JP2003036975A - Organic electric field light-emitting element - Google Patents

Organic electric field light-emitting element

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Publication number
JP2003036975A
JP2003036975A JP2001224085A JP2001224085A JP2003036975A JP 2003036975 A JP2003036975 A JP 2003036975A JP 2001224085 A JP2001224085 A JP 2001224085A JP 2001224085 A JP2001224085 A JP 2001224085A JP 2003036975 A JP2003036975 A JP 2003036975A
Authority
JP
Japan
Prior art keywords
layer
organic
emission
color adjusting
light
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2001224085A
Other languages
Japanese (ja)
Inventor
Mutsumi Suzuki
睦美 鈴木
Masao Fukuyama
正雄 福山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP2001224085A priority Critical patent/JP2003036975A/en
Publication of JP2003036975A publication Critical patent/JP2003036975A/en
Withdrawn legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide an organic electric field light-emitting element in which color purity is improved by improving element constitution of the organic electric field light-emitting element. SOLUTION: The organic electric field light-emitting element has a pair of electrodes and a layer composed of an organic substance of at least one layer or more sandwiched between them, and a light-emitting color adjusting layer is inserted between the organic layer and the electrode. By this, to improve the color purity becomes possible. Further, it is also enabled that the light- emitting color adjusting layer is made to have an absorbance in wavelength regions in addition to the desired emitting wavelength region, and by this, suppression of deteriorating the color purity becomes possible by absorbing unnecessary light emissions.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、各種の表示装置と
して広範囲に利用される発光素子であって、色純度に優
れた有機電界発光素子に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an organic electroluminescent element which is widely used as various display devices and has excellent color purity.

【0002】[0002]

【従来の技術】電界発光素子は、自己発光のために液晶
素子にくらべて明るく、鮮明な表示が可能であるため、
古くから多くの研究者によって研究されてきた。現在実
用レベルに達した電界発光素子としては、無機材料のZ
nSを用いた素子がある。しかし、この様な無機の電界
発光素子は、発光のための駆動電圧として50V以上が
必要であるため、広く使用されるには至っていない。
2. Description of the Related Art An electroluminescent device is brighter and clearer than a liquid crystal device due to self-luminous display.
It has been studied by many researchers since ancient times. As an electroluminescent device that has reached a practical level, Z, which is an inorganic material, is currently used.
There is an element using nS. However, such an inorganic electroluminescent device requires a driving voltage of 50 V or higher for light emission, and thus has not been widely used.

【0003】これに対して有機材料を用いた電界発光素
子である有機電界発光素子は、従来実用的なレベルから
はほど遠いものであったが、1987年にイーストマン
・コダック社のシー・ダブリュ・タン(C.W.Tan
g)らによって開発された積層構造素子によりその特性
が飛躍的に進歩した。彼らは蒸着膜の構造が安定で電子
を輸送することのできる蛍光体からなる層(電子輸送性
発光層)と、正孔を輸送することのできる有機物からな
る層(正孔輸送層)とを積層し、正孔と電子を蛍光体中
に注入して発光させることに成功した。これによって有
機電界発光素子の発光効率が向上し、10V以下の電圧
で1000cd/m2以上の発光が得られる様になっ
た。その後、電子輸送性発光層を発光層と電子輸送層に
分けるなど、素子を構成する層の機能分離が進められた
結果、現在では10000cd/m 2以上の発光特性が
得られている。
On the other hand, an electroluminescent element using an organic material
The organic electroluminescent device, which is a child
It was far from, but in 1987 Eastman
・ CW Tan of Kodak Company
g) The characteristics of the laminated structure element developed by
Has made great strides. They have a stable vapor-deposited film structure
Layer consisting of a phosphor that can transport
Light emitting layer) and an organic substance capable of transporting holes.
Layer (hole-transporting layer) to stack holes and electrons in the phosphor.
It was succeeded in injecting into and making it emit light. By this
The luminous efficiency of the electroluminescent device is improved and the voltage is 10 V or less.
1000 cd / m2The above light emission can be obtained
It was After that, the electron-transporting light-emitting layer was formed into a light-emitting layer and an electron-transporting layer.
The functional separation of the layers that make up the device was promoted.
As a result, at present 10,000 cd / m 2The above emission characteristics
Has been obtained.

