate, and 3 mol or more of ethylene oxide or propylene oxide added to 1 mol of trimethylolpropane. And tri (meth) acrylate in which the three hydroxyl groups of the triol obtained are substituted with a (meth) acryloyloxy group.

  Specific examples of the tetrafunctional (meth) acrylate include pentaerythritol tetra (meth) acrylate.

  Specific examples of the pentafunctional (meth) acrylate include dipentaerythritol penta (meth) acrylate.

  Specific examples of the hexafunctional (meth) acrylate include dipentaerythritol hexa (meth) acrylate.

  The polyfunctional (meth) acrylate may be a poly (meth) acrylate in which a plurality of hydroxyl groups of dipentaerythritol such as dipentaerythritol hexa (meth) acrylate are substituted with (meth) acryloyloxy groups.

  The (meth) acrylate compound may be a phosphoric acid group-containing ethylene oxide-modified phosphoric acid (meth) acrylate, ethylene oxide-modified alkyl phosphoric acid (meth) acrylate, or the like.

  Examples of the cationic photopolymerizable compound include an epoxy compound, an oxetane compound, and a vinyl ether compound.

  Examples of the epoxy compound include bisphenol A type epoxy compounds, bisphenol F type epoxy compounds, phenol novolac type epoxy compounds, trimethylolpropane polyglycidyl ether, and aliphatic epoxy compounds such as neopentyl glycol diglycidyl ether, 1,2-epoxy- And alicyclic epoxy compounds such as 4-vinylcyclohexane and 1-methyl-4- (2-methyloxiranyl) -7-oxabicyclo [4.1.0] heptane.

  It is also possible to use a commercial item as an epoxy compound. Examples of commercially available epoxy compounds include “Celoxide 2000”, “Celoxide 3000”, and “Celoxide 4000” manufactured by Daicel Chemical Industries, Ltd.

  Examples of the cationically polymerizable oxetane compound include 2-ethylhexyloxetane, 3-hydroxymethyl-3-methyloxetane, 3-hydroxymethyl-3-ethyloxetane, 3-hydroxymethyl-3-propyloxetane, and 3-hydroxymethyl-3. Normal butyl oxetane, 3-hydroxymethyl-3-phenyl oxetane, 3-hydroxymethyl-3-benzyl oxetane, 3-hydroxyethyl-3-methyl oxetane, 3-hydroxyethyl-3-ethyl oxetane, 3-hydroxyethyl- 3-propyloxetane, 3-hydroxyethyl-3-phenyloxetane, 3-hydroxypropyl-3-methyloxetane, 3-hydroxypropyl-3-ethyloxetane, 3-hydroxypropyl-3-propyloxeta , 3-hydroxypropyl-3-phenyl oxetane, 3-hydroxybutyl-3-methyl oxetane, and the like.

  Commercial products can be used as the oxetane compound. Examples of commercially available oxetane compounds include Aron Oxetane series (“OXT-101”, “OXT-212”, “OXT-121”, “OXT-221”, etc.) manufactured by Toa Gosei Co., Ltd.); “Celoxide 2021”, “Celoxide 2021A”, “Celoxide 2021P”, “Celoxide 2080”, “Celoxide 2081”, “Celoxide 2083”, “Celoxide 2085”, “Epolide GT300”, “Epolide GT301”, “Epolide GT302”, “Epolide GT400”, “Epolide GT401” and “Epolide GT403”; “Syracure UVR-6105”, “Syracure UVR-6107”, “Syracure UVR-6110” manufactured by Dow Chemical Japan Co., Ltd. , And the like can be used "CYRACURE UVR-6128", "ERL4289" and "ERL4299". Moreover, a well-known oxetane compound (For example, the oxetane compound as described in Unexamined-Japanese-Patent No. 2009-40830 etc.) can also be used.

  Examples of the vinyl ether compound include 2-hydroxyethyl vinyl ether, triethylene glycol vinyl monoether, tetraethylene glycol divinyl ether, trimethylolpropane trivinyl ether, and the like.

  In addition, as the photopolymerizable compound in the present embodiment, the photopolymerizable compounds described in paragraphs 0042 to 0049 of JP2013-182215A can also be used.

  In the ink composition of the present embodiment, when the curable component is composed of only a photopolymerizable compound or a main component thereof, the above-described photopolymerizable compound has a polymerizable functional group in one molecule. It is more preferable to use a bifunctional or higher polyfunctional photopolymerizable compound having 2 or more as an essential component because durability (strength, heat resistance, etc.) of the cured product can be further improved.

  The photopolymerizable compound may be insoluble in alkali from the viewpoint of easily obtaining a color filter pixel portion having excellent reliability. In the present specification, the photopolymerizable compound is alkali-insoluble means that the amount of the photopolymerizable compound dissolved in a 1% by mass aqueous potassium hydroxide solution at 25 ° C. is 30 based on the total mass of the photopolymerizable compound. It means that it is below mass%. The dissolution amount of the photopolymerizable compound is preferably 10% by mass or less, and more preferably 3% by mass or less.

  The content of the photopolymerizable compound is the viewpoint that an appropriate viscosity is easily obtained as an inkjet ink, the viewpoint that the curability of the ink composition is good, and the solvent resistance of the pixel portion (cured product of the ink composition). From the viewpoint of improving the wear resistance, it may be 10% by mass or more, 15% by mass or more, or 20% by mass or more based on the mass of the nonvolatile content of the ink composition. The content of the photopolymerizable compound is based on the mass of the non-volatile content of the ink composition from the viewpoint of easily obtaining an appropriate viscosity as an inkjet ink, and from the viewpoint of obtaining more excellent optical characteristics (leakage light). It may be 90% by mass or less, 80% by mass or less, 70% by mass or less, 60% by mass or less, or 50% by mass or less.

  The photopolymerizable compound has a crosslinkable group from the viewpoint of excellent stability of the pixel portion (cured product of the ink composition) (for example, it can suppress deterioration over time and is excellent in high-temperature storage stability and wet heat storage stability). You may do it. The crosslinkable group is a functional group that reacts with other crosslinkable groups by heat or active energy rays (for example, ultraviolet rays), such as an epoxy group, an oxetane group, a vinyl group, an acryloyl group, an acryloyloxy group, and a vinyl ether group. Is mentioned.

