JP2021122042A - 発光デバイス、発光装置、電子機器、照明装置および化合物 - Google Patents
発光デバイス、発光装置、電子機器、照明装置および化合物 Download PDFInfo
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- JP2021122042A JP2021122042A JP2020125993A JP2020125993A JP2021122042A JP 2021122042 A JP2021122042 A JP 2021122042A JP 2020125993 A JP2020125993 A JP 2020125993A JP 2020125993 A JP2020125993 A JP 2020125993A JP 2021122042 A JP2021122042 A JP 2021122042A
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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
- 239000003115 supporting electrolyte Substances 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 1
- 229910001936 tantalum oxide Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002230 thermal chemical vapour deposition Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000007736 thin film deposition technique Methods 0.000 description 1
- 238000000427 thin-film deposition 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
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229910000314 transition metal oxide Inorganic materials 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical group 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 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
- OYQCBJZGELKKPM-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O-2].[Zn+2].[O-2].[In+3] OYQCBJZGELKKPM-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
- ZVWKZXLXHLZXLS-UHFFFAOYSA-N zirconium nitride Chemical compound [Zr]#N ZVWKZXLXHLZXLS-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
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Abstract
Description
図1(A)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、少なくとも発光層113と電子輸送層114とを有する。
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。本実施の形態では、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、発光層113および電子輸送層114を含む構成を例に説明するが、EL層103に含まれる層については、正孔注入層、正孔輸送層、電子注入層、キャリアブロック層、励起子ブロック層、電荷発生層など、様々な層構造を適用することができる。
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よいし、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5(A)および図5(B)を参照しながら説明する。図5(B)は照明装置の上面図、図5(A)は図5(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4mm2(2mm×2mm)とした。
比較発光デバイス1は、発光デバイス1におけるPyA1PQを、上記構造式(vii)で表される2−{4−[9,10−ジ(ナフタレン−2−イル)−2−アントリル]フェニル}−1−フェニル−1H−ベンゾイミダゾール(略称:ZADN)に変えた他は、発光デバイス1と同様に作製した。
