WO2006022399A1 - Positive electrode for compound semiconductor light-emitting device - Google Patents
Positive electrode for compound semiconductor light-emitting device Download PDFInfo
- Publication number
- WO2006022399A1 WO2006022399A1 PCT/JP2005/015596 JP2005015596W WO2006022399A1 WO 2006022399 A1 WO2006022399 A1 WO 2006022399A1 JP 2005015596 W JP2005015596 W JP 2005015596W WO 2006022399 A1 WO2006022399 A1 WO 2006022399A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- emitting device
- positive electrode
- compound
- semiconductor light
- Prior art date
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 92
- 150000001875 compounds Chemical class 0.000 title description 17
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052709 silver Inorganic materials 0.000 claims abstract description 18
- 239000004332 silver Substances 0.000 claims abstract description 17
- 229910001316 Ag alloy Inorganic materials 0.000 claims abstract description 12
- 229910052751 metal Inorganic materials 0.000 claims description 42
- 239000002184 metal Substances 0.000 claims description 42
- 229910002601 GaN Inorganic materials 0.000 claims description 32
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 claims description 23
- 229910045601 alloy Inorganic materials 0.000 claims description 12
- 239000000956 alloy Substances 0.000 claims description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 8
- 229910052763 palladium Inorganic materials 0.000 claims description 6
- 239000010949 copper Substances 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 229910052741 iridium Inorganic materials 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 229910052703 rhodium Inorganic materials 0.000 claims description 4
- 229910052707 ruthenium Inorganic materials 0.000 claims description 4
- 229910052779 Neodymium Inorganic materials 0.000 claims description 3
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- 229910052762 osmium Inorganic materials 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 2
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims description 2
- 238000000034 method Methods 0.000 description 23
- 238000004544 sputter deposition Methods 0.000 description 23
- 239000000758 substrate Substances 0.000 description 17
- 239000000463 material Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 8
- 229910052594 sapphire Inorganic materials 0.000 description 7
- 239000010980 sapphire Substances 0.000 description 7
- 238000005530 etching Methods 0.000 description 6
- 238000009792 diffusion process Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 229910002704 AlGaN Inorganic materials 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000004767 nitrides Chemical class 0.000 description 3
- -1 platinum group metals Chemical class 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002019 doping agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 238000002248 hydride vapour-phase epitaxy Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 238000001451 molecular beam epitaxy Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000005477 sputtering target Methods 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
- RGGPNXQUMRMPRA-UHFFFAOYSA-N triethylgallium Chemical compound CC[Ga](CC)CC RGGPNXQUMRMPRA-UHFFFAOYSA-N 0.000 description 2
- OTRPZROOJRIMKW-UHFFFAOYSA-N triethylindigane Chemical compound CC[In](CC)CC OTRPZROOJRIMKW-UHFFFAOYSA-N 0.000 description 2
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 2
- XCZXGTMEAKBVPV-UHFFFAOYSA-N trimethylgallium Chemical compound C[Ga](C)C XCZXGTMEAKBVPV-UHFFFAOYSA-N 0.000 description 2
- IBEFSUTVZWZJEL-UHFFFAOYSA-N trimethylindium Chemical compound C[In](C)C IBEFSUTVZWZJEL-UHFFFAOYSA-N 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- 229910007264 Si2H6 Inorganic materials 0.000 description 1
- USZGMDQWECZTIQ-UHFFFAOYSA-N [Mg](C1C=CC=C1)C1C=CC=C1 Chemical compound [Mg](C1C=CC=C1)C1C=CC=C1 USZGMDQWECZTIQ-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- JFDAACUVRQBXJO-UHFFFAOYSA-N ethylcyclopentane;magnesium Chemical compound [Mg].CC[C]1[CH][CH][CH][CH]1.CC[C]1[CH][CH][CH][CH]1 JFDAACUVRQBXJO-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910000078 germane Inorganic materials 0.000 description 1
- QUZPNFFHZPRKJD-UHFFFAOYSA-N germane Chemical compound [GeH4] QUZPNFFHZPRKJD-UHFFFAOYSA-N 0.000 description 1
- 150000002291 germanium compounds Chemical class 0.000 description 1
- 229910052986 germanium hydride Inorganic materials 0.000 description 1
- 229910021478 group 5 element Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/36—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the electrodes
- H01L33/40—Materials therefor
- H01L33/405—Reflective materials
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/02—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies
- H01L33/26—Materials of the light emitting region
- H01L33/30—Materials of the light emitting region containing only elements of Group III and Group V of the Periodic Table
- H01L33/32—Materials of the light emitting region containing only elements of Group III and Group V of the Periodic Table containing nitrogen
Definitions
- the present invention relates to a positive electrode for a compound-semiconductor light-emitting device, a light-emitting device and a lamp using such a positive electrode and, particularly, to a positive electrode excellent in electrical characteristics and stability, as well as to a compound-semiconductor light- emitting device provided therewith and the inventions relating thereto.