[Photo radical polymerization initiator]
As the radical photopolymerization initiator, a molecular cleavage type or hydrogen abstraction type radical photopolymerization initiator is suitable.

  Examples of the molecular cleavage type photo radical polymerization initiator include benzoin isobutyl ether, 2,4-diethylthioxanthone, 2-isopropylthioxanthone, 2,4,6-trimethylbenzoyldiphenylphosphine oxide, 2-benzyl-2-dimethylamino- 1- (4-morpholinophenyl) -butan-1-one, bis (2,6-dimethoxybenzoyl) -2,4,4-trimethylpentylphosphine oxide, (2,4,6-trimethylbenzoyl) ethoxyphenyl Phosphine oxide and the like are preferably used. Other molecular cleavage type photo radical polymerization initiators include 1-hydroxycyclohexyl phenyl ketone, benzoin ethyl ether, benzyl dimethyl ketal, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1- (4 -Isopropylphenyl) -2-hydroxy-2-methylpropan-1-one and 2-methyl-1- (4-methylthiophenyl) -2-morpholinopropan-1-one may be used in combination.

  Examples of the hydrogen abstraction type photo radical polymerization initiator include benzophenone, 4-phenylbenzophenone, isophthalphenone, 4-benzoyl-4'-methyl-diphenyl sulfide, and the like. A molecular cleavage type photo radical polymerization initiator and a hydrogen abstraction type photo radical polymerization initiator may be used in combination.

[Photocationic polymerization initiator]
Examples of the cationic photopolymerization initiator include polyarylsulfonium salts such as triphenylsulfonium hexafluoroantimonate and triphenylsulfonium hexafluorophosphate; diphenyliodonium hexafluoroantimonate, P-nonylphenyliodonium hexafluoroantimony Examples thereof include polyaryl iodonium salts such as nates.

  A commercial item can also be used as a photocationic polymerization initiator. Commercially available products include sulfonium salt photocationic polymerization initiators such as “CPI-100P” manufactured by San Apro, acylphosphine oxide compounds such as “Lucirin TPO” manufactured by BASF, “Irgacure 907” manufactured by BASF, "Irgacure 819", "Irgacure 379EG", "Irgacure 184", "Irgacure PAG290", etc. are mentioned.

  The content of the photopolymerization initiator may be 0.1 parts by mass or more and 0.5 parts by mass or more with respect to 100 parts by mass of the photopolymerizable compound from the viewpoint of curability of the ink composition. It may be 1 part by mass or more. The content of the photopolymerization initiator may be 40 parts by mass or less and 30 parts by mass with respect to 100 parts by mass of the photopolymerizable compound from the viewpoint of temporal stability of the pixel part (cured product of the ink composition). Or 20 parts by mass or less.

  As mentioned above, although each component contained in the ink composition of this embodiment was demonstrated, in the range which does not inhibit the effect of this invention, a light emitting nanocrystal particle | grain, light-scattering particle | grains, and a polymer dispersing agent are included. , An organic ligand, a thermosetting component, and a component other than the photopolymerizable component may be further contained. Examples of other components include a sensitizer and a solvent.

  As the sensitizer, amines that do not cause an addition reaction with the thermosetting resin can be used. Examples of the sensitizer include trimethylamine, methyldimethanolamine, triethanolamine, p-diethylaminoacetophenone, ethyl p-dimethylaminobenzoate, isoamyl p-dimethylaminobenzoate, N, N-dimethylbenzylamine, 4, 4′-bis (diethylamino) benzophenone and the like can be mentioned. The content of the sensitizer may be 0.001% by mass or more and 1% by mass or less based on the mass of the nonvolatile content of the ink composition.

  Examples of the solvent include ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol dibutyl ether, diethyl adipate, dibutyl oxalate, dimethyl malonate, diethyl malonate, dimethyl succinate, and diethyl succinate. 1,4-butane all diacetate, glyceryl triacetate and the like. From the viewpoint of preparing the ink composition to be uniform and from the viewpoint of forming a color filter pixel portion (light conversion layer) with less unevenness by improving the fluidity of the ink composition, it is preferable to use a solvent.

  The boiling point of the solvent is preferably 180 ° C. or higher from the viewpoint of continuous ejection stability of the inkjet ink. Further, since it is necessary to remove the solvent from the ink composition before the ink composition is cured when the pixel portion is formed, the boiling point of the solvent is preferably 300 ° C. or less from the viewpoint of easy removal of the solvent.

  The ink composition described above can be applied as an ink used in a known and commonly used method for producing a color filter, but is necessary without wasting waste of relatively expensive materials such as luminescent nanocrystal particles and solvents. It is preferable that the color filter pixel portion (light conversion layer) can be formed only by using a necessary amount in such a place, and that it is appropriately prepared and used so as to be suitable for the inkjet method rather than for the photolithography method.

  The viscosity of the ink composition is, for example, 2 mPa · s or more, 5 mPa · s or more, or 7 mPa · s or more from the viewpoint of ejection stability during ink jet printing. The viscosity of the ink composition may be 20 mPa · s or less, 15 mPa · s or less, or 12 mPa · s or less. When the viscosity of the ink composition is 2 mPa · s or more, the meniscus shape of the ink composition at the tip of the ink discharge hole of the discharge head is stabilized, so that the discharge control of the ink composition (for example, the discharge amount and the discharge timing) Control). On the other hand, when the viscosity is 20 mPa · s or less, the ink composition can be smoothly discharged from the ink discharge hole. The viscosity of the ink composition is 2 to 20 mPa · s, 2 to 15 mPa · s, 2 to 12 mPa · s, 5 to 20 mPa · s, 5 to 15 mPa · 2 to 20 mPa · s, 7 to 15 mPa · s, 7 to 12 mPa · s. -S or 7-12 mPa * s may be sufficient. The viscosity of the ink composition is measured by, for example, an E-type viscometer. The viscosity of the ink composition can be adjusted to a desired range by changing, for example, the weight average molecular weight of the thermosetting resin, the content of the solvent, and the like.

