JP2010192431A - 発光素子、発光装置及び電子機器 - Google Patents
発光素子、発光装置及び電子機器 Download PDFInfo
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- JP2010192431A JP2010192431A JP2010010662A JP2010010662A JP2010192431A JP 2010192431 A JP2010192431 A JP 2010192431A JP 2010010662 A JP2010010662 A JP 2010010662A JP 2010010662 A JP2010010662 A JP 2010010662A JP 2010192431 A JP2010192431 A JP 2010192431A
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- Prior art keywords
- light
- emitting
- emitting layer
- organic compound
- emitting element
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- 239000000126 substance Substances 0.000 claims abstract description 186
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 120
- 239000000463 material Substances 0.000 claims description 59
- 150000001875 compounds Chemical class 0.000 claims description 51
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- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 125000005264 aryl amine group Chemical group 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 10
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- 238000000295 emission spectrum Methods 0.000 claims description 4
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- 238000004768 lowest unoccupied molecular orbital Methods 0.000 abstract description 52
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Abstract
【解決手段】第1の電極上に形成された第1の発光層と、第1の発光層上に第1の発光層と接して形成された第2の発光層と、第2の発光層上に形成された第2の電極と、を有し、第1の発光層は、第1の発光物質及び正孔輸送性の有機化合物を有し、第2の発光層は、第2の発光物質と電子輸送性の有機化合物を有する。第1と第2の発光物質の最低空軌道準位と、電子輸送性の有機化合物の最低空軌道準位と、の差は、それぞれ0.2eV以下であり、正孔輸送性の有機化合物の最高被占軌道準位と、第1と第2の発光物質の最高被占軌道準位と、の差は、それぞれ0.2eV以下であり、正孔輸送性の有機化合物の最低空軌道準位と、第1の発光物質の最低空軌道準位と、の差が、0.3eVより大きい物質を選択する。
【選択図】図1
Description
本実施の形態の発光素子110の概念図の一例を図1(A)に示す。本実施の形態の発光素子110は陽極100と陰極101との間に複数の層からなるEL層103を有している。EL層103は少なくとも発光層102を有しており、発光層102は陽極100側から第1の発光層102a、第2の発光層102bの2層を積層することによって構成されている。なお、当該2層は接して形成される。
本実施の形態では、実施の形態1で説明した発光素子を用いて作製される発光装置の一例として、パッシブマトリクス型の発光装置およびアクティブマトリクス型の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2で示した発光装置を用いて完成させた様々な電子機器および照明器具について、図6を用いて説明する。
以下に、実施例1乃至実施例3で使用した、構造式(11)で表される4−(10−フェニル−9−アントリル)−4’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミン(略称:PCBAPA)の合成方法の一例を記載する。
