JP2005044790A - Organic electroluminescent element, illuminator, and display device - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an organic electroluminescent element, an illuminator and a display device with restrained light emitting voltage, operating in low power consumption. <P>SOLUTION: The organic electroluminescent element having at least a light emitting layer containing a phosphorescent compound between an anode and a cathode is characterized by having an adjacent layer disposed between the light emitting layer and the cathode and adjacent to the light emitting layer, and including a compound represented by a general formula (1) in the adjacent layer. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an organic electroluminescence element, a lighting device, and a display device.

  Conventionally, there is an electroluminescence display (ELD) as a light-emitting electronic display device. Examples of constituent elements of ELD include inorganic electroluminescent elements and organic electroluminescent elements (hereinafter also referred to as organic EL elements). Inorganic electroluminescent elements have been used as planar light sources, but an alternating high voltage is required to drive the light emitting elements.

  On the other hand, an organic electroluminescence device has a structure in which a light emitting layer containing a compound that emits light is sandwiched between a cathode and an anode, and excitons (excitons) by injecting electrons and holes into the light emitting layer and recombining them. Is a device that emits light using the emission of light (fluorescence / phosphorescence) when this exciton is deactivated, and can emit light at a voltage of several volts to several tens of volts. Since it is a mold, it has a wide viewing angle, has high visibility, and is a thin-film complete solid-state device, and therefore has attracted attention from the viewpoints of space saving, portability, and the like.

  For the development of organic EL elements for practical use in the future, organic EL elements that emit light efficiently and with high brightness with lower power consumption are desired. For example, stilbene derivatives, distyrylarylene derivatives, or tris A technique for doping a styrylarylene derivative with a small amount of a phosphor to improve emission luminance and extend the lifetime of the device (see, for example, Patent Document 1), and using 8-hydroxyquinoline aluminum complex as a host compound, An organic light emitting layer having an organic light emitting layer doped with a small amount of a phosphor (see, for example, Patent Document 2), further comprising an 8-hydroxyquinoline aluminum complex as a host compound and doped with a quinacridone dye. There is a report on an element having the above (for example, see Patent Document 3).

  In the technique disclosed in the above document, when the emission from the excited singlet is used, the generation ratio of the singlet exciton and the triplet exciton is 1: 3, so the generation probability of the luminescent excited species is 25%. Since the light extraction efficiency is about 20%, the limit of the external extraction quantum efficiency (ηext) is set to 5%.

  However, since the University of Princeton reported on organic EL devices using phosphorescence emission from excited triplets (see, for example, Non-Patent Document 1), research on materials that exhibit phosphorescence at room temperature (for example, Non-Patent Documents). 2) is becoming active.

  When excited triplets are used, the upper limit of internal quantum efficiency is 100%, so in principle the luminous efficiency is four times that of excited singlets, and the performance is almost the same as that of cold cathode tubes. It can be applied to and is attracting attention.

  The 10th International Workshop on Inorganic and Organic Electroluminescence (EL'00, Hamamatsu) reports several reports on phosphorescent compounds. For example, Ikai et al. Uses a hole-transporting compound as a host of a phosphorescent compound. In addition, M.M. E. Thompson et al. Use various electron transport materials doped with a novel iridium complex as a host of a phosphorescent compound. Furthermore, Tsutsui et al. Have obtained high emission luminance by introducing a hole blocking layer (exciton blocking layer). Other examples of using a 5-coordinated aluminum complex as the hole blocking layer (see, for example, Patent Documents 4 and 5) and Ikai et al. Use a fluorine-substituted compound as the hole blocking layer (exciton blocking layer). Thus, highly efficient light emission is achieved (see, for example, Non-Patent Document 3).

However, since all of the conventional organic EL elements have a high emission voltage, there is a problem of high power consumption and high cost.
Japanese Patent No. 3093796 Japanese Unexamined Patent Publication No. 63-264692 JP-A-3-255190 JP 2001-284056 A Japanese Patent Laid-Open No. 2002-8860 M.M. A. Baldo et al. , Nature, 395, 151-154 (1998) M.M. A. Baldo et al. , Nature, 403, 17, 750-753 (2000) Appl. Phys. Lett. 79, 156 pages (2001)

  This invention is made | formed in view of the subject which concerns, and the objective of this invention is suppressing the light emission voltage and providing the organic electroluminescent element, illuminating device, and display apparatus which operate | move with low power consumption.

  The above object of the present invention has been achieved by the following configurations 1 to 9.

(Claim 1)
In an organic electroluminescence device having at least a light emitting layer containing a phosphorescent compound between an anode and a cathode,
Between the light emitting layer and the cathode and having an adjacent layer adjacent to the light emitting layer;
An organic electroluminescence device comprising a compound represented by the following general formula (1) in the adjacent layer.

(In the formula, L ₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Q ₁ is necessary for bonding to a nitrogen atom to form an aromatic heterocycle. Represents an atomic group, R ₁ represents a hydrogen atom or a substituent, and n1 represents an integer of 2 or more, a plurality of Q ₁ may be the same or different, and a plurality of R ₁ are the same or different; And at least one of the plurality of R ₁ represents a fluorine atom or a substituent containing a fluorine atom.)
(Claim 2)
The organic electroluminescent device according to claim 1, wherein the compound represented by the general formula (1) is a compound represented by the following general formula (1-1).

(In the formula, L ₁₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Y _{1 to} Y ₄ each independently represent a nitrogen atom or C—R ₁₁ (R ₁₁ represents a hydrogen atom or a substituent, and n11 represents an integer greater than or equal to 2. At least one of Y ₁ to Y ₄ is a C— group in which R ₁₁ is a fluorine atom or a substituent containing a fluorine atom. R _11. )
(Claim 3)
In an organic electroluminescence device having at least a light emitting layer containing a phosphorescent compound between an anode and a cathode,
Between the light emitting layer and the cathode, and having an adjacent layer adjacent to the light emitting layer;
An organic electroluminescence device comprising a compound represented by the following general formula (2) in the adjacent layer.

(In the formula, L ₂ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Q ₂ is necessary for bonding to a carbon atom to form an aromatic heterocycle. Represents an atomic group, R ₂ represents a hydrogen atom or a substituent, and n2 represents an integer of 2 or more, a plurality of Q ₂ may be the same or different, and a plurality of R ₂ are the same or different. And at least one of the plurality of R ₂ represents a fluorine atom or a substituent containing a fluorine atom.)
(Claim 4)
The organic electroluminescent device according to claim 1, wherein the compound represented by the general formula (2) is a compound represented by the following general formula (2-1).

(In the formula, L ₂₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Y _{5 to} Y ₇ each independently represents a nitrogen atom or C—R ₂₁ (R ₂₁ Represents a hydrogen atom or a substituent, R ₂₂ represents a hydrogen atom or a substituent, and n21 represents an integer of 2 or more, and at least one of Y ₅ to Y ₇ represents that R ₂₁ is a fluorine atom or a fluorine atom. C—R ₂₁ which is a substituent containing an atom, or R ₂₂ is a substituent containing a fluorine atom.)
(Claim 5)
The organic electroluminescence element according to any one of claims 1 to 4, wherein the light emission is blue.

(Claim 6)
The organic electroluminescence element according to claim 1, wherein the light emission is white.

(Claim 7)
A display device comprising the organic electroluminescence element according to claim 1.

(Claim 8)
An illuminating device comprising the organic electroluminescent element according to claim 1.

(Claim 9)
A display device comprising the illumination device according to claim 8 and a liquid crystal element as a display unit.

