This application is based on and claims the benefit of priority from the prior Japanese Patent Application No. 2017-010967, filed on Jan. 25, 2017, the entire contents of which are incorporated herein by reference.
An embodiment of the present invention relates to a light-emitting element, a display device including the light-emitting element, and a manufacturing method of the display device.
An EL (Electroluminescence) display device is represented as an example of a display device. An EL display device has a light-emitting element in each of a plurality of pixels formed over a substrate. A light-emitting element possesses an electroluminescence layer between a pair of electrodes (cathode and anode) and is driven by supplying a current to the pair of electrodes. A color provided by a light-emitting element is mainly determined by an emission wavelength of an emission material in an electroluminescence layer, and a variety of emission colors can be obtained by appropriately selecting an emission material. Full-color display can be realized by arranging, over a substrate, a plurality of light-emitting elements giving different emission colors. When an electroluminescence layer is mainly composed of an organic compound, a light-emitting element is called an organic light-emitting element or an organic EL element, and a display device including these elements is also called an organic EL display device.
An emission color of a light-emitting element can be also adjusted by utilizing a light-interference effect in a light-emitting element. For example, Japanese Patent Application Publication No. 2014-132525 discloses a method to improve efficiency of a light-emitting element in which light obtained from an electroluminescence layer is resonated between a pair of electrodes to increase luminance in a front direction.
An embodiment of the present invention is a display device having a first light-emitting element and a second light-emitting element. The first light-emitting element and the second light-emitting element each possess: a first electrode; a second electrode over and in contact with the first electrode; an electroluminescence layer over the second electrode; and a third electrode over the electroluminescence layer, the third electrode being shared by the first light-emitting element and the second light-emitting element. The first electrode of the first light-emitting element and the first electrode of the second light-emitting element respectively include a first metal and a second metal different from the first metal.
An embodiment of the present invention is a display device having a first light-emitting element and a second light-emitting element. The first light-emitting element and the second light-emitting element each possess: a first electrode; a second electrode over and in contact with the second electrode; an electroluminescence layer over the second electrode; and a third electrode over the electroluminescence layer, the third electrode being shared by the first light-emitting element and the second light-emitting element. The first electrodes of the first light-emitting element and the second light-emitting elements are different in thickness from each other.
Hereinafter, the embodiments of the present invention are explained with reference to the drawings. The invention can be implemented in a variety of different modes within its concept and should not be interpreted only within the disclosure of the embodiments exemplified below.
The drawings may be illustrated so that the width, thickness, shape, and the like are illustrated more schematically compared with those of the actual modes in order to provide a clearer explanation. However, they are only an example, and do not limit the interpretation of the invention. In the specification and the drawings, the same reference number is provided to an element that is the same as that which appears in preceding drawings, and a detailed explanation may be omitted as appropriate.
In the present invention, when a plurality of films is formed by processing one film, the plurality of films may have functions or rules different from each other. However, the plurality of films originates from a film formed as the same layer in the same process and has the same layer structure and the same material. Therefore, the plurality of films is defined as films existing in the same layer.
In the specification and the scope of the claims, unless specifically stated, when a state is expressed where a structure is arranged “over” another structure, such an expression includes both a case where the substrate is arranged immediately above the “other structure” so as to be in contact with the “other structure” and a case where the structure is arranged over the “other structure” with an additional structure therebetween.
In the present specification, the pixels 102 collectively mean the first pixel 102b, the second pixel 102g, and the third pixel 102r. The same is applied to other reference numbers without a subscript such as b, g, and r.
Light-emitting elements 104b, 104g, and 104r are disposed in the first to third pixels 102b, 102g, and 102r, respectively (
The first electrode 110 is disposed in each pixel 102 and configured to be independently applied with a potential. On the other hand, the second electrode 116 is continuously formed over and shared by the plurality of pixels 102 and the plurality of light-emitting elements 104. The display device 100 is configured so that a constant potential is applied to the second electrode 116. One of the first electrode 110 and the second electrode 116 functions as an anode, and the other serves as a cathode. In the present embodiment, an explanation is given to an example in which the first electrode 110 and the second electrode 116 respectively function as an anode and a cathode.
