JP2003201472A5 - - Google Patents
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- JP2003201472A5 JP2003201472A5 JP2002305258A JP2002305258A JP2003201472A5 JP 2003201472 A5 JP2003201472 A5 JP 2003201472A5 JP 2002305258 A JP2002305258 A JP 2002305258A JP 2002305258 A JP2002305258 A JP 2002305258A JP 2003201472 A5 JP2003201472 A5 JP 2003201472A5
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【0116】
実施例8〜34および比較例3〜6
洗浄したITO電極付きガラス板上に、4,4’−ビス[N−(1−ナフチル)−N−フェニルアミノ]ビフェニル(α−NPD)を真空蒸着して膜厚30nmの正孔注入層を形成した。次いで、表1の化合物を真空蒸着し、膜厚30nmの発光層を得た。さらに、ビス(2−メチル−8−ヒドロキシキノリナート)(フェノラート)ガリウム錯体を真空蒸着して膜厚30nmの電子注入層を作成し、その上に、マグネシウムと銀を10:1(重量比)で混合した合金で膜厚100nmの電極を形成して有機EL素子を得た。各層は10-6Torrの真空中で、基板温度室温の条件下で蒸着した。この素子の発光特性を表2に示す。本実施例の有機EL素子は全て、最大発光輝度35000(cd/m2)以上の高い輝度特性を示した。同様に比較例として、前記比較化合物A〜Dを成膜して用いる以外は、実施例8と同様の方法で有機EL素子を作製した。この素子の発光特性を表2に併せて示す。いずれの場合も、最大発光輝度、最大発光効率共に、本実施例で作成した素子よりも劣っていることは明らかである。[0116]
Examples 8 to 3 4 and Comparative Examples 3 to 6
4,4'-Bis [N- (1-naphthyl) -N-phenylamino] biphenyl (α-NPD) is vacuum-deposited on a cleaned glass plate with an ITO electrode to form a hole injection layer with a thickness of 30 nm. Formed. Next, the compounds shown in Table 1 were vacuum-deposited to obtain a light emitting layer having a film thickness of 30 nm. Further, a bis (2-methyl-8-hydroxyquinolinate) (phenolat) gallium complex is vacuum-deposited to form an electron-injected layer having a film thickness of 30 nm, and magnesium and silver are placed on the electron-injected layer in a 10: 1 (weight ratio). ) Was used to form an electrode having a film thickness of 100 nm to obtain an organic EL element. Each layer was deposited in a vacuum of 10-6 Torr under the conditions of substrate temperature room temperature. Table 2 shows the light emission characteristics of this device. All of the organic EL elements of this embodiment showed high brightness characteristics of a maximum emission brightness of 35,000 (cd / m 2 ) or more. Similarly, as a comparative example, an organic EL device was produced by the same method as in Example 8 except that the comparative compounds A to D were formed into a film and used. The emission characteristics of this device are also shown in Table 2. In either case, it is clear that both the maximum emission brightness and the maximum emission efficiency are inferior to the elements produced in this embodiment.
【0117】
【表2】
[0117]
[Table 2]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002305258A JP3797310B2 (en) | 2001-10-26 | 2002-10-21 | Material for organic electroluminescence device and organic electroluminescence device using the same |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001328710 | 2001-10-26 | ||
JP2001-328710 | 2001-10-26 | ||
JP2002305258A JP3797310B2 (en) | 2001-10-26 | 2002-10-21 | Material for organic electroluminescence device and organic electroluminescence device using the same |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004003764A Division JP3855999B2 (en) | 2001-10-26 | 2004-01-09 | Material for organic electroluminescence device and organic electroluminescence device using the same |
Publications (3)
Publication Number | Publication Date |
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JP2003201472A JP2003201472A (en) | 2003-07-18 |
JP2003201472A5 true JP2003201472A5 (en) | 2004-12-16 |
JP3797310B2 JP3797310B2 (en) | 2006-07-19 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2002305258A Expired - Fee Related JP3797310B2 (en) | 2001-10-26 | 2002-10-21 | Material for organic electroluminescence device and organic electroluminescence device using the same |
Country Status (1)
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JP (1) | JP3797310B2 (en) |
Families Citing this family (30)
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JP4795268B2 (en) * | 2006-04-20 | 2011-10-19 | キヤノン株式会社 | Organic light emitting device |
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US8829783B2 (en) | 2007-06-18 | 2014-09-09 | Idemitsu Kosan Co., Ltd. | Trinaphthyl monoamine or derivative thereof, organic electroluminescent device using the same, and organic electroluminescent material-containing solution |
KR20100038193A (en) * | 2007-08-06 | 2010-04-13 | 이데미쓰 고산 가부시키가이샤 | Aromatic amine derivative and organic electroluminescent device using the same |
US8367222B2 (en) * | 2009-02-27 | 2013-02-05 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent device |
JP6005925B2 (en) | 2011-11-18 | 2016-10-12 | ユー・ディー・シー アイルランド リミテッド | ORGANIC ELECTROLUMINESCENT ELEMENT, COMPOUND USED FOR THE ELEMENT, LIGHT EMITTING DEVICE, DISPLAY DEVICE AND LIGHTING DEVICE USING THE ELEMENT |
KR101921896B1 (en) * | 2011-12-12 | 2018-11-26 | 메르크 파텐트 게엠베하 | Compounds for electronic devices |
JP6307686B2 (en) * | 2012-12-05 | 2018-04-11 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | AMINE DERIVATIVE, ORGANIC LIGHT EMITTING MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME |
WO2016006629A1 (en) * | 2014-07-09 | 2016-01-14 | 保土谷化学工業株式会社 | Organic electroluminescent element |
EP3244462B1 (en) * | 2015-01-06 | 2020-11-11 | Hodogaya Chemical Co., Ltd. | Organic electroluminescent element |
US10566540B2 (en) * | 2015-02-03 | 2020-02-18 | Hodogaya Chemical Co., Ltd. | Organic electroluminescent device |
WO2016175211A1 (en) * | 2015-04-27 | 2016-11-03 | 保土谷化学工業株式会社 | Organic electroluminescent element |
KR20190052505A (en) * | 2017-11-08 | 2019-05-16 | 에스에프씨 주식회사 | Naphthalene derivatives having substituted amine groups and organic light-emitting diode including the same |
KR20190091409A (en) * | 2018-01-26 | 2019-08-06 | 삼성디스플레이 주식회사 | Organic electroluminescence device and monoamine compound for organic electroluminescence device |
JP7465062B2 (en) | 2018-01-26 | 2024-04-10 | 三星ディスプレイ株式會社 | Organic electroluminescent device and monoamine compound for organic electroluminescent device |
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2002
- 2002-10-21 JP JP2002305258A patent/JP3797310B2/en not_active Expired - Fee Related
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