JP2020205421A - 発光デバイス、発光装置、電子機器および照明装置 - Google Patents
発光デバイス、発光装置、電子機器および照明装置 Download PDFInfo
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- JP2020205421A JP2020205421A JP2020102027A JP2020102027A JP2020205421A JP 2020205421 A JP2020205421 A JP 2020205421A JP 2020102027 A JP2020102027 A JP 2020102027A JP 2020102027 A JP2020102027 A JP 2020102027A JP 2020205421 A JP2020205421 A JP 2020205421A
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- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
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- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 238000005011 time of flight secondary ion mass spectroscopy Methods 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
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- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- CJGUQZGGEUNPFQ-UHFFFAOYSA-L zinc;2-(1,3-benzothiazol-2-yl)phenolate Chemical compound [Zn+2].[O-]C1=CC=CC=C1C1=NC2=CC=CC=C2S1.[O-]C1=CC=CC=C1C1=NC2=CC=CC=C2S1 CJGUQZGGEUNPFQ-UHFFFAOYSA-L 0.000 description 1
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- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- 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]
- H10K50/14—Carrier transporting layers
- H10K50/16—Electron transporting layers
-
- 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]
- H10K50/14—Carrier transporting layers
- H10K50/16—Electron transporting layers
- H10K50/165—Electron transporting layers comprising dopants
-
- 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
- H05B33/20—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the material in which the electroluminescent material is embedded
-
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Abstract
Description
を有する電子機器である。
図1(A1)(A2)に、本発明の一態様の発光デバイスを表す図を示す。本発明の一態様の発光デバイスは、陽極101と、陰極102、EL層103を有しており、当該EL層は、正孔注入層111、正孔輸送層112、発光層113および電子輸送層114を有している。なお、正孔輸送層112は第1の正孔輸送層112−1および第2の正孔輸送層112−2を有することが好ましく、電子輸送層114は図1(A2)のように第1の電子輸送層114−1および第2の電子輸送層114−2を有していることが好ましい。
続いて、上述の発光デバイスの詳細な構造や材料の例について説明する。本発明の一態様の発光デバイスは、上述のように陽極101と陰極102の一対の電極間に複数の層からなるEL層103を有し、当該EL層103は少なくとも陽極101側より、正孔注入層111、第1の正孔輸送層112−1、第2の正孔輸送層112−2、発光層113および電子輸送層114を含む。
これら導電性材料は、真空蒸着法やスパッタリング法などの乾式法、インクジェット法、スピンコート法等を用いて成膜することが可能である。また、ゾル−ゲル法を用いて湿式法で形成しても良いし、金属材料のペーストを用いて湿式法で形成してもよい。
本実施の形態では、実施の形態1および実施の形態2に記載の発光デバイスを用いた発光装置について説明する。
本実施の形態では、実施の形態1および実施の形態2に記載の発光デバイスを照明装置として用いる例を、図8を参照しながら説明する。図8(B)は照明装置の上面図、図8(A)は図8(B)におけるe−f断面図である。
本実施の形態では、実施の形態1および実施の形態2に記載の発光デバイスをその一部に含む電子機器の例について説明する。実施の形態1および実施の形態2に記載の発光デバイスは寿命が良好であり、信頼性の良好な発光デバイスである。その結果、本実施の形態に記載の電子機器は、信頼性の良好な発光部を有する電子機器とすることが可能である。
まず、ガラス基板上に、酸化珪素を含むインジウム錫酸化物(ITSO)をスパッタリング法にて成膜し、陽極101を形成した。なお、その膜厚は70nmとし、電極面積は2mm×2mmとした。