The first electrode 110 of each light-emitting element 104 possesses two layers. Specifically, the first electrode 110 of each light-emitting element 104 has a reflective electrode 112 including a metal capable of reflecting emission which is obtained from the electroluminescence layer 120 and includes visible light as well as an electrode (hereinafter, referred to as a transparent electrode) 114 which is located over the reflective electrode 112 and able to transmit the emission. More specifically, the first electrode 110b of the first pixel 102b has a reflective electrode 112b and a transparent electrode 114b, the first electrode 110g of the second pixel 102g has a reflective electrode 112g and a transparent electrode 114g, and the first electrode 110r of the third pixel 102r has a reflective electrode 112r and a transparent electrode 114r. In each of the light-emitting elements 104, the reflective electrode 112 is in direct contact with and electrically connected to the transparent electrode 114. Note that the reflective electrode 112, the transparent electrode 114, and the second electrode 116 may be independently recognized as an electrode. In this case, they are respectively called a first electrode, a second electrode, and a third electrode.
As a metal included in the reflective electrode 112, a metal such as aluminum, silver, copper, gold, molybdenum, tungsten, tantalum, and nickel and an alloy thereof are represented and are selected so that the metals included in the reflective electrodes 112b, 112g, and 112r are different from one another or one of the metals is different from the other two metals. At least one of the reflective electrodes 112b, 112g, and 112r may be structured by stacked films of these metals.
The metals included in the reflective electrodes 112b, 112g, and 112r may be selected from a variety of metals so that a reflectance of the reflective electrode 112g is lower than that of the reflective electrode 112b and equal to or higher than that of the reflective electrode 112r. In other words, the reflective electrodes 112 may be configured so that the following relationship is established:
R
1b
>R
1g
≥R
1r
where the reflectances of the reflective electrodes 112b, 112g, and 112r are R1b, R1g, and R1r, respectively. For example, the reflective electrodes 112b, 112g, and 112r may include silver, aluminum, and an alloy of molybdenum and tungsten, respectively.
The transparent electrodes 114 may include a conductive oxide capable of transmitting at least part of visible light. As a conductive oxide, indium-tin oxide (ITO), indium-zinc oxide (IZO), and the like are exemplified. Silicon may be included in the oxide.
Thicknesses of the reflective electrodes 112 may be the same or different between the first to third light-emitting elements 104b, 104g, and 104r. Similarly, thicknesses of the transparent electrodes 114 may be the same or different between the first to third light-emitting elements 104b, 104g, and 104r. When the thicknesses of the transparent electrode 114 are arranged to be the same in the all light-emitting elements 104, the manufacturing process of the display device 100 can be simplified.
The second electrode 116 may be structured as a semi-transparent and semi-reflective electrode partly reflecting and partly transmitting visible light. For example, the second electrode 116 may be formed so as to include magnesium, lithium, silver, or an alloy thereof (e.g., Mg—Ag) at a thickness which allows visible light to partly pass therethrough. The thickness thereof may be selected in a range from 5 nm to 100 nm.
A partition wall 106 is disposed between the first electrodes 110 of the adjacent pixels 102. The partition wall 106 is an insulating film and covers edge portions of the first electrodes 110. With this structure, steps caused by the edge portions of the first electrodes 110 are retrieved, and the electroluminescence layer 120 and the second electrode 116 formed thereover can be prevented from being disconnected by the steps.
The electroluminescence layer 120 is formed so as to be in contact with and cover the first electrodes 110 and the partition wall 106. The second electrode 116 is disposed so as to be in contact with the electroluminescence layer 120. In the specification and claims, the electroluminescence layer 120 means the films sandwiched by the first electrode 110 and the second electrode 116.
