JP2005011610A - Organic electroluminescent element - Google Patents

Organic electroluminescent element Download PDF

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JP2005011610A
JP2005011610A JP2003172977A JP2003172977A JP2005011610A JP 2005011610 A JP2005011610 A JP 2005011610A JP 2003172977 A JP2003172977 A JP 2003172977A JP 2003172977 A JP2003172977 A JP 2003172977A JP 2005011610 A JP2005011610 A JP 2005011610A
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group
layer
transport layer
light
emitting layer
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Noriyuki Fukumatsu
Hiroshi Miyazaki
浩 宮崎
敬之 福松
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Nippon Steel Chem Co Ltd
新日鐵化学株式会社
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an organic electroluminescent element (organic EL element) which has improved luminous efficiency, fully ensures drive stability, and moreover has a simple constitution, while utilizing emission of phosphorescence. <P>SOLUTION: In the organic EL element, a positive electrode, an organic layer including a hole transport layer, a luminous layer and an electron transport layer, and a negative electrode are laminated on a substrate. The hole transport layer is formed between the luminous layer and the positive electrode, and the electron transport layer is formed between the luminous layer and the negative electrode. A hole-blocking layer is not formed between the electron transport layer and the luminous layer. The luminous layer contains as a host material a compound expressed by general formula (I), and as a guest material an organometallic complex, containing at least one metal selected from among Ru, Rh, Pd, Ag, Re, Os, Ir, Pt and Au. The hole transport layer contains triarylamine dimer having at least two condensed ring aryl groups. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

【0001】 [0001]
【発明の属する技術分野】 BACKGROUND OF THE INVENTION
本発明は有機電界発光素子(以下、有機EL素子という)に関するものであり、詳しくは、有機化合物からなる発光層に電界をかけて光を放出する薄膜型デバイスに関するものである。 The present invention is an organic electroluminescent device (hereinafter, referred to as organic EL device) is related, more particularly, to a thin film type device that emits light by applying an electric field to the light-emitting layer made of an organic compound.
【0002】 [0002]
【従来の技術】 BACKGROUND OF THE INVENTION
有機材料を用いた電界発光素子の開発は、電極からの電荷注入効率向上を目的として電極の種類の最適化し、芳香族ジアミンからなる正孔輸送層と8−ヒドロキシキノリンアルミニウム錯体(以下、Alq3という)からなる発光層とを電極間に薄膜として設けた素子の開発(Appl. Phys. Lett., 51巻, 913頁,1987年)により、従来のアントラセン等の単結晶を用いた素子と比較して大幅な発光効率の改善がなされたことから、自発光・高速応答性といったと特徴を持つ高性能フラットパネルへの実用を目指して進められてきた。 Development of electroluminescent devices using organic materials, and optimization of the types of electrodes for the purpose of charge injection efficiency from the electrode, the hole transport layer and 8-hydroxyquinoline aluminum complex composed of an aromatic diamine (hereinafter referred to as Alq3 ) development of device having a light emitting layer as a thin film between the electrodes consisting of (Appl. Phys. Lett., 51, pp. 913 pp., by 1987), compared with devices using a single crystal, such as a conventional anthracene substantial improvement of luminous efficiency Te from that which has been made, has been promoted with the aim of practical for high-performance flat panel having the features that said that self-luminous, high-speed response.
【0003】 [0003]
このような有機EL素子の効率を更に改善するため、上記の陽極/正孔輸送層/発光層/陰極の構成を基本とし、これに正孔注入層、電子注入層や電子輸送層を適宜設けたもの、例えば陽極/正孔注入層/正孔輸送層/発光層/陰極や、陽極/正孔注入層/発光層/電子輸送層/陰極や、陽極/正孔注入層/発光層/電子輸送層/電子注入層/陰極や、陽極/正孔注入層/正孔輸送層/発光層/正孔阻止層/電子輸送層/陰極などの構成のものが知られている。 To such further improve the efficiency of the organic EL elements, the configuration of the anode / hole transporting layer / light emitting layer / cathode as a basic, this provided a hole injection layer, an electron injection layer or an electron transport layer suitably ones, for example, anode / hole injection layer / and a hole transport layer / luminescent layer / cathode, anode / hole injection layer / light emitting layer / electron transporting layer / cathode or anode / hole injection layer / light emitting layer / electron transporting layer / or electron injection layer / cathode, anode / hole injection layer / hole transport layer / luminescent layer / hole blocking layer / electron transport layer / cathode having a structure, such as are known. この正孔輸送層は、正孔注入層から注入された正孔を発光層に伝達する機能を有し、また電子輸送層は、陰極より注入された電子を発光層に伝達する機能を有している。 The hole transport layer has a function of transporting holes injected from the hole injection layer to the light-emitting layer, also an electron-transporting layer has a function of transporting electrons injected from the cathode to the emission layer ing. なお、正孔注入層を陽極バッファ層というときもある。 Incidentally, also when the hole injection layer that anode buffer layer.
【0004】 [0004]
そして、この正孔輸送層を発光層と正孔注入層間に介在させることによって、より低い電界で多くの正孔が発光層に注入され、更に発光層に陰極又は電子輸送層より注入された電子は、正孔輸送層が電子を極めて流しにくいので、正孔輸送層と発光層との界面に蓄積され、発光効率が上昇することが知られている。 Then, by interposing the hole transport layer to the light-emitting layer and the hole injection layer, many holes are injected to the emitting layer at a lower electric field, which is further injected from the cathode or the electron transporting layer to the light emitting layer electron since the hole transport layer is not easily highly flowing electrons are accumulated at the interface between the hole transport layer and the light-emitting layer, the luminous efficiency is known to be elevated.
【0005】 [0005]
同様に、電子輸送層を発光層と電子注入層間に介在させることによって、より低い電界で多くの電子が発光層に注入され、更に発光層に陽極又は正孔輸送層より注入された正孔は、電子輸送層が正孔を流しにくいので、電子輸送層と発光層との界面に蓄積され、発光効率が上昇することが知られている。 Similarly, by interposing the electron transporting layer to the light-emitting layer and an electron injection layer, a number of electrons are injected to the emitting layer at a lower electric field, further holes injected from the anode or the hole transport layer to the light-emitting layer , electron-transporting layer is so hard flowing holes are accumulated at the interface between the electron transport layer and the light-emitting layer, the luminous efficiency is known to be elevated. こうした構成層の機能にあわせて、これまでに多くの有機材料の開発が進められてきた。 In accordance with the function of such a configuration layer, the development of many of the organic material has been advanced so far.
【0006】 [0006]
一方、上記の芳香族ジアミンからなる正孔輸送層とAlq3からなる発光層とを設けた素子をはじめとした多くの素子が蛍光発光を利用したものであったが、燐光発光を用いる、すなわち、三重項励起状態からの発光を利用すれば、従来の蛍光(一重項)を用いた素子と比べて、3倍程度の効率向上が期待される。 On the other hand, many elements that including device provided with a light emitting layer made of a hole transport layer and Alq3 composed of an aromatic diamine described above were those using fluorescence emission, using phosphorescent, i.e., by using the light emission from the triplet excited state, as compared to devices using conventional fluorescence (singlet), to enhance the luminous efficiency approximately three times is expected. この目的のためにクマリン誘導体やベンゾフェノン誘導体を発光層とすることが検討されてきたが(第51回応用物理学会連合講演会、28a−PB−7、1990年)、極めて低い輝度しか得られなかった。 It has been studied the use of coumarin derivatives and benzophenone derivatives and the light-emitting layer for the purpose (51st Applied Physics Society Association Lecture, 28a-PB-7, 1990 years), not obtained only very low brightness It was. その後、三重項状態を利用する試みとして、ユーロピウム錯体を用いることが検討されてきたが、これも高効率の発光には至らなかった。 Then, an attempt to utilize triplet state, although the use of a europium complex has been investigated, which also failed to emit light at high efficiency.
【0007】 [0007]
最近、白金錯体(T−1、PtOEP)を用いることで、高効率の赤色発光が可能なことが報告された(Nature, 395巻,151頁,1998年)。 Recently, by using the platinum complex (T-1, PtOEP), it can be red light emission with high efficiency has been reported (Nature, 395, pp. 151 pp., 1998). その後、イリジウム錯体(T−2、Ir(ppy)3)を発光層にドープすることで、緑色発光で効率が大きく改善されている(Appl. Phys. Lett., 75巻,4頁,1999年)。 Then, by doping the light emitting layer of an iridium complex (T-2, Ir (ppy) 3), efficiency in green light emission are greatly improved (Appl. Phys. Lett., 75, pp. 4, pp, 1999 ). 更に、これらのイリジウム錯体は発光層を最適化することにより、素子構造をより単純化しても極めて高い発光効率を示すことが報告されている(Appl. Phys. Lett., 77巻,904頁,2000年)。 Furthermore, by these iridium complexes to optimize light emitting layer, it has been reported to exhibit extremely high luminous efficiency even more simplified device structure (Appl. Phys. Lett., 77, pp. 904 pp., 2000).
【0008】 [0008]
なお、上記T−1及びT−2等の化学式は下記特許文献等に記載されているので、それが参照される。 The chemical formulas such as the T-1 and T-2 is because it is described in the following patent documents and the like, it is referred to. また、ホスト材、ゲスト材や、正孔注入層、電子輸送層等の有機層に一般的に使用される化合物の構造式、略号も下記特許文献に記載されているので、参照される。 The host material, and the guest material, a hole injection layer, the structural formula of the commonly used compound in an organic layer such as an electron-transporting layer, since they are described in abbreviations also following patent document, are referred to. 以下の説明で断りなく使用する略号は、この技術分野で一般的に使用される略号であって、下記特許文献等に記された略号を意味すると理解される。 Abbreviations used without notice in the following description, a abbreviations commonly used in the art, is understood to mean the abbreviations are described in the following patent documents and the like.
【特許文献1】特開2002−305083号公報【特許文献2】特開2001−313178号公報【特許文献3】特開2002−352957号公報【非特許文献1】C. [Patent Document 1] Japanese 2002-305083 Publication No. Patent Document 2] Japanese 2001-313178 Publication No. Patent Document 3] Japanese 2002-352957 Patent Publication Non-Patent Document 1] C. Adachi, et. Adachi, et. al. al. , Appl. , Appl. Phys. Phys. Lett. Lett. 77, 904(2000 ) 77, 904 (2000)
【0009】 [0009]
燐光有機電界発光素子開発においてホスト材料として提案されているのは、特許文献2で紹介されているカルバゾール化合物のCBPである。 What is proposed as a host material in phosphorescent organic electroluminescent device development is the CBP of carbazole compounds that are introduced in Patent Document 2. 緑色燐光発光材料のトリス(2−フェニルピリジン)イリジウム錯体(以下、Ir(ppy)3という)のホスト材としてCBPを用いると、CBPは正孔を流し易く電子を流しにくい特性上、電荷注入バランスが崩れ、過剰の正孔は電子輸送側に流出し、結果としてIr(ppy)3からの発光効率が低下する。 Green tris (2-phenylpyridine) of phosphorescent material iridium complex (hereinafter, Ir (ppy) of 3) is used CBP as the host material, CBP is difficult characteristics on which shed easily electrons flowing hole, charge injection balance collapses, the excess holes to flow out to the electron transport side, the luminous efficiency from the results as Ir (ppy) 3 drops.
