JP2002203677A - Photo-function element, organic el element and organic el display device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a photo-function element, an organic EL element and an organic EL display device in which an active matrix display device using a photo-function element is formed with simple structure, and which are of low cost, highly fine, and bright. SOLUTION: The photo-function element, organic EL element and organic EL display device comprise at least one or more layers of photoconductive layer 3 and luminous layer 2 between a negative electrode and a positive electrode, and have a thyristor property by the above photoconductive layer 3 and luminous layer 2.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an optical functional device, particularly an organic electroluminescent (EL) device, and a high-quality optical functional device suitable for a display device.

[0002]

2. Description of the Related Art Conventionally, in an organic EL device, a transparent electrode serving as an anode is formed on a transparent substrate in a predetermined stripe shape or the like, and an organic light emitting layer is formed thereon. Then, on the surface of the light emitting layer, MgA was applied in a direction orthogonal to the transparent electrode.
A striped cathode electrode made of a metal such as g is formed. When a voltage is applied between the transparent electrode and the cathode electrode, the intersection of the stripes formed by each electrode emits light. This is the pixel that forms the image.

A display device having such a shape is called a simple matrix, in which a cathode electrode side is used as a scanning electrode and is sequentially selected, and data of a pixel selected by each scanning line is parallel-connected to one transparent electrode. Is used. At this time, by making the scanning speed about 60 screens per second, a two-dimensional image can be displayed without flickering due to the characteristics of human eyes. At this time, the brightness of the obtained image corresponds to a value obtained by dividing the luminance output from the organic EL element at the selected time by the number of scanning lines.

On the other hand, in the case of an active matrix display device in which an organic EL element is driven by a circuit formed on a substrate, each EL pixel has a thin film transistor (TFT) for controlling a current supplied to the pixel. Like T
FTs (field effect transistors) are connected one by one. That is, a pair of a bias TFT for passing a drive current to the organic EL element and a switch TFT for indicating whether the bias TFT should be selected are connected one by one.

Conventional active matrix type organic E
An example of a circuit diagram of the L display device is shown in FIGS. The organic EL display device 50 includes a screen 51, X-direction signal lines X1, X2,..., Y-direction signal lines Y1, Y2,..., Power supply Vdd lines Vdd1, Vdd2. TFT) Ty11, Ty2, Ty2
1, 22,..., Current control transistor (TFT) M1
1, 12, M21, 22,..., Organic EL element EL110,
120, EL210, 220 ..., capacitors C11, 1
2, C21, 22,..., An X-direction peripheral drive circuit (shift register X-axis) 52, a Y-direction peripheral drive circuit (shift register Y-axis) 53, and the like.

A pixel is specified by the X-direction signal lines X1 and X2 and the Y-direction signal lines Y1 and Y2, and the switching TFT transistors Ty11, Ty12, T
The signals y21 and y22 are turned on, and the image data is held in the signal holding capacitors C11 and C12. Thereby, the current control transistors M11, M1
2, M21 and M22 are turned on, and the power lines Vdd1 and Vdd2
The organic EL elements EL110, 120, EL210,
A bias current corresponding to the image data flows through 220,
This emits light.

For example, when a signal corresponding to image data is output to the X-direction signal line X1 and a Y-direction scanning signal is output to the Y-direction signal line Y1, the switching transistor Ty11 of the specified pixel is turned on. And a current control TFT transistor M11 according to a signal corresponding to the image data.
Is conducted, and a light-emitting current corresponding to the image data flows through the organic EL element EL110 to control light emission. As described above, for each pixel, a thin-film EL element, a current control transistor for controlling light emission of the EL element, a capacitor for holding a signal connected to a gate electrode of the current control transistor, and the capacitor In an active matrix EL image display device having a switching transistor and the like for writing data to a device, the emission intensity of the EL element is controlled by a voltage stored in a signal holding capacitor, and a non-linear element for emission current control is used. (A66-in 201pi Electrol
uminescent Display TPBrody, FCLuo, et.al, IEEE Tr
ans ElectronI) evices, Vol.ED-22, No. 9, Sep. 1975, P.
739 ~ P749).

The capacity of the signal holding capacitor used at this time is equal to or less than the capacity that allows the pixel switch TFT transistor to sufficiently charge the electric charge within a minute selection time.
Further, it is required that the decrease in the holding voltage of the capacitor caused by the charge that the leak current when the pixel switch TFT transistor is not selected until the next writing time is lost does not adversely affect the image on the display panel. . At this time, since the organic EL element continues to emit light at all times, the brightness of the image obtained by the image display device of this system is the emission luminance of the organic EL element itself.

In Japanese Patent Application Laid-Open No. 2000-299192, an active element using an organic EL element realized by connecting a thyristor element formed on an insulating substrate and an organic EL element formed on a transparent substrate is disclosed separately. A matrix display is described.

In the above-described simple matrix display device, the brightness of an obtained image is reduced unless the luminance output from the organic EL element is increased during a selected time as the number of scanning lines increases.

This implies that a high-definition display device having the number of scanning lines that requires an output exceeding the maximum rating of the organic EL element while deteriorating the reliability of the organic EL element cannot be realized.

On the other hand, in an active matrix display device using a drive circuit formed on the substrate, the above-mentioned problem can be solved, but the display device becomes expensive because the TFT is expensive.

Furthermore, in an active matrix display device in which the thyristor element and the organic EL element separately provided are connected, it is difficult to manufacture a high-definition display device due to the connection accuracy. Further, when the thyristor element and the organic EL element are formed on the same substrate and then connected, the process becomes longer, the cost is increased, and the display device is also expensive.

[0014]

SUMMARY OF THE INVENTION It is an object of the present invention to form an active matrix display device using an optical function element with a simple structure, and to provide an inexpensive high-definition and bright optical function element, an organic EL element, and an organic EL display. It is to provide a device.

[0015]

To achieve the above object, the present invention is configured as follows.

(1) An optical functional device having at least one photoconductive layer and a light emitting layer between a cathode and an anode, and having a thyristor characteristic by the photoconductive layer and the light emitting layer.

(2) The optical function according to (1), wherein the photoconductive layer comprises an inorganic non-single-crystal film.

(3) The non-single-crystal film is made of Si-H, Si
-Ge-H, Si-OH, Si-C-H and Si-
The optical functional device according to the above (2), which is an amorphous or polycrystalline film of any of NH.

