WO2007080555A1 - Dispositif émetteur de lumière convertie par une substance fluorescente - Google Patents

Dispositif émetteur de lumière convertie par une substance fluorescente Download PDF

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Publication number
WO2007080555A1
WO2007080555A1 PCT/IB2007/050114 IB2007050114W WO2007080555A1 WO 2007080555 A1 WO2007080555 A1 WO 2007080555A1 IB 2007050114 W IB2007050114 W IB 2007050114W WO 2007080555 A1 WO2007080555 A1 WO 2007080555A1
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Prior art keywords
phosphor
light
light emitting
light emitted
disposed
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PCT/IB2007/050114
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English (en)
Inventor
Gerd O. Mueller
Regina B. Mueller-Mach
Thomas Juestel
Petra Huppertz
Detlef U. Wiechert
Dominik Uhlich
Original Assignee
Koninklijke Philips Electronics N.V.
Philips Lumileds Lighting Company, Llc
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Priority claimed from US11/623,068 external-priority patent/US7446343B2/en
Application filed by Koninklijke Philips Electronics N.V., Philips Lumileds Lighting Company, Llc filed Critical Koninklijke Philips Electronics N.V.
Priority to CN200780002475.2A priority Critical patent/CN101370906B/zh
Priority to EP07700585.8A priority patent/EP1979438B1/fr
Publication of WO2007080555A1 publication Critical patent/WO2007080555A1/fr

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Definitions

  • the present invention relates to phosphor-converted semiconductor light emitting devices.
  • LEDs light emitting diodes
  • RCLEDs resonant cavity light emitting diodes
  • VCSELs vertical cavity laser diodes
  • edge emitting lasers are among the most efficient light sources currently available.
  • Materials systems currently of interest in the manufacture of high-brightness light emitting devices capable of operation across the visible spectrum include Group III-V semiconductors, particularly binary, ternary, and quaternary alloys of gallium, aluminum, indium, and nitrogen, also referred to as Ill-nitride materials.
  • Ill-nitride light emitting devices are fabricated by epitaxially growing a stack of semiconductor layers of different compositions and dopant concentrations on a sapphire, silicon carbide, Ill-nitride, or other suitable substrate by metal-organic chemical vapor deposition (MOCVD), molecular beam epitaxy (MBE), or other epitaxial techniques.
  • MOCVD metal-organic chemical vapor deposition
  • MBE molecular beam epitaxy
  • the stack often includes one or more n-type layers doped with, for example, Si, formed over the substrate, one or more light emitting layers in an active region formed over the n-type layer or layers, and one or more p-type layers doped with, for example, Mg, formed over the active region. Electrical contacts are formed on the n- and p-type regions.
  • the light generated by III- nitride devices can be readily converted to produce light having a longer wavelength.
  • light having a first peak wavelength (the "primary light") can be converted into light having a longer peak wavelength (the “secondary light”) using a process known as luminescence/fluorescence.
  • the fluorescent process involves absorbing the primary light by a wavelength-converting material such as a phosphor and exciting the luminescent centers of the phosphor material, which emit the secondary light.
  • the peak wavelength of the secondary light will depend on the phosphor material.
  • the type of phosphor material can be chosen to yield secondary light having a particular peak wavelength.
  • the light emitting device and phosphor material are selected such that the combined primary and secondary light appear white.
  • a conventional white light phosphor converted LED a Ill-nitride die that emits blue light is combined with a phosphor that emits yellow light, such as YsAIsOi 2 )Ce 3+ .
  • Such white light devices typically have undesirable color rendering properties since the combined light is deficient in the red region of the visible light spectrum.
  • U.S. Patent 6,351,069 describes a phosphor-converted LED including two phosphors, a first phosphor that emits yellow light and a second phosphor that emits red light.
  • a phosphor converted light emitting device includes a semiconductor structure comprising a light emitting layer disposed between an n-type region and a p-type region, the light emitting layer being configured to emit light having a first peak wavelength; a first phosphor configured to emit light having a second peak wavelength; and a second phosphor configured to emit light having a third peak wavelength.
  • the second phosphor is an Eu + activated phosphor, configured such that in the excitation spectrum at 298K and 1.013 bar, a maximum intensity in a wavelength range between 460 nm and 470 nm is at least 5% of a maximum intensity in a wavelength range between 220 nm to 320 nm.