  According to the present invention, an organic electroluminescence element, an illumination device, and a display device that can operate with low power consumption while suppressing light emission voltage can be provided.

  In the organic electroluminescence element of the present invention (hereinafter also referred to as an organic EL element), the structure defined in any one of claims 1 to 6 suppresses the light emission voltage and operates with low power consumption. It turns out that an element can be provided. Moreover, the illuminating device and display apparatus which comprise the said organic EL element were able to be provided.

  Hereinafter, details of each component according to the present invention will be sequentially described.

  As a result of intensive studies, the present inventors, in an organic electroluminescent device having at least a light emitting layer containing a phosphorescent compound between the anode and the cathode, exist between the light emitting layer and the cathode and are adjacent to the light emitting layer. It is possible to obtain an organic EL element that suppresses the light emission voltage and operates with low power consumption by containing the adjacent layer that contains the compound represented by the general formula (1). I found it.

  That is, the layer containing the compound represented by the general formula (1) can be a layer having a low LUMO and a very high effect of blocking holes, and in particular, this layer is a cathode. It has been found that an organic EL element with a reduced emission voltage compared to the prior art can be obtained by providing as an adjacent layer adjacent to a light emitting layer containing a phosphorescent compound on the side.

  Further, as a result of intensive studies, the present inventors have found that an organic electroluminescence device having at least a light-emitting layer containing a phosphorescent compound between the anode and the cathode is present between the light-emitting layer and the cathode. The organic EL element which suppresses the light emission voltage and operates with low power consumption can be obtained by including the adjacent layer adjacent to the compound and containing the compound represented by the general formula (2) in the adjacent layer. I found what I could do.

  That is, the layer containing the compound represented by the general formula (2) can be a layer having a low LUMO and a very high effect of blocking holes, and this layer is particularly a cathode. It has been found that an organic EL element with a reduced emission voltage compared to the prior art can be obtained by providing as an adjacent layer adjacent to a light emitting layer containing a phosphorescent compound on the side.

In the general formula (1), L ₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Q ₁ is bonded to a nitrogen atom to form an aromatic heterocycle. Represents an atomic group necessary for the above, R ₁ represents a hydrogen atom or a substituent, and n1 represents an integer of 2 or more.

  The divalent or higher valent hydrocarbon linking group or the divalent or higher valent aromatic linking group may have a substituent.

A plurality of Q ₁ may be the same or different. A plurality of R ₁ may be the same or different, but at least one of the plurality of R ₁ represents a fluorine atom or a substituent containing a fluorine atom.

  The compound represented by the general formula (1) is preferably a compound represented by the general formula (1-1). Thereby, the light emission voltage can be suppressed and the operation can be performed with low power consumption.

In the general formula (1-1), L ₁₁ represents a divalent or higher hydrocarbon linking group or a divalent or higher aromatic linking group, and Y _{1 to} Y ₄ each independently represent a nitrogen atom, or C—R ₁₁ (R ₁₁ represents a hydrogen atom or a substituent), and n ₁₁ represents an integer of 2 or more. At least one of Y _{1 to} Y ₄ is C—R ₁₁ in which R ₁₁ is a fluorine atom or a substituent containing a fluorine atom.

  The divalent or higher valent hydrocarbon linking group or aromatic linking group may have a substituent.

In the general formula (2), L ₂ represents a divalent or higher valent hydrocarbon linking group or an aromatic linking group, and Q ₂ is necessary for bonding to a carbon atom to form an aromatic heterocycle. Represents an atomic group, R ₂ represents a hydrogen atom or a substituent, and n2 represents an integer of 2 or more. The divalent or higher valent hydrocarbon linking group or the divalent or higher valent aromatic linking group may have a substituent.

A plurality of Q ₂ may be the same or different. The plurality of R ₂ may be the same or different, but at least one of the plurality of R ₂ represents a fluorine atom or a substituent containing a fluorine atom.

  The compound represented by the general formula (2) is preferably a compound represented by the general formula (2-1). Thereby, the light emission voltage can be suppressed and the operation can be performed with low power consumption.

In the general formula (2-1), L ₂₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Y _{5 to} Y ₇ each independently represent a nitrogen atom or C -R ₂₁ (R ₂₁ represents a hydrogen atom or a substituent) represents, R ₂₂ represents a hydrogen atom or a substituent, n21 is an integer of 2 or more. At least one of Y _{5 to} Y ₇ is R ₂₁ is a fluorine atom or C—R ₂₁ which is a substituent containing a fluorine atom, or R ₂₂ is a substituent containing a fluorine atom.

  In the present invention, examples of the divalent or higher hydrocarbon linking group include a methylene linking group, an ethylene linking group, and an isopropylene linking group.

  In the present invention, examples of the divalent or higher valent aromatic linking group include a phenylene linking group and a naphthylene linking group.

  The divalent or higher valent hydrocarbon linking group or the divalent or higher valent aromatic linking group may have a substituent.

  The divalent or higher valent aromatic linking group may be formed by linking aromatic linking groups to form a divalent or higher valent linking group, and further, a hydrocarbon linking group and an aromatic linking group are linked, A divalent or higher valent linking group may be formed.