本合成例では、本発明の一態様の発光デバイスの電子輸送材料として用いることが可能な化合物である4−{4−[10−(3−ピリジル)−9−アントリル]フェニル}[1]ベンゾフロ[3,2−d]ピリミジン(略称:BfpmPPyA)の合成方法について説明する。BfpmPPyAの構造を以下に示す。
4−クロロ[1]ベンゾフロ[3,2−d]ピリミジン2.0g(9.7mmol)、4−クロロフェニルボロン酸1.8g(12mmol)、トリ(オルト−トリル)ホスフィン0.30g(0.97mmol)、炭酸カリウム2.7g(19mmol)を三口フラスコに入れた。この混合物にトルエン100mL、エタノール20mL、水10mLを加えて減圧下で攪拌して脱気した。そして、混合物に酢酸パラジウム(II)0.044g(0.19mmol)を加え、80℃で6時間攪拌した。さらに、酢酸パラジウム(II)0.027g(0.097mmol)、トリ(オルト−トリル)ホスフィン0.20g(0.44mmol)を加え、80℃で2時間攪拌した。
4−(4−クロロフェニル)[1]ベンゾフロ[3,2−d]ピリミジン2.5g(8.9mmol)、ビスピナコレートジボロン2.7g(11mmol)、酢酸カリウム2.6g(27mmol)、キシレン45mLを三口フラスコに入れて窒素置換した。この混合物に[1,1’−ビス(ジフェニルホスフィノ)フェロセン]パラジウム(II)ジクロリド ジクロロメタン付加物(略称:Pd(dppf)Cl2 ・CH2Cl2)0.36g(0.44mmol)を加え、120℃で17時間攪拌した。
200mL三口フラスコ内に3−(10−ブロモ−9−アントリル)ピリジン1.6g(4.8mmol)と4−[4−(4,4,5,5−テトラメチル−[1,3,2]ジオキサボロラン−2−イル)−フェニル]−[1]ベンゾフロ[3,2−d]ピリミジン2.0g(5.3mmol)、トリ(o−トリル)ホスフィン0.15g(0.48mmol)、炭酸カリウム1.3g(9.6mmol)を加えフラスコ内を窒素置換した。この混合物にトルエン50mLとエタノール10mLと水5mLを加え、減圧下で撹拌することにより脱気した。この混合物に酢酸パラジウム(II)22mg(0.096mmol)を加え、窒素気流下、80℃で11時間撹拌した。所定時間経過後、この混合物に水を加え、析出した固体を吸引ろ過により回収し、水、メタノールで洗浄した。得られた固体をシリカゲルカラムクロマトグラフィー(展開溶媒 トルエン:酢酸エチル=9:1)により精製し、さらにトルエンにて再結晶したところ、目的物の固体を1.4g(2.8mmol)、収率57%で得た。ステップ3の合成スキームを以下に示す。
本合成例では、本発明の一態様の発光デバイスの電子輸送材料として用いることが可能な化合物である2−{4−[10−(3−ピリジル)−9−アントリル]フェニル}ジベンゾ[f,h]キノキサリン(略称:DBqPPyA)の合成方法について説明する。DBqPPyAの構造を以下に示す。
150mL三口フラスコ内に3−(10−ブロモ−9−アントリル)ピリジン1.1g(3.2mmol)と2−(4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン−2−イル)ジベンゾ[f,h]キノキサリン1.5g(3.5mmol)、トリ(オルト−トリル)ホスフィン96mg(0.32mmol)、炭酸カリウム0.87g(6.3mmol)を加えフラスコ内を窒素置換した。この混合物にトルエン30mLとエタノール6.0mLと水3.0mLを加え、減圧下で撹拌することにより脱気した。この混合物に酢酸パラジウム(II)14mg(0.063mmol)を加え、窒素気流下、80℃で21時間撹拌した。所定時間経過後、この混合物に水を加え、固体を吸引ろ過により回収した。得られた固体にトルエンを加え、超音波を照射後、固体を回収した。
本合成例では、本発明の一態様の発光デバイスの電子輸送材料として用いることが可能な化合物である(9−{4−[10−(3−ピリジル)−9−アントリル]フェニル}ナフト[1’,2’:4,5]フロ[2,3−b]ピラジン)(略称:NfprPPyA)の合成方法について説明する。NfprPPyAの構造を以下に示す。
9−(4−クロロフェニル)−ナフト[1’,2’:4,5]フロ[2,3−b]ピラジン3.2g(9.7mmol)、ビスピナコレートジボロン3.0g(12mmol)、酢酸カリウム2.9g(29mmol)、キシレン50mLを三口フラスコに入れて減圧下で攪拌して脱気した。この混合物に[1,1’−ビス(ジフェニルホスフィノ)フェロセン]パラジウム(II)ジクロロメタン付加物(略称:Pd(dppf)Cl2)0.40g(0.49mmol)を加え、120℃で19時間攪拌した。
200mL三口フラスコ内に3−(10−ブロモ−9−アントリル)ピリジン1.4g(4.1mmol)と3−[4−(4,4,5,5−テトラメチル−[1,3,2]ジオキサボロラン−2−イル)−フェニル]ナフト[1’,2’:4,5]フロ[2,3−b]ピラジン1.9g(4.5mmol)、トリ(o−トリル)ホスフィン0.13g(0.41mmol)、炭酸カリウム1.1g(8.3mmol)を加えフラスコ内を窒素置換した。この混合物にトルエン40mLとエタノール8mLと水4mLを加え、減圧下で撹拌することにより脱気した。この混合物に酢酸パラジウム(II)19mg(0.083mmol)を加え、窒素気流下、80℃で10時間撹拌した。所定時間経過後、この混合物に水を加え、析出した固体を吸引ろ過により回収した。得られた固体は水、メタノールで洗浄した。得られた固体はシリカゲルカラムクロマトグラフィー(展開溶媒 トルエン:酢酸エチル=9:1)により精製し、さらにトルエンにて再結晶したところ、目的物の固体を1.3g(2.4mmol)、収率58%で得た。ステップ2の合成スキームを以下に示す。