【0010】 [0010]
上記の解決手段として、発光層と電子輸送層の間に正孔阻止層を設ける手段がある。 As the solution, there is a means for providing a hole blocking layer between the light-emitting layer and the electron transport layer. この正孔阻止層により正孔を発光層中に効率よく蓄積することによって、発光層中での電子との再結合確率を向上させ、発光の高効率化を達成することができる。 By efficiently accumulated in the light-emitting layer in the hole by the hole blocking layer improves the probability of recombination of the electrons in the light emitting layer, it is possible to achieve a high efficiency of light emission. 現状一般的に用いられている正孔阻止材料として、2,9−ジメチル−4,7−ジフェニル−1,10−フェナントロリン(以下、BCPという)及びp−フェニルフェノラート−ビス(2−メチル−8−キノリノラート−N1,O8)アルミニウム(以下、BAlqという)が挙げられる。 As hole blocking materials used in current general, 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (hereinafter referred to as BCP) and p- phenylphenolato - bis (2-methyl - 8-quinolinolato -N1, O8) aluminum (hereinafter referred to as BAlq). これにより電子輸送層で電子とホールの再結合が起こることを防止できるが、BCPは室温でも結晶化し易く材料としての信頼性に欠けるため、素子寿命が極端に短い。 Can prevent this by recombination of electrons and holes occurs in the electron-transporting layer, BCP is due to lack of reliability as easy material to crystallize even at room temperature, is extremely short life of the device. またBAlqはTgが約100℃と比較的良好な素子寿命結果が報告されているが、正孔阻止能力が十分でなく、Ir(ppy)3からの発光効率は低下する。 The BAlq is Tg is relatively excellent device lifetime results reported about 100 ° C., a hole blocking ability is not sufficient, the luminous efficiency from Ir (ppy) 3 decreases. 加えて、層構成が1層増すことから素子構造が複雑になり、コストが増加するという問題がある。 In addition, the layer configuration becomes complicated device structure from increasing one layer, there is a problem that the cost is increased.
また、CBP以外でも使用可能なホスト材料として、特許文献1には、発光層に、ホスト材料として含窒素複素環Ar1と芳香族環Ar2とを有する基と金属Mからなる錯体(−Ar −Ar −O−) Mを使用し、ゲスト材料として貴金属系の金属錯体を使用した有機EL素子が開示されている。 Further, as a host material usable other than CBP, Patent Document 1, the light-emitting layer, the complex (-Ar 1 consisting of base metal M and a nitrogen-containing heterocyclic Ar1 an aromatic ring Ar2 as a host material - using the Ar 2 -O-) n M, an organic EL device using the metal complexes of the noble metal is disclosed as a guest material. ここに例示されたホスト材料は膨大な数にのぼるが、Ar がベンゾキサゾール環で、Ar がベンゼン環である化合物が多数の中の一つとして例示されている。 Although tens of host material enormous exemplified herein, Ar 1 is at benzoxazole ring, compound Ar 2 is a benzene ring are illustrated as one among many. この中には、MがZnであって、nが2である化合物も例示されているが、それにとどまる。 This includes, M is a Zn, but n is even are exemplified compound is 2, remain in it. また、ゲスト材料として貴金属系の金属錯体も多数例示されている。 Further is it illustrated a number metal complexes of noble metal even as a guest material. ただし、特許文献1では正孔阻止層を有する4層構造素子のみでの使用が例示されているにとどまり、上記での問題点を解決できるまでには至っていない。 However, remain in use only in the four-layer structure device having a patent hole blocking layer in Document 1 is illustrated, not reached until can solve the problems above.
【0011】 [0011]
一方、特許文献3で紹介されている3−フェニル−4−(1'−ナフチル)−5−フェニル−1,2,4−トリアゾール(以下、TAZという)も燐光有機電界発光素子のホスト材として提案されているが、電子を流しやすく正孔を流しにくい特性上、発光領域が正孔輸送層側となる。 On the other hand, 3-phenyl-4 has been introduced in Patent Document 3 (1'-naphthyl) -5-phenyl-1,2,4-triazole (hereinafter, referred to as TAZ) as a host material for a phosphorescent organic electroluminescence device have been proposed, on the hard characteristic flowing easily holes flowing electrons, the light emitting region becomes the hole transport layer side. 従って正孔輸送層の材料によってはIr(ppy)3との相性問題により、Ir(ppy)3からの発光効率が低下することも考えられる。 Therefore the compatibility problem of the material of the hole transport layer and Ir (ppy) 3, also conceivable that the luminous efficiency from Ir (ppy) 3 drops. 例えば、正孔輸送層として高性能、高信頼性、高寿命の点から最も良く使用されている4,4'−ビス(N−(1−ナフチル)−N−フェニルアミノ)ビフェニル(以下、NPBという)は、Ir(ppy)3との相性が悪く、TAZからNPBにエネルギー遷移が起き、Ir(ppy)3からIr(ppy)3へのエネルギー遷移の効率が低下し、発光効率が低下するという問題がある。 For example, high performance as a hole transport layer, high reliability, best is used 4,4'-bis terms of long life (N-(1-naphthyl) -N- phenylamino) biphenyl (hereinafter, NPB ) has poor compatibility with Ir (ppy) 3, the energy transition occurred NPB from TAZ, the efficiency of energy transition is decreased from Ir (ppy) 3 to Ir (ppy) 3, luminous efficiency is reduced that there is a problem in that.
【0012】 [0012]
上記の解決手段として、4,4'−ビス(N,N'−(3−トルイル)アミノ)−3、3'−ジメチルビフェニル(以下、HMTPDという)のようなIr(ppy)3からエネルギー遷移が起こらない材料を正孔輸送層として用いる手段がある。 As the solution, 4,4'-bis (N, N '- (3- tolyl) amino) -3,3'-dimethyl-biphenyl (hereinafter, referred to as HMTPD) energy transition from an Ir (ppy) 3 as there is means to use a material does not occur as a hole-transporting layer.
非特許文献1では、発光層の主材料にTAZ、1,3−ビス(N,N−t−ブチル−フェニル)−1,3,4−オキサゾール(以下、OXD7という)又はBCPを使用し、ドーピング材にIr(ppy)3を使用し、電子輸送層にAlq3を使用し、正孔輸送層にHMTPDを使用することで燐光発光素子において3層構造で高効率発光を得ることが可能であり、特にTAZを用いた系で優れていると報告している。 In Non-Patent Document 1, TAZ the main material of the light-emitting layer, 1,3-bis (N, N-t-butyl - phenyl) -1,3,4-oxazole (hereinafter, referred OXD7) or using BCP, using Ir (ppy) 3 as a doping material, using Alq3 in the electron transport layer, it is possible to obtain a high efficiency light emission in the three-layer structure in phosphorescent device by using HMTPD in the hole transporting layer , it is reported to be excellent, especially in a system using the TAZ. しかし、HMTPDはTgが約50℃程度であるため、結晶化し易く材料としての信頼性に欠ける。 However, HMTPD since Tg is about 50 ° C., lacks reliability as easy material to crystallize. したがって、素子寿命が極端に短く、商業的応用は難しい上、駆動電圧が高いという問題点もある。 Accordingly, there is extremely short service life of the device, on the commercial application difficult, a problem that the driving voltage is high.
【0013】 [0013]
【発明が解決しようとする課題】 [Problems that the Invention is to Solve
有機EL素子をフラットパネル・ディスプレイ等の表示素子に応用するためには、素子の発光効率を改善すると同時に駆動時の安定性を十分に確保する必要がある。 In order to apply the organic EL devices to display devices such as flat panel displays, it is necessary to ensure sufficient stability during driving while improving the luminous efficiency of the device. 本発明は、上記現状に鑑み、高効率かつ長寿命、かつ簡略化された素子構成を可能ならしめる実用上有用な有機EL素子を提供することを目的とする。 In view of the above situation, and an object thereof is to provide a high efficiency and long life, and makes it possible a simplified device structure practically useful organic EL element.
【0014】 [0014]
【課題を解決するための手段】 In order to solve the problems]
すなわち、本発明は、基板上に、陽極、正孔輸送層、発光層及び電子輸送層を含む有機層並びに陰極が積層されてなり、発光層と陽極の間に正孔輸送層を有し、発光層と陰極の間に電子輸送層を有し、電子輸送層と発光層の間には正孔阻止層を有しない有機電界発光素子であって、発光層が、ホスト材料として下記一般式(I)で表わされる化合物を、ゲスト材料としてルテニウム、ロジウム、パラジウム、銀、レニウム、オスミウム、イリジウム、白金及び金から選ばれる少なくとも一つの金属を含む有機金属錯体を含有し、正孔輸送層が、少なくとも2個の縮合環アリール基を有するトリアリールアミンダイマーを含有することを特徴とする有機電界発光素子である。 That is, the present invention has, on a substrate, comprising an anode, a hole transport layer, an organic layer and a cathode comprises a light-emitting layer and an electron transporting layer stacked, a hole transport layer between the light emitting layer and the anode, an electron transporting layer between the light-emitting layer and the cathode, an organic electroluminescent element having no hole blocking layer between the electron transport layer and the light-emitting layer, light emitting layer, the following general formula as a host material ( the compounds represented by I), ruthenium as a guest material, rhodium, palladium, silver, rhenium, osmium, iridium, containing an organic metal complex containing at least one metal selected from platinum and gold, a hole transport layer, an organic electroluminescent device characterized by containing a triarylamine dimer having at least two fused rings aryl group.
【化3】 [Formula 3]
(式中、R 〜R は各々独立に、水素原子、アルキル基、アラルキル基、アルケニル基、シアノ基、アミノ基、アミド基、アルコキシカルボニル基、カルボキシル基、アルコキシ基、置換基を有していてもよい芳香族炭化水素基又は置換基を有していてもよい芳香族複素環基を示す) (Wherein, R 1 to R 8 each independently have a hydrogen atom, an alkyl group, an aralkyl group, an alkenyl group, a cyano group, an amino group, an amido group, an alkoxycarbonyl group, a carboxyl group, an alkoxy group, a substituent even though it represents an aromatic hydrocarbon group or an optionally substituted aromatic heterocyclic group)
【0015】 [0015]
ここで、トリアリールアミンダイマーとしては、下記一般式(II)で表わされる化合物が好ましいものとして挙げられる。 Here, the triarylamine dimer, be mentioned as the compound represented by the following general formula (II) are preferred.