- gallium nitride-based compound semiconductor represented by the formula Al x In y Gai- x - y N (0 ⁇ x ⁇ 1, 0 ⁇ y ⁇ 1, x+y ⁇ 1) has attracted much attention as a material for a light-emitting diode (LED) emitting ultraviolet to blue light, or green light.
- LED light-emitting diode
- Gallium nitride- based compound semiconductors are generally grown on a sapphire substrate. As this is an insulating substrate, unlike that for GaAs-based light-emitting devices, an electrode cannot be provided on rear surface of the substrate. Therefore, both negative and positive electrodes must be provided on the semiconductor grown as a crystal.
- a flip-chip-type structure in which the device is mounted with the electrode surface on the underside, and light is extracted from the side of the sapphire substrate, has attracted much attention.
- Fig. 1 is a schematic view showing an example of general structure of light-emitting device of this type.
- a light-emitting device has a buffer layer 2, a n- type semiconductor layer 3, a light-emitting layer 4, and a p-type semiconductor layer 5 successively grown as crystal on a substrate 1, with a portion of the light- emitting layer 4 and the p-type semiconductor layer 5 removed by etching so as to expose the n-type semiconductor layer 3, and a positive electrode 10 is formed on the p-type semiconductor layer 5 and a negative electrode 20 is formed on the n-type semiconductor layer 3.
- Such a light-emitting device is mounted, for example, with the surface having electrode formed thereon facing a lead frame, and then is bonded.
- a reflective metal is ⁇ used as the positive electrode 10, and is provided so as to cover the major portion of the p-type semiconductor layer 5 to thereby cause the light from the light- emitting layer toward the positive electrode to be reflected by the positive electrode 10 and to be extracted from the side of the substrate 1.
- material for the positive electrode has a low contact resistance with the p-type semiconductor layer and a high reflectance.
- silver has the highest reflectance. It has also been known, however, that Ag often causes electromigration to occur.
- Electromigration is a phenomenon in which a material is ionized and diffuses in the presence of water. For example, if electric current is supplied, in an atmosphere wherein water exists, to the electrode in which Ag is used, a deposit mainly composed of Ag is formed. If the deposit generated from the positive electrode reaches a negative electrode or the deposit couples a p-type semiconductor layer with an n-type semiconductor layer, the inverse voltage lowers to deteriorate the characteristic of the light-emitting device with time. Accordingly, when Ag is used as a reflective positive electrode, it is necessary to restrict the electromigration of Ag so that the characteristic is stabilized.
- Japanese Unexamined Patent Publication (Kokai) Nos. 11-186598 and 11-186599 propose means for using Ag as material of the positive electrode, wherein a silver layer is provided on a p-type nitride semiconductor layer and a stabilized layer is further provided on the silver layer. It is described that the stabilized layer serves to facilitate the mechanical and electrical characteristic of the silver layer.
- the Ag layer could be formed in a stable manner on the p-type nitride semiconductor layer by controlling a deposition rate of Ag layer and a temperature of a sapphire substrate during the deposition.
- An object of the present invention is to solve the above-mentioned problems when the silver is used as a material for a positive electrode, and provide a positive electrode for a compound-semiconductor light-emitting device high in inverse voltage and excellent in stability and productivity.
- the present invention is as follows:
- a positive electrode for a compound- semiconductor light-emitting device according to (1) or (2) above, wherein a content of silver in the silver alloy is in a range from 90 to 99.99 atomic %.
- a lamp comprising the compound-semiconductor light-emitting device according to (8) or (9) above.
- the positive electrode for the compound-semiconductor light-emitting device of the present invention it is possible to effectively restrict the electromigration of silver in comparison with the prior art reflective positive electrode using silver metal alone, since silver alloy is used in the reflective layer.