(4) The optical functional device according to any one of the above (1) to (3), having a P-type photoconductive layer on the cathode side and a light emitting layer on the anode side.

(5) The optical functional device according to any one of (1) to (3), having a light emitting layer on the cathode side and an N-type photoconductive layer on the anode side.

(6) The organic E in which the light emitting layer of the optical functional device according to any one of the above (1) to (5) is formed of an organic material.
L element.

(7) An organic EL display device having a plurality of the organic EL elements of (6) and operating as an active matrix.

[0023]

BEST MODE FOR CARRYING OUT THE INVENTION The optical functional device of the present invention has at least one photoconductive layer and a light emitting layer between a cathode and an anode, and has a thyristor characteristic by the photoconductive layer and the light emitting layer. is there.

As described above, since the light emitting element itself has the thyristor characteristics, a switching element, a driving circuit, and the like for driving the light emitting element become unnecessary, and an active matrix circuit can be formed without using a TFT or the like. .

The optical functional device of the present invention has thyristor characteristics due to the photoconductive layer and the light emitting layer. This thyristor characteristic is caused by a gap layer provided on the bonding surface between the photoconductive layer and the light emitting layer, or a gap layer provided on either side of the photoconductive layer or the light emitting layer, and a gap provided between the photoconductive layer and the light emitting layer. Can be obtained by layers. Here, a thyristor refers to an element that can maintain an on state and an off state without an external circuit. As such a thyristor element, for example, SC
R and Shockley diodes are known.

The operation principle of the optical functional device of the present invention will be described with reference to FIG. The device of the present invention has a structure in which the light emitting layer 2 and the photoconductive layer 3 are optically and electrically joined as shown in the illustrated example.

When a voltage is applied from the outside to the element having such a structure and an electric field is applied, a current flows when sufficient energy for the charge to cross the energy barrier in the photoconductive layer 3 is applied, and light is emitted. Light emission occurs due to recombination of electrons and holes in the layer 2. This emission includes return light 5 input to the photoconductive layer 3 in addition to the extraction light 4 extracted to the outside. The photoconductive layer has a power generation function by light, and charges are generated internally by the feedback light 5. Then, the generated charges are amplified to become a feedback current 6 and supplied to the light emitting layer 2. For this reason, the same effect as the apparent decrease in the energy barrier of the photoconductive layer 3 is obtained, and thereafter, even if the energy to be injected, that is, the voltage applied from the outside is reduced to some extent, the light emitting state is maintained.

In order to end the light emitting state, the energy applied from the outside, that is, the voltage, is set to a certain threshold value or less. When the voltage applied from the outside falls below a certain threshold value, the function of amplifying the charge generated by the photons is reduced, the feedback ratio for performing amplification cannot be maintained, and the light emitting state cannot be maintained, and the light is turned off.

Such a photoelectric feedback loop (amplification loop)
In order to maintain this, a carrier amplification mechanism is required. The mechanism for amplifying such a carrier is as follows: (1) Amplification by the avalanche effect. (2) A photoconductive layer having a carrier amplifying ability is used (for example, Me-PTC is used). (3) Apply a phototransistor. (4) A light emitting layer having a carrier amplifying ability is used. Although methods such as the above are conceivable, in the present invention, it is preferable to use amplification by the avalanche effect of (1).

When the amplification by the avalanche effect of (1) is performed, the electric charge generated by the light in the photoconductive layer 3 is accelerated by an electric field applied from the outside, and the avalanche effect is generated to generate the photocurrent 6, which is generated. It is provided to the light emitting layer again. That is, the charge derived from photons generated in the photoconductive layer 3 is:
It will be amplified by the external electric field. Since the amplifying effect by the avalanche effect is determined by the thickness of the photoconductive layer and the intensity of the electric field applied from the outside, it is easy to control and adjust.

The avalanche effect can be easily obtained by forming an interface between the light emitting layer and the photoconductive layer, an end of these layers, or a gap layer (insulating layer).

In the present invention, a photoconductive layer having a carrier amplifying ability by tunnel injection of (2) may be used (for example, Me-PTC is used).

The amplification factor necessary to maintain such a feedback loop is preferably 5 or more, particularly 6 or more, and more preferably 10 or more.

In order to maintain a photoelectric feedback loop,
Light lost by extraction, light / charge conversion efficiency, charge /
It is desirable to adjust the light conversion efficiency and the like so that the maximum efficiency can be obtained.

The photoconductive layer is not particularly limited as long as it has a photo-charge conversion function, and various inorganic and organic materials can be used. PbS-based materials such as PbS, PbSe, and PbTe; CdS
e or CdS containing impurities such as Cu and Cl
Although it is possible to use a system, InSb, or the like, Si, Ge, Ga
An amorphous semiconductor material using one or more of As and As is preferable. In particular, Si-H, Si-Ge-H,
A polycrystalline or amorphous material using one or more of Si-OH, Si-CH and Si-N-H is preferable.

Examples of the organic material include Me-PTC having a carrier amplifying ability, titanium oxide, tungsten pentoxide, strontium tungstate, niobium pentoxide, cadmium sulfide, zinc oxide, and zinc oxide used in dye-based solar cells. One or two or more known semiconductors such as tin oxide adsorbed with a dye material such as a cyanine dye, a merocyanine dye, a xanthene dye, a triphenylmethane dye, or a metal-free phthalocyanine dye are prescribed. And organic materials used in dye-based lasers.

The thickness of the photoconductive layer differs depending on the constituent materials, and may be adjusted to an optimum thickness in relation to the avalanche effect and the power supply voltage. Specifically, an energy gap is formed at the junction between the light emitting layer and the photoconductive layer, and Si-H, Si-Ge-H, Si-OH, Si-
When one or more of C—H and Si—N—H are used, 100 to 1000 nm, particularly 200 to 600 nm
It is.

The photoconductive layer may be P-type or N-type, and may have an optimum structure in designing a light-emitting layer or element to be combined.

The light-emitting layer is not particularly limited as long as it can emit light by the above-mentioned photocurrent or the like and can obtain sufficient luminous efficiency.

For example, a light emitting diode (LED), an organic EL element, or the like can be used. In the present invention, it is particularly preferable to use an organic EL element for the light-emitting layer because it can be formed by a thin-film process and is a surface light-emitting source.

The organic EL element has an organic layer containing at least an organic substance involved in a light emitting function between two electrodes. And the electrons and
The holes emit light by recombination in the organic layer.