【化4】 [Of 4]
(式中、Ar 及びAr は炭素数6〜14の1価の芳香族基であるが、少なくとも一方は炭素数10〜14の縮合環構造を有する芳香族基であり、Ar は炭素数6〜14の2価の芳香族基である) (Wherein, although Ar 1 and Ar 2 is a monovalent aromatic group having 6 to 14 carbon atoms, at least one is an aromatic group having a condensed ring structure 10 to 14 carbon atoms, Ar 3 carbon the number 6 to 14 of the divalent aromatic group)
また、ゲスト材料としては、緑色燐光発光性のトリス(2−フェニルピリジン)イリジウム錯体又は赤色発光性のビス(2−(2'−ベンゾ[4,5−α]チエニル)ピリジナト−N,C3')イリジウム(アセチルアセトナト)錯体が好ましいものとして例示される。 As the guest material, a green phosphorescent tris (2-phenylpyridine) iridium complex or red luminescent bis (2- (2'-benzo [4,5-α] thienyl) pyridinato -N, C3 ' ) iridium (acetylacetonate) are illustrated as complex.
【0016】 [0016]
【発明の実施の形態】 DETAILED DESCRIPTION OF THE INVENTION
本発明の有機EL素子は、発光層に、前記一般式(I)で表される化合物と、周期律表7〜11族から選ばれる少なくとも1つの金属を含む燐光性有機金属錯体とを含む、いわゆる燐光を利用した有機EL素子に関するが、主成分として一般式(I)で表される化合物を、また副成分としてルテニウム、ロジウム、パラジウム、銀、レニウム、オスミウム、イリジウム、白金及び金から選ばれる少なくとも一つの金属を含む有機金属錯体を含有する発光層を有する。 The organic EL device of the present invention includes the light-emitting layer, the compound represented by the general formula (I), and a phosphorescent organic metal complex containing at least one metal selected from the periodic table 7-11 group, relates to an organic EL device that utilizes a so-called phosphorescence, selected a compound represented by formula (I), also as an auxiliary component ruthenium, rhodium, palladium, silver, rhenium, osmium, iridium, platinum and gold as the main component having a light emitting layer containing an organic metal complex containing at least one metal.
【0017】 [0017]
ここで、主成分とは該層を形成する材料のうち50重量%以上を占めるものを意味し、副成分とは該層を形成する材料のうち50重量%未満を占めるものを意味する。 Here, the main component means that accounts for 50 wt% or more of the material forming the layer, the auxiliary component means one occupy less than 50% by weight of the material forming the layer. 本発明の有機電界発光素子において、発光層に含まれる一般式(I)で表される化合物は、該層に含まれる燐光性有機金属錯体の、励起三重項準位より高いエネルギー状態の励起三重項準位を有することが基本的に必要である。 In an organic electroluminescent device of the present invention, compounds represented by the general formula (I) in the light-emitting layer, the phosphorescent organic metal complex contained in the layer, the higher energy state than the excited triplet level excited triplet it is basically necessary to have a term level. また、安定な薄膜形状を与え、かつ/又は高いガラス転移温度(Tg)を有し、正孔及び/又は電子を効率よく輸送することができる化合物であることが必要である。 Further, given a stable thin film form, and / or have a high glass transition temperature (Tg), it is necessary to be a compound of the holes and / or electrons can be efficiently transported. 更に電気化学的かつ化学的に安定であり、トラップとなったり発光を消光したりする不純物が製造時や使用時に発生しにくい化合物であることが要求される。 Still more electrochemically and chemically stable, impurities or to quench the light emission or a trap that the compound is required to hardly occur during manufacture or use.
更に、燐光性有機錯体の発光が正孔輸送層の励起3重項準位に影響されにくくするため、発光領域が正孔輸送層界面よりも適度に距離を保てる正孔注入能力を有することも重要である。 Furthermore, since the light emission of the phosphorescent organic complex is hardly affected by the excited triplet level of the hole transport layer, it may have a hole injection ability emitting region can be kept reasonably distance than the hole transport layer interface is important.
【0018】 [0018]
これらの条件を満たす発光層を形成する材料として、本発明では前記一般式(I)で表わされる化合物をホスト材料として用いる。 As a material for forming these conditions are satisfied emitting layer, in the present invention using a compound represented by the general formula (I) as a host material. 一般式(I)において、R 〜R は各々独立に、水素原子、アルキル基、アラルキル基、アルケニル基、シアノ基、アミノ基、アミド基、アルコキシカルボニル基、カルボキシル基、アルコキシ基、置換基を有していてもよい芳香族炭化水素基又は置換基を有していてもよい芳香族複素環基を示す。 In the general formula (I), R 1 ~R 8 each independently represent a hydrogen atom, an alkyl group, an aralkyl group, an alkenyl group, a cyano group, an amino group, an amido group, an alkoxycarbonyl group, a carboxyl group, an alkoxy group, a substituted group the have a which may have aromatic hydrocarbon group or a substituent shown also aromatic heterocyclic group. アルキル基としては、炭素数1〜6のアルキル基(以下、低級アルキル基という)が好ましく例示され、アラルキル基としては、ベンジル基、フェネチル基が好ましく例示され、アルケニル基としては、炭素数1〜6の低級アルケニル基が好ましく例示され、アミノ基としては、−NR (Rは水素又は低級アルキル基)で表されるアミノ基が好ましく例示され、アミド基としては、−CONH が例示され、アルコキシカルボニル基及びアルコキシ基のアルコキシとしては、低級アルコキシが好ましく例示される。 As the alkyl group, alkyl group having 1 to 6 carbon atoms (hereinafter, referred to as lower alkyl group) is preferable, and examples of the aralkyl group, benzyl group, phenethyl group is preferable, and examples of the alkenyl group, 1 carbon atoms lower alkenyl groups 6 are preferably exemplified, as the amino group, -NR 2 (R is hydrogen or lower alkyl) amino group represented by is preferably exemplified as the amide group, -CONH 2 is illustrated, the alkoxy alkoxycarbonyl group and an alkoxy group, a lower alkoxy is preferably exemplified.
【0019】 [0019]
また、芳香族炭化水素基としては、フェニル基、ナフチル基、アセナフチル基、アントリル基等の芳香族炭化水素基が好ましく例示され、芳香族複素環基としては、ピリジル基、キノリル基、チエニル基、カルバゾル基、インドリル基、フリル基等の芳香族複素環基が好ましく例示される。 The aromatic hydrocarbon group, a phenyl group, a naphthyl group, acenaphthyl group, an aromatic hydrocarbon group such as an anthryl group are preferably exemplified, as the aromatic heterocyclic group, a pyridyl group, a quinolyl group, a thienyl group, carbazol group, an indolyl group, an aromatic heterocyclic group such as furyl group are preferably exemplified. これらが置換基を有する芳香族炭化水素基又は芳香族複素環基である場合は、置換基としては、低級アルキル基、低級アルコキシ基、フェノキシ基、トリオキシ基、ベンジルオキシ基、フェニル基、ナフチル基、ジメチルアミノ基等が挙げられる。 If they are aromatic hydrocarbon group or an aromatic heterocyclic group having a substituent, examples of the substituent include a lower alkyl group, a lower alkoxy group, a phenoxy group, Toriokishi group, a benzyloxy group, a phenyl group, a naphthyl group , dimethylamino group and the like.
【0020】 [0020]
一般式(I)で表わされる化合物は、より好ましくはR 〜R が水素原子、低級アルキル基又は低級アルコキシ基である化合物が選ばれる。 Compound represented by the general formula (I) is more preferably a compound R 1 to R 8 is a hydrogen atom, a lower alkyl group or a lower alkoxy group is selected. 更に、好ましくはR 〜R の内、6個以上が水素原子で、他が低級アルキル基である化合物であり、最も好ましくは全部が水素原子である化合物である。 Further, preferably of R 1 to R 8, with 6 or more hydrogen atoms, other is a compound which is a lower alkyl group, and most preferably is entirely hydrogen atom compounds.
【0021】 [0021]
この一般式(I)で表される化合物は、対応する金属塩と式(III)で表される化合物との間の錯体形成反応により合成される。 The compound represented by the general formula (I) is synthesized by complexation reaction between the compounds represented by the corresponding metal salt of the formula (III). 合成反応は、例えば、J. Synthesis reaction, for example, J. Chem. Chem. Soc. Soc. Perkin I,1291(1976). Perkin I, 1291 (1976). に示される方法により行われる。 It carried out by the method shown in. なお、式(III)において、R 〜R は一般式(I)のR 〜R と対応する。 In the equation (III), R 1 ~R 8 corresponds with R 1 to R 8 of general formula (I).
【化5】 [Of 5]
【0022】 [0022]
発光層におけるゲスト材料としては、ルテニウム、ロジウム、パラジウム、銀、レニウム、オスミウム、イリジウム、白金及び金から選ばれる少なくとも一つの金属を含む有機金属錯体を含有する。 The guest material in the light emitting layer contains ruthenium, rhodium, palladium, silver, rhenium, osmium, iridium, an organometallic complex containing at least one metal selected from platinum and gold. かかる有機金属錯体は、前記特許文献等で公知であり、これらが選択されて使用可能である。 Such organic metal complexes are the known in patent literature like, and can be selected from them and used.
【0023】 [0023]
好ましい有機金属錯体としては、下記一般式(IV)で表される化合物が挙げられる。 Preferred organometallic complexes include compounds represented by the following general formula (IV).
【化6】 [Omitted]
ここで、Mは上記金属を示し、nは該金属の価数を示す。 Here, M represents the metal, n represents shows the valence of the metal.