  The surface tension of the ink composition is preferably a surface tension suitable for an ink jet system, specifically, a range of 20 to 40 mN / m is preferable, and a range of 25 to 35 mN / m is more preferable. . By making the surface tension within this range, the occurrence of flight bending can be suppressed. Note that the flight bend means that when the ink composition is ejected from the ink ejection hole, the landing position of the ink composition deviates by 30 μm or more from the target position. When the surface tension is 40 mN / m or less, the meniscus shape at the tip of the ink discharge hole is stable, and thus the discharge control of the ink composition (for example, control of the discharge amount and discharge timing) becomes easy. On the other hand, when the surface tension is 20 mN / m or less, the occurrence of flight bending can be suppressed. That is, a pixel portion that is not accurately landed on the pixel portion formation region to be landed and is insufficiently filled with the ink composition, or a pixel portion formation region (or pixel portion) adjacent to the pixel portion formation region to be landed Thus, the ink composition does not land and the color reproducibility does not deteriorate. The surface tension of the ink composition can be adjusted to a desired range by using, for example, a silicon surfactant, a fluorine surfactant, an acetylene surfactant, and the like.

  By the way, the pixel portion forming process using the conventional ink composition is performed by a photolithography method, and the ink composition used for the photolithography method contains an alkali-soluble resin as a binder polymer. When the ink composition is used in a photographic system, first, the ink composition is applied onto a substrate, and when the ink composition contains a solvent, the ink composition is further dried to form a coating film. The coating film thus obtained is soluble in an alkali developer and is patterned by being treated with the alkali developer. At this time, since the alkali developer is mostly an aqueous solution from the viewpoint of easiness of waste liquid treatment of the developer, the coating film of the ink composition is treated with the aqueous solution. On the other hand, in the case of an ink composition using luminescent nanocrystal particles (quantum dots or the like), the luminescent nanocrystal particles are unstable with respect to water, and the luminescent property (for example, fluorescence) is impaired by moisture. On the other hand, when the pixel portion is formed by the ink jet method using the ink composition of the present embodiment, it is not necessary to perform treatment with an alkaline developer (aqueous solution), and the luminescent property of the luminescent nanocrystal particles may be impaired by moisture. Absent.

  Even when the coating film of the ink composition is not treated with an alkali developer, when the ink composition is alkali-soluble, the coating film of the ink composition easily absorbs moisture in the atmosphere, and the time As the time elapses, the light-emitting property (for example, fluorescence) of the light-emitting nanocrystal particles (quantum dots or the like) is impaired. From this point of view, in the present embodiment, the coating film of the ink composition is preferably insoluble in alkali. That is, the ink composition of the present embodiment is preferably an ink composition capable of forming an alkali-insoluble coating film. Such an ink composition can be obtained by using an alkali-insoluble thermosetting resin as the thermosetting resin. The coating film of the ink composition is insoluble in alkali. The amount of dissolution of the coating film of the ink composition at 25 ° C. in a 1% by mass potassium hydroxide aqueous solution is based on the total mass of the coating film of the ink composition. It means 30% by mass or less. The dissolution amount of the coating film of the ink composition is preferably 10% by mass or less, and more preferably 3% by mass or less. It should be noted that the ink composition is an ink composition capable of forming an alkali-insoluble coating film when it is applied to a substrate and then dried at 80 ° C. for 3 minutes when it contains a solvent. It can confirm by measuring the said dissolution amount of the coating film of thickness 1 micrometer obtained.

<Method for producing ink composition>
Next, a method for producing the ink composition of the above-described embodiment will be described. The ink composition can be obtained, for example, by mixing the constituent components of the ink composition described above and performing a dispersion treatment. Below, the manufacturing method of the ink composition which further contains a polymer dispersing agent is demonstrated as an example of the manufacturing method of an ink composition.

  The method for producing an ink composition includes, for example, a first step of preparing a dispersion of light scattering particles containing light scattering particles and a polymer dispersant, a dispersion of light scattering particles, and a light-emitting nanoparticle. A second step of mixing the crystal particles. In this method, the dispersion of light scattering particles may further contain a thermosetting resin, and in the second step, a thermosetting resin may be further mixed. According to this method, the light scattering particles can be sufficiently dispersed. For this reason, it is possible to reduce the leakage light in the pixel portion and easily obtain an ink composition having excellent ejection stability.

  In the step of preparing a dispersion of light-scattering particles, the light-scattering particles are dispersed by mixing the light-scattering particles, the polymer dispersant, and optionally a thermosetting resin, and performing a dispersion treatment. May be prepared. The mixing and dispersing treatment may be performed using a dispersing device such as a bead mill, a paint conditioner, a planetary stirrer or the like. It is preferable to use a bead mill or a paint conditioner from the viewpoint of good dispersibility of the light scattering particles and easy adjustment of the average particle diameter of the light scattering particles to a desired range.

  The method for producing an ink composition may further include a step of preparing a dispersion of luminescent nanocrystal particles containing the luminescent nanocrystal particles and a thermosetting resin before the second step. Good. In this case, in the second step, the dispersion of light scattering particles and the dispersion of luminescent nanocrystal particles are mixed. According to this method, the luminescent nanocrystal particles can be sufficiently dispersed. For this reason, it is possible to reduce the leakage light in the pixel portion and easily obtain an ink composition having excellent ejection stability. In the step of preparing a dispersion of luminescent nanocrystal particles, mixing and dispersion of the luminescent nanocrystal particles and the thermosetting resin are performed using the same dispersing device as the step of preparing the dispersion of light scattering particles. Processing may be performed.

  When the ink composition of this embodiment is used as an ink composition for an ink jet system, it is preferably applied to a piezo jet ink jet recording apparatus using a mechanical ejection mechanism using a piezoelectric element. In the piezo jet method, the ink composition is not instantaneously exposed to high temperatures during ejection, the luminescent nanocrystal particles are not easily altered, and the light emission characteristics as expected by the color filter pixel part (light conversion layer) Is easier to obtain.