  In the present invention, the substituent includes an alkyl group (for example, methyl group, ethyl group, propyl group, isopropyl group, tert-butyl group, pentyl group, hexyl group, octyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group). Etc.), a cycloalkyl group (eg, cyclopentyl group, cyclohexyl group, etc.), an alkenyl group (eg, vinyl group, allyl group, etc.), an alkynyl group (eg, ethynyl group, propargyl group, etc.), an aryl group (eg, phenyl group) Etc.), heteroaryl group (for example, furyl group, thienyl group, pyridyl group, pyridazyl group, pyrimidyl group, pyrazyl group, triazyl group, imidazolyl group, pyrazolyl group, thiazolyl group, quinazolyl group, phthalazyl group), heterocyclic group (For example, pyrrolidyl group, imidazolidyl group, morpholyl Oxazolidyl group, etc.), alkoxyl group (eg, methoxy group, ethoxy group, propyloxy group, pentyloxy group, hexyloxy group, octyloxy group, dodecyloxy group, etc.), cycloalkoxyl group (eg, cyclopentyloxy group, cyclohexyl). Oxy group etc.), aryloxy group (eg phenoxy group, naphthyloxy group etc.), alkylthio group (eg methylthio group, ethylthio group, propylthio group, pentylthio group, hexylthio group, octylthio group, dodecylthio group etc.), cycloalkylthio Groups (eg, cyclopentylthio group, cyclohexylthio group, etc.), arylthio groups (eg, phenylthio group, naphthylthio group, etc.), alkoxycarbonyl groups (eg, methyloxycarbonyl group, ethyloxycarbonyl, etc.) Butyloxycarbonyl group, octyloxycarbonyl group, dodecyloxycarbonyl group, etc.), aryloxycarbonyl group (eg, phenyloxycarbonyl group, naphthyloxycarbonyl group, etc.), sulfamoyl group (eg, aminosulfonyl group, methylaminosulfonyl group) Dimethylaminosulfonyl group, butylaminosulfonyl group, hexylaminosulfonyl group, cyclohexylaminosulfonyl group, octylaminosulfonyl group, dodecylaminosulfonyl group, phenylaminosulfonyl group, naphthylaminosulfonyl group, 2-pyridylaminosulfonyl group), acyl Groups (for example, acetyl group, ethylcarbonyl group, propylcarbonyl group, pentylcarbonyl group, cyclohexylcarbonyl group, octylcarbonyl group, 2 -Ethylhexylcarbonyl group, dodecylcarbonyl group, phenylcarbonyl group, naphthylcarbonyl group, pyridylcarbonyl group, etc.), acyloxy group (for example, acetyloxy group, ethylcarbonyloxy group, butylcarbonyloxy group, octylcarbonyloxy group, dodecylcarbonyloxy group) Group, phenylcarbonyloxy group, etc.), amide group (for example, methylcarbonylamino group, ethylcarbonylamino group, dimethylcarbonylamino group, propylcarbonylamino group, pentylcarbonylamino group, cyclohexylcarbonylamino group, 2-ethylhexylcarbonylamino group) Octylcarbonylamino group, dodecylcarbonylamino group, phenylcarbonylamino group, naphthylcarbonylamino group, etc.), carbamoyl group (eg Aminocarbonyl group, methylaminocarbonyl group, dimethylaminocarbonyl group, propylaminocarbonyl group, pentylaminocarbonyl group, cyclohexylaminocarbonyl group, octylaminocarbonyl group, 2-ethylhexylaminocarbonyl group, dodecylaminocarbonyl group, phenylaminocarbonyl Group, naphthylaminocarbonyl group, 2-pyridylaminocarbonyl group, etc.), ureido group (for example, methylureido group, ethylureido group, pentylureido group, cyclohexylureido group, octylureido group, dodecylureido group, phenylureido group naphthylureido group) 2-pyridylaminoureido group, etc.), sulfinyl group (for example, methylsulfinyl group, ethylsulfinyl group, butylsulfinyl group, cyclohexane) Silsulfinyl group, 2-ethylhexylsulfinyl group, dodecylsulfinyl group, phenylsulfinyl group, naphthylsulfinyl group, 2-pyridylsulfinyl group, etc.), alkylsulfonyl group (for example, methylsulfonyl group, ethylsulfonyl group, butylsulfonyl group, cyclohexylsulfonyl) Group, 2-ethylhexylsulfonyl group, dodecylsulfonyl group, etc.), arylsulfonyl group (phenylsulfonyl group, naphthylsulfonyl group, 2-pyridylsulfonyl group, etc.), amino group (for example, amino group, ethylamino group, dimethylamino group, Butylamino group, cyclopentylamino group, 2-ethylhexylamino group, dodecylamino group, anilino group, naphthylamino group, 2-pyridylamino group, etc.), halogen atom (for example, fluorine atom) Chlorine atom, bromine atom, etc.), fluorinated hydrocarbon group (eg, fluoromethyl group, trifluoromethyl group, pentafluoroethyl group, pentafluorophenyl group, etc.), cyano group, nitro group, hydroxyl group, mercapto group, Examples thereof include silyl groups (for example, trimethylsilyl group, triisopropylsilyl group, triphenylsilyl group, phenyldiethylsilyl group, etc.).

  These substituents may be further substituted with the above substituents. Moreover, the substituents may form a ring.

  The substituent is preferably a halogen atom, an alkyl group, an alkoxyl group, or an aryl group.

  Specific examples of the compound according to the present invention are shown below, but the present invention is not limited thereto.

  The light emitting layer according to the present invention contains a phosphorescent compound. Thereby, high luminous efficiency can be obtained.

  The phosphorescent compound contained in the light emitting layer according to the present invention can be appropriately selected from known materials used for the light emitting layer of the organic EL device. For example, an iridium complex listed in JP-A No. 2001-247859 or a formula shown in WO 00 / 70,655, pages 16 to 18, for example, tris (2-phenylpyridine) iridium, etc. Examples of the dopant include platinum complexes such as platinum complex, osmium complex, and 2,3,7,8,12,13,17,18-octaethyl-21H, 23H-porphyrin platinum complex. By using such a phosphorescent compound as a dopant, a light-emitting organic EL device with high internal quantum efficiency can be realized.

  The phosphorescent compound used in the present invention is preferably a complex compound containing a group 8 metal in the periodic table of elements, more preferably an iridium compound, an osmium compound, or a platinum compound (platinum complex system). Compound) and rare earth complexes, and most preferred is an iridium compound.

  Specific examples of the phosphorescent compound used in the present invention are shown below, but are not limited thereto. These compounds are described, for example, in Inorg. Chem. 40, 1704-1711, and the like.

  In addition, for example, J. et al. Am. Chem. Soc. 123, 4304-4312 (2001), WO00 / 70655, WO02 / 15645, JP2001-247859, JP2001-345183, JP2002-117978, JP2002-170684, special JP 2002-203678, JP 2002-235076, JP 2002-302671, JP 2002-324679, JP 2002-332291, JP 2002-332292, JP 2002-338588, etc. The iridium complex mentioned by general formula of this, the iridium complex mentioned as a specific example, the iridium complex represented by Formula (IV) of Unexamined-Japanese-Patent No. 2002-8860, etc. are mentioned.

  The phosphorescent compound according to the present invention has a phosphorescence quantum yield in solution of 0.001 or more at 25 ° C. Preferably, it is 0.01 or more. More preferably, it is 0.1 or more.

  The phosphorescence quantum yield can be measured by the method described in Spectroscopic II, page 398 (1992 edition, Maruzen) of the 4th edition, Experimental Chemistry Course 7.

  In the present invention, a triarylamine derivative having an electron-withdrawing group is contained in an adjacent layer adjacent to the light-emitting layer that exists between the light-emitting layer containing the phosphorescent compound and the cathode. In the organic EL element, the layer corresponds to an electron transport layer or a hole blocking layer described later.

  The hole blocking layer and the electron transport layer adjacent to the light emitting layer have a function of transporting electrons and play a role of blocking holes moving from the light emitting layer from reaching the cathode. By incorporating the compound represented by the general formula (1) or the compound represented by the general formula (2) into these layers adjacent to the light emitting layer containing the photoactive compound, phosphorous can be obtained in a state where LUMO is low. It has the effect of blocking the holes moving from the light emitting layer containing the photocompound from reaching the cathode, thereby suppressing the light emission voltage and providing an organic EL device that operates with low power consumption. Can do.

  Next, the constituent layers of the organic EL device of the present invention will be described in more detail.

In this invention, although the preferable specific example of the layer structure of an organic EL element is shown below, this invention is not limited to these.
(I) Anode / light emitting layer / electron transport layer / cathode (ii) Anode / hole transport layer / light emitting layer / electron transport layer / cathode (iii) Anode / hole transport layer / light emitting layer / hole blocking layer / electron Transport layer / cathode (iv) anode / hole transport layer / light emitting layer / hole blocking layer / electron transport layer / cathode buffer layer / cathode (v) anode / anode buffer layer / hole transport layer / light emitting layer / hole Blocking layer / electron transport layer / cathode buffer layer / cathode << Anode >>
As the anode in the organic EL element, an electrode material made of a metal, an alloy, an electrically conductive compound, or a mixture thereof having a high work function (4 eV or more) is preferably used. Specific examples of such electrode materials include metals such as Au, and conductive transparent materials such as CuI, indium tin oxide (ITO), SnO ₂ and ZnO. Alternatively, an amorphous material such as IDIXO (In ₂ O ₃ —ZnO) capable of forming a transparent conductive film may be used. For the anode, a thin film may be formed by depositing these electrode materials by a method such as vapor deposition or sputtering, and a pattern having a desired shape may be formed by a photolithography method, or when the pattern accuracy is not required (100 μm or more) Degree), a pattern may be formed through a mask having a desired shape when the electrode material is deposited or sputtered. When light emission is extracted from the anode, it is desirable that the transmittance is greater than 10%, and the sheet resistance as the anode is preferably several hundred Ω / □ or less. Further, although the film thickness depends on the material, it is usually selected in the range of 10 to 1000 nm, preferably 10 to 200 nm.