The two electrodes, that is, the first electrode and the second electrode can be made of a normal conductive material such as Al, Ni, Cr, Ag, Au, etc., but are at least on the organic EL side. The anode or the cathode may be a hole injection electrode or an electron injection electrode.

As the electron injection electrode, a substance having a low work function is preferable. For example, K, Li, Na, Mg, La, C
e, Ca, Sr, Ba, Al, Ag, In, Sn, Z
It is preferable to use a single metal element such as n or Zr, or a two-component or three-component alloy system containing them for improving the stability. As an alloy system, for example, Ag · Mg (A
g: 0.1 to 50 at%), Al.Li (Li: 0.01)
１４14 at%), In · Mg (Mg: 50 to 80 at%),
Al.Ca (Ca: 0.01 to 20 at%) and the like. Note that the electron injection electrode can also be formed by an evaporation method or a sputtering method.

The thickness of the electron injecting electrode thin film may be a certain thickness or more for sufficiently injecting electrons.
The thickness is preferably 1 nm or more, more preferably 3 nm or more. The upper limit is not particularly limited, but the thickness may be generally about 3 to 500 nm. An auxiliary electrode or a protection electrode may be further provided on the electron injection electrode.

The pressure during the deposition is preferably from 1 × 10 ⁻⁸ to 1
The heating temperature of the evaporation source is 100 to 1400 ° C. for a metal material and 100 to 50 ° C. for an organic material at × 10 ⁻⁵ Torr.
About 0 ° C. is preferable.

The hole injection electrode is preferably a transparent or translucent electrode for extracting emitted light. As the transparent electrode, ITO (tin-doped indium oxide), IZO
(Zinc-doped indium oxide), ZnO, SnO ₂ , I
Examples include n ₂ O ₃ , and preferably ITO (tin-doped indium oxide) and IZO (zinc-doped indium oxide). ITO usually contains In ₂ O ₃ and SnO in a stoichiometric composition, but the amount of O may slightly deviate from this. When transparency is not required, the hole injection electrode may be made of a known opaque metal material.

The thickness of the hole injecting electrode may be a certain thickness or more that can sufficiently inject holes, and is preferably 5 or more.
The range is preferably from 0 to 500 nm, more preferably from 50 to 300 nm. The upper limit is not particularly limited, but if the thickness is too large, there is a fear of peeling or the like. If the thickness is too small, there is a problem in the film strength at the time of manufacturing, the hole transport ability, and the resistance value.

The hole injecting electrode layer can be formed by a vapor deposition method or the like, but is preferably a sputtering method, particularly a pulse D method.
It is preferable to form by the C sputtering method.

The organic layer of the organic EL structure can have the following configuration.

The light emitting layer has a function of injecting holes (holes) and electrons, a function of transporting them, and a function of generating excitons by recombination of holes and electrons. It is preferable to use a relatively electronically neutral compound for the light emitting layer.

The hole injecting / transporting layer has a function of facilitating the injection of holes from the hole injecting electrode, a function of stably transporting holes, and a function of hindering electrons.
The electron injection transport layer has a function of facilitating injection of electrons from the electron injection electrode, a function of stably transporting electrons, and a function of preventing holes. These layers increase and confine holes and electrons injected into the light emitting layer, optimize the recombination region, and improve luminous efficiency.

The thickness of the light emitting layer, the thickness of the hole injecting and transporting layer, and the thickness of the electron injecting and transporting layer are not particularly limited, and vary depending on the forming method.
It is preferable that the thickness be in the range of 10 to 300 nm.

The thickness of the hole injecting and transporting layer and the thickness of the electron injecting and transporting layer depend on the design of the recombination / light emitting region, but may be about the same as the thickness of the light emitting layer or about 1/10 to 10 times. When the hole or electron injection layer and the transport layer are separated from each other, it is preferable that the injection layer has a thickness of 1 nm or more and the transport layer has a thickness of 1 nm or more. At this time, the upper limit of the thickness of the injection layer and the transport layer is usually about 500 nm for the injection layer and 500 nm for the transport layer.
It is about. Such a film thickness is the same when two injection / transport layers are provided.

The light emitting layer of the organic EL device contains a fluorescent substance which is a compound having a light emitting function. Examples of such a fluorescent substance include, for example, JP-A-63-26469.
No. 2 discloses at least one compound selected from compounds such as quinacridone, rubrene, and styryl dyes. Also, Tris (8
Quinolinol derivatives such as metal complex dyes having 8-quinolinol or a derivative thereof as a ligand, such as (quinolinolato) aluminum; tetraphenylbutadiene, anthracene, perylene, coronene, and 12-phthaloperinone derivatives. Further, phenylanthracene derivatives described in JP-A-8-12600 (Japanese Patent Application No. 6-110569), tetraarylethene derivatives described in JP-A-8-12969 (Japanese Patent Application No. 6-114456), and the like are used. be able to.

Further, it is preferable to use in combination with a host substance capable of emitting light by itself, and it is preferable to use it as a dopant. In such a case, the content of the dopant in the light emitting layer is preferably 0.01 to 20% by volume, more preferably 0.1 to 15% by volume. In particular, for a rubrene-based material, the content is preferably 0.01 to 20% by volume. By using in combination with the host substance,
The emission wavelength characteristic of the host material can be changed, light emission shifted to a longer wavelength becomes possible, and the emission efficiency and stability of the device are improved.

The host substance is preferably a quinolinolato complex, and more preferably an aluminum complex having 8-quinolinol or a derivative thereof as a ligand. Such an aluminum complex is disclosed in JP-A-63-26469.
No. 2, JP-A-3-255190, JP-A-5-7707
3, JP-A-5-258859, JP-A-6-2158
No. 74 and the like.

Specifically, first, tris (8-quinolinolato) aluminum, bis (8-quinolinolato) magnesium, bis (benzo {f} -8-quinolinolato) zinc, bis (2-methyl-8-quinolinolato) aluminum Oxide, tris (8-quinolinolato) indium,
Tris (5-methyl-8-quinolinolato) aluminum, 8-quinolinolatolithium, tris (5-chloro-
8-quinolinolato) gallium, bis (5-chloro-8-
Quinolinolato) calcium, 5,7-dichloro-8-quinolinolatoaluminum, tris (5,7-dibromo-
8-hydroxyquinolinolato) aluminum and poly [zinc (II) -bis (8-hydroxy-5-quinolinyl) methane].

