JP2016171047A - Light emission device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To enhance the charge generation efficiency of a charge generation layer in a light emission device in which the charge generation layer is sandwiched between plural organic layers.SOLUTION: Plural organic layers 120 are located between a first electrode 110 and a second electrode 130, and each of the organic layers 120 has a light emission layer. A charge generation layer 200 is located between the adjacent organic layers 120. In other words, the plurality of organic layers 120 are mutually stacked, and the charge generation layer 200 is provided between these plural organic layers 120. The charge generation layer 200 has first and second layers. The first layer contains an electron-transporting material, and the second layer contains a metal and a hole-transporting material. The charge generation layer contains electron injection material for enhancing the electron injection performance of the first layer at a position nearer to the first layer than the second layer.SELECTED DRAWING: Figure 1

Description

  The present invention relates to a light emitting device.

  In recent years, a light emitting device having an organic EL (Organic Electroluminescence) element in a light emitting portion has been developed. The organic EL element has a configuration in which an organic layer is sandwiched between a first electrode and a second electrode. The organic layer generally has a configuration in which a light emitting layer is sandwiched between a hole injection layer and an electron injection layer.

  On the other hand, as a method for increasing the luminance of the light emitting device, there is a method in which the above-described organic layers are stacked and a charge generation layer is disposed between adjacent organic layers, so-called multiphoton light emitting structure or tandem structure. For example, Patent Document 1 describes using a structure in which an n-doped organic layer, a metal compound layer, and a p-doped organic layer are stacked in this order as the charge generation layer. In Patent Document 1, as the metal compound layer, titanium, zirconium, hafnium, niobium, tantalum, molybdenum, tungsten, manganese, iron, ruthenium, rhodium, iridium, nickel, palladium, platinum, copper, zinc, silicon, germanium, or It is described that it can be carried out from these combinations of stoichiometric oxides or non-stoichiometric oxides.

  Patent Document 2 describes that LiF, Al, and 1,4,5,8,9,12-hexaazatriphenylenehexacarbonitrile (HATCN) are stacked as a charge generation layer.

Special table 2008-511100 gazette JP 2010-192719 A

  The charge generation efficiency in the charge generation layer directly affects the luminance of the light emitting device. For this reason, it is desired to improve the charge generation efficiency of the charge generation layer.

  An example of a problem to be solved by the present invention is to improve the charge generation efficiency of a charge generation layer in a light emitting device in which a charge generation layer is sandwiched between a plurality of organic layers.

The invention according to claim 1 is a first electrode;
A second electrode;
A plurality of organic layers located between the first electrode and the second electrode, each including a light emitting layer;
A charge generation layer located between two adjacent organic layers;
With
The charge generation layer includes
A first layer comprising an electron transporting material;
A second layer comprising a metal and a hole injection material;
Have
The charge generation layer is a light emitting device including an electron injecting material between the second layer and the first layer or in the first layer.

It is sectional drawing which shows the structure of the light-emitting device which concerns on embodiment. It is sectional drawing which shows the structure of an organic layer. It is sectional drawing which shows the structure of an electric charge generation layer. It is sectional drawing which shows the structure of the electric charge generation layer which concerns on 2nd Embodiment. It is sectional drawing which shows the structure of the electric charge generation layer which concerns on a modification. 1 is a plan view illustrating a configuration of a light emitting device according to Example 1. FIG. It is the figure which removed the 2nd electrode from FIG. It is the figure which removed the organic layer, the charge generation layer, and the insulating layer from FIG. It is AA sectional drawing of FIG. 4 is data showing current density and light emission efficiency in a light emitting device in which the charge generation layer has the structure shown in FIG. FIG. 5 is data showing current density and light emission efficiency in a light emitting device in which the charge generation layer has the structure shown in FIG. 4.

  Hereinafter, embodiments of the present invention will be described with reference to the drawings. In all the drawings, the same reference numerals are given to the same components, and the description will be omitted as appropriate.

