Method for fabrication of a luminescent structure
09590146 ยท 2017-03-07
Assignee
Inventors
- Josephus Paulus Augustinus Deeben (Eindhoven, NL)
- Patrick Henricus Johannes Van Stijn (Eindhoven, NL)
Cpc classification
H01L2224/16225
ELECTRICITY
H01L2924/00012
ELECTRICITY
H01L2924/00012
ELECTRICITY
International classification
H01L33/00
ELECTRICITY
Abstract
A method for fabricating an LED/phosphor structure is described where an array of blue light emitting diode (LED) dies are mounted on a submount wafer. A phosphor powder is mixed with an organic polymer binder, such as an acrylate or nitrocellulose. The liquid or paste mixture is then deposited over the LED dies or other substrate as a substantially uniform layer. The organic binder is then removed by being burned away in air, or being subject to an O.sub.2 plasma process, or dissolved, leaving a porous layer of phosphor grains sintered together. The porous phosphor layer is impregnated with a sol-gel (e.g., a sol-gel of TEOS or MTMS) or liquid glass (e.g., sodium silicate or potassium silicate), also known as water glass, which saturates the porous structure. The structure is then heated to cure the inorganic glass binder, leaving a robust glass binder that resists yellowing, among other desirable properties.
Claims
1. A method for fabricating a luminescent structure comprising: a. depositing phosphor layer on a surface, the phosphor layer comprising phosphor powder mixed with a first binder; b. removing the first binder and heating the phosphor layer, leaving a porous phosphor layer on the surface comprising phosphor grains sintered together; c. infusing the porous phosphor layer with a sol-gel or liquid glass; and d. curing the sol-gel or liquid glass to form an inorganic transparent glass binder.
2. The method of claim 1 wherein the step of removing the first binder comprises heating the first binder to evaporate the first binder.
3. The method of claim 1 wherein the first binder comprises nitrocellulose.
4. The method of claim 1 where the step of depositing the phosphor layer comprises depositing the phosphor powder and first binder on a transparent support substrate, the method further comprising singulating the transparent support structure to form luminescent tiles and affixing one of the tiles over a light emitting diode (LED) die.
5. The method of claim 4 wherein affixing one of the tiles over the LED die comprises affixing one of the tiles over another phosphor tile affixed over the LED die.
6. The method of claim 1 wherein the sol-gel or liquid glass, after curing, forms a layer of inorganic glass.
7. The method of claim 1 wherein the sol-gel or liquid glass, after curing, forms a layer of either TEOS, MTMS, or MTES.
8. The method of claim 1 where the step of depositing the phosphor layer comprises depositing the phosphor powder and first binder on a transparent support substrate, wherein the support structure is a transparent lens between a light emitting diode die and the phosphor layer.
9. The method of claim 1 wherein the step of depositing the phosphor layer comprises depositing the phosphor layer over a light emitting diode die.
10. The method of claim 1 where the step of depositing the phosphor layer comprises depositing the phosphor powder and first binder on a transparent support substrate, the method further comprising positioning the porous phosphor layer, infused with the glass binder, and the support structure over a light emitting diode (LED) die so the phosphor layer is not in direct contact with the LED die.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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(13) Elements that are the same or similar are labeled with the same numeral.
DETAILED DESCRIPTION
(14) Although the present invention of a phosphor layer does not rely on its use with any particular LED, an example of an LED structure will be described to illustrate the phosphor layer's use with an LED.
(15) Prior art
(16) In this disclosure, the term submount wafer is intended to mean a support for an array of LED dies, where electrical contacts on the wafer are bonded to electrodes on the LED dies, and the wafer is later singulated to form one or more LEDs on a single submount, where the submount has electrodes that are to be connected to a power supply.
(17) The LED die 10 is formed of semiconductor epitaxial layers, including an n-layer 14, an active layer 15, and a p-layer 16, grown on a growth substrate, such as a sapphire substrate. The growth substrate has been removed in
(18) A metal electrode 18 electrically contacts the p-layer 16, and a metal electrode 20 electrically contacts the n-layer 14. In one example, the electrodes 18 and 20 are gold pads that are ultrasonically welded to anode and cathode metal pads 22 and 24 on a ceramic submount wafer 12. The submount wafer 12 has conductive vias 24 leading to bottom metal pads 26 and 28 for bonding to a printed circuit board. Many LEDs are mounted on the submount wafer 12 and will be later singulated to form individual LEDs/submounts.
(19) Further details of LEDs can be found in the assignee's U.S. Pat. Nos. 6,649,440 and 6,274,399, and U.S. Patent Publications US 2006/0281203 A1 and 2005/0269582 A1, all incorporated herein by reference.
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(22) A phosphor layer 38 is shown over the wafer 12, which represents that either the phosphor layer 38 will be laminated over the wafer 12 or that the phosphor layer 38 will be a remote layer separated from the LED dies 10. In another embodiment, the phosphor layer 38 may be singulated to form tiles, and each tile is affixed over an LED die 10. Further, in another embodiment, the phosphor layer 38 is laminated over an LED wafer prior to the LEDs being singulated. In that way, there is little waste of phosphor. Other uses of the phosphor layer 38 are envisioned.
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(26) Initially, phosphor powder 42 is mixed with an organic polymer binder 44, such as an acrylate, nitrocellulose, or other commercially available binder that can be later evaporated or dissolved away. Due to the conventional small grain size of the phosphor powder 42 and its density in the binder 44, the distribution of phosphor powder 42 in binder 44 is fairly homogenous which should achieve good color uniformity across the phosphor layer 38. The phosphor grain size and density is not critical; however, the density should be such that the grains contact each other after the binder 44 is later removed.
