US20060014310A1 - Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal - Google Patents
Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal Download PDFInfo
- Publication number
- US20060014310A1 US20060014310A1 US11/227,416 US22741605A US2006014310A1 US 20060014310 A1 US20060014310 A1 US 20060014310A1 US 22741605 A US22741605 A US 22741605A US 2006014310 A1 US2006014310 A1 US 2006014310A1
- Authority
- US
- United States
- Prior art keywords
- layer
- etch
- growth substrate
- thinning
- stop layer
- 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.)
- Abandoned
Links
- 239000000758 substrate Substances 0.000 title claims description 72
- 238000000034 method Methods 0.000 claims abstract description 37
- 239000004065 semiconductor Substances 0.000 claims abstract description 12
- 238000005530 etching Methods 0.000 claims description 26
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- 229910002704 AlGaN Inorganic materials 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 120
- 229910052594 sapphire Inorganic materials 0.000 description 14
- 239000010980 sapphire Substances 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- 238000003892 spreading Methods 0.000 description 11
- 235000012431 wafers Nutrition 0.000 description 10
- 238000000605 extraction Methods 0.000 description 8
- 239000013078 crystal Substances 0.000 description 7
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 6
- 229910010271 silicon carbide Inorganic materials 0.000 description 6
- 229910052709 silver Inorganic materials 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- 239000004332 silver Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000003637 basic solution Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000005498 polishing Methods 0.000 description 4
- 238000002310 reflectometry Methods 0.000 description 4
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 238000003486 chemical etching Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 229910052593 corundum Inorganic materials 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000001312 dry etching Methods 0.000 description 2
- 229910052733 gallium Inorganic materials 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910003437 indium oxide Inorganic materials 0.000 description 2
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 description 2
- 229910000962 AlSiC Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910002601 GaN Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910003465 moissanite Inorganic materials 0.000 description 1
- 238000001451 molecular beam epitaxy Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 238000010943 off-gassing Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229910002059 quaternary alloy Inorganic materials 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000010944 silver (metal) Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229910002058 ternary alloy Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- -1 thin Cu foil Chemical class 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 238000003631 wet chemical etching Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10H—INORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
- H10H20/00—Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
- H10H20/80—Constructional details
- H10H20/862—Resonant cavity structures
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10H—INORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
- H10H20/00—Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
- H10H20/01—Manufacture or treatment
- H10H20/011—Manufacture or treatment of bodies, e.g. forming semiconductor layers
- H10H20/013—Manufacture or treatment of bodies, e.g. forming semiconductor layers having light-emitting regions comprising only Group III-V materials
- H10H20/0133—Manufacture or treatment of bodies, e.g. forming semiconductor layers having light-emitting regions comprising only Group III-V materials with a substrate not being Group III-V materials
- H10H20/01335—Manufacture or treatment of bodies, e.g. forming semiconductor layers having light-emitting regions comprising only Group III-V materials with a substrate not being Group III-V materials the light-emitting regions comprising nitride materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10H—INORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
- H10H20/00—Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
- H10H20/01—Manufacture or treatment
- H10H20/011—Manufacture or treatment of bodies, e.g. forming semiconductor layers
- H10H20/018—Bonding of wafers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10H—INORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
- H10H20/00—Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
- H10H20/80—Constructional details
- H10H20/81—Bodies
- H10H20/819—Bodies characterised by their shape, e.g. curved or truncated substrates
- H10H20/82—Roughened surfaces, e.g. at the interface between epitaxial layers
Definitions
- the present invention relates to III-nitride semiconductor light emitting devices.
- LEDs light emitting diodes
- 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 III-nitride materials.
- III-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, III-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
- Sapphire is often used as the growth substrate due to its wide commercial availability and relative ease of use.
- the stack grown on the growth substrate typically includes one or more n-type layers doped with, for example, Si, formed over the substrate, a light emitting or 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.
- U.S. Pat. No. 6,280,523 describes a III-nitride device formed by removing the growth substrate.
- the epitaxial stack is wafer bonded to a host substrate of GaP, GaAs, InP, or Si.
- the growth substrate is then removed by laser melting, wet chemical etching, or selective etching of a sacrificial layer. Removing the growth substrate permits the active region to be disposed between two dielectric distributed Bragg reflectors, in order to form a resonant cavity device.
- the use of a resonant cavity may increase control of the direction of emitted light, increase the amount of light extracted from the device, and increase the spectral purity of the light emitted normal to the device.
- III-nitride resonant cavity structures Needed in the art are improved III-nitride resonant cavity structures.
- a semiconductor light emitting device includes an n-type region, a p-type region, and light emitting region disposed between the n- and p-type regions.
- the n-type, p-type, and light emitting regions form a cavity having a top surface and a bottom surface. Both the top surface and the bottom surface of the cavity may have a rough surface. For example, the surface may have a plurality of peaks separated by a plurality of valleys.
- the thickness of the cavity is kept constant by incorporating an etch-stop layer into the device, then thinning the layers of the device by a process that terminates on the etch-stop layer.
- FIGS. 1 and 2 are a cross-sectional view and a plan view of a light emitting device according to embodiments of the present invention.
- FIG. 3 illustrates a method of fabricating the device of FIGS. 1 and 2 .
- FIG. 4 illustrates an epitaxial structure prior to bonding to a host substrate.
- FIG. 5 illustrates a method of bonding an epitaxial structure to a host substrate.
- FIG. 6 illustrates a method of removing a sapphire substrate from a III-nitride epitaxial structure.
- FIG. 7 illustrates photoelectrochemical etching to thin the epitaxial layers after growth substrate removal.
- FIG. 8 illustrates an embodiment of the present invention including trenches formed in the n-type region of the device.
- FIGS. 9, 10 , and 11 illustrate examples of arrangement of the etch vias of FIG. 8 .
- FIG. 12 is a plan view of an alternate embodiment of the present invention.
- FIG. 13 is a cross sectional view of the device of FIG. 12 .
- FIG. 14 is a cutaway plan view of a p-contact.
- FIG. 15 illustrates a substrate that may be removed by chemical etching.
- FIG. 16 illustrates substrate removal by photoelectrochemical etching.
- FIG. 17 illustrates a portion of a resonant cavity device formed by chemical mechanical polishing.
- FIG. 18 illustrates a portion of a resonant cavity device formed by photoelectrochemical etching.
- improved III-nitride resonant cavity devices are provided.
- a constant cavity thickness is created by incorporating an etch stop layer during growth.
- trenches are formed on the device to increase light extraction.
- grid contacts are provided.
- FIGS. 1 and 2 are cross sectional and plan views of a resonant cavity III-nitride device according to embodiments of the invention.
- An active region 112 is sandwiched between an n-type region 108 and a p-type region 116 .
- the embodiment of FIGS. 1 and 2 shows an n-contact 10 formed on a portion of n-type region 108 not covered by DBR 11 , through which light is extracted from the device.
- a reflective p-contact 12 is formed on p-type region 116 .
- P-contact 12 connects the epitaxial layers 20 to a host substrate 16 either directly or via optional bonding layers 14 .
- Host substrate 16 may be a semiconductor, requiring ohmic contacts 18 on the surface of host substrate.
- the device illustrated in FIGS. 1 and 2 is a large junction device, meaning that the device has an area of at least 200 ⁇ 200 ⁇ m 2 and operates at a current density of at least 100 A/cm 2 .
- N-contact 10 may surround the extraction surface, as illustrated in FIG. 2 , or may have an alternative configuration.
- the pattern of contacts may be chosen such that the largest distance between any point on p-contact 12 and n-contact 10 is less than the maximum current spreading distance characteristic of the particular device.
- the maximum current spreading distance may range from, for example, about 20 ⁇ m to about 250 ⁇ m. Increasing the electrical conductivity increases the spreading distance. Decreasing the epitaxial stack thickness decreases the spreading distance.
- current is blocked from the p-type region 116 in the area under n-contact 10 , in order to force current into the cavity formed by DBR 11 and reflective p-contact 12 .
- Current blocking may be accomplished by implanting the areas of p-type region 116 under n-contact 10 with H + at, for example, an energy of 10 keV and a dose of 2 ⁇ 10 14 cm 2 , to create highly resistive regions.
- the areas to be blocked may be covered with a non-ohmic metal such as Ti or an insulator such as an oxide or a nitride of silicon.
- the distance between the reflective p-contact and the active region may be selected to maximize extraction from the device.
- the electric field intensity in the cavity forms a standing wave.
- the center of the active region may be located near a maximum in the electric field intensity.
- any absorbing structures such as, for example, highly doped layers of a tunnel junction, are preferably located a minima in the field intensity.
- the resonant cavity is formed by DBR 11 and a reflective layer opposite the p-type region from the DBR; typically p-contact 12 , though the reflective layer may be optional bonding layers 14 , or host substrate 16 .
- the resonant cavity offers superior control of the light As described in “Impact of Planar Microcavity Effects on Light Extraction—Part I: Basic Concepts and Analytical Trends,” H Benisty, H. De Neve, and C. Weisbuch, IEEE Journal Of Quantum Electronics, Vol. 34, No. 9, September 1998, pp. 1612-1631, the resonant cavity offers potentially a higher internal efficiency, a higher extraction efficiency and greater control over the direction, i.e. radiation pattern, and spectrum of the emitted light.
- the principal variables of the device structure are the reflectivities of the top and bottom mirrors and the optical thickness of the structure. Generally, the thinner the cavity the fewer the waveguided modes. The light in these modes is trapped in the crystal and lost as heat. Shutting off this recombination process leaves more electron-hole pairs available for generation of usable light that is light generated within the escape cone of the crystal. Thus the wafers are processed as thin as possible, less than 1 ⁇ m, consistent with good device yield and adequate current spreading. In many embodiments, the thickness of the epitaxial layers 20 that form the resonant cavity is less than about 1 ⁇ m, often between about 0.5 and about 0.7 ⁇ m.