The structure of the electroluminescence layer 120 may be arbitrarily determined. In the display device 100 shown in
The hole-injection layer 122 has a function to promote hole injection to the electroluminescence layer 120 from the first electrode 110. The hole-injection layer 122 may be provided so as to be in contact with the first electrodes 110 and the partition wall 106. For the hole-injection layer 122, a compound to which holes are readily injected, that is, a compound readily oxidized (i.e., electron-donating compound) can be used. In other words, a compound whose level of the highest occupied molecular orbital (HOMO) is shallow can be used. For example, an aromatic amine such as a benzidine derivative and a triarylamine, a carbazole derivative, a thiophene derivative, a phthalocyanine derivative such as copper phthalocyanine, and the like can be used. Alternatively, a polymer material such as polythiophene, polyaniline, or a derivative thereof may be used. Poly(3,4-ethylenedioxydithiophene)/poly(styrenesulfonic acid) is represented as an example. A mixture of an electron-donating compound such as the aforementioned aromatic amine, carbazole derivative, or aromatic hydrocarbon with an electron acceptor may be used. As an electron acceptor, a transition-metal oxide such as vanadium oxide and molybdenum oxide, a nitrogen-containing heteroaromatic compound, an aromatic compound having a strong electron-withdrawing group such as a cyano group, and the like are represented.
The hole-transporting layer 124 has a function to transport holes injected to the hole-injection layer 122 to the emission layer 126, and a material the same as or similar to the material usable in the hole-injection layer 122 can be used. For example, it is possible to use a material having a deeper HOMO level than that of the hole-injection layer 122 and having a difference in HOMO level from the hole-injection layer 122 by approximately 0.5 eV or less. Typically, an aromatic amine such as a benzidine derivative can be used.
The emission layer 126 may be formed with a single compound or have the so-called host-guest type structure. In the case of the host-guest type structure, a stillbene derivative, a condensed aromatic compound such as an anthracene derivative, a carbazole derivative, a metal complex including a ligand having a benzoquinolinol as a basic skeleton, an aromatic amine, a nitrogen-containing heteroaromatic compound such as a phenanthroline derivative, and the like can be used as a host material, for example. A guest functions as an emission material, and a fluorescent material such as a coumarin derivative, a pyran derivative, a quinacridone derivative, a tetracene derivative, a pyrene derivative, and an anthracene derivative, or a phosphorescent material such as an iridium-based orthometal complex can be used. When the emission layer 126 is configured with a single compound, the above host material can be used as an emission material.
As shown in
The electron-transporting layer 128 has a function to transport electrons injected from the second electrode 116 through the electron-injection layer 130 to the emission layer 126. For the electron-transporting layer 128, a compound readily reduced (i.e., electron-accepting compound) can be used. In other words, a compound whose level of the lowest unoccupied molecular orbital (LUMO) is deep can be used. For example, a metal complex including a ligand having a benzoquinolinol as a basic skeleton, such as tris(8-quinolinolato)aluminum and tris(4-methyl-8-quinolinolato)aluminum, a metal complex including a ligand having an oxathiazole or thiazole as a basic skeleton, and the like are represented. In addition to these metal complexes, a compound with an electron-deficient heteroaromatic ring, such as an oxadiazole derivative, a thiazole derivative, a triazole derivative, and a phenanthroline derivative, can be used.
For the electron-injection layer 130, a compound which promotes electron injection to the electron-transporting layer 128 from the second electrode 116 can be used. For example, a mixture of a compound usable in the electron-transporting layer 128 with an electron donor such as lithium or magnesium can be used. Alternatively, an inorganic compound such as lithium fluoride and calcium fluoride may be used.
In the present specification and claims, a region from an upper surface of the first electrode 110 to a bottom surface of the emission layer 126 is defined as a hole-transporting region, and a region from an upper surface of the emission layer 126 to a bottom surface of the second electrode 116 is defined as an electron-transporting region. The hole-injection layer 122 and the hole-transporting layer 124 are included in the hole-transporting region, while the electron-transporting layer 128 and the electron-injection layer 130 are included in the electron-transporting region. Therefore, the electroluminescence layer 120 is structured with the hole-transporting region, the emission layer 126, and the electron-transporting region. When a layer (e.g., the hole-transporting layer 124 or the electron-transporting layer 128) other than the emission layer 126 functions as an emission layer, the electroluminescence layer 120 is structured with the hole-transporting region and the electron-transporting region.