9−フェニル−9H−カルバゾール−3−ボロン酸の合成スキームを下記反応式(a−1)に示す。
PCBAの合成スキームを下記反応式(a−2)に示す。
PCBAPAの合成スキームを下記反応式(a−3)に示す。
以下に、実施例1及び実施例3で使用した、構造式(12)で表される4−(1−ナフチル)−4’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミン(略称:PCBANB)の合成方法の一例を記載する。
3−(4−ブロモフェニル)−9−フェニル−9H−カルバゾールの合成スキームを下記反応式(b−1)に示す。
4−(1−ナフチル)ジフェニルアミンの合成スキームを下記反応式(b−2)に示す。
PCBANBの合成スキームを下記反応式(b−3)に示す。
以下に、実施例1乃至実施例3で使用した、構造式(14)で表される4−(1−ナフチル)−4’−(10−フェニル−9−アントリル)−4’’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミン(略称:PCBNAPA)の合成方法の一例を記載する。
4−(1−ナフチル)アニリンの合成スキームを下記反応式(c−1)に示す。
PCBNAの合成スキームを下記反応式(c−2)に示す。
PCBNAPAの合成スキームを下記反応式(c−3)に示す。
以下に、実施例2で使用した、構造式(17)で表される4−フェニル−4’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミン(略称:PCBA1BP)の合成方法の一例を記載する。
本測定例では、構造式(11)で表されるPCBAPAのHOMO準位及びLUMO準位について測定した。なお、PCBAPAは、発光素子1〜6、及び比較発光素子1において第1の発光物質として用いた。PCBAPAの薄膜状態におけるイオン化ポテンシャルを大気中の光電子分光法(理研計器社製、AC−2)で測定した結果、5.40eVであった。その結果、HOMO準位が−5.40eVであることがわかった。さらに、PCBAPAの薄膜の吸収スペクトルのデータを用い、直接遷移を仮定したTaucプロットから吸収端を求め、その吸収端を光学的エネルギーギャップとして見積もったところ、そのエネルギーギャップは2.82eVであった。得られたエネルギーギャップの値とHOMO準位からLUMO準位を求めたところ、−2.58eVであった。
本測定例では構造式(12)で表されるPCBANBの、HOMO準位及びLUMO準位について測定した。なお、PCBANBは、発光素子1、2、6及び比較発光素子2において正孔輸送性の有機化合物として用いた。PCBANBの薄膜状態におけるイオン化ポテンシャルを大気中の光電子分光法(理研計器社製、AC−2)で測定した結果、5.44eVであった。その結果、HOMO準位が−5.44eVであることがわかった。さらに、PCBANBの薄膜の吸収スペクトルのデータを用い、直接遷移を仮定したTaucプロットから吸収端を求め、その吸収端を光学的エネルギーギャップとして見積もったところ、そのエネルギーギャップは3.25eVであった。得られたエネルギーギャップの値とHOMO準位からLUMO準位を求めたところ、−2.19eVであった。
本測定例では、構造式(17)で表されるPCBA1BPの、HOMO準位及びLUMO準位について測定した。なお、PCBA1BPは、発光素子3〜5、及び比較発光素子3において正孔輸送性の有機化合物として用いた。PCBA1BPの薄膜状態におけるイオン化ポテンシャルを大気中の光電子分光法(理研計器社製、AC−2)で測定した結果、5.42eVであった。その結果、HOMO準位が−5.42eVであることがわかった。さらに、PCBA1BPの薄膜の吸収スペクトルのデータを用い、直接遷移を仮定したTaucプロットから吸収端を求め、その吸収端を光学的エネルギーギャップとして見積もったところ、そのエネルギーギャップは3.21eVであった。得られたエネルギーギャップの値とHOMO準位からLUMO準位を求めたところ、−2.21eVであった。
本測定例では、構造式(14)で表されるPCBNAPAの、HOMO準位及びLUMO準位について測定した。なお、PCBNAPAは、発光素子1〜6、及び比較発光素子1〜3において第2の発光物質として用いた。PCBNAPAの薄膜状態におけるイオン化ポテンシャルを大気中の光電子分光法(理研計器社製、AC−2)で測定した結果、5.47eVであった。その結果、HOMO準位が−5.47eVであることがわかった。さらに、PCBNAPAの薄膜の吸収スペクトルのデータを用い、直接遷移を仮定したTaucプロットから吸収端を求め、その吸収端を光学的エネルギーギャップとして見積もったところ、そのエネルギーギャップは2.92eVであった。得られたエネルギーギャップの値とHOMO準位からLUMO準位を求めたところ、−2.55eVであった。