【0004】このような有機電界発光素子は、発光層の
材料を変えることにより、赤・青・緑の発光色を揃える
ことができることから、フルカラーディスプレイへの応
用が検討されている。
Since such an organic electroluminescent device can make the emission colors of red, blue and green uniform by changing the material of the light emitting layer, its application to a full color display is under study.

【0005】[0005]

【発明が解決しようとする課題】電子機器などに使用す
るために、より表示品位の高いフルカラーディスプレイ
を実現するためには、それぞれの発光色の色純度を高く
しなくてはならないが、従来の有機電界発光素子には半
値幅の広い蛍光スペクトルを有する発光材料を用いるこ
とが多いため、得られる素子も色純度の低いものが多か
った。
In order to realize a full-color display having a higher display quality for use in electronic devices and the like, it is necessary to increase the color purity of each luminescent color. Since an organic electroluminescent element often uses a light emitting material having a fluorescence spectrum with a wide half-value width, many of the obtained elements have low color purity.

【0006】本発明は、かかる従来の問題点に鑑みてな
されたもので、その目的は、有機電界発光素子の素子構
成を改良することによって、色純度の改善された有機電
界発光素子を実現することにある。
The present invention has been made in view of such conventional problems, and an object thereof is to realize an organic electroluminescent device having improved color purity by improving the device structure of the organic electroluminescent device. Especially.

【0007】[0007]

【課題を解決するための手段】本発明の有機電界発光素
子は、一対の電極とその間に挟まれた少なくとも一層以
上の有機物からなる層を有しており、有機層と電極の間
に発光色調整層を挿入したことを特徴とするものであ
る。
The organic electroluminescence device of the present invention has a pair of electrodes and at least one layer made of an organic material sandwiched between the electrodes, and the luminescent color is provided between the organic layer and the electrodes. It is characterized in that an adjustment layer is inserted.

【0008】請求項1に記載の発明は、一対の電極と、
その間に挟まれた少なくとも一層以上の有機物からなる
層を有し、有機層と電極の間に発光色調整層を挿入した
ことを特徴とする有機電界発光素子であり、色純度を向
上するという作用を有する。
The invention according to claim 1 includes a pair of electrodes,
An organic electroluminescent device characterized by having at least one layer made of an organic substance sandwiched between them, and having an emission color adjusting layer inserted between the organic layer and an electrode, which has an effect of improving color purity. Have.

【0009】請求項2に記載の発明は、上記発光色調整
層が、所望する発光波長域以外の波長域に吸光度を有す
ることを特徴とするものであり、不要な発光を吸収する
ことによりいろ純度の低下を抑制するという作用を有す
る。
The invention according to claim 2 is characterized in that the emission color adjusting layer has an absorbance in a wavelength range other than a desired emission wavelength range, and it absorbs unnecessary emission. It has an effect of suppressing a decrease in purity.

【0010】請求項3に記載の発明は、上記発光色調整
層が、所望する発光波長域が強められるような膜厚に調
整されていることを特徴とするものであり、このことに
より所望の波長域に発光ピークをもつ有機電界発光素子
が実現できるという作用を有する。
The invention according to claim 3 is characterized in that the emission color adjusting layer is adjusted to have a film thickness capable of strengthening a desired emission wavelength region, and thereby the desired emission color adjusting layer is obtained. It has an effect of realizing an organic electroluminescence device having an emission peak in the wavelength range.

【0011】請求項4に記載の発明は、上記発光色調整
層が、電荷輸送材料と金属の混合層からなることを特徴
とするものであり、このことにより発光色調整層の電荷
輸送性が向上し、効率が高く、色純度の良い素子が実現
できるという作用を有する。
The invention according to claim 4 is characterized in that the emission color adjusting layer comprises a mixed layer of a charge transport material and a metal, whereby the charge transporting property of the emission color adjusting layer is improved. It has an effect that an element having improved and high efficiency and good color purity can be realized.