(First embodiment)
FIG. 1 is a cross-sectional view illustrating a configuration of a light emitting device 10 according to the embodiment. 2 is a cross-sectional view showing the configuration of the organic layer 120 shown in FIG. 1, and FIG. 3 is a cross-sectional view showing the configuration of the charge generation layer 200 shown in FIG. As shown in FIG. 1, the light emitting device 10 includes a first electrode 110, a second electrode 130, a plurality of organic layers 120, and a charge generation layer 200. The plurality of organic layers 120 are located between the first electrode 110 and the second electrode 130, and each has a light emitting layer 124 as shown in FIG. 2. The charge generation layer 200 is located between the adjacent organic layers 120. In other words, the plurality of organic layers 120 are stacked on each other, but the charge generation layer 200 is provided between the plurality of organic layers 120. Further, the organic layer 120 can also be expressed as a light emitting unit. The light emitting device 10 can also include a plurality of light emitting units having different emission colors via the charge generation layer 200. As shown in FIG. 3, the charge generation layer 200 includes a first layer 202 and a second layer 204. The first layer 202 includes an electron transport material, and the second layer 204 includes a metal and a hole injection material. In addition, the charge generation layer 200 includes an electron injection material that improves the electron injection property of the first layer 202 closer to the first layer 202 than the second layer 204. In the example shown in FIG. 3, the electron injection material is included in the first layer 202. Details will be described below.

The light emitting device 10 is formed using a substrate 100. When the light emitting device 10 is a bottom emission type, the substrate 100 is formed of a light transmissive material such as glass or a light transmissive resin. However, when the light emitting device 10 is a top emission type described later, the substrate 100 may be formed of a material that does not have translucency. The substrate 100 is, for example, a polygon such as a rectangle. The substrate 100 may have flexibility. In the case where the substrate 100 has flexibility, the thickness of the substrate 100 is, for example, not less than 10 μm and not more than 1000 μm. In particular, when the substrate 100 is glass, the thickness of the substrate 100 is, for example, 200 μm or less. When the substrate 100 is a resin, the substrate 100 is formed using, for example, PEN (polyethylene naphthalate), PES (polyethersulfone), PET (polyethylene terephthalate), or polyimide. In addition, when the substrate 100 is a resin, an inorganic barrier film such as SiN _x or SiON is formed on at least the light emitting surface side (preferably both surfaces) of the substrate 100 in order to suppress moisture from passing through the substrate 100. ing.

  A light emitting unit 140 is formed on the substrate 100. The light emitting unit 140 has an organic EL element. As shown in FIG. 1, the organic EL element has a configuration in which a first electrode 110, a plurality of organic layers 120, and a second electrode 130 are laminated in this order. A charge generation layer 200 is provided between the plurality of organic layers 120. In the example shown in FIG. 1, the light emitting device 10 has two organic layers 120. The charge generation layer 200 connects these two organic layers 120. If the organic layer 120 has a multi-photon structure, three (so-called tridem structure) or more may be formed. In this case, the charge generation layer 200 is provided at two locations between the organic layers 120.

  The first electrode 110 is a transparent electrode having optical transparency. The transparent conductive material constituting the transparent electrode is a metal-containing material, for example, a metal oxide such as ITO (Indium Tin Oxide), IZO (Indium Zinc Oxide), IWZO (Indium Tungsten Zinc Oxide), or ZnO (Zinc Oxide). is there. The thickness of the first electrode 110 is, for example, not less than 10 nm and not more than 500 nm. The first electrode 110 is formed using, for example, a sputtering method or a vapor deposition method. The first electrode 110 may be a carbon nanotube or a conductive organic material such as PEDOT / PSS.