"cathode"
On the other hand, as the cathode, a material having a low work function (4 eV or less) metal (referred to as an electron injecting metal), an alloy, an electrically conductive compound, and a mixture thereof as an electrode material is used. Specific examples of such electrode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al ₂ O ₃ ) Mixtures, indium, lithium / aluminum mixtures, rare earth metals and the like. Among these, a mixture of an electron injecting metal and a second metal which is a stable metal having a larger work function value than this, such as a magnesium / silver mixture, magnesium, from the viewpoint of electron injectability and durability against oxidation, etc. / Aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide (Al ₂ O ₃ ) mixtures, lithium / aluminum mixtures, aluminum and the like are preferred. The cathode can be produced by forming a thin film of these electrode materials by a method such as vapor deposition or sputtering. The sheet resistance as the cathode is preferably several hundred Ω / □ or less, and the film thickness is usually selected in the range of 10 nm to 5 μm, preferably 50 to 200 nm. In order to transmit the emitted light, if either the anode or the cathode of the organic EL element is transparent or translucent, the light emission luminance is improved, which is convenient.

  Moreover, after producing the said metal with a film thickness of 1-20 nm on a cathode, a transparent or semi-transparent cathode can be produced by producing the electroconductive transparent material quoted by description of the anode on it, By applying this, an element in which both the anode and the cathode are transmissive can be manufactured.

  Next, an injection layer, a blocking layer, an electron transport layer, and the like used as a constituent layer of the organic EL element of the present invention will be described.

<< Buffer layer >>: Anode buffer layer, cathode buffer layer An injection layer is provided as necessary, and includes a cathode buffer layer (electron injection layer) and an anode buffer layer (hole injection layer). You may exist between a positive hole transport layer and between a cathode and a light emitting layer or an electron carrying layer.

  The buffer layer is a layer provided between the electrode and the organic layer in order to lower the driving voltage and improve the light emission luminance. “The organic EL element and the forefront of its industrialization (published by NTT Corporation on November 30, 1998) 2), Chapter 2, “Electrode Materials” (pages 123 to 166) in detail, and includes an anode buffer layer and a cathode buffer layer.

  The details of the anode buffer layer (hole injection layer) are described in JP-A Nos. 9-45479, 9-260062, and 8-288069, and a specific example is represented by copper phthalocyanine. Examples thereof include a phthalocyanine buffer layer, an oxide buffer layer typified by vanadium oxide, an amorphous carbon buffer layer, and a polymer buffer layer using a conductive polymer such as polyaniline (emeraldine) or polythiophene.

  The details of the cathode buffer layer (electron injection layer) are described in JP-A-6-325871, 9-17574, 10-74586, and the like, and specifically, strontium, aluminum, and the like are representative. A metal buffer layer, an alkali metal compound buffer layer typified by lithium fluoride, an alkaline earth metal compound buffer layer typified by magnesium fluoride, and an oxide buffer layer typified by aluminum oxide. The buffer layer (injection layer) is desirably a very thin film, and although it depends on the material, the film thickness is preferably in the range of 0.1 nm to 5 μm.

<< Blocking Layer >>: Hole Blocking Layer, Electron Blocking Layer The hole blocking layer is an electron transporting layer in a broad sense, and is provided adjacent to the light emitting layer. The hole blocking layer is made of a hole blocking material that has a function of transporting electrons but has a very small ability to transport holes, and the probability of recombination of electrons and holes by blocking holes while transporting electrons. Can be improved.

  As described above, when the organic EL element has a hole blocking layer, the adjacent layer according to the present invention corresponds to the hole blocking layer. By using the compound represented by the above general formula (1) or the compound represented by the general formula (2) as the hole blocking material of the hole blocking layer, it is possible to suppress the light emission voltage and operate with low power consumption. it can.

  On the other hand, the electron blocking layer is a hole transport layer in a broad sense, made of a material that has a function of transporting holes and has a very small ability to transport electrons, and blocks electrons while transporting holes. Thus, the probability of recombination of electrons and holes can be improved.

<Light emitting layer>
The light emitting layer according to the present invention contains a phosphorescent compound, and is a layer that emits light by recombination of electrons and holes injected from the electrode or the electron transport layer and the hole transport layer. It may be in the light emitting layer or at the interface between the light emitting layer and the adjacent layer.

  By using a phosphorescent compound, an organic EL element with high emission efficiency can be obtained.

  As the phosphorescent compound, the aforementioned phosphorescent compound can be used.

  There are two types of light emission of phosphorescent compounds in principle. One is the recombination of carriers on the host compound to which carriers are transported to generate an excited state of the host compound, and this energy is phosphorescent. Energy transfer type to obtain light emission from the phosphorescent compound by transferring to the compound, the other is that the phosphorescent compound becomes a carrier trap, carrier recombination occurs on the phosphorescent compound, and from the phosphorescent compound In any case, the excited state energy of the phosphorescent compound is lower than the excited state energy of the host compound.

  In the present invention, the phosphorescent maximum wavelength of the phosphorescent compound is not particularly limited. In principle, the phosphorescent compound can be obtained by selecting a central metal, a ligand, a ligand substituent, and the like. However, it is preferable that the phosphorescent compound has a phosphorescent maximum wavelength of 380 to 480 nm. Examples of such phosphorescent emission wavelengths include organic EL elements that emit blue light and organic EL elements that emit white light. These elements should be operated with lower emission voltage and lower power consumption. Can do.

  In addition, by using a plurality of phosphorescent compounds, it is possible to mix different light emission, thereby obtaining an arbitrary emission color. White light emission is possible by adjusting the kind of phosphorescent compound and the amount of doping, and can also be applied to illumination and backlight.

  The light emitting layer may contain a host compound in addition to the phosphorescent compound.

  In the present invention, the host compound is a compound having a phosphorescence quantum yield of phosphorescence emission of less than 0.01 at room temperature (25 ° C.) among compounds contained in the light emitting layer.

  In this invention, it is preferable to use the organic EL element material of this invention mentioned above as a host compound. Thereby, the luminous efficiency can be further increased.

  Furthermore, a plurality of known host compounds may be used in combination. By using a plurality of types of host compounds, it is possible to adjust the movement of charges, and the organic EL element can be made highly efficient. As these known host compounds, compounds having a hole transporting ability and an electron transporting ability, preventing the emission of longer wavelengths, and having a high Tg (glass transition temperature) are preferable.

  Specific examples of known host compounds include compounds described in the following documents.

  JP 2001-257076, JP 2002-308855, JP 2001-313179, JP 2002-319491, JP 2001-357777, JP 2002-334786, JP 2002-8860, JP 2002-334787, JP 2002-15871, JP2002-334788, JP2002-43056, JP2002-334789, JP2002-756645, JP2002-338579, JP2002-105445, JP2002-343568, JP2002 141173, JP2002-352957, JP2002203683, JP2002-363227, JP2002-231453, JP2003-3165, JP2002-234888, JP2003-27048, JP200. -255934, JP 2002-260861, JP 2002-280183, JP 2002-299060, JP 2002-302516, JP 2002-305083, JP 2002-305084, 2002-308837, etc. JP.