When a potential difference is provided between the first electrode 110 and the second electrode 116, holes and electrons are injected to the electroluminescence layer 120 from the former and the latter, respectively. Holes are transported to the emission layer 126 through the hole-injection layer 122 and the hole-transporting layer 124, while electrons are transported to the emission layer 126 through the electron-injection layer 130 and the electron-transporting layer 128. Holes and electrons are recombined in the emission layer 126, by which an excited state of the emission material included in the emission layer 126 is produced. When the excited state relaxes to a ground state, light having a wavelength corresponding to an energy difference between the excited state and the ground state is radiated and observed as the light emission from each light-emitting element 104.
Each layer included in the electroluminescence layer 120 may be formed by applying a wet-type film-formation method such as an ink-jet method, a spin-coating method, a printing method, and a dip-coating method or a dry-type film-formation method such as an evaporation method.
Detailed structures of the light-emitting elements 104 are illustrated in
When an odd multiple of one fourth of λ (λ/4) is the same as or close to the optical distance L where λ is an emission peak wavelength of the electroluminescence layer 120, the light having this wavelength λ is inconsistent with the optical distance L and attenuated. On the other hand, when an integral multiple of one half of λ (λ/2), that is, an integral multiple of a half wavelength is the same as or close to the optical distance L, the light having this wavelength λ is consistent with the optical distance L and amplified. Therefore, the thickness of each layer in the electroluminescence layer 120 and the thickness of the transparent electrode 114 may be controlled so that the optical distance L is an integral multiple of λ/2 in each of the first to third light-emitting elements 104b, 104g, and 104r. It is not necessary to arrange the optical distance L to completely match an integral multiple of λ/2, and the thickness of each layer in the electroluminescence layer 120 and the thickness of the transparent electrode 114 may be controlled so that the optical distance L ranges from 0.8 times to 1.2 times as long as an integral multiple of λ/2.
A plane in which light is mainly generated in the emission layer 126 is defined as an emission plane. The light emission is suppressed when this plane is located at an anti-node of the interfering light, while the light emission is amplified when the emission plane is located at a node. Specifically, the light emission is attenuated in a case where an optical distance d from the emission plane to the upper surface of the reflective electrode 122 or an optical distance from the emission plane to the bottom surface of the second electrode 116 is an odd multiple of one fourth of λ (λ/4). On the other hand, the light emission is amplified when the optical distance d from the emission plane to the upper surface of the reflective electrode 122 or the optical distance from the emission plane to the bottom surface of the second electrode 116 is an integral multiple of one half of λ (λ/2). Therefore, the thickness of each layer in the electroluminescence layer 120 and the thickness of the transparent electrode 114 may be controlled so that the optical distance d is an integral multiple of λ/2 in each of the first to third light-emitting elements 104b, 104g, and 104r. Note that it is not necessary to arrange the optical distance d to completely match an integral multiple of λ/2, and the thickness of each layer in the electroluminescence layer 120 and the thickness of the transparent electrode 114 may be controlled so that the optical distance d ranges from 0.8 times to 1.2 times as long as an integral multiple of λ/2. It is not always easy to determine the position of the emission plane. Hence, the thickness of each layer in the electroluminescence layer 120 and the thickness of the transparent electrode 114 may be controlled so that an optical distance from the upper surface of the reflective electrode 112 to a point arbitrarily selected in the emission layer 126 is an integral multiple of λ/2.
Moreover, a reflectance R2 of the second electrode 116 may be adjusted by appropriately selecting a material or adjusting a thickness thereof.
According to the traditional design concept, the resonance in a light-emitting element is controlled by appropriately adjusting these parameters, i.e., the optical distance L of the resonance structure formed in a light-emitting element, the optical distance d from the emission plane to the upper surface of the reflective electrode, the emission peak wavelength of the emission layer, and the reflectance R2 of the second electrode, by which intensity, a full-width half-maximum, and color purity of the emission extracted from the light-emitting element 104 are controlled and improved. However, although the control of only these parameters realizes an increase of emission intensity in a front direction and a decrease of a full-width half-maximum, viewing-angle dependence is contrarily decreased, resulting in a significant reduction in luminance and a considerable change in emission color when a viewing angle is increased. Additionally, a difference in viewing-angle dependence of the emission intensity and the emission wavelength is caused between the light-emitting elements with different structures. For example, as schematically demonstrated by the left diagram of
The difference in behavior between the first to third light-emitting elements 104b, 104g, and 104r is caused by the increase in viewing-angle dependence of emission intensity with decreasing emission wavelength. The emission intensity Ecav(λ) of the light-emitting element 104 is expressed by the following equation:
where Enc(λ) is the emission intensity of the light-emitting element 104 in the absence of a resonance structure, and ϕ1 and ϕ2 are wavelength-dependent phase changes on reflection at the reflective electrode 112 and the second electrode 116, respectively. Other variables are described above. As revealed by this equation, the terms including the angle θ increase with decreasing λ, resulting in the viewing-angle dependence of the emission intensity between the light-emitting elements 104 having different emission colors.
