Light-emitting device
US-12155019-B2 · Nov 26, 2024 · US
US9905738B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9905738-B2 |
| Application number | US-201514643620-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 10, 2015 |
| Priority date | Mar 11, 2014 |
| Publication date | Feb 27, 2018 |
| Grant date | Feb 27, 2018 |
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Provided are a composition for an encapsulant having a viscosity of about 4,000 to about 9,500 mPa·s when measured using a Brookfield (DV-II+pro) spindle No. 52 at a torque of about 90% under atmospheric pressure at about 23° C., whereby maintaining a phosphor precipitation degree within about 18% when including a phosphor and allowed to stand at about 23° C. for greater than or equal to about 2 hours, and including at least one first siloxane compound having a silicon-bonded hydrogen (Si—H) and at least one second siloxane compound having a silicon-bonded alkenyl group (Si-Vi), an encapsulant obtained by curing the composition, and an electronic device including the encapsulant.
Opening claim text (preview).
What is claimed is: 1. A phosphor-containing mixture, comprising: a composition comprising: a first siloxane compound having a silicon-bonded hydrogen, and a second siloxane compound having a silicon-bonded alkenyl group, wherein: the first siloxane compound is included in an amount of less than about 50wt % based on the total amount of the first siloxane compound and the second siloxane compound, and the second siloxane compound is included in an amount of greater than about 50wt % based on the total amount of the first siloxane compound and the second siloxane compound, and a siloxane mixture consisting of the first siloxane compound, the second siloxane compound, and a hydrosilylation catalyst has a viscosity of about 4,000 to about 10,000 mPa·s when measured using a Brookfield (DV-II+pro) spindle No. 52 at a torque of about 90% under atmospheric pressure at about 23° C.; and a phosphor having a density of about 3.5 g/cm 3 to about 6.5 g/cm 3 , the phosphor being present in an amount of about 5% to about 40% based on the weight of the composition, wherein the siloxane mixture, when combined with the phosphor and allowed to stand at about 23° C. for greater than or equal to about 2 hours, exhibits a phosphor precipitation degree of about 18% or less. 2. The phosphor-containing mixture according to claim 1 , wherein the phosphor precipitation degree is determined by: measuring a light back scattering spectrum of the siloxane mixture of the composition and the phosphor, the light back scattering spectrum being evaluated in a vertical direction over time using a Turbiscan equipment, comparing each measurement value with an initial spectrum, and evaluating the changed degree. 3. The phosphor-containing mixture according to claim 1 , wherein the composition has a transmittance, after curing the composition, of greater than or equal to about 90% at a wavelength of about 450 nm. 4. The phosphor-containing mixture according to claim 1 , wherein the composition has a refractive index, before curing the composition, of greater than or equal to about 1.40 at 589 nm. 5. The phosphor-containing mixture according to claim 1 , wherein the first siloxane compound is represented by Chemical Formula 1: (R 7 R 8 R 9 SiO 1/2 ) M2 (R 10 R 11 SiO 2/2 ) D3 (R 12 SiO 3/2 ) T2 (SiO 3/2 —Y 1 —SiO 3/2 ) T3 (SiO 4/2 ) Q2 [Chemical Formula 1] wherein, in Chemical Formula 1, R 7 to R 12 are independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 carbonyl group, a hydroxy group, or a combination thereof, at least one of R 7 to R 12 includes hydrogen, Y 1 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C2 to C20 alkynylene group, or a combination thereof, 0<M2<1, 0≦D3<1, 0≦T2<1, 0≦T3<1, 0≦Q2<1, and M2+D3+T2+T3+Q2=1. 6. The phosphor-containing mixture according to claim 5 , wherein at least one of the R 7 to R 12 includes a substituted or unsubstituted C6 to C30 aryl group. 7. The phosphor-containing mixture according to claim 1 , wherein the second siloxane compound is represented by Chemical Formula 2: (R 13 R 14 R 15 SiO 1/2 ) M3 (R 16 R 17 SiO 2/2 ) D4 (R 18 SiO 3/2 ) T4 (SiO 3/2 —Y 2 —SiO 3/2 ) T5 (SiO 4/2 ) Q3 [Chemical Formula 2] wherein, in Chemical Formula 2, R 13 to R 18 are independently a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 carbonyl group, a hydroxy group, or a combination thereof, at least one of R 13 to R 18 includes a substituted or unsubstituted C2 to C30 alkenyl group, Y 2 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C2 to C20 alkynylene group, or a combination thereof, 0<M3<1, 0≦D4<1, 0≦T4<1, 0≦T5<1, 0≦Q3<1, and M3+D4+T4+T5+Q3=1. 8. The phosphor-containing mixture according to claim 7 , wherein at least one of the R 13 to R 18 includes a substituted or unsubstituted C6 to C30 aryl group. 9. The phosphor-containing mixture according to claim 1 , wherein the siloxane mixture has a viscosity of about 4,000 to about 9,500 mPa·s when measured using a Brookfield (DV-II+pro) spindle No. 52 at a torque of about 90% under atmospheric pressure at about 23° C. 10. An encapsulant obtained by curing the phosphor-containing mixture according to claim 1 . 11. An electronic device comprising the encapsulant as according to claim 10 .
containing silicon bound to unsaturated aliphatic groups · CPC title
Electricity · mapped topic
Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond · CPC title
Siloxanes having aromatic substituents, e.g. phenyl side groups · CPC title
Polysiloxanes · CPC title
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