COLOR CONVERSION FILM MATERIAL, COLOR CONVERSION FILM, AND DISPLAY DEVICE
20220220371 · 2022-07-14
Assignee
Inventors
Cpc classification
G02B6/0056
PHYSICS
G02F1/133614
PHYSICS
G02F1/133382
PHYSICS
G02B6/0026
PHYSICS
G02F1/133615
PHYSICS
G02B6/0036
PHYSICS
C09K11/025
CHEMISTRY; METALLURGY
International classification
C09K11/02
CHEMISTRY; METALLURGY
Abstract
A color conversion film material, a color conversion film, and a display device are provided. The material of the color conversion film includes a first compound and a second compound, and a mass ratio of the first compound and the second compound is (0.4-1.6):(0.3-1.7). A heat stability of the color conversion film is enhanced by using the color conversion film made of the material of the color conversion film. Moreover, a color gamut of the display device is improved, and costs thereof are reduced by applying the color conversion film to the display device.
Claims
1. A material of a color conversion film, comprising: a first compound and a second compound, wherein a structural formula of the first compound is ##STR00017## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, and R.sub.11 are respectively and independently selected from one of a halogen atom, —CN, a tert-butyl group, a non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group; wherein a structural formula of the second compound is ##STR00018## wherein R.sub.12, R.sub.13, R.sub.14, and R.sub.15 are one of —F, —Cl, Br, —I, —NH.sub.2, —COOH, —OH, —SH, —COH, —COO—, —COCl, —COBr, —CN, —NO.sub.2, —NH.sub.2, ═NH, ≡N, a benzene, a phenol ring, an non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group, R.sub.16 is an non-conjugated structure, and X.sup.− is one of F.sup.−, Cl.sup.−, Br, CN.sup.−, ClO.sub.4.sup.−, CF.sub.3SO.sub.3.sup.−, CF.sub.2HSO.sub.3.sup.−, and CFH.sub.2SO.sub.3.sup.−; and wherein a mass ratio of the first compound and the second compound is (0.4-1.6):(0.3-1.7).
2. The material of the color conversion film according to claim 1, wherein the material of the color conversion film further includes a dispersion system, the first compound and the second compound are dispersed in the dispersion system, the dispersion system is a pressure sensitive adhesive, and a mass ratio of the first compound, the second compound, and the dispersion system is (0.4-1.6):(0.3-1.7):(100-1000).
3. The material of the color conversion film according to claim 1, wherein the material of the color conversion film further includes a dispersion system, the first compound and the second compound are dispersed in the dispersion system, the dispersion system includes an acrylic resin, an acrylic monomer, and a photoinitiator, and a mass ratio of the first compound, the second compound, the acrylic resin, the acrylic monomer, and the photoinitiator is (0.4-1.6):(0.3-1.7):(24-300):(74-500):(2-200).
4. The material of the color conversion film according to claim 1, wherein the non-conjugated structure is selected from one of an ester group containing a chain structure, —C.sub.nH.sub.2n+1, —OC.sub.yH.sub.2y+1, and —FC.sub.mH.sub.2m, and n=1-40, y=1-40, and m=1-40.
5. The material of the color conversion film according to claim 1, wherein the conjugated structure formed by the connection of the alkoxy group and the ester group further includes a heterocyclic group, and the heterocyclic group includes one of a five-membered heterocyclic group, a six-membered heterocyclic group, and a benzoheterocyclic group.
6. The material of the color conversion film according to claim 5, wherein the five-membered heterocyclic group includes one of furan, thiophene, pyrrole, imidazole, and thiazole.
7. The material of the color conversion film according to claim 5, wherein the six-membered heterocyclic group includes one of pyridine, pyrazine, pyrimidine, and pyridazine.
8. The material of the color conversion film according to claim 5, wherein the benzoheterocyclic group includes one of indole, quinoline, pteridine, and acridine.