  • Fig. 1 shows an excitation spectrum of a Y 2 ⁇ 3 :Eu material with weak absorption at wavelengths greater than 300 nm.
  • Fig. 2 shows an emission spectrum of the material of Fig. 1.
  • Fig. 3 shows an excitation spectrum of a first example of an Eu-comprising material according to embodiments of the present invention.
  • Fig. 4 shows an emission spectrum of the material of Fig. 3.
  • Fig. 5 shows an excitation spectrum of a second example of an Eu-comprising material according to embodiments of the present invention.
  • Fig. 6 shows an emission spectrum of the material of Fig. 5.
  • Fig. 7 shows an excitation spectrum of a third example of an Eu-comprising material according to embodiments of the present invention.
  • Fig. 8 shows an emission spectrum of the material of Fig. 7.
  • Fig. 9 shows an excitation spectrum of a fourth example of an Eu-comprising material according embodiments of the present invention.
  • Fig. 10 shows an emission spectrum of the material of Fig. 9.
  • Figs. 11 and 12 show emission spectra of devices according to embodiments of the present invention.
  • Fig. 13 illustrates a device including an LED, a luminescent ceramic, and a phosphor disposed in a transparent layer.
  • Fig. 14 illustrates a device including an LED and two luminescent ceramics.
  • Fig. 15 illustrates a device including an LED, a conformal phosphor layer, and a phosphor disposed in a transparent layer.
  • Fig. 16 is an exploded view of a packaged light emitting device.
  • Eu 2+ activated red emitting phosphors are undesirably unstable because of the tendency OfEu 2+ to oxidize or react with other components present in the light emitting device.
  • Another drawback Of Eu 2+ activated red-emitting phosphors is their relatively wide emission band, which results in a low lumen equivalent.
  • Eu + activated red-emitting phosphors are generally more stable over their lifetime as compared to Eu 2+ activated phosphors, but Eu 3+ activated phosphors generally are strongly absorbing only in the very short wavelength UV-C and VUV spectral ranges, while the absorption is very weak at longer wavelengths, particularly visible wavelengths. Poor absorption at longer wavelengths disfavors the application of such Eu 3+ phosphors in phosphor-converted light emitting devices, since the emission wavelength of efficient high brightness LEDs used in such devices is generally within the near UV-A spectral range above 350nm or within the blue spectral range, much longer wavelengths than the wavelength range in which such Eu 3+ activated phosphors are strongly absorbing.
  • a phosphor converted light emitting device includes an Eu 3+ activated red emitting phosphor with an excitation spectrum suitable for use with a blue-emitting LED.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm at least 5% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • the term "intensity" denotes the amount of absorbed light (corresponding to an absorption strength).
  • the Eu 3+ activated red phosphor at least 90%, more preferably at least 95%, and more preferably at least 98% of the Eu atoms in the phosphor are in the form Of Eu 3+ .
  • the spectral (absorption and emission) properties Of Eu 3+ materials are more stable over time as compared to Eu 2+ materials, since Eu 3+ does not oxidize as readily as Eu 2+ . Accordingly, the fewer Eu 2+ atoms, the better the lifetime behavior of the phosphor material.
  • a light-emitting device may be operated efficiently with LEDs with blue primary light.
  • the absorption strength of a converting element depends on the absorption strength of the material itself and on the thickness of the converting element in the primary light propagation direction.
  • a more effective light conversion material (high absorption strength of the material itself) according to embodiments of the invention may enable the application of thinner phosphor materials for more compact devices, and/or may reduce the risk of re-absorption of the secondary light and following radiation-less transition, leading to an enhanced efficiency of the light emitting device due to a thinner converting element.
  • LEDs emitting within the UV-A spectral range may also be combined with a phosphor material according to the embodiments of the present invention.
  • the peak area in the wavelength range between 680 nm to 720 nm is at least 15% of the peak area in the wavelength range between 570 nm to 720 nm.
  • Such devices show deep red emission characteristics in that for some applications efficiencies of 100 - 200 Lumen/Watt are feasible. Such devices may also show improved color point stability due to the stability of the red phosphor.
  • the term "peak area" denotes the integral amount of light within the specified wavelength range.
  • the atomic dopant level (in atom-% of the trivalent cation of the host lattice) of Eu in the Eu 3+ activated phosphor material is up to and including 20%.
