Patent Application
20230172057
This application claims the priority of Chinese patent application No. 202111452323.0, filed on Nov. 30, 2021, the entirety of which is incorporated herein by reference.
The present disclosure generally relates to the field of organic electroluminescent material technology and, more particularly, relates to a heterocyclic compound containing heteroatom substituted fluorene and an optoelectronic device.
According to a direction of light emitted by an organic light-emitting layer, organic light-emitting diode (OLED) display can be divided into a bottom-emitting OLED display and a top-emitting OLED display. In the bottom-emitting OLED display, light emits towards a direction facing the substrate, a reflective electrode is formed over the organic light-emitting layer, and a transparent electrode is formed under the organic light-emitting layer. If the OLED display is an active matrix OLED display, a portion of the thin film transistors formed therein does not transmit light, such that a light-emitting area is reduced. On the other hand, in the top-emitting OLED display, the transparent electrode is formed over the organic light-emitting layer, and the reflective electrode is formed under the organic light-emitting layer, such that light emits towards a direction opposite to the substrate, thereby increasing the light transmission area and improving the brightness.
Currently, a refractive index of an OLED device cannot meet market demand, and the light extraction effect is insufficient. The difference in measured refractive indices for respective wavelength regions of the blue light, green light, and red light is substantially large. Therefore, not all the light emitted by the blue, green, and red light-emitting devices can simultaneously obtain the high light extraction efficiency.
In view of the low light extraction efficiency of an existing OLED device, a capping layer (CPL), e.g., a light extraction material, needs to be added in the device structure. According to the principles of optical absorption and refraction, a refractive index of a material of the surface capping layer is as high as possible.
One aspect of the present disclosure provides a heterocyclic compound containing heteroatom substituted fluorene. The heterocyclic compound includes a structure in Formula I:
where Y is selected from O or S; at least one of X1, X2, X3, X4, X5, X6, X7 and X8 is a N atom, and rest are CR2; L1, L2, and L3 are independently selected from single bond, substituted or unsubstituted aromatic groups; Ar1 and Ar2 are independently selected from substituted or unsubstituted aromatic groups or heteroaryl groups; R1 is selected from a hydrogen atom, a deuterium atom, or an aromatic group or a heteroaryl group condensed with adjacent groups; and R2 is selected from a hydrogen atom, a deuterium atom, a substituted or unsubstituted C1-C5 alkyl group, a halogen, a cyano group, or an amino group.
Another aspect of the present disclosure provides a display panel. The display panel includes an organic light-emitting device. The organic light-emitting device includes an anode, a cathode, and an organic thin layer disposed between the anode and the cathode. The cathode is covered with a capping layer, and the capping layer includes any one or a combination of at least two of heterocyclic compounds. Each heterocyclic compound includes a structure in Formula I:
where Y is selected from O or S; at least one of X1, X2, X3, X4, X5, X6, X7 and X8 is a N atom, and rest are CR2; L1, L2, and L3 are independently selected from single bond, substituted or unsubstituted aromatic groups; Ar1 and Ar2 are independently selected from substituted or unsubstituted aromatic groups or heteroaryl groups; R1 is selected from a hydrogen atom, a deuterium atom, or an aromatic group or a heteroaryl group condensed with adjacent groups; and R2 is selected from a hydrogen atom, a deuterium atom, a substituted or unsubstituted C1-C5 alkyl group, a halogen, a cyano group, or an amino group.
Another aspect of the present disclosure provides a display device. The display device includes a display panel. The display panel includes an organic light-emitting device. The organic light-emitting device includes an anode, a cathode, and an organic thin layer disposed between the anode and the cathode. The cathode is covered with a capping layer, and the capping layer includes any one or a combination of at least two of heterocyclic compounds. Each heterocyclic compound includes a structure in Formula I:
where Y is selected from O or S; at least one of X1, X2, X3, X4, X5, X6, X7 and X8 is a N atom, and rest are CR2; L1, L2, and L3 are independently selected from single bond, substituted or unsubstituted aromatic groups; Ar1 and Ar2 are independently selected from substituted or unsubstituted aromatic groups or heteroaryl groups; R1 is selected from a hydrogen atom, a deuterium atom, or an aromatic group or a heteroaryl group condensed with adjacent groups; and R2 is selected from a hydrogen atom, a deuterium atom, a substituted or unsubstituted C1-C5 alkyl group, a halogen, a cyano group, or an amino group.
Other aspects of the present disclosure can be understood by those skilled in the art in light of the description, the claims, and the drawings of the present disclosure.
To more clearly illustrate the embodiments of the present disclosure, the drawings will be briefly described below. The drawings in the following description are certain embodiments of the present disclosure, and other drawings may be obtained by a person of ordinary skill in the art in view of the drawings provided without creative efforts.
Reference will now be made in detail to exemplary embodiments of the disclosure, which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or the alike parts. The described embodiments are some but not all of the embodiments of the present disclosure. Based on the disclosed embodiments, persons of ordinary skill in the art may derive other embodiments consistent with the present disclosure, all of which are within the scope of the present disclosure.