The inventor focused on a fact that the variables relating to the angle θ include not only the emission peak wavelength λ and the reflectance R2 of the second electrode 116 but also the reflectance R1 of the reflective electrode 112. When the reflectance R2 of the second electrode 116 is constant, the contribution of the angle θ is decreased with decreasing reflectance R1 of the reflective electrode 112, resulting in a reduction of the viewing-angle dependence. However, if the reflectances R1b, R1g, and R1r of the reflective electrodes 112 are the same in all of the first to third light-emitting elements 104b, 104g, and 104r, the viewing-angle dependence cannot be canceled because the emission wavelengths of these light-emitting elements 104 are different. On the basis of this consideration, the inventor found that not only the viewing angle dependence can be decreased but also the behavior of the change of the emission intensity with the viewing angle can be the same in all of the light-emitting elements 104 by independently controlling the reflectances R1b, R1g, and R1r of the reflective electrodes 112 so as to correspond to the emission wavelengths of the light-emitting elements 104b, 104g, and 104r.
Specifically, in addition to the parameters including the optical distance L, the optical distance d, the emission peak wavelength λ, and the reflectance R2 of the second electrode 116, the reflectances R1 of the reflective electrodes 112 are individually changed for the light-emitting elements 104 giving different emission colors as described above. Accordingly, as demonstrated by the left diagram in
In the present embodiment, display devices 170 and 172 with different structures from those of the display device 100 of the First Embodiment are explained. An explanation of the structures the same as those of the First Embodiment may be omitted.
As shown in
A material included in the optical adjustment layer 140 can be selected from materials having a refractive index higher than that of the second electrode 116. Specifically, a material with a high transmittance and a relatively high refractive index in the visible region is represented. As an example of such a material, an organic compound is given. As an organic compound, a polymer material is representative, and a polymer material including sulfur, halogen, or phosphorous is exemplified. As a polymer including sulfur, a polymer having a substituent such as a thioether, a sulfone, and a thiophene in the main or side chain is given. As a polymer material including phosphorous, a polymer material including a phosphorous acid, a phosphoric acid, or the like in the main or side chain, a polyphosphazene, or the like is represented. As a polymer material including halogen, a polymer material including bromine, iodine, or chlorine as a substituent is exemplified. The polymer material may be intermolecularly or intramolecularly cross-linked.
As another example, an inorganic material is represented, and titanium oxide, zirconium oxide, chromium oxide, aluminum oxide, indium oxide, ITO, IZO, lead sulfide, zinc sulfide, silicon nitride, and the like are exemplified. A mixture of the inorganic compound and the polymer material may be used.
The optical adjustment layer 140 further possesses a function to allow the light passing through the second electrode 116 to interfere therein. Therefore, a thickness of the optical adjustment layer 140 may be varied between the first to third pixels 102b, 102g, and 102r. For example, as demonstrated by the display device 172 shown in
Similar to the First Embodiment, the reflectances R1 of the reflective electrodes 112 are different between the first to third light-emitting elements 104b, 104g, and 104r in the display devices 170 and 172. Therefore, it is possible to provide the light-emitting elements 104 having low viewing-angle dependence and excellent color purity of the emitted light. Moreover, the use of such light-emitting elements 104 allows production of a display device having small viewing-angle dependence and high color reproducibility.
In the present embodiment, display devices 174 and 176 different in structure from those of the display devices 100, 170, and 172 of the First and Second Embodiments are explained. An explanation regarding the structures the same as those of the First and Second Embodiments may be omitted.