<Light conversion layer and color filter>
Next, details of the light conversion layer and the color filter using the ink composition of the above-described embodiment will be described with reference to the drawings. In the following description, the same reference numerals are used for the same or corresponding elements, and duplicate descriptions are omitted.

  FIG. 1 is a schematic cross-sectional view of a color filter according to an embodiment. As shown in FIG. 1, the color filter 100 includes a base material 40 and a light conversion layer 30 provided on the base material 40. The light conversion layer 30 includes a plurality of pixel units 10 and a light shielding unit 20.

  The light conversion layer 30 includes, as the pixel unit 10, a first pixel unit 10a, a second pixel unit 10b, and a third pixel unit 10c. The first pixel unit 10a, the second pixel unit 10b, and the third pixel unit 10c are arranged in a lattice pattern so as to be repeated in this order. The light shielding unit 20 is provided between adjacent pixel units, that is, between the first pixel unit 10a and the second pixel unit 10b, between the second pixel unit 10b and the third pixel unit 10c, and third. The pixel portion 10c and the first pixel portion 10a are provided. In other words, these adjacent pixel portions are separated from each other by the light shielding portion 20.

  The first pixel portion 10a and the second pixel portion 10b each include a cured product of the ink composition of the above-described embodiment. The cured product contains luminescent nanocrystal particles, light scattering particles, and a curing component. The curing component is a cured product of a thermosetting resin, and specifically, a cured product obtained by crosslinking of the thermosetting resin. That is, the first pixel unit 10a includes the first cured component 13a and the first light-emitting nanocrystal particles 11a and the first light-scattering particles 12a dispersed in the first cured component 13a. Including. Similarly, the second pixel portion 10b includes a second cured component 13b, second luminescent nanocrystal particles 11b and second light-scattering particles 12b dispersed in the second cured component 13b, respectively. including. In the first pixel portion 10a and the second pixel portion 10b, the first cured component 13a and the second cured component 13b may be the same or different, and the first light scattering particles 12a The second light scattering particles 12b may be the same or different.

  The first light-emitting nanocrystal particles 11a are red light-emitting nanocrystal particles that absorb light having a wavelength in the range of 420 to 480 nm and emit light having an emission peak wavelength in the range of 605 to 665 nm. That is, the first pixel unit 10a may be rephrased as a red pixel unit for converting blue light into red light. The second light-emitting nanocrystal particles 11b are green light-emitting nanocrystal particles that absorb light having a wavelength in the range of 420 to 480 nm and emit light having an emission peak wavelength in the range of 500 to 560 nm. That is, the second pixel unit 10b may be rephrased as a green pixel unit for converting blue light into green light.

  The content of the luminescent nanocrystal particles in the pixel portion including the cured product of the ink composition is 5% by mass or more based on the total mass of the cured product of the ink composition from the viewpoint of excellent leakage light reduction effect. It may be 10% by mass or more, 15% by mass or more, 20% by mass or more, 30% by mass or more, and 40% by mass or more. Also good. From the viewpoint of excellent reliability of the pixel portion, the content of the luminescent nanocrystal particles may be 70% by mass or less based on the total mass of the cured product of the ink composition, and may be 60% by mass or less. It may be 55% by mass or less, or 50% by mass or less.

  The content of the light-scattering particles in the pixel portion including the cured product of the ink composition is 0.1% by mass or more based on the total mass of the cured product of the ink composition, from the viewpoint of excellent leakage light reduction effect. 1 mass% or more, 5 mass% or more, 7 mass% or more, 10 mass% or more, or 12 mass% or more. May be. The content of the light scattering particles may be 60% by mass or less based on the total mass of the cured product of the ink composition from the viewpoint of excellent leakage light reduction effect and excellent reliability of the pixel portion. 50% by mass or less, 40% by mass or less, 30% by mass or less, 25% by mass or less, or 20% by mass or less, It may be 15% by mass or less.

  The third pixel portion 10c has a transmittance of 30% or more for light with a wavelength in the range of 420 to 480 nm. Therefore, the third pixel unit 10c functions as a blue pixel unit when a light source that emits light having a wavelength in the range of 420 to 480 nm is used. The 3rd pixel part 10c contains the hardened | cured material of the composition containing the above-mentioned thermosetting resin, for example. The cured product contains a third curing component 13c. The 3rd hardening component 13c is a hardened | cured material of a thermosetting resin, and is specifically a hardened | cured material obtained by bridge | crosslinking of a thermosetting resin. That is, the third pixel portion 10c includes the third curing component 13c. When the third pixel portion 10c includes the above-described cured product, the composition containing the thermosetting resin has the above-described ink as long as the transmittance with respect to light having a wavelength in the range of 420 to 480 nm is 30% or more. Among the components contained in the composition, components other than the thermosetting resin may be further contained. Note that the transmittance of the third pixel portion 10c can be measured by a microspectroscopic device.

  The thickness of the pixel portion (the first pixel portion 10a, the second pixel portion 10b, and the third pixel portion 10c) may be, for example, 1 μm or more, 2 μm or more, or 3 μm or more. May be. The thickness of the pixel portion (the first pixel portion 10a, the second pixel portion 10b, and the third pixel portion 10c) may be, for example, 30 μm or less, 20 μm or less, or 15 μm or less. May be.

  The light shielding unit 20 is a so-called black matrix provided for the purpose of preventing color mixture by separating adjacent pixel units and preventing light leakage from the light source. The material constituting the light-shielding part 20 is not particularly limited, and curing of a resin composition containing light-shielding particles such as carbon fine particles, metal oxides, inorganic pigments, organic pigments in a binder polymer in addition to a metal such as chromium. A thing etc. can be used. As the binder polymer used here, polyimide resin, acrylic resin, epoxy resin, polyacrylamide, polyvinyl alcohol, gelatin, casein, cellulose, or a mixture of two or more resins, photosensitive resin, O / W An emulsion type resin composition (for example, an emulsion of reactive silicone) can be used. The thickness of the light shielding part 20 may be, for example, 0.5 μm or more and 10 μm or less.

