Field of the Invention
This invention relates fabricating semiconductor devices and in particular methods for coating light emitting diodes (LEDs) and LEDs coated using the method.
Description of the Related Art
Light emitting diodes (LED or LEDs) are solid state devices that convert electric energy to light, and generally comprise one or more active layers of semiconductor material sandwiched between oppositely doped layers. When a bias is applied across the doped layers, holes and electrons are injected into the active layer where they recombine to generate light. Light is emitted from the active layer and from all surfaces of the LED.
Conventional LEDs cannot generate white light from their active layers. Light from a blue emitting LED has been converted to white light by surrounding the LED with a yellow phosphor, polymer or dye, with a typical phosphor being cerium-doped yttrium aluminum garnet (YAG:Ce). The surrounding phosphor material “downconverts” the wavelength of some of the LED's blue light, changing its color to yellow. Some of the blue light passes through the phosphor without being changed while a substantial portion of the light is downconverted to yellow. The LED emits both blue and yellow light, which combine to provide a white light. In another approach light from a violet or ultraviolet emitting LED has been converted to white light by surrounding the LED with multicolor phosphors or dyes.
One conventional method for coating an LED with a phosphor layer utilizes a syringe or nozzle for injecting a phosphor mixed with epoxy resin or silicone polymers over the LED. Using this method, however, it can be difficult to control the phosphor layer's geometry and thickness. As a result, light emitting from the LED at different angles can pass through different amounts of conversion material, which can result in an LED with non-uniform color temperature as a function of viewing angle. Because the geometry and thickness is hard to control, it can also be difficult to consistently reproduce LEDs with the same or similar emission characteristics.
Another conventional method for coating an LED is by stencil printing, which is described in European Patent Application EP 1198016 A2 to Lowery. Multiple light emitting semiconductor devices are arranged on a substrate with a desired distance between adjacent LEDs. The stencil is provided having openings that align with the LEDs, with the holes being slightly larger than the LEDs and the stencil being thicker than the LEDs. A stencil is positioned on the substrate with each of the LEDs located within a respective opening in the stencil. A composition is then deposited in the stencil openings, covering the LEDs, with a typical composition being a phosphor in a silicone polymer that can be cured by heat or light. After the holes are filled, the stencil is removed from the substrate and the stenciling composition is cured to a solid state.
Like the syringe method above, using the stencil method can be difficult to control the geometry and layer thickness of the phosphor containing polymer. The stenciling composition may not fully fill the stencil opening such that the resulting layer is not uniform. The phosphor containing composition can also stick to the stencil opening which reduces the amount of composition remaining on the LED. The stencil openings may also be misaligned to the LED. These problems can result in LEDs having non-uniform color temperature and LEDs that are difficult to consistently reproduce with the same or similar emission characteristics.
Various coating processes of LEDs have been considered, including spin coating, spray coating, electrostatic deposition (ESD), and electrophoretic deposition (EPD). Processes such as spin coating or spray coating typically utilize a binder material during the phosphor deposition, while other processes require the addition of a binder immediately following their deposition to stabilize the phosphor particles/powder.
With these approaches the key challenge is accessing the wire bond pad on the device after the coating process. Accessing the wire bond by standard wafer fabrication techniques is difficult with typical silicone binding material, as well as other binder materials such as epoxies or glass. Silicones are not compatible with commonly used wafer fabrication materials such as acetone, as well as some developers, and resist strippers. This can limit the options and choices for the particular silicones and process steps. Silicones are also cured at high temperature (greater than 150° C.), which is beyond the glass transition temperature of commonly used photoresists. Cured silicone films with phosphor are also difficult to etch and have a very slow etch rate in chlorine and CF4 plasma, and wet etching of cured silicones is typically inefficient.
As a result, typical LEDs are singulated from a wafer, mounted in a package, wire bonded and then coated with a phosphor. With this approach, the phosphor incorporation occurs at the package level, instead of the wafer level. This can result in a process that is costly, difficult to control and is sensitive to packaging geometry effects such as the placement of the wire bond.
The present invention discloses new methods for fabricating semiconductor devices such as LED chips at the wafer level, and discloses LED chips and LED chip wafers fabricated using the methods. The new methods are particularly applicable to coating LEDs at the wafer level while still leaving the wire bond pads accessible for wire bonding. In accordance with certain aspects of the present invention, the coating can include phosphor particles that downconvert at least some of the light emitted from the active region of the LED chip to produce white light, thereby producing a white LED chip.
One embodiment of a method for fabricating semiconductor devices according to the present invention comprises providing a plurality of semiconductor devices on a substrate and forming a contact on at least some of the semiconductor devices. A containment structure is formed on at least some of the semiconductor devices having a contact with each containment structure defining a deposition area excluding its contact. A coating material is then deposited within the deposition area, with the coating material not covering the contact.
One embodiment of a light emitting diode (LED) chip wafer according to the present invention comprises a plurality of LEDs on a substrate wafer with at least some of the LEDs having a contact. A plurality of containment structures, each of which is associated with a respective one of the plurality of LEDs. Each of the containment structures is at least partially on its respective one of the LEDs and defines a deposition area on its respective one of the LEDs. The deposition area excludes the contact. A coating is included in each of the deposition areas.
One embodiment of a light emitting diode (LED) chip according to the present invention comprises an LED and a contact on the LED. A containment structure is included that is associated with the LED, with the containment structure at least partially on the LED and defining a deposition area on the LED excluding the contact. A coating is included in the deposition area and on the surface of said LED.
These and other aspects and advantages of the invention will become apparent from the following detailed description and the accompanying drawings which illustrate by way of example the features of the invention.
The present invention provides fabrication methods that are particularly applicable to wafer level coating of semiconductor devices such as LEDs. The present invention also provides semiconductor devices, such as LEDs fabricated using these methods. The present invention allows for repeatable and consistent coating of LEDs at the wafer level with a down-converter layer (e.g. phosphor loaded silicone) while still allowing access to one or more of the contacts for wire bonding. The phosphor can be applied to the LED chip at the wafer level (prior to dicing) in a defined area, and then fixed in place with a transparent binder such as silicone. This is accomplished while leaving the upper wire bond pad (e.g. n-type bond pad) uncovered by the phosphor and the silicone binder. After testing and dicing, the individual LED chips can be mounted and wire bonded in an LED package using conventional mounting and wire bonding methods without the need for further processing to coat with a down converting phosphor.
