[go: up one dir, main page]

WO2018114744A1 - Source de lumière à semi-conducteur émettant de la lumière blanche - Google Patents

Source de lumière à semi-conducteur émettant de la lumière blanche Download PDF

Info

Publication number
WO2018114744A1
WO2018114744A1 PCT/EP2017/083206 EP2017083206W WO2018114744A1 WO 2018114744 A1 WO2018114744 A1 WO 2018114744A1 EP 2017083206 W EP2017083206 W EP 2017083206W WO 2018114744 A1 WO2018114744 A1 WO 2018114744A1
Authority
WO
WIPO (PCT)
Prior art keywords
light source
light
emitting
primary
source according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2017/083206
Other languages
English (en)
Inventor
Ralf Petry
Ingo Koehler
Thomas Juestel
Matthias Mueller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Patent GmbH
Original Assignee
Merck Patent GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck Patent GmbH filed Critical Merck Patent GmbH
Publication of WO2018114744A1 publication Critical patent/WO2018114744A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
    • C09K11/77Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
    • C09K11/7728Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing europium
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
    • C09K11/77Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
    • C09K11/77Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
    • C09K11/7715Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing cerium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J29/00Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
    • H01J29/02Electrodes; Screens; Mounting, supporting, spacing or insulating thereof
    • H01J29/10Screens on or from which an image or pattern is formed, picked up, converted or stored
    • H01J29/18Luminescent screens
    • H01J29/20Luminescent screens characterised by the luminescent material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02BCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
    • Y02B20/00Energy efficient lighting technologies, e.g. halogen lamps or gas discharge lamps