A schematic cross-sectional view of the display device 174 is shown in
As described in the First Embodiment, the light emission is attenuated when the optical distance d from the emission plane to the upper surface of the reflective electrode 112 is an odd multiple of one fourth of the emission peak wavelength λ (λ/4) of the emission layer 126, while the light emission is amplified when the optical distance d is an integral multiple of one half of the emission peak wavelength λ (λ/2). As demonstrated by the display device 174, the thickness of the emission layer 126 is controlled in each light-emitting element 104, by which the optical distance d can be adjusted and optimized in each pixel 102. For example, the optical adjustment can be accomplished by arranging the thickness of the emission layer 126g to be larger than the thickness of the emission layer 126b and smaller than the thickness of the emission layer 126r.
In the display device 176, thicknesses of the hole-transporting regions are further different between the pixels 102. As shown in
Similar to the First Embodiment, the reflectances R1 of the reflective electrodes 112 are different between the first to third light-emitting elements 104b, 104g, and 104r in the display device 174 and 176. Therefore, it is possible to provide the light-emitting elements 104 having low viewing-angle dependence and excellent color purity of the emitted light. Moreover, the use of such light-emitting elements 104 allows production of a display device having small viewing-angle dependence and high color reproducibility.
In the present embodiment, a display device 180 different in structure from those of the display devices 100, 170, 172, 174, and 176 of the First to Third Embodiments is explained. An explanation regarding the structures the same as those of the First to Third Embodiments may be omitted.
Similar to the display device 100, the first electrode 110 of each light-emitting element 104 of the display device 180 has the reflective electrode 112 and the transparent electrode 114 over the reflective electrode 112 as shown in
T
b
>T
g
≥T
r
where the thicknesses of the reflective electrodes 112b, 112g, and 112r are respectively Tb, Tg, and Tr. The metals included in the reflective electrodes 112 can be selected from the metals exemplified in the First Embodiment.
The thickness Tb is selected so that the light generated in the emission layer 126b does not pass through the reflective electrode 112 and a reflectance as high as possible can be obtained in the first light-emitting element 104b. For example, the thickness Tb is equal to or more than 100 nm and equal to or less than 300 nm or equal to or more than 120 nm and equal to or less than 200 nm, and typically 130 nm. On the other hand, the thickness Tr is selected so that the reflectance of the reflective electrode 112r is decreased by allowing part of the light generated in the emission layer 126r to pass through the reflective electrode 112r in the third light-emitting element 104r. For example, the thickness Tr is equal to or more than 10 nm and equal to or less than 80 nm or equal to or more than 30 nm and equal to or less than 60 nm, and typically 50 nm. Similar to the third pixel 102r, the thickness Tg is selected so that the reflectance of the reflective electrode 112g is decreased by allowing part of the light generated in the emission layer 126g to pass through the reflective electrode 112g in the second light-emitting element 104g. However, the thickness of Tg is selected so that the reflectance of the reflective electrode 112g is equal to or higher than the reflectance of the reflective electrode 112r and smaller than the reflectance of the reflective electrode 112b. For example, the thickness Tg is equal to or more than 30 nm and equal to or less than 100 nm or equal to or more than 50 nm and equal to or less than 80 nm, and typically 70 nm. Hence, the following relationships are established:
R
1b
>R
1g
≥R
1r
T
1r
≥T
1g
≥T
1g
where the reflectances of the reflective electrodes 112b, 112g, and 112r are respectively R1b, R1g, and R1r and the transmittances thereof are respectively T1b, T1g, and T1r. T1g may be 0 (zero).
Accordingly, similar to the First Embodiment, the behavior of the change of the emission intensity can be the same between the first to third light-emitting elements 104b, 104g, and 104r in the display device 180 even if the angle θ is varied. Moreover, the dependence of the chromaticity of x and y on angle θ can be decreased in the first to third light-emitting elements 104b, 104g, and 104r. As a result, it is possible to provide the light-emitting elements 104 having low viewing-angle dependence and excellent color purity of the emitted light. Moreover, the use of such light-emitting elements 104 allows production of a display device having small viewing-angle dependence and high color reproducibility.