- the light-emitting device using the inventive positive electrode is high in inverse voltage and excellent in stability as well as productivity.
- silver alloy generally has a reflectance higher than pure silver metal, if suitable compositions are selected. Accordingly, the light-emitting device using the inventive positive electrode also facilitates the device output.
- FIG. 1 is a schematic view showing general structure of a flip chip type compound semiconductor light-emitting device according to prior art.
- Fig. 2 is a schematic view showing an example of a flip chip type gallium nitride-based compound semiconductor light-emitting device according to the present invention.
- Best Modes for Carrying Out the Invention As a compound-semiconductor light-emitting device using the inventive positive electrode, a structure, shown in Fig. 1 and wherein a buffer layer 2, an n-type semiconductor layer 3, a light-emitting layer 4 and a p- type semiconductor layer 5 are sequentially crystallized and grown on a substrate 1, and a negative electrode and a positive electrode are provided on the n-type semiconductor layer 3 and the p-type semiconductor layer 5 can be used without limitation.
- the positive electrode comprises a reflective layer consisting of silver (Ag) alloy.
- the inventor of the present invention found that the electromigration of silver can be restricted by alloying silver. Although how the electromigration is restricted due to the alloying of silver is not yet clear, it is supposed on one hand that the aggregation of Ag is suppressed in an alloy film to result in a smoother surface. On the other hand, it is supposed that a metal alloyed with silver forms an oxide film (such as Bi 2 Oa) on the surface. In view of such a supposition, the metal alloyed with silver is preferably that easily forming the oxide film. More concretely, Nd, Pd, Cu or Bi is particularly desirable as the metal alloyed with silver.
- a ratio of Ag in the reflective layer is preferably at least 90 atomic %, more preferably at least 95 atomic %, most preferably at least 97 atomic %. If the percentage of Ag is too low, the reflectance largely lowers. On the contrary, if the percentage of Ag is too high, the restriction of the electromigration becomes unfavorable, whereby the ratio of Ag is preferably 99.99 atomic % or less, more preferably 99.9 atomic % or less, most preferably 99.5 atomic % or less.
- Alloyed Ag has a better reflectance than pure Ag metal. This is also supposed to be because the aggregation of Ag is suppressed to smooth the surface.
- a ratio of metal alloyed with silver is 1 to 2%, the reflectance becomes higher than pure Ag metal if the mating metal is suitably selected. On the contrary, the reflectance becomes lower if the alloyed ratio is high.
- the device output is also enhanced by the improvement in reflectance.
- a film thickness of the reflective layer is preferably in a range from 30 to 500 nm. If the film thickness is too small, the reflectance becomes insufficient, and, on the contrary, if the film thickness is too large, the productivity is lowered. As a result, the film thickness is more preferably in a range from 50 to 300 nm, most preferably in a range from 60 to 250 nm.
- the positive electrode according to the present invention may be formed solely of a reflective layer consisting of Ag alloy, a contact metal layer having a low contact resistance and excellent in light- transmission property may be provided between the p-type semiconductor layer and the reflective layer. Also, a bonding pad layer is generally provided as the uppermost layer, for the electric connection with a circuit board or a lead frame.
- the contact metal layer operates also as means for preventing Ag from diffusing from the reflective layer to the p-type semiconductor layer, resulting in avoiding a reduction of inverse voltage.
- a metal having a high work function As material for the contact metal layer, in order to achieve low contact resistance to the p-type semiconductor layer, it is preferable to use a metal having a high work function and, specifically, platinum group metals such as Pt, Ir, Rh, Pd, Ru and Os and alloys containing platinum group metals. Pt, Ir, Rh, and Ru are more preferable, and Pt is particularly preferable.
- the contact metal layer also has a role as a diffusion suppression layer for suppressing diffusion of Ag from the reflective layer to p-type semiconductor layer, it is preferable to use a metal of a dense structure and a high melting point. Specifically, a metal or an alloy with higher melting point than Ag is preferable. From this standpoint also, platinum group metals are preferable as materials for the contact metal layer.
- the thickness of the contact metal layer is preferably 1 nm or greater, more preferably 2 nm or greater, and most preferably 3 nm or greater. In order to obtain sufficient light-transmission property, thickness of the contact metal layer is preferably 30 nm or less, more preferably 20 nm or less, and most preferably 10 nm or less.