Definitions

  • This present invention relates to specific solid state light sources with incandescent dimming behaviour, and more particularly to
  • LEDs semiconductor light emitting diodes
  • LDs laser diodes
  • OLEDs organic light emitting diodes
  • white light emitting solid state light sources mostly comprises a high brightness blue light emitting semiconductor chip based on (In.Ga)N [see S. Nakamura et al., Appl. Phys. Lett. 67, p 1868 (1995)] and a luminescent screen.
  • the light source works as an efficient pump exciting a luminescent material which returns to its ground state by emitting green, yellow, or red light.
  • Additive colour mixing results in a broadband emission spectrum which is perceived as white light.
  • the principle of this colour conversion process is well-founded in the pronounced Stokes Shift (electron-phonon coupling) between absorption and emission of
  • Nichia Chemical Industries Ltd. introduced a white LED, that uses a luminescent layer comprising YsAlsO ⁇ Ce (YAG:Ce) or Y3(Al i -x Ga x )5Oi 2:Ce (YAGaG:Ce) to convert blue light emitted by an (ln,Ga)N LED into a broad band yellow emission spectrum, that peaks at about 565 nm.
  • the emission band is sufficiently broad to produce white light in the colour temperature range from about 5,000 to about 8,000 K, and a colour rendering index (CRI) of about 77 - 85.
  • a first object of the present invention is directed to is a white light emitting solid state light source exhibiting an incandescent-like dimming behaviour which is adapted to be operated at an excitation density of about 0.1 to about 100 W/mm 2 , preferably about 0.5 to about 50 W/mm 2 and most preferred about 1 to about 20 W/mm 2 comprising or consisting of
  • said luminescent layer comprises at least one phosphor that is activated by at least two cations selected from the group consisting of Ce 3+ , Mn 2+ , Pr 3+ and Eu 2+ .
  • excitation density is determined according to DIN 50564/VDE 0705-2301 ("Messunglac
  • a solid light source according to the present invention comprising a phosphor in its luminescent layer that is co-activated by specific ion couples comprising Ce 3+ , Mn 2+ , Pr 3+ and Eu 2+ display luminescence in the green to red spectral range, whereby the long decay time of Mn 2+ results in bleaching of the Mn 2+ upon a high excitation density.
  • the claimed light source exhibits spectral properties and dimming behaviour similar to those known from incandescent lamps.
  • the colour temperature is rather low, typically below 3,000 K, while dimming behaviour is equal to that of
  • the present invention fulfils all requirements to solve the problem as described above.
  • the primary light source of the present invention is either a semiconductor LED, a semiconductor laser diode (LD) or an organic light emitting diode (OLED). More particularly preferred are those sources emitting light within the spectral range of about 385 to about 480 nm, preferably about 390 to about 450 nm and most preferred about 400 to 440 nm.
  • the light sources according to the present invention are in particular characterized by
  • LED Light emitting diodes
  • a light-emitting diode (LED) forming a first group of suitable primary light sources is a two-lead semiconductor light source. It is a p-n junction diode, which emits light when activated. When a suitable voltage is applied to the leads, electrons are able to recombine with electron holes within the device, releasing energy in the form of photons. This effect is called electroluminescence, and the colour of the light (corresponding to the energy of the photon) is determined by the energy band gap of the semiconductor.
  • a p-n junction can convert absorbed light energy into a proportional electric current.
  • the same process is reversed here (i.e. the p-n junction emits light when electrical energy is applied to it).
  • This phenomenon is generally called electroluminescence, which can be defined as the emission of light from a semi-conductor under the influence of an electric field.
  • the charge carriers recombine in a forward-biased p-n junction as the electrons cross from the n-region and recombine with the holes existing in the p- region. Free electrons are in the conduction band of energy levels, while holes are in the valence energy band. Thus the energy level of the holes will be lesser than the energy levels of the electrons. Some portion of the energy must be dissipated in order to recombine the electrons and the holes. This energy is emitted in the form of heat and light.
  • the electrons dissipate energy in the form of heat for silicon and germanium diodes but in gallium arsenide phosphide (GaAsP) and gallium phosphide (GaP) semiconductors, the electrons dissipate energy by emitting photons. If the semiconductor is translucent, the junction becomes the source of light as it is emitted, thus becoming a light-emitting diode, but when the junction is reverse biased no light will be produced by the LED and, on the contrary, the device may also be damaged.
  • GaAsP gallium arsenide phosphide
  • GaP gallium phosphide
  • the LED consists of a chip of semiconducting
  • the wavelength of the light emitted, and thus its colour, depends on the band gap energy of the materials forming the p-n junction.
  • the electrons and holes usually recombine by a non-radiative transition, which produces no optical emission, because these are indirect band gap materials.
  • the materials used for the LED have a direct band gap with energies corresponding to near-infrared, visible, or near-ultraviolet light.
  • LEDs are usually built on an n-type substrate, with an electrode attached to the p-type layer deposited on its surface. P-type substrates, while less common, occur as well. Many commercial LEDs, especially GaN/lnGaN, also use sapphire substrate.
  • bare uncoated semiconductors such as silicon exhibit a very high refractive index relative to open air, which prevents passage of photons arriving at sharp angles relative to the air-contacting surface of the semiconductor due to total internal reflection. This property affects both the light-emission efficiency of LEDs as well as the light-absorption efficiency of photovoltaic cells.
  • the refractive index of silicon is 3.96 (at 590 nm), while air is 1 .0002926.
  • a flat-surface uncoated LED semiconductor chip will emit light only perpendicular to the semiconductor's surface, and a few degrees to the side, in a cone shape referred to as the light cone, cone of light, or the escape cone. The maximum angle of incidence is referred to as the critical angle. When this angle is exceeded, photons no longer escape the semiconductor but are instead reflected internally inside the
  • a convoluted chip surface with angled facets similar to a jewel or Fresnel lens can increase light output by allowing light to be emitted perpendicular to the chip surface while far to the sides of the photon emission point.
  • the ideal shape of a semiconductor with maximum light output would be a microsphere with the photon emission occurring at the exact centre, with electrodes penetrating to the centre to contact at the emission point. All light rays emanating from the centre would be
  • a hemispherical semiconductor would also work, with the flat back-surface serving as a mirror to back-scattered photons.
  • a preferred embodiment of the present invention encompasses so-called “Chip-on-board” (COB) LED comprising one or more chips.
  • COB Chip-on-board
  • COB COB according to the following geometry: diameter of the ring: about 1 to about 10 and preferably about 5 mm around the ring. Once the ring is filled its height is about 0.5 mm resulting in a volume of ab 10 mm 3 .
  • said chips show a feed size of about 800 to about 1 ,200 ⁇ and preferably of about 1 ,000 ⁇ corresponding to an area of about 1 mm 2 .
  • the free space above the chip amounts to about 200 to about 300 ⁇ and preferably about 250 ⁇ , which is equivalent to the magnitude of the phosphor layer above the surface of said chips.
  • the phosphors useful for operating COB chips comprise about 10 to about 100 mg and preferably about 20 mg silicones corresponding to an amount of up to 50 % of said phosphor or a mass of up to 10 mg, which are distributed over an area of about 10 mm 2 and a volume of about 20 mm 3 .
  • a laser diode, or LD also known as injection laser diode or ILD, is an electrically pumped semiconductor laser in which the active laser medium is formed by a p-n junction of a semiconductor diode similar to that found in a light-emitting diode.
  • the laser diode is the most common type of laser produced with a wide range of uses that include fibre optic communications, barcode readers, laser pointers, CD/DVD/Blu-ray Disc reading and recording, laser printing, laser scanning and increasingly directional lighting sources.
  • a laser diode is a PIN diode.
  • the active region of the laser diode is in the intrinsic (I) region and the carriers (electrons and holes) are pumped into that region from the N and P regions respectively.
  • I intrinsic
  • the carriers electrospray
  • the carriers and the photons are confined in order to maximize their chance for recombination and light generation.
  • the goal for a laser diode is to recombine all carriers in the I region, and produce light.
  • laser diodes are fabricated using direct bandgap semiconductors.
  • the laser diode epitaxial structure is grown using one of the crystal growth techniques, usually starting from an N doped substrate, and growing the I doped active layer, followed by the P doped cladding, and a contact layer.
  • the active layer most often consists of quantum wells, which provide lower threshold current and higher efficiency.
  • Laser diodes form a subset of the larger classification of
  • diode lasers are semiconductor devices, they may also be classified as semiconductor lasers. Either designation distinguishes diode lasers from solid-state lasers.
  • OPSL Optically pumped semiconductor lasers
