This invention relates generally to the planar emissive device field, and more specifically to a new and useful plasma lamp and method of manufacture in the planar emissive device field.
Flat fluorescent lamps are planar “light bulbs” that produce light over their entire surface area. Many operate as dielectric barrier discharge lamps, which are constructed of two sheets of glass with external or dielectric-encapsulated internal planar electrodes that are used to produce a plasma discharge. The plasma is energized by a high voltage applied to the electrodes, which produces a breakdown in the gas. The gas breakdown products cause luminescence, usually in a phosphor, such that the lamp produces light.
Conventional flat fluorescent lamp designs rely on complex geometries and structures that require expensive and complex fabrication processes, such as those used for plasma display panel (PDP) production. These processes may include the use of thick film dielectric paste screening and firing, MgO thin film deposition, and photolithography-patterned metal electrodes. The complex construction and expensive manufacturing processes used to make these conventional lamps drive up the costs of the lamp. To be competitive with the ubiquitous light bulb, there is a great need in the planar plasma lamp field to create a new and useful plasma lamp and method of manufacture that reduces lamp costs.
The following description of the preferred embodiments of the invention is not intended to limit the invention to these preferred embodiments, but rather to enable any person skilled in the art to make and use this invention.
1. System.
As shown in
The construction and manufacture of this lamp 100 can impart several benefits. First, the lamp 100 can yield light output of high quality: the light can be bright, dimmable, of uniform luminance across the surface, have uniform color quality at various emission angles and intensity levels, have a high color rendering index (CRI), have a wide range of available chromaticity, and have good luminous efficacy. Second, the lamp 100 can have a lower manufacturing cost due to a reduced number of parts requiring fewer and less complex manufacturing equipment, and/or a reduced number of manufacturing steps. For example, the lamp substrate 200 functions as the dielectric of the lamp 100, reducing or eliminating the need for an additional dielectric component. As another example, the phosphor coatings 400 can be screen printed, reducing the manufacturing cost through step and equipment reduction. Furthermore, in one variation of the lamp 100, the transparent conductive oxide (TCO) or transparent conductive film can be used as the electrodes 300. Not only does using TCO allow for the buss electrode 340 to be screen-printed without subsequent photolithography processes, but using TCO also reduces the material cost of the lamp 100.
The lamp 100 is preferably utilized with a bipolar-pulsed voltage source using a MOS-FET H-bridge switching topology. A programmable microcontroller produces timing signals to trigger drivers for the MOS-FETs. In one variation, the rail voltage is produced by a power factor correction (PFC) circuit, which converts a universal AC input voltage to about 370 VDC. Dimming can be accomplished by adjusting the pulse repetition frequency (PRF) through 0-10 VDC input to the microcontroller. However, any other suitable voltage source and control circuitry can be used.
The first and second lamp substrates 200 of the lamp 100 support the electrodes 300 and phosphor layers 400, and can additionally function as the dielectric for the lamp 100. The lamp substrates 200 are preferably substantially similar, and preferably have the same dimensions, material, treatments, and dielectric constants. Alternatively, the first and second lamp substrates 200 can have differing parameters. The lamp substrates 200 are preferably planar and prismatic, with two opposing broad faces. The lamp substrates 200 are preferably plates (e.g. rectangular prisms), but can alternatively be curved (e.g. with complimentary curvatures) or have any other suitable geometry. The lamp substrates 200 are preferably glass, more preferably chemically strengthened glass. In one variation, the lamp substrates 200 are made of soda-lime float glass that has been chemically strengthened by sodium ion-potassium ion exchange. However, the lamp substrates 200 can be made of soda-lime container glass, borosilicate glass, any suitable sheet glass, a polymer, or any other suitable material. The lamp substrates 200 can be unstrengthened or strengthened, wherein strengthening can include chemical strengthening, such as ion exchange, lamination, annealing, or any other suitable strengthening method.