  • Higher Eu 3+ concentration may lead to pronounced energy transfer of the absorbed energy to the surface and defect sites and thus to quenching of the Eu + luminescence, a phenomenon known as concentration quenching.
  • the Eu + activated phosphor material further comprises a co-dopant M selected from the group comprising Bi, In, Tl, Sb or mixtures thereof.
  • M co-dopant
  • these additional dopants are elements with a large number of electrons on d-orbitals, which increases the electron density to enhance the absorption capability of Eu 3+ within the host lattice.
  • the atomic dopant concentration of M (in atom-%) in the Eu 3+ activated material is up to 20%. Higher M 3+ concentration may lead to pronounced energy transfer of the absorbed energy to the surface and defect sites and thus to quenching of the activator luminescence.
  • the ratio of Eu (in atom-%) to M (in atom-%) in the Eu 3+ activated material is 0.1 : 1 to 10 : 1. If more than one co-dopant is present, in the above ratio of Eu:M, M may represent the sum of all co-dopants.
  • the Eu 3+ activated phosphor material is selected from the group of oxides, oxyhalogenides, garnets, vanadates, tungstates, borates, silicates, germanates or mixtures thereof. These materials offer a high electron density at the sites of the oxygen anions within the host lattice, leading to improved absorption properties OfEu 3+ .
  • the Eu 3+ activated phosphor material is selected from the group of (Gdi_ x _ z Lu x )2 ⁇ 3:Eu z , (Y 1-x-y- z Gd x Lu y ) 3 Al 5 0i2:Eu z , Ba 2 (Yi-X- Y -ZGd x LUy) 2 Si 4 OiSiEUz, (Y 1-x- y -zGd x Luy)VO 4 :Euz, (Yi- x -y-zGd x Lu y )OF:Eu z , (Yi- x - y .
  • a light-emitting device may be of use in a broad variety of systems and/or applications, including one or more of the following: office lighting systems, household application systems, shop lighting systems, home lighting systems, accent lighting systems, spot lighting systems, theater lighting systems, fiber-optic application systems, projection systems, self-lit display systems, pixelated display systems, segmented display systems, warning sign systems, medical lighting application systems, indicator sign systems, decorative lighting systems, portable systems, automotive applications, and green house lighting systems.
  • Figs. 1 and 2 show the excitation and emission spectra of an Y 2 OsIEu material with a Eu-doping level of 5%. While the absorption of the Eu + phosphor in the UV-C and VUV spectral range is strong, it is very weak below the low energy edge of the charge transfer state around 300nm. This weak absorption at wavelengths greater than 300 nm prevents the application Of Eu 3+ phosphors with spectra as illustrated in Figs. 1 and 2 in phosphor converted light emitting diodes, since the minimum emission wavelength for efficient high brightness LEDs is generally at least 370nm, which is outside the strong absorption wavelength range the Y 2 OsIEu phosphor material.
  • the absorption lines around 395nm ( 7 Fo - 5 Ds) and 465nm ( 7 Fo - 5 D 2 ) are spin forbidden 4f-4f transitions and therefore very weak absorption lines.
  • Red line-emitting Eu 3+ phosphors according to embodiments of the invention have relatively strong absorption of UV-A radiation and/or blue radiation due to the enhancement of the weak absorption lines at around 395nm ( 7 Fo - 5 Ds) and 465nm ( 7 Fo - 5 D 2 ). This is achieved by using lattices with a high covalency or by co-doping the host lattice by ions having the [Ar]3d 10 , [Kr]4d 10 or [Xe ⁇ f 14 Sd 10 electron configuration.
  • the spin forbidden character of the 4 f-4f transitions of Eu + is relaxed to a certain extent, which results in an enhanced absorption strength of these transitions.
  • the improved absorption properties enable the efficient application of these materials as a color converter for organic or inorganic state of the art light emitting diodes with emission wavelengths in the UV-A and/or blue spectral range.