Other host materials are disclosed in
Phenylanthracene derivative described in JP-A-12600 (Japanese Patent Application No. 6-110569) and JP-A-8-1296
No. 9 (Japanese Patent Application No. 6-114456) is also preferable.

The light emitting layer may also serve as an electron injection / transport layer. In such a case, it is preferable to use tris (8-quinolinolato) aluminum or the like. These fluorescent substances may be deposited.

The light emitting layer is preferably a mixed layer of at least one kind of hole injecting and transporting compound and at least one kind of electron injecting and transporting compound, if necessary.
Further, it is preferable that a dopant is contained in the mixed layer. The content of the dopant in such a mixed layer is preferably 0.01 to 20% by volume, more preferably 0.1 to 15% by volume.

In the mixed layer, a hopping conduction path of carriers is formed, so that each carrier moves in a polarly advantageous substance, and carrier injection of the opposite polarity is less likely to occur, so that the organic compound is less likely to be damaged. This has the advantage that the element life is extended. Further, by including the above-described dopant in such a mixed layer, the emission wavelength characteristics of the mixed layer itself can be changed, the emission wavelength can be shifted to a longer wavelength, and the emission intensity is increased, The stability of the device can be improved.

The hole injecting and transporting compound and the electron injecting and transporting compound used in the mixed layer may be selected from the compounds for the hole injecting and transporting layer and the compounds for the electron injecting and transporting layer described below, respectively. Among them, as the compound capable of injecting and transporting holes, it is preferable to use an amine derivative having strong fluorescence, for example, a triphenyldiamine derivative which is a hole transporting material, further a styrylamine derivative, or an amine derivative having an aromatic condensed ring. .

As the compound capable of injecting and transporting electrons, it is preferable to use a quinoline derivative, furthermore a metal complex having 8-quinolinol or a derivative thereof as a ligand, particularly tris (8-quinolinolato) aluminum (Alq3). It is also preferable to use the above-mentioned phenylanthracene derivatives and tetraarylethene derivatives.

The mixing ratio of the mixed layer depends on the respective carrier mobility and carrier concentration. In general, the weight ratio of the compound of the hole injecting and transporting compound / the compound having the electron injecting and transporting function is 1/99 to less. 99/1, more preferably 10/90 to 90/10, particularly preferably 20/80 to
It is preferable that the ratio be approximately 80/20.

The thickness of the mixed layer is preferably not less than the thickness of one molecular layer and less than the thickness of the organic compound layer. Specifically, the thickness is preferably 1 to 85 nm, more preferably 5 to 60 nm, particularly preferably 5 to 50 nm.

As a method for forming the mixed layer, co-evaporation in which evaporation is performed from different evaporation sources is preferable. However, when the vapor pressures (evaporation temperatures) are the same or very close, the mixed layers are previously mixed in the same evaporation board. Alternatively, it can be deposited. In the mixed layer, it is preferable that the compounds are uniformly mixed, but in some cases, the compounds may exist in an island shape. The light-emitting layer is generally formed to a predetermined thickness by vapor-depositing an organic fluorescent substance or by dispersing and coating the resin in a resin binder.

The hole injecting and transporting layer is described in, for example,
JP-A-3-295695, JP-A-2-191694, JP-A-3-792, JP-A-5-234681
JP, JP-A-5-239455, JP-A-5-5-2
JP-A-99174, JP-A-7-126225, JP-A-7-126226, JP-A-8-100172
Various organic compounds described in JP-A No. 06509555 A1 and the like can be used. For example, a tetraarylbendicine compound (triaryldiamine or triphenyldiamine: TPD), an aromatic tertiary amine,
Examples include hydrazone derivatives, carbazole derivatives, triazole derivatives, imidazole derivatives, oxadiazole derivatives having an amino group, and polythiophene. These compounds may be used alone or in combination of two or more. When two or more kinds are used in combination, they may be stacked as separate layers or mixed.

When the hole injecting and transporting layer is divided into a hole injecting layer and a hole transporting layer, a preferable combination can be selected from the compounds for the hole injecting and transporting layer. At this time, it is preferable to laminate the compounds in order from the hole injecting electrode (ITO or the like) with the smallest ionization potential. Further, it is preferable to use a compound having a good thin film property on the surface of the hole injection electrode. Such a stacking order is the same when two or more hole injection transport layers are provided. With such a stacking order, the driving voltage is reduced, and the occurrence of current leakage and the occurrence and growth of dark spots can be prevented. In addition, in the case of forming an element, since a thin film of about 1 to 10 nm can be made uniform and pinhole-free because evaporation is used,
Even if a compound having a small ionization potential and having absorption in the visible region is used for the hole injection layer, it is possible to prevent a change in the color tone of the emission color and a decrease in efficiency due to reabsorption. The hole injecting and transporting layer can be formed by vapor deposition of the above compound in the same manner as the light emitting layer and the like.

A quinoline derivative such as an organometallic complex having 8-quinolinol such as tris (8-quinolinolato) aluminum (Alq3) or a derivative thereof as a ligand, an oxadiazole derivative, a perylene derivative, etc. A pyridine derivative, a pyrimidine derivative, a quinoxaline derivative, a diphenylquinone derivative, a nitro-substituted fluorene derivative, or the like can be used. The electron injection / transport layer may also serve as the light emitting layer. In such a case, it is preferable to use tris (8-quinolinolato) aluminum or the like. The electron injecting and transporting layer may be formed by vapor deposition or the like, similarly to the light emitting layer.

When the electron injecting and transporting layer is divided into an electron injecting layer and an electron transporting layer, a preferred combination can be selected from the compounds for the electron injecting and transporting layer. At this time, it is preferable to stack the compounds in descending order of the electron affinity value from the electron injection electrode side. Such a stacking order is the same when two or more electron injection / transport layers are provided.

For forming the hole injection transport layer, the light emitting layer and the electron injection transport layer, a uniform thin film can be formed.
It is preferable to use a vacuum deposition method. When vacuum deposition is used, the amorphous state or the crystal grain size is 0.2 μm
The following homogeneous thin film is obtained. If the crystal grain size exceeds 0.2 μm, the light emission becomes non-uniform, the driving voltage of the device must be increased, and the charge injection efficiency is significantly reduced.

The conditions for vacuum deposition are not particularly limited.
The degree of vacuum is 0 ^-4 Pa or less, and the deposition rate is 0.01 to 1 nm /
It is preferable to set it to about sec. Further, it is preferable to form each layer continuously in a vacuum. If they are formed continuously in a vacuum, impurities can be prevented from adsorbing at the interface between the layers, so that high characteristics can be obtained. Further, the driving voltage of the element can be reduced, and the occurrence and growth of dark spots can be suppressed.