(27) The phosphor powder 42 may be any conventional phosphor, including YAG, red, green, yellow, blue, or orange phosphor, or combinations thereof, depending on the application and the LED.
(28) Since the polymer binder 44 does not have to have good optical properties, it may be much less expensive than silicone. Silicone for use with phosphors is about $900 US/kg.
(29) The mixed binder/phosphor may form a paste or viscous liquid that is spray coated, dip coated, spun on, or screen printed onto the substrate 40. The thickness is not critical for the invention, but the thickness and density of the phosphor powder 42 affects the emitted light color. The deposited layer should have a thickness accuracy of +/2% to achieve good color uniformity.
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(32) After the saturation step, the liquid glass or sol-gel is cured to dehydrate the material, leaving a robust glass binder 48 surrounding the phosphor powder 42. In some cases, curing is performed by heat or dehydrating at a longer time at room temperature, or performed using a chemical curing agent.
(33) Liquid glass (sodium silicate or potassium silicate) is made by fusing varying portions of sand (SiO2) and soda ash (Na2CO3), where CO2 is driven off. The ratio of these portions determines the properties of the final product. This product is specified as a ratio of SiO2/Na2O and as a concentration in water. The sodium may also be replaced by potassium or lithium in order to obtain different properties. After applying liquid glass as a thin film, the water is evaporated, leaving a solid glass coating behind. Lower SiO2/Na2O ratios tend to retain water better and hence evaporate slower. Higher ratio solutions (approx. 2.8-3.22) are preferred if increased durability is desired. Complete dehydration typically requires heat during the drying process. The silicate layers may be cured at a temperature of 250 C., which is well below the temperature that luminescent materials can stand (nitride-based luminescent materials can stand temperatures up to 350 C. and YAG-based luminescent materials even much higher).
(34) Another method to make the coatings durable is to make use of chemical setting. Chemical setting agents that can be used in this manner include mineral and organic acids, CO2 gas, and acid salts such as sodium bicarbonate.
(35) When silicate films are completely dehydrated, they provide excellent resistance to high temperatures. Most silicates have flow points around 850 C. In LEDs, such temperatures will never be reached.
(36) Liquid glass is transparent for visible light, and the transmission drops off rapidly below 400 nm, exhibiting a value of approximately 40% at 325 nm. For LEDs that convert blue to white light, this range is sufficient.
(37) Silicate coatings may be brittle. If a higher degree of flexibility is required, typically 5% by weight of glycerine can be added. Glycerine has a very high transparency for blue light. Other materials may be added, such as ethyelene glycol, propylene glycol, an alcohol, etc.
(38) There are many suitable sol-gel materials, such as TEOS (tetraethylorthosilicate), MTMS (methyltrimethoxysilane), and MTES (triethoxysilane), all generally referred to as glass materials. Sol-gel is relatively inexpensive (less than $20 US/kg), so the resulting phosphor layer is less expensive than phosphor powder in a silicone binder. Glass has high thermo and photo-thermal stability and resists yellowing in the presence of the high heat and flux of an LED. Forming a sol-gel of such materials is well known for depositing the materials on a substrate.
(39) The sol-gel process is a wet-chemical technique commonly used for the fabrication of a glassy coating. In this process, the sol (or solution) evolves gradually towards the formation of a gel-like network containing both a liquid phase and a solid phase. The micron-size or sub-micron-size glass particles become linked, forming the gel. The formation of a TEOS, MTMS, MTES, or other glass layer using sol-gel is well-known and need not be described in detail.
(40) The drying process serves to remove the liquid phase from the gel, yielding an amorphous glass (a linked silica network or matrix). Subsequent thermal treatment (firing) may be performed in order to densify the glass to enhance its mechanical properties.
(41) Since there will be shrinkage after dehydration, the thickness of the sol-gel or liquid glass should be adjusted to ensure complete coverage of the phosphor powder 42 after dehydration. Multiple applications and curing of the sol-gel or liquid glass may be desirable for complete coverage.
(42) The glass layer may be formed to have a relatively high index of refraction, comparable to that of high index silicones, to provide good light extraction.
(43) As an alternative to depositing the film of
(44) In one embodiment, a flexible layer of the polymer binder 44 and phosphor power 42 mixture is formed on a releasable film (an embodiment of substrate 40). The layer may be tested to determine its luminescent properties and matched to a particular bin of LED dies that emit a particular narrow range of blue light. As shown in
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(48) In step 70, an LED wafer is fabricated, such as a wafer containing GaN-based blue LEDs.
(49) In step 71, the LED wafer is diced, and a submount wafer is populated with the LED dies.
(50) In step 72, a mixture of phosphor powder and an organic binder is created as a paste or a liquid for screen printing or other type of deposition, or created as a lamination layer.
(51) In step 73, the phosphor/binder mixture is printed or laminated on a glass plate (e.g., for a remote phosphor) or other substrate or over the LED dies.
(52) In step 74, the organic binder is removed by heating or subjecting the binder to an O2 plasma or other treatment, leaving a porous, sintered phosphor powder layer.
(53) In step 75, the phosphor web is impregnated with liquid glass, a sol-gel, or other suitable material by spray coating, dip coating, or other process.
(54) In step 76, the liquid glass or sol-gel is cured such as by heating to cross-link the sol-gel layer and/or evaporate any solution, such as water in the liquid glass.
(55) Steps 75 and 76 may be performed multiple times due to shrinkage.
(56) While particular embodiments of the present invention have been shown and described, it will be obvious to those skilled in the art that changes and modifications may be made without departing from this invention in its broader aspects and, therefore, the appended claims are to encompass within their scope all such changes and modifications as fall within the true spirit and scope of this invention.