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4mm2(2mm×2mm)とした。
発光デバイス3は、発光デバイス2におけるBfpmPPyAを、上記構造式(ix)で表される2−{4−[10−(3−ピリジル)−9−アントリル]フェニル}ジベンゾ[f,h] キノキサリン(略称:DBqPPyA)に変えた他は発光デバイス2と同様に作製した。
発光デバイス4は、発光デバイス2における電子輸送層114を、上記構造式(x)で表される(9−{4−[10−(3−ピリジル)−9−アントリル]フェニル}ナフト[1’,2’:4,5]フロ[2,3−b]ピラジン)(略称:NfprPPyA)とLiqとを重量比1:2(=NfprPPyA:Liq)となるように12.5nm共蒸着した後、重量比2:1(=NfprPPyA:Liq)となるように12.5nm共蒸着して形成した他は発光デバイス2と同様に作製した。
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。
≪合成例4≫
本参考例では、実施例1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
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
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
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
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 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 (38)
- 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、発光層と電子輸送層とを有し、
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、
前記電子輸送層は、電子輸送材料を有し、
前記電子輸送材料は、第1の骨格と、第2の骨格と、第3の骨格とを有する有機化合物であり、
前記第1の骨格は、電子を輸送する機能を有し、
前記第2の骨格は、正孔を受容する機能を有し、
前記第3の骨格は、単環、且つπ電子不足型である複素芳香族環を有する発光デバイス。 - 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、発光層と、電子輸送層とを有し、
前記電子輸送層は、電子輸送材料を有し、
前記電子輸送材料は、第1の骨格と、第2の骨格と、第3の骨格とを有する有機化合物であり、
前記第1の骨格は、電子を輸送する機能を有し、
前記第2の骨格は、正孔を受容する機能を有し、
前記第2の骨格は、2環以上の縮合芳香族炭化水素環を有し、
前記第3の骨格は、単環、且つ、π電子不足型である複素芳香族環を有する発光デバイス。 - 請求項2において、
前記第2の骨格が、3環以上の縮合芳香族炭化水素環を有する発光デバイス。 - 請求項2において、
前記第2の骨格が3環または4環の縮合芳香族炭化水素環である発光デバイス。 - 請求項1乃至請求項4のいずれか一項において、
前記第2の骨格の環を形成する炭素の数が14以上である発光デバイス。 - 請求項1乃至請求項5のいずれか一項において、
前記縮合芳香族炭化水素環が6員環のみで構成されている発光デバイス。 - 請求項2において、
前記第2の骨格が、アントラセン環、フェナントレン環、ベンゾフルオレン環、テトラセン環、クリセン環、トリフェニレン環およびピレン環のいずれか一を含む発光デバイス。 - 請求項2において、
前記第2の骨格がアントラセン環である発光デバイス。 - 請求項1乃至請求項8のいずれか一項において、前記電子輸送層が、金属、金属塩、金属酸化物、または有機金属塩をさらに有する発光デバイス。
- 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、正孔輸送材料と、アクセプタ材料とを有し、
前記電子輸送層は、電子輸送材料と、金属、金属塩、金属酸化物、または有機金属塩と、を有し、
前記正孔輸送材料は、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、
前記アクセプタ材料は、前記正孔輸送材料に電子受容性を示す物質であり、
前記電子輸送材料は、第1の骨格と、第2の骨格と、第3の骨格とを有する有機化合物であり、
前記第1の骨格は、電子を輸送する機能を有し、