- the extraction efficiency of the generated light may be increased by fine tuning the cavity thickness.
- the angle of the generated light is a sensitive function of wavelength and cavity thickness.
- the radiation pattern may be fitted to the escape cone of the crystal, i.e. less than 25° from normal, by careful selection of cavity thickness. Therefore within the less than 1 ⁇ m thickness requirement stated above is an additional requirement that the optical thickness across the device corresponds to a desired resonance to optimize the extraction efficiency or surface brightness.
- a resonance requires control to within 15 nm, e.g. 570+/ ⁇ 15 nm or 675+/ ⁇ 15 nm thickness.
- the epitaxial layers are generally thinned after growth to the desired cavity thickness.
- the epitaxial layer may be thinned by conventional etching processes or chemical mechanical polishing.
- FIG. 17 illustrates a portion of a device where the cavity is thinned by chemical mechanical polishing.
- Such conventional thinning processes present two problems. First, with conventional processes it can be difficult to control the stopping point of the thinning process with the 15 nm precision required to make an efficient resonant cavity.
- III-nitride layers due to the lattice mismatch between the growth substrate on which the epitaxial layers are grown and between the epitaxial layers themselves, it is difficult to grow flat III-nitride layers.
- the presence of crystal defects generally results in III-nitride layers with an uneven surface, as illustrated by active region 112 of FIG. 17 .
- the surfaces of the III-nitride layers may have a cross section including peaks separated by valleys.
- the “peaks” are slanted crystal planes 5 , separated by the “valleys” formed by steps 7 between the individual planes.
- Planes 5 may be, for example, 1 to 150 microns long, and are often about 100 microns long.
- Steps 7 may have a height, for example, on the order of about ⁇ /4, where ⁇ is the wavelength in the crystal of light emitted by active region 112 .
- steps 7 may have a height between about 15 nm and about 100 nm.
- Regions 108 , 112 , and 116 are thin enough that strain within these regions causes each to have the same peak-and-valley surface, as illustrated at the interfaces between active region 112 and p-type region 116 , and between active region 112 and n-type region 108 .
- the conventional thinning processes described above typically result in a flat surface, as illustrated at the interface between n-type region 108 and mirror 11 .
- forming a resonant cavity device by conventional processes results in a cavity with one uneven surface (the interface between p-type region 116 and p-contact 12 , resulting from growth) and one flat surface (the interface between n-type region 108 and mirror 11 , resulting from etching or chemical mechanical polishing).
- the difference in the surfaces on either side of the resonant cavity results in variations in the cavity thickness as illustrated by arrows 3 and 4 .
- only portions of the cavity are appropriately tuned. Such variations can decrease the efficiency of the device.
- the thickness of the resonant cavity is kept constant by incorporating an etch stop layer into the epitaxial layers during growth.
- the etch stop layer is grown just before or within one micron of the epitaxial layers forming the cavity. Since the epitaxial layers grown over the etch stop layer are thin, they retain the surface of the etch stop layer, resulting in a constant resonant cavity thickness.
- the device is thinned by a process that terminates on the etch stop layer, resulting in a cavity with a constant thickness since the top cavity surface is identical to the bottom cavity surface.
- both surfaces of the cavity, the interface between n-type region 108 and mirror 11 and the interface between p-type region 116 and p-contact 12 have the same surface shape, resulting in a cavity of constant thickness.
- the thickness of the cavity varies less than ⁇ /8 from an average thickness of the cavity, or less than 5% from the average thickness of the cavity.
- a device with a constant cavity thickness may be fabricated by the method illustrated in FIG. 3 .
- stage 31 epitaxial layers 20 are grown on a conventional growth substrate.
- the epitaxial layers are then attached to a host substrate in stage 33 , such that the growth substrate can be removed in stage 35 .
- the epitaxial layers are thinned in stage 37 , then a contact and optional mirror are formed on the exposed surface of the epitaxial layers in stage 39 .
- FIG. 4 illustrates stage 31 of FIG. 3 in more detail.
- Epitaxial layers 20 of the device of FIG. 1 are grown on a substrate 40 such as sapphire, SiC, or GaN.
- Optional preparation layers 41 which may include, for example, buffer layers or nucleation layers, may be grown first on substrate 40 to provide a suitable growth substrate.
- One or more etch-stop layers 42 may then be grown.
- the epitaxial layers 20 are then grown to the desired cavity thickness over etch-stop layer 42 .
- Epitaxial layers 20 include n-type region 108 , active region 112 , and p-type region 116 . Usually, the n-type region is grown first, followed by the active region and the p-type region.
- a reflective p-contact 12 is formed on the surface of p-type region 116 .
- P-contact 12 may be a single layer or may include multiple layers such as an adhesion layer, an ohmic contact layer, a reflective layer, and a guard metal layer.
- the reflective layer is usually silver or aluminum.
- the guard metal may include, for example, nickel, titanium, or tungsten. The guard metal may be chosen to prevent the reflective metal layer from migrating, particularly in the case of a silver reflective layer, and to provide an adhesion layer for a bonding layer 14 A, used to bond the epitaxial structure to a host substrate.
- FIG. 5 illustrates stage 33 of FIG. 3 , attaching the epitaxial layers to a host substrate, in more detail.
- Bonding layers 14 A and 14 B typically metal, serve as compliant materials for thermo-compression bonding between the epitaxial structure and the host substrate.
- suitable bonding layer metals include gold and silver. If silver is used, the guard metal in p-contact 12 may be eliminated.
- 14 A and 14 B can be a mixture of metals such that when bonding at elevated temperatures, the eutectic temperature is met, and 14 A and 14 B melt while bonding.
- Host substrate 16 provides mechanical support to the epitaxial layers after the growth substrate is removed, and provides electrical contact to p-contact 12 .
- Host substrate 16 is selected to be electrically conductive (i.e.
- Suitable materials include, for example, metals such as thin Cu foil, Mo, Cu/Mo, and Cu/W; semiconductors with metal contacts (layers 46 and 18 of FIG. 6 ), such as Si with ohmic contacts and GaAs with ohmic contacts including, for example, one or more of Pd, Ge, Ti, Au, Ni, Ag; and composite metal-ceramics such as AlSiC or cobalt diamond.
- Table 1 below lists the properties of some suitable host substrates, as well as the properties of GaN and Al 2 O 3 for comparison: Thermal conduc- Material CTE (10 ⁇ 6 /K) tivity (W/m K) Electrical resistance ( ⁇ cm) GaN 4.8 130 0.01 Al 2 O 3 6.8 40 Very high Si 2.7 150 0.01 plus contact resistance GaAs 5.7 59 0.01 plus contact resistance Mo 4.8 140 5 ⁇ 10 ⁇ 6
- Host substrate structure 49 and epitaxial structure 48 are pressed together at elevated temperature and pressure to form a durable metal bond between bonding layers 14 A and 14 B.
- bonding is done on a wafer scale, before a wafer with an epitaxial structure is diced into individual devices.
- the temperature and pressure ranges for bonding are limited on the lower end by the strength of the resulting bond, and on the higher end by the stability of the host substrate structure and the epitaxial structure and CTE mismatch.
- high temperatures and/or high pressures can cause decomposition of the epitaxial layers in structure 48 , delamination of p-contact 12 , failure of diffusion barriers, for example in p-contact 12 , outgassing of the component materials in the epitaxial layers, and wafer bowing.
- a suitable temperature range is, for example, about 200° C. to about 500° C.
- a suitable pressure range is, for example, about 100 psi to about 300 psi.
- FIG. 6 illustrates a method of removing a sapphire growth substrate, stage 35 in FIG. 3 .
- Portions of the interface between sapphire substrate 40 and the III-nitride layers 45 are exposed, through the sapphire substrate, to a high fluence ultraviolet laser 70 pulsed in a step and repeat pattern, or fired synchronously with continuous motion.
- the photon energy of the laser is above the band gap of the III-nitride layer adjacent to the sapphire (GaN in some embodiments), thus the pulse energy is effectively converted to thermal energy within the first 100 nm of epitaxial material adjacent to the sapphire.
- sufficiently high fluence i.e.
- the resulting structure includes epitaxial layers 45 bonded to host substrate structure 49 .
- Exposure to the laser pulse results in large temperature gradients and mechanical shock waves traveling outward from the exposed region, resulting in thermal and mechanical stress within the epitaxial material sufficient to cause cracking of the epitaxial material and failure of wafer bond 14 , which limits the yield of the substrate removal process.
- the damage caused by thermal and mechanical stresses may be reduced by patterning the epitaxial structure down to the sapphire substrate or down to a suitable depth of the epitaxial structure, to form trenches between individual devices on the wafer.
- the trenches are formed by conventional masking and dry etching techniques, before the wafer is bonded to the host substrate structure.
- the laser exposure region is then matched to the pattern of trenches on the wafer.
- the trench isolates the impact of the laser pulse to the semiconductor region being exposed and provides a preferred path for stress relaxation.
- a sapphire substrate or other suitable substrate may be removed by photoelectrochemical etching.
- Substrate removal by photoelectrochemical etching is illustrated in FIG. 16 .
- trenches 6 may be formed in the epitaxial layers of the device and a portion of substrate 40 (for example, the 30 microns of substrate 40 closest to the epitaxial layers) by laser scribing as is known in the art, or any other suitable technique.
- the epitaxial layers are then bonded to host substrate structure 49 through p-contact 12 and bonding layers 14 A and 14 B.
- Growth substrate 40 may then be thinned by conventional means such as grinding to expose the trench 6 to ambient.
- the structure is immersed in a solution suitable for photoelectrochemical etching that flows into trenches 6 , and the structure is exposed through substrate 40 to light 8 with an energy greater than the band gap of sacrificial layer 41 . Exposure to the light generates electron-hole pairs in sacrificial layer 41 , which break the bonds of sacrificial layer 41 , undercutting and releasing substrate 40 from the epitaxial structure.