本測定例では、構造式(13)で表されるCzPAの、HOMO準位及びLUMO準位について測定した。なお、CzPAは、発光素子1〜6、及び比較発光素子1〜3において電子輸送性の有機化合物として用いた。CzPAの薄膜状態におけるイオン化ポテンシャルを大気中の光電子分光法(理研計器社製、AC−2)で測定した結果、5.64eVであった。その結果、HOMO準位が−5.64eVであることがわかった。さらに、CzPAの薄膜の吸収スペクトルのデータを用い、直接遷移を仮定したTaucプロットから吸収端を求め、その吸収端を光学的エネルギーギャップとして見積もったところ、そのエネルギーギャップは2.95eVであった。得られたエネルギーギャップの値とHOMO準位からLUMO準位を求めたところ、−2.69eVであった。
以下に、実施例6で使用した、構造式(18)で表される4,4’−ジ(1−ナフチル)−4’’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミン(略称:PCBNBB)の合成例を示す。
4,4’−ジブロモトリフェニルアミンの合成スキームを下記反応式(K−1)に示す。
4,4’−ジ(1−ナフチル)トリフェニルアミンの合成スキームを下記反応式(K−2)に示す。
4−ブロモ−4’,4’’−ジ(1−ナフチル)トリフェニルアミンの合成スキームを下記反応式(K−3)に示す。
4,4’−ジ(1−ナフチル)−4’’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミンの合成スキームを下記反応式(K−4)に示す。
101 陰極
102 発光層
102a 第1の発光層
102b 第2の発光層
103 EL層
104 正孔注入層
105 正孔輸送層
106 電子輸送層
107 電子注入層
110 発光素子
122 HOMO準位
124 HOMO準位
128 HOMO準位
142 LUMO準位
144 LUMO準位
146 LUMO準位
148 LUMO準位
601 基板
602 絶縁層
603 電極
604 隔壁
605 開口部
606 隔壁
607 EL層
608 電極
703 走査線
705 領域
706 隔壁
708 データ線
709 接続配線
710 入力端子
711a FPC
711b FPC
712 入力端子
801 素子基板
802 画素部
803 駆動回路部
804 駆動回路部
805 シール材
806 封止基板
807 配線
808 FPC
809 nチャネル型TFT
810 pチャネル型TFT
811 スイッチング用TFT
812 電流制御用TFT
813 陽極
814 絶縁物
815 EL層
816 陰極
817 発光素子
818 空間
1001 照明装置
1002 照明装置
1003 卓上照明器具
9100 テレビジョン装置
9100 テレビジョン装置
9101 筐体
9103 表示部
9105 スタンド
9107 表示部
9109 操作キー
9110 リモコン操作機
9201 本体
9202 筐体
9203 表示部
9204 キーボード
9205 外部接続ポート
9206 マウス
9301 筐体
9302 筐体
9303 連結部
9304 表示部
9305 表示部
9306 スピーカ部
9307 記録媒体挿入部
9308 LEDランプ
9309 操作キー
9310 接続端子
9311 センサ
9312 マイクロフォン
9401 照明部
9402 傘
9403 可変アーム
9404 支柱
9405 台
9406 電源
9500 携帯電話機
9501 筐体
9502 表示部
9502 表示部
9503 操作ボタン
9504 外部接続ポート
9505 スピーカ
9506 マイク
Claims (10)
- 第1の電極と、
前記第1の電極上に形成された第1の発光層と、
前記第1の発光層上に、前記第1の発光層と接して形成された第2の発光層と、
前記第2の発光層上に形成された第2の電極と、を有し、
前記第1の発光層は、第1の発光物質と、正孔輸送性の有機化合物と、を有し、
前記第2の発光層は、第2の発光物質と、電子輸送性の有機化合物と、を有し、
前記第1の発光物質の最低空軌道準位と、前記第2の発光物質の最低空軌道準位と、前記電子輸送性の有機化合物の最低空軌道準位と、の差は、いずれも0.2eV以下であり、
前記正孔輸送性の有機化合物の最高被占軌道準位と、前記第1の発光物質の最高被占軌道準位と、前記第2の発光物質の最高被占軌道準位と、の差は、いずれも0.2eV以下であり、
前記正孔輸送性の有機化合物の最低空軌道準位と、前記第1の発光物質の最低空軌道準位と、の差は、0.3eVより大きい発光素子。 - 第1の電極と、
前記第1の電極上に形成された第1の発光層と、
前記第1の発光層上に、前記第1の発光層と接して形成された第2の発光層と、
前記第2の発光層上に形成された第2の電極と、を有し、
前記第1の発光層は、第1の発光物質と、正孔輸送性の有機化合物と、を有し、
前記第2の発光層は、第2の発光物質と、電子輸送性の有機化合物と、を有し、