The first and second lamp substrates 200 are preferably hermetically sealed together, and cooperatively define an internal chamber 102. The first and second lamp substrates are preferably sealed together by glass frit 210, but can alternatively be sealed in any suitable manner. The distance between the first and second lamp substrates 200 is preferably substantially uniform, and is preferably maintained by spacers 220. This distance is approximately 1.1 mm, but can alternatively be larger or smaller. The distance is preferably maintained by spherical spacers, wherein the spacers 220 preferably have a diameter substantially similar to the desired separation distance (e.g. 1.1 mm, 0.5 mm, etc.). However, rectangular prismatic, cylindrical, or any other suitable spacer can be used. Alternatively, the spacing may be accomplished by molding the back glass substrate with pre-formed spacers (e.g. bumps) that maintain the spacing between the front and back glass. The spacers 220 are preferably glass, more preferably the same glass as the lamp substrates 200, but can be any suitable material. The spacers 220 are preferably evenly distributed over the active area of the lamp 100 (e.g. across the broad face of the first and second lamp substrates 200), but can alternatively be confined to the lamp/lamp substrate perimeter. As shown in
As shown in
As shown in
As shown in
The working gas of the lamp 100 functions to form plasma in response to the high voltage generated between the electrodes 300. The working gas is preferably hermetically sealed in the internal volume defined between the first and second lamp substrates 200. The working gas is preferably a noble gas or a noble gas mixture and can include other materials, such as metal halides, sodium, mercury, or sulfur. In one variation of the lamp, the working gas includes only noble gas, and does not include metal halides, mercury, or sulfur. In another variation of the lamp, the working gas includes neon (Ne) and xenon (Xe), wherein the working gas composition includes 50-100% neon gas and 50-100% xenon gas at a pressure of 100-600 torr. However, the working gas can additionally/alternatively include helium (He), argon (Ar), or krypton (Kr), and can have any other suitable composition.
2. Method of Manufacturing.
As shown in
Applying a first and second phosphor layer to a broad face of a first and second lamp substrate S100 functions to apply the first and second phosphor coating 400 over the interior surfaces of the lamp substrates 200. The phosphor layers 400 are preferably screen-printed (silkscreened, serigraphed, serigraph printed) onto the broad faces of the lamp substrates 200, but the broad faces can be otherwise coated with phosphor (e.g. sprayed, dipped, painted, etc.). As shown in
Joining the first and second lamp substrates together S300 functions to form a substantially hermetic seal between the perimeters of the first and second lamp substrates 200 and to define the internal chamber 102 that contains a working gas. The lamp substrates 200 are preferably joined together after phosphor layer application. As shown in
Positioning the spacers S320 preferably defines the final separation distance (gap distance) between the first and second lamp substrates 200. The spacers 220 are preferably spherical spacers with a diameter substantially equivalent to the desired separation distance, but can alternatively be prismatic spacers 220 or have any other suitable geometry. The spacers 220 are preferably positioned in an even distribution over the broad face of a lamp substrate 200, such as in a grid pattern, but can alternatively be only positioned along the perimeter of the broad face, positioned in a random distribution, or positioned in any suitable manner. Positioning spacers 220 on a broad face of a lamp substrate 200 preferably includes placing the spacers 220 in the desired distribution onto a wet phosphor layer 400 that covers a broad face of a lamp substrate 200, before the phosphor layer 400 has been dried. The spacers 220 are preferably placed on one lamp substrate 200, but can alternatively be placed on both lamp substrates 200. One variation of the method includes pressing the spacers 220 into the wet phosphor layer 400 of the second lamp substrate 204 in the desired distribution, then drying the second phosphor layer 404. Alternatively, the spacers 220 can be included in the frit paste, wherein application of the frit paste during glass frit bonding simultaneously positions the spacers 220 on the broad face of a lamp substrate 200. Alternatively, the spacers 220 can be positioned on a phosphor-coated broad face after the phosphor layer 400 has been dried.
Joining the lamp substrates together using glass frit bonding S340 functions to form a substantially hermetic perimeter seal between the two lamp substrates 200. Glass frit bonding preferably includes: applying a bead of frit paste to the perimeter of a phosphor-coated broad face S342; drying the frit paste; aligning the first and second lamp substrates S344; applying a substantially normal, compressive force against the broad faces of first and second lamp substrates S346; and heating the assembly to flow the frit. The frit paste is preferably applied to the phosphor-coated broad faces of both the first and second lamp substrates 200, but can alternatively be applied to only the phosphor-coated broad face of the first lamp substrate 202 or only the phosphor-coated broad face of the second lamp substrate 204. The frit paste preferably traces substantially the entirety of the broad face perimeter, wherein the frit bead is preferably substantially continuous, but the frit paste can alternatively be applied as a plurality of beads or strips. Frit paste application can additionally include imbedding spacers 220 into the wet frit paste before drying. In one variation of the method, the frit bead is approximately 2-3 mm wide. Aligning the first and second lamp substrates 200 preferably includes aligning the edges of the lamp substrates 200, wherein the first and second lamp substrates 200 preferably have substantially the same geometry. The lamp substrates 200 are preferably arranged with the phosphor-coated faces proximal each other (e.g. on the interior), but can alternatively be arranged with the phosphor-coated faces on the exterior. The lamp substrates 200 can be aligned by placing the first and second lamp substrates 200 in a guide, or aligned in any suitable manner. The normal, compressive force is preferably applied to the lamp substrates 200 after lamp substrate alignment. The normal, compressive force is preferably substantially evenly applied to the perimeter of the lamp substrates 200, more preferably over the area including the frit paste. Alternatively, the compressive force can be substantially evenly distributed over the broad faces of the lamp substrates 200. The compressive force is preferably applied by a plurality of clips (e.g. evenly distributed about the assembly perimeter), but can alternatively be applied by a pressure plate, by a pressurized chamber, or any other suitable pressure application mechanism. Heating the assembly to flow the frit preferably includes heating the assembly (e.g. in an oven) above either the sintering or flow temperature for the frit paste.
