Protective layers produced by sol gel processes

US10473968B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10473968-B2
Application numberUS-201615353453-A
CountryUS
Kind codeB2
Filing dateNov 16, 2016
Priority dateNov 16, 2015
Publication dateNov 12, 2019
Grant dateNov 12, 2019

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Abstract

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Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and/or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. For example, rhodamine-based fluorescent compounds are used in matrices produced by sol gel processes and/or UV (ultraviolet) curing processes which are configured to stabilize the compounds and extend their lifetime—to provide the required emission specifications of the color conversion films. Film integration and display configurations further enhance the display performance with color conversion films utilizing various color conversion elements.

First claim

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The invention claimed is: 1. A color conversion film for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, the color conversion film configured to absorb illumination from a backlight source of the LCD and having at least one of a R emission peak and a G emission peak, wherein the color conversion film further comprises a protective coating prepared by a sol gel process; wherein the color conversion film further comprises at least one rhodamine-based fluorescent (RBF) compound selected to absorb illumination from the backlight source of the LCD and have the at least one of a R emission peak and a G emission peak; and wherein the at least one RBF compound is defined by at least one of Formula 1 and Formula 4: wherein R 1 is COOR, NO 2 , COR, COSR, CO(N-heterocycle), CON(R) 2 , or CN; R 2 each is independently selected from H, halide, N(R) 2 , COR, CN, CON(R) 2 , CO(N-heterocycle), NCO, NCS, OR, SR, SO 3 H, SO 3 M and COOR; R 3 each is independently selected from H, halide, N(R) 2 , COR, CN, CON(R) 2 , CO(N-heterocycle), NCO, NCS, OR, SR, SO 3 H, SO 3 M and COOR; R 4 -R 16 and R 4′ -R 16′ are each independently selected from H, CF3, alkyl, haloalkyl, cycloalkyl, heterocycloalkyl, alkenyl, alkynyl, aryl, benzyl, halide, NO 2 , OR, N(R) 2 , COR, CN, CON(R) 2 , CO(N-Heterocycle) and COOR; R is H, alkyl, cycloalkyl, heterocycloalkyl, alkenyl, alkynyl, aryl, benzyl, —(CH 2 CH 2 O) r CH 2 CH 2 OH, —(CH 2 ) p OC(O)NH(CH 2 ) q Si(Oalkyl) 3 , —(CH 2 ) p OC(O)CH═CH 2 or —(CH 2 ) p Si(Oalkyl) 3 ; n and m are each independently an integer between 1-4; p and q are each independently an integer between 1-6; r is an integer between 0-10; M is a monovalent cation; and X is an anion; and wherein: R 1 each is independently H, Q 1 , OQ 1 , CF 3 , C(O)OQ 1 , C(O)NQ 1 Q 2 , NHC(O)Q 1 , C(O)Q 1 , NQ 1 Q 2 , NO 2 , CN, SQ 1 , —NQ 1 Q 2 CONQ 3 Q 4 , NCO, NCS, —OC(O)OQ 1 , SO 3 —, SO 3 Q 1 , or halide; n is an integer between 1-5; R 3 , R 3′ , R 6 and R 6′ are each independently selected from H, CF 3 , alkyl, alkenyl, alkynyl, haloalkyl, heterocycloalkyl, cycloalkyl, aryl and benzyl; R 2 , R 2′ , R 4 , R 4′ , R 5 and R 5′ are each independently selected from H, Q 1 , OQ 1 , CF 3 , NQ 1 Q 2 , NO 2 , CN, SO 3 − , SO 3 Q 1 and halide; Q 1 and Q 2 are each independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, azide, haloalkyl, heterocycloalkyl, cycloalkyl, aryl, benzyl, —(CH 2 ) p OC(O)NH(CH 2 ) q Si(Oalkyl) 3 , —(CH 2 ) p OC(O)CH═CH 2 , —(CH 2 ) p Si(Oalkyl) 3 , —OC(O)N(H)Q 4 , —OC(S)N(H)Q 4 , —N(H)C(O)N(Q 3 ) 2 and —N(H)C(S)N(Q 3 ) 2 ; Q 3 and Q 4 are each independently selected from H, alkyl, haloalkyl, heterocycloalkyl, cycloalkyl, aryl and benzyl; X − is an anion. 2. The color conversion film of claim 1 , wherein the sol gel process is carried out with at least one of: ZPH, MMA, trimethoxysilane derivative, and an ESOR. 3. The color conversion film of claim 1 , wherein the color conversion film is produced by at least one of a sol gel process and a UV (ultraviolet) curing process. 4. An LCD comprising at least one color conversion film of claim 1 , wherein the LCD comprises a backlight unit comprising the backlight source and a LCD panel having the RGB color filters, wherein the at least one color conversion film is positioned in the LCD panel and is patterned with respect to a patterning of the RGB color filters to yield a spatial correspondence between film regions with R and G emission peaks and respective R and G color filter. 5. An LCD comprising at least one color conversion film of claim 1 , wherein the LCD comprises a backlight unit comprising the backlight source and a LCD panel having the RGB color filters, wherein an intensity of the R and G emission peaks of the at least one color conversion film are adjusted to fine tune a white point of the LCD to be at a center of an expected line of deterioration of the intensity within given LCD specifications. 6. An LCD comprising at least one color conversion film of claim 1 , wherein the LCD comprises a backlight unit comprising the backlight source and a LCD panel having the RGB color filters, wherein the RBF compounds in the film are at least partially self-assembled to at least partially provide polarized emission, and wherein the at least one color conversion film replaces at least one polarizer film in the LCD.

Assignees

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Classifications

  • having cover layers or intermediate layers, e.g. subbing layers {(G03F7/091 - G03F7/093, B41N3/03 take precedence)} · CPC title

  • in non photosensitive layers or as additives, e.g. for dry lithography · CPC title

  • Dyes containing a substituent, which contains a silicium atom · CPC title

  • containing a diaryl- or triarylmethane dye · CPC title

  • Filters, e.g. additive colour filters; Components for display devices · CPC title

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What does patent US10473968B2 cover?
Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and/or red emission at h…
Who is the assignee on this patent?
Storedot Ltd
What technology area does this patent fall under?
Primary CPC classification G02F1/133514. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Nov 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).