- the epitaxial structure may include an etch-stop layer 42 , which terminates the photoelectrochemical etch. Further details of photoelectrochemical etching and suitable etch stop layers 42 are described below in reference to FIG. 7 .
- FIG. 15 illustrates an example of a substrate 40 that may be removed by chemical etching.
- Substrate 40 of FIG. 15 includes a SiC layer 40 C grown or processed onto a Si base 40 A.
- An optional SiO x layer 41 B may be disposed between base 40 A and SiC layer 40 C.
- Si base layer 40 A and oxide layer 40 B may be easily removed by conventional silicon processing techniques.
- SiC layer 40 C may be thin enough, for example, less than 0.5 ⁇ m thick, to be removed entirely by known dry etching or abrasive techniques.
- P-contact 12 may then be formed on the exposed surface of epitaxial layers 45 . Alternatively, p-contact 12 may be formed in holes etched in SiC layer 40 C.
- the remaining epitaxial layers are thinned to the etch stop layer 42 by, for example, photoelectrochemical etching (PEC) as illustrated in FIG. 7 .
- PEC photoelectrochemical etching
- the host substrate and epitaxial layers (structure 53 ) are immersed in a basic solution 50 .
- An example of a suitable basic solution is 0.2 M KOH, though many other suitable basic or acidic solutions may be used and depend on the composition of the material to be etched and the desired surface texture.
- the epitaxial surface of structure 53 generally an n-type GaN layer, is exposed to light with energy greater than the band gap of the surface layer. In the example illustrated in FIG.
- the etch stop layer may have a composition selected for a band gap greater than that of the layer to be etched.
- the etched layer may be GaN
- the etch stop layer may be AlGaN.
- the light source used to expose structure 53 is selected to have an energy greater than the band gap of the layer to be etched, but less than the band gap of the etch stop layer. Accordingly, exposure to the light does not generate electron-hole pairs in the etch stop layer, effectively halting the etch once the etch stop layer is reached.
- InGaN may be used as the etch stop layer.
- Indium oxide, formed as the InGaN decomposes, is insoluble in the etchant solution and coats the surface of the etched layer, terminating the etch.
- the etch stop layer may optionally be removed, for example, by continuing photoelectrochemical etching with light of a different energy in the case of an AlGaN etch stop layer, or by agitating the solution to disturb the indium oxide coating the surface of the etched layer in the case of an InGaN etch stop layer.
- the device may include multiple etch stop layers, a first etch stop layer close to the growth substrate to control the etch during growth substrate removal, and a second etch stop layer close to the active region to control the etch during thinning.
- the growth substrate is removed by photoelectrochemical etching, then a portion of n-type region 108 is removed by a conventional etch, such as a reactive ion etch.
- the resonant cavity is formed by further thinning n-type region 108 in a second photoelectrochemical etch.
- n-type region 108 may be patterned such that the portion under contact 10 is thicker than the portion under mirror 11 , in order to minimize the thickness of the cavity, while providing enough n-type material under contact 10 for adequate current spreading, optimal contact resistance, and mechanical strength.
- a structure also permits testing during pauses in the etching process to check for optimum etch depth based on reflectivity and radiometric measurements of output light.
- contact 10 and mirror 11 are deposited on the exposed surface of epitaxial structure 20 .
- mirror 11 is not conductive (a dielectric DBR for example)
- an optional current spreading layer 70 of, for example, conductive indium tin oxide or a heavily doped III-nitride material may be included between mirror 11 and n-type region 108 in order to spread current from contact 10 under mirror 11 .
- the current spreading layer may be contacted by removing portions of mirror 11 down to the current spreading layer to create channels and extending contact 10 into the channel or depositing an additional conductive material in the channels that makes electrical contact with contact 10 .
- FIG. 8 is a cross sectional view of a portion of a resonant cavity device including trenches, according embodiments of the invention.
- Etch vias 72 are etched through DBR 11 into n-type region 108 in order to interrupt the waveguide at the interface of n-type region 108 and DBR 11 .
- Etch vias 72 may thus enhance extraction from the device by limiting the number of modes in the device.
- Etch vias 72 are typically confined to n-type region 108 and generally do not extend into active region 112 .
- Etch vias 72 may have a depth between about 0.1 ⁇ m and about 2.5 ⁇ m and may be spaced about 1 ⁇ m to about 10 ⁇ m apart. A usual distance between two adjacent trenches is about 3 ⁇ m.
- Trenches 72 may form a pattern of broken lines to facilitate current spreading in the etched layer.
- FIGS. 9, 10 , and 11 illustrate examples of patterns of trenches 72 .
- Trenches 72 may be formed by conventional
- DBR 11 on the surface of n-type region 108 is divided into multiple regions separated by metal contacts, instead of a single DBR 11 , as illustrated in FIG. 1 .
- FIGS. 12 and 13 are a plan view and a cross sectional view of a portion of such a device.
- Each region of DBR 11 may be, for example, about 50 ⁇ m to about 150 ⁇ m across. Though the regions shown are square, other shapes may be used.
- Each DBR region is separated by, for example, about 1 ⁇ m to about 10 ⁇ m.
- the areas between DBR regions 11 are filled with n-contact 10 .
- an optional current spreading layer 70 which may be, for example, indium tin oxide or RuO, is disposed between n-type region 108 and DBR regions 11 and n-contact regions 11 .
- Current injection in the regions of epitaxial layers 20 beneath n-contacts 10 may be blocked by hydrogen implantation as described above, in order to confine light emission to the areas underlying DBR regions 11 .
- p-contact 12 may be a single, continuous reflective sheet, as illustrated in FIG. 13 , or may have regions of high reflectivity opposite DBR regions 11 .
- FIG. 14 is a cutaway plan view of a p-contact 12 .
- Mirror regions 80 are aligned with DBR regions 11 , illustrated in FIG. 12 .
- Mirror regions 80 are optimized for high reflectivity and are separated by contact regions 82 , which may be optimized for good adhesion.
- Mirror regions 80 may be, for example, silver, and contact regions 82 may be, for example, nickel.
Landscapes
- Led Devices (AREA)
- Semiconductor Lasers (AREA)
Abstract
Description
- This application is a division of application Ser. No. 10/861,745, filed Jun. 3, 2004 and incorporated herein by reference.
- 1. Field of Invention
- The present invention relates to III-nitride semiconductor light emitting devices.
- 2. Description of Related Art
- Semiconductor light-emitting devices including light emitting diodes (LEDs) 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 III-nitride materials. Typically, III-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, III-nitride, or other suitable substrate by metal-organic chemical vapor deposition (MOCVD), molecular beam epitaxy (MBE), or other epitaxial techniques. Sapphire is often used as the growth substrate due to its wide commercial availability and relative ease of use. The stack grown on the growth substrate typically includes one or more n-type layers doped with, for example, Si, formed over the substrate, a light emitting or 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.
- Since sapphire is not conductive, contacts to both the p- and n-sides of the active region must be formed on the top side of the device, requiring that a portion of the active region and p-type region be etched away to expose a portion of the buried n-type region. The device is thus a non-planar surface with narrow insulating blocking layers separating the n- and p-contacts, a geometry that is difficult to package. Also, much of the area of the active region is lost to the n-contact and insulating regions, providing a poor fill factor.
- U.S. Pat. No. 6,280,523 describes a III-nitride device formed by removing the growth substrate. The epitaxial stack is wafer bonded to a host substrate of GaP, GaAs, InP, or Si. The growth substrate is then removed by laser melting, wet chemical etching, or selective etching of a sacrificial layer. Removing the growth substrate permits the active region to be disposed between two dielectric distributed Bragg reflectors, in order to form a resonant cavity device. The use of a resonant cavity may increase control of the direction of emitted light, increase the amount of light extracted from the device, and increase the spectral purity of the light emitted normal to the device.
- Needed in the art are improved III-nitride resonant cavity structures.
- In accordance with embodiments of the invention, a semiconductor light emitting device includes an n-type region, a p-type region, and light emitting region disposed between the n- and p-type regions. The n-type, p-type, and light emitting regions form a cavity having a top surface and a bottom surface. Both the top surface and the bottom surface of the cavity may have a rough surface. For example, the surface may have a plurality of peaks separated by a plurality of valleys. In some embodiments, the thickness of the cavity is kept constant by incorporating an etch-stop layer into the device, then thinning the layers of the device by a process that terminates on the etch-stop layer.
-
FIGS. 1 and 2 are a cross-sectional view and a plan view of a light emitting device according to embodiments of the present invention. -
FIG. 3 illustrates a method of fabricating the device ofFIGS. 1 and 2 . -
FIG. 4 illustrates an epitaxial structure prior to bonding to a host substrate. -
FIG. 5 illustrates a method of bonding an epitaxial structure to a host substrate. -
FIG. 6 illustrates a method of removing a sapphire substrate from a III-nitride epitaxial structure. -
FIG. 7 illustrates photoelectrochemical etching to thin the epitaxial layers after growth substrate removal. -
FIG. 8 illustrates an embodiment of the present invention including trenches formed in the n-type region of the device. -
FIGS. 9, 10 , and 11 illustrate examples of arrangement of the etch vias ofFIG. 8 . -
FIG. 12 is a plan view of an alternate embodiment of the present invention. -
FIG. 13 is a cross sectional view of the device ofFIG. 12 . -
FIG. 14 is a cutaway plan view of a p-contact. -
FIG. 15 illustrates a substrate that may be removed by chemical etching. -
FIG. 16 illustrates substrate removal by photoelectrochemical etching. -
FIG. 17 illustrates a portion of a resonant cavity device formed by chemical mechanical polishing. -
FIG. 18 illustrates a portion of a resonant cavity device formed by photoelectrochemical etching. - In accordance with embodiments of the invention, improved III-nitride resonant cavity devices are provided. A constant cavity thickness is created by incorporating an etch stop layer during growth. In some embodiments of the invention, trenches are formed on the device to increase light extraction. In some embodiments, grid contacts are provided.