  • Suitable Eu-comprising phosphor materials for the absorption enhancement according to the present invention are high covalent lattices such as (Gdi_ x Lu x ) 2 Os:Eu, (Y 1-x- y Gd x Lu y ) 3 Al 5 0i 2 :Eu, (Yi_ x _ y Gd x Luy)VO 4 :Eu, (Yi_ x _ y Gd x Lu y )OF:Eu z , (Yi_ x _ y Gd x Lu y )OCl:Eu, Ba(Yi_ x _yGd x Lu y )B 9 Oi6:Eu, Ba 3 (Yi- x -yGd x Luy)(BO 3 )s :Eu, (Yi_ x _ y Gd x Lu y ) 2 Si0 5 :Eu, (Cai_ a Sr a
  • Eu 3+ is surrounded by ions with high negative charge density. Suitable Eu-doping levels are up to atomic 20%. Within these materials, Eu 3+ exhibits a strong covalent interaction with the host lattice influencing the transition probability of the spin forbidden transition in comparison to atomic transition probabilities.
  • the covalent interaction of Eu 3+ with the host lattices can be even more enhanced by co-doping of the host lattice with other triple positive charged ions such as Bi 3+ , In 3+ , Tl 3+ or Sb 3+ or mixtures thereof.
  • suitable In 3+ co-doping levels are up to atomic 10%.
  • the atomic dopant level of M in the Eu-comprising phosphor material is up to 5%.
  • the atomic dopant level of M in the Eu-comprising phosphor material is up to 1%.
  • the ratio in atom% of Eu to M in the Eu-comprising phosphor material is between 0.5:1 and 5:1. According to an embodiment of the present invention, the ratio in atom% of Eu to M in the Eu-comprising phosphor material is 1 : 1 to 3 : 1. When more than one co-dopant M is present, the M term in the above ratios represents the sum of all co-dopants.
  • the absorbed excitation energy is generally released by secondary radiation with longer wavelength.
  • the excited D-levels relax radiation- less to the excited D-ground state 5 Do.
  • transitions to the 7 F 2 state are allowed, while transitions to the 7 F 4 state leading to a deep red emission are spin- forbidden.
  • deep red emission with wavelengths around 700nm are preferred.
  • the high electron density of the Eu 3+ -comprising phosphor materials according to the present invention also influences the emission properties, where the spin forbidden transition 5 Do ⁇ 7 F4 is enhanced in comparison to the allowed transition 5 Do ⁇ 7 F 2 .
  • Figs. 3 and 4 show the excitation and emission spectra of LaOChEu.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is about 21% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • the peak area in the wavelength range between 680 nm and 720 nm is 22% of the peak area in the wavelength range between 570 nm and 720 nm.
  • Figs. 5 and 6 show the excitation and emission spectra of Sr3ln2Ge3 ⁇ i2:Eu.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is about 25% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • Fig. 5 shows the excitation and emission spectra of Sr3ln2Ge3 ⁇ i2:Eu.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is about 25% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • the peak area in the wavelength range between 680 nm and 720 nm is 25% of the peak area in the wavelength range between 570 nm and 720 nm.
  • Figs. 7 and 8 show the excitation and emission spectra OfY 2 SiOsIEu.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is about 11% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • the peak area in the wavelength range between 680 nm and 720 nm is 21% of the peak area in the wavelength range between 570 nm and 720 nm.
  • Figs. 9 and 10 show the excitation and emission spectra of Ca3Ga2Ge3 ⁇ i2:Eu.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is about 11% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • the peak area in the wavelength range between 680 nm and 720 nm is 27% of the peak area in the wavelength range between 570 nm and 720 nm.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is at least 10% of the maximum intensity in the wavelength range between 220 nm and 320 nm, as shown for examples III and IV above.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is at least 15% of the maximum intensity in the wavelength range between 220 nm and 320 nm.
  • the maximum intensity in the wavelength range between 460 nm and 470 nm is at least 20% of the maximum intensity in the wavelength range between 220 nm and 320 nm, as shown for examples I and II above.
  • the peak area in the wavelength range between 680 nm and 720 nm is at least 20% of the peak area in the wavelength range between 570 nm and 720 nm, as shown for examples I, II, III, and IV above.
  • Other Eu-comprising phosphor materials may exhibit different peak area ratios.
  • Fig. 11 shows an emission spectrum of an LED according to an embodiment of the present invention.
  • the LED was manufactured as follows: a powder mixture of 20% (Y,Gd)3Al 5 Oi2:Ce and 80% Y 2 SiOsIEu was suspended in a fluid silicone precursor compound. A drop of this silicone precursor was placed on an LED die emitting light of the wavelength 465 nm, then the silicone was polymerized. The LED was then sealed with a plastic lens.