- thickness is preferably 0.5 nm or greater from this viewpoint, more preferably 1 nm or greater.
- the contact metal layer is a continuous layer.
- a thickness thereof is preferably in a range from 100 to 1000 nm. As the bondability becomes higher as the thickness of the bonding pad increases in view of the characteristic thereof, 300 nm or more is preferable. Further, in view f the production cost, the thickness is preferably 500 nm or less.
- the reflective layer, the contact metal layer and the bonding pad layer may be formed by any of well-known method such as sputtering or vacuum deposition. Of them, the sputtering method is preferably used because a reflective layer excellent in reflectivity and a contact metal layer low in contact resistance are obtainable.
- a sputtering film forming method using RF discharge, is used for forming the contact metal layer on the p-type semiconductor layer.
- a sputtering film forming method using RF discharge an electrode with lower contact resistance can be obtained as compared to a vapor deposition method or a sputtering film forming method using DC discharge.
- the reflective layer is preferably formed by a sputtering film forming method using DC discharge.
- the difference in the film obtained by the RF discharge sputtering method from that obtained by the DC discharge sputtering method resides in the crystallinity.
- the film obtained by the DC discharge sputtering method has a prismatic structure and is dense, while the film obtained by the RF discharge sputtering method has no prismatic structure and is coarse.
- the contact metal layer is formed initially by the RF discharge to be as thin as possible so that the light-transmission property is facilitated while maintaining the contact resistance at a low level, and then the reflective layer is formed thereon by the DC discharge.
- Sputtering may be carried out using any known conventional sputtering apparatus under any suitably selected conditions conventionally known.
- a substrate having compound semiconductor layers laminated thereon is placed in the chamber, and temperature of the substrate is set in the range from room temperature to 500°C. Although heating of the substrate is not particularly required, the substrate may be suitably heated.
- the chamber is evacuated to the degree of vacuum in the range of 10 '4 ⁇ 10 '7 Pa. He, Ne, Ar, Kr, Xe, etc. can be used as the sputtering gas. Ar is preferred in view of availability.
- One of these gases is introduced into the chamber up to the pressure of 0.1 ⁇ 10 Pa, and then, discharge is performed. Preferably the pressure is in the range of 0.2 ⁇ 5 Pa.
- Supplied electric power is preferably in the range of 0.2 ⁇ 2.0 kW.
- the content of oxygen in the required target used for sputtering is preferably 10,000 ppm or less in order to reduce the oxygen content of the formed layer, and is more preferably 6,000 ppm or less.
- the substrate may be made of any of transparent materials including the known ones such as sapphire or SiC.
- Various compound-semiconductors of gallium nitride type have been known in the art, represented by the following general formula.
- gallium nitride type compound-semiconductors are usable without any limitations.
- a gallium nitride-based semiconductor laminate having a buffer layer 2 consisting of AlN layer, a contact layer 3a consisting of n-type GaN layer, a lower clad layer 3b consisting of n-type GaN layer, a light-emitting layer 4 consisting of InGaN layer, an upper clad layer 5b consisting of p-type AlGaN layer, and a contact layer 5a consisting of p-type GaN layer successively laminated on a sapphire substrate 1 in this order, can be used.
- a part of the contact layer 5a, the upper clad layer 5b, the light-emitting layer 4 and the lower clad layer 3b of gallium nitride-based compound semiconductor is removed by etching, and a negative electrode 20 of, for example, Ti/Au is provided on the contact layer 3a by a well-known method in the art, and a positive electrode 10 is provided on the contact layer 5a.
- Group III nitride semiconductor such as MOCVD (metal- organic chemical vapor deposition) , HVPE (hydride vapor phase epitaxy) , or MBE (molecular beam epitaxy) . From the viewpoints of layer thickness controllability and mass productivity, MOCVD is preferably employed.
- H 2 hydrogen
- N 2 nitrogen
- trimethylgallium (TMG) or triethylgallium (TEG) is employed as a Ga (Group III element) source
- trimethylaluminum (TMA) or triethylaluminum (TEA) is employed as an Al (Group III element) source
- trimethylindium (TMI) or triethylindium (TEI) is employed as an In (Group III element) source
- ammonia (NH 3 ) , hydrazine (N 2 H 4 ) , or the like is employed as an N (Group V element) source.