-
FIGS. 1 and 2 are cross sectional and plan views of a resonant cavity III-nitride device according to embodiments of the invention. Anactive region 112 is sandwiched between an n-type region 108 and a p-type region 116. The embodiment ofFIGS. 1 and 2 shows an n-contact 10 formed on a portion of n-type region 108 not covered byDBR 11, through which light is extracted from the device. A reflective p-contact 12 is formed on p-type region 116. P-contact 12 connects theepitaxial layers 20 to ahost substrate 16 either directly or viaoptional bonding layers 14.Host substrate 16 may be a semiconductor, requiringohmic contacts 18 on the surface of host substrate. In some embodiments of the invention, the device illustrated inFIGS. 1 and 2 is a large junction device, meaning that the device has an area of at least 200×200 μm2 and operates at a current density of at least 100 A/cm2. - N-
contact 10 may surround the extraction surface, as illustrated inFIG. 2 , or may have an alternative configuration. The pattern of contacts may be chosen such that the largest distance between any point on p-contact 12 and n-contact 10 is less than the maximum current spreading distance characteristic of the particular device. The maximum current spreading distance may range from, for example, about 20 μm to about 250 μm. Increasing the electrical conductivity increases the spreading distance. Decreasing the epitaxial stack thickness decreases the spreading distance. In some embodiments, current is blocked from the p-type region 116 in the area under n-contact 10, in order to force current into the cavity formed byDBR 11 and reflective p-contact 12. Current blocking may be accomplished by implanting the areas of p-type region 116 under n-contact 10 with H+ at, for example, an energy of 10 keV and a dose of 2×1014 cm2, to create highly resistive regions. Alternatively, the areas to be blocked may be covered with a non-ohmic metal such as Ti or an insulator such as an oxide or a nitride of silicon. - The distance between the reflective p-contact and the active region may be selected to maximize extraction from the device. Generally the electric field intensity in the cavity forms a standing wave. The center of the active region may be located near a maximum in the electric field intensity. Conversely, any absorbing structures, such as, for example, highly doped layers of a tunnel junction, are preferably located a minima in the field intensity. Calculation of the optimal separation between the reflective p-contact and the active region is analogous to the calculations described in more detail in U.S. Pat. No. 6,903,376, titled “Selective Placement Of Quantum Wells In Flip-Chip Light Emitting Diodes For Improved Light Extraction” and incorporated herein by reference.
- The resonant cavity is formed by
DBR 11 and a reflective layer opposite the p-type region from the DBR; typically p-contact 12, though the reflective layer may be optional bonding layers 14, orhost substrate 16. The resonant cavity offers superior control of the light As described in “Impact of Planar Microcavity Effects on Light Extraction—Part I: Basic Concepts and Analytical Trends,” H Benisty, H. De Neve, and C. Weisbuch, IEEE Journal Of Quantum Electronics, Vol. 34, No. 9, September 1998, pp. 1612-1631, the resonant cavity offers potentially a higher internal efficiency, a higher extraction efficiency and greater control over the direction, i.e. radiation pattern, and spectrum of the emitted light. The principal variables of the device structure are the reflectivities of the top and bottom mirrors and the optical thickness of the structure. Generally, the thinner the cavity the fewer the waveguided modes. The light in these modes is trapped in the crystal and lost as heat. Shutting off this recombination process leaves more electron-hole pairs available for generation of usable light that is light generated within the escape cone of the crystal. Thus the wafers are processed as thin as possible, less than 1 μm, consistent with good device yield and adequate current spreading. In many embodiments, the thickness of theepitaxial layers 20 that form the resonant cavity is less than about 1 μm, often between about 0.5 and about 0.7 μm. - For devices with typical spectral width less than about 140 meV, the extraction efficiency of the generated light may be increased by fine tuning the cavity thickness. Internal to the crystal, the angle of the generated light is a sensitive function of wavelength and cavity thickness. The radiation pattern may be fitted to the escape cone of the crystal, i.e. less than 25° from normal, by careful selection of cavity thickness. Therefore within the less than 1 μm thickness requirement stated above is an additional requirement that the optical thickness across the device corresponds to a desired resonance to optimize the extraction efficiency or surface brightness. Typically a resonance requires control to within 15 nm, e.g. 570+/−15 nm or 675+/−15 nm thickness.
- In order to achieve the desired cavity thickness, the epitaxial layers are generally thinned after growth to the desired cavity thickness. The epitaxial layer may be thinned by conventional etching processes or chemical mechanical polishing.
FIG. 17 illustrates a portion of a device where the cavity is thinned by chemical mechanical polishing. Such conventional thinning processes present two problems. First, with conventional processes it can be difficult to control the stopping point of the thinning process with the 15 nm precision required to make an efficient resonant cavity. - Second, due to the lattice mismatch between the growth substrate on which the epitaxial layers are grown and between the epitaxial layers themselves, it is difficult to grow flat III-nitride layers. The presence of crystal defects generally results in III-nitride layers with an uneven surface, as illustrated by
active region 112 ofFIG. 17 . The surfaces of the III-nitride layers may have a cross section including peaks separated by valleys. The “peaks” are slantedcrystal planes 5, separated by the “valleys” formed by steps 7 between the individual planes.Planes 5 may be, for example, 1 to 150 microns long, and are often about 100 microns long. Steps 7 may have a height, for example, on the order of about λ/4, where λ is the wavelength in the crystal of light emitted byactive region 112. For example, steps 7 may have a height between about 15 nm and about 100 nm.Regions active region 112 and p-type region 116, and betweenactive region 112 and n-type region 108. The conventional thinning processes described above typically result in a flat surface, as illustrated at the interface between n-type region 108 andmirror 11. Accordingly, forming a resonant cavity device by conventional processes results in a cavity with one uneven surface (the interface between p-type region 116 and p-contact 12, resulting from growth) and one flat surface (the interface between n-type region 108 andmirror 11, resulting from etching or chemical mechanical polishing). The difference in the surfaces on either side of the resonant cavity results in variations in the cavity thickness as illustrated byarrows - In accordance with embodiments of the invention, the thickness of the resonant cavity is kept constant by incorporating an etch stop layer into the epitaxial layers during growth. In order for the etch stop layer to be conformal to the layers that form the resonant cavity, the etch stop layer is grown just before or within one micron of the epitaxial layers forming the cavity. Since the epitaxial layers grown over the etch stop layer are thin, they retain the surface of the etch stop layer, resulting in a constant resonant cavity thickness. The device is thinned by a process that terminates on the etch stop layer, resulting in a cavity with a constant thickness since the top cavity surface is identical to the bottom cavity surface.
FIG. 18 illustrates a portion of a device where the cavity is thinned by a process that terminates on an etch stop layer grown before the cavity layers. As illustrated inFIG. 18 , both surfaces of the cavity, the interface between n-type region 108 andmirror 11 and the interface between p-type region 116 and p-contact 12, have the same surface shape, resulting in a cavity of constant thickness. In some embodiments, at any point in the cavity, the thickness of the cavity varies less than λ/8 from an average thickness of the cavity, or less than 5% from the average thickness of the cavity. - A device with a constant cavity thickness may be fabricated by the method illustrated in
FIG. 3 . Instage 31, epitaxial layers 20 are grown on a conventional growth substrate. The epitaxial layers are then attached to a host substrate instage 33, such that the growth substrate can be removed instage 35. The epitaxial layers are thinned instage 37, then a contact and optional mirror are formed on the exposed surface of the epitaxial layers instage 39. -
FIG. 4 illustratesstage 31 ofFIG. 3 in more detail. Epitaxial layers 20 of the device ofFIG. 1 are grown on asubstrate 40 such as sapphire, SiC, or GaN. Optional preparation layers 41, which may include, for example, buffer layers or nucleation layers, may be grown first onsubstrate 40 to provide a suitable growth substrate. One or more etch-stop layers 42 may then be grown. The epitaxial layers 20 are then grown to the desired cavity thickness over etch-stop layer 42. Epitaxial layers 20 include n-type region 108,active region 112, and p-type region 116. Usually, the n-type region is grown first, followed by the active region and the p-type region. A reflective p-contact 12 is formed on the surface of p-type region 116. P-contact 12 may be a single layer or may include multiple layers such as an adhesion layer, an ohmic contact layer, a reflective layer, and a guard metal layer. The reflective layer is usually silver or aluminum. The guard metal may include, for example, nickel, titanium, or tungsten. The guard metal may be chosen to prevent the reflective metal layer from migrating, particularly in the case of a silver reflective layer, and to provide an adhesion layer for abonding layer 14A, used to bond the epitaxial structure to a host substrate. -
FIG. 5 illustratesstage 33 ofFIG. 3 , attaching the epitaxial layers to a host substrate, in more detail.Bonding layers contact 12 may be eliminated. Alternatively 14A and 14B can be a mixture of metals such that when bonding at elevated temperatures, the eutectic temperature is met, and 14A and 14B melt while bonding.Host substrate 16 provides mechanical support to the epitaxial layers after the growth substrate is removed, and provides electrical contact to p-contact 12.Host substrate 16 is selected to be electrically conductive (i.e. less than about 0.1 Ωcm), to be thermally conductive, to have a coefficient of thermal expansion (CTE) matched to that of the epitaxial layers, and to be flat (i.e. with an RMS roughness less than about 100 nm) enough to form a strong wafer bond. Suitable materials include, for example, metals such as thin Cu foil, Mo, Cu/Mo, and Cu/W; semiconductors with metal contacts (layers FIG. 6 ), such as Si with ohmic contacts and GaAs with ohmic contacts including, for example, one or more of Pd, Ge, Ti, Au, Ni, Ag; and composite metal-ceramics such as AlSiC or cobalt diamond. Table 1 below lists the properties of some suitable host substrates, as well as the properties of GaN and Al2O3 for comparison:Thermal conduc- Material CTE (10−6/K) tivity (W/m K) Electrical resistance (Ωcm) GaN 4.8 130 0.01 Al2O3 6.8 40 Very high Si 2.7 150 0.01 plus contact resistance GaAs 5.7 59 0.01 plus contact resistance Mo 4.8 140 5 × 10−6 -