  The second electrode 130 is made of, for example, a metal selected from the first group consisting of Al, Au, Ag, Pt, Mg, Sn, Zn, and In or an alloy of a metal selected from the first group. Contains a metal layer. In this case, the second electrode 130 has a light shielding property. The thickness of the second electrode 130 is, for example, not less than 10 nm and not more than 500 nm. However, the second electrode 130 may be formed using the material exemplified as the material of the first electrode 110. The second electrode 130 is formed using, for example, a sputtering method or a vapor deposition method.

  Note that the materials of the first electrode 110 and the second electrode 130 described above are examples in which light is transmitted through the substrate 100, that is, light emission from the light emitting device 10 is performed through the substrate 100 (bottom emission type). It is. In other cases, light may pass through the side opposite to the substrate 100. That is, the light emission from the light emitting device 10 is performed without passing through the substrate 100 (top emission type). The top emission type includes two types of laminated structures: a reverse product type and a forward product type. In the reverse product type, the material of the first electrode 110 and the material of the second electrode 130 are opposite to those of the bottom emission type. That is, the material of the second electrode 130 is used as the material of the first electrode 110, and the material of the first electrode 110 is used as the material of the second electrode 130. In the other product type, the material of the first electrode 110 is formed on the material of the second electrode 130 described above, the organic layer is further formed thereon, and the second electrode 130 is formed on the organic layer. Thus, the light is extracted from the side opposite to the substrate 100. The light emitting device 10 according to the present embodiment may be of any structure of a bottom emission type and the above two types of top emission types.

  As shown in FIG. 2, the organic layer 120 has a light emitting layer 124. Specifically, the organic layer 120 has a configuration in which a hole injection layer 122, a light emitting layer 124, and an electron injection layer 126 are stacked. A hole transport layer may be formed between the hole injection layer 122 and the light emitting layer 124. An electron transport layer may be formed between the light emitting layer 124 and the electron injection layer 126. The organic layer 120 may be formed by a vacuum deposition method. In addition, at least one layer of the organic layer 120, for example, a layer in contact with the first electrode 110 (the hole injection layer 122 in the example shown in FIG. 2) is applied by an application method such as an inkjet method, a printing method, or a spray method. May be formed. The remaining layers of the organic layer 120 may be formed by a vacuum evaporation method or may be formed by a coating method. In addition, for example, the first electrode 110 side is formed by a coating method, and the second electrode 130 side through the charge generation layer 200 is formed by a vacuum evaporation method. 120 may be formed by different methods.

  As shown in FIG. 3, the charge generation layer 200 includes a first layer 202 and a second layer 204. The first layer 202 and the second layer 204 are formed using, for example, a vacuum evaporation method.

The first layer 202 includes an electron transport material. This electron transporting material is, for example, Bphen (4,7-Diphenyl-1,10-phenanthroline). However, other electron transporting materials may be used for the first layer 202. Examples of other organic compounds having an electron transporting property include metal complexes having at least one 8-quinolinolato or a derivative thereof such as Alq ₃ [tris (8-quinolinolato) aluminum] as a ligand, TAZ [3- ( Triazole compounds such as 4-biphenyl) -5- (4-t-butylphenyl) -4-phenyl-1,2,4-triazole], PBD [2- (4-biphenyl) -5- (4-t Oxadiazole compounds such as (butyl) -1,3,4-oxadiazole] can be used. However, it is not limited to these materials. Further, in the structure shown in this drawing, the first layer 202 includes an electron injection material that enhances the electron injection property of the electron transport material in addition to the electron transport material described above. As this electron injection material, for example, Liq (8-Hydroxyquinolinolato-lithium) can be used. However, the electron injection material is not limited to this. Electron injection materials further include oxides and fluorides of alkaline metals and alkaline earth metals such as LiF, Li ₂ O, and Li ₂ CO ₃ , carbonates, alkali metals such as lithium, sodium, calcium, and cesium, Alkaline earth metals can be used. Further, the thickness of the first layer 202 is, for example, not less than 5 nm and not more than 150 nm, preferably not less than 10 nm and not more than 50 nm.