  • an electron and a hole When an electron and a hole are present in the same region, they may recombine or "annihilate" producing a spontaneous emission— i.e., the electron may re-occupy the energy state of the hole, emitting a photon with energy equal to the difference between the electron's original state and hole's state.
  • the energy released from the recombination of electrons and holes is carried away as phonons, i.e., lattice vibrations, rather than as photons.
  • Spontaneous emission below the lasing threshold produces similar properties to an LED. Spontaneous emission is necessary to initiate laser oscillation, but it is one among several sources of inefficiency once the laser is oscillating.
  • photon-emitting semiconductor laser and a conventional phonon-emitting (non-light-emitting) semiconductor junction diode lies in the type of semiconductor used, one whose physical and atomic structure confers the possibility for photon emission.
  • These photon-emitting semiconductors are the so-called "direct bandgap" semiconductors.
  • Other materials, the so-called compound semiconductors have virtually identical crystalline structures as silicon or germanium but use alternating
  • Gallium arsenide, indium phosphide, gallium antimonide, and gallium nitride are all examples of compound semiconductor materials that can be used to create junction diodes that emit light.
  • recombination energy can cause recombination by stimulated emission.
  • This generates another photon of the same frequency, polarization, and phase , travelling in the same direction as the first photon.
  • stimulated emission will cause gain in an optical wave (of the correct wavelength) in the injection region, and the gain increases as the number of electrons and holes injected across the junction increases.
  • the gain region is surrounded with an optical cavity to form a laser.
  • an optical waveguide is made on that crystal's surface, such that the light is confined to a relatively narrow line.
  • the two ends of the crystal are cleaved to form perfectly smooth, parallel edges, forming a Fabry-Perot resonator.
  • Photons emitted into a mode of the waveguide will travel along the waveguide and be reflected several times from each end face before they exit.
  • a light wave passes through the cavity, it is amplified by stimulated emission, but light is also lost due to absorption and by incomplete reflection from the end facets.
  • the diode begins to "lase".
  • Some important properties of laser diodes are determined by the geometry of the optical cavity. Generally, the light is contained within a very thin layer, and the structure supports only a single optical mode in the direction perpendicular to the layers. In the transverse direction, if the waveguide is wide compared to the wavelength of light, then the waveguide can support multiple transverse optical modes, and the laser is known as "multi-mode". These transversely multi-mode lasers are adequate in cases where one needs a very large amount of power, but not a small diffraction- limited beam; for example in printing, activating chemicals,
  • the waveguide In applications where a small focused beam is needed, the waveguide must be made narrow, on the order of the optical wavelength. This way, only a single transverse mode is supported and one ends up with a diffraction-limited beam.
  • Such single spatial mode devices are used for optical storage, laser pointers, and fiber optics. Note that these lasers may still support multiple longitudinal modes, and thus can lase at multiple wavelengths simultaneously.
  • the wavelength emitted is a function of the band-gap of the semiconductor material and the modes of the optical cavity. In general, the maximum gain will occur for photons with energy slightly above the band-gap energy, and the modes nearest the peak of the gain curve will lase most strongly.
  • Single spatial mode lasers that can support multiple longitudinal modes are called Fabry Perot (FP) lasers.
  • An FP laser will work at multiple cavity modes within the gain bandwidth of the lasing medium.
  • the number of lasing modes in an FP laser is usually unstable, and can fluctuate due to changes in current or temperature.
  • Single spatial mode diode lasers can be designed so as to operate on a single longitudinal mode. These single frequency diode lasers exhibit a high degree of stability, and are used in spectroscopy and metrology, and as frequency references.
  • Single frequency diode lasers classed as either distributed feedback (DFB) lasers or distributed Bragg reflector (DBR) lasers.
  • DBR distributed Bragg reflector
  • Double heterostructure laser (DH Laser).
  • a layer of low bandgap material is sandwiched between two high bandgap layers.
  • One commonly-used pair of materials is gallium arsenide (GaAs) with aluminium gallium arsenide (Al x Ga(i -X )As).
  • GaAs gallium arsenide
  • Al x Ga(i -X )As aluminium gallium arsenide
  • Each of the junctions between different bandgap materials is called a heterostructure, hence the name "double heterostructure laser” or DH laser.
  • the kind of laser diode described in the first part of the article may be referred to as
  • a homojunction laser for contrast with these more popular devices.
  • the advantage of a DH laser is that the region where free electrons and holes exist simultaneously— the active region— is confined to the thin middle layer. This means that many more of the electron-hole pairs can contribute to amplification— not so many are left out in the poorly amplifying periphery. In addition, light is reflected from the heterojunction; hence, the light is confined to the region where the amplification takes place.
  • Quantum Well Lasers If the middle layer is made thin enough, it acts as a quantum well. This means that the vertical variation of the electron's wave-function, and thus a component of its energy, is quantized.
  • the efficiency of a quantum well laser is greater than that of a bulk laser because the density of states function of electrons in the quantum well system has an abrupt edge that concentrates electrons in energy states that contribute to laser action.
  • Lasers containing more than one quantum well layer are known as multiple quantum well lasers. Multiple quantum wells improve the overlap of the gain region with the
  • optical waveguide mode Further improvements in the laser efficiency have also been demonstrated by reducing the quantum well layer to a quantum wire or to a "sea" of quantum dots.
  • Quantum Cascade Lasers In a quantum cascade laser, the difference between quantum well energy levels is used for the laser transition instead of the bandgap. This enables laser action at relatively long wavelengths, which can be tuned simply by altering the thickness of the layer. They are heterojunction lasers.
  • Interband Cascade Lasers An interband cascade laser (ICL) is a type of laser diode that can produce coherent radiation over a large part of the mid-infrared region of the electromagnetic spectrum.
  • ICL interband cascade laser
  • the problem with the simple quantum well diode described above is that the thin layer is simply too small to effectively confine the light.
  • another two layers are added on, outside the first three. These layers have a lower refractive index than the centre layers, and hence confine the light effectively.
  • Such a design is called a separate confinement heterostructure (SCH) laser diode. Almost all commercial laser diodes since the 1990s have been SCH quantum well diodes.
  • SCH confinement heterostructure
  • a distributed Bragg reflector laser is a type of single frequency laser diode. It is characterized by an optical cavity consisting of an electrically or optically pumped gain region between two mirrors to provide feedback. One of the mirrors is a broadband reflector and the other mirror is wavelength selective so that gain is favoured on a single longitudinal mode, resulting in lasing at a single resonant frequency.
  • the broadband mirror is usually coated with a low reflectivity coating to allow emission.
  • the wavelength selective mirror is a periodically structured diffraction grating with high reflectivity. The diffraction grating is within a non-pumped, or passive region of the cavity.
  • a DBR laser is a monolithic single chip device with the grating etched into the semiconductor. DBR lasers can be edge emitting lasers or VCSELs.
  • DFL Distributed Feedback Laser
  • a distributed feedback laser is a type of single frequency laser diode. DFBs are the most common transmitter type in DWDM-systems.
  • a diffraction grating is etched close to the p-n junction of the diode. This grating acts like an optical filter, causing a single wavelength to be fed back to the gain region and lase. Since the grating provides the feedback that is required for lasing, reflection from the facets is not required. Thus, at least one facet of a DFB is anti-reflection coated.
  • the DFB laser has a stable wavelength that is set during manufacturing by the pitch of the grating, and can only be tuned slightly with temperature.
  • DFB lasers are widely used in optical communication applications where a precise and stable wavelength is critical.
  • the threshold current of this DFB laser based on its static characteristic, is around 1 1 mA.
  • the appropriate bias current in a linear regime could be taken in the middle of the static characteristic (50 mA).
  • VCSEL Vertical-cavity surface-emitting lasers
  • the active region length is very short compared with the lateral dimensions so that the radiation emerges from the surface of the cavity rather than from its edge.
  • VCSELs have lower output powers when compared to edge-emitting lasers.
  • Edge- emitters cannot be tested until the end of the production process. If the edge-emitter does not work, whether due to bad contacts or poor material growth quality, the production time and the processing materials have been wasted.