  Moreover, the light emitting layer may contain the host compound which has a fluorescence maximum wavelength further as a host compound. In this case, the energy transfer from the other host compound and the phosphorescent compound to the fluorescent compound allows electroluminescence as an organic EL element to be emitted from the other host compound having a fluorescence maximum wavelength. A host compound having a fluorescence maximum wavelength is preferably a compound having a high fluorescence quantum yield in a solution state. Here, the fluorescence quantum yield is preferably 10% or more, particularly preferably 30% or more. Specific host compounds having a maximum fluorescence wavelength include coumarin dyes, pyran dyes, cyanine dyes, croconium dyes, squalium dyes, oxobenzanthracene dyes, fluorescein dyes, rhodamine dyes, and pyrylium dyes. Perylene dyes, stilbene dyes, polythiophene dyes, and the like. The fluorescence quantum yield can be measured by the method described in 362 (1992, Maruzen) of Spectroscopic II of the Fourth Edition Experimental Chemistry Course 7.

  The color emitted in this specification is the spectral radiance meter CS-1000 (Minolta) in FIG. 4.16 on page 108 of “New Color Science Handbook” (Edited by the Japan Society for Color Science, University of Tokyo Press, 1985). It is determined by the color when the measured result is applied to the CIE chromaticity coordinates.

  The light emitting layer can be formed by forming the above compound by a known thinning method such as a vacuum deposition method, a spin coating method, a casting method, an LB method, or an ink jet method. Although the film thickness as a light emitting layer does not have a restriction | limiting in particular, Usually, 5 nm-5 micrometers, Preferably it is chosen in the range of 5 nm-200 nm. The light emitting layer may have a single layer structure in which these phosphorescent compounds and host compounds are composed of one or more kinds, or may have a laminated structure composed of a plurality of layers having the same composition or different compositions. Good.

《Hole transport layer》
The hole transport layer is made of a hole transport material having a function of transporting holes, and in a broad sense, a hole injection layer and an electron blocking layer are also included in the hole transport layer. The hole transport layer can be provided as a single layer or a plurality of layers.

  The hole transport material has any one of hole injection or transport and electron barrier properties, and may be either organic or inorganic. For example, triazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives and pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, amino-substituted chalcone derivatives, oxazole derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbenes Derivatives, silazane derivatives, aniline copolymers, conductive polymer oligomers, particularly thiophene oligomers, and the like can be given.

  As the hole transport material, those described above can be used, but it is preferable to use a porphyrin compound, an aromatic tertiary amine compound and a styrylamine compound, particularly an aromatic tertiary amine compound.

  Representative examples of aromatic tertiary amine compounds and styrylamine compounds include N, N, N ′, N′-tetraphenyl-4,4′-diaminophenyl; N, N′-diphenyl-N, N′— Bis (3-methylphenyl)-[1,1′-biphenyl] -4,4′-diamine (TPD); 2,2-bis (4-di-p-tolylaminophenyl) propane; 1,1-bis (4-di-p-tolylaminophenyl) cyclohexane; N, N, N ′, N′-tetra-p-tolyl-4,4′-diaminobiphenyl; 1,1-bis (4-di-p-tolyl) Aminophenyl) -4-phenylcyclohexane; bis (4-dimethylamino-2-methylphenyl) phenylmethane; bis (4-di-p-tolylaminophenyl) phenylmethane; N, N'-diphenyl-N, N ' − (4-methoxyphenyl) -4,4'-diaminobiphenyl; N, N, N ', N'-tetraphenyl-4,4'-diaminodiphenyl ether; 4,4'-bis (diphenylamino) quadriphenyl; N, N, N-tri (p-tolyl) amine; 4- (di-p-tolylamino) -4 '-[4- (di-p-tolylamino) styryl] stilbene; 4-N, N-diphenylamino- (2-diphenylvinyl) benzene; 3-methoxy-4′-N, N-diphenylaminostilbenzene; N-phenylcarbazole, and two more described in US Pat. No. 5,061,569 Having a condensed aromatic ring of, for example, 4,4'-bis [N- (1-naphthyl) -N-phenylamino] biphenyl (NPD), JP-A-4-308 4,4 ', 4 "-tris [N- (3-methylphenyl) -N-phenylamino] triphenylamine (MTDATA) in which three triphenylamine units described in No. 88 are linked in a starburst type ) And the like.

  Furthermore, a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used. In addition, inorganic compounds such as p-type-Si and p-type-SiC can also be used as the hole injection material and the hole transport material.

  The hole transport layer can be formed by thinning the hole transport material by a known method such as a vacuum deposition method, a spin coating method, a casting method, a printing method including an ink jet method, or an LB method. it can. Although there is no restriction | limiting in particular about the film thickness of a positive hole transport layer, Usually, 5 nm-about 5 micrometers, Preferably it is 5-200 nm. This hole transport layer may have a single layer structure composed of one or more of the above materials.

《Electron transport layer》
The electron transport layer is made of a material having a function of transporting electrons, and in a broad sense, an electron injection layer and a hole blocking layer are also included in the electron transport layer. The electron transport layer can be provided as a single layer or a plurality of layers.

  Further, as in (i) and (ii) of the layer structure, the organic EL element is not provided with a hole blocking layer, and is adjacent to the light emitting layer is an electron transport layer (in this case, the electron transport layer is also a hole blocking layer). If the compound represented by the general formula (1) or the compound represented by the general formula (2) is used as the electron transport material of the electron transport layer, the emission voltage can be reduced. It can be operated with low power consumption.

  When the hole blocking layer is provided adjacent to the light emitting layer of the organic EL element as in the layer configurations (iii), (iv), and (v), the electron transport layer is a conventional electron transport layer. The electron transport material used in the above can be used. The electron transport material only needs to have a function of transmitting electrons injected from the cathode to the light emitting layer, and the material can be selected and used from conventionally known compounds. Examples include nitro-substituted fluorene derivatives, diphenylquinone derivatives, thiopyran dioxide derivatives, carbodiimides, fluorenylidenemethane derivatives, anthraquinodimethane and anthrone derivatives, oxadiazole derivatives, and the like. Furthermore, in the above oxadiazole derivative, a thiadiazole derivative in which the oxygen atom of the oxadiazole ring is substituted with a sulfur atom, and a quinoxaline derivative having a quinoxaline ring known as an electron withdrawing group can also be used as an electron transport material.

  In addition, a compound represented by the general formula (1) or a compound represented by the general formula (2) may be used.

  Furthermore, a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used.

  In addition, metal complexes of 8-quinolinol derivatives such as tris (8-quinolinol) aluminum (Alq), tris (5,7-dichloro-8-quinolinol) aluminum, tris (5,7-dibromo-8-quinolinol) aluminum, Tris (2-methyl-8-quinolinol) aluminum, tris (5-methyl-8-quinolinol) aluminum, bis (8-quinolinol) zinc (Znq), etc., and the central metals of these metal complexes are In, Mg, Cu , Ca, Sn, Ga, or Pb can also be used as an electron transport material. In addition, metal-free or metal phthalocyanine, or those having terminal ends substituted with an alkyl group or a sulfonic acid group can be preferably used as the electron transporting material. In addition, the distyrylpyrazine derivative exemplified as the material of the light emitting layer can also be used as an electron transport material, and similarly to the hole injection layer and the hole transport layer, inorganic such as n-type-Si and n-type-SiC can be used. A semiconductor can also be used as an electron transport material.