【0024】 [0024]
また、環A は置換基を有していてもよい芳香族炭化水素環基又は芳香族複素環基を表わし、好ましくは、フェニル基、ビフェニル基、ナフチル基、アントリル基、チエニル基、ピリジル基、キノリル基、又はイソキノリル基を表す。 Furthermore, ring A 1 represents which may have an aromatic hydrocarbon ring group or an aromatic heterocyclic group the substituent is preferably a phenyl group, a biphenyl group, a naphthyl group, an anthryl group, a thienyl group, a pyridyl group represents a quinolyl group, or an isoquinolyl group. これらが有していてもよい置換基としては、フッ素原子等のハロゲン原子;メチル基、エチル基等の炭素数1〜6のアルキル基;ビニル基等の炭素数2〜6のアルケニル基;メトキシカルボニル基、エトキシカルボニル基等の炭素数2〜6のアルコキシカルボニル基;メトキシ基、エトキシ基等の炭素数1〜6のアルキル基;ビニル基等の炭素数2〜6のアルケニル基;メトキシカルボニル基、エトキシカルボニル基等の炭素数2〜6のアルコキシカルボニル基;メトキシ基、エトキシ基等の炭素数1〜6のアルコキシ基;フェノキシ基、ベンジルオキシ基などのアリールオキシ基;ジメチルアミノ基、ジエチルアミノ基等のジアルキルアミノ基;アセチル基等のアシル基;トリフルオロメチル基等のハロアルキル基;シアノ基等が挙げられ Examples of the substituent that the they have, a halogen atom such as a fluorine atom; a methyl group, an alkyl group having 1 to 6 carbon atoms such as ethyl group, an alkenyl group having 2 to 6 carbon atoms such as a vinyl group; methoxy carbonyl group, an alkoxycarbonyl group having 2 to 6 carbon atoms such as an ethoxycarbonyl group; methoxy group, an alkyl group having 1 to 6 carbon atoms such as an ethoxy group; a methoxycarbonyl group; an alkenyl group having 2 to 6 carbon atoms such as a vinyl group , alkoxycarbonyl group having 2 to 6 carbon atoms such as an ethoxycarbonyl group; methoxy group, an alkoxy group having 1 to 6 carbon atoms such as an ethoxy group; a phenoxy group, an aryloxy group such as a benzyloxy group; a dimethylamino group, a diethylamino group haloalkyl group such as trifluoromethyl group; an acyl group such as an acetyl group; a dialkylamino group such as a cyano group and the like .
【0025】 [0025]
環A は置換基を有していてもよい、窒素を複素環形成原子として含有する芳香族複素環基を表わし、好ましくは、ピリジル基、ピリミジル基、ピラジン基、トリアジン基、ベンゾチアゾール基、ベンゾオキサゾール基、ベンゾイミダゾール基、キノリル基、イソキノリル基、キノキサリン基、又はフェナントリジン基を表す。 Ring A 2 may have a substituent, nitrogen represent an aromatic heterocyclic group containing as the hetero ring-forming atoms, preferably, a pyridyl group, a pyrimidyl group, a pyrazine group, a triazine group, benzothiazole group, benzoxazole group, benzimidazole group, quinolyl group, isoquinolyl group, quinoxaline group or phenanthridine group.
【0026】 [0026]
これらが有していてもよい置換基としては、フッ素原子等のハロゲン原子;メチル基、エチル基等の炭素数1〜6のアルキル基;ビニル基等の炭素数2〜6のアルケニル基;メトキシカルボニル基、エトキシカルボニル基等の炭素数2〜6のアルコキシカルボニル基;メトキシ基、エトキシ基等の炭素数1〜6のアルコキシ基;フェノキシ基、ベンジルオキシ基などのアリールオキシ基;ジメチルアミノ基、ジエチルアミノ基等のジアルキルアミノ基;アセチル基等のアシル基;トリフルオロメチル基等のハロアルキル基;シアノ基等が挙げられる。 Examples of the substituent that the they have, a halogen atom such as a fluorine atom; a methyl group, an alkyl group having 1 to 6 carbon atoms such as ethyl group, an alkenyl group having 2 to 6 carbon atoms such as a vinyl group; methoxy carbonyl group, an alkoxycarbonyl group having 2 to 6 carbon atoms such as an ethoxycarbonyl group; methoxy group, an alkoxy group having 1 to 6 carbon atoms such as an ethoxy group, a dimethylamino group; a phenoxy group, an aryloxy group such as a benzyl group haloalkyl group such as trifluoromethyl group; an acyl group such as an acetyl group; a dialkylamino group such as a diethylamino group and a cyano group.
【0027】 [0027]
なお、環A が有する置換基と環A が有する置換基が結合して、一つの縮合環を形成してもよく、7,8−ベンゾキノリン基等が挙げられる。 Incidentally, bonded substituents substituent and the ring A 2 which ring A 1 has has, may form one condensed ring, 7,8-benzoquinoline group. 環A 及び環A の置換基として、より好ましくはアルキル基、アルコキシ基、芳香族炭化水素環基又はシアノ基が挙げられる。 As the substituent of ring A 1 and ring A 2, and more preferably an alkyl group, an alkoxy group, an aromatic hydrocarbon ring group or a cyano group. 式(IV)におけるMとして好ましくは、ルテニウム、ロジウム、パラジウム、銀、レニウム、オスミウム、イリジウム、白金又は金が挙げられる。 It preferred as M in Formula (IV), ruthenium, rhodium, palladium, silver, rhenium, osmium, iridium, platinum or gold. 前記一般式(IV)で示される有機金属錯体の具体例を以下に示すが、下記の化合物に限定されるわけではない。 Specific examples of the organic metal complex represented by the general formula (IV) below, but is not limited to the following compounds.
【0028】 [0028]
【化7】 [Omitted]
【0029】 [0029]
本発明の有機EL素子は、発光層と陽極の間に正孔輸送層を有し、正孔輸送層に含有される正孔輸送材料として、少なくとも2個の縮合環アリール基を有するトリアリールアミンダイマーを含有する。 The organic EL device of the present invention has a hole transport layer between the light-emitting layer and the anode, as a hole transport material contained in the hole transport layer, triaryl amines having at least two fused rings aryl group containing dimer. なお、トリアリールアミンダイマーは、(−Ar−NAr で表わされる化合物を意味し、ここでArはアリール又はアリーレン基を示す。 Incidentally, triarylamine dimer, (- Ar-NAr 2) means a compound represented by 2, wherein Ar represents an aryl or arylene group.
【0030】 [0030]
かかるトリアリールアミンダイマーとしては、上記一般式(II)で表わされる化合物が好ましく挙げられる。 Such triarylamine dimer compound represented by the above general formula (II) may be preferably mentioned. 一般式(II)において、Ar 及びAr は炭素数6〜14の1価の芳香族基であるが、少なくとも一方は炭素数10〜14の縮合環構造を有する芳香族基である。 In formula (II), Ar 1 and Ar 2 is a monovalent aromatic group having 6 to 14 carbon atoms, at least one is an aromatic group having a condensed ring structure 10 to 14 carbon atoms. 縮合環構造を有する芳香族基としては、ナフチル基、低級アルキル置換ナフチル基等の2〜3環の縮合環構造を有する芳香族基が好ましく挙げられる。 The aromatic group having a condensed ring structure, a naphthyl group, an aromatic group having a condensed ring structure 2-3 rings such as lower alkyl-substituted naphthyl group are preferred. 縮合環構造を有する芳香族基以外の芳香族基としては、フェニル基、低級アルキル置換フェニル基、ビフェニリル基等のベンゼン環を有する芳香族基が好ましく挙げられる。 The aromatic group other than aromatic group having a fused ring structure, a phenyl group, a lower alkyl-substituted phenyl group, an aromatic group having a benzene ring such as biphenylyl group are preferred. Ar は炭素数6〜14の2価の芳香族基であるが、フェニレン基、低級アルキル置換フェニレン基等が好ましく挙げられる。 Although Ar 3 is a divalent aromatic group having 6 to 14 carbon atoms, a phenylene group, such as lower alkyl-substituted phenylene group is preferred.
好ましいトリアリールアミンダイマーとしては、具体的には、NPB、4,4'−ビス(N−(9−フェナントリル)−N−フェニルアミノ)ビフェニル(以下、PPBという)等が挙げられる。 Preferred triarylamine dimer, specifically, NPB, 4,4'-bis (N-(9-phenanthryl) -N- phenylamino) biphenyl (hereinafter, referred to as PPB), and the like.
【0031】 [0031]
本発明では、発光層のホスト材料として、前記一般式(I)で表される化合物を使用し、正孔輸送材料として縮合環を有するトリアリールアミンダイマーを使用する。 In the present invention, as a host material of the light-emitting layer, using the above formula (I) compounds, using a triarylamine dimer having a condensed ring as a hole-transporting material. 正孔輸送材料として、縮合環を有さないN,N'−ジフェニル−N,N'−ビス(3−メチルフェニル)−[1,1'−ビフェニル]−4,4'−ジアミン(以下、TPDという)、HMTPDはそれぞれTg=60℃、50℃で結晶化しやすく、寿命等の性能が劣るだけでなく、量産実績もない。 As a hole transport material, N having no fused rings, N'- diphenyl -N, N'- bis (3-methylphenyl) - [1,1'-biphenyl] -4,4'-diamine (hereinafter, as TPD), HMTPD each Tg = 60 ° C., tends to crystallize at 50 ° C., not only inferior performance life, etc., there is no mass production performance. 一方、縮合環を有するNPBは安定で、性能が優れるだけでなく、量産実績がある。 Meanwhile, NPB having a condensed ring is a stable, well performance is excellent, there is a mass production performance. しかし、発光層のホスト材料としてTAZを使用した場合、正孔輸送材料としてNPBを使用すると正孔輸送層/発光層界面で、Ir錯体からNPBにエネルギー移動するため、消光してしまい発光効率が良くないので、Ir錯体からエネルギー移動しないHMTPDを使用している。 However, when using TAZ as a host material of the light emitting layer, using NPB as a hole transporting material in the hole transport layer / light-emitting layer interface, to energy transfer to the NPB from Ir complexes, the emission efficiency will be quenched so not good, they are using the HMTPD not energy transfer from the Ir complex. 本発明のように発光層のホスト材料として、前記一般式(I)で表される化合物を使用し、正孔輸送材料としてNPBを使用すると、これらの問題が解決された優れた性能の有機EL素子が得られる。 As a host material for the light emitting layer as in the present invention, using the above formula (I) compounds, using NPB as a hole transporting material, an organic EL superior performance of these problems have been resolved element can be obtained.
【0032】 [0032]
本発明で発光層に使用するホスト材料は、電子と正孔をほぼ均等に流すことができるので、発光層の中央で発光させる事ができる。 The host materials used in the light emitting layer in the present invention, can flow electrons and holes substantially uniformly, it can emit light at the center of the light-emitting layer. 従って、TAZの様に正孔輸送側で発光し、正孔輸送層にエネルギー遷移が発生し効率低下を招くことはないし、CPBの様に電子輸送層側で発光し、電子輸送層にエネルギー遷移して効率を落とすこともなく、正孔輸送層としてNPB、電子輸送層としてAlq3の様な信頼性が高い材料を使用できる。 Therefore, light emission in the hole transport side as the TAZ, to energy transition to the hole transport layer will not lead to reduced efficiency occurs, emitted in the electron transport layer side as the CPB, the energy transition in the electron transport layer without lowering the efficiency, NPB, the material has high reliability, such as Alq3 as an electron transport layer can be used as a hole-transporting layer.