Host substrate structure 49 andepitaxial structure 48 are pressed together at elevated temperature and pressure to form a durable metal bond betweenbonding layers structure 48, delamination of p-contact 12, failure of diffusion barriers, for example in p-contact 12, outgassing of the component materials in the epitaxial layers, and wafer bowing. A suitable temperature range is, for example, about 200° C. to about 500° C. A suitable pressure range is, for example, about 100 psi to about 300 psi. -
FIG. 6 illustrates a method of removing a sapphire growth substrate,stage 35 inFIG. 3 . Portions of the interface betweensapphire substrate 40 and the III-nitride layers 45 are exposed, through the sapphire substrate, to a highfluence ultraviolet laser 70 pulsed in a step and repeat pattern, or fired synchronously with continuous motion. The photon energy of the laser is above the band gap of the III-nitride layer adjacent to the sapphire (GaN in some embodiments), thus the pulse energy is effectively converted to thermal energy within the first 100 nm of epitaxial material adjacent to the sapphire. At sufficiently high fluence (i.e. greater than about 1.5 J/cm2) and a photon energy above the band gap of GaN and below the absorption edge of sapphire (i.e. between about 3.44 and about 6 eV), the temperature within the first 100 nm rises on a nanosecond scale to a temperature greater than 1000° C., high enough for the GaN to dissociate into gallium and nitrogen gasses, releasing theepitaxial layers 45 fromsubstrate 40. The resulting structure includesepitaxial layers 45 bonded to hostsubstrate structure 49. - Exposure to the laser pulse results in large temperature gradients and mechanical shock waves traveling outward from the exposed region, resulting in thermal and mechanical stress within the epitaxial material sufficient to cause cracking of the epitaxial material and failure of
wafer bond 14, which limits the yield of the substrate removal process. The damage caused by thermal and mechanical stresses may be reduced by patterning the epitaxial structure down to the sapphire substrate or down to a suitable depth of the epitaxial structure, to form trenches between individual devices on the wafer. The trenches are formed by conventional masking and dry etching techniques, before the wafer is bonded to the host substrate structure. The laser exposure region is then matched to the pattern of trenches on the wafer. The trench isolates the impact of the laser pulse to the semiconductor region being exposed and provides a preferred path for stress relaxation. - As an alternative to laser lift off as described above, a sapphire substrate or other suitable substrate may be removed by photoelectrochemical etching. Substrate removal by photoelectrochemical etching is illustrated in
FIG. 16 . After growth ofepitaxial layers 20 ongrowth substrate 40,trenches 6 may be formed in the epitaxial layers of the device and a portion of substrate 40 (for example, the 30 microns ofsubstrate 40 closest to the epitaxial layers) by laser scribing as is known in the art, or any other suitable technique. The epitaxial layers are then bonded to hostsubstrate structure 49 through p-contact 12 andbonding layers Growth substrate 40 may then be thinned by conventional means such as grinding to expose thetrench 6 to ambient. The structure is immersed in a solution suitable for photoelectrochemical etching that flows intotrenches 6, and the structure is exposed throughsubstrate 40 tolight 8 with an energy greater than the band gap ofsacrificial layer 41. Exposure to the light generates electron-hole pairs insacrificial layer 41, which break the bonds ofsacrificial layer 41, undercutting and releasingsubstrate 40 from the epitaxial structure. The epitaxial structure may include an etch-stop layer 42, which terminates the photoelectrochemical etch. Further details of photoelectrochemical etching and suitable etch stop layers 42 are described below in reference toFIG. 7 . - Growth substrates other than sapphire may be removed with ordinary chemical etchants, and thus may not require the laser exposure substrate removal procedure described above.
FIG. 15 illustrates an example of asubstrate 40 that may be removed by chemical etching.Substrate 40 ofFIG. 15 includes aSiC layer 40C grown or processed onto aSi base 40A. An optional SiOx layer 41B may be disposed betweenbase 40A andSiC layer 40C.Si base layer 40A andoxide layer 40B may be easily removed by conventional silicon processing techniques.SiC layer 40C may be thin enough, for example, less than 0.5 μm thick, to be removed entirely by known dry etching or abrasive techniques. P-contact 12 may then be formed on the exposed surface of epitaxial layers 45. Alternatively, p-contact 12 may be formed in holes etched inSiC layer 40C. - After the growth substrate is removed, the remaining epitaxial layers are thinned to the
etch stop layer 42 by, for example, photoelectrochemical etching (PEC) as illustrated inFIG. 7 . The host substrate and epitaxial layers (structure 53) are immersed in abasic solution 50. An example of a suitable basic solution is 0.2 M KOH, though many other suitable basic or acidic solutions may be used and depend on the composition of the material to be etched and the desired surface texture. The epitaxial surface ofstructure 53, generally an n-type GaN layer, is exposed to light with energy greater than the band gap of the surface layer. In the example illustrated inFIG. 7 , ultraviolet light with a wavelength of about 365 nm and an intensity between about 10 and about 100 mW/cm2 is used. Exposure to the light generates electron-hole pairs in the surface semiconductor layer. The holes migrate to the surface of the epitaxial layers under the influence of the electric field in the n-type semiconductor. The holes then react with the GaN at the surface andbasic solution 50 to break the GaN bonds, according to the equation
2GaN+60H−+6e +=2Ga(OH)3+N2.
An external electric potential may be applied acrosselectrodes - The etch stop layer may have a composition selected for a band gap greater than that of the layer to be etched. For example, the etched layer may be GaN, and the etch stop layer may be AlGaN. The light source used to expose
structure 53 is selected to have an energy greater than the band gap of the layer to be etched, but less than the band gap of the etch stop layer. Accordingly, exposure to the light does not generate electron-hole pairs in the etch stop layer, effectively halting the etch once the etch stop layer is reached. In some embodiments, InGaN may be used as the etch stop layer. Indium oxide, formed as the InGaN decomposes, is insoluble in the etchant solution and coats the surface of the etched layer, terminating the etch. After thinning, the etch stop layer may optionally be removed, for example, by continuing photoelectrochemical etching with light of a different energy in the case of an AlGaN etch stop layer, or by agitating the solution to disturb the indium oxide coating the surface of the etched layer in the case of an InGaN etch stop layer. - In embodiments where a substrate is removed by photoelectrochemical etching then thinned by photoelectrochemical etching, the device may include multiple etch stop layers, a first etch stop layer close to the growth substrate to control the etch during growth substrate removal, and a second etch stop layer close to the active region to control the etch during thinning. In some embodiments, the growth substrate is removed by photoelectrochemical etching, then a portion of n-
type region 108 is removed by a conventional etch, such as a reactive ion etch. The resonant cavity is formed by further thinning n-type region 108 in a second photoelectrochemical etch. - Though the embodiment illustrated in
FIG. 1 shows a uniformly thick n-type region, in some embodiments a three dimensional structure may be formed on n-type region 108 during thinning. For example, n-type region 108 may be patterned such that the portion undercontact 10 is thicker than the portion undermirror 11, in order to minimize the thickness of the cavity, while providing enough n-type material undercontact 10 for adequate current spreading, optimal contact resistance, and mechanical strength. Such a structure also permits testing during pauses in the etching process to check for optimum etch depth based on reflectivity and radiometric measurements of output light. - After thinning the epitaxial layers, contact 10 and
mirror 11 are deposited on the exposed surface ofepitaxial structure 20. Ifmirror 11 is not conductive (a dielectric DBR for example), an optional current spreadinglayer 70 of, for example, conductive indium tin oxide or a heavily doped III-nitride material may be included betweenmirror 11 and n-type region 108 in order to spread current fromcontact 10 undermirror 11. The current spreading layer may be contacted by removing portions ofmirror 11 down to the current spreading layer to create channels and extendingcontact 10 into the channel or depositing an additional conductive material in the channels that makes electrical contact withcontact 10. -
FIG. 8 is a cross sectional view of a portion of a resonant cavity device including trenches, according embodiments of the invention. Etch vias 72 are etched throughDBR 11 into n-type region 108 in order to interrupt the waveguide at the interface of n-type region 108 andDBR 11. Etch vias 72 may thus enhance extraction from the device by limiting the number of modes in the device. Etch vias 72 are typically confined to n-type region 108 and generally do not extend intoactive region 112. Etch vias 72 may have a depth between about 0.1 μm and about 2.5 μm and may be spaced about 1 μm to about 10 μm apart. A usual distance between two adjacent trenches is about 3 μm.Trenches 72 may form a pattern of broken lines to facilitate current spreading in the etched layer.FIGS. 9, 10 , and 11 illustrate examples of patterns oftrenches 72.Trenches 72 may be formed by conventional etching steps after depositingmirror 11. - In some embodiments of the invention,
DBR 11 on the surface of n-type region 108 is divided into multiple regions separated by metal contacts, instead of asingle DBR 11, as illustrated inFIG. 1 .FIGS. 12 and 13 are a plan view and a cross sectional view of a portion of such a device. Each region ofDBR 11 may be, for example, about 50 μm to about 150 μm across. Though the regions shown are square, other shapes may be used. Each DBR region is separated by, for example, about 1 μm to about 10 μm. The areas betweenDBR regions 11 are filled with n-contact 10. In some embodiments, an optional current spreadinglayer 70, which may be, for example, indium tin oxide or RuO, is disposed between n-type region 108 andDBR regions 11 and n-contact regions 11. Current injection in the regions ofepitaxial layers 20 beneath n-contacts 10 may be blocked by hydrogen implantation as described above, in order to confine light emission to the areas underlyingDBR regions 11. - In the device illustrated in
FIGS. 12 and 13 , p-contact 12 may be a single, continuous reflective sheet, as illustrated inFIG. 13 , or may have regions of high reflectivity oppositeDBR regions 11.FIG. 14 is a cutaway plan view of a p-contact 12.Mirror regions 80 are aligned withDBR regions 11, illustrated inFIG. 12 .Mirror regions 80 are optimized for high reflectivity and are separated by contact regions 82, which may be optimized for good adhesion.Mirror regions 80 may be, for example, silver, and contact regions 82 may be, for example, nickel. - Having described the invention in detail, those skilled in the art will appreciate that, given the present disclosure, modifications may be made to the invention without departing from the spirit of the inventive concept described herein. Therefore, it is not intended that the scope of the invention be limited to the specific embodiments illustrated and described.
