Electroluminescent light sources emit light when a voltage is applied. Currently, electroluminescence-based light sources are limited to back light units in television and lighting for signage due to low achievable light emission intensities. A typical electroluminescent device consists of an active layer that is sandwiched directly between two insulating layers, and the active layer consists of a phosphor material. When a high enough voltage is applied across the active layer, electrons accelerated by the electric field collide with the phosphor material to emit light from the active layer. Emission intensity is limited by the electron density, which is very low.
Embodiments of the subject invention relate to electroluminescent devices, methods of manufacturing the same, and methods of using the same. An electroluminescent device can include an active layer directly in contact with a semiconductor p-n junction (e.g., with a semiconductor layer of a p-n junction).
In an embodiment, an electroluminescent device can include an active layer and at least one p-n junction in physical contact with the active layer, wherein the at least one p-n junction includes a first semiconductor layer and a second semiconductor layer. Either the first semiconductor layer or the second semiconductor layer is a p-type semiconductor layer, and the other is an n-type semiconductor layer.
In another embodiment, a method of forming an electroluminescent device can include: forming a second semiconductor layer directly on and in physical contact with a first semiconductor layer; forming an active layer directly on and in physical contact with the second semiconductor layer; forming a third semiconductor layer directly on and in physical contact with the active layer; and forming a fourth semiconductor layer directly on and in physical contact with the third semiconductor layer. Either the first semiconductor layer or the second semiconductor layer is a p-type semiconductor layer, and the other is an n-type semiconductor layer. Also, either the third semiconductor layer or the fourth semiconductor layer is a p-type semiconductor layer, and the other is an n-type semiconductor layer.
In yet another embodiment, a method of generating light can include providing an electroluminescent device. The device can include an active layer and at least one p-n junction in physical contact with the active layer, wherein the at least one p-n junction includes a first semiconductor layer and a second semiconductor layer. Either the first semiconductor layer or the second semiconductor layer is a p-type semiconductor layer, and the other is an n-type semiconductor layer.
When the terms “on” or “over” are used herein, when referring to layers, regions, patterns, or structures, it is understood that the layer, region, pattern or structure can be directly on another layer or structure, or intervening layers, regions, patterns, or structures may also be present. When the terms “under” or “below” are used herein, when referring to layers, regions, patterns, or structures, it is understood that the layer, region, pattern or structure can be directly under the other layer or structure, or intervening layers, regions, patterns, or structures may also be present. When the term “directly on” is used herein, when referring to layers, regions, patterns, or structures, it is understood that the layer, region, pattern or structure is directly on another layer or structure, such that no intervening layers, regions, patterns, or structures are present. When the term “direct contact” is used herein, when referring to layers, regions, patterns, or structures in contact with other layers, regions, patterns, or structures, it is understood that the layer, region, pattern or structure is in direct, physical contact with the other layer, region, pattern, or structure, such that no intervening layers, regions, patterns, or structures are present.
When the term “about” is used herein, in conjunction with a numerical value, it is understood that the value can be in a range of 95% of the value to 105% of the value, i.e. the value can be +/−5% of the stated value. For example, “about 1 kg” means from 0.95 kg to 1.05 kg.
Embodiments of the subject invention relate to electroluminescent devices, methods of manufacturing the same, and methods of using the same. An electroluminescent device can include an active layer directly in contact with a semiconductor layer of a p-n junction.
In a typical electroluminescent device, an active layer is sandwiched between two insulating layers. When a high enough voltage is applied across the active layer, electrons at the interface of the active layer and the insulator are accelerated to high energy and collide with phosphor in the active layer to emit light from the active layer. However, emission intensity is limited by the electron density, which is very low in a typical electroluminescent device. Embodiments of the subject invention provide a completely new device architecture that sandwiches the active layer between two semiconductor layers and/or between two semiconductor p-n junctions.