- monosilane (SiH 4 ) or disilane (Si 2 H 6 ) serving as an Si source, or germane (GeH 4 ) or an organic germanium compound serving as a Ge source is employed as an n-type dopant
- germane (GeH 4 ) or an organic germanium compound serving as a Ge source is employed as an n-type dopant
- bis (cyclopentadienyl)magnesium (Cp 2 Mg) or bis (ethylcyclopentadienyl)magnesium ((EtCp) 2 Mg) serving as an Mg source is employed as a p-type dopant.
- a gallium-nitride-based compound semiconductor light-emitting device exhibiting excellent characteristics and stability can be produced.
- a high-luminance LED can be produced on the basis of the technique.
- electronic devices such as mobile phones and display panels, each employing a chip fabricated on the basis of the technique; and machines and apparatuses such as automobiles, computers, and game machines, each employing any of the electronic device, can be driven at low electric power and realize excellent characteristics. Particularly, an electric power saving effect is remarkably attained in mobile phones, game machines, toys, and automotive parts, which are driven by a battery.
- Table 1 indicates the compositions of the reflective layers and the contact metal layers used in Examples and Comparative Examples, the initial characteristics of the devices and results of aging tests obtained therefrom.
- the aging tests have been carried out, while using 10 samples in the respective Example, in an environment at 25°C and 40 to 60% RH while continuously supplying a current of 30 mA for 100 hours, after which the number of samples resulting in the reduction of inverse voltage; i.e., the occurrence of electromigration; is counted.
- the driving voltage and the output power are initial values measured at a current of 20 mA.
- Fig. 2 is a schematic view showing a gallium nitride-based compound semiconductor light-emitting device fabricated in the present Example.
- the gallium nitride-based compound semiconductor was formed by laminating a buffer layer 2 of AlN layer on a sapphire substrate 1, and by successively laminating thereon a contact layer 3a of n-type GaN layer, a lower clad layer 3b of n-ty ⁇ e GaN layer, a light-emitting layer 4 of InGaN layer, an upper clad layer 5b of p-type AlGaN layer, a contact layer 5a of p-type GaN layer.
- the contact layer 3a is n-type GaN layer doped with Si at 7 x 10 18 /cm 3
- lower clad layer 3b is n-type GaN layer doped with Si at 5 x 10 18 /cm 3
- the light-emitting layer 4 has single quantum well structure, and the composition of InGaN is Ino. 95 Gao.o 5 N.
- the upper clad layer 5b is p- type AlGaN doped with Mg at 1 x 10 18 /cm 3 , and the composition is Al 0 . 25 Ga 0 ⁇ sN.
- the contact layer 5a is p- type GaN layer doped with Mg at 5 x 10 19 /cm 3 . Lamination of these layers was carried out by MOCVD method under the usual conditions well known to those skilled in the art.
- a flip chip type gallium nitride-based compound semiconductor light-emitting device was fabricated by providing a positive electrode 10 and negative electrode 20 to this gallium nitride-based compound semiconductor laminate following the procedure as described below.
- the contact layer 3a of the negative electrode forming region was exposed in the above- described gallium nitride-based compound semiconductor laminate.
- the procedure is as follows. Using known lithographic technology and lift-off technology, an etching mask was formed on the region other than the negative electrode forming region on the p-contact layer 5a.
- the laminate was taken out from the etching apparatus, and the etching mask was removed by washing with acetone.
- a positive electrode 10 was formed as follows. After the device was treated in boiling concentrated HCl for 10 minutes in order to remove an oxide film on the surface of the contact layer 5a, a positive electrode was formed on the contact layer 5a. First, a reflective layer was formed. The procedure for forming these layers is as follows.
- a resist is coated uniformly, and known lithographic technique was used to remove the resist from a positive electrode forming region.
- BHF buffered hydrofluoric acid
- a reflective layer was formed in a vacuum sputtering 'apparatus. Operating conditions for forming this layer by sputtering method are as follows.
- the chamber was evacuated so that the degree of vacuum became lower than 10 "4 PA.
- the above-mentioned gallium nitride type compound-semiconductor laminate was accommodated in the chamber.