【0012】[0012]

【発明の実施の形態】以下、本発明の実施の形態につい
て、図面を用いて説明する。図1は本発明の一実施の形
態による有機電界発光素子の概略構成を示す断面図であ
る。この有機電界発光素子は、ベースとなるガラス基板
1上に電極である陽極2を形成し、この陽極2の上に、
上記ガラス基板1および陽極2の側から正孔輸送層3、
発光層4、電子輸送層5、発光色調整層6、陰極7を形
成して成るものである。そして、この実施の形態に係る
有機電界発光素子は、電子輸送層5と陰極7との間の場
所に本発明による発光色調整層6が形成されている点が
特徴である。
BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described below with reference to the drawings. FIG. 1 is a sectional view showing a schematic configuration of an organic electroluminescence device according to an embodiment of the present invention. In this organic electroluminescence device, an anode 2 which is an electrode is formed on a glass substrate 1 which is a base, and on the anode 2,
From the side of the glass substrate 1 and the anode 2, the hole transport layer 3,
The light emitting layer 4, the electron transport layer 5, the emission color adjusting layer 6, and the cathode 7 are formed. The organic electroluminescent element according to this embodiment is characterized in that the emission color adjusting layer 6 according to the present invention is formed between the electron transport layer 5 and the cathode 7.

【0013】陽極2には透明電極としてインジウム錫酸
化物(ITO)や半透明電極としての金薄膜を用いるこ
とができる。
For the anode 2, indium tin oxide (ITO) as a transparent electrode or a gold thin film as a semitransparent electrode can be used.

【0014】電荷輸送層は、正孔輸送層3と電子輸送層
5とに大別される。それぞれ、電極からの電荷の注入を
容易にし、注入された電荷を発光領域まで輸送するとい
う働きをする。電荷輸送層と電極の間に電荷注入層を設
ける場合もある。正孔注入層のための材料としては、陽
極2からの正孔の注入を容易にするため、HOMOレベ
ルの小さい材料が使用される。具体的には、銅フタロシ
アニン(CuPc)やトリス{4−[(3-メチルフェニ
ル)フェニルアミノ]フェニル}アミン(m−MTDA
TA)などがあげられる。また正孔輸送層3としては、
正孔輸送性の強い材料が使用され、具体的には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(TPD)
などのトリフェニルアミン誘導体などを用いることがで
きる。
The charge transport layer is roughly classified into a hole transport layer 3 and an electron transport layer 5. Each of them has a function of facilitating the injection of charges from the electrodes and transporting the injected charges to the light emitting region. A charge injection layer may be provided between the charge transport layer and the electrode. As a material for the hole injection layer, a material having a low HOMO level is used in order to facilitate injection of holes from the anode 2. Specifically, copper phthalocyanine (CuPc) and tris {4-[(3-methylphenyl) phenylamino] phenyl} amine (m-MTDA
TA) and the like. Further, as the hole transport layer 3,
A material having a strong hole transporting property is used. Specifically, N, N
'-Diphenyl-N, N'-bis (3-methylphenyl)
1,1'-biphenyl-4,4'-diamine (TPD)
A triphenylamine derivative or the like can be used.

【0015】一方、電子輸送層5としては電子輸送性の
強い材料が用いることができ、具体的にはフェナントロ
リン誘導体,オキサジアゾール誘導体やトリス(8−ヒ
ドロキシキノリノール)アルミニウム(Alq)などに
代表されるキノリノール金属錯体などの使用が検討され
ている。さらに電子注入層としてはポルフィリン誘導体
や上記電子輸送材料と金属との混合膜を用いることが検
討されている。
On the other hand, a material having a strong electron-transporting property can be used for the electron-transporting layer 5, and specific examples thereof include a phenanthroline derivative, an oxadiazole derivative and tris (8-hydroxyquinolinol) aluminum (Alq). The use of quinolinol metal complexes and the like is being investigated. Furthermore, it has been studied to use a porphyrin derivative or a mixed film of the above-mentioned electron transport material and a metal as the electron injection layer.

【0016】発光層4としては数多くの化合物群が検討
されているが、基本的には電子・正孔の注入が可能でか
つ蛍光・りん光を有する物質であれば使用できる。ま
た、成膜性に優れた材料の中に色素を少量分散させた膜
を発光層4として用いることにより、有機電界発光素子
の高効率化、長寿命化および発光色の調整をすることも
検討されている。この手法は、単独では結晶化しやす
い、あるいは濃度消光を起こしやすい蛍光色素、りん光
色素に対して非常に有効である。
A large number of compounds have been studied as the light emitting layer 4, but basically any substance capable of injecting electrons / holes and having fluorescence / phosphorescence can be used. Further, by using a film in which a small amount of a dye is dispersed in a material having excellent film-forming property as the light emitting layer 4, it is considered to improve the efficiency and the life of the organic electroluminescent device and adjust the emission color. Has been done. This method is very effective for fluorescent dyes and phosphorescent dyes that are easily crystallized or cause concentration quenching by themselves.