In the present embodiment, a manufacturing method of the display device 170 is explained. An explanation of the structures the same as those of the First to Fourth Embodiments may be omitted.
One or all of the scanning-line driver circuits 206 and the data-line driver circuit 208 may not be directly formed over the substrate 200. A driver circuit formed over a substrate (e.g., semiconductor substrate) different from the substrate 200 may be mounted on the substrate 200 or the connector, and the pixels 102 may be controlled with the driver circuit. In
The substrate 200 and the opposing substrate 202 may be a substrate without flexibility or a substrate having flexibility. A structure may be employed in which a resin film or an optical film such as a circular polarizing plate is bonded instead of the opposing substrate 202. There is no particular limitation to the arrangement of the pixels 102, and a stripe arrangement, a delta arrangement, and the like may be applied.
First, as shown in
When flexibility is provided to the display device 100, a base material (not illustrated) is formed over the substrate 200, and then the base film 212 is provided. In this case, the substrate 200 may be called a supporting substrate or a carrier substrate. The base material is an insulating film with flexibility and may include a material selected from polymer materials exemplified by a polyimide, a polyamide, a polyester, and a polycarbonate. The base material can be formed by applying a wet-type film-forming method such as a printing method, an ink-jet method, a spin-coating method, and a dip-coating method or a lamination method.
The base film 212 is a film having a function to prevent impurities such as an alkaline metal from diffusing to the transistor 220 and the like from the substrate 200 (and the base material) and may include a silicon-containing inorganic compound such as silicon nitride, silicon oxide, silicon nitride oxide, and silicon oxynitride. The base film 212 can be formed to have a single-layer or stacked-layer structure by applying a chemical vapor deposition method (CVD method), a sputtering method, or the like.
Next, a semiconductor film 222 is formed (
When the semiconductor film 222 includes silicon, the semiconductor film 222 may be prepared with a CVD method by using a silane gas and the like as a raw material. A heat treatment or application of light such as a laser may be performed on amorphous silicon obtained to conduct crystallization. When the semiconductor film 222 includes an oxide semiconductor, the semiconductor film 222 can be formed by utilizing a sputtering method and the like.
Next, a gate insulating film 214 is prepared so as to cover the semiconductor film 222 (
Next, a gate (gate electrode) 224 is formed over the gate insulating film 214 with a sputtering method or a CVD method (
Next, an interlayer film 216 is formed over the gate 224 (
Next, etching is performed on the interlayer film 216 and the gate insulating film 214 to form openings 228 reaching the semiconductor film 222 (
Next, a metal film is formed to cover the openings 228 and processed with etching to form a source/drain (source/drain electrodes) 226 (
Next, a leveling film 230 is formed so as to cover the transistor 220 (
After that, etching is performed on the leveling film 230 to form an opening 234 exposing one of the source/drain 226 of the transistor 220 (
Next, a metal film is formed over the leveling film 230 and processed with etching to form one of the electrodes 242 of the supplementary capacitance 240 (
Next, an insulating film 244 is formed over the leveling film 230 and the electrode 242 (
Next, the reflective electrode 112g of the first electrode 110 is formed to cover the opening 236 as shown in
Next, the reflective electrode 112b of the first pixel 102b is formed as shown in
Next, the transparent electrodes 114 are fabricated so as to cover the reflective electrodes 112b, 112g, and 112r (
In the present embodiment, an example is demonstrated in which the transparent electrodes 114b, 114g, and 114r are formed after forming the reflective electrodes 112b, 112g, and 112r. However, the formation order of these electrodes is not limited. For example, the reflective electrode 112 and the transparent electrode 114 of one pixel 102 is first fabricated, and then the reflective electrodes 112 and the transparent electrodes 114 of other pixels 102 may be sequentially formed. In this case, the reflective electrodes 112 and the transparent electrodes 114 can be sequentially formed, by which oxidation of surfaces of the reflective electrodes 112 can be inhibited.
The supplementary capacitor 240 is formed by the first electrode 110, the insulating film 244, and the electrode 242. A potential of the gate 224 of the transistor 220 can be maintained for a longer time by forming the supplementary capacitor 240. The structure of the first electrode 110 is the same as that described in the First Embodiment, and the first electrode 110 can be formed by using a sputtering method, a CVD method, or the like.