According to one aspect of the invention, a patterned surface feature or containment structure can be formed on or around each LED at the wafer level, with the containment structure acting to define the coverage area of the phosphor coating and transparent binder. The containment structure is preferably arranged to prevent phosphor or binder coverage of the wire bond pad. The present invention allows for fabrication, testing and binning of LEDs at the wafer level independent of type of LED lamp packages that the chip will eventually be mounted in. The method can also be scaled to smaller or larger device sizes, and the present invention also eliminates complex wafer fabrication processes to access wire bond pads covered by phosphor and binder coating.
The present invention is described herein with reference to certain embodiments but it is understood that the invention can be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. In particular, the present invention is described below in regards to coating LEDs with a down-converter coating that typically comprises a phosphor loaded binder (“phosphor/binder coating”), but it is understood that the present invention can be used to coat LEDs with other materials for down-conversion, protection, light extraction or scattering. It is also understood that the phosphor binder can have scattering or light extraction particles or materials, and that the coating can be electrically active.
The methods according to the present invention can also be used for coating other semiconductor devices with different materials. Additionally, single or multiple coatings and/or layers can be formed on the LEDs. A coating may comprise one or more phosphors, scattering particles and/or other materials. A coating may also comprise a material such as an organic dye that provides down-conversion. With multiple coatings and/or layers, each one can include different phosphors, different scattering particles, different optical properties, such as transparency, index of refraction, and/or different physical properties, as compared to other layers and/or coatings.
It is also understood that when an element such as a layer, region or substrate is referred to as being “on” another element, it can be directly on the other element or intervening elements may also be present. Furthermore, relative terms such as “inner”, “outer”, “upper”, “above”, “lower”, “beneath”, and “below”, and similar terms, may be used herein to describe a relationship of one layer or another region. It is understood that these terms are intended to encompass different orientations of the device in addition to the orientation depicted in the figures.
Although the terms first, second, etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms are only used to distinguish one element, component, region, layer or section from another region, layer or section. Thus, a first element, component, region, layer or section discussed below could be termed a second element, component, region, layer or section without departing from the teachings of the present invention.
Embodiments of the invention are described herein with reference to cross-sectional view illustrations that are schematic illustrations of idealized embodiments of the invention. As such, variations from the shapes of the illustrations as a result, for example, of manufacturing techniques and/or tolerances are expected. Embodiments of the invention should not be construed as limited to the particular shapes of the regions illustrated herein but are to include deviations in shapes that result, for example, from manufacturing. A region illustrated or described as square or rectangular will typically have rounded or curved features due to normal manufacturing tolerances. Thus, the regions illustrated in the figures are schematic in nature and their shapes are not intended to illustrate the precise shape of a region of a device and are not intended to limit the scope of the invention.
Each of the LED chips 10 in the wafer comprises a semiconductor LED 12 that can have many different semiconductor layers arranged in different ways. The fabrication and operation of LEDs is generally known in the art and only briefly discussed herein. The layers of the LED 12 can be fabricated using known processes with a suitable process being fabrication using metal organic chemical vapor deposition (MOCVD). The layers of the LEDs 12 generally comprise an active layer/region 14 sandwiched between first and second oppositely doped epitaxial layers 16, 18, all of which can be arranged successively on a substrate 20. In this embodiment the LEDs 12 are shown as separate devices on the substrate 20. This separation can be achieved by having portions of the active region 14 and doped layers 16, 18 etched down to the substrate 20 to form the open areas between the LEDs 12. In other embodiments the active layer 14 and doped layers 16, 18 can remain continuous layers on the substrate 20 and can be separated into individual devices when the LED chips are singulated.
It is understood that additional layers and elements can also be included in the LEDs 12, including but not limited to buffer, nucleation, contact and current spreading layers as well as light reflective and extraction layers and elements. The active region 14 can comprise single quantum well (SQW), multiple quantum well (MQW), double heterostructure or super lattice structures. In one embodiment, the first epitaxial layer 16 is an n-type doped layer and the second epitaxial layer 18 is a p-type doped layer, although in other embodiments the first layer 16 can be p-type doped and the second layer 18 n-type doped. The first and second epitaxial layers 16, 18 are hereinafter referred to as n-type and p-type layers, respectively.
The active region 14 and the n- and p-type layers 16, 18 may be fabricated from different material systems, with preferred material systems being Group-III nitride based material systems. Group-III nitrides refer to those semiconductor compounds formed between nitrogen and the elements in the Group III of the periodic table, usually aluminum (Al), gallium (Ga), and indium (In). The term also refers to ternary and quaternary compounds such as aluminum gallium nitride (AlGaN) and aluminum indium gallium nitride (AlInGaN). In one embodiment, the n- and p-type layers 16, 18 are gallium nitride (GaN) and the active region 14 is InGaN. In alternative embodiments the n- and p-type layers 16, 18 may be AlGaN, aluminum gallium arsenide (AlGaAs) or aluminum gallium indium arsenide phosphide (AlGaInAsP).
The substrate 20 can comprise the growth substrate and can be made of many materials such at sapphire, silicon carbide, aluminum nitride (AlN), GaN, with a suitable substrate being a 4H polytype of silicon carbide, although other silicon carbide polytypes can also be used including 3C, 6H and 15R polytypes. Silicon carbide has certain advantages, such as a closer crystal lattice match to Group III nitrides than sapphire and results in Group III nitride films of higher quality. Silicon carbide also has a very high thermal conductivity so that the total output power of Group-III nitride devices on silicon carbide is not limited by the thermal dissipation of the substrate (as may be the case with some devices formed on sapphire). SiC substrates are available from Cree Research, Inc., of Durham, N.C. and methods for producing them are set forth in the scientific literature as well as in a U.S. Pat. Nos. Re. 34,861; 4,946,547; and 5,200,022. In the embodiment shown, the substrate 20 is at the wafer level, with the plurality of LEDs 12 formed on the wafer substrate 20.