  The base material 40 is a transparent base material having optical transparency. For example, the base material 40 is a transparent glass substrate such as quartz glass, Pyrex (registered trademark) glass, or a synthetic quartz plate, a transparent resin film, an optical resin film, or the like. A flexible base material etc. can be used. Among these, it is preferable to use the glass substrate which consists of an alkali free glass which does not contain an alkali component in glass. Specifically, “7059 glass”, “1737 glass”, “Eagle 200” and “Eagle XG” manufactured by Corning, “AN100” manufactured by Asahi Glass, “OA-10G” manufactured by Nippon Electric Glass, and “ OA-11 "is preferred. These are materials having a small coefficient of thermal expansion, and are excellent in dimensional stability and workability in high-temperature heat treatment.

  The color filter 100 including the above light conversion layer 30 is preferably used when a light source that emits light having a wavelength in the range of 420 to 480 nm is used.

  For example, the color filter 100 is formed by forming the light-shielding portion 20 on the base material 40 in a pattern, and then forming the ink composition (in the above-described embodiment) on the pixel portion forming region partitioned by the light-shielding portion 20 on the base material 40. Ink-jet ink) can be selectively deposited by an ink-jet method and can be produced by a method of curing the ink composition by irradiation with active energy rays or heating. In a conventional method of forming a pixel portion by a photolithography method, since development is usually performed using an alkaline developer, an alkali-soluble polymer is used as a binder polymer, and in principle, approximately 2/3 or more of the material is used. The material is wasted. As described above, the inkjet method is superior to the photolithography method in terms of material use efficiency.

  The light shielding part 20 is formed by forming a metal thin film such as chromium or a resin composition thin film containing light shielding particles in a region serving as a boundary between a plurality of pixel parts on one side of the substrate 40. And a method of patterning the thin film. The metal thin film can be formed by, for example, a sputtering method, a vacuum deposition method, or the like, and the thin film of the resin composition containing the light-shielding particles can be formed by, for example, a method such as coating or printing. Examples of the patterning method include a photolithography method.

  Examples of the inkjet method include a bubble jet (registered trademark) method using an electrothermal transducer as an energy generating element, a piezo jet method using a piezoelectric element, and the like.

When the ink composition is cured by irradiation with active energy rays (for example, ultraviolet rays), for example, a mercury lamp, a metal halide lamp, a xenon lamp, an LED, or the like may be used. The wavelength of the irradiated light may be, for example, 200 nm or more and 440 nm or less. The exposure amount may be, for example, 10 mJ / cm ² or more and may be 4000 mJ / cm ² or less.

  The heating temperature for curing the ink composition may be, for example, 110 ° C. or higher and 250 ° C. or lower. The heating time may be, for example, 10 minutes or more and 120 minutes or less.

  As mentioned above, although one embodiment of the color filter, the light conversion layer, and the manufacturing method thereof has been described, the ink composition of the above-described embodiment can be used in, for example, a photolithography method in addition to the ink jet method. In this case, the ink composition contains an alkali-soluble resin as a binder polymer.

  For example, the light conversion layer may be a pixel portion including a cured product of an ink composition containing blue light-emitting nanocrystal particles instead of or in addition to the third pixel portion 10c. A blue pixel portion). The light conversion layer may include a pixel portion (for example, a yellow pixel portion) including a cured product of an ink composition containing nanocrystal particles that emit light of a color other than red, green, and blue. In these cases, each of the luminescent nanocrystal particles contained in each pixel portion of the light conversion layer preferably has an absorption maximum wavelength in the same wavelength region.

  In addition, at least a part of the pixel portion of the light conversion layer may include a cured product of a composition containing a pigment other than the light-emitting nanocrystal particles.

  The color filter may include an ink repellent layer made of a material having an ink repellency narrower than that of the light shielding portion on the pattern of the light shielding portion. Also, instead of providing an ink repellent layer, a photocatalyst-containing layer as a wettability variable layer is formed in a solid shape in a region including the pixel portion formation region, and then light is passed through the photocatalyst-containing layer through a photomask. Exposure may be performed by irradiation to selectively increase the ink affinity of the pixel portion formation region. Examples of the photocatalyst include titanium oxide.

  The color filter may include an ink receiving layer containing hydroxypropyl cellulose or the like between the base material and the pixel portion.

  The color filter may include a protective layer on the pixel portion. This protective layer flattens the color filter and prevents elution of components contained in the pixel portion, or components contained in the pixel portion and components contained in the photocatalyst containing layer into the liquid crystal layer. It is provided. As the material constituting the protective layer, those used as known color filter protective layers can be used.

  In manufacturing the color filter and the light conversion layer, the pixel portion may be formed by a photolithography method instead of the ink jet method. In this case, first, the ink composition is applied to the base material in layers to form an ink composition layer. Next, the ink composition layer is exposed in a pattern and then developed using a developer. In this way, a pixel portion made of a cured product of the ink composition is formed. Since the developer is usually alkaline, an alkali-soluble polymer is used as the binder polymer. However, the ink jet method is superior to the photolithography method in terms of material use efficiency. This is because, in the photolithography method, approximately 2/3 or more of the material is removed in principle, and the material is wasted. For this reason, in this embodiment, it is preferable to form a pixel part by an inkjet system using inkjet ink.

  In addition to the above-described luminescent nanocrystal particles, the pixel portion of the light conversion layer of the present embodiment may further contain a pigment having substantially the same color as the luminescent color of the luminescent nanocrystal particles. For example, when a pixel portion containing luminescent nanocrystal particles that absorb blue light and emit light is used as the pixel portion of the liquid crystal display element, blue light or quasi-white light having a peak at 450 nm as light from the light source However, when the concentration of the light-emitting nanocrystal particles in the pixel portion is not sufficient, light from the light source passes through the light conversion layer when the liquid crystal display element is driven. The transmitted light (blue light, leakage light) from this light source and the light emitted from the light-emitting nanocrystal particles are mixed. From the viewpoint of preventing the color reproducibility from being deteriorated due to the occurrence of such color mixing, a pigment may be contained in the pixel portion of the light conversion layer. In order to contain the pigment in the pixel portion, the ink composition may contain a pigment.