In the case where a plurality of compounds are contained in one layer when a vacuum evaporation method is used to form each of these layers, it is preferable to co-deposit each boat containing the compounds by individually controlling the temperature.

In the present invention, instead of or in addition to the electron transport layer, a high-resistance inorganic electron injection / transport layer having an electron conduction path and having a function of blocking holes can be provided.

As described above, by providing a high-resistance inorganic electron injecting and transporting layer having an electron conduction path and having a function of blocking holes between the organic light emitting layer and the electron injecting electrode, the organic light emitting layer is provided. Electrons can be efficiently injected into the layer, so that the luminous efficiency can be improved and the driving voltage can be reduced. Furthermore, the thickness of the element can be reduced by providing a high-resistance inorganic electron injecting and transporting layer having an electron conduction path and a function of blocking holes.

The high resistance inorganic electron injecting and transporting layer preferably has a work function of 4 eV or less as a first component, more preferably 1 eV or less.
４4 eV, preferably Li, Na, K, Rb, C
one or more alkali metal elements selected from s and Fr, or one or more alkaline earth metal elements preferably selected from Mg, Ca and Sr, or 1 preferably selected from La and Ce Contains oxides of any one or more of the lanthanoid elements. Of these, lithium oxide, magnesium oxide, calcium oxide, and cerium oxide are particularly preferred. When these are mixed and used, the mixing ratio is arbitrary. Lithium oxide is 50 mol% in terms of Li ₂ O in these mixtures.
It is preferable to contain the above.

The high-resistance inorganic electron injection layer further contains, as a second component, at least one element selected from Zn, Sn, V, Ru, Sm and In. In this case, the content of the second component is preferably 0.2 to 40 mol%, more preferably 1 to 20 mol%. If the content is small, the electron injection function is reduced, and if the content is large, the hole blocking function is reduced. When two or more kinds are used in combination, the total content is preferably in the above range. The second component may be in a metal element state or an oxide state.

As described above, in the first component having high resistance,
As the second component, Zn, Sn, V, Ru, Sm and I
n or more elements selected from the group consisting of
By forming the conductive path at a content of 40 mol%, electrons can be efficiently injected from the electron injection electrode into the organic light emitting layer. This is considered to be due to the fact that the inclusion of the second component in the first component causes the conductive material to be present in the form of islands in the insulating material, thereby forming a hopping path for electron injection. .

In the first component, the second component is added in an amount of 0.2 to 40.
By containing mol%, the movement of holes from the organic light emitting layer to the electron injection electrode can be further suppressed, and the holes and electrons can be efficiently recombined in the organic light emitting layer. .

When a high-resistance inorganic electron injecting and transporting layer is provided, it is equivalent to a conventional organic electron injecting and transporting layer, an organic electron injecting layer, and an organic EL element having an organic electron transporting layer. In addition, higher brightness can be obtained, and the heat resistance and weather resistance are high, so the life is long, and the connectivity with the electron injection electrode, which is an inorganic material, is also good. There is also an advantage that there is less. Furthermore, unlike relatively expensive organic materials, the inorganic materials for forming the inorganic electron injecting and transporting layer are inexpensive, easily available, and easy to form. The manufacturing cost of the device can be reduced.

The resistivity of the high-resistance inorganic electron injection / transport layer is:
1-1 × 10 ¹¹ Ω · cm, especially 1 × 10 ³ -1 × 10 ⁸ Ω
・ It is cm. By setting the resistivity of the inorganic electron injecting and transporting layer in such a range, electron injection efficiency can be dramatically improved while maintaining high hole blocking properties.

The oxide of the first component usually has a stoichiometric composition, but it deviates somewhat from this, and a non-stoichiometric composition is obtained.
ry). The same applies to the oxide of the second component.

The high resistance inorganic electron injecting and transporting layer further comprises
As impurities, H, Ne used as a sputtering gas,
Ar, Kr, Xe and the like may be contained in a total of 5 at% or less.

The inorganic electron injecting and transporting layer having high and low resistance is usually in an amorphous state.

The high resistance inorganic electron injecting and transporting layer has a thickness of 0.2 to
It preferably has a thickness of 30 nm,
It is particularly preferable that the film has a thickness of 0. Even if the thickness of the high-resistance inorganic electron injecting and transporting layer is less than 0.2 nm, it is 30 nm.
, The function of electron injection cannot be sufficiently exhibited.

The high-resistance inorganic electron injecting and transporting layer can be formed by various physical or chemical thin film forming methods such as sputtering and vapor deposition, but is preferably formed by sputtering. In particular, it is preferable to form the inorganic electron injecting and transporting layer by a multi-source sputtering method in which the first component and the second component are used as targets and sputtering is performed separately. According to the multi-source sputtering method, sputtering can be performed under conditions suitable for each target. Further, an inorganic electron injecting and transporting layer can be formed by a single sputtering method using a mixed target of the first component and the second component.

When a high-resistance inorganic electron injecting and transporting layer is formed by a sputtering method, the pressure of a sputtering gas is
It is preferable to set the range of 0.1 to 1 Pascal.
As a sputtering gas, an inert gas usually used in a sputtering method, for example, Ar, Ne, Xe, K
r or the like can be used, and if necessary, nitrogen gas can be used. At the time of sputtering, an oxygen gas of 1 to 99% may be mixed in addition to these sputtering gases.

As the sputtering method, a high frequency sputtering method using an RF power source or a DC sputtering method can be used. The power of the high frequency sputtering using the RF power source is preferably in the range of 0.1 to 10 W / cm 2, The deposition rate is 0.5 to 10 nm / min.
A range of 1 to 5 nm is preferred.

The substrate temperature during film formation is about 25 to 150 ° C.

Further, the organic EL device of the present invention may have a high-resistance inorganic hole injecting and transporting layer, similarly to the high-resistance inorganic electron injecting and transporting layer.

As described above, by arranging the high-resistance inorganic hole injection / transport layer having a hole conduction path and capable of blocking electrons between the organic layer and the hole injection electrode, holes can be efficiently injected into the light emitting layer. In addition, the luminous efficiency is improved and the driving voltage is reduced. By using such a high-resistance inorganic hole injection / transport layer, an organic EL
The film thickness of the entire device can be reduced, and a thin film device having an extremely small thickness can be obtained in combination with the thinning of the color filter layer.