In the embodiment shown, the substrate 20 is not a growth substrate but is instead a carrier substrate with the LED chips flip-wafer bonded to a carrier substrate 20. In this embodiment, the growth substrate can comprise the materials described above for growth substrate 20, but in this embodiment the growth substrate is removed after (or before) flip-wafer bonding, with the substrate removed using known grinding and/or etching processes. The LEDs 12 are wafer mounted to the carrier substrate 20 by mounting layer 22, which is typically one or more bond/metal layers, and which can also serve to reflect light incident on it. In other embodiments, the growth substrate or at least portions thereof can remain on the LEDs. The growth substrate or the remaining portions can be shaped or textured to enhance light extraction from the LEDs.
Each of the LEDs 12 can have first and second contacts 24, 26. In the embodiment shown, the LEDs have a vertical geometry with the first contact 24 on the substrate 20 and the second contact 26 on the n-type layer 16 and serving as a wire bond pad. The first contact 24 is shown as one layer on the substrate, but when the LED chips are singulated from the wafer the first contact 24 will also be separated such that each LED chip 10 has its own portion of the first contact 24. An electrical signal applied to the first contact 24 spreads through the substrate 20 and into the p-type layer 18 and a signal applied to the second contact 26 spreads into the n-type layer 16.
In the case of Group-III nitride devices where the order of the layers is reversed and a p-type layer is the top layer, a thin transparent or semitransparent current spreading layer typically covers some or all of the p-type layer to assist in spreading current from the first contact into the p-type layer. It is understood that the spreading layer can comprise a metal such as platinum (Pt) or a transparent conductive oxide such as indium tin oxide (ITO). The first and second contacts 24, 26 are hereinafter referred to as the n-type and p-type contacts respectively.
As further described below, the present invention can also be used with LEDs having lateral geometry wherein both contacts are on the top of the LEDs. This geometry is typically utilized in embodiments having the p-type layer as the first or upper epitaxial layer and the n-type layer is the second or lower epitaxial layer. A portion of the p-type layer and active region is removed, such as by etching, to expose a contact mesa on the n-type layer. Contacts can then be deposited on the p-type layer and the n-type layer on its contact mesa and the contacts can comprise known materials deposited using known deposition techniques.
Referring now to
As shown in
Referring now to
Referring now to
Many different phosphors can be used in the coating 34 according to the present invention. The present invention is particularly adapted to LED chips emitting white light. In one embodiment according to the present invention LEDs 12 emit light in the blue wavelength spectrum and the phosphor absorbs some of the blue light and re-emits yellow. The LED chips 10 emit a white light combination of blue and yellow light. In one embodiment the phosphor comprises commercially available YAG:Ce, although a full range of broad yellow spectral emission is possible using conversion particles made of phosphors based on the (Gd,Y)3(Al,Ga)5O12:Ce system, such as the Y3Al5O12:Ce (YAG). Other yellow phosphors that can be used for white emitting LED chips include:
First and second phosphors can also be combined for higher CRI white of different white hue (warm white) with the yellow phosphors above combined with red phosphors. Different red phosphors can be used including:
Other phosphors can be used to create saturated color emission by converting substantially all light to a particular color. For example, the following phosphors can be used to generate green saturated light:
The following lists some additional suitable phosphors used as conversion particles in LED chips 10, although others can be used. Each exhibits excitation in the blue and/or UV emission spectrum, provides a desirable peak emission, has efficient light conversion, and has acceptable Stokes shift:
Yellow/Green
Different sized phosphor particles can be used including but not limited to 10-100 nanometer(nm)-sized particles to 20-30 μm sized particles, or larger. Smaller particle sizes typically scatter and mix colors better than larger sized particles to provide a more uniform light. Larger particles are typically more efficient at converting light compared to smaller particles, but emit a less uniform light. In one embodiment, the particle sizes are in the range of 2-5 μm. In other embodiments, the coating 34 can comprise different types of phosphors or can comprise multiple phosphor coatings for monochromatic or polychromatic light sources.
During deposition of the phosphor coating 34, phosphor particles can deposit over the edge of the window 32. To prevent these phosphor particles from covering the containment structure 30, the mask layer 28 can comprise a set-back 36 from the containment structure 30 so that the window starts at a point inside of said containment structure. The set-back is formed from the mask layer 28 and comprises a section of dielectric material between the containment structure 30 to the window 32. The set-back 36 is sized such that any spill-over of phosphor particles during deposition of the coating material builds up on the set back 36 and not on the containment structure 30. The allows the containment structure to have an uncovered “corner” to interact with binder material, as described below.
Referring now to
The binder 38 is deposited in liquid form and then cured using many different curing methods depending on different factors such as the type of binder used. Different curing methods include but are not limited to heat, ultraviolet (UV), infrared (IR) or air curing. Although the binder 38 is deposited in liquid form, preferably does not flow out of the containment structure 30 and over other portions of the LED 12 or wafer. The surface tension between the binder 38 when it is in liquid form and the corner 40 of the containment structure 30 holds the binder 38 in a dome shape over the phosphor coating 34. The binder 38 can then be cured in the dome shape. It is understood, that the shape of the binder will be influenced by the same of the containment structure 30. For example, if the containment structure is square or rectangle shaped the dome shape will have a square or rectangular influence. It is further understood that while the corner 40 is depicted as a right angle, its actual shape can be much more general. The shape can include but is not limited to an angle larger or smaller than a right angle, and smoothly varying or curved rather than abrupt.
Different factors determine the amount of LED light that will be absorbed by the phosphor/binder coating in the final LED chips, including but not limited to the size of the phosphor particles, the percentage of phosphor loading, the type of binder material, the efficiency of the match between the type of phosphor and wavelength of emitted light, and the thickness of the phosphor/binding layer. These different factors can be controlled to control the emission wavelength of the LED chips according to the present invention.
Referring now to
It is understood that LED chips according to the present invention can be fabricated using different steps and processes than those described above, and the fabrication steps can be performed in different sequences. For example, the n- and p-type contacts can be deposited at a later processing point such as after curing of the binder. The n-type contact can be deposited in an opening etched in the mask layer and the p-type contact can be deposited on the substrate.