比較発光デバイス1は、発光層113におけるαN−βNPAnthを上記構造式(vii)で表される7−[4−(10−フェニル−9−アントリル)フェニル]−7H−ジベンゾ[c,g]カルバゾール(略称:cgDBCzPA)に変え、電子輸送層114を上記構造式(viii)で表される2−[3’−(ジベンゾチオフェン−4−イル)ビフェニル−3−イル]ジベンゾ[f,h]キノキサリン(略称:2mDBTBPDBq−II)を15nm蒸着した後、上記構造式(ix)で表される2,9−ジ(2−ナフチル)−4,7−ジフェニル−1,10−フェナントロリン(略称:NBPhen)を10nm蒸着して形成した他は発光デバイス1と同様に作製した。
った。
本参考例では、各実施例で用いた有機化合物のHOMO準位、LUMO準位および電子移動度の算出方法について説明する。
本参考例では、実施例2において用いた2−フェニル−3−{4−[10−(3−ピリジル)−9−アントリル]フェニル}キノキサリン(略称:PyA1PQ)の合成方法について説明する。PyA1PQの構造を以下に示す。
102 陰極
103 EL層
111 正孔注入層
112 正孔輸送層
112−1 第1の正孔輸送層
112−2 第2の正孔輸送層
113 発光層
113−1 再結合領域
114 電子輸送層
114−1 第1の電子輸送層
114−2 第2の電子輸送層
115 電子注入層
116 電荷発生層
117 P型層
118 電子リレー層
119 電子注入バッファ層
120 非発光再結合領域
201 陽極
202 陰極
210 第1の層
211 第2の層
212 第3の層
400 基板
401 陽極
403 EL層
404 陰極
405 シール材
406 シール材
407 封止基板
408 空間
412 パッド
420 ICチップ
501 陽極
502 陰極
511 第1の発光ユニット
512 第2の発光ユニット
513 電荷発生層
601 駆動回路部(ソース線駆動回路)
602 画素部
603 駆動回路部(ゲート線駆動回路)
604 封止基板
605 シール材
607 空間
608 配線
609 FPC(フレキシブルプリントサーキット)
610 素子基板
611 スイッチング用FET
612 電流制御用FET
613 陽極
614 絶縁物
616 EL層
617 陰極
618 発光デバイス
951 基板
952 電極
953 絶縁層
954 隔壁層
955 EL層
956 電極
1001 基板
1002 下地絶縁膜
1003 ゲート絶縁膜
1006 ゲート電極
1007 ゲート電極
1008 ゲート電極
1020 第1の層間絶縁膜
1021 第2の層間絶縁膜
1022 電極
1024W 陽極
1024R 陽極
1024G 陽極
1024B 陽極
1025 隔壁
1028 EL層
1029 陰極
1031 封止基板
1032 シール材
1033 透明な基材
1034R 赤色の着色層
1034G 緑色の着色層
1034B 青色の着色層
1035 ブラックマトリクス
1036 オーバーコート層
1037 第3の層間絶縁膜
1040 画素部
1041 駆動回路部
1042 周辺部
2001 筐体
2002 光源
2100 ロボット
2110 演算装置
2101 照度センサ
2102 マイクロフォン
2103 上部カメラ
2104 スピーカ
2105 ディスプレイ
2106 下部カメラ
2107 障害物センサ
2108 移動機構
3001 照明装置
5000 筐体
5001 表示部
5002 第2の表示部
5003 スピーカ
5004 LEDランプ
5006 接続端子
5007 センサ
5008 マイクロフォン
5012 支持部
5013 イヤホン
5100 掃除ロボット
5101 ディスプレイ
5102 カメラ
5103 ブラシ
5104 操作ボタン
5150 携帯情報端末
5151 筐体
5152 表示領域
5153 屈曲部
5120 ゴミ
5200 表示領域
5201 表示領域
5202 表示領域
5203 表示領域
7101 筐体
7103 表示部
7105 スタンド
7107 表示部
7109 操作キー
7110 リモコン操作機
7201 本体
7202 筐体
7203 表示部
7204 キーボード
7205 外部接続ポート
7206 ポインティングデバイス
7210 第2の表示部
7401 筐体
7402 表示部
7403 操作ボタン
7404 外部接続ポート
7405 スピーカ
7406 マイク
9310 携帯情報端末
9311 表示パネル
9313 ヒンジ
9315 筐体
Claims (14)
- 陽極と、
陰極と、
前記陽極と、前記陰極との間に位置するEL層を有し、
前記EL層は、正孔注入層と、発光層と、電子輸送層とを有し、
前記正孔注入層は、前記陽極と前記発光層との間に位置し、
前記電子輸送層は、前記発光層と前記陰極との間に位置し、
前記正孔注入層は、第1の物質と、第2の物質とを有し、
前記第1の物質は、正孔輸送性を有し、且つそのHOMO準位が−5.7eV以上−5.4eV以下の有機化合物であり、
前記第2の物質は、前記第1の物質に電子受容性を示す物質であり、
前記電子輸送層が、電流を流すことによって抵抗値が小さくなる材料により構成されている発光デバイス。 - 請求項1において、
前記電流を流すことによって抵抗値が小さくなる材料が、アルカリ金属またはアルカリ土類金属の有機金属錯体を含む発光デバイス。 - 請求項1において、
前記電流を流すことによって抵抗値が小さくなる材料が、電子輸送性を有する有機化合物と、アルカリ金属またはアルカリ土類金属の有機金属錯体を含む発光デバイス。 - 請求項2または請求項3において、
前記アルカリ金属またはアルカリ土類金属の有機金属錯体が、クラスタを形成する発光デバイス。 - 請求項2乃至請求項4のいずれか一項において、
前記アルカリ金属またはアルカリ土類金属の有機金属錯体が、窒素及び酸素を有する配位子と、アルカリ金属またはアルカリ土類金属と、を有する金属錯体である発光デバイス。 - 請求項2乃至請求項4のいずれか一項において、
前記アルカリ金属またはアルカリ土類金属の有機金属錯体が、8−ヒドロキシキノリナト構造を含む配位子と1価の金属イオンとを有する金属錯体である発光デバイス。 - 請求項2乃至請求項4のいずれか一項において、