  • VCSELs emit the beam perpendicular to the active region of the laser as opposed to parallel as with an edge emitter, tens of thousands of VCSELs can be processed simultaneously on a three- inch gallium arsenide wafer.
  • the yield can be controlled to a more predictable outcome. However, they normally show a lower power output level.
  • VECSEL Vertical external-cavity surface-emitting lasers, or VECSELs, are similar to VCSELs. In VCSELs, the mirrors are typically grown epitaxially as part of the diode structure, or grown separately and bonded directly to the semiconductor containing the active region.
  • VECSELs are distinguished by a construction in which one of the two mirrors is external to the diode structure. As a result, the cavity includes a free-space region. A typical distance from the diode to the external mirror would be 1 cm.
  • One of the most interesting features of any VECSEL is the small thickness of the semiconductor gain region in the direction of propagation, less than 100 nm.
  • a conventional in-plane semiconductor laser entails light propagation over distances of from 250 ⁇ upward to 2 mm or longer. The significance of the short propagation distance is that it causes the effect of "anti-guiding" nonlinearities in the diode laser gain region to be minimized.
  • VECSELs include projection displays, served by frequency doubling of near-IR VECSEL emitters to produce blue and green light.
  • External Cavity Diode Lasers EDL
  • external-cavity diode lasers are tunable lasers which use mainly double heterostructure diodes of the Al x Ga(i-x)As type.
  • the first external-cavity diode lasers used intracavity etalons and simple tuning Littrow gratings.
  • Other designs include gratings in grazing-incidence configuration and multiple-prism grating configurations.
  • OLED Organic Light Emitting Diodes
  • a third group of suitable primary light sources encompasses so-called organic light emitting diodes (OLED) in which the emissive electroluminescent layer is a film of organic compound that emits light in response to an electric current.
  • This layer of organic semiconductor is situated between two electrodes; typically, at least one of these electrodes is transparent.
  • OLEDs are used to create digital displays in devices such as television screens, computer monitors, portable systems such as mobile phones, handheld game console sand PDAs.
  • a major area of research is the development of white OLED devices for use in solid-state
  • OLED displays can use either passive- matrix (PMOLED) or active-matrix (AMOLED) addressing schemes. Active- matrix OLEDs (AMOLED) require a thin-film transistor backplane to switch each individual pixel on or off, but allow for higher resolution and larger display sizes.
  • An OLED display works without a backlight; thus, it can display deep black levels and can be thinner and lighter than a liquid crystal display (LCD). In low ambient light conditions (such as a dark room), an OLED screen can achieve a higher contrast ratio than an LCD, regardless of whether the LCD uses cold cathode fluorescent lamps or an LED backlight.
  • a typical OLED is composed of a layer of organic materials situated between two electrodes, the anode and cathode, all deposited on
  • the organic molecules are electrically conductive as a result of derealization of pi electrons caused by conjugation over part or all of the molecules. These materials have conductivity levels ranging from insulators to conductors, and are therefore considered organic semiconductors.
  • the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO) of organic semiconductors are analogous to
  • OLEDs Originally, the most basic polymer OLEDs consisted of a single organic layer. However, multilayer OLEDs can be fabricated with two or more layers in order to improve device efficiency. As well as conductive properties, different materials may be chosen to aid charge injection at electrodes by providing a more gradual electronic profile or block a charge from reaching the opposite electrode and being wasted. Many modern OLEDs incorporate a simple bilayer structure, consisting of a conductive layer and an emissive layer. More recent developments in OLED
  • graded heterojunction architecture improve quantum efficiency (up to 19%) by using a graded heterojunction.
  • the composition of hole and electron-transport materials varies continuously within the emissive layer with a dopant emitter.
  • a voltage is applied across the OLED such that the anode is positive with respect to the cathode.
  • Anodes are picked based upon the quality of their optical transparency, electrical conductivity, and chemical stability.
  • a current of electrons flows through the device from cathode to anode, as electrons are injected into the LUMO of the organic layer at the cathode and withdrawn from the HOMO at the anode. This latter process may also be described as the injection of electron holes into the HOMO.
  • Electrostatic forces bring the electrons and the holes towards each other and they recombine forming an exciton, a bound state of the electron and hole. This happens closer to the emissive layer, because in organic semiconductors holes are generally more mobile than electrons.
  • the decay of this excited state results in a relaxation of the energy levels of the electron, accompanied by emission of radiation whose frequency is in the visible region.
  • the frequency of this radiation depends on the band gap of the material, in this case the difference in energy between the HOMO and LUMO.
  • an exciton may either be in a singlet state or a triplet state depending on how the spins of the electron and hole have been combined. Statistically three triplet excitons will be formed for each singlet exciton. Decay from triplet states (phosphorescence) is spin forbidden, increasing the timescale of the transition and limiting the internal efficiency of fluorescent
  • Phosphorescent organic light-emitting diodes make use of spin- orbit interactions to facilitate intersystem crossing between singlet and triplet states, thus obtaining emission from both singlet and triplet states and improving the internal efficiency.
  • ITO Indium tin oxide
  • a typical conductive layer may consist of PEDOTPSS as the HOMO level of this material generally lies between the work function of ITO and the HOMO of other commonly used polymers, reducing the energy barriers for hole injection.
  • Metals such as barium and calcium are often used for the cathode as they have low work functions which promote injection of electrons into the LUMO of the organic layer. Such metals are reactive, so they require a capping layer of aluminium to avoid degradation.
  • anode/hole transport layer (HTL) interface topography plays a major role in the efficiency, performance, and lifetime of organic light emitting diodes.
  • Imperfections in the surface of the anode decrease anode- organic film interface adhesion, increase electrical resistance, and allow for more frequent formation of non-emissive dark spots in the OLED material adversely affecting lifetime.
  • Mechanisms to decrease anode roughness for ITO/glass substrates include the use of thin films and self-assembled monolayers.
  • alternative substrates and anode materials are being considered to increase OLED performance and lifetime. Possible examples include single crystal sapphire substrates treated with gold (Au) film anodes yielding lower work functions, operating voltages, electrical resistance values, and increasing lifetime of OLEDs.
  • Single carrier devices are typically used to study the kinetics and charge transport mechanisms of an organic material and can be useful when trying to study energy transfer processes.
  • As current through the device is composed of only one type of charge carrier, either electrons or holes, recombination does not occur and no light is emitted.
  • electron only devices can be obtained by replacing ITO with a lower work function metal which increases the energy barrier of hole injection.
  • hole only devices can be made by using a cathode made solely of aluminium, resulting in an energy barrier too large for efficient electron injection.
  • OLEDs using small molecules were first developed by C.W. Tang et al. at Eastman Kodak.
  • the term OLED traditionally refers specifically to this type of device, though the term SM-OLED is also in use.
  • Molecules commonly used in OLEDs include organometallic chelates (for example Alq3, used in the organic light-emitting device reported by Tang et a/.), fluorescent and phosphorescent dyes and conjugated dendrimers.
  • organometallic chelates for example Alq3, used in the organic light-emitting device reported by Tang et a/.
  • fluorescent and phosphorescent dyes and conjugated dendrimers.
  • a number of materials are used for their charge transport properties, for example triphenylamine and derivatives are commonly used as materials for hole transport layers.
  • Fluorescent dyes can be chosen to obtain light emission at different wavelengths, and
  • Alq3 has been used as a green emitter, electron transport material and as a host for yellow and red emitting dyes.
  • PLED Polymer light-emitting diodes
  • LEP light-emitting polymers
  • Vacuum deposition is not a suitable method for forming thin films of polymers.
  • polymers can be processed in solution, and spin coating is a common method of depositing thin polymer films. This method is more suited to forming large-area films than thermal evaporation. No vacuum is required, and the emissive materials can also be applied on the substrate by a technique derived from commercial inkjet printing.
  • the metal cathode may still need to be deposited by thermal evaporation in vacuum.
  • An alternative method to vacuum deposition is to deposit a Langmuir-Blodgett film.
  • Typical polymers used in pleaded displays include derivatives of poly(p-phenylene vinylene) and polyfluorene. Substitution of side chains onto the polymer backbone may determine the colour of emitted light or the stability and solubility of the polymer for performance and ease of processing.