The LED chips 50, however, are not covered by a single dielectric mask layer that is etched to form the containment structure. Instead, they are covered by a dielectric phosphor “mask” layer 52 that is etched to form the window 54. The containment structure 56 is not etched from the mask layer 52, but is instead formed on the mask layer from the same or different material as the mask layer 52. The mask layer 52 is formed of the same materials as the mask layer 28 described above and can be etched using the etching processes described above. The electric field formed during electrophoretic deposition is blocked by the mask layer 52 except for through the window 54. As described above, this encourages deposition of the phosphor particles in and around the window 54. Because the containment structure is formed separately from the mask layer 52, it can be formed of any rigid material that can be deposited, formed or placed on the mask layer 52. This can include insulating, semiconductor or metal materials. In other embodiments, the containment structure can be formed separately from the LED chips and placed or bonded in place on the mask layer 52. The containment structure 56 functions to hold the phosphor coating 58 and the binder 60 as described above, with the corner of the containment structure 56 holding the binder 60 in a dome over the phosphor coating 58 until the binder 60 is cured.
In alternative embodiments of a wafer level LED chips according to the present invention, the containment structure can be filled with phosphor and binder using different processes.
The containment structure 76 can be filled with binder phosphor mixture 78 in liquid form that can be dispensed into the containment structure by known processes such as micro-dispense, inkjet, screen or stencil printing. The surface tension between the binder/phosphor mixture and the outside corner 80 of the containment structure 76 holds the mixture 78 in a dome over and between the containment structure 76 and over the window 74. The mixture 78 can then be cured using the curing methods described above.
The binding/phosphor mixture can have different concentrations or loading of phosphor materials in the binder, with a typical concentration being in range of 30-70% by weight. In one embodiment, the phosphor concentration is approximately 65% by weight, and is preferably uniformly dispersed throughout the binder. Still in other embodiments the coating can comprise multiple layers of different concentrations of types of phosphors, or a first coat of clear silicone can be deposited followed by phosphor loaded layers.
In other embodiments the wafer level LED chips can be fabricated using other features of the LED chip as the containment structure. These alternative features typically comprise a corner, edge or similar feature to cooperate with the surface tension of the binder to hold the binder in a dome over the phosphor coating.
A phosphor coating 96 is deposited on the LED 12 at the window 94 using the methods described above, with some of the phosphor coating 96 spilling over onto the surface of the mask layer 92 around the window 94. The phosphor coating 96 comprises a coating edge 98 that forms a corner or containment feature. A binder 100 can be deposited over the phosphor coating 96, with the binder comprising the materials described above and being deposited using the methods described above. The binder 100 is deposited in liquid form and then cured using one of the different curing methods described above. Although the binder 100 is deposited in liquid form, it does not flow over the entire mask layer 92. The surface tension between the liquid binder 100 and the coating edge holds the binder 100 in a dome shape over the phosphor coating 96. The binder 100 can then be cured in the dome shape. The mask layer 92 can be further etched to reveal the second contact 26 using the methods described above, and the LED chips 90 can be singulated and mounted in packages as described above.
Many different LED chip structures and other semiconductor devices can be fabricated according to the present invention.
In lateral geometry embodiments, each LED 122 is etched through its p-type layer 128 and active region 124 to form an n-type mesa 132. A first p-type contact 134 is formed on the p-type layer 128 and a second n-type contact 136 is formed on the n-type mesa 132. A current spreading layer (not shown can also be included on the p-type layer 128 to spread current from the first contact 134 into the p-type layer 128, with the preferred current spreading layer being a transparent conductor such as those described above.
A dielectric mask layer 138 is deposited over the LEDs 122 covering the exposed surfaces of the LEDs 122 including the first and second contacts 134, 136. The dielectric mask layer 138 is then etched using the methods described above to form a containment structure 140 and window 142. A phosphor and binder can be depositing over the window and within the containment structure using any of the methods described above. As shown in
The mask layer 138 can then be etched using the known etching processes described above, but in this embodiment the mask etching is completed to reveal the first contact 124 and the second contact 126. The LED chips can then be singulated from the wafer and can be mounted in a package, or to a submount or printed circuit board (PCB) without the need for further processing to add phosphor. Each of the individual chips can be mounted and wire bonded in an LED package using conventional mounting and wire bonding methods. In this embodiment, however, two wire bonds are used, one for the first contact 134 and the other for the second contact 136. A conventional encapsulation can then surround the LED chip and electrical connections. In another embodiment, the LED chip can be enclosed by a hermetically sealed cover with an inert atmosphere surrounding the LED chip at or below atmospheric pressure.
In other embodiments the containment structure can be in different locations on the LED chips to provide for tailored phosphor coverage of the LEDs.
A dielectric mask layer 162 is included over LEDs 12, and the surface of the carrier substrate 20 between adjacent LEDs 12. A containment structure 164 is etched in the layer 162 primarily on the carrier substrate 20 surrounding the LED 12. Each containment structure 164 passes over its respective LED 12 at the location of its second contact 26 so that the second contact is not within the containment structure 164. A window can then be etched in the mask layer 162 to reveal most of the top surface of the LED 12. As shown in
The placement of the containment structure 164 allows for substantially all of the LED 12 to be covered by the phosphor coating 168 with the only uncovered area being the area covered by the second contact 26. The mask layer 162 can be further etched to reveal the second contact 26 and the LED chips 160 can be singulated and packaged as described above.
The placement of the containment structure sections 184a, 184b also allows for substantially all of the LED 12 to be covered by the phosphor coating 188 while accommodating the placement of the second contact 26 in the center of the LED. The only area uncovered by the phosphor coating is the area at the center of the LED 12 covered by the second contact 26. The mask layer 182 can be further etched to reveal the second contact 26 and the LED chips 180 can be singulated and packaged as described above.
The LED chips according to the present invention can also comprise features and layers to enhance light extraction. A reflective layer can be arranged that is arranged to reflect light emitted from the active region toward the carrier or substrate, back toward the top of the LED chips. This reflective layer reduces the emission of light from the LEDs that does not pass through conversion material before emitting from the LED chips, such as through the substrate, and encourages emission toward the top of the LED chips and through the phosphor coating.