  The second layer 204 includes a metal and a hole injection material. As the hole injection material, for example, a compound containing a hexaazatriphenylene derivative such as HATCN (1,4,5,8,9,12-hexaazatriphenylenehexacarbonitrile) can be used. The chemical formula of HATCN is represented by the following chemical formula (1).

  The metal contained in the second layer 204 is preferably a second group metal such as Mg or Ca. In order to form the second layer 204, the metal and the hole injection material may be heated and deposited on the substrate 100 in the same vacuum deposition apparatus. Here, as a heat source for depositing the hole injection material, a resistance heating type heat source can be used. When Mg is used as the metal contained in the second layer 204, a resistance heating type heating source can be used as a heating source when the metal is deposited. For this reason, when the metal contained in the second layer 204 is Mg, when the organic layer 120 is formed by a resistance heating type vacuum vapor deposition method, it is not necessary to invest new equipment, and the manufacturing cost of the light emitting device 10 is reduced. Can be lowered.

  FIG. 10 shows data indicating current density and light emission efficiency in the light emitting device 10. The lower data in the graph is data of a light emitting element in which the second layer 204 is formed on the first layer 202 without containing metal, in other words, the second layer 204 is formed only of the hole injection material. (HATCN layer). The upper data in the graph is the same as the lower data in the graph for the first layer 202, and the second layer 204 contains a metal material (specifically, Mg) in a volume ratio of 10%. It is data of a light emitting element. Note that the structure of the first layer 202 is the same in each light emitting element, and the thickness of the second layer 204 is 20 nm. It can be seen that the light-emitting element to which the metal material is added has higher light emission efficiency than the light-emitting element in which the metal material is not added to the second layer 204. That is, it can be seen that when a metal material is added to the second layer 204, the merit (increase in luminance) of the tandem structure is increased.

  The thickness of the second layer 204 is, for example, not less than 20 nm and not more than 50 nm, but may be thinner than this. For example, the thickness of the second layer 204 may be 1 nm or more and 10 nm or less. Further, the volume content of the metal (for example, Mg) contained in the second layer 204 is preferably 10% or more, and more preferably 50% or more. The volume content is, for example, 90% or less. As a method for calculating the volume content of Mg, for example, secondary ion mass spectrometry (SIMS) or X-ray fluorescence analysis (XRF) can be used.

  Next, a method for manufacturing the light emitting device 10 will be described. First, the first electrode 110 is formed on the substrate 100. Next, the organic layer 120, the charge generation layer 200, and the organic layer 120 are formed in this order. Note that the charge generation layer 200 and the organic layer 120 may be further formed at least once on the upper organic layer 120. Next, the second electrode 130 is formed on the uppermost organic layer 120.

  As described above, according to the present embodiment, the charge generation layer 200 includes the first layer 202 and the second layer 204. The first layer 202 includes an electron transport material, and the second layer 204 includes a metal and a hole injection material. With such a configuration, the charge generation efficiency in the charge generation layer 200 is increased. For this reason, even if the plurality of organic layers 120 are stacked between the first electrode 110 and the second electrode 130, the light emission efficiency of each of the organic layers 120 is unlikely to decrease. Therefore, the luminance of the light emitting unit 140 can be increased.

  Further, when a metal or a metal compound having a high melting point (high evaporation temperature in high vacuum) is used as a material included in the second layer 204, an electron beam evaporation source is used when forming the second layer 204. It is necessary to use it. However, in this embodiment, when Mg is used as the metal contained in the second layer 204, the melting point of Mg (evaporation temperature in high vacuum) is lower than that of other metal materials. Can be formed using only a resistance heating deposition source. Therefore, when the organic layer 120 is formed by a resistance heating method deposition source, an additional deposition source becomes unnecessary. Therefore, the manufacturing cost of the charge generation layer 200 can be reduced.