  • PNVs that are soluble in organic solvents or water have been prepared via ring opening metathesis polymerization.
  • CPEs conjugated poly electrolytes
  • Phosphorescent organic light emitting diodes use the principle of electrophosphorescence to convert electrical energy in an OLED into light in a highly efficient manner, with the internal quantum efficiencies of such devices approaching 100%.
  • a polymer such as poly(N-vinylcarbazole) is used as a host material to which an organometallic complex is added as a
  • Iridium complexes such as lr(mppy)3 are currently the focus of research, although complexes based on other heavy metals such as platinum have also been used.
  • the heavy metal atom at the centre of these complexes exhibits strong spin-orbit coupling, facilitating intersystem crossing between singlet and triplet states.
  • both singlet and triplet excitons will be able to decay radiatively, hence improving the internal quantum efficiency of the device compared to a standard pleaded where only the singlet states will contribute to emission of light.
  • the organic electroluminescent device according to the invention particularly preferably has the following structure: anode / orange- or red- phosphorescent emitter layer / interlayer 1 / interlayer 2 / cathode.
  • Suitable matrix materials for the phosphorescent compound are various materials as used in accordance with the prior art as matrix materials for phosphorescent compounds.
  • Suitable matrix materials for the phosphorescent emitter are aromatic ketones, in particular selected from compounds of the formula (1 ) depicted above or aromatic phosphine oxides or aromatic sulfoxides or sulfones, for example in accordance with WO 04/013080, WO 04/093207 or WO 06/005627, triarylamines, carbazole derivatives, for example CBP ( ⁇ , ⁇ -biscarbazolylbiphenyl), mCBP or the carbazole derivatives disclosed in WO 05/039246, US 2005/0069729, JP 2004/288381 , EP 1205527 or WO 08/086851 , indolocarbazole derivatives, for example in accordance with WO 07/063754 or WO
  • Semiconductors forming an essential part of the light sources of the present invention are selected from the group of species capable of emitting radiation in the blue spectral range, such as for example ZnSe, or SiC.
  • the preferred semiconductors are chosen either from GaN or (ln,Ga)N.
  • the most preferred OLED are based on lr 3+ , Pt 2+ , or Cu + emitters.
  • the luminescent layer according to the present invention is capable of emitting primary radiation in the green to red spectral range (about 500 to about 700 nm).
  • said luminescent layer comprises at least one phosphor containing two different activator ions for the application as a colour conversion screen onto blue light emitting radiation sources, e.g. based onto an InGaN LED, an InGaN laser diode, or onto an organic light emitting diode (OLED).
  • the phosphors used in the luminescent layer give rise to good LED qualities.
  • the LED quality is described here via conventional parameters, such as the colour rendering index (CRI), the correlated colour temperature (CCT), lumen equivalent, absolute lumen flux, or the colour point in
  • the colour rendering index is a dimensionless lighting quantity, familiar to the person skilled in the art, which compares the colour reproduction faithfulness of an artificial light source with that of solar light or filament light sources (the latter two have a CRI of 100).
  • the correlated colour temperature is a lighting quantity, familiar to the person skilled in the art, with the unit Kelvin. The higher the numerical value, the higher the blue content of the light and the colder the white light from an artificial radiation source appears to the observer.
  • the CCT follows the concept of the black body radiator, whose colour temperature describes the so-called Planck curve in the CIE diagram.
  • the lumen equivalent is a lighting quantity, familiar to the person skilled in the art, with the unit Im/W which describes the magnitude of the photometric luminous flux in lumens of a light source at a certain
  • radiometric radiation power with the unit watt The higher the lumen equivalent, the more efficient a light source.
  • the lumen is a photometric lighting quantity, familiar to the person skilled in the art, which describes the luminous flux of a light source, which is a measure of the total visible radiation emitted by a radiation source. The greater the luminous flux, the brighter the light source appears to the observer.
  • CIE x and CIE y stand for the coordinates in the standard CIE colour chart (here standard observer 1931 ), familiar to the person skilled in the art, by means of which the colour of a light source is described.
  • UV light denotes light whose emission maximum is ⁇ 400 nm
  • near UV light denotes light whose emission maximum is between 370-400nm
  • violet light denotes light whose emission maximum is between 401 and 430 nm
  • blue light denotes light whose emission maximum is between 431 and 470 nm
  • cyan-coloured light denotes light whose emission maximum is between 471 and 505 nm
  • green light denotes light whose emission maximum is between 506 and 560 nm
  • yellow light denotes light whose emission maximum is between 561 and 575 nm
  • orange light denotes light whose emission maximum is between 576 and 600 nm
  • red light denotes light whose emission maximum is between 601 and 700 nm.
  • Luminescent compositions doped by one of these ion couples solely absorb blue light due to the sensitizing ions, i.e. Eu 2+ and Ce 3+ , respectively, since Mn 2+ does not exhibit states in the blue spectral range with sufficient absorption cross section.
  • the luminescent compositions can be excited over a broad range, which extends from about 300 nm to 440 nm, preferably 350 nm to about 420 nm.
  • the maximum of the excitation curve is usually at about 350 to 400 nm, depending on the exact
  • halophosphates is not dependent on the fluorescent lamp driving conditions, since the excitation density is in all kind of lamps not higher than 0.1 W/mm 2 and thus much too low for the saturation of the Mn 2+ emission, which would result in a blue shift of the colour point.
  • the luminescent layer which is deposited onto a blue-emitting semiconductor LED, is exposed to a very high excitation density, viz. 0.1 - 100 W/mm 2 , and thus saturation of the Mn 2+ emission will be observed. Therefore, a blue shift of the colour point by enhancing the driving current can be expected. This will be even more pronounced, if laser diodes will be used as a pump source.
  • the present invention is exemplified by a white light emitting pcLED employing CaS:Ce,Mn as a colour converter.
  • suitable phosphors are selected from the group consisting of oxides, nitrides, oxynitrides, sulphides, oxysulfides and their mixtures.
  • silicates, alumosilicates and garnets preferably selected from the group consisting of (Y,Gd,Tb,Lu)3Al5- xSixOi2-xN x :X,Y (0 ⁇ x ⁇ 5), BaMgAli 0 Oi 7 :X,Y, SrAI 2 O 4 :X,Y, Sr 4 Ah 4 O 2 5:X,Y, (Ca,Sr,Ba)Si 2 N 2 O 2 :Eu, SrSiAI 2 O 3 N 2 :X,Y, (Ca,Sr,Ba) 2 Si 5 N 8 :X,Y,
  • the phosphors may be coated.
  • Suitable for this purpose are all coating methods as are known to the person skilled from the prior art and are used for phosphors.
  • Suitable materials for the coating are, in particular, metal oxides and nitrides, in particular alkaline-earth metal oxides, such as AI2O3, and alkaline-earth metal nitrides, such as AIN, as well as S1O2.
  • the coating can be carried out here, for example, by fluidised-bed methods or by wet-chemical methods. Suitable coating methods are disclosed, for example, in JP 04-304290, WO 91 /10715, WO 99/27033, US 2007/0298250, WO 2009/065480 and WO 2010/075908.
  • the aim of the coating can on the one hand be higher stability of the phosphors, for example to air or moisture. However, the aim may also be improved coupling-in and -out of light through a suitable choice of the surface of the coating and the refractive indices of the coating material.
  • the phosphors may also be coated with organic materials, for example with siloxanes. This may have advantages with respect to the dispersibility in a resin during production of the LEDs.
  • Another object of the present invention refers to a method for providing a cosy indoor illumination comprising the following steps:
  • a luminescent layer comprising at least one phosphor that is activated by at least two cations selected from the group consisting of Ce 3+ , Mn 2+ , Pr 3+ and Eu 2+ being capable of emitting primary radiation, said luminescent layer being deposited on said primary light source, and
  • said primary light source is either a semiconductor LED, a semiconductor laser diode (LD) or an organic light emitting diode (OLED).
  • LD semiconductor laser diode
  • OLED organic light emitting diode
  • a final object of the present invention is related to the use of the light source as claimed above for indoor illumination purposes.
  • the following example illustrates the present invention by means of a white LED light source comprising a 460 nm emitting (ln,Ga)N die and a luminescence layer comprising CaS:CeMn as a colour converter.
  • CaS:Ce(0.1 %)Mn(1 .0%) is suspended into a silicone precursor, typically used for the packaging of InGaN LEDs.
  • concentration in the suspension is selected that between 10 and 300 g of the phosphor is deposited onto the semiconductor chip having a surface area of about 1 mm 2 .
  • a catalyst is added to polymerize the silicon precursor, and the LED is sealed by a transparent plastic cap.
  • Fig. 1 Principle of sensitizer-mediated excitation.
  • Fig. 2 Emission spectra of a white light emitting pcLED as function of the driving current.
  • Fig. 3 CIE 1931 colour point of a white LED comprising
  • Fig. 4 Emission spectra of CaS:Ce(0.1 )Mn(x%) as function of the Mn 2+ concentration.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Luminescent Compositions (AREA)