The reflective layer can be arranged in different ways and in different locations in the LED chip. In one embodiment it can be arranged between the n-type layer and the substrate. The layer can also extend on the substrate beyond the edge of the LEDs. In other embodiments the reflective layer is only between the n-type layer and the substrate. The layer can comprise different materials including but not limited to a metal or a semiconductor reflector such as a distributed Bragg reflector (DBR). In other embodiments, the surfaces of the LED chips, including the cured binder, can be roughened to enhance light extraction. These surfaces can be textured by different methods such as by laser texturing, mechanical shaping, etching (chemical or plasma), or other processes, to enhance light extraction. Texturing results in surface features that are 0.1-5 μm tall or deep, and preferably 0.2-1 μm. In other embodiments, the surface of the LEDs 12 can also be textured or shaped for improved light extraction.
It is understood that the present invention can be used to coat different semiconductor devices with different material and should not be limited to coating LEDs with phosphors and binders.
A dielectric mask layer 202 is deposited over each of the LEDs and a containment structure 204 and window 206 is formed in the mask layer 202 as described above. In this embodiment a phosphor/binder combination is not deposited in the containment structure, but instead a binder 208 only, such as silicone, is deposited. The corner 210 of the containment structure 204 holds the binder 208 in a dome over the window 206 until it is cured. The mask layer 202 can be further etched to reveal the second contact 26, and the LED chips 200 can be singulated and packaged.
This embodiment is particularly applicable to monochromatic LEDs and provides the advantage of high reliability silicone being adjacent to the LEDs emitting surface. This is the region that can experience light and heat induced discoloration, which can be reduced by the presence of the silicone binder 100.
Although the present invention has been described in detail with reference to certain preferred configurations thereof, other versions are possible. Therefore, the spirit and scope of the invention should not be limited to the versions described above.
This invention was made with Government support under Contract DOC/NIST 70-NANB4H3037. The Government has certain rights in this invention.
| Number | Name | Date | Kind |
|---|---|---|---|
| 4308114 | Das et al. | Dec 1981 | A |
| 4733335 | Serizawa et al. | Mar 1988 | A |
| 4902535 | Garg et al. | Feb 1990 | A |
| 4918497 | Edmond | Apr 1990 | A |
| 4935665 | Murata | Jun 1990 | A |
| 4946547 | Palmour et al. | Aug 1990 | A |
| 4966862 | Edmond | Oct 1990 | A |
| 5027168 | Edmond | Jun 1991 | A |
| 5200022 | Kong et al. | Apr 1993 | A |
| 5210051 | Carter, Jr. | May 1993 | A |
| 5277840 | Osaka et al. | Jan 1994 | A |
| 5338944 | Edmond et al. | Aug 1994 | A |
| RE34861 | Davis et al. | Feb 1995 | E |
| 5393993 | Edmond et al. | Feb 1995 | A |
| 5416342 | Edmond et al. | May 1995 | A |
| 5523589 | Edmond et al. | Jun 1996 | A |
| 5604135 | Edmond et al. | Feb 1997 | A |
| 5614131 | Mukerji et al. | Mar 1997 | A |
| 5631190 | Negley | May 1997 | A |
| 5739554 | Edmond et al. | Apr 1998 | A |
| 5766987 | Mitchell et al. | Jun 1998 | A |
| 5767573 | Noda et al. | Jun 1998 | A |
| 5813753 | Vriens | Sep 1998 | A |
| 5858278 | Itoh et al. | Jan 1999 | A |
| 5912477 | Negley | Jun 1999 | A |
| 5923053 | Jakowetz et al. | Jul 1999 | A |
| 5959316 | Lowery | Sep 1999 | A |
| 5988925 | Baggett | Nov 1999 | A |
| 6001671 | Fjelstad | Dec 1999 | A |
| 6066861 | Horn et al. | May 2000 | A |
| 6069440 | Shimizu et al. | May 2000 | A |
| 6087202 | Exposito et al. | Jul 2000 | A |
| 6120600 | Edmond et al. | Sep 2000 | A |
| 6132072 | Turnbull et al. | Oct 2000 | A |
| 6139304 | Centofante | Oct 2000 | A |
| 6153448 | Takahashi | Nov 2000 | A |
| 6187606 | Edmond et al. | Feb 2001 | B1 |
| 6188230 | Birk | Feb 2001 | B1 |
| 6201262 | Edmond et al. | Mar 2001 | B1 |
| 6252254 | Soules et al. | Jun 2001 | B1 |
| 6323480 | Tran et al. | Nov 2001 | B1 |
| 6329224 | Nguyen et al. | Dec 2001 | B1 |
| 6331063 | Kamada et al. | Dec 2001 | B1 |
| 6338813 | Hsu et al. | Jan 2002 | B1 |
| 6376277 | Corisis | Apr 2002 | B2 |
| 6395564 | Huang | May 2002 | B1 |
| 6404125 | Garbuzou | Jun 2002 | B1 |
| 6501100 | Srivastava | Dec 2002 | B1 |
| 6522065 | Srivastava | Feb 2003 | B1 |
| 6531328 | Chen | Mar 2003 | B1 |
| 6577073 | Shimizu et al. | Jun 2003 | B2 |
| 6583444 | Fjelstad | Jun 2003 | B2 |
| 6610563 | Waitl et al. | Aug 2003 | B1 |
| 6624058 | Kazama | Sep 2003 | B1 |
| 6635363 | Duclos et al. | Oct 2003 | B1 |