Next, the partition wall 106 is formed so as to cover the edge portions of the first electrodes 110 (
Next, the electroluminescence layer 120 and the second electrode 116 are formed so as to cover the first electrodes 110 and the partition wall 106. The structures of these elements are the same as those described in the First Embodiment. Specifically, the hole-injection layer 122 is first formed to cover the transparent electrodes 114 of the first electrodes 110 and the partition wall 106, and then the hole-transporting layer 124 is prepared over the hole-injection layer 122 (
Although not shown, it is possible to prepare the emission layer 126 so as to have the same structure and the same material in the first to third pixels 102b, 102g, and 102r. In this case, the emission layer 126 is prepared continuously in the first to third pixels 102b, 102g, and 102r and shared by the first to third pixels 102b, 102g, and 102r. In this case, the emission layer 126 may be configured to give white emission.
The electron-transporting layer 128 and the electron-injection layer 130 are successively formed over the emission layers 126, and the second electrode 116 is fabricated over the electron-injection layer 130 (
Next, the optical adjustment layer 140 is formed over the second electrode 116 (
The display device 170 may having a passivation film (sealing film) and the like as an optional structure. The passivation film may be composed of a single layer or a plurality of layers. For example, the passivation film 160 in which a first layer 162, a second layer 164, and a third layer 166 are stacked may be formed as shown in
In this case, the first layer 162 is first formed over the optical adjustment layer 140. The first layer 162 may include a silicon-containing inorganic compound or the like and may be prepared with a CVD method or a sputtering method, for example.
Next, the second layer 164 is formed. The second layer 164 may contain an organic resin including an acrylic resin, a polysiloxane, a polyimide, a polyester, and the like. Furthermore, as shown in
After that, the third layer 168 is formed. The third layer 168 may have the same structure as the first layer 162 and can be formed with the same method as that of the first layer 162. Through these processes, the passivation film 160 is fabricated. When the passivation film 160 is a single layer, the passivation film 160 can be formed with a material the same as that of the first layer 162. When the passivation film 160 is composed of a plurality of layers, the uppermost layer and the lowest layer may be formed with a material the same as that of the first layer 162.
After that, the opposing substrate 202 is fixed through the adhesion layer 250 (
Although not shown, a polarizing plate (circular polarizing plate) may be formed instead of the opposing substrate 202 as described above. Alternatively, a polarizing plate may be arranged over or under the opposing substrate 202. In addition, an electrode, a functional film including an electrode, or a functional substrate (e.g., a touch panel) may be disposed.
As described above, in the display devices disclosed in the present specification, the reflectances of the reflective electrodes 112 are individually varied in the light-emitting elements 104. Therefore, even if the emission intensity of the light-emitting elements 104 is changed with the change of the angle θ, the behavior of this change can be the same between the first to third light-emitting elements 104b, 104g, and 104r. Moreover, the dependence of the chromaticity of x and y on angle θ can be decreased in each light-emitting element 104. As a result, it is possible to provide the light-emitting elements 104 having low viewing-angle dependence and excellent color purity of the emitted light. Moreover, the use of such light-emitting elements 104 allows production of a display device having small viewing-angle dependence and high color reproducibility.
The aforementioned modes described as the embodiments of the present invention can be implemented by appropriately combining with each other as long as no contradiction is caused. Furthermore, any mode which is realized by persons ordinarily skilled in the art through the appropriate addition, deletion, or design change of elements or through the addition, deletion, or condition change of a process is included in the scope of the present invention as long as they possess the concept of the present invention.
In the specification, although the cases of the organic EL display device are exemplified, the embodiments can be applied to any kind of display devices of the flat panel type such as other self-emission type display devices, liquid crystal display devices, and electronic paper type display device having electrophoretic elements and the like. In addition, it is apparent that the size of the display device is not limited, and the embodiment can be applied to display devices having any size from medium to large.
It is properly understood that another effect different from that provided by the modes of the aforementioned embodiments is achieved by the present invention if the effect is obvious from the description in the specification or readily conceived by persons ordinarily skilled in the art.
Number | Date | Country | Kind |
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2017-010967 | Jan 2017 | JP | national |