Claims (11)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/227,416 US20060014310A1 (en) | 2004-06-03 | 2005-09-14 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/861,745 US6956246B1 (en) | 2004-06-03 | 2004-06-03 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
US11/227,416 US20060014310A1 (en) | 2004-06-03 | 2005-09-14 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/861,745 Division US6956246B1 (en) | 2004-06-03 | 2004-06-03 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
Publications (1)
Publication Number | Publication Date |
---|---|
US20060014310A1 true US20060014310A1 (en) | 2006-01-19 |
Family
ID=34939988
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/861,745 Expired - Lifetime US6956246B1 (en) | 2004-06-03 | 2004-06-03 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
US11/227,416 Abandoned US20060014310A1 (en) | 2004-06-03 | 2005-09-14 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/861,745 Expired - Lifetime US6956246B1 (en) | 2004-06-03 | 2004-06-03 | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal |
Country Status (4)
Country | Link |
---|---|
US (2) | US6956246B1 (en) |
EP (1) | EP1603171B1 (en) |
JP (1) | JP5007027B2 (en) |
TW (1) | TWI392176B (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060154391A1 (en) * | 2005-01-11 | 2006-07-13 | Tran Chuong A | Light emitting diodes (LEDs) with improved light extraction by roughening |
US20100032699A1 (en) * | 2008-08-05 | 2010-02-11 | Dicon Fiberoptics Inc. | System for High Efficiency Solid-State Light Emissions and Method of Manufacture |
US20100081256A1 (en) * | 2008-09-30 | 2010-04-01 | Toyoda Gosei Co., Ltd. | Method for producing group III nitride compound semiconductor element |
WO2012049607A1 (en) | 2010-10-12 | 2012-04-19 | Koninklijke Philips Electronics N.V. | Pec biasing technique for leds |
US20130050686A1 (en) * | 2011-08-25 | 2013-02-28 | Palo Alto Research Center Incorporated | Gap distributed bragg reflectors |
KR101256755B1 (en) * | 2010-11-12 | 2013-04-24 | 세미엘이디즈 옵토일렉트로닉스, 컴퍼니 리미티드 | Vertical Light Emitting Diode (VLED) Die Having N-Type Confinement Structure With Etch Stop Layer And Method Of Fabrication |
US10748762B2 (en) | 2018-07-13 | 2020-08-18 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Process for fabricating at least one semiconductor structure comprising a step of separation relative to the growth substrate |
EP3910663A1 (en) * | 2020-05-14 | 2021-11-17 | The Boeing Company | Fabricating a silicon carbide and nitride structures on a carrier substrate |
WO2022104595A1 (en) * | 2020-11-18 | 2022-05-27 | 苏州晶湛半导体有限公司 | Light-emitting device and preparation method therefor |
US11361964B2 (en) | 2020-05-14 | 2022-06-14 | The Boeing Company | Fabricating a silicon carbide and nitride structures on a carrier substrate |
US11714231B2 (en) | 2020-05-14 | 2023-08-01 | The Boeing Company | Silicon carbide and nitride structures on a substrate |
Families Citing this family (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7361938B2 (en) | 2004-06-03 | 2008-04-22 | Philips Lumileds Lighting Company Llc | Luminescent ceramic for a light emitting device |
US20070267646A1 (en) * | 2004-06-03 | 2007-11-22 | Philips Lumileds Lighting Company, Llc | Light Emitting Device Including a Photonic Crystal and a Luminescent Ceramic |
US7256483B2 (en) * | 2004-10-28 | 2007-08-14 | Philips Lumileds Lighting Company, Llc | Package-integrated thin film LED |
US20060204865A1 (en) * | 2005-03-08 | 2006-09-14 | Luminus Devices, Inc. | Patterned light-emitting devices |
TWI251357B (en) * | 2005-06-21 | 2006-03-11 | Epitech Technology Corp | Light-emitting diode and method for manufacturing the same |
US7384808B2 (en) * | 2005-07-12 | 2008-06-10 | Visual Photonics Epitaxy Co., Ltd. | Fabrication method of high-brightness light emitting diode having reflective layer |
US20070019699A1 (en) * | 2005-07-22 | 2007-01-25 | Robbins Virginia M | Light emitting device and method of manufacture |
DE102005055293A1 (en) * | 2005-08-05 | 2007-02-15 | Osram Opto Semiconductors Gmbh | Method for producing semiconductor chips and thin-film semiconductor chip |
DE102005046942A1 (en) | 2005-09-30 | 2007-04-05 | Osram Opto Semiconductors Gmbh | Method for connecting several layers made from a semiconductor material and a replacement substrate used in thin layer technology comprises using a joining layer formed by thermal compression |
US8257987B2 (en) * | 2006-02-02 | 2012-09-04 | Trustees Of Boston University | Planarization of GaN by photoresist technique using an inductively coupled plasma |
DE102007004303A1 (en) | 2006-08-04 | 2008-02-07 | Osram Opto Semiconductors Gmbh | Thin-film semiconductor device and device composite |
JP2008041937A (en) * | 2006-08-07 | 2008-02-21 | Yokogawa Electric Corp | Surface emitting laser |
US20080132081A1 (en) * | 2006-12-04 | 2008-06-05 | Shaheen Mohamad A | Thin III-V semiconductor films with high electron mobility |
US8110838B2 (en) * | 2006-12-08 | 2012-02-07 | Luminus Devices, Inc. | Spatial localization of light-generating portions in LEDs |
DE102007004304A1 (en) * | 2007-01-29 | 2008-07-31 | Osram Opto Semiconductors Gmbh | Thin-film light emitting diode chip, has layer stack made of primary radiation surfaces lying opposite to each other so that thin-film light emitting diode chip has two primary radiation directions |
DE102007030129A1 (en) * | 2007-06-29 | 2009-01-02 | Osram Opto Semiconductors Gmbh | Method for producing a plurality of optoelectronic components and optoelectronic component |
KR100949571B1 (en) * | 2008-01-21 | 2010-03-25 | 포항공과대학교 산학협력단 | Photon laser and its manufacturing method |
JP2009188249A (en) * | 2008-02-07 | 2009-08-20 | Nanoteco Corp | Light-emitting diode and method of manufacturing the same, and light-emitting diode array |
JP5326643B2 (en) * | 2009-02-20 | 2013-10-30 | 日亜化学工業株式会社 | Method of manufacturing nitride semiconductor device |
US8247886B1 (en) | 2009-03-09 | 2012-08-21 | Soraa, Inc. | Polarization direction of optical devices using selected spatial configurations |
JP5182189B2 (en) * | 2009-03-27 | 2013-04-10 | 富士通株式会社 | Manufacturing method of semiconductor device |
US8299473B1 (en) | 2009-04-07 | 2012-10-30 | Soraa, Inc. | Polarized white light devices using non-polar or semipolar gallium containing materials and transparent phosphors |
US8791499B1 (en) | 2009-05-27 | 2014-07-29 | Soraa, Inc. | GaN containing optical devices and method with ESD stability |
JP5397042B2 (en) * | 2009-06-26 | 2014-01-22 | 富士通株式会社 | Manufacturing method of semiconductor device |
US8507304B2 (en) * | 2009-07-17 | 2013-08-13 | Applied Materials, Inc. | Method of forming a group III-nitride crystalline film on a patterned substrate by hydride vapor phase epitaxy (HVPE) |
US20110027973A1 (en) * | 2009-07-31 | 2011-02-03 | Applied Materials, Inc. | Method of forming led structures |
US8148241B2 (en) * | 2009-07-31 | 2012-04-03 | Applied Materials, Inc. | Indium surfactant assisted HVPE of high quality gallium nitride and gallium nitride alloy films |
US9000466B1 (en) | 2010-08-23 | 2015-04-07 | Soraa, Inc. | Methods and devices for light extraction from a group III-nitride volumetric LED using surface and sidewall roughening |
US8207554B2 (en) | 2009-09-11 | 2012-06-26 | Soraa, Inc. | System and method for LED packaging |
US9293667B2 (en) | 2010-08-19 | 2016-03-22 | Soraa, Inc. | System and method for selected pump LEDs with multiple phosphors |
CN102630349B (en) | 2009-09-18 | 2017-06-13 | 天空公司 | Method power led and using current density operation |
US9583678B2 (en) | 2009-09-18 | 2017-02-28 | Soraa, Inc. | High-performance LED fabrication |
US9293644B2 (en) | 2009-09-18 | 2016-03-22 | Soraa, Inc. | Power light emitting diode and method with uniform current density operation |
US8933644B2 (en) | 2009-09-18 | 2015-01-13 | Soraa, Inc. | LED lamps with improved quality of light |
US8575642B1 (en) | 2009-10-30 | 2013-11-05 | Soraa, Inc. | Optical devices having reflection mode wavelength material |
EP2330697A1 (en) * | 2009-12-07 | 2011-06-08 | S.O.I.Tec Silicon on Insulator Technologies | Semiconductor device having an InGaN layer |
US20110186874A1 (en) * | 2010-02-03 | 2011-08-04 | Soraa, Inc. | White Light Apparatus and Method |
US8905588B2 (en) | 2010-02-03 | 2014-12-09 | Sorra, Inc. | System and method for providing color light sources in proximity to predetermined wavelength conversion structures |