| 6642652 | Collins, III et al. | Nov 2003 | B2 |
| 6653765 | Levinson | Nov 2003 | B1 |
| 6733711 | Durocher et al. | May 2004 | B2 |
| 6747406 | Bortscheller et al. | Jun 2004 | B1 |
| 6756058 | Brubaker | Jun 2004 | B2 |
| 6759266 | Hoffman | Jul 2004 | B1 |
| 6791119 | Slater, Jr. et al. | Sep 2004 | B2 |
| 6791259 | Stokes | Sep 2004 | B1 |
| 6793371 | Lamke et al. | Sep 2004 | B2 |
| 6812500 | Reeh et al. | Nov 2004 | B2 |
| 6841934 | Wang et al. | Jan 2005 | B2 |
| 6853010 | Slater, Jr. et al. | Feb 2005 | B2 |
| 6860621 | Bachl et al. | Mar 2005 | B2 |
| 6891259 | Im et al. | May 2005 | B2 |
| 6919683 | Jang | Jul 2005 | B1 |
| 6939481 | Srivastava | Sep 2005 | B2 |
| 6958497 | Emerson et al. | Oct 2005 | B2 |
| 7023019 | Maeda et al. | Apr 2006 | B2 |
| 7029935 | Negley et al. | Apr 2006 | B2 |
| 7049159 | Lowery | May 2006 | B2 |
| 7051965 | Nishimura | May 2006 | B2 |
| 7122937 | Hatakeyama et al. | Oct 2006 | B2 |
| 7126273 | Sorg | Oct 2006 | B2 |
| 7176612 | Omoto et al. | Feb 2007 | B2 |
| 7183587 | Negley et al. | Feb 2007 | B2 |
| 7195944 | Tran et al. | Mar 2007 | B2 |
| 7202598 | Juestel et al. | Apr 2007 | B2 |
| 7260123 | Sato | Aug 2007 | B2 |
| 7286296 | Chaves et al. | Oct 2007 | B2 |
| 7312106 | Raben | Dec 2007 | B2 |
| 7361938 | Mueller et al. | Apr 2008 | B2 |
| 7371603 | Kim et al. | May 2008 | B2 |
| 7510890 | Ott et al. | Mar 2009 | B2 |
| 7535089 | Fitzgerald | May 2009 | B2 |
| 7601550 | Bogner | Oct 2009 | B2 |
| 7646035 | Loh et al. | Jan 2010 | B2 |
| 7655957 | Loh et al. | Feb 2010 | B2 |
| 7804103 | Zhai et al. | Sep 2010 | B1 |
| 7858403 | Hiller et al. | Dec 2010 | B2 |
| 7910938 | Hussell et al. | Mar 2011 | B2 |
| 7994531 | Lin et al. | Aug 2011 | B2 |
| 8207546 | Harada et al. | Jun 2012 | B2 |
| 20020001869 | Fjelstad | Jan 2002 | A1 |
| 20020006040 | Kamada et al. | Jan 2002 | A1 |
| 20020070449 | Yagi et al. | Jun 2002 | A1 |
| 20020096789 | Bolken | Jul 2002 | A1 |
| 20020105266 | Juestel et al. | Aug 2002 | A1 |
| 20020123164 | Slater, Jr. et al. | Sep 2002 | A1 |
| 20020185965 | Collins, III et al. | Dec 2002 | A1 |
| 20030006418 | Emerson et al. | Jan 2003 | A1 |
| 20030038596 | Ho | Feb 2003 | A1 |
| 20030042852 | Chen | Mar 2003 | A1 |
| 20030066311 | Li et al. | Apr 2003 | A1 |
| 20030121511 | Hashimura et al. | Jul 2003 | A1 |
| 20030141510 | Brunner et al. | Jul 2003 | A1 |
| 20030207500 | Pichler et al. | Nov 2003 | A1 |
| 20040004435 | Hsu | Jan 2004 | A1 |
| 20040037949 | Wright | Feb 2004 | A1 |
| 20040038442 | Kinsman | Feb 2004 | A1 |
| 20040041222 | Loh | Mar 2004 | A1 |
| 20040056260 | Slater, Jr. et al. | Mar 2004 | A1 |
| 20040080939 | Braddell et al. | Apr 2004 | A1 |
| 20040106234 | Sorg et al. | Jun 2004 | A1 |
| 20040124429 | Stokes et al. | Jul 2004 | A1 |
| 20040164307 | Mueller-Mach et al. | Aug 2004 | A1 |
| 20040012958 | Hashimoto | Dec 2004 | A1 |
| 20040264193 | Okumura | Dec 2004 | A1 |
| 20050002168 | Narhi et al. | Jan 2005 | A1 |
| 20050021191 | Taniguchi et al. | Jan 2005 | A1 |
| 20050057813 | Hasei et al. | Mar 2005 | A1 |
| 20050077529 | Shen | Apr 2005 | A1 |
| 20050122031 | Itai et al. | Jun 2005 | A1 |
| 20050196886 | Jager et al. | Sep 2005 | A1 |
| 20050221519 | Leung et al. | Oct 2005 | A1 |
| 20050265404 | Ashdown | Dec 2005 | A1 |
| 20050280894 | Hartkop et al. | Dec 2005 | A1 |
| 20060001046 | Batres et al. | Jan 2006 | A1 |
| 20060003477 | Braune et al. | Jan 2006 | A1 |
| 20060034082 | Park et al. | Feb 2006 | A1 |
| 20060091788 | Yan | May 2006 | A1 |
| 20060102914 | Smits et al. | May 2006 | A1 |
| 20060157721 | Tran et al. | Jul 2006 | A1 |
| 20060258028 | Paolini et al. | Nov 2006 | A1 |
| 20070012940 | Suh et al. | Jan 2007 | A1 |
| 20070018573 | Shioi | Jan 2007 | A1 |
| 20070040503 | Chase | Feb 2007 | A1 |
| 20070096131 | Chandra | May 2007 | A1 |
| 20070120135 | Soules | May 2007 | A1 |
| 20070158669 | Lee et al. | Jul 2007 | A1 |
| 20070165403 | Park | Jul 2007 | A1 |
| 20070205425 | Harada | Sep 2007 | A1 |
| 20070295975 | Omae | Dec 2007 | A1 |
| 20080006815 | Wang et al. | Jan 2008 | A1 |
| 20080006839 | Lin | Jan 2008 | A1 |
| 20080173884 | Chitnis et al. | Jul 2008 | A1 |
| 20080203410 | Brunner et al. | Aug 2008 | A1 |
| 20090001473 | Ibbetson et al. | Jan 2009 | A1 |
| 20090057690 | Chakraborty | Mar 2009 | A1 |
| 20090065791 | Yen et al. | Mar 2009 | A1 |
| 20090086475 | Caruso et al. | Apr 2009 | A1 |
| 20090117672 | Caruso et al. | May 2009 | A1 |
| 20090261358 | Chitnis et al. | Oct 2009 | A1 |
| 20100155750 | Donofrio | Jun 2010 | A1 |
| 20100308361 | Beeson et al. | Dec 2010 | A1 |
| 20110070668 | Hiller et al. | Mar 2011 | A1 |
| 20110070669 | Hiller et al. | Mar 2011 | A1 |
| 20110180829 | Cho | Jul 2011 | A1 |
| Number | Date | Country |