Preferably, a metal or semimetal oxide such as silicon or germanium is used as the main component of the high-resistance inorganic hole injecting and transporting layer, and the work function is 4.5.
forming a conductive path by containing a metal or semimetal and / or any one or more of these oxides, carbides, nitrides, silicides, and borides of eV or more, preferably 4.5 to 6 eV; Accordingly, holes can be efficiently injected from the hole injection electrode into the organic layer on the light emitting layer side. In addition, the transfer of electrons from the organic layer to the hole injection electrode can be suppressed, and the recombination of holes and electrons in the light emitting layer can be performed efficiently. Further, an organic EL device having both the advantages of the inorganic material and the advantages of the organic material can be obtained. In addition, luminance equal to or higher than that of a device having a conventional organic hole injecting layer can be obtained, and since the heat resistance and the weather resistance are high, the life is longer than that of the conventional device, and the occurrence of leaks and dark spots is reduced. Also, by using not only relatively expensive organic substances, but also inorganic materials that are inexpensive, easily available, and easy to manufacture,
Manufacturing costs can also be reduced.

The high-resistance inorganic hole injecting and transporting layer preferably has a resistivity of 1 to 1 × 10 ¹¹ Ω · cm, particularly 1 × 10 ¹¹ Ω · cm.
^{It is 3} to 1 × 10 ⁸ Ω · cm. By setting the resistivity of the high-resistance inorganic hole injection / transport layer in the above range, the hole injection efficiency can be dramatically improved while maintaining high electron blocking properties. The resistivity of the high-resistance inorganic hole injecting and transporting layer can also be determined from the sheet resistance and the film thickness. In this case, the sheet resistance can be measured by a four-terminal method or the like.

The material of the main component is an oxide of silicon or germanium. Preferably, in (Si _1-x Ge _x ) O _y , 0 ≦ x ≦ 1, 1.7 ≦ y ≦ 2.2, preferably 1 0.7 ≦ y ≦ 1.99. The main component of the high-resistance inorganic hole injecting and transporting layer may be silicon oxide or germanium oxide, or a mixed thin film thereof. If y is larger or smaller than this, the hole injection function tends to decrease. The composition may be determined by, for example, Rutherford backscattering or chemical analysis.

The high-resistance inorganic hole injecting and transporting layer further contains, in addition to the main components, oxides, carbides, nitrides, silicides, and borides of metals (including semimetals) having a work function of 4.5 eV or more. Is preferred. Work function 4.5 eV or more,
Preferably the metal at 4.5-6 eV is preferably Au, C
u, Fe, Ni, Ru, Sn, Cr, Ir, Nb, P
At least one of t, W, Mo, Ta, Pd and Co. These are generally present as metals or in the form of oxides. Moreover, these carbides, nitrides, silicides, and borides may be used. When these are mixed and used, the mixing ratio is arbitrary. Their content is preferably from 0.2 to 40 mol%, more preferably from 1 to 2 mol%.
0 mol%. If the content is less than this, the hole injection function is reduced, and if the content exceeds this, the electron blocking function is reduced. When two or more kinds are used in combination, the total content is preferably in the above range.

The oxides, carbides, nitrides, silicides and borides of the above metals or metals (including semimetals) are usually dispersed in a high-resistance inorganic hole injecting and transporting layer.
The particle size of the dispersed particles is usually about 1 to 5 nm.
It is considered that a hopping path for transporting holes between the dispersed particles as conductors via the high-resistance main component is formed.

In the high-resistance inorganic hole injecting and transporting layer, H, Ne or A used as a sputtering gas is additionally used as an impurity.
r, Kr, Xe and the like may be contained in a total of 5 at% or less.

The average value of the whole high-resistance inorganic hole injecting and transporting layer is not necessarily uniform as long as it has such a composition, and a structure having a concentration gradient in the film thickness direction may be employed.

The high-resistance inorganic hole injecting and transporting layer is usually
It is in an amorphous state.

The thickness of the high-resistance inorganic hole injecting and transporting layer is preferably 0.3 to 100 nm, more preferably 1 to 100 nm.
The thickness is preferably about 100 to 100 nm, particularly about 5 to 30 nm. Even if the high-resistance inorganic hole injecting and transporting layer is thinner or thicker, the function as the hole injecting layer cannot be sufficiently exhibited.

The method for manufacturing the above-described high-resistance inorganic hole injection / transport layer is the same as that for the above-described high-resistance inorganic electron injection / transport layer.

In the present invention, a substrate on which an element is formed is an amorphous substrate such as glass or quartz, and a crystalline substrate such as Si, GaAs, ZnSe, ZnS, Ga, or the like.
P, InP, etc., and a substrate in which a crystalline, amorphous or metal buffer layer is formed on these crystalline substrates can also be used. As the metal substrate, Mo,
Al, Pt, Ir, Au, Pd and the like can be used. Further, a resin material such as plastic or a material having flexibility can be used. The substrate material is preferably a glass substrate or a resin material. When the substrate is on the light extraction side, it is preferable that the substrate has the same light transmittance as the above-mentioned electrodes.

As the glass material, an alkali glass is preferable from the viewpoint of cost, but in addition, a glass composition such as soda lime glass, lead alkali glass, borosilicate glass, aluminosilicate glass, and silica glass is also preferable. In particular, soda glass, which has no surface treatment, can be used at low cost.

Further, in order to prevent oxidation of the organic layers and electrodes of the element, it is preferable to seal the element with a sealing plate or the like. The sealing plate adheres and seals the sealing plate using an adhesive resin layer in order to prevent moisture from entering. The sealing gas is A
An inert gas such as r, He, N ₂ or the like is preferable. Further, the moisture content of the sealing gas is preferably 100 ppm or less, more preferably 10 ppm or less, and particularly preferably 1 ppm or less. Although there is no particular lower limit for the water content, it is usually about 0.1 ppm.

Next, a method of driving an image display device using the element of the present invention will be described. First, the elements of the present invention are arranged in a matrix as shown in FIG.

Now, the elements D11 and D22 are turned on and the elements D11 and D22 are turned on.
12, D21 When trying to display an image with the lights turned off, the waveforms shown in the timing chart shown in FIG. 3 are input to the scanning electrodes Y1 and Y2 and the data electrodes X1 and X2.