In an embodiment, an electroluminescent device can include an active layer directly in contact with at least one semiconductor layer. Each semiconductor layer in direct contact with the active layer can be part of a p-n junction. For example, the active layer can be between two semiconductor layers, such that the active layer is in contact with both semiconductor layers. In certain embodiments, the active layer can be sandwiched between two semiconductor p-n junctions, such that the top surface of the active layer is in contact with a semiconductor layer and the bottom surface of the active layer is in contact with a semiconductor layer. Each semiconductor layer in direct contact with the active layer can be part of a p-n junction, leading to an enhancement in electron density, thereby generating much higher light intensities than typical electroluminescent devices. This advantageous arrangement also provides an avenue for current injection that can further increase emission intensity.
In many embodiments, the active layer of the electroluminescent device can be a phosphor layer. In a further embodiment, the active layer can include a coating of a phosphor material and/or a coating of phosphor particles embedded in a host material. The host material in which the phosphor particles can be embedded can be crystalline or amorphous. In addition, the host material in which the phosphor particles can be embedded can be inorganic or organic. The phosphor layer, phosphor coating, or phosphor particles can include, for example, zinc sulfide (ZnS), manganese, calcium sulfide (CaS), ZnS nanocrystals, and/or CaS nanocrystals, though embodiments are not limited thereto. In an embodiment of the subject invention, an active layer of an electroluminescent device can include Mn-doped ZnS (ZnS:Mn). In another embodiment, the active layer can include ZnS/CaS nanocrystals. In a further embodiment, the active layer can include ZnS with ZnS/CaS nanocrystal inclusions
The availability of large numbers of phosphors that radiate in a variety of wavelengths and bandwidths, from deep-blue to far-red, enables the development of light sources in many specific wavelength regions. There are two main methods of exciting phosphors; one is optical excitation by a UV source (e.g., UV-LED) followed by emission in higher wavelengths. This method suffers from Stokes down-conversion, where the energy of the emitted photon is much smaller than the energy of the absorbed photon. Another method of exciting phosphors is impact excitation by high energy electrons, and theoretical efficiency for this process is very high. The main loss mechanism is the non-radiative electron-hole recombination. These losses can be compensated by increasing the density of electrons available for excitation.
In an embodiment, a phosphor layer can include a host material impurity ions as active ions. The crystal field energy of the host structure can cause splitting of the energy level in the active ions leading to an absorption line in blue and emission lines at longer wavelengths with long lifetimes (phosphorescence). The host material can be, for example, an oxide, a nitride, or a sulfide material, though embodiments are not limited thereto. The impurity ions can be, for example, any of the following elements or any combination of the following elements, though embodiments are not limited thereto: cerium (Ce), europium (Eu), terbium (Tb), manganese (Mn), copper (Cu), silver (Ag), lead (Pb), and bismuth (Bi). The host material can include a small percentage of impurity ions, for example 0.001% to 10% by weight or by volume, preferably 0.1% to 5% by weight, more preferably 0.5% to 2% by weight, and even more preferably 1% or about 1% by weight. In a particular embodiment, the host material can include about 1% by volume of impurity ions. Other examples of phosphor materials that can be used in the subject invention include some well-known phosphor materials: Ce3+ and/or Eu2+ doped Y3Al5O12 (YAG: Ce3+, Eu2+), Y2O3:Eu2+, Ba3MgSi2O8:Eu2+, Mn2+, ZnS:Mn, CaS:Cu, CaS:Pb2+, CaS:Eu2+.
In an embodiment, the phosphor material can be ZnS:Mn. Electrons that are accelerated in the conduction band of the ZnS semiconductor interact with Mn ions to produce emission in the orange region. However, most of the phosphor hosts that emit radiation in other wavelengths are oxides, nitrides, or sulfides, which are highly insulating. Embedding particles of these phosphors in a wide band gap semiconductor such as ZnS can increase emission intensities. Phosphor materials fabricated by solid state sintering methods are in micrometer scale, and thus light scattering at grain boundaries can be significant. Light scattering can reduces the extraction efficiency of the source. When the phosphor particle size is few tens of nanometers, much smaller than the wavelength of light (400-800 nm), the effect of light scattering can be significantly reduced. The Mie scattering cross-section of particles below 50 nm is very small. In addition, when the phosphor particle size is reduced to the scale of tens of nanometers, the surface area-to-volume ratio of the material is increased, leading to an increase in the luminous efficiency.