前記アルカリ金属またはアルカリ土類金属の有機金属錯体が、8−ヒドロキシキノリナト構造を含む配位子を有するリチウム錯体である発光デバイス。 - 請求項2乃至請求項7のいずれか一項において、
前記電子輸送層が、第1の層と第2の層とを有し、
前記第1の層は前記発光層と前記第2の層との間に位置し、
前記第2の層は、前記第1の層と前記陰極との間に位置し、
前記第1の層と、前記第2の層に含まれるアルカリ金属またはアルカリ土類金属の有機金属錯体の濃度が異なる発光デバイス。 - 請求項8において、
前記第1の層のアルカリ金属またはアルカリ土類金属の有機金属錯体の濃度が、前記第2の層のアルカリ金属またはアルカリ土類金属の有機金属錯体の濃度よりも高い発光デバイス。 - 請求項1乃至請求項9のいずれか一項において、
前記第2の物質が、有機化合物である発光デバイス。 - 請求項1乃至請求項10のいずれか一項において、
前記発光層は、ホスト材料と、発光物質とを有し、
前記発光物質は、青色の蛍光を発する発光デバイス。 - 請求項1乃至請求項11のいずれか一項に記載の発光デバイスと、センサ、操作ボタン、スピーカ、または、マイクと、
を有する電子機器。 - 請求項1乃至請求項11に記載の発光デバイスと、トランジスタ、または、基板と、を有する発光装置。
- 請求項1乃至請求項11に記載の発光デバイスと、筐体と、を有する照明装置。
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KR20150115622A (ko) | 2014-04-04 | 2015-10-14 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
KR101537500B1 (ko) | 2014-04-04 | 2015-07-20 | 주식회사 엘지화학 | 유기 발광 소자 |
KR101537499B1 (ko) | 2014-04-04 | 2015-07-16 | 주식회사 엘지화학 | 유기 발광 소자 |
JP6262849B2 (ja) | 2014-09-23 | 2018-01-17 | ホアウェイ・テクノロジーズ・カンパニー・リミテッド | 送信機、受信機、および同期信号を送信/受信するための方法 |
US9773832B2 (en) | 2014-12-10 | 2017-09-26 | Semiconductor Energy Laboratory Co., Ltd. | Semiconductor device and electronic device |
CN104659070B (zh) * | 2015-03-13 | 2018-11-16 | 上海天马有机发光显示技术有限公司 | 一种显示面板、显示装置及显示面板的制造方法 |
KR102257063B1 (ko) | 2016-01-29 | 2021-05-27 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 |
US10388900B2 (en) | 2016-07-28 | 2019-08-20 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
TWI804474B (zh) * | 2016-09-14 | 2023-06-11 | 日商半導體能源研究所股份有限公司 | 有機化合物、發光元件、發光裝置、電子裝置及照明設備 |
JP2019016788A (ja) | 2017-07-03 | 2019-01-31 | 三星電子株式会社Samsung Electronics Co.,Ltd. | 有機発光素子 |
KR102499281B1 (ko) | 2018-09-26 | 2023-02-13 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 디바이스, 발광 장치, 전자 기기, 및 조명 장치 |
KR20200036959A (ko) * | 2018-09-28 | 2020-04-08 | 삼성디스플레이 주식회사 | 유기 전계 발광 소자 및 유기 전계 발광 소자용 아민 화합물 |
DE112019005070T5 (de) | 2018-10-10 | 2021-07-15 | Semiconductor Energy Laboratory Co., Ltd. | Licht emittierende Vorrichtung, Licht emittierende Einrichtung, elektronisches Gerät und Beleuchtungsvorrichtung |
KR20200081978A (ko) * | 2018-12-28 | 2020-07-08 | 엘지디스플레이 주식회사 | 유기발광다이오드 및 이를 포함하는 유기발광장치 |
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2020
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- 2020-06-11 DE DE102020115543.3A patent/DE102020115543A1/de active Pending
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DE102020115543A1 (de) | 2020-12-17 |
TW202110778A (zh) | 2021-03-16 |
US20200395568A1 (en) | 2020-12-17 |
KR20200143283A (ko) | 2020-12-23 |
US11974447B2 (en) | 2024-04-30 |
US20230104201A1 (en) | 2023-04-06 |
CN112086567A (zh) | 2020-12-15 |
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