【0017】陰極7は有機膜に電子が注入できることが
必要であり、アルカリ金属またはアルカリ土類金属また
はその化合物を構成材料の一つとして用いることが多
い。具体的にはリチウム、マグネシウムやカルシウム、
あるいはこれらの金属や化合物を他の金属と組み合わせ
て用いることができる。
The cathode 7 needs to be capable of injecting electrons into the organic film, and an alkali metal, an alkaline earth metal or a compound thereof is often used as one of the constituent materials. Specifically, lithium, magnesium and calcium,
Alternatively, these metals and compounds can be used in combination with other metals.

【0018】本発明によれば、上記電子輸送層5と陰極
7との間に発光色調整層6を設けることにより、所望す
る発光領域の光のみを素子の外部に取り出すことが可能
となり、有機電界発光素子の色純度を向上させることが
できる。この発光色調整層6には所望する発光波長領域
以外に吸光度を有する材料を使用する。適当な発光材料
と発光色調整層6とを組み合わせることにより、発光層
4からの光の一部を吸収し、色純度を上げることが可能
となる。例えば、青色の発光材料を用いる場合、発光色
調整層6に500nmより長波長の領域に吸収を有する有機
材料を用いることによって、500nm以上の光が吸収さ
れ、緑色の発光成分がカットされることにより色純度が
向上する。また、発光領域と電極間の膜厚を変化させる
と干渉効果によりスペクトルが変化するため、発光色調
整層6を適当な膜厚にすることにより、発光色を変化さ
せることができる。
According to the present invention, by providing the luminescent color adjusting layer 6 between the electron transport layer 5 and the cathode 7, it becomes possible to extract only the light in the desired luminescent area to the outside of the device. The color purity of the electroluminescent element can be improved. For the emission color adjusting layer 6, a material having an absorbance outside the desired emission wavelength range is used. By combining an appropriate luminescent material and the luminescent color adjusting layer 6, part of the light from the luminescent layer 4 can be absorbed and the color purity can be increased. For example, when a blue light emitting material is used, by using an organic material having absorption in a wavelength region longer than 500 nm for the emission color adjusting layer 6, light of 500 nm or more is absorbed and a green light emitting component is cut off. This improves the color purity. Further, when the film thickness between the light emitting region and the electrode is changed, the spectrum changes due to the interference effect. Therefore, the emission color can be changed by setting the light emission color adjusting layer 6 to an appropriate film thickness.

【0019】また、この発光色調整層6は電荷輸送性を
兼ね備えていることが重要である。そのためには、電荷
輸送材料と金属の混合層を発光色調整層6として用いる
ことが有効である。
It is important that the luminescent color adjusting layer 6 also has a charge transporting property. For that purpose, it is effective to use a mixed layer of a charge transport material and a metal as the emission color adjusting layer 6.

【0020】なお、以上の説明では陰極7と有機層であ
る電子輸送層5との間に発光色調整層6を設けた場合に
ついて説明をしたが、陽極2と有機層である正孔輸送層
3との間に発光色調整層6を設けた場合についても同様
な考え方で実施することができる。
In the above description, the case where the emission color adjusting layer 6 is provided between the cathode 7 and the electron transporting layer 5 which is an organic layer has been described, but the anode 2 and the hole transporting layer which is an organic layer. The same idea can be applied to the case where the emission color adjusting layer 6 is provided between the light emitting element 3 and the light emitting element 3.

【0021】[0021]

【実施例】次に、本発明の具体例を説明する。EXAMPLES Next, specific examples of the present invention will be described.