Referring to
In many embodiments, the active layer 60 and at least one of the second semiconductor layer 50 and the third semiconductor layer 70 are present, and the active layer 60 is in direct contact with each of these layers that is present. In an embodiment, the active layer 60 is directly on the second semiconductor layer 50, the second semiconductor layer 50 is directly on the first semiconductor layer 40, and the third 70 and fourth 80 semiconductor layers are not present. The first 40 and second 50 semiconductor layers can be different types (i.e., the first semiconductor layer 40 can be an n-type semiconductor layer and the second semiconductor layer 50 can be a p-type semiconductor layer, or the first semiconductor layer 40 can be a p-type semiconductor layer and the second semiconductor layer 50 can be an n-type semiconductor layer). In an alternative embodiment, the third semiconductor layer 70 is directly on the active layer 60, the fourth semiconductor layer 80 is directly on the third semiconductor layer 70, and the first 40 and second 50 semiconductor layers are not present. The third 70 and fourth 80 semiconductor layers can be different types (i.e., the third semiconductor layer 70 can be a p-type semiconductor layer and the fourth semiconductor layer 80 can be an n-type semiconductor layer, or the third semiconductor layer 70 can be an n-type semiconductor layer and the fourth semiconductor layer 80 can be a p-type semiconductor layer).
Each semiconductor layer 40, 50, 70, 80 (if present) can be either an n-type semiconductor layer or a p-type semiconductor layer. In an embodiment, the first semiconductor layer 40 and the fourth semiconductor layer 80 can be the same type (p-type or n-type), and the second semiconductor layer 50 and the third semiconductor layer 70 can be the same type (p-type or n-type). For example, the first semiconductor layer 40 can be an n-type semiconductor layer, the second semiconductor layer 50 can be a p-type semiconductor layer, the third semiconductor layer 70 can be a p-type semiconductor layer, and the fourth semiconductor layer 80 can be an n-type semiconductor layer. As another example, the first semiconductor layer 40 can be a p-type semiconductor layer, the second semiconductor layer 50 can be an n-type semiconductor layer, the third semiconductor layer 70 can be an n-type semiconductor layer, and the fourth semiconductor layer 80 can be a p-type semiconductor layer.
The active layer 60 can then be sandwiched between two p-n junctions, and the active layer 60 can be in direct contact with two semiconductor layers (e.g., 50 and 70), one semiconductor layer from one of the p-n junctions and one semiconductor layer from the other p-n junction. In addition, each semiconductor layer in direct contact with the active layer 60 can be of the same type (n-type or p-type). For example, the active layer 60 can be directly on a p-type semiconductor layer (e.g., the second semiconductor layer 50) and directly under and in direct contact with a p-type semiconductor layer (e.g., the third semiconductor layer 70). As another example, the active layer 60 can be in directly on an n-type semiconductor layer (e.g., the second semiconductor layer 50) and directly under and in direct contact with an n-type semiconductor layer (e.g., the third semiconductor layer 70).
In another embodiment, the first semiconductor layer 40 and the third semiconductor layer 70 can be the same type (p-type or n-type), and the second semiconductor layer 50 and the fourth semiconductor layer 80 can be the same type (p-type or n-type). The semiconductor layers in direct contact with the active layer 60 can be of different types (n-type or p-type). For example, the active layer 60 can be in directly on a p-type semiconductor layer (e.g., the second semiconductor layer 50) and directly under and in direct contact with an n-type semiconductor layer (e.g., the third semiconductor layer 70). As another example, the active layer 60 can be in directly on an n-type semiconductor layer (e.g., the second semiconductor layer 50) and directly under and in direct contact with a p-type semiconductor layer (e.g., the third semiconductor layer 70).