9. A color conversion film, comprising: the material of the color conversion film according to claim 1.
10. A display device, comprising: an optical structure including a color conversion film; wherein a material of the color conversion film includes a first compound and a second compound; wherein a structural formula of the first compound is ##STR00019## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, and R.sub.11 are respectively and independently selected from one of a halogen atom, —CN, a tert-butyl group, an non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group; wherein a structural formula of the second compound is ##STR00020## wherein R.sub.12, R.sub.13, R.sub.14, and R.sub.15 are one of —F, —Cl, Br, —I, —NH.sub.2, —COOH, —OH, —SH, —COH, —COO—, —COCl, —COBr, —CN, —NO.sub.2, —NH.sub.2, ═NH, ≡N, a benzene, a phenol ring, an non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group, R.sub.16 is a non-conjugated structure, and X.sup.− is one of F.sup.−, Cl.sup.−, Br, CN.sup.−, ClO.sub.4.sup.−, CF.sub.3SO.sub.3.sup.−, CF.sub.2HSO.sub.3.sup.−, and CFH.sub.2SO.sub.3.sup.−; and wherein a mass ratio of the first compound and the second compound is (0.4-1.6):(0.3-1.7).
11. The display device according to claim 10, wherein the display device further includes a backlight source and a back plate; wherein the backlight source is disposed near a lateral side of the optical structure, and the back plate is disposed under a bottom of the optical structure; wherein the optical structure is a light guiding plate, and the color conversion film is disposed at a side of the light guiding plate close to the backlight source; and wherein the light guiding plate further includes a reflective layer, the reflective layer is disposed at a lower surface of the light guiding plate close to the back plate, and the reflective layer includes a plurality of reflective portions.
12. The display device according to claim 10, wherein the display device further includes a backlight source and a back plate; wherein the backlight source is disposed near a lateral side of the optical structure, and the back plate is disposed under a bottom of the optical structure; wherein the optical structure is a light guiding plate, and the color conversion film is disposed at a lower surface of the light guiding plate close to the back plate; and wherein the light guiding plate further includes a reflective layer, the reflective layer is disposed at a lower surface of the color conversion film close to the back plate, and the reflective layer includes a plurality of reflective portions.
13. The display device according to claim 10, wherein the optical structure is a polarizer, and the color conversion film is disposed in the polarizer.
14. The display device according to claim 11, wherein the display device further includes a heat dissipation plate, and the heat dissipation plate is disposed at a side of the backlight source away from the optical structure.
15. The display device according to claim 11, wherein the display device further includes a light transmitting layer, and the light transmitting layer is disposed at a side of the color conversion film away from the light guiding plate.
16. The display device according to claim 11, wherein the display device further includes a baffle, and the baffle is located under a lower surface of the reflective layer close to the back plate.
17. The display device according to claim 16, wherein the display device further includes a barrier layer, and the barrier layer is located near a side of the backlight source away from the baffle.
18. The display device according to claim 13, wherein the polarizer includes a peeling protection film and a surface protection film, and the color conversion film is disposed between the peeling protection film and the surface protection film.
Description
DESCRIPTION OF DRAWINGS
[0036] In order to clearly illustrate technical solutions in the present disclosure, the drawings required for using in the description of the embodiments is briefly described below. Obviously, the drawings in the following description are only some of the embodiments of the present disclosure. For those skilled in the art, other drawings may also be obtained in accordance with these drawings without making for creative efforts.
[0037]
[0038]
[0039]
[0040]
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
[0041] In combination with accompanying drawings in embodiments of the present disclosure below, technical solutions in the embodiments of the present disclosure are clearly and completely described. Obviously, the described embodiments are merely a part of the embodiments of the present disclosure, rather than all the embodiments. Based on the embodiments in the present disclosure, all of other embodiments obtained by those skilled in the art without making for creative efforts belong to the scope protected by the present disclosure.