Similar reference numbers and letters represent similar terms in the following FIGURES, such that once an item is defined in one FIGURE, it does not need to be further discussed in subsequent FIGURES.
The present disclosure provides a heterocyclic compound containing heteroatom substituted fluorene. The heterocyclic compound containing heteroatom substituted fluorene may have a structure shown in Formula I:
where Y may be selected from O or S; at least one of X1, X2, X3, X4, X5, X6, X7 and X8 may be a N atom, and the rest may be CR2; L1, L2, and L3 may be independently selected from single bond, substituted or unsubstituted aromatic groups; Ar1 and Ar2 may be independently selected from substituted or unsubstituted aromatic groups or heteroaryl groups; R1 may be selected from a hydrogen atom, a deuterium atom, or an aromatic group or a heteroaryl group condensed with adjacent groups; and R2 may be selected from a hydrogen atom, a deuterium atom, a substituted or unsubstituted C1-C5 alkyl group, a halogen, a cyano group, or an amino group.
The present disclosure provides a heterocyclic compound containing heteroatom substituted fluorene and an optoelectronic device. The prepared heterocyclic compound may have a substantially high refractive index in the entire visible light region. The difference in measured refractive indices of the heterocyclic compound for respective wavelength regions of blue light, green light, and red light may be substantially small, and the light extraction efficiency of the heterocyclic compound in a blue light device, a green light device and a red light device may be substantially high, thereby achieving a substantially high device efficiency. In the present disclosure, by introducing heteroatom substituted fluorene in the molecular structure, although the molecular volume change is substantially small, the polarizability of the molecule may be greatly improved, which may comprehensively improve the refractive index of the heterocyclic compound in wavelength regions of the blue light, green light, and red light.
In one embodiment, the substituent of the aromatic group or heteroaryl group may be selected from a C1-C10 alkyl group or a C1-C10 alkoxy group.
In one embodiment, any one, two or three of X1, X2, X3, X4, X5, X6, X7, and X8 may be a N atom, and the rest may be CR2.
In one embodiment, the R2 may be a hydrogen atom, a deuterium atom, F, Cl, Br, a cyano group, or a trifluoromethyl group.
In one embodiment, the heteroatom substituted fluorene in Formula I may have any one of the following structures:
where Y may be selected from O or S, and the above structure may be connected to L1 through any carbon atom.
In one embodiment, the heteroatom substituted fluorene in Formula I may have any one of the following structures:
where Y may be selected from O or S, and the above structure may be connected to L1 through any carbon atom.
In one embodiment, the heteroatom substituted fluorene in Formula I may have any one of the following structures:
where Y may be selected from O or S, and the above structure may be connected to L1 through any carbon atom.
In one embodiment, the heteroatom substituted fluorene in Formula I may have any one of the following structures:
where Y may be selected from O or S, and the above structure may be connected to L1 through any carbon atom.
The above heteroatom substituted fluorene may refer to the following structure in the structural formula:
In one embodiment, the heterocyclic compound may have any one of the following structures:
In one embodiment, the L1, L2, and L3 may be independently selected from single bond, substituted or unsubstituted aromatic groups. The substituent of the aromatic group may be selected from deuterium atom.
In one embodiment, the L1, L2, and L3 may be independently selected from phenylene, biphenylene, terphenylene, naphthylene, anthrylene, phenanthrylene, pyrenylene, fluoranthene, triphenylene or fluorenylene.
In one embodiment, the L1, L2, and L3 may be independently selected from any one of the following structures:
where # may represent a connection position.
In one embodiment, the Ar1 and Ar2 may be independently selected from substituted or unsubstituted aromatic groups or heteroaryl groups. The substituent of the aforementioned aromatic group or heteroaryl group may be selected from a deuterium atom.
In one embodiment, the Ar1 and Ar2 may be independently selected from substituted or unsubstituted condensed aromatic groups or condensed heteroaryl groups. The substituent of the aforementioned condensed aromatic group or condensed heteroaryl group may be selected from a deuterium atom.
In one embodiment, the Ar1 and Ar2 may be independently selected from phenyl, biphenyl, terphenyl, naphthyl, anthracenyl, phenanthryl, pyrenyl, fluoranthene, triphenylene, fluorenyl, pyrrolyl, furyl, thienyl, pyridyl, pyrimidinyl, pyridazinyl, triazinyl, benzofuranyl, benzothienyl, dibenzofuranyl, dibenzothienyl, oxazolyl, oxadiazolyl, thiazolyl, thiadiazolyl, benzoxazolyl, benzothiazolyl, imidazolyl, pyrazolyl, indolyl, quinolinyl, isoquinolinyl, purinyl, isoxazolyl, isothiazole, pyrone, pyrazinyl, thienofuranyl, thienopyrrolyl, pyrrolopyridyl, pyridopyrimidinyl, pyrazolooxazolyl, pyrazinopyridazinyl, imidazothiazolyl or coumarin.
In one embodiment, the Ar1 and Ar2 may be independently selected from any one of the following structures:
where # may represent a connection position.