前記第1の発光層における前記第1の発光物質の割合は、30wt%以上70wt%以下であり、
前記第1の発光物質の最低空軌道準位と、前記第2の発光物質の最低空軌道準位と、前記電子輸送性の有機化合物の最低空軌道準位と、の差は、いずれも0.2eV以下であり、
前記正孔輸送性の有機化合物の最高被占軌道準位と、前記第1の発光物質の最高被占軌道準位と、前記第2の発光物質の最高被占軌道準位と、の差は、いずれも0.2eV以下であり、
前記正孔輸送性の有機化合物の最低空軌道準位と、前記第1の発光物質の最低空軌道準位と、の差は、0.3eVより大きい発光素子。 - 第1の電極と、
前記第1の電極上に形成された第1の発光層と、
前記第1の発光層上に、前記第1の発光層と接して形成された第2の発光層と、
前記第2の発光層上に形成された第2の電極と、を有し、
前記第1の発光層は、第1の発光物質と、正孔輸送性の有機化合物と、を有し、
前記第2の発光層は、第2の発光物質と、電子輸送性の有機化合物と、を有し、
前記正孔輸送性の有機化合物は、アリールアミン骨格を有する化合物であり、
前記電子輸送性の有機化合物は、3環以上6環以下の多環芳香族炭化水素骨格を有する化合物であり、
前記第1の発光物質及び前記第2の発光物質は、3環以上6環以下の多環芳香族炭化水素骨格及びアリールアミン骨格を有する化合物である発光素子。 - 第1の電極と、
前記第1の電極上に形成された第1の発光層と、
前記第1の発光層上に、前記第1の発光層と接して形成された第2の発光層と、
前記第2の発光層上に形成された第2の電極と、を有し、
前記第1の発光層は、第1の発光物質と、正孔輸送性の有機化合物と、を有し、
前記第2の発光層は、第2の発光物質と、電子輸送性の有機化合物と、を有し、
前記正孔輸送性の有機化合物は、下記一般式(1)で表される化合物であり、
前記電子輸送性の有機化合物は、3環以上6環以下の多環芳香族炭化水素骨格を有する化合物であり、
前記第1の発光物質及び前記第2の発光物質は、下記一般式(2)で表される化合物である発光素子。
- 第1の電極と、
前記第1の電極上に形成された第1の発光層と、
前記第1の発光層上に、前記第1の発光層と接して形成された第2の発光層と、
前記第2の発光層上に形成された第2の電極と、を有し、
前記第1の発光層は、第1の発光物質と、正孔輸送性の有機化合物と、を有し、
前記第2の発光層は、第2の発光物質と、電子輸送性の有機化合物と、を有し、
前記正孔輸送性の有機化合物は、下記一般式(3)で表される化合物であり、
前記電子輸送性の有機化合物は、3環以上6環以下の多環芳香族炭化水素骨格を有する化合物であり、
前記第1の発光物質及び前記第2の発光物質は、下記一般式(4)で表される化合物である発光素子。
- 請求項3乃至5のいずれか一において、
前記第1の発光層における前記第1の発光物質の割合は、30wt%以上70wt%以下である発光素子。 - 請求項1乃至6のいずれか一において、
前記第1の発光層と、前記第2の発光層と、は、同じ発光色を呈する発光素子。 - 請求項1乃至6のいずれか一において、
前記第1の発光層及び前記第2の発光層からの発光スペクトルの最大ピークは、430nm以上470nm以下の領域に位置する発光素子。 - 請求項1乃至8のいずれか一に記載の発光素子を含む発光装置。
- 請求項9に記載の発光装置を含む電子機器。
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JP2014099641A (ja) | 2014-05-29 |
KR20100085839A (ko) | 2010-07-29 |
CN101789495B (zh) | 2015-09-02 |
KR101424797B1 (ko) | 2014-07-31 |
JP5788031B2 (ja) | 2015-09-30 |
TW201043086A (en) | 2010-12-01 |
TWI528862B (zh) | 2016-04-01 |
CN102832349A (zh) | 2012-12-19 |
US20100181562A1 (en) | 2010-07-22 |
KR101998738B1 (ko) | 2019-07-10 |
TWI583253B (zh) | 2017-05-11 |
US8324615B2 (en) | 2012-12-04 |
CN101789495A (zh) | 2010-07-28 |
CN102832349B (zh) | 2016-01-06 |
US9147854B2 (en) | 2015-09-29 |
TW201311043A (zh) | 2013-03-01 |
JP5751755B2 (ja) | 2015-07-22 |
KR20120103524A (ko) | 2012-09-19 |
US20130161593A1 (en) | 2013-06-27 |
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