[0042] The present disclosure provides a material of a color conversion film. The material of the color conversion film includes a first compound and a second compound. A structural formula of the first compound is
##STR00005##
wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, and R.sub.11 are respectively and independently selected from one of a halogen atom, —CN, a tert-butyl group, a non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group. A structural formula of the second compound is
##STR00006##
wherein R.sub.12, R.sub.13, R.sub.14, and R.sub.15 are one of —F, —Cl, Br, —I, —NH.sub.2, —COOH, —OH, —SH, —COH, —COO—, —COCl, —COBr, —CN, —NO.sub.2, —NH.sub.2, ═NH, ≡N, a benzene, a phenol ring, an non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group, and R.sub.10 is an non-conjugated structure. Specifically, the non-conjugated structure is selected from one of an ester group containing a chain structure, —C.sub.nH.sub.2n+1, —OC.sub.yH.sub.2y+1, and —FC.sub.mH.sub.2m, and n=1-40, y=1-40, and m=1-40. In an embodiment, the conjugated structure formed by the connection of the alkoxy group and the ester group further includes a heterocyclic group, and the heterocyclic group includes one of a five-membered heterocyclic group, a six-membered heterocyclic group, and a benzoheterocyclic group. The five-membered heterocyclic group includes one of furan, thiophene, pyrrole, imidazole, thiazole, and the like. The six-membered heterocyclic group includes one of pyridine, pyrazine, pyrimidine, pyridazine, and the like. The benzoheterocyclic group includes one of indole, quinoline, pteridine, and acridine. X.sup.− is one of F.sup.−, Cl.sup.−, Br, CN.sup.−, ClO.sub.4.sup.−, CF.sub.3SO.sub.3.sup.−, CF.sub.2HSO.sub.3.sup.−, and CFH.sub.2SO.sub.3.sup.−. A mass ratio of the first compound and the second compound is (0.4-1.6):(0.3-1.7). Specifically, the mass ratio of the first compound and the second compound may be one of 0.5:0.6, 0.7:0.9, 1:1, 1:1.2, or 1.4:1.6.
[0043] In an embodiment, the R.sub.1 is —Br, the R.sub.2 is —CN, the R.sub.3 is —C.sub.2H.sub.5, the R.sub.4 is —FC.sub.3H.sub.6, the R.sub.5 is —I, the R.sub.6 is —Cl, the R.sub.7 is —OC.sub.3H.sub.7, as well as the R.sub.8, the R.sub.9, the R.sub.10, and the R.sub.11 are the tert-butyl group. The structural formula of the first compound may be
##STR00007##
The R.sub.12 is —COOH, the R.sub.13 is —COH, the R.sub.14 is —COH, the R.sub.15 is the benzene, and the R.sub.16 is —C.sub.nH.sub.2n+1, in which when n=1, the R.sub.16 is —CH.sub.3. The X.sup.− is CF.sub.3SO.sub.3.sup.−. The structural formula of the second compound may be
##STR00008##
[0044] In an embodiment, the R.sub.1 is the five-membered heterocyclic group formed by connecting the alkoxy group with the ester group, for example, thiophene formed by connecting the alkoxy group with the ester group. The R.sub.2 is —CN, the R.sub.3 is —C.sub.2H.sub.5, the R.sub.a is —FC.sub.3H.sub.6, the R.sub.5 is —I, the R.sub.6 is —Cl, the R.sub.7 is —OC.sub.3H.sub.7, as well as the R.sub.8, the R.sub.9, the R.sub.10, and the R.sub.11 are the tert-butyl group. The structural formula of the first compound may be
##STR00009##
The R.sub.12 is —COOH, the R.sub.13 is —SH, the R.sub.14 is the phenol ring, the R.sub.15 is the benzene, and the R.sub.16 is —OC.sub.yH.sub.2y+1, in which when y=2, the R.sub.16 is —OC.sub.2H.sub.5. The X.sup.− is ClO.sub.4.sup.−. The structural formula of the second compound may be
##STR00010##
[0045] In an embodiment, the R.sub.1 is the conjugated structure formed by connecting the alkoxy group with the ester group, for example,
##STR00011##
The R.sub.2 is —CN, the R.sub.3 is —C.sub.2H.sub.5, the R.sub.4 is —FC.sub.3H.sub.6, the R.sub.5 is —I, the R.sub.6 is —Cl, the R.sub.7 is —OC.sub.3H.sub.7, as well as the R.sub.8, the R.sub.9, the R.sub.10, and the R.sub.11 are the tert-butyl group. The structural formula of the first compound may be
##STR00012##
The R.SUB.12 .is
[0046] ##STR00013##
the R.sub.13 is —SH, R.sub.14 is the phenol ring, the R.sub.15 is the benzene, and the R.sub.16 is —OC.sub.yH.sub.2y+1, in which when y=1, the R.sub.16 is —OC.sub.2H.sub.5. The X.sup.− is ClO.sub.4.sup.−. The structural formula of the first compound may be
##STR00014##
[0047] In another embodiment, the material of the color conversion film further includes a dispersion system. The first compound and the second compound are dispersed in the dispersion system. The dispersion system is a pressure sensitive adhesive. A mass ratio of the first compound, the second compound, and the dispersion system is (0.4-1.6):(0.3-1.7):(100-1000). Specifically, the dispersion system is the pressure sensitive adhesive. The mass ratio of the first compound, the second compound, and the dispersion system may be one of 0.5:0.6:150, 1:1:300, 1:1.2:500, or 1:1:900.