In a further embodiment, the second 50 and fourth 80 semiconductor layers are not present, and the first 40 and third 70 semiconductor layers are different types (n-type or p-type). For example, the first semiconductor layer 40 can be an n-type semiconductor layer and the third semiconductor layer 70 can be a p-type semiconductor layer, or the first semiconductor layer 40 can be a p-type semiconductor layer and the third semiconductor layer 70 can be an n-type semiconductor layer. The active layer 60 can be in direct contact with both the first semiconductor layer 40 and the third semiconductor layer 70.
Each semiconductor layer (40, 50, 70, and 80) can be any semiconductor layer known in the art, including an inorganic layer or an organic layer. For example, one or more semiconductor layers (40, 50, 70, and 80) can be ZnS, ZnO, an n-type polymer, a p-type polymer, or any combination thereof, though embodiments are not limited thereto.
The first conducting layer 20 (if present) can be either transparent or opaque, and the second conducting layer 100 (if present) can be either transparent or opaque. For example, the first 20 and second conducting layers 100 can either or both be a transparent electrode, such as a layer including indium tin oxide (ITO), carbon nanotubes (CNTs), indium zinc oxide (IZO), and/or a silver nanowire, though embodiments are not limited thereto.
The first insulating layer 30 (if present) and the second insulating layer 90 (if present) can each include any suitable insulating material known in the art, for example, barium titanium oxide (BaTiO3), a polymer with nanoparticle inclusions (e.g., BaTiO3 nanoparticle inclusions), silicon dioxide, or any combination thereof, though embodiments are not limited thereto. In an embodiment, the first insulating layer 30 and the second insulating layer 90 can include different materials. In an alternative embodiment, the first insulating layer 30 and the second insulating layer 90 can include the same material or materials.
In an embodiment, the substrate 10 (if present) can include a curved aluminum side and a modulated polymer side (e.g., a curved aluminum back and a modulated polymer front). In further embodiments, the substrate 10 (if present) can be any suitable substrate known in the art, such as a silicon substrate, a metal substrate, a polymer substrate, a glass substrate, or any combination thereof, though embodiments are not limited thereto.
In an embodiment, the electroluminescent device can include a first semiconductor layer 40, a second semiconductor layer 50, an active layer 60, a third semiconductor layer 70, and a fourth semiconductor layer 80. The active layer can be in direct contact with both the second 50 and third 70 semiconductor layers. The first 40 and fourth 80 semiconductor layers can each be n-type semiconductor layers, such as n-type zinc oxide (n-ZnO), and the second 50 and third 70 semiconductor layers can each be p-type semiconductor layers, such as p-type zinc sulfide (p-ZnS). The active layer 60 can include ZnS/CaS nanocrystals.
The high density of electrons increases the fraction of the available electrons that take part in excitation (ηexc) and the fraction of radiating atoms (ηlum) due to high probability of collision. Since energy expenditure on electrons tapped at interfacial sites are no longer needed, most of the electrons will have high energies and therefore the fraction of the hot electrons that have sufficient energy to excite the dopants (ηhot) is increased.
The overall efficiency of an electroluminescent device depends on four main contributions: (a) the fraction of the excited dopants that radiatively de-excite (ηlum), which strongly depends on the density of dopants and the density of electrons available for excitation; (b) the fraction of the generated radiation that is extracted due to scattering losses and total-internal-reflection (ηout); (c) the fraction of the available electrons that take part in excitation (ηexc); and (d) the fraction of the hot electrons that have sufficient energy to excite the dopants (ηhot), which depends on the binding energy of the localized electrons in interfacial traps and the applied voltage. Therefore the overall efficiency (ηtotal), can be given by Equation 1.
ηtotal=ηlum+ηout+ηexc+ηhot Equation (1).
Electroluminescent devices according to embodiments of the subject invention affect all four contributions and thus enhance the device performance significantly.