  • Fig. 11 illustrates that the resulting LED shows good optical characteristics with a T c value of 3000 K.
  • Fig. 12 shows an emission spectrum of an LED according to an embodiment of the present invention.
  • the LED was manufactured as follows: a powder mixture of 20% (Y,Gd)3Al 5 Oi2:Ce and 80% LaOCl:Eu was suspended in a fluid silicone precursor compound. A drop of this silicone precursor was placed on an LED die emitting light of the wavelength 465 nm, then the silicone was polymerized. The LED is then sealed with a plastic lens.
  • Fig. 12 illustrates that the resulting LED shows good optical characteristics with a T c value of 3100 K.
  • Eu-doping levels different from 5atom% can be chosen in order to adapt for instance the converting element size or the spectral properties of the converting element to the desired application.
  • the spectra of the Eu-comprising materials according to the present invention were measured with an in-house built spectrofluorimeter system.
  • the light source of this spectrofluorimeter system is a 150W Xe-lamp in an airflow-cooled housing.
  • the lamp output is focused on the entrance slit of the excitation monochromator (Bentham) with a focal length of 0.5 m.
  • the escaping light from the exit slit of the excitation monochromator is fed into a sample chamber and focused onto the sample material under test via several mirrors. While the sample under test is oriented horizontally, the optical axis of the excitation and the emission branch are oriented vertically and nearly parallel. This geometric orientation ensures reliable and quantitative comparative measurements of different samples.
  • the sample chamber is coupled optically to the emission monochromator (Bentham, focal length 0.5m) via a mirror system. Detection of the emitted light occurs with a thermo-electrically cooled photomultiplier tube (PMT) unit mounted to the exit slit of the emission monochromator.
  • PMT thermo-electrically cooled photomultiplier tube
  • the sample under test is shaped as a powder layer of 2 mm thickness and the spot size of the excitation light beam is approximately 2x3 mm 2 .
  • the spectral resolution of the excitation and emission branch was in the order of 1-2 nm.
  • a 1 nm step size was chosen for the determination of the excitation and emission spectra.
  • the Eu 3+ activated red emitting phosphors described above are particularly promising for use in phosphor converted LEDs configured to emit white light.
  • a blue emitting LED may combined with a yellow or green emitting phosphor and a red emitting Eu + activated phosphor; or a UV emitting LED may be combined with a blue emitting phosphor, a yellow or green emitting phosphor, and a red emitting Eu + activated phosphor.
  • Suitable yellow or green emitting phosphors include aluminum garnet phosphors with the general formula (Lui_ x _ y _ a _bY x Gdy)3(Ali_ z Ga z ) 5 Oi2:Ce a Prb wherein 0 ⁇ x ⁇ 1, 0 ⁇ y ⁇ 1, 0 ⁇ z ⁇ 0.1, 0 ⁇ a ⁇ 0.2 and 0 ⁇ b ⁇ 0.1, such as Lu 3 Al 5 Oi 2 :Ce 3+ and Y 3 Al 5 Oi 2 :Ce 3+ ; SrSi 2 N 2 O 2 :Eu 2+ ; (Sri_ u _ v _ x Mg u Ca v Ba x )(Ga 2 .
  • Suitable blue-emitting phosphors include, for example, MgSrSiO 4 .
  • the Eu + activated red phosphors described above may offer advantages over other red phosphors.
  • the excitation spectrum of the Eu 3+ activated red phosphors is generally limited to a sharp line (i.e., narrow wavelength range) in the visible spectrum, as illustrated in Figs. 3, 5, 7 and 9, the Eu 3+ activated red phosphor does not absorb light emitted by any yellow or green emitting phosphor in the device.
  • the Eu 3+ activated red phosphors do not need to be separated from the yellow or green emitting phosphor, permitting great flexibility in the implementation of a white light phosphor-converted LED including an Eu + activated red phosphor.
  • the color rendering properties of the white light in a device including an Eu 3+ activated red phosphor may be boosted by the line emission (i.e. narrow wavelength range) from the red phosphor, as illustrated in Figs. 4, 6, 8, and 10.
  • the composite light emitted from such devices may have a correlated color temperature (CCT) between 2800 and 3300K, with a color rendering index Ra between 80 and 87.