(Second Embodiment)
FIG. 4 is a cross-sectional view illustrating a configuration of the charge generation layer 200 included in the light emitting device 10 according to the second embodiment. FIG. 4 corresponds to FIG. 3 of the first embodiment. The light emitting device 10 according to the present embodiment has the same configuration as that of the light emitting device 10 according to the first embodiment except for the configuration of the charge generation layer 200.

  In the example shown in FIG. 4, the charge generation layer 200 has a configuration in which a first layer 202, a second layer 204, and a third layer 206 are stacked. The configuration of the first layer 202 and the configuration of the second layer 204 are the same as those in the first embodiment. However, the thickness of the second layer 204 may be thinner than that of the first embodiment, and is, for example, 1 nm to 30 nm, and more preferably 1 nm to 10 nm.

  The third layer 206 is formed using a hole injection material. This hole injection material is, for example, the same as the hole injection material included in the second layer 204, but may be another material. The third layer 206 is formed using, for example, a vacuum evaporation method. The thickness of the third layer 206 is, for example, not less than 1 nm and not more than 100 nm. The third layer 206 does not contain the metal contained in the second layer 204. However, the above-described metal may diffuse from the second layer 204 to the third layer 206. Even in this case, the metal content of the third layer 206 is lower than the metal content of the second layer 204. The metal concentration in the third layer 206 decreases as the distance from the second layer 204 increases.

  Note that when the hole injection material constituting the third layer 206 is the same as the hole injection material included in the second layer 204, the second layer 204 and the third layer 206 are continuously formed using the same vapor deposition apparatus. Can be formed. Specifically, the second layer 204 is formed by depositing a metal while depositing a hole injection material. Then, when the thickness of the formed film reaches a necessary thickness as the second layer 204, the vapor deposition of the metal is finished while continuing the vapor deposition of the hole injection material. When such a method is used, it may be difficult to confirm the interface between the second layer 204 and the third layer 206.

  Also in this embodiment, since the charge generation layer 200 includes the second layer 204, the charge generation efficiency in the charge generation layer 200 is increased as in the first embodiment. Therefore, the luminance of the light emitting unit 140 can be increased. In addition, since the third layer 206 is formed on the second layer 204, the second layer 204 (that is, a layer containing a metal) can be made thinner than in the first embodiment. By reducing the thickness of the second layer 204, the light transmittance of the charge generation layer 200 can be increased. Therefore, not only the light emission from the organic layer 120 on the second electrode 130 side of the opaque electrode on the bottom emission side described above, but also the light emission from the organic layer 120 on the first electrode 110 side reflects the opaque electrode. Since the light is extracted outside, the light extraction efficiency of the light emitting device 10 is improved.

  FIG. 11 is a graph showing the relationship between the light emission efficiency and the current density of the light emitting device 10 according to this embodiment. Here, the film thickness of the second layer 204 was changed between 2 nm and 20 nm, and the Mg volume ratio was changed between 10%, 50%, and 80%. From this graph, it can be seen that the luminous efficiency of the light emitting device 10 increases when the thickness of the second layer 204 is changed from 5 nm to 2 nm.

(Modification)
FIG. 5 is a cross-sectional view illustrating a configuration of the charge generation layer 200 included in the light emitting device 10 according to the modification. FIG. 5 corresponds to FIG. 4 of the second embodiment. The light emitting device 10 according to this embodiment has the same configuration as that of the light emitting device 10 according to the first embodiment or the second embodiment, except for the configuration of the charge generation layer 200. This figure shows a case similar to that of the second embodiment.

In the present embodiment, the first layer 202 does not contain an electron injection material. Instead, the charge generation layer 200 includes an electron injection layer 208 below the second layer 204 (for example, between the first layer 202 and the second layer 204). The electron injection layer 208 is formed using, for example, Liq. However, the electron injection layer 208 is formed using another electron injection material such as an alkali metal or alkaline earth metal oxide or fluoride such as Li ₂ O, LiF, or Li ₂ CO ₃ , or a carbonate alkali metal compound. May be.