Abstract

Il est proposé une source de lumière à semi-conducteur émettant de la lumière blanche présentant un comportement de gradation de type incandescent qui fonctionne à une densité d'excitation d'environ 0,1 à environ 100 W/mm2, comprenant ou consistant en (a) une source de lumière primaire ; (b) une couche luminescente pouvant émettre un rayonnement primaire déposé sur ladite source de lumière primaire ; et (c) un écran luminescent pouvant convertir ledit rayonnement primaire en un rayonnement adapté à l'éclairage concerné, ladite couche luminescente comprenant au moins un luminophore qui est activé par au moins deux cations choisis dans le groupe constitué de Ce3+, Mn2+, Pr3+, et Eu2+.
PCT/EP2017/083206 2016-12-20 2017-12-18 Source de lumière à semi-conducteur émettant de la lumière blanche Ceased WO2018114744A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP16205570 2016-12-20
EP16205570.1 2016-12-20

Publications (1)

Publication Number Publication Date
WO2018114744A1 true WO2018114744A1 (fr) 2018-06-28

Family

ID=57570876

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2017/083206 Ceased WO2018114744A1 (fr) 2016-12-20 2017-12-18 Source de lumière à semi-conducteur émettant de la lumière blanche

Country Status (2)

Country Link
TW (1) TW201830688A (fr)
WO (1) WO2018114744A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11215753B2 (en) * 2020-02-27 2022-01-04 Taiwan Semiconductor Manufacturing Company, Ltd. Photonic semiconductor device and method

Citations (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991010715A1 (fr) 1990-01-22 1991-07-25 Gte Laboratories Incorporated Phosphores presentant une amelioration du flux lumineux et lampes realisees a partir de ceux-ci
JPH04304290A (ja) 1991-03-29 1992-10-27 Nichia Chem Ind Ltd 蛍光体及びその製造方法
KR930010521B1 (ko) * 1990-09-26 1993-10-25 삼성전관 주식회사 황색 형광체
EP0652273A1 (fr) 1993-11-09 1995-05-10 Shinko Electric Industries Co. Ltd. Matériau organique pour dispositif électroluminescent et dispositif électroluminescent
WO1999027033A1 (fr) 1997-11-26 1999-06-03 Minnesota Mining And Manufacturing Company Couches de carbone en forme de losange recouvrant des phosphores inorganiques
WO2000070655A2 (fr) 1999-05-13 2000-11-23 The Trustees Of Princeton University Dispositifs electroluminescents organiques a tres haute performance utilisant l'electrophosphorescence
WO2001041512A1 (fr) 1999-12-01 2001-06-07 The Trustees Of Princeton University Complexes de forme l2mx en tant que dopants phosphorescents pour del organiques
WO2002002714A2 (fr) 2000-06-30 2002-01-10 E.I. Du Pont De Nemours And Company Composes d'iridium electroluminescents contenant des phenylpyridines fluores, des phenylpyrimidines et des phenylquinolines, et dispositifs fabriques avec ces composes
WO2002015645A1 (fr) 2000-08-11 2002-02-21 The Trustees Of Princeton University Composes organometalliques et electrophosphorescence organique presentant un deplacement d'emission
EP1191613A2 (fr) 2000-09-26 2002-03-27 Canon Kabushiki Kaisha Dispositif luminescent, dispositif d'affichage et composé complexe d'un métal
EP1191612A2 (fr) 2000-09-26 2002-03-27 Canon Kabushiki Kaisha Dispositif luminescent, dispositif d'affichage et composé complexe d'un métal
EP1191614A2 (fr) 2000-09-26 2002-03-27 Canon Kabushiki Kaisha Dispositif luminescent et composé complexe d'un métal utilisé pour ce dispositif
EP1205527A1 (fr) 2000-03-27 2002-05-15 Idemitsu Kosan Co., Ltd. Dispositif a electroluminescence organique
WO2004013080A1 (fr) 2002-08-01 2004-02-12 Covion Organic Semiconductors Gmbh Derives de spirobifluorene, leur preparation et leurs utilisations
WO2004081017A1 (fr) 2003-03-11 2004-09-23 Covion Organic Semiconductors Gmbh Complexes metalliques
JP2004288381A (ja) 2003-03-19 2004-10-14 Konica Minolta Holdings Inc 有機エレクトロルミネッセンス素子
WO2004093207A2 (fr) 2003-04-15 2004-10-28 Covion Organic Semiconductors Gmbh Melanges de semi-conducteurs organiques aptes a l'emission et de matieres matricielles, leur utilisation et composants electroniques contenant ces melanges
US20050069729A1 (en) 2003-09-30 2005-03-31 Konica Minolta Holdings, Inc. Organic electroluminescent element, illuminator, display and compound
WO2005033244A1 (fr) 2003-09-29 2005-04-14 Covion Organic Semiconductors Gmbh Complexes metalliques
WO2005042550A1 (fr) 2003-10-30 2005-05-12 Merck Patent Gmbh Complexes metalliques a ligands bipodes
WO2005111172A2 (fr) 2004-05-11 2005-11-24 Merck Patent Gmbh Nouveaux melanges de materiaux pour applications electroluminescentes
WO2005113563A1 (fr) 2004-05-19 2005-12-01 Merck Patent Gmbh Complexes metalliques
JP2005347160A (ja) 2004-06-04 2005-12-15 Konica Minolta Holdings Inc 有機エレクトロルミネッセンス素子、照明装置及び表示装置
EP1617711A1 (fr) 2003-04-23 2006-01-18 Konica Minolta Holdings, Inc. Dispositif organique electroluminescent et affichage
WO2006005627A1 (fr) 2004-07-15 2006-01-19 Merck Patent Gmbh Derives oligomeres de spirobifluorene, leur elaboration et leur utilisation
WO2006008069A1 (fr) 2004-07-16 2006-01-26 Merck Patent Gmbh Complexes metalliques
US7053543B2 (en) * 2000-03-01 2006-05-30 Koninklijke Philips Electronics N.V. Plasma picture screen with blue phospor
JP2006140262A (ja) * 2004-11-11 2006-06-01 Nemoto & Co Ltd 半導体発光装置
WO2006061182A1 (fr) 2004-12-09 2006-06-15 Merck Patent Gmbh Complexes metalliques et leur utilisation en tant que composants d'emission dans des elements electroniques, notamment dans des dispositifs d'affichage electroluminescents
WO2006081973A1 (fr) 2005-02-03 2006-08-10 Merck Patent Gmbh Complexes metalliques
WO2006117052A1 (fr) 2005-05-03 2006-11-09 Merck Patent Gmbh Dispositif electroluminescent organique, et derives d'acide boronique et d'acide borinique utilises pour produire ce dispositif electroluminescent organique
EP1731584A1 (fr) 2004-03-31 2006-12-13 Konica Minolta Holdings, Inc. Matériau de dispositif électroluminescent organique, dispositif électroluminescent organique, écran et dispositif d'éclairage
US20070046176A1 (en) * 2005-04-27 2007-03-01 Spudnik,Inc. Phosphor Compositions For Scanning Beam Displays
WO2007063754A1 (fr) 2005-12-01 2007-06-07 Nippon Steel Chemical Co., Ltd. Compose pour element electroluminescent organique et element electroluminescent organique
WO2007137725A1 (fr) 2006-05-31 2007-12-06 Merck Patent Gmbh Nouveaux matériaux pour dispositifs électroluminescents organiques
US20070298250A1 (en) 2006-06-22 2007-12-27 Weimer Alan W Methods for producing coated phosphor and host material particles using atomic layer deposition methods
WO2008056746A1 (fr) 2006-11-09 2008-05-15 Nippon Steel Chemical Co., Ltd. Composé pour un dispositif électroluminescent organique et dispositif électroluminescent organique
WO2008086851A1 (fr) 2007-01-18 2008-07-24 Merck Patent Gmbh Dérivés de carbazole pour des dispositifs électroluminescents organiques
WO2009062578A1 (fr) 2007-11-12 2009-05-22 Merck Patent Gmbh Dispositifs organiques électroluminescents contenant des complexes azométhine/métal
WO2009065480A1 (fr) 2007-11-22 2009-05-28 Merck Patent Gmbh Substances luminescentes à surface modifiée
DE102008036982A1 (de) 2008-08-08 2010-02-11 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
DE102008056688A1 (de) 2008-11-11 2010-05-12 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
WO2010075908A1 (fr) 2008-12-08 2010-07-08 Merck Patent Gmbh Substances luminescentes à surface modifiée à base de silicate
US8946982B2 (en) 2007-11-12 2015-02-03 Merck Patent Gmbh Coated phosphor particles with refractive index adaption
DE102014113068A1 (de) * 2014-09-10 2016-03-10 Seaborough Ip I B.V. Lichtemittierende Vorrichtung
WO2016092743A1 (fr) * 2014-12-12 2016-06-16 パナソニックIpマネジメント株式会社 Dispositif électroluminescent