  In addition, one or two of the red pixel portion (R), the green pixel portion (G), and the blue pixel portion (B) in the light conversion layer of the present embodiment are not included in the luminescent nanocrystal particles. The pixel portion may contain a color material. A known color material can be used as the color material that can be used here. For example, the color material used for the red pixel portion (R) includes a diketopyrrolopyrrole pigment and / or an anionic red organic dye. Examples of the color material used for the green pixel portion (G) include at least one selected from the group consisting of a halogenated copper phthalocyanine pigment, a phthalocyanine green dye, and a mixture of a phthalocyanine blue dye and an azo yellow organic dye. Examples of the color material used for the blue pixel portion (B) include an ε-type copper phthalocyanine pigment and / or a cationic blue organic dye. When used in the light conversion layer, these coloring materials are used in an amount of 1 to 5 masses based on the total mass of the pixel portion (cured product of the ink composition) from the viewpoint of preventing a decrease in transmittance. % Is preferred.

  Hereinafter, the present invention will be described specifically by way of examples. However, the present invention is not limited only to the following examples. Note that all the materials used in the examples were those in which argon gas was introduced and dissolved oxygen was replaced with nitrogen gas. The titanium oxide used was heated at 120 ° C. for 2 hours under reduced pressure of 1 mmHg and allowed to cool in an argon gas atmosphere before mixing. The liquid material used in the examples was dehydrated with Molecular Sieves 3A for 48 hours or more in advance before mixing.

<Preparation of InP / ZnSeS / ZnS nanocrystal particle dispersion (non-volatile content: 30% by mass)>
[Synthesis of red light emitting nanocrystalline particle core (InP core)]
5 g of trioctylphosphine oxide (TOPO), 1.46 g (5 mmol) of indium acetate, and 3.16 g (15.8 mmol) of lauric acid were added to the reaction flask to obtain a mixture. The mixture was heated at 160 ° C. for 40 minutes under a nitrogen environment, and then heated at 250 ° C. for 20 minutes under vacuum. Subsequently, the reaction temperature (temperature of the mixture) was raised to 300 ° C. under a nitrogen (N ₂ ) environment. At this temperature, a mixture of 3 g 1-octadecene (ODE) and 0.25 g (1 mmol) tris (trimethylsilyl) phosphine was rapidly introduced into the reaction flask and the reaction temperature was maintained at 260 ° C. After 5 minutes, the reaction was stopped by removing the heater, and the resulting reaction solution was cooled to room temperature. Next, 8 ml of toluene and 20 ml of ethanol were added to the reaction solution in the glove box. Subsequently, centrifugation was performed to precipitate InP nanocrystal particles, and then InP nanocrystal particles were obtained by decanting the supernatant. Next, the obtained InP nanocrystal particles were dispersed in hexane.

[Preparation of indium laurate precursor solution]
10 g of 1-octadecene (ODE), 146 mg (0.5 mmol) of indium acetate and 300 mg (1.5 mmol) of lauric acid were added to the reaction flask to obtain a mixture. The mixture was heated at 140 ° C. for 2 hours under vacuum to obtain a transparent solution (indium laurate precursor solution). This precursor solution was kept in the glove box at room temperature until needed. Since indium laurate is low in solubility at room temperature and easily precipitates, when using the precursor solution, the precipitated indium laurate in the precursor solution (ODE mixture) is heated to about 90 ° C. to be transparent. After forming the solution, the desired amount was weighed and used.

[Synthesis of Red Light-Emitting Nanocrystalline Particle Shell (ZnSeS / ZnS Shell)]
A hexane solution of InP nanocrystal particles (InP core) and an indium laurate precursor solution were added to the reaction flask to obtain a mixture. The amounts of InP core hexane solution and precursor solution added were adjusted so that the InP core was 25 mg and the indium laurate was 5 g. After allowing the mixture to stand for 10 minutes at room temperature under vacuum, the temperature of the mixture was raised to 230 ° C. and held at that temperature for 2 hours.

  The reaction temperature (mixture temperature) was then lowered to room temperature, 0.7 g of oleic acid was added to the reaction flask and the temperature was raised to 80 ° C. Next, 14 mg of diethylzinc dissolved in 1 ml of ODE, 8 mg of bis (trimethylsilyl) selenide and 7 mg of hexamethyldisilathiane (ZnSeS precursor solution) were dropped into the reaction mixture to form a 0.5 monolayer thick ZnSeS. A shell was formed.

  After the dropwise addition of the ZnSeS precursor solution, the reaction temperature was maintained at 80 ° C. for 10 minutes. The temperature was then raised to 140 ° C. and held for 30 minutes. Next, 69 mg of diethylzinc dissolved in 2 ml of ODE and 66 mg of hexamethyldisilathian (ZnS precursor solution) were dropped into this reaction mixture to form a ZnS shell having a thickness of 2 monolayers. Ten minutes after the dropwise addition of the ZnS precursor solution, the reaction was stopped by removing the heater. Next, the reaction mixture was cooled to room temperature, and the resulting white precipitate was removed by centrifugation, thereby obtaining a transparent nanocrystal particle solution (ODE solution) in which InP / ZnSeS / ZnS nanocrystal particles were dispersed.

[Synthesis of Ligands for Luminescent Nanocrystal Particles]
JEFAMINE M-1000 (manufactured by Huntsman) was charged into the flask, and then JEFAMINE M-1000 and an equimolar amount of succinic anhydride (manufactured by Sigma-Aldrich) were added thereto while stirring in a nitrogen gas environment. The internal temperature of the flask was raised to 80 ° C. and stirred for 8 hours to obtain a ligand represented by the following formula (1A) as a pale yellow viscous oil.