US8740413B1 (en) | 2010-02-03 | 2014-06-03 | Soraa, Inc. | System and method for providing color light sources in proximity to predetermined wavelength conversion structures |
US10147850B1 (en) | 2010-02-03 | 2018-12-04 | Soraa, Inc. | System and method for providing color light sources in proximity to predetermined wavelength conversion structures |
CN101792106B (en) * | 2010-04-08 | 2011-09-07 | 长春理工大学 | Etching solution for processing N-type silicon microchannel array by photon-assisted electrochemical etching method |
US8293551B2 (en) | 2010-06-18 | 2012-10-23 | Soraa, Inc. | Gallium and nitrogen containing triangular or diamond-shaped configuration for optical devices |
US9450143B2 (en) | 2010-06-18 | 2016-09-20 | Soraa, Inc. | Gallium and nitrogen containing triangular or diamond-shaped configuration for optical devices |
US8541951B1 (en) | 2010-11-17 | 2013-09-24 | Soraa, Inc. | High temperature LED system using an AC power source |
US8896235B1 (en) | 2010-11-17 | 2014-11-25 | Soraa, Inc. | High temperature LED system using an AC power source |
US8786053B2 (en) | 2011-01-24 | 2014-07-22 | Soraa, Inc. | Gallium-nitride-on-handle substrate materials and devices and method of manufacture |
US8686431B2 (en) | 2011-08-22 | 2014-04-01 | Soraa, Inc. | Gallium and nitrogen containing trilateral configuration for optical devices |
US9488324B2 (en) | 2011-09-02 | 2016-11-08 | Soraa, Inc. | Accessories for LED lamp systems |
US8912025B2 (en) | 2011-11-23 | 2014-12-16 | Soraa, Inc. | Method for manufacture of bright GaN LEDs using a selective removal process |
WO2013123241A1 (en) | 2012-02-17 | 2013-08-22 | The Regents Of The University Of California | Method for the reuse of gallium nitride epitaxial substrates |
EP2823515A4 (en) | 2012-03-06 | 2015-08-19 | Soraa Inc | LIGHT EMITTING DIODE WITH LOW REFRACTIVE INDEX TO REDUCE LIGHT GUIDING EFFECTS |
US8985794B1 (en) | 2012-04-17 | 2015-03-24 | Soraa, Inc. | Providing remote blue phosphors in an LED lamp |
US8971368B1 (en) | 2012-08-16 | 2015-03-03 | Soraa Laser Diode, Inc. | Laser devices having a gallium and nitrogen containing semipolar surface orientation |
US9978904B2 (en) | 2012-10-16 | 2018-05-22 | Soraa, Inc. | Indium gallium nitride light emitting devices |
US8802471B1 (en) | 2012-12-21 | 2014-08-12 | Soraa, Inc. | Contacts for an n-type gallium and nitrogen substrate for optical devices |
US9761763B2 (en) | 2012-12-21 | 2017-09-12 | Soraa, Inc. | Dense-luminescent-materials-coated violet LEDs |
US8748324B1 (en) * | 2013-02-26 | 2014-06-10 | The Boeing Company | Systems and methods for separating components of a multilayer stack of electronic components |
JP2013128150A (en) * | 2013-03-26 | 2013-06-27 | Toyoda Gosei Co Ltd | Method of manufacturing group-iii nitride semiconductor light-emitting element |
US8994033B2 (en) | 2013-07-09 | 2015-03-31 | Soraa, Inc. | Contacts for an n-type gallium and nitrogen substrate for optical devices |
US9419189B1 (en) | 2013-11-04 | 2016-08-16 | Soraa, Inc. | Small LED source with high brightness and high efficiency |
US20150372096A1 (en) * | 2014-06-20 | 2015-12-24 | Ishiang Shih | High Electron Mobility Transistors and Integrated Circuits with Improved Feature Uniformity and Reduced defects for Microwave and Millimetre Wave Applications |
US11025031B2 (en) * | 2016-11-29 | 2021-06-01 | Leonardo Electronics Us Inc. | Dual junction fiber-coupled laser diode and related methods |
CN110854154B (en) * | 2019-11-18 | 2024-04-30 | 佛山市国星半导体技术有限公司 | Silicon-based micro LED chip and manufacturing method thereof |
Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5390210A (en) * | 1993-11-22 | 1995-02-14 | Hewlett-Packard Company | Semiconductor laser that generates second harmonic light with attached nonlinear crystal |
US5838707A (en) * | 1996-12-27 | 1998-11-17 | Motorola, Inc. | Ultraviolet/visible light emitting vertical cavity surface emitting laser and method of fabrication |
US5862167A (en) * | 1994-07-19 | 1999-01-19 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride compound |
US5985687A (en) * | 1996-04-12 | 1999-11-16 | The Regents Of The University Of California | Method for making cleaved facets for lasers fabricated with gallium nitride and other noncubic materials |
US6061381A (en) * | 1995-09-29 | 2000-05-09 | British Telecommunications Public Limited Company | Optically resonant structure |
US6071795A (en) * | 1998-01-23 | 2000-06-06 | The Regents Of The University Of California | Separation of thin films from transparent substrates by selective optical processing |
US6111272A (en) * | 1997-09-29 | 2000-08-29 | Siemens Aktiengesellschaft | Semiconductor light source formed of layer stack with total thickness of 50 microns |
US6113685A (en) * | 1998-09-14 | 2000-09-05 | Hewlett-Packard Company | Method for relieving stress in GaN devices |
US6177359B1 (en) * | 1999-06-07 | 2001-01-23 | Agilent Technologies, Inc. | Method for detaching an epitaxial layer from one substrate and transferring it to another substrate |
US6280523B1 (en) * | 1999-02-05 | 2001-08-28 | Lumileds Lighting, U.S., Llc | Thickness tailoring of wafer bonded AlxGayInzN structures by laser melting |
US6320206B1 (en) * | 1999-02-05 | 2001-11-20 | Lumileds Lighting, U.S., Llc | Light emitting devices having wafer bonded aluminum gallium indium nitride structures and mirror stacks |
US20030045120A1 (en) * | 2001-09-04 | 2003-03-06 | Hu Evelyn L. | Photoelectrochemical undercut etching of semiconductor material |
US6559075B1 (en) * | 1996-10-01 | 2003-05-06 | Siemens Aktiengesellschaft | Method of separating two layers of material from one another and electronic components produced using this process |
US20030092212A1 (en) * | 2001-05-09 | 2003-05-15 | Margaret Buchanan | Method for micro-fabricating a pixelless infrared imaging device |
US20030222263A1 (en) * | 2002-06-04 | 2003-12-04 | Kopin Corporation | High-efficiency light-emitting diodes |
US20040023468A1 (en) * | 2002-01-22 | 2004-02-05 | Bruno Ghyselen | Method for manufacturing a free-standing substrate made of monocrystalline semi-conductor material |
US20040046180A1 (en) * | 2001-03-21 | 2004-03-11 | Kabushiki Kaisha Toshiba | Resonant-cavity light-emitting diode and optical transmission module using the light-emitting diode |
US20050139847A1 (en) * | 2003-12-24 | 2005-06-30 | Taeyoub Kim | Silicon-based light emitting diode |
US20050205884A1 (en) * | 2004-03-19 | 2005-09-22 | Lumileds Lighting U.S., Llc | Semiconductor light emitting devices including in-plane light emitting layers |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1174562A (en) * | 1997-06-30 | 1999-03-16 | Nichia Chem Ind Ltd | Nitride semiconductor element |
US6903376B2 (en) * | 1999-12-22 | 2005-06-07 | Lumileds Lighting U.S., Llc | Selective placement of quantum wells in flipchip light emitting diodes for improved light extraction |
TW445507B (en) * | 2000-07-20 | 2001-07-11 | United Epitaxy Co Ltd | Roughened interface of light emitting device |
JP2003092426A (en) * | 2001-09-18 | 2003-03-28 | Nichia Chem Ind Ltd | Nitride compound semiconductor light emitting element and its manufacturing method |
JP2002185043A (en) * | 2001-10-19 | 2002-06-28 | Sumitomo Chem Co Ltd | Method for manufacturing group 3-5 compound semiconductor light emitting device |
US7279718B2 (en) * | 2002-01-28 | 2007-10-09 | Philips Lumileds Lighting Company, Llc | LED including photonic crystal structure |
DE10208171A1 (en) * | 2002-02-26 | 2003-09-18 | Osram Opto Semiconductors Gmbh | Radiation-emitting semiconductor component with a vertical emission direction and production method therefor |
KR101030068B1 (en) | 2002-07-08 | 2011-04-19 | 니치아 카가쿠 고교 가부시키가이샤 | Nitride semiconductor device manufacturing method and nitride semiconductor device |
US7102175B2 (en) * | 2003-04-15 | 2006-09-05 | Matsushita Electric Industrial Co., Ltd. | Semiconductor light-emitting device and method for fabricating the same |
-
2004
- 2004-06-03 US US10/861,745 patent/US6956246B1/en not_active Expired - Lifetime
-
2005
- 2005-05-27 EP EP05104535.9A patent/EP1603171B1/en active Active
- 2005-05-31 JP JP2005160075A patent/JP5007027B2/en active Active
- 2005-05-31 TW TW094117898A patent/TWI392176B/en active
- 2005-09-14 US US11/227,416 patent/US20060014310A1/en not_active Abandoned
Patent Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5390210A (en) * | 1993-11-22 | 1995-02-14 | Hewlett-Packard Company | Semiconductor laser that generates second harmonic light with attached nonlinear crystal |