Patent Citations (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991010715A1 (fr) 1990-01-22 1991-07-25 Gte Laboratories Incorporated Phosphores presentant une amelioration du flux lumineux et lampes realisees a partir de ceux-ci
KR930010521B1 (ko) * 1990-09-26 1993-10-25 삼성전관 주식회사 황색 형광체
JPH04304290A (ja) 1991-03-29 1992-10-27 Nichia Chem Ind Ltd 蛍光体及びその製造方法
EP0652273A1 (fr) 1993-11-09 1995-05-10 Shinko Electric Industries Co. Ltd. Matériau organique pour dispositif électroluminescent et dispositif électroluminescent
WO1999027033A1 (fr) 1997-11-26 1999-06-03 Minnesota Mining And Manufacturing Company Couches de carbone en forme de losange recouvrant des phosphores inorganiques
WO2000070655A2 (fr) 1999-05-13 2000-11-23 The Trustees Of Princeton University Dispositifs electroluminescents organiques a tres haute performance utilisant l'electrophosphorescence
WO2001041512A1 (fr) 1999-12-01 2001-06-07 The Trustees Of Princeton University Complexes de forme l2mx en tant que dopants phosphorescents pour del organiques
US7053543B2 (en) * 2000-03-01 2006-05-30 Koninklijke Philips Electronics N.V. Plasma picture screen with blue phospor
EP1205527A1 (fr) 2000-03-27 2002-05-15 Idemitsu Kosan Co., Ltd. Dispositif a electroluminescence organique
WO2002002714A2 (fr) 2000-06-30 2002-01-10 E.I. Du Pont De Nemours And Company Composes d'iridium electroluminescents contenant des phenylpyridines fluores, des phenylpyrimidines et des phenylquinolines, et dispositifs fabriques avec ces composes
WO2002015645A1 (fr) 2000-08-11 2002-02-21 The Trustees Of Princeton University Composes organometalliques et electrophosphorescence organique presentant un deplacement d'emission
EP1191613A2 (fr) 2000-09-26 2002-03-27 Canon Kabushiki Kaisha Dispositif luminescent, dispositif d'affichage et composé complexe d'un métal
EP1191612A2 (fr) 2000-09-26 2002-03-27 Canon Kabushiki Kaisha Dispositif luminescent, dispositif d'affichage et composé complexe d'un métal
EP1191614A2 (fr) 2000-09-26 2002-03-27 Canon Kabushiki Kaisha Dispositif luminescent et composé complexe d'un métal utilisé pour ce dispositif
WO2004013080A1 (fr) 2002-08-01 2004-02-12 Covion Organic Semiconductors Gmbh Derives de spirobifluorene, leur preparation et leurs utilisations
WO2004081017A1 (fr) 2003-03-11 2004-09-23 Covion Organic Semiconductors Gmbh Complexes metalliques
JP2004288381A (ja) 2003-03-19 2004-10-14 Konica Minolta Holdings Inc 有機エレクトロルミネッセンス素子
WO2004093207A2 (fr) 2003-04-15 2004-10-28 Covion Organic Semiconductors Gmbh Melanges de semi-conducteurs organiques aptes a l'emission et de matieres matricielles, leur utilisation et composants electroniques contenant ces melanges
EP1617711A1 (fr) 2003-04-23 2006-01-18 Konica Minolta Holdings, Inc. Dispositif organique electroluminescent et affichage
EP1617710A1 (fr) 2003-04-23 2006-01-18 Konica Minolta Holdings, Inc. Materiau pour dispositif electroluminescent organique, dispositif electroluminescent organique, dispositif d'eclairage et affichage
WO2005033244A1 (fr) 2003-09-29 2005-04-14 Covion Organic Semiconductors Gmbh Complexes metalliques
US20050069729A1 (en) 2003-09-30 2005-03-31 Konica Minolta Holdings, Inc. Organic electroluminescent element, illuminator, display and compound
WO2005039246A1 (fr) 2003-09-30 2005-04-28 Konica Minolta Holdings, Inc. Dispositif electroluminescent organique, dispositif d'eclairage et afficheur
WO2005042550A1 (fr) 2003-10-30 2005-05-12 Merck Patent Gmbh Complexes metalliques a ligands bipodes
EP1731584A1 (fr) 2004-03-31 2006-12-13 Konica Minolta Holdings, Inc. Matériau de dispositif électroluminescent organique, dispositif électroluminescent organique, écran et dispositif d'éclairage
WO2005111172A2 (fr) 2004-05-11 2005-11-24 Merck Patent Gmbh Nouveaux melanges de materiaux pour applications electroluminescentes
WO2005113563A1 (fr) 2004-05-19 2005-12-01 Merck Patent Gmbh Complexes metalliques
JP2005347160A (ja) 2004-06-04 2005-12-15 Konica Minolta Holdings Inc 有機エレクトロルミネッセンス素子、照明装置及び表示装置
WO2006005627A1 (fr) 2004-07-15 2006-01-19 Merck Patent Gmbh Derives oligomeres de spirobifluorene, leur elaboration et leur utilisation
WO2006008069A1 (fr) 2004-07-16 2006-01-26 Merck Patent Gmbh Complexes metalliques
JP2006140262A (ja) * 2004-11-11 2006-06-01 Nemoto & Co Ltd 半導体発光装置
WO2006061182A1 (fr) 2004-12-09 2006-06-15 Merck Patent Gmbh Complexes metalliques et leur utilisation en tant que composants d'emission dans des elements electroniques, notamment dans des dispositifs d'affichage electroluminescents
WO2006081973A1 (fr) 2005-02-03 2006-08-10 Merck Patent Gmbh Complexes metalliques
US20070046176A1 (en) * 2005-04-27 2007-03-01 Spudnik,Inc. Phosphor Compositions For Scanning Beam Displays
WO2006117052A1 (fr) 2005-05-03 2006-11-09 Merck Patent Gmbh Dispositif electroluminescent organique, et derives d'acide boronique et d'acide borinique utilises pour produire ce dispositif electroluminescent organique
WO2007063754A1 (fr) 2005-12-01 2007-06-07 Nippon Steel Chemical Co., Ltd. Compose pour element electroluminescent organique et element electroluminescent organique
WO2007137725A1 (fr) 2006-05-31 2007-12-06 Merck Patent Gmbh Nouveaux matériaux pour dispositifs électroluminescents organiques
US20070298250A1 (en) 2006-06-22 2007-12-27 Weimer Alan W Methods for producing coated phosphor and host material particles using atomic layer deposition methods
WO2008056746A1 (fr) 2006-11-09 2008-05-15 Nippon Steel Chemical Co., Ltd. Composé pour un dispositif électroluminescent organique et dispositif électroluminescent organique
WO2008086851A1 (fr) 2007-01-18 2008-07-24 Merck Patent Gmbh Dérivés de carbazole pour des dispositifs électroluminescents organiques
WO2009062578A1 (fr) 2007-11-12 2009-05-22 Merck Patent Gmbh Dispositifs organiques électroluminescents contenant des complexes azométhine/métal
US8946982B2 (en) 2007-11-12 2015-02-03 Merck Patent Gmbh Coated phosphor particles with refractive index adaption
WO2009065480A1 (fr) 2007-11-22 2009-05-28 Merck Patent Gmbh Substances luminescentes à surface modifiée
DE102008036982A1 (de) 2008-08-08 2010-02-11 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
DE102008056688A1 (de) 2008-11-11 2010-05-12 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
WO2010075908A1 (fr) 2008-12-08 2010-07-08 Merck Patent Gmbh Substances luminescentes à surface modifiée à base de silicate
DE102014113068A1 (de) * 2014-09-10 2016-03-10 Seaborough Ip I B.V. Lichtemittierende Vorrichtung
WO2016092743A1 (fr) * 2014-12-12 2016-06-16 パナソニックIpマネジメント株式会社 Dispositif électroluminescent