|---|---|---|
| 102005062514 | Mar 2007 | DE |
| 0732740 | Sep 1996 | EP |
| 1059678 | Dec 2000 | EP |
| 1138747 | Oct 2001 | EP |
| 1198016 | Apr 2002 | EP |
| 1367655 | Dec 2003 | EP |
| 1385215 | Jan 2004 | EP |
| 1724848 | Nov 2006 | EP |
| 1724848 | Nov 2006 | EP |
| 2704690 | Nov 1994 | FR |
| 2704690 | Nov 1994 | FR |
| H0428265 | Jan 1992 | JP |
| 11-040858 | Feb 1999 | JP |
| 11040848 | Feb 1999 | JP |
| H1140848 | Feb 1999 | JP |
| 2000002802 | Jan 2000 | JP |
| 2000208820 | Jul 2000 | JP |
| 2000-315823 | Nov 2000 | JP |
| 2000315823 | Nov 2000 | JP |
| 2001-181613 | Jul 2001 | JP |
| 2002009097 | Jan 2002 | JP |
| 2002009347 | Jan 2002 | JP |
| 2002-050799 | Feb 2002 | JP |
| 2002-50799 | Feb 2002 | JP |
| 2002-050799 | Feb 2002 | JP |
| 2002-076446 | Mar 2002 | JP |
| 2002-093830 | Mar 2002 | JP |
| 2002-531955 | Sep 2002 | JP |
| 2002-531956 | Sep 2002 | JP |
| 2003-197973 | Jul 2003 | JP |
| 2003-258011 | Sep 2003 | JP |
| 2003-526212 | Sep 2003 | JP |
| 2003-303999 | Oct 2003 | JP |
| 2003-318448 | Nov 2003 | JP |
| 2003-533852 | Nov 2003 | JP |
| 2004-501512 | Jan 2004 | JP |
| 2004087812 | Mar 2004 | JP |
| 2004179343 | Jun 2004 | JP |
| 2004-221185 | Aug 2004 | JP |
| 2004363343 | Dec 2004 | JP |
| 2005033138 | Feb 2005 | JP |
| 2005508093 | Mar 2005 | JP |
| 20055080093 | Mar 2005 | JP |
| 2005298817 | Oct 2005 | JP |
| 2006054209 | Feb 2006 | JP |
| 2006303303 | Nov 2006 | JP |
| 2006303373 | Nov 2006 | JP |
| 2007324608 | Dec 2007 | JP |
| WO 0033390 | Jun 2000 | WO |
| WO 0124283 | Apr 2001 | WO |
| WO 0124283 | Apr 2001 | WO |
| WO 03021668 | Mar 2003 | WO |
| WO 03021691 | Mar 2003 | WO |
| WO 2005101909 | Oct 2005 | WO |
| WO 2006033695 | Mar 2006 | WO |
| WO 2006036251 | Apr 2006 | WO |
| WO 2002018560 | Feb 2007 | WO |
| WO 2007049187 | May 2007 | WO |
| WO 2008003176 | Jan 2008 | WO |
| Entry |
|---|
| International Search Report and Written Opinion from related PCT Application No. PCT/US2009/001572, dated Jul. 17, 2009. |
| Office Action from related U.S. Appl. No. 11/982,276, dated Dec. 7, 2009. |
| Office Action from related U.S. Appl. No. 12/077,638, dated Dec. 8, 2009. |
| Official Notice of Rejection re related Japanese Patent Application No. 2007-533459, dated Jul. 29, 2008. |
| From related application. Japanese Patent Application No. 2006-526964, Official Notice of Rejection, dated Feb. 16, 2010. |
| Official Notice of Final Decision of Rejection re: related Japanese Patent Application No. 2007-533459, dated Dec. 26, 2008. |
| Rejection Decision re: related Chinese Patent Application No. 200580031382.3, dated: Feb. 2, 2009. |
| Communication pursuant to Article 94(3) EPC re: related European Application No. 05808825.3, dated Feb. 18, 2009. |
| Notice on Reexamination for Chinese Patent Application No. 200580031382.3 dated May 28, 2010. |
| Examination of related European Application No. 05 808 825.3-2203, dated Mar. 18, 2009. |
| PCT International Search Report and Written Opinion, PCT/US2007/024366,dated Jul. 15, 2008. |
| Official Notice of Rejection dated Jul. 29, 2008, Japanese Patent Application No. 2007-533459. |
| NPO-30394 Electrophoretic Deposition for Fabricating Microbatteries p. 1-2, NASA Tech Briefs Issue May 3, 2003. |
| Patent Abstracts of Japan vol. 2000, No. 10, Nov. 17, 2000. |
| Patent Abstracts of Japan vol. 2002, No. 05, May 3, 2002. |
| Nichia Corp. White LED Part No. NSPW300BS, Specification for Nichia White LED, Model NSPW300BS Jan. 14, 2004. |
| Nichia Corp. White LED Part No. NSPW312BS, Specification for Nichia White LED, Model NSPW312BS Jan. 14, 2004. |
| Lau, John, “Flip-Chip Technologies”, Mcgraw Hill, 1996. |
| International Materials Reviews “Materials for Field Emission Displays”, A.P. Burden 2001. |
| Office Action re related U.S. Appl. No. 10/666,399, dated Sep. 5, 2008. |
| International Search Report for PCT/US2007/024367, dated Oct. 22, 2008. |
| PCT Search Report and Written Opinion dated Oct. 31, 2007. |
| Office Action from Japanese Patent Application No. 2007-533459 (Appeal No. 2009-006588) dated Jul. 16, 2010. |
| Office Action from Chinese Patent Application No. 200780012387.0 dated Jun. 30, 2010. |
| Summons for Oral Proceedings for European Patent Application No. 05808825.3 dated Sep. 9, 2010. |
| Notification of the First Office Action for Chinese Patent Application No. 200780050127.2 dated Aug. 8, 2010. |
| Notice of Rejection for Japanese Patent Application No. 2006-526964 dated Oct. 5, 2010. |
| Notification of the First Office Action for Chinese Patent Application No. 200780050197.8 dated Sep. 9, 2010. |
| Reexamination Decision No. 27346 for Chinese Patent Application No. 200580031382.3 dated Oct. 27, 2010. |
| First Office Action for European Patent Application No. 07754163.9 dated Feb. 28, 2011. |