  The electron transport layer can be formed by thinning the electron transport material by a known method such as a vacuum deposition method, a spin coating method, a casting method, a printing method including an ink jet method, or an LB method. Although there is no restriction | limiting in particular about the film thickness of an electron carrying layer, Usually, 5 nm-about 5 micrometers, Preferably it is 5-200 nm. The electron transport layer may have a single layer structure composed of one or more of the above materials.

<< Substrate (also referred to as substrate, substrate, support, etc.) >>
The organic EL device of the present invention is preferably formed on a substrate.

  The substrate of the organic EL device of the present invention is not particularly limited to the type of glass, plastic, etc., and is not particularly limited as long as it is transparent. Examples of substrates that are preferably used include glass, quartz, A light transmissive resin film can be mentioned. A particularly preferable substrate is a resin film that can give flexibility to the organic EL element.

  Examples of the resin film include polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polyethersulfone (PES), polyetherimide, polyetheretherketone, polyphenylene sulfide, polyarylate, polyimide, polycarbonate (PC), and cellulose triacetate. Examples thereof include films made of (TAC), cellulose acetate propionate (CAP) and the like. An inorganic or organic film or a hybrid film of both may be formed on the surface of the resin film.

  The external extraction efficiency at room temperature for light emission of the organic electroluminescence device of the present invention is preferably 1% or more, more preferably 5% or more. Here, the external extraction quantum efficiency (%) = the number of photons emitted to the outside of the organic EL element / the number of electrons sent to the organic EL element × 100.

  In addition, a hue improvement filter such as a color filter may be used in combination, or a color conversion filter that converts the emission color from the organic EL element into multiple colors using a phosphor. In the case of using a color conversion filter, the λmax of light emission of the organic EL element is preferably 480 nm or less.

<< Method for producing organic EL element >>
As an example of the method for producing the organic EL device of the present invention, a method for producing an organic EL device comprising an anode / anode buffer layer / hole transport layer / light emitting layer / hole blocking layer / electron transport layer / cathode buffer layer / cathode. explain.

  First, a thin film made of a desired electrode material, for example, an anode material is formed on a suitable substrate by a method such as vapor deposition or sputtering so as to have a film thickness of 1 μm or less, preferably 10 to 200 nm, thereby producing an anode. To do. Next, an organic compound thin film of an anode buffer layer, a hole transport layer, a light emitting layer, a hole blocking layer, an electron transport layer, and a cathode buffer layer, which are organic EL element materials, is formed thereon.

As a method for thinning the organic compound thin film, there are a vapor deposition method and a wet process (spin coating method, casting method, ink jet method, printing method) as described above, but it is easy to obtain a uniform film and a pinhole. From the point of being difficult to form, a vacuum deposition method, a spin coating method, an ink jet method, and a printing method are particularly preferable. Further, different film forming methods may be applied for each layer. When employing a vapor deposition method for film formation, the vapor deposition conditions vary depending on the type of compound used, but generally a boat heating temperature of 50 to 450 ° C., a vacuum degree of 10 ⁻⁶ to 10 ⁻² Pa, and a vapor deposition rate of 0.01 It is desirable to select appropriately within a range of ˜50 nm / second, a substrate temperature of −50 to 300 ° C., and a film thickness of 0.1 nm to 5 μm, preferably 5 to 200 nm.

  After these layers are formed, a thin film made of a cathode material is formed thereon by a method such as vapor deposition or sputtering so as to have a thickness of 1 μm or less, preferably in the range of 50 to 200 nm, and a cathode is provided. Thus, a desired organic EL element can be obtained. The organic EL element is preferably produced from the hole injection layer to the cathode consistently by a single evacuation, but may be taken out halfway and subjected to different film forming methods. At that time, it is necessary to consider that the work is performed in a dry inert gas atmosphere.

  The multicolor display device of the present invention is provided with a shadow mask only when the light emitting layer is formed, and the other layers are common, so that patterning of the shadow mask or the like is unnecessary, and the evaporation method, the casting method, the spin coating method, the ink jet method on one side. A film can be formed by a method or a printing method.

  When patterning is performed only on the light-emitting layer, the method is not limited, but a vapor deposition method, an inkjet method, and a printing method are preferable. In the case of using a vapor deposition method, patterning using a shadow mask is preferable.

  Moreover, it is also possible to produce the cathode, the cathode buffer layer, the electron transport layer, the hole transport layer, the light emitting layer, the hole transport layer, the anode buffer layer, and the anode in this order by reversing the order of production. When a DC voltage is applied to the multicolor display device thus obtained, light emission can be observed by applying a voltage of about 2 to 40 V with the positive polarity of the anode and the negative polarity of the cathode. An alternating voltage may be applied. The alternating current waveform to be applied may be arbitrary.

  The display device of the present invention can be used as a display device, a display, and various light emission sources. In a display device or a display, full-color display is possible by using three types of organic EL elements of blue, red, and green light emission.

  Examples of the display device and display include a television, a personal computer, a mobile device, an AV device, a character broadcast display, and an information display in an automobile. In particular, it may be used as a display device for reproducing still images and moving images, and the driving method when used as a display device for reproducing moving images may be either a simple matrix (passive matrix) method or an active matrix method.

  The lighting device of the present invention includes home lighting, interior lighting, clock and liquid crystal backlights, billboard advertisements, traffic lights, light sources of optical storage media, light sources of electrophotographic copying machines, light sources of optical communication processors, light sensors Although a light source etc. are mentioned, it is not limited to this.

  Further, the organic EL element according to the present invention may be used as an organic EL element having a resonator structure.

  Examples of the purpose of use of the organic EL element having such a resonator structure include a light source of an optical storage medium, a light source of an electrophotographic copying machine, a light source of an optical communication processing machine, and a light source of an optical sensor. It is not limited. Moreover, you may use for the said use by making a laser oscillation.

<Display device>
The organic EL element of the present invention may be used as one kind of lamp for illumination or exposure light source, a projection device for projecting an image, or a display for directly viewing a still image or a moving image. It may be used as a device (display). When used as a display device for reproducing moving images, the driving method may be either a simple matrix (passive matrix) method or an active matrix method. Alternatively, a full-color display device can be manufactured by using three or more organic EL elements of the present invention having different emission colors. Alternatively, it is possible to make one color emission color, for example, white emission, into BGR by using a color filter to achieve full color. Furthermore, it is possible to convert the emission color of the organic EL to another color by using a color conversion filter, and in this case, λmax of the organic EL emission is preferably 480 nm or less.

  An example of a display device composed of the organic EL element of the present invention will be described below with reference to the drawings.

  FIG. 1 is a schematic diagram illustrating an example of a display device including organic EL elements. It is a schematic diagram of a display such as a mobile phone that displays image information by light emission of an organic EL element.

  The display 1 includes a display unit A having a plurality of pixels, a control unit B that performs image scanning of the display unit A based on image information, and the like.

  The control unit B is electrically connected to the display unit A, and sends a scanning signal and an image data signal to each of the plurality of pixels based on image information from the outside. The pixels for each scanning line are converted into image data signals by the scanning signal. In response to this, light is sequentially emitted and image scanning is performed to display image information on the display unit A.

  FIG. 2 is a schematic diagram of the display unit A.

  The display unit A includes a wiring unit including a plurality of scanning lines 5 and data lines 6, a plurality of pixels 3 and the like on a substrate. The main members of the display unit A will be described below. FIG. 2 shows a case where the light emitted from the pixel 3 is extracted in the direction of the white arrow (downward).