Applying electrodes to the exteriors of the first and second lamp substrates S500 couples the electrodes 300 to the lamp exterior. As shown in
Electrode application to the lamp exterior S500 preferably includes laminating the broad face of electrodes 300 to the uncoupled broad faces of the first and/or second broad face of the lamp exterior. The electrodes 300 are preferably laminated to the uncoupled broad faces with adhesive, but can alternatively be laminated using any other suitable lamination method. In one variation, UV-curable adhesive, such as optical grade UV-curable epoxy, is used; however, any other suitable epoxy or adherent can be used. In one variation of the method, electrode application includes applying epoxy, aligning the electrode 300 and the uncoupled broad face of the lamp substrate 200, applying a compressive force on the electrode 300 against the broad face of the lamp substrate 200, and curing the epoxy. The epoxy can be applied to the electrode 300, the uncoupled broad face and/or the side of the electrode substrate 360 that includes the electrode 300. The electrodes 300 are preferably aligned by aligning the electrode substrates 360 with the uncoupled broad face of the lamp substrate 200. Clips, guides, or any other suitable alignment mechanism can be used. The alignment mechanisms used in glass frit sealing the first and second lamp substrates together are preferably used, but other alignment mechanisms can alternatively be used. The electrodes 300 are preferably aligned with the electrodes 300 proximal the uncoupled broad face of the lamp substrate 200 and the electrode substrates 360 distal the uncoupled broad face of the lamp substrate 200. Force is preferably applied to the electrode 300 in a substantially normal direction, but can alternatively be applied at an angle relative to normal. Force is preferably applied to the face of the electrode substrate 360 opposing that supporting the electrode 300, but can alternatively be applied to any suitable face. Force is preferably applied by a pressure plate, but can alternatively be applied by a roller or any other suitable force application mechanism. Curing the epoxy preferably includes exposing the assembly to UV light, but can alternatively include exposing the epoxy to oxygen or any other suitable curing reagent or catalyst.
However, the electrodes 300 can be directly formed on the uncoupled broad faces or joined to the uncoupled broad face of the lamp substrates 200 in any suitable manner.
Applying the electrodes 300 to the uncoupled broad face can additionally include forming the electrodes before electrode application S520. The electrodes 300 are preferably formed from electrode substrates 360 that have been pre-coated with conductive material (e.g. TCO-coated glass substrates from a manufacturer), wherein the conductive material functions as the discharge electrode 320. In one variation, the electrode substrates 360 are pre-coated with conductive material during the glass manufacturing process. For example, a TCO film can be produced on the glass float line at the same time that the glass electrode substrate 360 is being made. However, the electrodes 300 can be formed from uncoated electrode substrates 360, wherein forming the electrodes 300 further includes depositing conductive material on the electrode substrates S522 to form discharge electrodes 320. Depositing conductive material on the electrode substrates S522 can include screen-printing a blanket film of conductive material on the electrode substrate 360, screen-printing an electrode pattern onto the electrode substrate 360 (e.g. using a pattern that prevents the conductive material from being applied to the perimeter of the electrode substrate 360), patterning electrodes 320 (e.g. copper electrodes) onto the electrode substrate 360 using photolithography techniques on blanket films produced using particle deposition, metal organic chemical vapor deposition (MOCVD), metal organic molecular beam deposition (MOMBD), spray pyrolysis, and pulsed laser deposition (PLD), sputtering (e.g. magnetron sputtering) or any other suitable electrode forming technique.
As shown in
As shown in
When the electrode substrate 360 is a film, applying the electrodes 300 to the first and second substrates can additionally include coupling a protective substrate to the electrode S540, as shown in
The method can additionally include providing the internal chamber with a working gas S400. Providing the internal chamber with a working gas preferably includes: providing an opening to the internal chamber S420; evacuating the internal chamber S440, filling the internal chamber with a working gas S460, and sealing the opening S480. Providing the internal chamber 102 with a working gas is preferably performed after phosphor layer application but before electrode application.