前記第2の骨格は、正孔を受容する機能を有し、
前記第3の骨格は、単環、且つ、π電子不足型である複素芳香族環を有する発光デバイス。 - 請求項10において、
前記第2の骨格が2環以上4環以下の縮合芳香族炭化水素環である発光デバイス。 - 請求項10において、
前記第2の骨格が3環または4環の縮合芳香族炭化水素環である発光デバイス。 - 請求項10において、
前記第2の骨格が、ナフタレン環、フルオレン環、アントラセン環、フェナントレン環、テトラセン環、クリセン環、トリフェニレン環およびピレン環のいずれか一を含む発光デバイス。 - 請求項10乃至請求項13のいずれか一項において、
前記第2の骨格の環を形成する炭素の数が14以上である発光デバイス。 - 請求項10乃至請求項14のいずれか一項において、
前記縮合芳香族炭化水素環が6員環のみで構成されている発光デバイス。 - 請求項10において、
前記第2の骨格がアントラセン環である発光デバイス。 - 請求項10乃至請求項16のいずれか一項において、
前記アクセプタ材料が、有機化合物である発光デバイス。 - 請求項3乃至請求項12のいずれか一項において、
前記金属、金属塩、金属酸化物、または有機金属塩が、アルカリ金属またはアルカリ土類金属を有する金属錯体である発光デバイス。 - 請求項9乃至請求項18のいずれか一項において、
前記金属、金属塩、金属酸化物、または有機金属塩が、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9乃至請求項18のいずれか一項において、
前記金属、金属塩、金属酸化物、または有機金属塩が、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9乃至請求項18のいずれか一項において、
前記金属、金属塩、金属酸化物、または有機金属塩が、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1乃至請求項21のいずれか一項において、
前記電子輸送材料における前記第1の骨格と前記第3の骨格とが、前記第2の骨格を介して結合する発光デバイス。 - 請求項1乃至請求項22のいずれか一項において、
前記電子輸送材料におけるLUMOが、前記第1の骨格に主として分布している発光デバイス。 - 請求項1乃至請求項23のいずれか一項において、
前記第1の骨格が、窒素を含む縮合芳香環またはトリアジン環を含む発光デバイス。 - 請求項1乃至請求項24のいずれか一項において、
前記第1の骨格が2個以上の窒素原子を有する発光デバイス。 - 請求項1乃至請求項25のいずれか一項において、
前記第1の骨格が、キノキサリン環、ジベンゾ[h,g]キノキサリン環、トリアジン環およびベンゾフロピリミジン環のいずれか一を含む骨格である発光デバイス。 - 請求項1乃至請求項26のいずれか一項において、
前記第1の骨格がキノキサリン環を含む骨格である発光デバイス。 - 請求項1乃至請求項27のいずれか一項において、
前記電子輸送材料におけるHOMOが、前記第2の骨格に主として分布している発光デバイス。 - 請求項1乃至請求項28のいずれか一項において、
前記第3の骨格が、窒素原子を有する六員環である複素芳香族環を含む発光デバイス。 - 請求項1乃至請求項29のいずれか一項において、
前記第3の骨格が、ピリジン環、ピリミジン環、ピラジン環およびトリアジン環のいずれか一である発光デバイス。 - 請求項30において、
前記第3の骨格が、前記第2の骨格に結合している炭素に対するβ位が窒素となるように前記第2の骨格と結合している発光デバイス。 - 請求項30において、
前記第3の骨格が3位で置換したピリジン環、5位で置換したピリミジン環、またはピラジン環である発光デバイス。 - 請求項1乃至請求項32のいずれか一項において、
前記電子輸送層が前記陰極に接する発光デバイス。 - 請求項1乃至請求項33のいずれか一項において、
前記発光層は、ホスト材料と、発光材料とを有し、
前記発光材料は、青色の蛍光を発する発光デバイス。 - 請求項1乃至請求項34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34のいずれか一項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34のいずれか一項に記載の発光デバイスと、筐体と、を有する照明装置。
- 第1の骨格と、第2の骨格と、第3の骨格とを有し、電子輸送層に用いられる化合物であって、
前記第1の骨格は、電子を輸送する機能を有し、
前記第2の骨格は、正孔を受容する機能を有し、
前記第3の骨格は、単環、且つπ電子不足型である複素芳香族環を有する化合物。
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DE102020119439A1 (de) | 2021-01-28 |
KR20210012965A (ko) | 2021-02-03 |
CN112310294A (zh) | 2021-02-02 |
US20210028371A1 (en) | 2021-01-28 |
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