  The scanning lines 5 and the plurality of data lines 6 in the wiring portion are each made of a conductive material, and the scanning lines 5 and the data lines 6 are orthogonal to each other in a lattice shape and are connected to the pixels 3 at the orthogonal positions (details are shown in FIG. Not shown).

  When a scanning signal is applied from the scanning line 5, the pixel 3 receives an image data signal from the data line 6 and emits light according to the received image data. Full color display is possible by appropriately arranging pixels in the red region, the green region, and the blue region that emit light on the same substrate.

  Next, the light emission process of the pixel will be described.

  FIG. 3 is a schematic diagram of a pixel.

  The pixel includes an organic EL element 10, a switching transistor 11, a driving transistor 12, a capacitor 13, and the like. A full color display can be performed by using red, green, and blue light emitting organic EL elements as the organic EL elements 10 in a plurality of pixels, and juxtaposing them on the same substrate.

  In FIG. 3, an image data signal is applied from the control unit B to the drain of the switching transistor 11 through the data line 6. When a scanning signal is applied from the control unit B to the gate of the switching transistor 11 via the scanning line 5, the driving of the switching transistor 11 is turned on, and the image data signal applied to the drain is supplied to the capacitor 13 and the driving transistor 12. Is transmitted to the gate.

  By transmitting the image data signal, the capacitor 13 is charged according to the potential of the image data signal, and the drive of the drive transistor 12 is turned on. The drive transistor 12 has a drain connected to the power supply line 7 and a source connected to the electrode of the organic EL element 10, and the power supply line 7 connects to the organic EL element 10 according to the potential of the image data signal applied to the gate. Current is supplied.

  When the scanning signal is moved to the next scanning line 5 by the sequential scanning of the control unit B, the driving of the switching transistor 11 is turned off. However, even if the driving of the switching transistor 11 is turned off, the capacitor 13 maintains the potential of the charged image data signal, so that the driving of the driving transistor 12 is kept on and the next scanning signal is applied. Until then, the light emission of the organic EL element 10 continues. When the scanning signal is next applied by sequential scanning, the driving transistor 12 is driven according to the potential of the next image data signal synchronized with the scanning signal, and the organic EL element 10 emits light.

  That is, the organic EL element 10 emits light by the switching transistor 11 and the drive transistor 12 that are active elements for the organic EL element 10 of each of the plurality of pixels, and the light emission of the organic EL element 10 of each of the plurality of pixels 3. It is carried out. Such a light emitting method is called an active matrix method.

  Here, the light emission of the organic EL element 10 may be light emission of a plurality of gradations by a multi-value image data signal having a plurality of gradation potentials, or on / off of a predetermined light emission amount by a binary image data signal. But you can.

  The potential of the capacitor 13 may be held continuously until the next scanning signal is applied, or may be discharged immediately before the next scanning signal is applied.

  In the present invention, not only the active matrix method described above, but also a passive matrix light emission drive in which the organic EL element emits light according to the data signal only when the scanning signal is scanned.

  FIG. 4 is a schematic view of a passive matrix display device. In FIG. 4, a plurality of scanning lines 5 and a plurality of image data lines 6 are provided in a lattice shape so as to face each other with the pixel 3 interposed therebetween.

  When the scanning signal of the scanning line 5 is applied by sequential scanning, the pixels 3 connected to the applied scanning line 5 emit light according to the image data signal. In the passive matrix system, the pixel 3 has no active element, and the manufacturing cost can be reduced.

  The organic EL material according to the present invention can also be applied to an organic EL element that emits substantially white light as a lighting device. A plurality of light emitting colors are simultaneously emitted by a plurality of light emitting materials to obtain white light emission by color mixing. The combination of a plurality of emission colors may include three emission maximum wavelengths of three primary colors of blue, green, and blue, or two using a complementary color relationship such as blue and yellow, blue green and orange, etc. The thing containing the light emission maximum wavelength may be used.

  In addition, a combination of light emitting materials for obtaining a plurality of emission colors includes a combination of a plurality of phosphorescent or fluorescent materials (light emitting dopants), a light emitting material that emits fluorescent or phosphorescent light, and the light emission. Any combination of a dye material that emits light from the material as excitation light may be used, but in the white organic electroluminescence device according to the present invention, a method of combining a plurality of light-emitting dopants is preferable.

  As a layer structure of an organic electroluminescence device for obtaining a plurality of emission colors, a method of having a plurality of emission dopants in one emission layer, a plurality of emission layers, and an emission wavelength in each emission layer And a method of forming minute pixels emitting light having different wavelengths in a matrix.

  In the white organic electroluminescence device according to the present invention, patterning may be performed by a metal mask, an ink jet printing method, or the like at the time of film formation, if necessary. When patterning, only the electrode may be patterned, the electrode and the light emitting layer may be patterned, or the entire element layer may be patterned.

  The light emitting material used for the light emitting layer is not particularly limited. For example, in the case of a backlight in a liquid crystal display element, the platinum complex according to the present invention is known so as to be suitable for the wavelength range corresponding to the CF (color filter) characteristics. Any one of the light emitting materials may be selected and combined to be whitened.

  Thus, in addition to the display device and display, the white light-emitting organic EL element of the present invention can be used as various light sources, lighting devices, household lighting, interior lighting, and a kind of lamp such as an exposure light source. It is also useful for display devices such as backlights for liquid crystal display devices.

  Others such as backlights for watches, signboard advertisements, traffic lights, light sources for optical storage media, light sources for electrophotographic copying machines, light sources for optical communication processors, light sources for optical sensors, etc. There are a wide range of uses such as household appliances.

  EXAMPLES Hereinafter, although an Example demonstrates this invention, the embodiment of this invention is not limited to these.

Example 1
<Preparation of organic EL elements 1-1 to 15>
Transparent support provided with this ITO transparent electrode after patterning on a substrate (NH45 manufactured by NH Techno Glass Co., Ltd.) formed by depositing 100 nm of ITO (indium tin oxide) on a glass substrate of 100 mm × 100 mm × 1.1 mm as an anode The substrate was ultrasonically cleaned with isopropyl alcohol, dried with dry nitrogen gas, and subjected to UV ozone cleaning for 5 minutes. This transparent support substrate is fixed to a substrate holder of a commercially available vacuum deposition apparatus, while 200 mg of m-MTDATXA is put in a molybdenum resistance heating boat, and 200 mg of CBP is put in another molybdenum resistance heating boat, and another molybdenum resistance 200 mg of A-30 was put in a heating boat, 100 mg of Ir-12 was put in another resistance heating boat made of molybdenum, and 200 mg of Alq ₃ was put in another resistance heating boat made of molybdenum, and attached to a vacuum deposition apparatus.

Next, the pressure in the vacuum chamber was reduced to 4 × 10 ⁻⁴ Pa, and the heating boat containing m-MTDATXA was heated and heated, and deposited on the transparent support substrate at a deposition rate of 0.1 nm / second to form a 50 nm hole. A transport layer was provided. Further, the heating boat containing CBP and Ir-12 was energized and heated, and co-deposited on the hole transport layer at a deposition rate of 0.2 nm / second and 0.012 nm / second, respectively, to form a 30 nm light emitting layer. Was established.

  Further, the heating boat containing A-30 was energized and heated, and was deposited on the light emitting layer at a deposition rate of 0.1 nm / second to provide a 10 nm thick hole blocking layer.

  Further, the heating boat containing Alq3 was energized and heated, and deposited on the hole blocking layer at a striking speed of 0.1 nm / second to provide an electron transport layer having a thickness of 40 nm.