In many embodiments, the active layer 60 can be a ZnS film embedded with nanocrystals. The nanocrystals can be, for example, CaS:Pb2+, La2O3:Bi, CaS:Eu2+, or any combination thereof. CaS:Pb2+, La2O3:Bi can emit in blue, and CaS:Eu2+ can emit in red.
In an embodiment, the active layer 60 can be adjacent to an n-type ZnO layer (either the second semiconductor layer 50 or the third semiconductor layer 70), which can be made n-type by oxygen vacancies, and a p-type ZnS layer can be present, which can be made slightly p-type by nitrogen doping during growth. In an alternative embodiment, the ZnO and ZnS layers can be reversed.
Referring to
The source 200 provides further increase in electron density. When the electrodes (e.g., the two outer electrodes, such as the first 40 and fourth 80 semiconductor layers) are biased with a high voltage, a potential difference exists between these two layers (e.g., these two n-type layers or these two p-type layers). Electrons are injected into the device from the source 200 due to this voltage difference. The amount of current is controlled by an external circuit (not shown), and this allows control of the device power consumption according to the light output required. Any suitable external circuit known in the art can be used.
Advantageously, electroluminescent devices according to embodiments of the subject invention can generate power outputs in a range of 1300 to 1500 μW/cm2 (13 to 15 W/m2).
Referring again to
In many embodiments, the active layer 60 and at least one of the second semiconductor layer 50 and the third semiconductor layer 70 are present, and the active layer 60 is in direct contact with each of these layers that is present. In an embodiment, the second semiconductor layer 50 is formed directly on the first semiconductor layer 40, the active layer 60 is formed directly on the second semiconductor layer 50, and the third 70 and fourth 80 semiconductor layers are not formed. The first 40 and second 50 semiconductor layers can be different types (i.e., the first semiconductor layer 40 can be an n-type semiconductor layer and the second semiconductor layer 50 can be a p-type semiconductor layer, or the first semiconductor layer 40 can be a p-type semiconductor layer and the second semiconductor layer 50 can be an n-type semiconductor layer). In an alternative embodiment, the third semiconductor layer 70 is formed directly on the active layer 60, the fourth semiconductor layer 80 is formed directly on the third semiconductor layer 70, and the first 40 and second 50 semiconductor layers are not formed. The third 70 and fourth 80 semiconductor layers can be different types (i.e., the third semiconductor layer 70 can be a p-type semiconductor layer and the fourth semiconductor layer 80 can be an n-type semiconductor layer, or the third semiconductor layer 70 can be an n-type semiconductor layer and the fourth semiconductor layer 80 can be a p-type semiconductor layer).
In an embodiment, the active layer 60 can be sandwiched between two p-n junctions, and the active layer 60 can be in direct contact with two semiconductor layers (e.g., 50 and 70), one semiconductor layer from one of the p-n junctions and one semiconductor layer from the other p-n junction. In addition, each semiconductor layer in direct contact with the active layer 60 can be of the same type (n-type or p-type). For example, the active layer 60 can be directly on a p-type semiconductor layer (e.g., the second semiconductor layer 50) and directly under and in direct contact with a p-type semiconductor layer (e.g., the third semiconductor layer 70). As another example, the active layer 60 can be in directly on an n-type semiconductor layer (e.g., the second semiconductor layer 50) and directly under and in direct contact with an n-type semiconductor layer (e.g., the third semiconductor layer 70).
In an embodiment, the electroluminescent device can include a first semiconductor layer 40, a second semiconductor layer 50, an active layer 60, a third semiconductor layer 70, and a fourth semiconductor layer 80. The active layer can be in direct contact with both the second 50 and third 70 semiconductor layers. The first 40 and fourth 80 semiconductor layers can each be n-type semiconductor layers, such as n-ZnO, and the second 50 and third 70 semiconductor layers can each be p-type semiconductor layers, such as p-ZnS. The active layer 60 can include ZnS/CaS nanocrystals.
Referring again to
In an embodiment, a method of generating light can include providing an electroluminescent device as described herein.