[0048] In another embodiment, the dispersion system includes an acrylic resin, an acrylic monomer, and a photoinitiator. The first compound and the second compound are dispersed in the dispersion system. A mass ratio of the first compound, the second compound, the acrylic resin, the acrylic monomer, and the photoinitiator is (0.4-1.6):(0.3-1.7):(24-300):(74-500):(2-200). Specifically, the mass ratio of the first compound, the second compound, the acrylic resin, the acrylic monomer, and the photoinitiator may be one of 0.5:0.6:30:120:130, 1:1:80:150:160, 1:1.2:50:90:100, or 1:1:25:75:3.
[0049] In the present disclosure, the material of the color conversion film includes the first compound and the second compound. The first compound is a boron fluoride dipyrrole derivative which may absorb cyan light at 480 nm-510 nm, and then emit green light. The second compound is a rhodamine 101 derivative which may absorb yellow-orange light at 560 nm-610 nm, and then emit red light. The first compound and the second compound are mixed in the dispersion system to form the material of the color conversion film, thus improving a color gamut of the display device.
[0050] The present disclosure further provides a color conversion film. The color conversion film is made of the material of the color conversion film which includes all the above-mentioned technical features.
[0051] In the present disclosure, a color conversion film is provided. The first compound is the boron fluoride dipyrrole derivative which may absorb the cyan light at 480 nm-510 nm, and then emit the green light, and the second compound is the rhodamine 101 derivative which may absorb the yellow-orange light at 560 nm-610 nm, and then emit the red light. The first compound and the second compound are mixed in the dispersion system to form the material of the color conversion film. Since the first compound, the second compound, and the dispersion system are employed to form the color conversion film, a heat stability of the color conversion film is enhanced, costs of production are reduced, and the color gamut of the display device is improved.
[0052] Referring to
[0053] The optical structure 20 includes a color conversion film 21. The color conversion film includes a first compound and a second compound. A structural formula of the first compound is
##STR00015##
wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, and R.sub.11 are respectively and independently selected from one of a halogen atom, —CN, a tert-butyl group, a non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group. A structural formula of the second compound is
##STR00016##
wherein R.sub.12, R.sub.13, R.sub.14, and R.sub.15 are one of —F, —Cl, Br, —I, —NH.sub.2, —COOH, —OH, —SH, —COH, —COO—, —COCl, —COBr, —CN, —NO.sub.2, —NH.sub.2, ═NH, ≡N, a benzene, a phenol ring, an non-conjugated structure, and a conjugated structure formed by connecting an alkoxy group with an ester group, R.sub.16 is an non-conjugated structure, and X.sup.− is one of F.sup.−, Cl.sup.−, Br, CN.sup.−, ClO.sub.4.sup.−, CF.sub.3SO.sub.3.sup.−, CF.sub.2HSO.sub.3.sup.−, and CFH.sub.2SO.sub.3.sup.−. A mass ratio of the first compound and the second compound is (0.4-1.6):(0.3-1.7). The optical structure may be one of a light guiding plate and a polarizer.