  • CCT correlated color temperature
  • Fig. 13 is a cross sectional view of a portion of a device including a blue emitting LED combined with a yellow or green emitting phosphor formed as a luminescent ceramic and an Eu + activated red phosphor as described above.
  • a III -nitride semiconductor structure 18 including at least one light emitting layer 20 disposed between an n-type region and a p-type region is grown on a growth substrate (not shown). Portions of semiconductor structure 18 may be etched to expose regions of each conductivity type, such that p- and n-contacts may be formed on the same side of the device and the device may be mounted as a flip chip.
  • Semiconductor structure 18 is connected to a mount 12, which may be, for example, ceramic or Si-based, by metal interconnects 14 and 16, which connect the mount to the p- and n-contacts (not shown) on semiconductor structure 18.
  • the growth substrate may remain a part of the device (disposed between semiconductor structure 18 and luminescent ceramic 22) or may be removed from the semiconductor structure.
  • One or both of the p- and n-contacts may be reflective to light generated by light emitting layer 20 such that a majority of light that escapes the semiconductor structure escapes through the top surface of semiconductor structure 18, in the orientation shown in Fig. 13.
  • a yellow or green emitting phosphor in the form of a luminescent ceramic 22 is disposed over the top surface of semiconductor structure 18.
  • Luminescent ceramics are described in more detail in U.S. Patent Application Publication 2005-0269582, which is incorporated herein by reference.
  • a suitable YsAIsOi 2 )Ce 3+ ceramic may be produced as follows: 40 g Y 2 O 3 (99.998%), 32 g Al 2 O 3 (99.999%), and 3.44 g CeO 2 are milled with 1.5 kg high purity alumina balls (2 mm diameter) in isopropanol on a roller bench for 12 hrs. The dried precursor powder is then calcined at 1300 0 C for two hours under CO atmosphere.
  • the YAG powder obtained is then deagglomerated with a planet ball mill (agate balls) under ethanol.
  • the ceramic slurry is then slip cast to obtain a ceramic green body after drying.
  • the green bodies are then sintered between graphite plates at 1700 0 C for two hours.
  • Luminescent ceramic 22 may be attached to semiconductor structure 18 by, for example, direct wafer bonding or by an adhesive such as an organic material such as epoxy, acrylic, or silicone; one or more high index inorganic materials; or a sol-gel glass.
  • an adhesive such as an organic material such as epoxy, acrylic, or silicone; one or more high index inorganic materials; or a sol-gel glass.
  • high index materials include high index optical glasses such Schott glass SF59, Schott glass LaSF 3, Schott glass LaSF Nl 8, and mixtures thereof. These glasses are available from Schott Glass Technologies Incorporated, of Duryea, Pa.
  • high index chalcogenide glass such as (Ge,Sb, Ga)(S, Se) chalcogenide glasses, III-V semiconductors including but not limited to GaP, InGaP, GaAs, and GaN, II-VI semiconductors including but not limited to ZnS, ZnSe, ZnTe, CdS, CdSe, and CdTe, group IV semiconductors and compounds including but not limited to Si and Ge, organic semiconductors, metal oxides including but not limited to tungsten oxide, titanium oxide, nickel oxide, zirconium oxide, indium tin oxide, and chromium oxide, metal fluorides including but not limited to magnesium fluoride and calcium fluoride, metals including but not limited to Zn, In,
  • sol-gel glasses are described in more detail in U.S. Patent 6,642,618, which is incorporated herein by reference.
  • one or more materials such as oxides of titanium, cerium, lead, gallium, bismuth, cadmium, zinc, barium, or aluminum may be included in the SiO 2 sol-gel glass to increase the index of refraction of the glass in order to more closely match the index of the glass with the indices of the luminescent ceramic and the surface of the semiconductor structure to which the luminescent ceramic is attached.
  • the luminescent ceramic can be textured or molded, ground, machined, hot stamped, or polished into shapes that are desirable, for example, for increased light extraction.
  • a luminescent ceramic may be shaped into a lens such as a dome lens or Fresnel lens, roughened, or textured with a photonic crystal structure, such as a periodic lattice of holes formed in the ceramic.
  • the shaped ceramic layer may be smaller than, the same size as, or larger than the surface to which it is attached.