【0022】(実施例1)基板にはガラス上に透明な陽
極としてインジウム錫酸化膜(ITO)をあらかじめ形
成し、電極の形にパターニングしたもの用いた。このガ
ラス基板1を充分に洗浄した後、蒸着する材料と一緒に
真空装置内にセットし、10-4Paまで真空排気した。
その後、正孔輸送層3としてN,N'-ビス[4'-(N,N-ジフェ
ニルアミノ)-4-ビフェニリル]-N,N'-ジフェニルベンジ
ジン(TPT)を50nm製膜した。その後、発光層4
兼電子輸送層5としてAlqを50nm製膜した。その
後、発光色調整層6として銅フタロシアニン(CuP
c)とリチウム金属の共蒸着膜を140nm製膜した。
CuPcとリチウム金属の混合比はモル比で1:1とし
た。その後、陰極7としてAl/Li混合膜を150n
mの厚さで製膜し、有機電界発光素子を作成した。Cu
Pc/Li混合膜およびAl/Li混合膜は2種類の材料
をそれぞれ独立な蒸着元から蒸発させる共蒸着法によっ
て作製した。これらの製膜は一度も真空を破ることな
く、連続して行った。なお、膜厚は水晶振動子によって
モニターした。有機電界発光素子作製後、直ちに乾燥窒
素中で電極の取り出しを行い、引き続き特性測定を行っ
た。得られた有機電界発光素子に電圧を印加したとこ
ろ、均一な緑色の発光が得られた。発光スペクトルは5
20nmにピークがあり、スペクトル半値幅は81n
m、XYZ表色系における色度座標はx=0.27y=
0.58であった。
(Example 1) As a substrate, an indium tin oxide film (ITO) was previously formed on a glass as a transparent anode and patterned into an electrode shape. After thoroughly cleaning the glass substrate 1, the glass substrate 1 was set in a vacuum apparatus together with the material to be vapor-deposited, and vacuum exhausted to 10 −4 Pa.
After that, as the hole transport layer 3, N, N′-bis [4 ′-(N, N-diphenylamino) -4-biphenylyl] -N, N′-diphenylbenzidine (TPT) was deposited to a thickness of 50 nm. Then, the light emitting layer 4
Alq was formed into a film of 50 nm as the electron-transporting layer 5. Then, copper phthalocyanine (CuP) is used as the emission color adjusting layer 6.
A co-deposited film of c) and lithium metal was formed to a thickness of 140 nm.
The mixing ratio of CuPc and lithium metal was 1: 1 in terms of molar ratio. After that, an Al / Li mixed film as a cathode 7 is formed to a thickness of 150 n.
A film having a thickness of m was formed to prepare an organic electroluminescence device. Cu
The Pc / Li mixed film and the Al / Li mixed film were produced by a co-evaporation method in which two kinds of materials are evaporated from independent evaporation sources. These film formations were continuously performed without breaking the vacuum even once. The film thickness was monitored by a crystal oscillator. Immediately after manufacturing the organic electroluminescent device, the electrode was taken out in dry nitrogen, and the characteristics were measured. When a voltage was applied to the obtained organic electroluminescence device, uniform green light emission was obtained. Emission spectrum is 5
There is a peak at 20 nm, and the spectral half width is 81 n.
m, chromaticity coordinates in the XYZ color system are x = 0.27y =
It was 0.58.

【0023】(実施例2)基板にはガラス上に透明な陽
極としてインジウム錫酸化膜(ITO)をあらかじめ形
成し、電極の形にパターニングしたもの用いた。このガ
ラス基板1を充分に洗浄した後、蒸着する材料と一緒に
真空装置内にセットし、10-4Paまで真空排気した。
その後、正孔輸送層3としてTPTを50nm製膜し
た。その後、発光層4として化1に示す化合物(1)を
25nm、電子輸送層5としてAlqを25nm製膜し
た。
Example 2 As a substrate, an indium tin oxide film (ITO) was previously formed as a transparent anode on glass and patterned into an electrode shape. After thoroughly cleaning the glass substrate 1, the glass substrate 1 was set in a vacuum apparatus together with the material to be vapor-deposited, and vacuum exhausted to 10 −4 Pa.
After that, TPT having a thickness of 50 nm was formed as the hole transport layer 3. Then, 25 nm of the compound (1) shown in Chemical formula 1 was formed as the light emitting layer 4, and 25 nm of Alq was formed as the electron transporting layer 5.