[Preparation of InP / ZnSeS / ZnS nanocrystal particle dispersion 1 by ligand exchange]
30-50 mg of the ligand obtained above was added to 1 ml of the nanocrystal particle solution obtained above. Subsequently, ligand exchange was performed by heating at 90 ° C. for 3 to 15 hours. 6 ml of ethanol was added to 1 ml of nanocrystal particle solution after ligand exchange. Subsequently, centrifugation was performed to precipitate the nanocrystal particles, and then the supernatant was decanted and dried under vacuum to form nanocrystal particles (InP / ZnSeS / ZnS nanoparticle modified with a ligand represented by the above formula (1A)). Crystalline particles) were obtained. By dispersing the obtained nanocrystal particles in the solvent 1, a nanocrystal particle dispersion 1 (nonvolatile content: 30% by mass) was obtained.

<Preparation of thermosetting resin>
As a thermosetting resin, an acrylic resin having an epoxy group (trade name: Fine Dick A-254, manufactured by DIC Corporation, “Fine Dick” is a registered trademark) was prepared.

<Preparation of curing agent>
As the acid anhydride curing agent, 1-methylcyclohexane-4,5-dicarboxylic acid anhydride (reagent, manufactured by Tokyo Chemical Industry Co., Ltd.) was prepared.

<Preparation of curing catalyst>
Dimethylbenzylamine (reagent, manufactured by Tokyo Chemical Industry Co., Ltd.) was prepared as a curing catalyst.

<Preparation of thermosetting resin solution>
0.28 g of the thermosetting resin, 0.09 g of the curing agent, and 0.004 g of the curing catalyst are dissolved in 1,4-butanediol diacetate, and the thermosetting resin solution 1 (nonvolatile content: 30% by mass) was obtained.

<Preparation of light scattering particles>
The following titanium oxides 1 to 6 were prepared as light scattering particles.
Titanium oxide 1: MPT-141 (trade name, manufactured by Ishihara Sangyo Co., Ltd., average particle diameter (volume average diameter): 100 nm, crystal type: rutile type, surface treatment: alumina)
Titanium oxide 2: CR-60-2 (trade name, manufactured by Ishihara Sangyo Co., Ltd., average particle diameter (volume average diameter): 210 nm, crystal type: rutile type, surface treatment: alumina, organic matter)
Titanium oxide 3: A-220 (trade name, manufactured by Ishihara Sangyo Co., Ltd., average particle diameter (volume average diameter): 160 nm, crystal type: anatase type, surface treatment: alumina)
Titanium oxide 4: TIO14PB (trade name, manufactured by Kojundo Chemical Laboratory Co., Ltd., average particle diameter (volume average diameter): 2000 nm, crystal type: rutile type, surface treatment: none)
Titanium oxide 5: JR (trade name, manufactured by Teika Co., Ltd., average particle diameter (volume average diameter): 270 nm, crystal type: rutile type, surface treatment: none)
Titanium oxide 6: JA-1 (trade name, average particle diameter (volume average diameter): 180 nm, crystal type: anatase type, surface treatment: none, manufactured by Teika Co., Ltd.)

<Preparation of polymer dispersant>
DISPERBYK-2164 (trade name manufactured by BYK, “DISPERBYK” is a registered trademark) was prepared as a polymer dispersant.

<Preparation of light scattering particle dispersion>
In a container filled with argon gas, 2.4 g of titanium oxide 1, 0.4 g of a polymer dispersant, and 1,4-butanediol diacetate were mixed, and the resulting nonvolatile content was 44%. Add zirconia beads (diameter: 1.25 mm) to the mixture, shake the mixture for 2 hours using a paint conditioner, disperse the mixture, and disperse the light-scattering particles by removing the zirconia beads with a polyester mesh filter. Body 1 was obtained. Moreover, except having used titanium oxide 2-6 as a titanium oxide, it carried out similarly to the above, and obtained the light-scattering particle dispersions 2-6, respectively.

<Example 1>
(1) Preparation of Ink Composition (Inkjet Ink) 2.25 g of the luminescent nanocrystal particle dispersion 1, 0.75 g of the light scattering particle dispersion 1, and 1.25 g of the thermosetting resin solution 1 Were mixed, and the mixture was filtered through a filter having a pore size of 5 μm to obtain an ink composition. The average particle diameter (volume average diameter MV) of the light-scattering particles in the ink composition was 0.235 μm. In this example, the average particle diameter (volume average diameter MV) of the light scattering particles in the ink composition is a dynamic light scattering nanotrack particle size distribution meter (trade name “manufactured by Nikkiso Co., Ltd.”). Nanotrack ")).

(2) Evaluation Using the ink composition obtained in the above (1), the dispersion stability of the light scattering particles, the sedimentation separation property, and the ejection stability of the ink composition were evaluated in the following procedure. . The results are shown in Table 1.

[Evaluation of dispersion stability of light scattering particles]
The volume of the light-scattering particles immediately after the production of the ink composition (hereinafter also referred to as “dispersion” in this test) using a dynamic light-scattering particle size distribution measuring apparatus (Nanotrack UPA150 manufactured by Nikkiso Co., Ltd.). The average diameter (MV ₀ ) and the volume average diameter (MV ₁ ) after storage at 40 ° C. for 5 days after preparing the dispersion were measured, and the dispersion stability of the light scattering particles was evaluated. The evaluation criteria for the dispersion stability of the light-scattering particles are as follows. The rate of change of the volume average diameter is the ratio of the volume average diameter before and after storage (MV ₁ -MV ₀ ) to the volume average diameter before storage (MV ₀ ) (MV ₁ -MV ₀ ) / MV. ₀ × 100).
A: The volume average diameter immediately after the preparation of the dispersion is less than 1 μm and the change rate of the volume average diameter is 15% or less B: The volume average diameter immediately after the preparation of the dispersion is less than 1 μm and the change ratio of the volume average diameter is 15 Exceeding% C: Volume average diameter immediately after production of dispersion is 1 μm or more

[Evaluation of sedimentation separation of light scattering particles]
Moreover, immediately after preparation of the said dispersion, it left still at 25 degreeC for 3 days, and evaluated sedimentation separation property. The evaluation criteria for the sedimentation separation of the light scattering particles are as follows.
a: When sedimentation did not occur b: When phase separation occurred and sedimentation was confirmed

