JP4328704B2 - 有機エレクトロルミネッセンス素子及びこれを用いた表示装置 - Google Patents
有機エレクトロルミネッセンス素子及びこれを用いた表示装置 Download PDFInfo
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- JP4328704B2 JP4328704B2 JP2004299928A JP2004299928A JP4328704B2 JP 4328704 B2 JP4328704 B2 JP 4328704B2 JP 2004299928 A JP2004299928 A JP 2004299928A JP 2004299928 A JP2004299928 A JP 2004299928A JP 4328704 B2 JP4328704 B2 JP 4328704B2
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- 238000005401 electroluminescence Methods 0.000 title claims description 41
- 150000002894 organic compounds Chemical class 0.000 claims description 32
- 239000000463 material Substances 0.000 claims description 21
- 230000005525 hole transport Effects 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 8
- 101150094912 TFB4 gene Proteins 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 64
- 239000000758 substrate Substances 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- VFUDMQLBKNMONU-UHFFFAOYSA-N 9-[4-(4-carbazol-9-ylphenyl)phenyl]carbazole Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 VFUDMQLBKNMONU-UHFFFAOYSA-N 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000004696 coordination complex Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-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
- 230000000903 blocking effect Effects 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- ZNOVTXRBGFNYRX-UHFFFAOYSA-N 2-[[4-[(2-amino-5-methyl-4-oxo-1,6,7,8-tetrahydropteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid Chemical compound C1NC=2NC(N)=NC(=O)C=2N(C)C1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 ZNOVTXRBGFNYRX-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- -1 aluminum quinolinol Chemical compound 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- DCZNSJVFOQPSRV-UHFFFAOYSA-N n,n-diphenyl-4-[4-(n-phenylanilino)phenyl]aniline Chemical class C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 DCZNSJVFOQPSRV-UHFFFAOYSA-N 0.000 description 1
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1022—Heterocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/188—Metal complexes of other metals not provided for in one of the previous groups
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/10—OLED displays
- H10K59/12—Active-matrix OLED [AMOLED] displays
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Inorganic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
Description
図1(b)に示す有機化合物層が3層の有機EL素子を作製した。先ず、ガラス基板(透明基板15)上に100nm厚のITO電極(透明電極14)をパターニングして、対向する電極面積が3mm2になるようにした。そのITO電極基板上に、以下の有機化合物層と電極層を10-4Paの真空チャンバー内で抵抗加熱による真空蒸着し、連続成膜した。比較例として有機化合物層2についてCBP(4,4’−N,N’−ジカルバゾール−ビフェニル)をドープしない系も作製した。
有機化合物層1(ホール輸送層13)(40nm):TFB4
有機化合物層2(発光層12)(20nm):有機化合物4+CBP(質量比=70:30)
有機化合物層3(電子輸送層16)(50nm):Bphen
金属電極層1(1nm):KF
金属電極層2(100nm):Al
縦75mm、横75mm、厚さ1.1mmのガラス基板上に透明電極(陽極側)として約100nm厚のITO膜をスパッタ法にて形成後、単純マトリクス電極としてライン/スペース=100μm/40μmの間隔で100ラインをパターニングした。次に、実施例1と同様の条件で3層からなる有機化合物層を作成した。
12 発光層
13 ホール輸送層
14 透明電極
15 透明基板
16 電子輸送層
20 画素回路
21 走査信号ドライバ
22 情報信号ドライバ
23 電流供給源
25 ゲート走査線
26 情報戦
27 電流供給線
31,32 TFT
33 容量
34 有機EL素子
35 アノード
40 ガラス基板
41 ソース領域
42 ドレイン領域
43 チャネル領域
44 p−Si層
45 ゲート電極
46 ドレイン電極
47 ソース電極
48 ゲート絶縁膜
49,52,53 絶縁層
50 ITO電極
51 有機化合物層
52 陰極層
111 ガラス基板
112 透明電極
113 有機化合物層
114 金属電極
Claims (4)
- 前記発光層に含まれる、他の化合物がCBPであることを特徴とする請求項1に記載の有機エレクトロルミネッセンス素子。
- 前記電子輸送層がBphenであることを特徴とする請求項1または2に記載の有機エレクトロルミネッセンス素子。