また、本材料の組み合わせでは、ドーピング材として緑発光のIr(ppy)3のみならず、赤色発光のビス(2−(2'−ベンゾ[4,5−α]チエニル)ピリジナト−N,C3')イリジウム(アセチルアセトナト)錯体(以下、btp Ir(acac)という)も使用できる。 Further, the combination of this material, not a green light emission of Ir (ppy) 3 only as a doping material, the red light-bis (2- (2'-benzo [4,5-α] thienyl) pyridinato -N, C3 ' ) iridium as (acetylacetonato) complex (hereinafter, btp 2 Ir (acac)) it can also be used. 赤色発光には、CBPをホスト材としてIrbtpをゲスト材として、CBPが正孔を流し易い欠点を補うために、BCPなどの正孔阻止層を施す技術が知られているが、本発明の材料の組み合わせを用いると、正孔阻止層なしで、同等の性能を得ることができる。 The red emission, the Irbtp the CBP as the host material as a guest material, in order to compensate for the likely disadvantage CBP is flowing hole, but a technique for performing a hole blocking layer, such as BCP are known, the material of the present invention using a combination of, without a hole blocking layer, it is possible to obtain an equivalent performance.
【0033】 [0033]
以下、本発明の有機EL素子について、図面を参照しながら説明する。 Hereinafter, the organic EL device of the present invention will be described with reference to the drawings. 図1は本発明に用いられる一般的な有機EL素子の構造例を模式的に示す断面図であり、1は基板、2は陽極、3は正孔注入層、4は正孔輸送層、5は発光層、6は電子輸送層、7は陰極を各々表わす。 Figure 1 is a sectional view showing a structural example of a general organic EL element used in the present invention schematically, 1 denotes a substrate, 2 anode, 3 hole-injecting layer, 4 hole-transporting layer, 5 the light-emitting layer, 6 electron-transporting layer, 7 represents each cathode. 本発明の有機EL素子では、基板、陽極、正孔輸送層、発光層、電子輸送層及び陰極を必須の層として有するが、必須の層以外の層、例えば、正孔注入層は省略可能であり、また必要により他の層を設けてもよい。 In the organic EL device of the present invention includes a substrate, an anode, a hole transport layer, light emitting layer, has an electron-transporting layer and the essential layers of the cathode, essential layers other than the layer, for example, a hole injection layer is optional There also may be provided other layers as necessary. しかし、本発明の有機EL素子は、正孔阻止層は必要としない。 However, the organic EL device of the present invention, the hole blocking layer is not required. 正孔阻止層を設けないことにより、層構造が簡素化され、製造上、性能上の利点をもたらす。 By not providing the hole-blocking layer, which simplifies the layer construction, manufacturing, offers advantages in performance.
【0034】 [0034]
基板1は有機電界発光素子の支持体となるものであり、石英やガラスの板、金属板や金属箔、プラスチックフィルムやシートなどが用いられる。 Substrate 1 is to be a support for an organic electroluminescent device, a quartz or glass plate, a metal plate or foil, or a plastic film or sheet. 特にガラス板や、ポリエステル、ポリメタクリレート、ポリカーボネート、ポリスルホンなどの透明な合成樹脂の板が好ましい。 In particular, a glass plate, polyester, polymethacrylate, polycarbonate, transparent synthetic resin plate such as polysulfone preferred. 合成樹脂基板を使用する場合にはガスバリア性に留意する必要がある。 When a synthetic resin substrate is used it is necessary to pay attention to the gas barrier property. 基板のガスバリヤ性が小さすぎると、基板を通過した外気により有機電界発光素子が劣化することがあるので好ましくない。 If gas barrier property of the substrate is too small, undesirable organic electroluminescent device may deteriorate by the outside air passing through the substrate. このため、合成樹脂基板の少なくとも片面に緻密なシリコン酸化膜等を設けてガスバリア性を確保する方法も好ましい方法の一つである。 Therefore, a method of securing the gas barrier property provide a dense silicon oxide film on at least one surface of the synthetic resin substrate is also one of preferred methods.
【0035】 [0035]
基板1上には陽極2が設けられるが、陽極は正孔輸送層への正孔注入の役割を果たすものである。 On the substrate 1 anode 2 is provided but the anode plays a role of injecting holes into the hole-transporting layer. この陽極は、通常、アルミニウム、金、銀、ニッケル、パラジウム、白金等の金属、インジウム及び/又はスズの酸化物などの金属酸化物、ヨウ化銅などのハロゲン化金属、カーボンブラック、あるいは、ポリ(3−メチルチオフェン)、ポリピロール、ポリアニリン等の導電性高分子などにより構成される。 The anode is usually, aluminum, gold, silver, nickel, palladium, a metal such as platinum, a metal oxide such as indium and / or tin oxide, a metal halide such as copper iodide, carbon black or poly (3-methylthiophene), polypyrrole, etc. an electrically conductive polymer such as polyaniline. 陽極の形成は通常、スパッタリング法、真空蒸着法などにより行われることが多い。 Formation of the anode is usually formed by a sputtering method, it is often performed by a vacuum deposition method. また、銀などの金属微粒子、ヨウ化銅などの微粒子、カーボンブラック、導電性の金属酸化物微粒子、導電性高分子微粉末などの場合には、適当なバインダー樹脂溶液に分散し、基板1上に塗布することにより陽極2を形成することもできる。 The metal particles such as silver, fine particles of copper iodide, carbon black, conductive metal oxide fine particles, in the case of a conductive polymer fine powder is dispersed in a suitable binder resin solution, on the substrate 1 it is also possible to form the anode 2 by coating. 更に、導電性高分子の場合は電解重合により直接基板1上に薄膜を形成したり、基板1上に導電性高分子を塗布して陽極2を形成することもできる(Appl.Phys.Lett.,60巻,2711頁,1992年)。 Furthermore, in the case of the conductive polymer can be formed or a thin film is formed directly on the substrate 1 by electrolytic polymerization, the anode 2 by coating a conductive polymer on a substrate 1 (Appl. , Vol. 60, pp. 2711, 1992). 陽極は異なる物質で積層して形成することも可能である。 The anode can also be formed by laminating different materials. 陽極の厚みは、必要とする透明性により異なる。 The thickness of the anode varies with the requirement for transparency. 透明性が必要とされる場合は、可視光の透過率を、通常、60%以上、好ましくは80%以上とすることが望ましく、この場合、厚みは、通常、5〜1000nm、好ましくは10〜500nm程度である。 When transparency is required, the transmittance of visible light, usually at least 60%, preferably not less that 80% or more, in this case, the thickness, usually, 5 to 1000 nm, preferably 10 to it is about 500nm. 不透明でよい場合は陽極2は基板1と同一でもよい。 Where opaqueness is the anode 2 may be the same as the substrate 1. また、更には上記の陽極2の上に異なる導電材料を積層することも可能である。 Moreover, even it is possible to laminate a different conductive material on the anode 2 described above.
【0036】 [0036]
陽極2の上には正孔輸送層4が設けられる。 The hole transport layer 4 is provided on the anode 2. 両者の間には、正孔注入層3を設けることもできる。 Between the two, it may be provided a hole injection layer 3. 正孔輸送層の材料に要求される条件としては、陽極からの正孔注入効率が高く、かつ、注入された正孔を効率よく輸送することができる材料であることが必要である。 The conditions required for the material of the hole transport layer, high efficiency of hole injection from the anode, and it is necessary the injected holes is a material that can be efficiently transported. そのためには、イオン化ポテンシャルが小さく、可視光の光に対して透明性が高く、しかも正孔移動度が大きく、更に安定性に優れ、トラップとなる不純物が製造時や使用時に発生しにくいことが要求される。 For this purpose, a small ionization potential, high transparency to visible light, high hole mobility, to be further excellent in stability, impurities to be traps hardly occurs during manufacture or use is required. また、発光層5に接するために発光層からの発光を消光したり、発光層との間でエキサイプレックスを形成して効率を低下させないことが求められる。 You can also quench the emission from the light-emitting layer in order to contact with the light-emitting layer 5, it does not reduce the efficiency by forming an exciplex with the luminescent layer is obtained. 上記の一般的要求以外に、車載表示用の応用を考えた場合、素子には更に耐熱性が要求される。 Besides the aforementioned general requirements, when application for vehicle display, further heat resistance is required for the device. 従って、Tgとして85℃以上の値を有する材料が望ましい。 Therefore, a material having a value of 85 ° C. or more as Tg is desirable.
【0037】 [0037]
本発明の有機EL素子では、正孔輸送材料として、前記のNPB、PPBのようなトリアリールアミンダイマーを使用する。 In the organic EL device of the present invention, as a hole transport material, wherein the NPB, using the triarylamine dimer such as PPB.
【0038】 [0038]
なお、必要によりその他の正孔輸送材料として公知の化合物をトリアリールアミンダイマーと併用することもできる。 Incidentally, a known compound may be used in combination with a triarylamine dimer Other hole transporting material as required. 例えば、2個以上の3級アミンを含み2個以上の縮合芳香族環が窒素原子に置換した芳香族ジアミン(特開平5−234681号公報)、4,4',4”−トリス(1−ナフチルフェニルアミノ)トリフェニルアミン等のスターバースト構造を有する芳香族アミン化合物(J. Lumin., 72−74巻、985頁、1997年)、トリフェニルアミンの四量体からなる芳香族アミン化合物(Chem.Commun., 2175頁、1996年)、2,2',7,7'−テトラキス−(ジフェニルアミノ)−9,9'−スピロビフルオレン等のスピロ化合物(Synth. Metals, 91巻、209頁、1997年)等が挙げられる。これらの化合物は、単独で用いてもよいし、必要に応じて、各々、混合して用いてもよい。 For example, two or more aromatic diamines in which two or more fused aromatic rings include tertiary amine has been substituted with nitrogen atoms (JP-A-5-234681), 4,4 ', 4 "- tris (1- aromatic amine compounds having a starburst structure, such as naphthyl phenylamino) triphenylamine (J. Lumin., 72-74, pp. 985 pp., 1997), an aromatic amine compound made of a tetramer of triphenylamine ( . Chem.Commun, pp 2175, 1996), 2,2 ', 7,7'-tetrakis -. (diphenylamino) -9,9'-spirobifluorene, etc. spiro compounds of (Synth Metals, 91, pp. 209 pages include 1997), and the like. these compounds may be used alone, if necessary, each may be mixed.
また、上記の化合物以外に、正孔輸送層の材料として、ポリビニルカルバゾール、ポリビニルトリフェニルアミン(特開平7−53953号公報)、テトラフェニルベンジジンを含有するポリアリーレンエーテルサルホン(Polym. Adv. Tech., 7巻、33頁、1996年)等の高分子材料が挙げられる。 In addition to the above compounds, as the material of the hole transport layer, polyvinylcarbazole, polyvinyl triphenylamine (Japanese Patent Laid-Open No. 7-53953), polyarylene ether sulfone containing tetraphenylbenzidine (Polym. Adv. Tech ., Vol. 7, page 33, and polymer materials in 1996) and the like.