The invention includes, but is not limited to, the following embodiments:
An electroluminescent device, including:
The electroluminescent device according to embodiment 1, wherein the device includes:
wherein the first p-n junction includes the first semiconductor layer and the second semiconductor layer,
wherein the second p-n junction includes a third semiconductor layer and a fourth semiconductor layer, and
wherein one of the third semiconductor layer and the fourth semiconductor layer is a p-type semiconductor layer and the other is an n-type semiconductor layer.
The electroluminescent device according to embodiment 2, further including:
wherein the first p-n junction is on the first insulating layer.
The electroluminescent device according to any of embodiments 2-3, wherein the active layer includes zinc sulfide/calcium sulfide nanocrystals (ZnS/CaS nanocrystals),
wherein the first semiconductor layer includes n-type zinc oxide (n-ZnO),
wherein the second semiconductor layer is directly under and in physical contact with the active layer and includes p-type zinc sulfide (p-ZnS),
wherein the third semiconductor layer is directly on and in physical contact with the active layer and includes p-ZnS, and
wherein the fourth semiconductor layer includes n-ZnO.
The electroluminescent device according to any of embodiments 2-4, further including a current source connected between the first semiconductor layer and the fourth semiconductor layer.
The electroluminescent device according to any of embodiments 2-5, further including at least one layer selected from the following group:
a first insulating layer directly under and in physical contact with the first p-n junction; and
a second insulating layer directly on and in physical contact with the second p-n junction.
The electroluminescent device according to any of embodiments 2-6, further including at least one layer selected from the following group:
a first conducting layer under the first p-n junction; and
a second conducting layer on the second p-n junction.
The electroluminescent device according to embodiment 7, wherein each conducting layer is transparent.
The electroluminescent device according to any of embodiments 1-8, wherein the active layer includes at least one material selected from the following group:
The electroluminescent device according to any of embodiments 1-5 and 7-9, further including an insulating layer in physical contact with at least one p-n junction.
A method of forming an electroluminescent device, including:
The method according to embodiment 11, wherein the active layer includes at least one material selected from the following group:
The method according to any of embodiments 11-12, further including connecting a current source connected between the first semiconductor layer and the fourth semiconductor layer.
The method according to any of embodiments 11-13, further including:
The method according to any of embodiments 11-14, wherein the active layer includes ZnS/CaS nanocrystals,
wherein the first semiconductor layer includes n-ZnO,
wherein the second semiconductor includes p-ZnS,
wherein the third semiconductor layer includes p-ZnS, and
wherein the fourth semiconductor layer includes n-ZnO.
A method of generating light, including:
providing an electroluminescent device, wherein the device includes:
The method according to embodiment 16, wherein the device includes:
wherein the first p-n junction includes the first semiconductor layer and the second semiconductor layer,
wherein the second p-n junction includes a third semiconductor layer and a fourth semiconductor layer,
wherein one of the third semiconductor layer and the fourth semiconductor layer is a p-type semiconductor layer and the other is an n-type semiconductor layer, and
The method according to any of embodiments 16-17, wherein the active layer includes at least one material selected from the following group:
phosphor particles embedded in a host material, wherein the host material is crystalline or amorphous.
The method according to any of embodiments 16-18, further including:
All patents, patent applications, provisional applications, and publications referred to or cited herein are incorporated by reference in their entirety, including all figures and tables, to the extent they are not inconsistent with the explicit teachings of this specification.
Following are examples that illustrate procedures for practicing the invention. These examples should not be construed as limiting. All percentages are by weight and all solvent mixture proportions are by volume unless otherwise noted.