- 請求項1乃至3のいずれか1項に記載の有機エレクトロルミネッセンス素子を用いたことを特徴とする表示装置。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004299928A JP4328704B2 (ja) | 2004-10-14 | 2004-10-14 | 有機エレクトロルミネッセンス素子及びこれを用いた表示装置 |
EP05795228A EP1805279A1 (en) | 2004-10-14 | 2005-10-12 | Organic electroluminescent device and display apparatus using the same |
CNA2005800218602A CN1977028A (zh) | 2004-10-14 | 2005-10-12 | 有机电致发光器件及使用该器件的显示设备 |
PCT/JP2005/019155 WO2006041189A1 (en) | 2004-10-14 | 2005-10-12 | Organic electroluminescent device and display apparatus using the same |
US11/578,068 US20070207344A1 (en) | 2004-10-14 | 2005-10-12 | Organic Electroluminescent Device and Display Apparatus Using the Same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004299928A JP4328704B2 (ja) | 2004-10-14 | 2004-10-14 | 有機エレクトロルミネッセンス素子及びこれを用いた表示装置 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2006114663A JP2006114663A (ja) | 2006-04-27 |
JP2006114663A5 JP2006114663A5 (ja) | 2007-01-18 |
JP4328704B2 true JP4328704B2 (ja) | 2009-09-09 |
Family
ID=36148473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004299928A Expired - Fee Related JP4328704B2 (ja) | 2004-10-14 | 2004-10-14 | 有機エレクトロルミネッセンス素子及びこれを用いた表示装置 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20070207344A1 (ja) |
EP (1) | EP1805279A1 (ja) |
JP (1) | JP4328704B2 (ja) |
CN (1) | CN1977028A (ja) |
WO (1) | WO2006041189A1 (ja) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007294402A (ja) * | 2006-03-28 | 2007-11-08 | Canon Inc | 有機エレクトロルミネッセンス素子及び表示装置 |
JP2007269735A (ja) * | 2006-03-31 | 2007-10-18 | Canon Inc | 金属錯体、発光素子及び表示装置 |
JP2008007500A (ja) * | 2006-06-02 | 2008-01-17 | Canon Inc | 金属錯体及び有機発光素子 |
JP5084204B2 (ja) * | 2006-09-06 | 2012-11-28 | キヤノン株式会社 | 発光素子及び高分子混合金属錯体 |
JP5127206B2 (ja) * | 2006-11-28 | 2013-01-23 | キヤノン株式会社 | 金属錯体化合物、有機発光素子及び表示装置 |
JP4886870B2 (ja) * | 2010-03-08 | 2012-02-29 | 株式会社東芝 | 有機電界発光素子、表示装置および照明装置 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG54160A1 (en) * | 1987-11-04 | 1998-11-16 | Igen Inc | Electrochemiluminescent rhenium moeities and methods |
JP4505162B2 (ja) * | 2000-09-21 | 2010-07-21 | 富士フイルム株式会社 | 発光素子および新規レニウム錯体 |
JP2002203681A (ja) * | 2000-12-27 | 2002-07-19 | Fuji Photo Film Co Ltd | 発光素子 |
JPWO2003076549A1 (ja) * | 2002-03-08 | 2005-07-07 | キヤノン株式会社 | 金属配位化合物を用いた電界発光素子 |
AU2003211786A1 (en) * | 2002-03-08 | 2003-09-22 | Canon Kabushiki Kaisha | Organic light-emitting device |
GB0206169D0 (en) * | 2002-03-15 | 2002-04-24 | Isis Innovation | Rhenium compounds |
JP2003332074A (ja) * | 2002-05-09 | 2003-11-21 | Canon Inc | 金属配位化合物を用いた発光素子 |
CN100439469C (zh) * | 2002-08-27 | 2008-12-03 | 富士胶片株式会社 | 有机金属配位化合物、有机el元件及有机el显示器 |
JP4164317B2 (ja) * | 2002-08-28 | 2008-10-15 | キヤノン株式会社 | 有機発光素子 |
JP4557651B2 (ja) * | 2003-10-01 | 2010-10-06 | キヤノン株式会社 | 発光性銅配位化合物及び有機発光素子 |
-
2004
- 2004-10-14 JP JP2004299928A patent/JP4328704B2/ja not_active Expired - Fee Related
-
2005
- 2005-10-12 EP EP05795228A patent/EP1805279A1/en not_active Withdrawn
- 2005-10-12 WO PCT/JP2005/019155 patent/WO2006041189A1/en active Application Filing
- 2005-10-12 CN CNA2005800218602A patent/CN1977028A/zh active Pending
- 2005-10-12 US US11/578,068 patent/US20070207344A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20070207344A1 (en) | 2007-09-06 |
CN1977028A (zh) | 2007-06-06 |
JP2006114663A (ja) | 2006-04-27 |
WO2006041189A1 (en) | 2006-04-20 |
EP1805279A1 (en) | 2007-07-11 |
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