【0039】 [0039]
正孔輸送層を塗布法で形成する場合は、正孔輸送材料を1種又は2種以上と、必要により正孔のトラップにならないバインダー樹脂や塗布性改良剤などの添加剤とを添加し、溶解して塗布溶液を調製し、スピンコート法などの方法により陽極2上に塗布し、乾燥して正孔輸送層4を形成する。 When forming the hole transport layer by a coating method, by adding the one or more hole transport material, an additive such as a binder resin and a coating improving agent as not to hole trapping necessary, dissolved to a coating solution was prepared, by a method such as spin coating is coated on the anode 2 and dried to form the hole transport layer 4. バインダー樹脂としては、ポリカーボネート、ポリアリレート、ポリエステル等が挙げられる。 The binder resin, polycarbonate, polyarylate, polyester, and the like. バインダー樹脂は添加量が多いと正孔移動度を低下させるので、少ない方が望ましく、通常、50重量%以下が好ましい。 Since the binder resin lowers the hole mobility and the addition amount is large, it is desirable small, usually preferably 50 wt% or less.
【0040】 [0040]
真空蒸着法で形成する場合は、正孔輸送材料を真空容器内に設置されたルツボに入れ、真空容器内を適当な真空ポンプで10 −4 Pa程度にまで排気した後、ルツボを加熱して、正孔輸送材料を蒸発させ、ルツボと向き合って置かれた、陽極が形成された基板上に正孔輸送層4を形成させる。 When forming a vacuum deposition method, it puts a hole-transporting material to the installation crucible in a vacuum vessel, after evacuating to about 10 -4 Pa vacuum vessel with an appropriate vacuum pump, heating the crucible to evaporate the hole transporting material, it is placed opposite the crucible to form a hole transport layer 4 on the substrate with the anode formed. 正孔輸送層4の膜厚は、通常、5〜300nm、好ましくは 10〜100nmである。 The thickness of the hole transport layer 4 is usually, 5 to 300 nm, preferably from 10 to 100 nm. この様に薄い膜を一様に形成するためには、一般に真空蒸着法がよく用いられる。 To uniformly form such a thin film, vacuum deposition process is generally used for.
【0041】 [0041]
正孔輸送層4の上には発光層5が設けられる。 Emitting layer 5 is provided on the hole transport layer 4. 発光層5は、前記一般式(I)で表される化合物と、前述した周期律表7ないし11族から選ばれる金属を含む有機金属錯体を含有し、電界を与えられた電極間において、陽極から注入されて正孔輸送層を移動する正孔と、陰極から注入されて電子輸送層6を移動する電子との再結合により励起されて、強い発光を示す。 Emitting layer 5, the compound represented by the general formula (I), containing an organic metal complex containing a metal selected from the periodic table 7 to Group 11 described above, in an electrical field between the electrodes, an anode and holes are injected to move the hole transport layer from being injected from the cathode are excited by recombination of electrons traveling through the electron transport layer 6, showing a strong emission. なお発光層5は、本発明の性能を損わない範囲で、他のホスト材料(一般式(I)と同様の働きを行う)や蛍光色素など、他成分を含んでいてもよい。 Note emitting layer 5 is a performance not deteriorated the scope of the present invention, (performs the same function as the general formula (I)) other host materials and fluorescent dyes, may contain other ingredients.
【0042】 [0042]
前記有機金属錯体が発光層中に含有される量は、0.1〜30重量%の範囲にあることが好ましい。 The amount of the organometallic complex is contained in the light-emitting layer is preferably in the range of 0.1 to 30 wt%. 0.1重量%以下では素子の発光効率向上に寄与できず、30重量%を越えると有機金属錯体同士が2量体を形成する等の濃度消光が起き、発光効率の低下に至る。 Is 0.1 wt% or less can not contribute to light emission efficiency of the device, it occurs concentration quenching of such organometallic complexes each other exceeds 30% by weight to form a dimer, leading to reduction of luminous efficiency. 従来の蛍光(1重項)を用いた素子において、発光層に含有される蛍光性色素(ドーパント)の量より、若干多い方が好ましい傾向がある。 In devices using a conventional fluorescence (singlet), than the amount of fluorescent dye contained in the light-emitting layer (dopant) somewhat larger there is a preferred tendency. 有機金属錯体が発光層中に膜厚方向に対して部分的に含まれたり、不均一に分布してもよい。 The organic metal complex or partially included in direction of the film thickness in the light emitting layer may be non-uniformly distributed.
発光層5の膜厚は、通常10〜200nm、好ましくは20〜100nmである。 The thickness of the light-emitting layer 5 is usually 10 to 200 nm, preferably 20 to 100 nm. 正孔輸送層4と同様の方法にて薄膜形成される。 It is a thin film formed in the same manner as the hole transport layer 4.
【0043】 [0043]
素子の発光効率を更に向上させることを目的として、発光層5と陰極7の間に電子輸送層6が設けられる。 For the purpose of further improving the luminous efficiency of the device, the electron-transporting layer 6 is provided between the light-emitting layer 5 and the cathode 7. 電子輸送層6は、電界を与えられた電極間において陰極から注入された電子を効率よく発光層5の方向に輸送することができる化合物より形成される。 Electron transport layer 6 is formed of a compound capable of transporting electrons injected from the cathode efficiently in the direction of the light-emitting layer 5 between the energized electrodes. 電子輸送層6に用いられる電子輸送性化合物としては、陰極7からの電子注入効率が高く、かつ、高い電子移動度を有し注入された電子を効率よく輸送することができる化合物であることが必要である。 The electron-transporting compounds for the electron-transporting layer 6, high electron injection efficiency from the cathode 7, and to be a compound capable of efficiently transporting the injected electrons have a high electron mobility is necessary.
【0044】 [0044]
このような条件を満たす電子輸送材料としては、Alq3などの金属錯体(特開昭59−194393号公報)、10−ヒドロキシベンゾ[h]キノリンの金属錯体、オキサジアゾール誘導体、ジスチリルビフェニル誘導体、シロール誘導体、3−又は5−ヒドロキシフラボン金属錯体、ベンズオキサゾール金属錯体、ベンゾチアゾール金属錯体、トリスベンズイミダゾリルベンゼン(米国特許第 5,645,948号)、キノキサリン化合物(特開平6−207169号公報)、フェナントロリン誘導体(特開平5−331459号公報)、2−t−ブチル−9,10−N,N'−ジシアノアントラキノンジイミン、n型水素化非晶質炭化シリコン、n型硫化亜鉛、n型セレン化亜鉛などが挙げられる。 Such satisfy electron transporting material, a metal complex such as Alq3 (JP 59-194393 JP), 10-hydroxy-benzo [h] quinoline metal complexes, oxadiazole derivatives, distyrylbiphenyl derivatives, silole derivatives, 3- or 5-hydroxyflavone metal complexes, benzoxazole metal complexes, benzothiazole metal complex, tris benzimidazolyl benzene (U.S. Pat. No. 5,645,948), quinoxaline compounds (JP-a-6-207169) , phenanthroline derivatives (JP-A-5-331459), 2-t- butyl--9,10-n, N'-dicyanoanthraquinonediimine, n-type hydrogenated amorphous silicon carbide, n-type zinc sulfide, n-type such as zinc selenide, and the like. 電子輸送層6の膜厚は、通常、5〜200nm、好ましくは10〜100 nmである。 The thickness of the electron transport layer 6 is usually, 5 to 200 nm, preferably from 10 to 100 nm.
電子輸送層6は、正孔輸送層4と同様にして塗布法あるいは真空蒸着法により発光層5上に積層することにより形成される。 Electron transport layer 6 is formed by laminating on the light-emitting layer 5 by in the same manner as the hole transport layer 4 coating method or vacuum deposition method. 通常は、真空蒸着法が用いられる。 Typically, a vacuum deposition method is used.
【0045】 [0045]
正孔注入の効率を更に向上させ、かつ、有機層全体の陽極への付着力を改善させる目的で、正孔輸送層4と陽極2との間に正孔注入層3を挿入することも行われている。 Hole injection further improve the efficiency of, and, for the purpose of improving the adhesion to the whole organic layer anode, also the row to insert a hole injection layer 3 between the hole transport layer 4 and the anode 2 are we. 正孔注入層3を挿入することで、初期の素子の駆動電圧が下がると同時に、素子を定電流で連続駆動した時の電圧上昇も抑制される効果がある。 By inserting the hole injection layer 3, and at the same time the initial driving voltage of the device decreases, the effect of the voltage rise when the continuously driven element at a constant current is suppressed. 正孔注入層に用いられる材料に要求される条件としては、陽極とのコンタクトがよく均一な薄膜が形成でき、熱的に安定、すなわち、融点及びガラス転移温度が高く、融点としては 300℃以上、ガラス転移温度としては 100℃以上が要求される。 The conditions required for the material used for the hole injection layer, the anode and the contact can be well uniform thin film is formed, thermally stable, i.e., melting point and glass transition temperature is high, 300 ° C. or higher as the melting point , as the glass transition temperature is required more than 100 ° C.. 更に、イオン化ポテンシャルが低く陽極からの正孔注入が容易なこと、正孔移動度が大きいことが挙げられる。 Further, ionization potential is easy injection of holes from the anode low, and high hole mobility.
【0046】 [0046]
この目的のために、これまでに銅フタロシアニン等のタロシアニン化合物(特開昭63−295695号公報)、ポリアニリン(Appl. Phys. Lett., 64巻、1245頁,1994年)、ポリチオフェン(Optical Materials, 9巻、125頁、1998年)等の有機化合物や、スパッタ・カーボン膜(Synth. Met., 91巻、73頁、1997年)や、バナジウム酸化物、ルテニウム酸化物、モリブデン酸化物等の金属酸化物(J.Phys. D, 29巻、2750頁、1996年)が報告されている。 For this purpose, this Taroshianin compounds of copper phthalocyanine before (JP 63-295695 JP), polyaniline (Appl. Phys. Lett., 64, pp. 1245, 1994), polythiophene (Optical Materials, Volume 9, page 125, and an organic compound of 1998), etc., sputtered carbon film (Synth. Met., 91, pp. 73 pp., 1997) or, vanadium oxide, ruthenium oxide, a metal such as molybdenum oxide oxide (J.Phys. D, 29, pp. 2750, 1996) have been reported. 正孔注入層の場合も、正孔輸送層と同様にして薄膜形成可能であるが、無機物の場合には、更に、スパッタ法や電子ビーム蒸着法、プラズマCVD法が用いられる。 In the case of the hole injection layer is susceptible thin film formation in the same manner as the hole transport layer, the case of inorganic materials, sputtering or electron beam evaporation, plasma CVD method is used. 以上の様にして形成される陽極バッファ層3の膜厚は、通常、3〜100nm、好ましくは 5〜50nmである。 The thickness of the anode buffer layer 3 formed in the manner described above, usually, 3 to 100 nm, preferably from 5 to 50 nm.