Hereinafter, description will be given in chronological order. An L level voltage (for example, 0 V) is applied to all the electrodes for about 1 μs as a RESET period. This resets all the elements to the OFF state. For about 1 μs as the Y1 scanning period, the lighting voltage H1 (for example, 15 V) is input to Y1, and the hold voltage H2 (for example, 12V) is input to the other scanning electrodes. At the same time, an L level voltage (for example, 0 V) is applied to the data electrode X1,
An H level voltage (for example, 6 V) is applied to X2. At this time, the voltage applied between the organic EL elements D11 to D22 is D11 = H1-L (15V) and D12 = H1-
H (9V), D21 = H2-L (12V), D22 = H
2-H (6V). Therefore, only the organic EL element of D11 is turned on and starts lighting, and the other organic EL elements are turned off.
Keep state. A lighting voltage H1 (15 V) is applied to the Y2 scanning period during a time Y2 of about 1 μs, and a hold voltage H2 (12 V) is applied to the other scanning electrodes. At the same time, an H level voltage (6V) is applied to the data electrode X1, and an L level voltage (0V) is applied to X2. At this time, the voltage applied between the organic EL elements D11 to D22 is D11 = H2-H
(6V), D12 = H2-L (12V), D21 = H1
-H (9V), D22 = H1-L (15V). For this reason, the organic EL element of the element D22 shifts to the ON state and starts lighting. On the other hand, the organic EL element of the element D11 keeps the ON state and continues lighting, and the other organic EL elements maintain the OFF state. For about 16 ms as the HOLD period, the scanning electrode Y
1, hold voltage H2 (12V), data electrode X
1. An L level voltage (0 V) is input to X2. At this time, all the voltages applied between the organic EL elements of the elements D11 to D22 become the hold voltage H2-L (12 V), and the elements D11 and D22 keep the ON state and continue lighting. On the other hand, the elements D12 and D21 maintain the OFF state. Return to the operation again.

In the case of driving according to the above procedure, since the RESET period and the HOLD period are sufficiently longer than the scanning periods of all the scanning lines Y, the brightness of the obtained image is 10 to 10 times of the HOLD period.
0 cd / m ² , which eliminates the need to emit light with high luminance in a short period of time unlike a passive display device. Further, as described above, the fabrication of the optical functional device of the present invention is extremely simple, and the cost can be reduced. In addition, since the element of the present invention has thyristor characteristics, it is not necessary to separately form and connect thyristor elements.

The above driving conditions are merely examples, and various modifications and applications are possible without departing from the spirit of the present invention. In particular, the voltage applied during the hold period strongly depends on the thickness of the a-Si film because carriers generated by light in the a-Si film need to be amplified by a high electric field. The amplification factor required at that time is a
-It depends on the light absorption efficiency of Si and the efficiency of the organic EL element.

When an amorphous film is used for the photoconductive layer, carriers may be accumulated in the amorphous film by continuously applying a voltage to one of them, and a phenomenon in which the characteristics may change may appear. Such a change in characteristics affects the reliability of the display device. Therefore, during the reset time, a negative voltage is applied to all the Y-side electrodes, and a positive voltage is applied to all the X-side electrodes, so that the organic EL element is reverse-biased and the accumulated carriers are extracted. It is possible to relax.

When driven by the above procedure, 60
Since the number of images can be updated, it is possible to sufficiently cope with the display of a moving image.

[0112]

EXAMPLES Specific examples of the present invention will be described below. (1) As shown in FIG. 4, an ITO film 1000 is formed as an anode 102 on a transparent or translucent glass substrate 101.
Was formed by a sputtering method.

Conditions DC sputtering method Power density: 1 w / m ² Pressure: 0.4 (Pa) Ar: 50 SCCM H ₂ O: 0.5 SCCM (2) Next, as shown in FIG. The edge cover 10 having a Taber angle of 60 ° C. or less is used for patterning using a process to limit the light emitting portion.
No. 3 was formed with a resist. (3) Next, as shown in FIG. 6, a partition wall 104 for separating a cathode from elements was formed. For example, a structure having an overhang (reverse taper) as shown in the drawing can be formed by overetching the partition wall 103 using, for example, a photoresist. (4) Next, UV is applied to the substrate 101 on which the partition walls 103 are formed.
After the ozone treatment, white organic EL elements 105 were continuously formed by a vacuum evaporation method. The degree of vacuum during film formation is 1 ×
The test was performed at a pressure of 10 ⁻⁵ (Pa) to 1 × 10 ⁻⁴ (Pa) at a rate of 0.05 ° / sec to 1 ° / sec.

The organic layer 105 of the white organic EL is first formed as shown in FIG.
As shown in FIG.
{Then, the first light emitting layer prepared by adding 3% lube to triphenyldiamine (TPD) is 300}, and the second light emitting layer is doped with diphenylanthracene by a 5% distyrylarylene derivative (ID102, manufactured by Idemitsu). A film was formed at a thickness of 500 [deg.], And then trisquinolino aluminum (Alq3) for an electron injection / transport layer was formed at a thickness of 200 [deg.]. Thereafter, AgMg was formed at 50 ° as a light-transmissive cathode.

Next, a P-type a-
SiH was formed to a film thickness of 3000 °. Film formation conditions Plasma CVD method 0.1% B ₂ H ₆ / SiH ₄ : 50 SCCM Pressure: 20 (Pa) Temperature: 90 ° C. Power: 500 (w), 13.56 MHz Finally, 3000 と し て Al is deposited as electrode wiring 107 Formed.

FIG. 9 shows the IL characteristics of the thyristor-type organic EL device thus formed, and FIG. 10 shows the IL-V characteristics of 1 mm ² .

Even if the voltage applied to the organic EL element is increased later from 0 V, almost no current flows up to 14 V, and no light is emitted. However, when the applied voltage exceeded V14 V, light emission started at the same time as the current began to flow rapidly. At this point, gradually reduce the applied voltage.
The current gradually decreased until 5 V, but continued to flow, and light emission continued. When the applied voltage was lower than ５5 V, the current rapidly decreased and almost no current flowed, and light emission stopped.
Thereafter, even if the applied voltage was increased again, the current returned to a state where almost no current flowed up to １４14V.

As a result, the organic EL device of this embodiment is
ON state by applying V or more; OFF state by applying V or less 2
It can be seen that the thyristor has a stable thyristor characteristic. These characteristics were remarkably observed when the N-type photoconductive film was provided on the anode side, which is a transparent electrode, and when the P-type photoconductive film was provided on the cathode side.