US5862167A (en) * | 1994-07-19 | 1999-01-19 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride compound |
US6061381A (en) * | 1995-09-29 | 2000-05-09 | British Telecommunications Public Limited Company | Optically resonant structure |
US5985687A (en) * | 1996-04-12 | 1999-11-16 | The Regents Of The University Of California | Method for making cleaved facets for lasers fabricated with gallium nitride and other noncubic materials |
US6559075B1 (en) * | 1996-10-01 | 2003-05-06 | Siemens Aktiengesellschaft | Method of separating two layers of material from one another and electronic components produced using this process |
US5838707A (en) * | 1996-12-27 | 1998-11-17 | Motorola, Inc. | Ultraviolet/visible light emitting vertical cavity surface emitting laser and method of fabrication |
US6111272A (en) * | 1997-09-29 | 2000-08-29 | Siemens Aktiengesellschaft | Semiconductor light source formed of layer stack with total thickness of 50 microns |
US6071795A (en) * | 1998-01-23 | 2000-06-06 | The Regents Of The University Of California | Separation of thin films from transparent substrates by selective optical processing |
US6113685A (en) * | 1998-09-14 | 2000-09-05 | Hewlett-Packard Company | Method for relieving stress in GaN devices |
US6280523B1 (en) * | 1999-02-05 | 2001-08-28 | Lumileds Lighting, U.S., Llc | Thickness tailoring of wafer bonded AlxGayInzN structures by laser melting |
US6320206B1 (en) * | 1999-02-05 | 2001-11-20 | Lumileds Lighting, U.S., Llc | Light emitting devices having wafer bonded aluminum gallium indium nitride structures and mirror stacks |
US6177359B1 (en) * | 1999-06-07 | 2001-01-23 | Agilent Technologies, Inc. | Method for detaching an epitaxial layer from one substrate and transferring it to another substrate |
US20040046180A1 (en) * | 2001-03-21 | 2004-03-11 | Kabushiki Kaisha Toshiba | Resonant-cavity light-emitting diode and optical transmission module using the light-emitting diode |
US20030092212A1 (en) * | 2001-05-09 | 2003-05-15 | Margaret Buchanan | Method for micro-fabricating a pixelless infrared imaging device |
US20030045120A1 (en) * | 2001-09-04 | 2003-03-06 | Hu Evelyn L. | Photoelectrochemical undercut etching of semiconductor material |
US20040023468A1 (en) * | 2002-01-22 | 2004-02-05 | Bruno Ghyselen | Method for manufacturing a free-standing substrate made of monocrystalline semi-conductor material |
US20030222263A1 (en) * | 2002-06-04 | 2003-12-04 | Kopin Corporation | High-efficiency light-emitting diodes |
US20050139847A1 (en) * | 2003-12-24 | 2005-06-30 | Taeyoub Kim | Silicon-based light emitting diode |
US20050205884A1 (en) * | 2004-03-19 | 2005-09-22 | Lumileds Lighting U.S., Llc | Semiconductor light emitting devices including in-plane light emitting layers |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7186580B2 (en) * | 2005-01-11 | 2007-03-06 | Semileds Corporation | Light emitting diodes (LEDs) with improved light extraction by roughening |
US20060154391A1 (en) * | 2005-01-11 | 2006-07-13 | Tran Chuong A | Light emitting diodes (LEDs) with improved light extraction by roughening |
US20100032699A1 (en) * | 2008-08-05 | 2010-02-11 | Dicon Fiberoptics Inc. | System for High Efficiency Solid-State Light Emissions and Method of Manufacture |
US7919780B2 (en) * | 2008-08-05 | 2011-04-05 | Dicon Fiberoptics, Inc. | System for high efficiency solid-state light emissions and method of manufacture |
US8324083B2 (en) * | 2008-09-30 | 2012-12-04 | Toyoda Gosei Co., Ltd. | Method for producing group III nitride compound semiconductor element |
US20100081256A1 (en) * | 2008-09-30 | 2010-04-01 | Toyoda Gosei Co., Ltd. | Method for producing group III nitride compound semiconductor element |
US8912049B2 (en) | 2010-10-12 | 2014-12-16 | Koninklijke Philips N.V. | PEC biasing technique for LEDs |
TWI514627B (en) * | 2010-10-12 | 2015-12-21 | Koninkl Philips Electronics Nv | Photoelectrochemical (PEC) bias technology for light-emitting diodes |
CN103155190A (en) * | 2010-10-12 | 2013-06-12 | 皇家飞利浦电子股份有限公司 | Pec biasing technique for LEDs |
WO2012049607A1 (en) | 2010-10-12 | 2012-04-19 | Koninklijke Philips Electronics N.V. | Pec biasing technique for leds |
KR101256755B1 (en) * | 2010-11-12 | 2013-04-24 | 세미엘이디즈 옵토일렉트로닉스, 컴퍼니 리미티드 | Vertical Light Emitting Diode (VLED) Die Having N-Type Confinement Structure With Etch Stop Layer And Method Of Fabrication |
US9912121B2 (en) | 2011-08-25 | 2018-03-06 | Palo Alto Research Center Incorporated | Gap distributed Bragg reflectors |
US9335262B2 (en) * | 2011-08-25 | 2016-05-10 | Palo Alto Research Center Incorporated | Gap distributed Bragg reflectors |
US20130050686A1 (en) * | 2011-08-25 | 2013-02-28 | Palo Alto Research Center Incorporated | Gap distributed bragg reflectors |
US10748762B2 (en) | 2018-07-13 | 2020-08-18 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Process for fabricating at least one semiconductor structure comprising a step of separation relative to the growth substrate |
EP3910663A1 (en) * | 2020-05-14 | 2021-11-17 | The Boeing Company | Fabricating a silicon carbide and nitride structures on a carrier substrate |
US11361964B2 (en) | 2020-05-14 | 2022-06-14 | The Boeing Company | Fabricating a silicon carbide and nitride structures on a carrier substrate |
US11714231B2 (en) | 2020-05-14 | 2023-08-01 | The Boeing Company | Silicon carbide and nitride structures on a substrate |
EP4459684A3 (en) * | 2020-05-14 | 2025-01-22 | The Boeing Company | Fabricating a silicon carbide and nitride structures on a carrier substrate |
WO2022104595A1 (en) * | 2020-11-18 | 2022-05-27 | 苏州晶湛半导体有限公司 | Light-emitting device and preparation method therefor |
TWI825507B (en) * | 2020-11-18 | 2023-12-11 | 中國商蘇州晶湛半導體有限公司 | Light-emitting device and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
EP1603171A2 (en) | 2005-12-07 |
TWI392176B (en) | 2013-04-01 |
JP2005347747A (en) | 2005-12-15 |
US6956246B1 (en) | 2005-10-18 |
EP1603171B1 (en) | 2016-09-14 |
TW200616299A (en) | 2006-05-16 |
JP5007027B2 (en) | 2012-08-22 |
EP1603171A3 (en) | 2011-04-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6956246B1 (en) | Resonant cavity III-nitride light emitting devices fabricated by growth substrate removal | |
US7675084B2 (en) | Photonic crystal light emitting device | |
KR101203365B1 (en) | LIFT-OFF PROCESS FOR GaN FILMS FORMED ON SiC SUBSTRATE AND DEVICES FABRICATED USING THE METHOD | |
JP5468203B2 (en) | Method of manufacturing a group 3 nitride device and device manufactured using the method | |
JP4860024B2 (en) | InXAlYGaZN light emitting device and manufacturing method thereof | |
KR100707955B1 (en) | Light emitting diode and manufacturing method for the same | |
US8093607B2 (en) | Optoelectronic semiconductor component | |
JP2013102240A (en) | Group iii nitride light emitting device having light emitting region with double hetero-structure | |
EP2973755B1 (en) | Semiconductor structure comprising a porous reflective contact | |
JP2006344971A (en) | Method for removing growth substrate of semiconductor light emitting device | |
JP2006005369A (en) | Light-emitting device with transparent submount with backside via | |
US20110121358A1 (en) | P-type layer for a iii-nitride light emitting device | |
KR101991961B1 (en) | Reflective contact for a semiconductor light emitting device | |
KR101499954B1 (en) | fabrication of vertical structured light emitting diodes using group 3 nitride-based semiconductors and its related methods | |
KR100729759B1 (en) | Light emitting diodes and method for manufacturing same | |
JP2008288538A (en) | p-TYPE LAYER FOR GROUP III NITRIDE LIGHT EMITTING DEVICE | |
JP2013207108A (en) | Light-emitting diode element and manufacturing method of the same | |
KR20090115830A (en) | Group III-nitride semiconductor light emitting diode device of vertical structure and manufacturing method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |
|
AS | Assignment |
Owner name: LUMILEDS LIGHTING, U.S. LLC, CALIFORNIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:EPLER, JOHN E.;KRAMES, MICHAEL R.;WIERER, JONATHAN J.;REEL/FRAME:045473/0931 Effective date: 20040830 |
|
AS | Assignment |
Owner name: PHILIPS LUMILEDS LIGHTING COMPANY LLC, CALIFORNIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:LUMILEDS LIGHTING, U.S. LLC;REEL/FRAME:045530/0395 Effective date: 20110215 |
|
AS | Assignment |
Owner name: LUMILEDS LLC, CALIFORNIA Free format text: CHANGE OF NAME;ASSIGNOR:PHILIPS LUMILEDS LIGHTING COMPANY LLC;REEL/FRAME:046623/0038 Effective date: 20150326 |