  In addition, the substrate temperature at the time of vapor deposition was room temperature.

  Then, 0.5 nm of lithium fluoride was vapor-deposited as a cathode buffer layer, and also aluminum 110nm was vapor-deposited, the cathode was formed, and the organic EL element 1-1 was produced.

  In the production of the organic EL element 1-1, 1-2-3 was performed in the same manner as the organic EL element 1-1 except that the hole blocking layer was formed by replacing A-30 with the materials for organic EL elements shown in Table 1. -15 was produced. The structure of the compound used above is shown below.

<Evaluation of Organic EL Elements 1-1 to 1-15>
The organic EL elements 1-1 to 1-15 produced as described below were evaluated, and the results are shown in Table 1.

(Light emission voltage)
The voltage at the start of light emission was measured at a temperature of 23 ° C. under an atmosphere of nitrogen gas. Note that the voltage at the start of light emission was measured when the luminance was 50 cd / m ² or more. A spectral radiance meter CS-1000 (manufactured by Minolta) was used for the measurement of luminance.

  The light emission voltage in Table 1 was expressed as a relative value when the organic EL element 1-1 was 100.

  From Table 1, it was found that the organic EL device of the present invention has a low emission voltage, low power consumption, and very low cost.

Example 2
<Production of full-color display device>
<Full-color display device (1)>
(Blue light emitting organic EL device)
The organic EL element 1-14 produced in Example 1 was used.

(Green light-emitting organic EL device)
In the organic EL element 1-13 produced in Example 1, the organic EL element 1-13G produced by the same method as the organic EL element 1-13 was used except that Ir-1 was used instead of Ir-12. It was.

(Red light emitting organic EL device)
In the organic EL element 1-3 produced in Example 1, the organic EL element 1-3R produced by the same method as the organic EL element 1-3 was used except that Ir-9 was used instead of Ir-12. It was.

  The red, green and blue light-emitting organic EL elements are juxtaposed on the same substrate to produce an active matrix type full-color display device having the form shown in FIG. 1, and FIG. Only the schematic diagram of part A is shown. That is, a wiring portion including a plurality of scanning lines 5 and data lines 6 on the same substrate, and a plurality of juxtaposed pixels 3 (light emission color is a red region pixel, a green region pixel, a blue region pixel, etc.) The scanning lines 5 and the plurality of data lines 6 in the wiring portion are each made of a conductive material, and the scanning lines 5 and the data lines 6 are orthogonal to each other in a lattice shape and are connected to the pixels 3 at the orthogonal positions ( Details are not shown). The plurality of pixels 3 are driven by an active matrix system provided with an organic EL element corresponding to each emission color, a switching transistor as an active element, and a driving transistor, and a scanning signal is applied from a scanning line 5. Then, an image data signal is received from the data line 6 and light is emitted according to the received image data. In this manner, a full color display device was produced by appropriately juxtaposing the red, green, and blue pixels.

  By driving the full-color display device, it was confirmed that the power consumption was low and the cost was very low.

Example 3
In the organic EL element 1-14 produced in Example 1, the organic EL element 1 was used except that Ir-6 and Ir-12 (Ir-6: Ir-12 = 1: 4) were used instead of Ir-12. Organic EL element 1-14W produced by the same method as -14 was produced.

  The non-light-emitting surface of the organic EL element 1-14W was covered with a glass case to obtain a lighting device. The illumination device can be used as a thin illumination device that consumes less power and emits white light at a very low cost.

  FIG. 5 is a schematic view of the lighting device, and FIG. 6 is a cross-sectional view of the lighting device. The organic EL element 101 is covered with a glass cover 102 and connected with a power line (anode) 103 and a power line (cathode) 104. 105 is a cathode and 106 is an organic EL layer. The glass cover 102 is filled with nitrogen gas 108 and a water replenisher 109 is provided.

It is the schematic diagram which showed an example of the display apparatus comprised from an organic EL element. It is a schematic diagram of a display part. It is a schematic diagram of a pixel. It is a schematic diagram of a passive matrix type full-color display device. It is the schematic of an illuminating device. It is sectional drawing of an illuminating device.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Display 3 Pixel 5 Scan line 6 Data line 7 Power supply line 10 Organic EL element 11 Switching transistor 12 Drive transistor 13 Capacitor A Display part B Control part 102 Glass cover 103 Power supply line (anode)
104 Power line (cathode)
105 Cathode 106 Organic EL layer 107 Glass substrate with transparent electrode 108 Nitrogen gas 109 Water trapping agent

Claims (9)

In an organic electroluminescence device having at least a light emitting layer containing a phosphorescent compound between an anode and a cathode,
Between the light emitting layer and the cathode and having an adjacent layer adjacent to the light emitting layer;
An organic electroluminescence device comprising a compound represented by the following general formula (1) in the adjacent layer.

(In the formula, L ₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Q ₁ is necessary for bonding to a nitrogen atom to form an aromatic heterocycle. Represents an atomic group, R ₁ represents a hydrogen atom or a substituent, and n1 represents an integer of 2 or more, a plurality of Q ₁ may be the same or different, and a plurality of R ₁ are the same or different; And at least one of the plurality of R ₁ represents a fluorine atom or a substituent containing a fluorine atom.) The organic electroluminescent device according to claim 1, wherein the compound represented by the general formula (1) is a compound represented by the following general formula (1-1).

(In the formula, L ₁₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Y _{1 to} Y ₄ each independently represent a nitrogen atom or C—R ₁₁ (R ₁₁ represents a hydrogen atom or a substituent, and n11 represents an integer greater than or equal to 2. At least one of Y ₁ to Y ₄ is a C— group in which R ₁₁ is a fluorine atom or a substituent containing a fluorine atom. R _11. ) In an organic electroluminescence device having at least a light emitting layer containing a phosphorescent compound between an anode and a cathode,
Between the light emitting layer and the cathode, and having an adjacent layer adjacent to the light emitting layer;
An organic electroluminescence device comprising a compound represented by the following general formula (2) in the adjacent layer.

(In the formula, L ₂ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Q ₂ is necessary for bonding to a carbon atom to form an aromatic heterocycle. Represents an atomic group, R ₂ represents a hydrogen atom or a substituent, and n2 represents an integer of 2 or more, a plurality of Q ₂ may be the same or different, and a plurality of R ₂ are the same or different. And at least one of the plurality of R ₂ represents a fluorine atom or a substituent containing a fluorine atom.) The organic electroluminescent device according to claim 1, wherein the compound represented by the general formula (2) is a compound represented by the following general formula (2-1).

(In the formula, L ₂₁ represents a divalent or higher valent hydrocarbon linking group or a divalent or higher valent aromatic linking group, and Y _{5 to} Y ₇ each independently represents a nitrogen atom or C—R ₂₁ (R ₂₁ Represents a hydrogen atom or a substituent, R ₂₂ represents a hydrogen atom or a substituent, and n21 represents an integer of 2 or more, and at least one of Y ₅ to Y ₇ represents that R ₂₁ is a fluorine atom or a fluorine atom. C—R ₂₁ which is a substituent containing an atom, or R ₂₂ is a substituent containing a fluorine atom.) The organic electroluminescence element according to any one of claims 1 to 4, wherein the light emission is blue. The organic electroluminescence element according to claim 1, wherein the light emission is white. A display device comprising the organic electroluminescence element according to claim 1. An illuminating device comprising the organic electroluminescent element according to claim 1. A display device comprising: the illumination device according to claim 8; and a liquid crystal element as a display unit.

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