【0047】 [0047]
電子輸送層6は、発光層5の上に積層されるが、この間には正孔阻止層は存在させない。 Electron transport layer 6 is laminated on the luminescent layer 5, no hole blocking layer is present during this time. 電子輸送層6は電界を与えられた電極間において陰極から注入された電子を効率よく発光層の方向に輸送することができる化合物より形成される。 Electron transport layer 6 is formed from a compound which is capable of transporting electrons injected from the cathode in an electrical field between the electrodes efficiently in the direction of the light-emitting layer. 電子輸送層に用いられる電子輸送性化合物としては、陰極7からの電子注入効率が高く、かつ、高い電子移動度を有し注入された電子を効率よく輸送することができる化合物であることが必要である。 Electrons as the electron transporting compound used in the transport layer, high electron injection efficiency from the cathode 7, and it is necessary and high electron mobility compound capable of efficiently transporting the injected electrons have it is.
【0048】 [0048]
このような条件を満たす材料としては、Alq3などの金属錯体(特開昭59−194393号公報)、10−ヒドロキシベンゾ[h]キノリンの金属錯体、オキサジアゾール誘導体、ジスチリルビフェニル誘導体、シロール誘導体、3−又は5−ヒドロキシフラボン金属錯体、ベンズオキサゾール金属錯体、ベンゾチアゾール金属錯体、トリスベンズイミダゾリルベンゼン、キノキサリン化合物、フェナントロリン誘導体、2−t−ブチル−9,10−N,N'−ジシアノアントラキノンジイミン、n型水素化非晶質炭化シリコン、n型硫化亜鉛、n型セレン化亜鉛などが挙げられる。 As the materials satisfying these requirements include metal complexes such as Alq3 (JP 59-194393 JP), 10-hydroxy-benzo [h] quinoline metal complexes, oxadiazole derivatives, distyrylbiphenyl derivatives, silole derivatives , 3- or 5-hydroxyflavone metal complexes, benzoxazole metal complexes, benzothiazole metal complex, tris benzimidazolyl benzene, quinoxaline compounds, phenanthroline derivatives, 2-t-butyl--9,10-N, N'-dicyano-anthraquinone diisopropyl Min, n-type hydrogenated amorphous silicon carbide, n-type zinc sulfide, etc. n-type zinc selenide. 電子輸送層6の膜厚は、通常、5〜200nm、好ましくは10〜100nmである。 The thickness of the electron transport layer 6 is usually, 5 to 200 nm, preferably from 10 to 100 nm.
電子輸送層7は、正孔輸送層4と同様にして塗布法あるいは真空蒸着法により正孔阻止層6上に積層することにより形成される。 The electron transport layer 7 is formed by laminating on the hole blocking layer 6 by in the same manner as the hole transport layer 4 coating method or vacuum deposition method. 通常は、真空蒸着法が用いられる。 Typically, a vacuum deposition method is used.
【0049】 [0049]
陰極7は、発光層5に電子を注入する役割を果たす。 Cathode 7 plays a role of injecting electrons into the light emitting layer 5. 陰極として用いられる材料は、前記陽極2に使用される材料を用いることが可能であるが、効率よく電子注入を行なうには、仕事関数の低い金属が好ましく、スズ、マグネシウム、インジウム、カルシウム、アルミニウム、銀等の適当な金属又はそれらの合金が用いられる。 Material used as a cathode, the it is possible to use a material used for the anode 2, efficiently perform the electron injection, the low metals are preferred work function, tin, magnesium, indium, calcium, aluminum , suitable metals or alloys thereof such as silver, are used. 具体例としては、マグネシウム−銀合金、マグネシウム−インジウム合金、アルミニウム−リチウム合金等の低仕事関数合金電極が挙げられる。 Specific examples include magnesium - silver alloy, a magnesium - indium alloy, aluminum - include low work function alloy electrodes such as lithium alloy.
陰極7の膜厚は通常、陽極2と同様である。 The thickness of the cathode 7 is usually the same as that anode 2. 低仕事関数金属からなる陰極を保護する目的で、この上に更に、仕事関数が高く大気に対して安定な金属層を積層することは素子の安定性を増す。 The purpose of protecting the cathode made of a low work function metal, further thereon, laminating the metal layer stable against high atmospheric work function increases the stability of the device. この目的のために、アルミニウム、銀、銅、ニッケル、クロム、金、白金等の金属が使われる。 For this purpose, aluminum, silver, copper, nickel, chromium, gold, metals such as platinum are used.
更に、陰極と電子輸送層の間にLiF 、MgF 、Li O等の極薄絶縁膜(0.1〜5nm)を、電子注入層として挿入することも素子の効率を向上させる有効な方法である。 Further, LiF between the cathode and the electron transport layer, MgF 2, Li 2 ultrathin insulating film O or the like (0.1 to 5 nm), an effective method is also to improve the efficiency of the device can be inserted as an electron injection layer it is.
【0050】 [0050]
なお、図1とは逆の構造、すなわち、基板1上に陰極7、電子輸送層6、発光層5、正孔輸送層4、陽極2の順に積層することも可能であり、既述したように少なくとも一方が透明性の高い2枚の基板の間に本発明の有機EL素子を設けることも可能である。 Incidentally, the reverse of the structure to the FIG. 1, i.e., the cathode 7 on the substrate 1, an electron transport layer 6, the light emitting layer 5, a hole transport layer 4, it is also possible to laminate in the order of the anode 2, as already described it is also possible to provide at least one of the organic EL device of the present invention during the high two substrates transparent to. この場合も、必要により層を追加したり、省略したりすることが可能である。 Again, adding layers as needed, it is possible or omitted.
【0051】 [0051]
本発明は、有機EL素子が、単一の素子、アレイ状に配置された構造からなる素子、陽極と陰極がX−Yマトリックス状に配置された構造のいずれにおいても適用することができる。 The present invention relates to an organic EL element is a single element, it can also be applied in any device consisting of its structure arranged in array, an anode and a cathode of the deployed structure onto the X-Y matrix. 本発明の有機EL素子によれば、発光層に特定の骨格を有する化合物と、燐光性の金属錯体を含有させることにより、従来の一重項状態からの発光を用いた素子よりも発光効率が高くかつ駆動安定性においても大きく改善された素子が得られ、フルカラーあるいはマルチカラーのパネルへの応用において優れた性能を発揮できる。 According to the organic EL device of the present invention, a compound having a specific skeleton to the light emitting layer, by incorporating a phosphorescent metal complex, high luminous efficiency than devices using light emission from conventional singlet state and driving stability greatly improved element can be obtained even in, it can exhibit excellent performance in applications to full-color or multicolor panels.
【0052】 [0052]
【実施例】 【Example】
次に、本発明を、合成例及び実施例によって更に詳しく説明するが、本発明はその要旨を超えない限り、以下の実施例の記載に限定されるものではない。 Next, the present invention, Synthesis Examples and Examples will be described in more detail, the present invention unless departing from the gist of the present invention is not limited to the following examples.
【0053】 [0053]
合成例1 Synthesis Example 1
酢酸亜鉛二水和物3.0gをメタノール100mlに溶解させた。 The zinc acetate dihydrate 3.0g was dissolved in methanol 100 ml. これを、2−(2‐ヒドロキシフェニル)ベンゾオキサゾール5.8gの溶けたメタノール溶液600mlにゆっくり滴下し、50℃にて3時間撹拌した。 This was slowly added dropwise to a methanol solution 600ml of dissolved 2- (2-hydroxyphenyl) benzoxazole 5.8 g, was stirred for 3 hours at 50 ° C.. 生じた沈殿物を濾取し、50℃温水、NaHCO3飽和水、メタノール、ヘキサンの順で洗浄を行った。 The precipitates were collected by filtration was, 50 ° C. Hot water, NaHCO? Saturated water, methanol, washed successively with hexane was performed. これを、減圧乾燥して淡黄色粉末5.8gを得た。 This gave a pale yellow powder 5.8g and dried under reduced pressure. この化合物は一般式(I)において、R 〜R の全てがHである2−(2−ヒドロキシフェニル)ベンゾオキサゾール亜鉛錯体(以下、Zn(BOX)2という)であり、この一部を昇華精製し、素子作成に用いた。 In this compound the general formula (I), all R 1 to R 8 is a H 2-(2-hydroxyphenyl) benzoxazole zinc complex (hereinafter, Zn (BOX) of 2), and the part sublimation purification was used in the element created.
【0054】 [0054]
参考例1 Reference Example 1
ガラス基板上に真空蒸着法にて、真空度4.0×10 −4 Paで蒸着を行い、Zn(BOX)2、TAZ、ビス(8−ヒドロキシキノリラート)亜鉛(以下、Znq2という)又はAlq3を蒸着速度1.0Å/sにて1000Åの厚さに形成した。 By vacuum deposition on a glass substrate, subjected to degree of vacuum of 4.0 × 10 -4 Pa, Zn ( BOX) 2, TAZ, bis (8-hydroxyquinolinate acrylate) zinc (hereinafter, referred to Znq2) or the Alq3 at a deposition rate of 1.0 Å / s to a thickness of 1000 Å. これを大気中、室温で放置し、結晶化する時間を測定することにより、薄膜安定性に関する検討を行った。 This atmosphere, left at room temperature, by measuring the time for crystallization, were examined about the film stability. 結果を表1に示す。 The results are shown in Table 1.
【0055】 [0055]
【表1】 [Table 1]
【0056】 [0056]
参考例2 Reference Example 2
ガラス基板上に発光層のみを蒸着し、Ir(ppy)3のHost材料として適応できるかの検討を行った。 Depositing only luminescent layer on a glass substrate, was one of the study can be adapted as a Host material Ir (ppy) 3.
ガラス基板上に真空蒸着法にて、真空度4.0×10 −4 Pa の条件にてZn(BOX)2とIr(ppy)3とを異なる蒸着源から蒸着し、Ir(ppy)3の濃度が7.0 %であるような薄膜を500Åの厚さで形成した。 On a glass substrate by vacuum deposition at a vacuum degree of 4.0 × 10 -4 Pa conditions deposited from Zn (BOX) 2 and Ir (ppy) 3 and different deposition source, Ir (ppy) 3 of the concentration to form a thin film such as a 7.0% to a thickness of 500 Å. また、同様にして、薄膜主成分をTAZ、Znq2及びAlq3に変えて薄膜を作成した。 In the same manner, it was a thin film by changing the film main component TAZ, Znq2 and Alq3.