[Discharge stability of ink composition]
The ink composition was subjected to a discharge test using an inkjet printer (trade name “DMP-2850” manufactured by Fujifilm Dimatix). In the ejection test, the ink composition was ejected continuously for 10 minutes. In addition, 16 nozzles were formed in the head portion for ejecting ink of the ink jet printer, and the amount of ink composition used per ejection per nozzle was 10 pL. The discharge stability was evaluated according to the following criteria. The results are shown in Table 1.
I: Continuous discharge possible (continuous discharge possible with 10 nozzles or more out of 16 nozzles)
II: Continuous discharge not possible (out of 16 nozzles, the number of nozzles that can be continuously discharged is 9 or less)
III: Discharge not possible

<Example 2>
An ink composition was obtained in the same manner as in Example 1 except that the light scattering particle dispersion 2 was used as the light scattering particle dispersion. The average particle diameter of the light-scattering particles in the ink composition (volume average diameter MV immediately after preparation) was 0.206 μm. Using the obtained ink composition, in the same manner as in Example 1, the dispersion stability of the light scattering particles, the sedimentation separation property, and the ejection stability of the ink composition were evaluated. The results are shown in Table 1.

<Example 3>
An ink composition was obtained in the same manner as in Example 1 except that the light scattering particle dispersion 3 was used as the light scattering particle dispersion. The average particle diameter (volume average diameter MV immediately after production) of the light-scattering particles in the ink composition was 0.271 μm. Using the obtained ink composition, in the same manner as in Example 1, the dispersion stability of the light scattering particles, the sedimentation separation property, and the ejection stability of the ink composition were evaluated. The results are shown in Table 2.

<Comparative Example 1>
An ink composition was obtained in the same manner as in Example 1 except that the light scattering particle dispersion 4 was used as the light scattering particle dispersion. The average particle diameter of the light-scattering particles in the ink composition (volume average diameter MV immediately after preparation) was 1.082 μm. Using the obtained ink composition, in the same manner as in Example 1, the dispersion stability of the light scattering particles, the sedimentation separation property, and the ejection stability of the ink composition were evaluated. The results are shown in Table 2.

<Comparative example 2>
An ink composition was obtained in the same manner as in Example 1 except that the light scattering particle dispersion 5 was used as the light scattering particle dispersion. The average particle diameter of the light-scattering particles in the ink composition (volume average diameter MV immediately after production) was 0.417 μm. Using the obtained ink composition, in the same manner as in Example 1, the dispersion stability of the light scattering particles, the sedimentation separation property, and the ejection stability of the ink composition were evaluated. The results are shown in Table 2.

<Comparative Example 3>
An ink composition was obtained in the same manner as in Example 1 except that the light scattering particle dispersion 6 was used as the light scattering particle dispersion. The average particle diameter of the light scattering particles in the ink composition (volume average diameter MV immediately after preparation) was 0.240 μm. Using the obtained ink composition, in the same manner as in Example 1, the dispersion stability of the light scattering particles, the dispersion stability, the sedimentation separation property, and the ejection stability of the ink composition were evaluated. The results are shown in Table 2.

  DESCRIPTION OF SYMBOLS 10 ... Pixel part, 10a ... 1st pixel part, 10b ... 2nd pixel part, 10c ... 3rd pixel part, 11a ... 1st luminescent nanocrystal particle, 11b ... 2nd luminescent nanocrystal particle , 12a ... first light scattering particles, 12b ... second light scattering particles, 20 ... light-shielding part, 30 ... light conversion layer, 40 ... base material, 100 ... color filter.

Claims (18)

Luminescent nanocrystal particles,
Light scattering particles having at least part of the surface covered with alumina;
An ink composition containing a polymer dispersant.   The ink composition according to claim 1, wherein the light-scattering particles include titanium oxide.   The ink composition according to claim 1, wherein the light scattering particles have an average particle size of 0.05 to 1.0 μm.   The ink composition according to claim 1, wherein the polymer dispersant has a weight average molecular weight of 1000 or more.   The ink composition according to any one of claims 1 to 4, further comprising a thermosetting resin.   The ink composition according to claim 5, wherein the thermosetting resin is alkali-insoluble.   The ink composition according to any one of claims 1 to 4, further comprising a photopolymerizable compound.   The ink composition according to claim 7, wherein the photopolymerizable compound is insoluble in alkali.   The ink composition according to any one of claims 1 to 8, which is capable of forming an alkali-insoluble coating film.   The ink composition according to claim 1, wherein the surface tension is 20 to 40 mN / m.   The ink composition according to any one of claims 1 to 10, wherein the viscosity is 2 to 20 mPa · s.   The ink composition according to any one of claims 1 to 11, further comprising a solvent having a boiling point of 180 ° C or higher.   The ink composition according to any one of claims 1 to 12, which is used for a color filter.   The ink composition according to any one of claims 1 to 13, which is used in an inkjet method. A light conversion layer comprising a plurality of pixel portions,
The plurality of pixel portions are light conversion layers having pixel portions including a cured product of the ink composition according to any one of claims 1 to 14. A light shielding part provided between the plurality of pixel parts;
The plurality of pixel portions are
The light-emitting nanocrystal particles containing the cured product and containing the light-emitting nanocrystal particles that absorb light having a wavelength in the range of 420 to 480 nm and emit light having an emission peak wavelength in the range of 605 to 665 nm are included. A first pixel portion;
The light-emitting nanocrystal particles containing the cured product and containing the light-emitting nanocrystal particles that absorb light having a wavelength in the range of 420 to 480 nm and emit light having a light emission peak wavelength in the range of 500 to 560 nm. A second pixel portion;
The light conversion layer according to claim 15, comprising:   17. The light conversion layer according to claim 16, wherein the plurality of pixel portions further include a third pixel portion having a transmittance of 30% or more for light having a wavelength in a range of 420 to 480 nm.   A color filter provided with the light conversion layer as described in any one of Claims 15-17.

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