- Ar gas was introduced in the chamber as a sputtering gas so that the interior pressure became 0.5 Pa, and the sputtering was carried out by the DC discharge to form a reflective layer.
- a supplied power was 0.5 kW, and the reflective layer was formed of Ag/Cu alloy (Cu: 1 atomic %) of 200 nm thick.
- the composition of alloy in the reflective layer was controlled by preliminarily preparing a piece of alloy having this composition and using the same as a target.
- an 300 nm thick Au film was formed as a bonding pad layer by the sputtering of DC discharge at the same pressure and supply power as described above. After the sample was taken out from the sputtering apparatus, a portion of the metallic film other than the positive electrode was removed together with the resist by using the lift-off technique.
- a negative electrode 20 was formed on the contact layer 3a.
- the procedure for forming the negative electrode 20 is as follows. After a resist was coated uniformly all over the surface, on the region exposed up to contact layer 3a, known lithographic technique was used to open a window for negative electrode region, and vapor deposition method was used to deposit Ti and Au films in thickness of 100 nm and 300 ran, respectively. Metal films other than that on the negative electrode region were removed together with the resist. (4) Then, a protective film was formed. The procedure is as follows.
- SiO 2 film was formed to a thickness of 200 nm by above- mentioned sputtering method. An SiO 2 film other than that on the protective film region was removed together with the resist.
- the wafer was cut into pieces, to thereby fabricate the gallium nitride-based compound semiconductor light-emitting device of the present invention.
- the obtained gallium nitride type compound- semiconductor light-emitting device was mounted to TO-18 and the initial device characteristics were measured.
- a gallium nitride type semiconductor light-emitting device was prepared in the same manner as in Example 1, except for changing a material for the reflective layer, and estimated in the same manner as in Example 1. The results thereof were indicated also in Table 1. (Example 7)
- a gallium nitride type semiconductor light-emitting device was prepared in the same manner as in Example 1, except that a 4 nm thick Pt contact metal layer was formed, and estimated in the same manner as in Example 1. Results thereof were indicated also in Table 1. As is apparent from Table 1, it was found that, by the provision of the contact metal layer, the driving voltage was largely reduced although the output power became slightly smaller, and the reduction of inverse voltage was also largely reduced in the aging test.
- the contact metal layer was formed by using Ar gas for the RF discharge sputtering at a pressure of 3 Pa and a supplied power of 0.5 kW.
- a gallium nitride type semiconductor light-emitting device was prepared in the same manner as in Example 1, except that the reflective layer is formed of Ag metal, and estimated in the same manner as in Example 1. Results thereof are indicated in Table 1. As is apparent from Table 1, it was found that the inverse voltage reduced in all the samples, showing that the generation of electromigration is more significant than in the present invention. Table 1
- the gallium nitride-based compound semiconductor light-emitting device provided by the present invention has excellent characteristics and stability, and is useful as a material for a light-emitting diode and lamp, etc.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Led Devices (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/660,040 US7544974B2 (en) | 2005-08-23 | 2005-08-23 | Positive electrode for compound semiconductor light-emitting device |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004244054 | 2004-08-24 | ||
JP2004-244054 | 2004-08-24 | ||
US60550204P | 2004-08-31 | 2004-08-31 | |
US60/605,502 | 2004-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006022399A1 true WO2006022399A1 (en) | 2006-03-02 |
Family
ID=35967599
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/015596 WO2006022399A1 (en) | 2004-08-24 | 2005-08-23 | Positive electrode for compound semiconductor light-emitting device |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006022399A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013174579A1 (en) * | 2012-05-25 | 2013-11-28 | Osram Opto Semiconductors Gmbh | Method for producing an optoelectronic semiconductor chip, and optoelectronic semiconductor chip |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11191641A (en) * | 1997-10-14 | 1999-07-13 | Matsushita Electron Corp | Semiconductor light-emitting element, semiconductor light-emitting device using the same and manufacture thereof |