  • Second phosphor layer 24 may include particles 28 of one or more red phosphors, including at least one Eu 3+ activated red emitting phosphor as described above, disposed in a transparent binder material 26 such as resin, silicone, or epoxy.
  • Fig. 14 is a cross sectional view of a portion of a device including a blue emitting LED combined with a yellow or green emitting phosphor and an Eu 3+ activated red emitting phosphor, formed as separate luminescent ceramic layers.
  • a Ill-nitride semiconductor structure including a light emitting region configured to emit blue light is mounted on a mount 12.
  • a yellow or green emitting phosphor in the form of a luminescent ceramic 22 is disposed over the top surface of semiconductor structure 18.
  • An Eu 3+ activated red emitting phosphor in the form of a luminescent ceramic 30 is disposed over the top surface of luminescent ceramic 22.
  • Luminescent ceramics 30 and 22 may be connected to each other by, for example, direct wafer bonding or by an adhesive such as an organic material such as epoxy, acrylic, or silicone; one or more high index inorganic materials; or a sol-gel glass, as described above.
  • the positions of luminescent ceramics 30 and 22 relative to semiconductor structure 18 may be reversed.
  • Luminescent ceramics 30 and 22 may each have a thickness between 100 ⁇ m and 300 ⁇ m.
  • An Eu 3+ activated red phosphor may be formed into a luminescent ceramic by heating powder phosphor material until the surface of the powder particles begin to form a strong bond or neck at the contact points of the particles.
  • the temperature and pressure under which sintering occurs may depend on the particular phosphor material used.
  • the partially connected particles form a rigid agglomerate that further decreases its porosity by further neck growth. Grain boundaries are formed and move so that some grains grow at the expense of others.
  • This stage of sintering continues while the pore channels are connected (open porosity) until the pores are isolated (closed porosity). In the last stage of sintering, the pores become closed and are slowly eliminated along grain boundaries until the desired degree of densification is achieved.
  • Fig. 15 is a cross sectional view of a portion of a device including a blue emitting LED combined with a yellow or green emitting phosphor formed as a conformal layer and an Eu 3+ activated red emitting phosphor.
  • a yellow or green emitting phosphor is formed over the top of growth substrate 34 and the sides of growth substrate 34 and semiconductor structure 18 as a conformal layer 32.
  • Conformal phosphor layer 32 may be formed by, for example, stenciling as described in U.S. Patent 6,650,044, or by electrophoretic deposition as described in U.S. Patent 6,576,488. Both of U.S. Patents 6,650,044 and 6,576,488 are incorporated herein by reference. As in Fig.
  • Fig. 16 is an exploded view of a packaged light emitting device, as described in more detail in U.S. Patent 6,274,924.
  • a heat-sinking slug 100 is placed into an insert- molded leadframe.
  • the insert-molded leadframe is, for example, a filled plastic material 105 molded around a metal frame 106 that provides an electrical path.
  • Slug 100 may include an optional reflector cup 102.
  • the light emitting device die 104 which may be any of the devices described in the embodiments above, is mounted directly or indirectly via a thermally conducting mount 103 to slug 100.
  • a cover 108 which may be an optical lens, may be added.
  • the LED and the phosphors included in a white light device may be chosen to achieve a desired gamut through a preferred set of color filters, for example when the device is used as a backlight for an RGB display.

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Abstract

Dispositif émetteur de lumière convertie par une substance fluorescente comprenant une structure semi-conductrice comprenant une couche émettrice de lumière disposée entre une zone de type n et une zone de type p, la couche émettrice de lumière étant configurée pour émettre une lumière présentant une première longueur d’onde de pic ; une première substance fluorescente configurée pour émettre de la lumière présentant une seconde longueur d’onde de pic ; et une seconde substance fluorescente configurée pour présenter une troisième longueur d’onde de pic. La seconde substance fluorescente est une substance fluorescente activée à l'Eu3+, configurée de sorte que, dans le spectre d’excitation à 298K et 1,013 bar, une intensité maximale dans une plage de longueurs d'onde comprise entre 460 nm et 470 nm s'élève au moins à 5% d'une intensité maximal dans une plage de longueur d'onde comprise entre 220 nm et 320 nm.
PCT/IB2007/050114 2006-01-16 2007-01-15 Dispositif émetteur de lumière convertie par une substance fluorescente WO2007080555A1 (fr)

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