作成した薄膜を、蛍光測定装置にて評価した。 A thin film that was created, was evaluated by fluorescence measurement device. 励起波長はZn(BOX)2、TAZ、Znq2又はAlq3の極大吸収波長であり、そのときに出てくる光を観察した。 Excitation wavelength Zn (BOX) 2, TAZ, a maximum absorption wavelength of Znq2 or Alq3, was observed light emerging at that time. 結果を表2に示す。 The results are shown in Table 2.
【0057】 [0057]
【表2】 [Table 2]
発光層の主たる材料にTAZやZn(BOX)2を用いた場合、Ir(ppy)3にエネルギーが遷移し、燐光が発生するが、Znq2やAlq3を用いた場合は、Ir(ppy)3にエネルギーが遷移せず、Znq2やAlq3自身が蛍光を発することがうかがえる。 When using TAZ and Zn (BOX) 2 to a main material of the light-emitting layer, energy is shifted to the Ir (ppy) 3, although phosphorescence occurs, the case of using the Znq2 and Alq3, the Ir (ppy) 3 energy does not transition, Znq2 and Alq3 itself suggests that fluoresce.
【0058】 [0058]
実施例1 Example 1
図1において、正孔注入層を省略し、電子注入層を追加した構成の有機EL素子を作成した。 In Figure 1, omitting the hole injection layer, thereby constructing an organic EL device of the added forming the electron injection layer. 膜厚150 nmのITOからなる陽極が形成されたガラス基板上に、各薄膜を真空蒸着法にて、真空度4.0×10 −4 Paで積層させた。 The thickness 0.99 nm on a glass substrate with the anode formed consisting of ITO, and the respective thin films by vacuum vapor deposition, are stacked in a vacuum of 4.0 × 10 -4 Pa. まず、ITO上に正孔輸送層としてNPBを蒸着速度1.0Å/sにて600Åの厚さに形成した。 First, NPB was deposited as a hole transport layer on ITO at a deposition rate of 1.0 Å / s to a thickness of 600 Å.
次に、正孔輸送層上に、発光層としてZn(BOX) とIr(ppy) とを異なる蒸着源から、共に蒸着速度1.0Å/sにて共蒸着し、250Åの厚さに形成した。 Next, on the hole transport layer, a Zn (BOX) 2 and Ir (ppy) 3 and different deposition sources as the light emitting layer, both were co-evaporated at a deposition rate of 1.0 Å / s, to a thickness of 250Å the formed. この時、Ir(ppy) の濃度は7.0 %であった。 At this time, the concentration of Ir (ppy) 3 was 7.0%. 次に、電子輸送層としてAlq3を蒸着速度1.0Å/sにて500Åの厚さに形成した。 It was then formed to a thickness of 500Å to Alq3 as an electron transport layer at a deposition rate of 1.0 Å / s. 更に、電子輸送層上に、電子注入層としてフッ化リチウム(LiF)を蒸着速度0.5Å/sにて5Åの厚さに形成した。 Further, the electron transport layer was formed to a thickness of 5Å in lithium fluoride (LiF) the deposition rate 0.5 Å / s as the electron injection layer. 最後に、電子注入層上に、電極としてアルミニウム(Al)を蒸着速度15Å/sにて1700Åの厚さに形成し、有機EL素子を作成した。 Finally, on the electron injection layer, aluminum (Al) was formed to a thickness of 1700Å at a deposition rate of 15 Å / s as an electrode, thereby constructing an organic EL device.
【0059】 [0059]
得られた有機EL素子に外部電源を接続し直流電圧を印加したところ、表3のような発光特性を有することが確認された。 When the obtained organic EL device was connected to an outside power source, it was confirmed that the light emission characteristics shown in Table 3. 表3において、輝度、電圧及び発光効率は、10mA/cm での値を示す。 In Table 3, the luminance, voltage, and luminous efficiency were measured at 10 mA / cm 2. なお、素子発光スペクトルの極大波長は517 nmであり、Ir(ppy) からの発光が得られていることがわかった。 Incidentally, maximum wavelength of the element emission spectrum was 517 nm, it was found that light emission from Ir (ppy) 3 is obtained.
【0060】 [0060]
比較例1 Comparative Example 1
正孔輸送層としてHMTPDを、発光層の主成分としてTAZを用いた以外は実施例1と同様にして有機EL素子を作成した。 The HMTPD as a hole transport layer, thereby constructing an organic EL device except for using the TAZ as the main component of the light-emitting layer in the same manner as in Example 1.
【0061】 [0061]
比較例2 Comparative Example 2
発光層の主成分として、TAZを用いた以外は実施例1と同様にして有機EL素子を作成した。 As a main component of the light-emitting layer An organic EL device was fabricated except using TAZ in the same manner as in Example 1.
【0062】 [0062]
実施例2 Example 2
発光層の副成分としてbtp Ir(acac)を用いた以外は実施例1と同様にして有機EL素子を作成した。 Except for using btp 2 Ir (acac) as a sub-component of the light-emitting layer An organic EL device was fabricated in the same manner as in Example 1. 得られた有機EL素子の特性をまとめて表3に示す。 Collectively characteristics of the obtained organic EL device shown in Table 3.
【0063】 [0063]
【表3】 [Table 3]
【0064】 [0064]
実施例1は、高効率、低電圧を達成している。 Example 1, high efficiency, and achieve a low voltage. 実施例2は、赤色発光にも適用可能である。 Example 2 is also applicable to red emission.
【0065】 [0065]
【発明の効果】 【Effect of the invention】
本発明の有機電界発光素子は、低電圧において高輝度・高効率で発光させることが可能となり、更には高温保存時の劣化の少ない素子を得ることができる。 The organic electroluminescent device of the present invention, it is possible to emit light at low voltage with high brightness, high efficiency, and further can be obtained with less elements of deterioration during high temperature storage. 従って、本発明による有機電界発光素子はフラットパネル・ディスプレイ(例えばOAコンピュータ用や壁掛けテレビ)、車載表示素子、携帯電話表示や面発光体としての特徴を生かした光源(例えば、複写機の光源、液晶ディスプレイや計器類のバックライト光源)、表示板、標識灯への応用が考えられ、その技術的価値は大きいものである。 Accordingly, the organic electroluminescent device according to the present invention is a flat panel display (e.g. OA computers use or wall-mounted television), vehicle display devices, light sources utilizing the characteristics as a mobile phone display or a surface light emitter (e.g., a copying machine the light source, backlight sources of liquid crystal displays and instruments), display board, and a beacon light is considered, its technical value is larger.
【図面の簡単な説明】 BRIEF DESCRIPTION OF THE DRAWINGS
【図1】有機電界発光素子の一例を示した模式断面図。 Figure 1 is a schematic sectional view showing an example of an organic electroluminescent device.
【符号の説明】 DESCRIPTION OF SYMBOLS
1 基板、2 陽極、3 正孔注入層、4 正孔輸送層、5 発光層、6 電子輸送層、7 陰極 1 substrate, 2 anode, 3 hole-injecting layer, 4 hole-transporting layer, 5 light-emitting layer, 6 electron-transporting layer, 7 cathode

Claims (3)

  1. 基板上に、陽極、正孔輸送層、発光層及び電子輸送層を含む有機層並びに陰極が積層されてなり、発光層と陽極の間に正孔輸送層を有し、発光層と陰極の間に電子輸送層を有し、電子輸送層と発光層の間には正孔阻止層を有しない有機電界発光素子であって、発光層が、ホスト材料として下記一般式(I)で表わされる化合物を、ゲスト材料としてルテニウム、ロジウム、パラジウム、銀、レニウム、オスミウム、イリジウム、白金及び金から選ばれる少なくとも一つの金属を含む有機金属錯体を含有し、正孔輸送層が、少なくとも2個の縮合環アリール基を有するトリアリールアミンダイマーを含有することを特徴とする有機電界発光素子。 On a substrate, an anode, a hole transport layer, an organic layer and a cathode comprises a light-emitting layer and an electron transporting layer stacked, has a hole transport layer between the light-emitting layer and the anode, between the light-emitting layer and the cathode in an electron transport layer, an organic electroluminescence device having no hole blocking layer between the electron transport layer and the light-emitting layer, the light emitting layer is a compound represented by the following general formula as a host material (I) the ruthenium as a guest material, containing rhodium, palladium, silver, rhenium, osmium, iridium, an organometallic complex containing at least one metal selected from platinum and gold, a hole transport layer, at least two fused rings the organic electroluminescent device characterized by containing a triarylamine dimer having an aryl group.
    (式中、R 〜R は各々独立に、水素原子、アルキル基、アラルキル基、アルケニル基、シアノ基、アミノ基、アミド基、アルコキシカルボニル基、カルボキシル基、アルコキシ基、置換基を有していてもよい芳香族炭化水素基又は置換基を有していてもよい芳香族複素環基を示す) (Wherein, R 1 to R 8 each independently have a hydrogen atom, an alkyl group, an aralkyl group, an alkenyl group, a cyano group, an amino group, an amido group, an alkoxycarbonyl group, a carboxyl group, an alkoxy group, a substituent even though it represents an aromatic hydrocarbon group or an optionally substituted aromatic heterocyclic group)
  2. トリアリールアミンダイマーが、下記一般式(II)で表わされる化合物である請求項1記載の有機電界発光素子。 Triarylamine dimer, organic electroluminescent device of claim 1, wherein a compound represented by the following general formula (II).
    (式中、Ar 及びAr は炭素数6〜14の1価の芳香族基であるが、少なくとも一方は炭素数10〜14の縮合環構造を有する芳香族基であり、Ar は炭素数6〜14の2価の芳香族基である) (Wherein, although Ar 1 and Ar 2 is a monovalent aromatic group having 6 to 14 carbon atoms, at least one is an aromatic group having a condensed ring structure 10 to 14 carbon atoms, Ar 3 carbon the number 6 to 14 of the divalent aromatic group)
  3. ゲスト材料が、緑色燐光発光性のトリス(2−フェニルピリジン)イリジウム錯体又は赤色発光性のビス(2−(2'−ベンゾ[4,5−α]チエニル)ピリジナト−N,C3')イリジウム(アセチルアセトナト)錯体である請求項1又は2記載の有機電界発光素子。 Guest material, a green phosphorescent tris (2-phenylpyridine) iridium complex or red luminescent bis (2- (2'-benzo [4,5-α] thienyl) pyridinato -N, C3 ') iridium ( acetylacetonato) the organic electroluminescent device according to claim 1 or 2, wherein a complex.
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WO2007078184A1 (en) * 2006-01-06 2007-07-12 Industry-University Cooperation Foundation, Hanyang University Metallic compound and organic electroluminescence device comprising the same
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