【化1】 ・・・・(化1)[Chemical 1] ... (Chemical formula 1)

【0024】その後、発光色調整層6としてキナクリド
ン(Qd)とリチウム金属の共蒸着膜を125nm製膜
した。Qd中のリチウム金属の含有量はモル比で1:1と
した。その後、陰極7としてAl/Li混合膜を150
nmの厚さで製膜し、有機電界発光素子を作製した。Q
d/Li混合膜およびAl/Li混合膜は2種類の材料を
それぞれ独立な蒸着元から蒸発させる共蒸着法によって
作製した。これらの製膜は一度も真空を破ることなく、
連続して行った。なお、膜厚は水晶振動子によってモニ
ターした。有機電界発光素子作製後、直ちに乾燥窒素中
で電極の取り出しを行い、引き続き特性測定を行った。
得られた有機電界発光素子子に電圧を印加したところ、
均一な緑色の発光が得られた。発光スペクトルは470
nmにピークがあり、スペクトル半値幅は69nm、X
YZ表色系における色度座標はx=0.15y=0.1
6であった。
After that, a co-evaporated film of quinacridone (Qd) and lithium metal was formed to a thickness of 125 nm as the emission color adjusting layer 6. The content of lithium metal in Qd was 1: 1 in molar ratio. After that, an Al / Li mixed film is formed as the cathode 7 by 150
A film having a thickness of nm was formed to produce an organic electroluminescence device. Q
The d / Li mixed film and the Al / Li mixed film were produced by a co-evaporation method in which two kinds of materials are evaporated from independent evaporation sources. These film formations never break the vacuum,
It went continuously. The film thickness was monitored by a crystal oscillator. Immediately after manufacturing the organic electroluminescent device, the electrode was taken out in dry nitrogen, and the characteristics were measured.
When a voltage was applied to the obtained organic electroluminescent element,
A uniform green emission was obtained. The emission spectrum is 470
There is a peak at nm, the spectral half width is 69 nm, X
The chromaticity coordinate in the YZ color system is x = 0.15y = 0.1
It was 6.

【0025】(比較例1)比較例1として、発光色調整
層6を設けず、発光層4兼電子輸送層5であるAlq上
に直接陰極7のAl/Li混合層を積層したこと以外は
実施例1と同様に有機電界発光素子を作製した。この有
機電界発光素子に電圧を印加したところ、均一な黄緑色
の発光が得られた。発光スペクトルは526nmにピー
クがあり、スペクトル半値幅は100nm、XYZ表色
系における色度座標はx=0.32y=0.56であっ
た。
(Comparative Example 1) As Comparative Example 1, except that the emission color adjusting layer 6 is not provided and the Al / Li mixed layer of the cathode 7 is directly laminated on Alq which is the light emitting layer 4 and the electron transport layer 5. An organic electroluminescence device was produced in the same manner as in Example 1. When a voltage was applied to this organic electroluminescent device, uniform yellow-green light emission was obtained. The emission spectrum had a peak at 526 nm, the spectrum half width was 100 nm, and the chromaticity coordinate in the XYZ color system was x = 0.32y = 0.56.

【0026】(比較例2)比較例2として、発光色調整
層6を設けず、電子輸送層5であるAlq上に直接陰極
7のAl/Li混合層を積層したこと以外は実施例2と
同様に有機電界発光素子を作製した。この有機電界発光
素子に電圧を印加したところ、均一な黄緑色の発光が得
られた。発光スペクトルは477nmにピークがあり、
スペクトル半値幅は75nm、XYZ表色系における色
度座標はx=0.15y=0.20であった。
Comparative Example 2 As Comparative Example 2, the same as Example 2 except that the emission color adjusting layer 6 was not provided and the Al / Li mixed layer of the cathode 7 was directly laminated on the electron transport layer 5 of Alq. Similarly, an organic electroluminescent device was produced. When a voltage was applied to this organic electroluminescent device, uniform yellow-green light emission was obtained. The emission spectrum has a peak at 477 nm,
The spectrum half width was 75 nm, and the chromaticity coordinate in the XYZ color system was x = 0.15y = 0.20.

【0027】実施例1、2および比較例1、2に示した
結果より、本実施例で得られた有機電界発光素子は発光
スペクトルの半値幅が狭くなっており、色純度が向上し
ていることが明らかとなった。
From the results shown in Examples 1 and 2 and Comparative Examples 1 and 2, the organic electroluminescent elements obtained in this Example have a narrow half-width of emission spectrum and improved color purity. It became clear.