[0054] In another embodiment, the display device 10 further includes a backlight source 30 and a back plate 40. The backlight source 30 is disposed near a lateral side of the optical structure 20. The optical structure 20 is the light guiding plate. The color conversion film 21 is disposed at a side of the light guiding plate 22 close to the backlight source 30. The back plate 40 is disposed under a bottom of the optical structure 20. The light guiding plate 22 further includes a reflective layer 23, the reflective layer 23 is disposed at a lower surface of the light guiding plate 22 close to the back plate 40. The reflective layer 23 includes a plurality of reflective portions 231, and is used to improve a uniformity of light.
[0055] In another embodiment, the display device 10 further includes an outer frame 50, a plastic frame 60, an aluminum extrusion 70, a heat dissipation plate 80, a barrier layer 90, a fixation structure 100, a light transmitting layer 110, and a baffle 120. The outer frame 50 is located near a side of the optical structure 20 close to the backlight source 30. An end of the outer frame 50 close to the backlight source 30 is connected with the plastic frame 60, thus playing a role of supporting the display device and protecting the structures in the display device from damage. Another end of the outer frame 50 away from the backlight source 30 is connected with the back plate 40. The aluminum extrusion 70 is located between the plastic frame 60 and the outer frame 50. The heat dissipation plate 80 is disposed at a surface of the aluminum extrusion 70 close to the optical structure 20. The backlight source 30 is disposed at a surface of the heat dissipation plate 80 close to the optical structure 20. The fixation structure 100 is used to fix the aluminum extrusion 70 to the outer frame 50. The barrier layer 90 is disposed at a surface of the plastic frame 60 close to the backlight source. The barrier layer 90 is used to reflect light emitted from the backlight source 30 to the barrier layer 90, and the reflected light passes through the light transmitting layer 110 and is subsequently emitted to the optical structure 20. The color conversion film 21 is disposed at a surface of the light guiding plate 22 close to the backlight source 30. When white light emitted by the backlight source 30 passes the color conversion film 21, the cyan light and the yellow-orange light in the white light are absorbed, so that the light emitted by the backlight source 30 is purified, thus improving the color gamut of the display device 10. The light transmitting layer 110 is disposed at a surface of the color conversion film 21 close to the backlight source 30. The baffle 120 is located under a lower surface of the reflective layer 23 close to the back plate 40.
[0056] In the present disclosure, when the white light emitted by the backlight source passes the color conversion film, the cyan light and the yellow-orange light in the white light are absorbed, so that the light emitted by the backlight source is purified, thus improving the color gamut of the display device.
[0057] Referring to
[0058] Referring to
[0059] Referring to
[0060] In the present disclosure, the color conversion film is disposed in the polarizer. When the light passes the polarizer, the cyan light and the yellow-orange light in the light are absorbed by the color conversion film in the polarizer, thus purifying the emitted light and improving the color gamut of the display device.
[0061] The present disclosure provides a color conversion film, a material thereof, and a display device. The material of the color conversion film includes the first compound and the second compound. The first compound is the boron fluoride dipyrrole derivative which may absorb the cyan light at 480 nm-510 nm, and then emit the green light, and the second compound is the rhodamine 101 derivative which may absorb the yellow-orange light at 560 nm-610 nm, and then emit the red light. The heat stability of the color conversion film is enhanced by using the color conversion film made of the material of the color conversion film. Moreover, the color gamut of the display device is improved, and the costs thereof are reduced by applying the color conversion film to the display device.
[0062] The embodiments of the present disclosure are introduced in detail above. Specific examples herein are used to set forth the principles and the implementation of the present disclosure. The illustration of the foregoing embodiments is only used to facilitate understanding the present disclosure. Moreover, for those skilled in the art, both of the specific embodiments and the application scope can still be modified in accordance with the idea of the present disclosure. In summary, the content of the specification should not be construed as the limitation to the present disclosure.