  Also according to this modification, since the charge generation layer 200 includes the second layer 204, the charge generation efficiency in the charge generation layer 200 is increased as in the first embodiment. Therefore, the luminance of the light emitting unit 140 can be increased.

Example 1
FIG. 6 is a plan view illustrating the configuration of the light emitting device 10 according to the first embodiment. FIG. 7 is a view in which the second electrode 130 is removed from FIG. 6. FIG. 8 is a diagram in which the organic layer 120, the charge generation layer 200, and the insulating layer 150 are removed from FIG. 9 is a cross-sectional view taken along the line AA in FIG.

  In this embodiment, the light emitting device 10 is a lighting device, and includes a substrate 100 and a light emitting unit 140. The structure of the board | substrate 100 and the light emission part 140 is as the embodiment. Therefore, a plurality of organic layers 120 and a charge generation layer 200 are formed between the first electrode 110 and the second electrode 130.

  The edge of the first electrode 110 is covered with an insulating layer 150. The insulating layer 150 is made of, for example, a photosensitive resin material such as polyimide, and surrounds a portion of the first electrode 110 that becomes a light emitting region of the light emitting unit 140. By providing the insulating layer 150, it is possible to suppress a short circuit between the first electrode 110 and the second electrode 130 at the edge of the first electrode 110. The insulating layer 150 is formed, for example, by applying a resin material to be the insulating layer 150 and then exposing and developing the resin material.

  In addition, the light emitting device 10 includes a first terminal 112 and a second terminal 132. The first terminal 112 is connected to the first electrode 110, and the second terminal 132 is connected to the second electrode 130. For example, the first terminal 112 and the second terminal 132 include a layer formed of the same material as that of the first electrode 110. A lead wiring may be provided between the first terminal 112 and the first electrode 110. In addition, a lead wiring may be provided between the second terminal 132 and the second electrode 130.

  Next, a method for manufacturing the light emitting device 10 will be described. First, the first electrode 110 is formed on the substrate 100. In this step, the first terminal 112 and the second terminal 132 are also formed. Next, the insulating layer 150, the organic layer 120, the charge generation layer 200, and the second electrode 130 are formed in this order.

  Also in this example, since the charge generation layer 200 includes the second layer 204, the charge generation efficiency in the charge generation layer 200 is increased as in the first embodiment. Therefore, the luminance of the light emitting unit 140 can be increased.

  As mentioned above, although embodiment and the Example were described with reference to drawings, these are illustrations of this invention and can also employ | adopt various structures other than the above.

10 light emitting device 100 substrate 110 first electrode 120 organic layer 124 light emitting layer 130 second electrode 140 light emitting unit 200 charge generation layer 202 first layer 204 second layer 206 third layer 208 electron injection layer

Claims (7)

A first electrode;
A second electrode;
A plurality of organic layers located between the first electrode and the second electrode, each including a light emitting layer;
A charge generation layer located between two adjacent organic layers;
With
The charge generation layer includes
A first layer comprising an electron transporting material;
A second layer comprising a metal and a hole injection material;
Have
The light-emitting device, wherein the charge generation layer includes an electron injecting material between the second layer and the first layer or in the first layer. The light-emitting device according to claim 1.
The light emitting device, wherein the metal is a metal belonging to Group 2. The light-emitting device according to claim 2.
The light emitting device wherein the metal is Mg. The light emitting device according to claim 3.
The light emitting device wherein the volume content of Mg in the second layer is 50% or more. In the light-emitting device as described in any one of Claims 1-4,
The light emitting device having a thickness of the second layer of 1 nm to 10 nm. In the light-emitting device as described in any one of Claims 1-5,
The light-emitting device in which the electron injection material is included in the first layer. In the light-emitting device as described in any one of Claims 1-6,
A light emitting device having an electron injection layer containing the electron injection material between the second layer and the organic layer.

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