An electroluminescent device was prepared including an active layer sandwiched between two p-n junctions. A first conducting layer was formed on a substrate, a first insulating layer was formed on the first conducting layer, an n-ZnO layer was formed on the first conducting layer, a p-ZnS layer was formed on the n-ZnO layer, an active layer including ZnS/CaS nanocrystals was formed on the p-ZnS layer, another p-ZnS layer was formed on the active layer, another n-ZnO layer was formed on the p-ZnS layer, a second insulating layer was formed on the n-ZnO layer, and a second conducting layer was formed on the second insulating layer. The band diagram for the p-n junctions and the active layer is shown in
A microwave plasma system for nanoparticle growth was used and consisted of three main regions: (1) nebulizer for 1-1.5 μm aerosol droplets of a precursor; (2) plasma reaction zone where microwave energy generates a high temperature reaction zone for evaporation of solvents and reaction of the chemicals in droplets and plasma gas to form nanophosphors; and (3) substrate placed above the plasma zone for deposition of nanophosphors. The system was modified to accommodate chemical vapor deposition (CVD) of ZnO and ZnS. ZnO coatings were grown by introducing zinc acetylacetonate (Zn(acac)2) vapor as precursor near the substrate. Vapor was generated by heating granules of Zn(acac)2 in a container to 160° C. and pushing the vapor with gas that contained a mixture of argon (Ar) and oxygen. Dimethylzinc and H2S were used for the growth of ZnS films. For safe handling of the chemicals involved, the entire system was place in a fume hood, a picture of which is shown in
The starting point in the fabrication of this structure, a cross section of which is similar to that depicted in
ZnO films were also grown by the CVD process within the microwave plasma system on sputtered BTO films. Growth by CVD is much simpler and cost effective than sputtering. ZnS films were deposited by CVD process with dimethylzinc and H2S gas.
The two phosphor materials to be used to generate blue and red radiation were La2O3:Bi (blue) and CaS:Eu2+ (red), respectively. La2O3:Bi nanoparticles were grown by the microwave plasma process with starting precursors containing aqueous solutions of the nitrates of lanthanum (La) and bismuth (Bi) salts. Depending on the starting concentration, particles of sizes from 5 nm to 100 nm were deposited. Spectrum of light emitted by devices with the two phosphors (separately) and the comparison with a chlorophyll absorption spectrum are shown in
The microwave plasma process allows control of nanophosphor particle sizes by controlling the precursor concentration. La2O3:Bi nanophosphors were deposited in single crystal form with sizes from 5 nm to 100 nm by changing the starting concentration. Transmission Electron Microscopy (TEM) images in
The second BTO layer was sputter deposited at low temperature. Silver ink was used as the back electrode. Each coating was analyzed by X-ray diffraction for crystallinity and absorption spectroscopy for light transmission.
Light output measurements: One of the devices fabricated by the steps outlined above and the observed blue and red emission from these devices are shown in
Light emitting from each excited doped ion is directed radially in 3D. The light falling on the opaque back contact is reflected to the front. The percentage of light that is extracted from the front surface can be dependent on the refractive indices of the layers. The refractive indices of the materials forming the layers, (e.g., ZnS, CdS, ZnO, BTO, and ITO), are in the range of 2.01 to 2.3. The refractive index of BTO nanoparticle embedded polyimide, which can be spin-coated as the transparent insulating layer, can approach values closer to 1.99. Therefore, the critical angles for total internal reflection are large and most of the light is directed towards the glass substrate. However, the critical angle at the glass-air interface is closer to about 45.6°, which corresponds to an angle of about 28° at the film-glass interface.
Therefore, referring to
The BTO, ZnO, ZnS, and/or phosphor/ZnS composite coatings can be evaluated by one or more of the following methods: Morphological and Structural evaluation, such as atomic force microscopy (AFM), scanning electron microscopy (SEM-EDX), and X-ray diffraction (XRD); Optical characterization, such as emission, absorption, and photoluminescence spectroscopy (PL); and/or Optical emission intensity, such as being measured by an integrated sphere.
It should be understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application. In addition, any elements or limitations of any invention or embodiment thereof disclosed herein can be combined with any and/or all other elements or limitations (individually or in any combination) or any other invention or embodiment thereof disclosed herein, and all such combinations are contemplated with the scope of the invention without limitation thereto.
This application claims the benefit of U.S. Provisional Application Ser. No. 61/666,461, filed Jun. 29, 2012, which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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61666461 | Jun 2012 | US |