【0028】[0028]

【発明の効果】以上のように本発明によれば、一対の電
極と、その間に挟まれた少なくとも一層以上の有機物か
らなる層を有し、有機層と電極の間に発光色調整層を挿
入したため、色純度を向上させることが可能になるとい
う効果が得られる。
As described above, according to the present invention, a pair of electrodes and at least one layer made of an organic material sandwiched between the electrodes are provided, and an emission color adjusting layer is inserted between the organic layer and the electrodes. Therefore, the effect that the color purity can be improved can be obtained.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明における電界発光素子の構成の断面図FIG. 1 is a cross-sectional view of a structure of an electroluminescent device according to the present invention.

【符号の説明】[Explanation of symbols]

1 ガラス基板 2 陽極 3 正孔輸送層 4 発光層 5 電子輸送層 6 発光色調整層 7 陰極 1 glass substrate 2 anode 3 Hole transport layer 4 Light emitting layer 5 Electron transport layer 6 Emission color adjustment layer 7 cathode

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 一対の電極と、その間に挟まれた少なく
とも一層以上の有機物からなる層を有する有機電界発光
素子において、有機層と電極の間に発光色調整層を挿入
したことを特徴とする有機電界発光素子。
1. An organic electroluminescence device having a pair of electrodes and at least one layer made of an organic material sandwiched between the electrodes, wherein an emission color adjusting layer is inserted between the organic layer and the electrodes. Organic electroluminescent device.
【請求項2】 上記発光色調整層が、所望する発光波長
域以外の波長域に吸光度を有することを特徴とする、請
求項1に記載の有機電界発光素子。
2. The organic electroluminescent element according to claim 1, wherein the emission color adjusting layer has an absorbance in a wavelength range other than a desired emission wavelength range.
【請求項3】 上記発光色調整層が、所望する発光波長
域が強められるような膜厚に調整されていることを特徴
とする請求項1または2に記載の有機電界発光素子。
3. The organic electroluminescent element according to claim 1, wherein the emission color adjusting layer is adjusted to have a film thickness that enhances a desired emission wavelength range.
【請求項4】 上記発光色調整層が、電荷輸送材料と金
属の混合層からなることを特徴とする請求項1または2
に記載の有機電界発光素子。
4. The emission color adjusting layer comprises a mixed layer of a charge transport material and a metal.
The organic electroluminescent element as described in 1.
JP2001224085A 2001-07-25 2001-07-25 Organic electric field light-emitting element Withdrawn JP2003036975A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001224085A JP2003036975A (en) 2001-07-25 2001-07-25 Organic electric field light-emitting element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001224085A JP2003036975A (en) 2001-07-25 2001-07-25 Organic electric field light-emitting element

Publications (1)

Publication Number Publication Date
JP2003036975A true JP2003036975A (en) 2003-02-07

Family

ID=19057313

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001224085A Withdrawn JP2003036975A (en) 2001-07-25 2001-07-25 Organic electric field light-emitting element

Country Status (1)

Country Link
JP (1) JP2003036975A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005129289A (en) * 2003-10-22 2005-05-19 Hitachi Displays Ltd Organic el display device
JP2005353316A (en) * 2004-06-08 2005-12-22 Seiko Epson Corp Organic el device, manufacturing method of organic el device, and electronic apparatus
WO2006061954A1 (en) * 2004-12-08 2006-06-15 Fuji Electric Holdings Co., Ltd. Organic el element
JP2013033728A (en) * 2011-07-01 2013-02-14 Semiconductor Energy Lab Co Ltd Light-emitting device, electronic appliance, and illumination device
JP2013175485A (en) * 2013-06-11 2013-09-05 Rohm Co Ltd Organic el element

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005129289A (en) * 2003-10-22 2005-05-19 Hitachi Displays Ltd Organic el display device
JP2005353316A (en) * 2004-06-08 2005-12-22 Seiko Epson Corp Organic el device, manufacturing method of organic el device, and electronic apparatus
WO2006061954A1 (en) * 2004-12-08 2006-06-15 Fuji Electric Holdings Co., Ltd. Organic el element
GB2436226A (en) * 2004-12-08 2007-09-19 Fuji Electric Holdings Co Organic EL element
JP2013033728A (en) * 2011-07-01 2013-02-14 Semiconductor Energy Lab Co Ltd Light-emitting device, electronic appliance, and illumination device
JP2013175485A (en) * 2013-06-11 2013-09-05 Rohm Co Ltd Organic el element

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