| Notice of Rejection from Japanese Patent Application No. 2009-504205, dated Aug. 17, 2011. |
| Second Office Action from Chinese Patent Application No. 200780012387.0, dated Sep. 5, 2012. |
| Decision of Rejection for Japanese Patent Application No. 2009-504205, dated Jul. 31, 2012. |
| First Office Action from Chinese Patent Application No. 200980121201.4, dated Jul. 4, 2012. |
| International Search Report and Written Opinion from PCT Appl. No. PCT/US2012/050794, dated Jan. 10, 2013. |
| Notice of Reasons for Rejection from Japanese Patent Application No. 2011-502981, dated Feb. 5, 2013. |
| Office Action from Korean Patent Application No. 10-2008-7026531. dated Feb. 14, 2013. |
| Office Action from U.S. Appl. No. 11/775,958, dated Oct. 24, 2013. |
| Office Action from U.S. Appl. No. 12/414,457, dated Jul. 18, 2013. |
| Response to OA from U.S. Appl. No. 12/414,457, filed Oct. 17, 2013. |
| Third Office Action from Chinese Patent Appl. No. 2007800123870. dated Feb. 14, 2013. |
| Office Action from U.S. Appl. No. 11/398,214, dated Jun. 10, 2013. |
| Office Action from U.S. Appl. No. 11/775,958, dated Apr. 8, 2013. |
| Office Action from U.S. Appl. No. 13/192,293, dated Mar. 27, 2013. |
| Response to OA from U.S. Appl. No. 13/192,293. filed Jun. 20, 2013. |
| Office Action from U.S. Appl. No. 13/219,486. dated Feb. 8, 2013. |
| Response to OA from U.S. Appl. No. 13/219,486, filed May 2, 2013. |
| Office Action from U.S. Appl. No. 13/219,486, dated Aug. 21, 2012. |
| Response to OA from U.S. Appl. No. 13/219,486, filed Dec. 18, 2012. |
| Office Action from U.S. Appl. No. 13/219,486, dated Apr. 19, 2012. |
| Response to OA from U.S. Appl. No. 13/219,486, filed Jul. 12, 2012. |
| Office Action from U.S. Appl. No. 11/398,214, dated Apr. 25, 2011. |
| Response to OA from U.S. Appl. No. 11/398,214, filed Aug. 23, 2011. |
| Office Action from U.S. Appl. No. 12/414,457, dated Apr. 1, 2011. |
| Response to OA from U.S. Appl. No. 12/414,457, file Jul. 1, 2011. |
| Office Action from U.S. Appl. No. 12/414,457, dated Nov. 12, 2010. |
| Response to OA from U.S. Appl. No. 12/414,457, file Jan. 11, 2011. |
| Office Action from U.S. Appl. No. 12/414,457, dated Jun. 29, 2010. |
| Response to OA from U.S. Appl. No. 12/414,457, file Oct. 25, 2010. |
| Rejection Decision from Chinese Patent Appl. No. 200980121201.4, dated Sep. 23, 2013. |
| Decision of Rejection from Japanese Patent Appl. No. 2011-502981, dated Sep. 10, 2013. |
| Examination Report from European Patent Appl. No. 07 754 163.9-1564, dated Oct. 14, 2013. |
| Second Office Action from Chinese Application No. 200980121201.4, dated Mar. 5, 2013. |
| Interrogatory from Japanese Patent Appl. No. 2009-504205, dated Mar. 19, 2013. |
| Office Action from U.S. Appl. No. 11/396,214, dated Mar. 7, 2014. |
| Office Action from U.S. Appl. No. 11/398,214, dated Nov. 22, 2013. |
| Response to OA from U.S. Appl. No. 11/398,214, filed Jan. 14, 2014. |
| Office Action from Taiwanese Patent Appl. No. 096111808, dated Nov. 7, 2013. |
| Allowed Claims from Taiwanese Patent Appl. No. 096111808, dated Jun. 6, 2014. |
| Extended European Search Report from European Patent Appl. No. 08160051.2-1551, dated Apr. 24, 2014. |
| Office Action from U.S. Appl. No. 11/398,214, dated Jun. 12, 2014. |
| Examination Report from European Patent Appl. No. 09726236.8, dated Aug. 6, 2014. |
| Office Action from U.S. Appl. No. 11/775,958, dated Oct. 1, 2014. |
| Notice of Reexamination from Chinese Patent Appl. No. 200980121201.4, dated Jan. 16, 2015. |
| Examination Report from European Appl. No. 09 728 238.8, dated Jan. 5, 2015. |
| Office Action from U.S. Appl. No. 11/775,958, dated Jan. 7, 2015. |
| Office Action from Korean Patent Appl. No. 10-2010-7024150, dated Mar. 16, 2015. |
| Office Action from U.S. Appl. No. 11/775,958, dated Apr. 17, 2015. |
| Notice of Reasons for Rejection from Japanese Appl. No. 2011-502981, dated May 12, 2015. |
| Summons to attend oral proceedings from European Patent Appl. No. 07754163.9, dated Oct. 8, 2015. |
| Third Office Action from Chinese Patent Appl. No. 200980121201.4, dated Oct. 9, 2015. |
| Office Action from U.S. Appl. No. 11/775,958, dated Oct. 23, 2015. |
| Decision of Grant from Japanese Patent Appl. No 2011-502981, dated Sep. 1, 2015. |
| Office Action for Application No. 07754163.9; dated Apr. 8, 2016. |
| Office Action for Application No. 200980121201.4; dated Mar. 4, 2016. |
| Office Action for application No. 08160049.6; dated May 6, 2016. |
| European Office Action for Application No. 09728238.8-1453; dated Aug. 8, 2016. |
| European Office Action for Application No. 08160049.6-1551; dated Jul. 7, 2017. |
| Number | Date | Country | |
|---|---|---|---|
| 20090014736 A1 | Jan 2009 | US |