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
S. NAKAMURA ET AL., APPL. PHYS. LETT., vol. 67, 1995, pages 1868
ZIHAN XU ET AL: "Full color control and white emission from CaZnOS:Ce 3+ ,Na + ,Mn 2+ phosphors via energy transfer", JOURNAL OF MATERIALS CHEMISTRY C: MATERIALS FOR OPTICAL AND ELECTRONIC DEVICES, vol. 4, no. 41, 1 January 2016 (2016-01-01), UK, pages 9711 - 9716, XP055462523, ISSN: 2050-7526, DOI: 10.1039/C6TC03016E *

Also Published As

Publication number Publication date
TW201830688A (zh) 2018-08-16

Similar Documents

Publication Publication Date Title
US5966393A (en) Hybrid light-emitting sources for efficient and cost effective white lighting and for full-color applications
Kozlov et al. Temperature independent performance of organic semiconductor lasers
Heeger Light emission from semiconducting polymers: light-emitting diodes, light-emitting electrochemical cells, lasers and white light for the future
JP5176459B2 (ja) 白色発光素子
Gupta et al. Low-threshold amplified spontaneous emission in blends of conjugated polymers
Zhao et al. Efficient short‐wave infrared light‐emitting diodes based on heavy‐metal‐free quantum dots
Nakamura GaN-based blue/green semiconductor laser
US8237152B2 (en) White light emitting device based on polariton laser
Li et al. White-light-emitting diodes using semiconductor nanocrystals
KR20200063221A (ko) 다층 양자점 led 및 이를 제조하는 방법
CN101461069A (zh) 多量子阱结构、发射辐射的半导体本体和发射辐射的器件
Nakamura InGaN‐based blue/green LEDs and laser diodes
Feng et al. Light‐Emitting Device Based on Amplified Spontaneous Emission
JP6058946B2 (ja) 複数の活性層を有する窒化物半導体素子、窒化物半導体発光素子、窒化物半導体受光素子、及び、窒化物半導体素子の製造方法
Shei et al. Emission mechanism of mixed-color InGaN/GaN multi-quantum-well light-emitting diodes
US20240172462A1 (en) Organic electroluminescent devices
Chang et al. Si and Zn co-doped InGaN-GaN white light-emitting diodes
US7151282B2 (en) Light emitting diode
Mei et al. Tunable InGaN quantum dot microcavity light emitters with 129 nm tuning range from yellow-green to violet
WO2018114744A1 (fr) Source de lumière à semi-conducteur émettant de la lumière blanche
US6665329B1 (en) Broadband visible light source based on AllnGaN light emitting diodes
Stath et al. The status and future development of innovative optoelectronic devices based on III-nitrides on SiC and on III-antimonides
JP5060823B2 (ja) 半導体発光素子
US12068583B2 (en) Surface emitting laser device and light emitting device including the same
Peng 6 Organic/Polymer Luminescent

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17821557

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17821557

Country of ref document: EP

Kind code of ref document: A1