JP2000294837A (en) * | 1999-04-05 | 2000-10-20 | Stanley Electric Co Ltd | Gallium nitride compound semiconductor light emitting element |
JP2002237618A (en) * | 2001-02-08 | 2002-08-23 | Sony Corp | Display device and it manufacturing method |
JP2003168823A (en) * | 2001-09-18 | 2003-06-13 | Toyoda Gosei Co Ltd | Iii nitride based compound semiconductor light emitting element |
JP2003534668A (en) * | 2000-05-26 | 2003-11-18 | オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | Luminescent diode chip having a GaN-based epitaxy continuous layer emitting radiation and method of manufacturing the same |
JP2004063732A (en) * | 2002-07-29 | 2004-02-26 | Matsushita Electric Ind Co Ltd | Light-emitting element |
JP2004193338A (en) * | 2002-12-11 | 2004-07-08 | Sharp Corp | Nitride based compound semiconductor light emitting element and its manufacturing method |
-
2005
- 2005-08-23 WO PCT/JP2005/015596 patent/WO2006022399A1/en active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11191641A (en) * | 1997-10-14 | 1999-07-13 | Matsushita Electron Corp | Semiconductor light-emitting element, semiconductor light-emitting device using the same and manufacture thereof |
JP2000294837A (en) * | 1999-04-05 | 2000-10-20 | Stanley Electric Co Ltd | Gallium nitride compound semiconductor light emitting element |
JP2003534668A (en) * | 2000-05-26 | 2003-11-18 | オスラム オプト セミコンダクターズ ゲゼルシャフト ミット ベシュレンクテル ハフツング | Luminescent diode chip having a GaN-based epitaxy continuous layer emitting radiation and method of manufacturing the same |
JP2002237618A (en) * | 2001-02-08 | 2002-08-23 | Sony Corp | Display device and it manufacturing method |
JP2003168823A (en) * | 2001-09-18 | 2003-06-13 | Toyoda Gosei Co Ltd | Iii nitride based compound semiconductor light emitting element |
JP2004063732A (en) * | 2002-07-29 | 2004-02-26 | Matsushita Electric Ind Co Ltd | Light-emitting element |
JP2004193338A (en) * | 2002-12-11 | 2004-07-08 | Sharp Corp | Nitride based compound semiconductor light emitting element and its manufacturing method |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013174579A1 (en) * | 2012-05-25 | 2013-11-28 | Osram Opto Semiconductors Gmbh | Method for producing an optoelectronic semiconductor chip, and optoelectronic semiconductor chip |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2244311B1 (en) | Gallium nitride-based compound semiconductor light-emitting device | |
US8097478B2 (en) | Method for producing light-emitting diode | |
US7498611B2 (en) | Transparent electrode for semiconductor light-emitting device | |
EP2012372B1 (en) | Method for manufacturing gallium nitride compound semiconductor light emitting element | |
WO2007119822A1 (en) | Method for manufacturing semiconductor light emitting element, semiconductor light emitting element and lamp provided with the semiconductor light emitting element | |
WO2006011672A1 (en) | Positive electrode for semiconductor light-emitting device | |
JP2007165611A (en) | Gallium-nitride compound semiconductor light-emitting element and manufacturing method therefor | |
US20090263922A1 (en) | Reflective Positive Electrode And Gallium Nitride-Based Compound Semiconductor Light-Emitting Device Using The Same | |
JP4807983B2 (en) | Positive electrode for compound semiconductor light emitting device, light emitting device and lamp using the positive electrode | |
US7544974B2 (en) | Positive electrode for compound semiconductor light-emitting device | |
KR20070007784A (en) | Gallium nitride-based compound semiconductor light-emitting device | |
TW200524187A (en) | Gallium nitride-based compound semiconductor light-emitting device and negative electrode thereof | |
WO2006022399A1 (en) | Positive electrode for compound semiconductor light-emitting device | |
KR100895453B1 (en) | Positive electrode for compound semiconductor light-emitting device | |
JP4999278B2 (en) | Gallium nitride compound semiconductor light emitting device | |
US20070080365A1 (en) | Gallium nitride-based compound semiconductor light-emitting device, positive electrode for the device, light-emitting diode and lamp using the device | |
US20070126008A1 (en) | Gallium nitride-based compound semiconductor light-emitting device, positive electrode for the device, light-emitting diode and lamp using the device | |
JP2005142545A (en) | Gallium nitride-based compound semiconductor light emitting element, its positive electrode, light emitting diode using it, and lamp using it |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 11660040 Country of ref document: US Ref document number: 2007181907 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020077003805 Country of ref document: KR |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWP | Wipo information: published in national office |
Ref document number: 11660040 Country of ref document: US |
|
122 | Ep: pct application non-entry in european phase |