Next, an image display device as shown in FIG. 2 was manufactured using the thyristor type organic EL device.

Then, D11 and D22 are turned on, and D12,
In order to display an image with D21 turned off, waveforms shown in a timing chart shown in FIG. 3 were input to Y1 and Y2 serving as scanning electrodes and X1 and X2 serving as data electrodes. First, 0 V was applied to all electrodes for about 1 μs as a RESET period. As a result, the threshold voltage becomes 5 V or less as described above, and the thyristor type organic
All the L elements were reset to the OFF state. Next, for a period of about 1 μs as the Y1 scanning period, 15 V as the lighting signal H1 was input to the scanning electrode Y1, and 12 V as the hold signal H2 was input to the other scanning electrodes. At the same time, 0 V is applied to the data electrode X1 as an L level voltage.
, X2 were applied with an H level voltage of 6V. At this time, the voltages applied between the organic EL elements D11 to D22 are D11 = 15V, D12 = 9V, and D21 = 1.
2V, D22 = 6V. For this reason, only the thyristor type organic EL element of the element D11 was turned on to start lighting, and the other organic EL elements were kept off. Next, for about 1 μs as the Y2 scanning period, 15 V as the lighting signal H1 was applied to the scanning electrode Y2, and 12 V as the hold signal H2 was applied to the other scanning electrodes. At the same time, an H level signal of 6 V, X2 is applied to the data electrode X1.
Applied an L level signal of 0V. At this time, the elements D11 to D11
The voltage applied between the organic EL elements of D22 is D11
= 6V, D12 = 12V, D21 = 9V, D22 = 15
V. Therefore, the organic EL element of D22 was turned on and started lighting. On the other hand, the organic EL element of D11 keeps the ON state and continues lighting, and the other organic EL elements are turned off.
The F state was maintained. For about 16 ms as the HOLD period, the scanning electrode Y
1, Y2 hold signal 12V, data electrodes X1, X2
L level 0V was input to the. At this time, the elements D11 to D22
All the voltages applied between the respective organic EL elements became 12 V, which is the hold voltage, and D11 and D22 kept the ON state and continued lighting. On the other hand, D12 and D21 kept the OFF state. At this time, it can be seen from FIG. 9 that the luminance of the lit organic EL elements D11 and D22 is １００100 cd / m ² . Return to the operation again.

When driven by the above procedure, RESET
Since the HOLD period is sufficiently longer than the period and all Y scanning periods, the brightness of the obtained image is ~ 100 cd of the HOLD period.
/ M ² , indicating that it is not necessary to emit light with high luminance in a short time as in a passive display device. Further, as described above, the fabrication of the organic EL device of this embodiment is extremely simple, and the cost can be reduced. In addition, since the organic EL device of this example itself has thyristor characteristics, it can be seen that the process of separately forming and connecting the thyristor device is unnecessary.

In addition, when driving according to the above-described procedure, 60 images can be updated per second, so that it can be understood that moving images can be displayed sufficiently.

[0123]

As described above, according to the present invention, the element itself has a thyristor characteristic, and an active matrix display device can be formed using the thyristor characteristic. Therefore, a high-definition, high-reliability, high-luminance image display can be realized. An apparatus can be provided. Further, the manufacturing process is simple, and a low-cost optical functional element, organic EL element, and organic EL display device can be provided.

[0124]

[Brief description of the drawings]

[0125]

FIG. 1 is a conceptual diagram showing a basic configuration of an optical functional device of the present invention.

[0126]

FIG. 2 is a wiring diagram showing a state in which the optical functional elements of the present invention are arranged in a matrix.

[0127]

FIG. 3 is a timing chart for driving the display device of FIG. 2;

[0128]

FIG. 4 is a partial cross-sectional view showing a step of manufacturing the optical functional element of the present invention.

[0129]

FIG. 5 is a partial cross-sectional view showing a step of manufacturing the optical functional element of the present invention.

[0130]

FIG. 6 is a partial cross-sectional view showing a step of manufacturing the optical functional element of the present invention.

[0131]

FIG. 7 is a partial cross-sectional view showing a step of manufacturing the optical functional element of the present invention.

[0132]

FIG. 8 is a partial cross-sectional view illustrating a manufacturing process of the optical functional element of the present invention.

[0133]

FIG. 9 is a graph showing IL characteristics of a thyristor type organic EL device according to an example of the present invention.

[0134]

FIG. 10 is a diagram showing the IL-V characteristics of 1 mm ² of the thyristor type organic EL device according to the embodiment of the present invention.

[0135]

FIG. 11 shows a conventional active matrix type organic EL.
FIG. 1 is a schematic configuration diagram illustrating an example of a circuit diagram of a display device.

[0136]

FIG. 12 is an enlarged view of a portion A in FIG. 11;

[0137]

[Explanation of symbols]

 2 light emitting layer 3 photoconductive layer 4 outgoing light 5 return light 6 return current

Continued on the front page (51) Int.Cl. ⁷ Identification symbol FI Theme coat II (reference) H05B 33/08 H01L 29/28 33/22 29/74 VE F term (reference) 3K007 AB02 AB11 AB18 BA06 CA01 CB01 DA01 DB03 EA02 EB00 5C094 AA05 AA10 AA31 AA43 AA45 AA56 BA04 BA27 CA19 DA13 DB01 DB04 EA04 EA05 EB02 FA01 FA02 FB01 FB02 FB12 FB14 GA10 GB10 5F005 BA02 BB01 FA03

Claims (7)

[Claims] 1. An optical functional device having at least one or more photoconductive layers and a light emitting layer between a cathode and an anode, wherein the photoconductive layer and the light emitting layers have thyristor characteristics. 2. The optical functional device according to claim 1, wherein said photoconductive layer comprises an inorganic non-single-crystal film. 3. The non-single-crystal film is made of Si—H, Si—Ge.
-H, Si-OH, Si-CH and Si-NH
3. The optical functional device according to claim 2, which is an amorphous or polycrystalline film. 4. The optical functional device according to claim 1, further comprising a P-type photoconductive layer on the cathode side and a light emitting layer on the anode side. 5. The optical functional device according to claim 1, further comprising a light emitting layer on the cathode side and an N-type photoconductive layer on the anode side. 6. An organic EL device according to claim 1, wherein the light emitting layer of the optical function device according to claim 1 is formed of an organic material. 7. An organic EL display device comprising a plurality of the organic EL elements according to claim 6, and operating as an active matrix.