Providing an opening into the internal chamber S420 functions to allow fluid access to the internal chamber 102 after the perimeter of the first and second lamp substrates 200 have been sealed together. In one variation, as shown in
Providing the opening can additionally include joining a tube to the opening S430, which functions to provide a fluid path to the internal chamber 102 after sealing the perimeters of the first and second lamp substrates together. The tube 120 can additionally function as an opening sealant. The tube 120 is preferably a hollow, flared tube, but can alternatively be a hollow cylindrical tube or have any suitable geometry. The tube 120 is preferably glass, more preferably substantially the same glass as the lamp substrate 200, but can alternatively be a polymer or any other suitable material. In one variation, as shown in
As shown in
As shown in
Sealing the opening S480 preferably functions to hermetically seal the working gas between the first and second lamp substrates 200, and can additionally function to provide a substantially smooth surface for electrode application. As shown in
The method can additionally include processing the lamp substrates, preferably after providing the opening 110 but alternatively before. Substrate processing preferably includes strengthening the substrate, but can include buffing the substrate, clarifying the substrate, or any other suitable processing step. In one variation of the method, processing the lamp substrate includes strengthening a glass substrate by immersion in a potassium salt bath, such as a potassium nitrate solution, with or without potassium silicate, at elevated temperatures. This is preferably used when the lamp substrate 200 includes soda-lime glass. In another variation of the method, processing the lamp substrate includes both chemical strengthening and glass lamination. However lamination, heat treatment, or any other suitable method can additionally/alternatively be used to strengthen the lamp substrates.
One variation of the method includes: screen-printing a first and second phosphor layer on a broad face of a first and second glass plate, respectively; coupling the phosphor-coated faces of the first and second glass plates together; screen-printing a first and second electrode buss onto an electrode substrate; and coupling the first and second electrode to the uncoupled broad faces of the first and second electrode, respectively.
Another variation of the method includes: providing a first and second glass plate; drilling a hole through the corner of the second glass plate; cleaning the first and second glass plates; strengthening the first and second glass plates by immersion in a potassium nitrate salt bath; cleaning the first and second glass plates; screen-printing a broad face of each of the first and second glass plates with phosphor, wherein the broad face of the first glass plate is coated with a phosphor monolayer, and the broad face of the second glass plate is coated with a phosphor layer having a thickness greater than the phosphor monolayer; placing internal spacers into the phosphor layer coating the broad face of the second glass plate; drying the phosphor monolayer and the phosphor layer; applying a bead of frit about the perimeters of the phosphor-coated broad faces; aligning and coupling the phosphor-coated broad faces of the first and second glass plates; applying a normal, compressive force to the uncoupled faces of the glass plates; applying a bead of frit to a glass tube; coaxially aligning the tube with the hole, with the frit proximal the uncoupled face of the second glass plate; heating the assembly to frit flow temperatures to seal the first and second glass plates and to seal the tube to the second glass plate; evacuating the interior chamber defined between the sealed first and second substrates through the tube; backfilling the interior chamber with a working gas through the tube; sealing the hole by locally heating the free end of the tube, such that the tube collapses radially inward; removing transparent conductive oxide (TCO) from the perimeter of a first and second TCO-coated glass substrate; screen-printing a first and second silver buss electrode about the perimeter of the first and second TCO-coated glass substrates, wherein the buss electrodes extend onto the TCO-coated portions of the glass substrates; firing the buss electrodes; soldering leads to solder pads on the buss electrodes; and laminating the first and second TCO-coated substrates against the uncoupled broad faces of the first and second glass plates, respectively, wherein the buss electrodes and TCO layers are proximal the respective glass plate.
Another variation of the method is substantially similar to that described above, but uses PET films with copper electrodes instead of TCO-coated glass substrates. In this variation, the method includes the additional steps of laminating a first and second piece of protective glass over the uncoupled broad faces of the first and second PET films, respectively.
However, any suitable combination of the aforementioned actions in any suitable order can be utilized to manufacture a lamp.
As a person skilled in the art will recognize from the previous detailed description and from the figures and claims, modifications and changes can be made to the preferred embodiments of the invention without departing from the scope of this invention defined in the following claims.
This application claims the benefit of U.S. Provisional Application No. 61/487,617, filed 18 May 2011, which is incorporated in its entirety by this reference.
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