In one embodiment, the heterocyclic compound may have any one of the following structures:
The above disclosed heterocyclic compound in the present disclosure may be prepared by the existing method, and those skilled in the art may select a specific synthesis method according to conventional technical knowledge. The present disclosure may merely provide an exemplary synthesis route, which may not be limited by the present disclosure.
A representative synthetic route of the compound shown in Formula I in the present disclosure may include following:
In one embodiment, the above-disclosed compound in the present disclosure may be applied to the CPL layer of a top-emitting OLED device. In another embodiment, the above-disclosed compound may be used as an optical auxiliary layer such as a hole transport layer, an electron blocking layer, etc.
The present disclosure also provides a display panel including an organic light-emitting device. The organic light-emitting device may include an anode, a cathode, and an organic thin layer disposed between the anode and the cathode. The cathode may be covered with a capping layer, and the capping layer may include any one or a combination of at least two of the above-disclosed heterocyclic compounds.
The present disclosure also provides a display panel including an organic light-emitting device. The organic light-emitting device may include an anode, a cathode, and an organic thin layer disposed between the anode and the cathode. The organic thin layer may include a hole transport layer, and the hole transport layer may include any one or a combination of at least two of the above-disclosed heterocyclic compounds.
The present disclosure also provides a display panel including an organic light-emitting device. The organic light-emitting device may include an anode, a cathode, and an organic thin layer disposed between the anode and the cathode. The organic thin layer may include an electron blocking layer, and the electron blocking layer may include any one or a combination of at least two of the above-disclosed heterocyclic compounds.
The organic light-emitting device in the present disclosure may include a substrate, an indium-tin oxide (ITO) anode, a first hole transport layer, a second hole transport layer, an electron blocking layer, a light-emitting layer, a first electron transport layer, a second electron transport layer, a cathode (Mg—Ag electrode, a mass ratio of Mg over Ag may be approximately 1:9), and a capping layer (CPL) that are stacked in sequence.
In one embodiment, the anode material of the organic light-emitting device may be selected from a metal, a metal oxide, and a conductive polymer. The metal may include copper, gold, silver, iron, chromium, nickel, manganese, palladium, and platinum, or an alloy thereof, etc. The metal oxide may include indium oxide, zinc oxide, indium-tin oxide (ITO), indium-zinc oxide (IZO), etc. The conductive polymer may include polyaniline, polypyrrole, poly(3-methylthiophene), etc. In addition to the above materials and combinations that facilitate the hole injection, the anode material may further include any other suitable material.
In one embodiment, the cathode material of the organic light-emitting device may be selected from a metal, and a multilayer metal material. The metal may include aluminum, magnesium, silver, indium, tin, titanium, or an alloy thereof, etc. The multilayer metal material may include LiF/Al, LiO2/Al, BaF2/Al, etc. In addition to the above materials and combinations that facilitate electron injection, the cathode material may further include any other suitable material.
In one embodiment, the organic thin layer of the organic light-emitting device may include at least one light-emitting layer (EML), and may further include other functional layers, including a hole injection layer (HIL), a hole transport layer (HTL), an electron blocking layer (EBL), a hole blocking layer (HBL), an electron transport layer (ETL), and an electron injection layer (EIL).
In one embodiment, the organic light-emitting device may be prepared according to the following method. An anode may be formed on a transparent or an opaque smooth substrate, an organic thin layer may be formed on the anode, and a cathode may be formed on the organic thin layer.
In one embodiment, forming the organic thin layer may include evaporation, sputtering, spin coating, dipping, ion plating, or any other known film formation method.
The present disclosure also provides a display device including the above-disclosed display panel.
In the present disclosure, an organic light-emitting device (OLED device) may be applied to the display device. The organic light-emitting display device may include a mobile phone display, a computer display, a TV display, a smart watch display, a smart car display panel, VR or AR helmet display, or display of various smart devices, etc.
A synthetic route of compound M001 and detailed preparation method may include following:
(1) The M001-1 (0.5 mmol), M001-2 (0.75 mmol), K2CO3 (0.5 mmol), PdCl2 (5×104 mmol), TPPDA (5×104 mmol) may be added into 3 mL o-xylene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 100° C. for 24 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M001-3 may be obtained through column chromatography.
(2) M001-3 (0.5 mmol), M001-4 (1.5 mmol), KO(t-Bu) (0.75 mmol), [Pd(cinnamyl)Cl]2 (2 mol %), Ligand (1.5 mol %) may be added into 3 mL toluene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 110° C. for 12 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M001 may be obtained through column chromatography.
Through the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS (m/z)), the structure of the target product M001 may be obtained as C47H30N4O with a calculated value of 666.2 and a test value of 666.1.
Elemental analysis: theoretical value C, 84.66, H, 4.54, N, 8.40; test value C, 84.66, H, 4.53, N, 8.40.
A synthetic route of compound M029 and detailed preparation method may include following:
(1) M001-3 (0.5 mmol), M029-1 (1.5 mmol), KO(t-Bu) (0.75 mmol), [Pd(cinnamyl)Cl]2 (2 mol %), Ligand (1.5 mol %) may be added into 3 mL toluene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 110° C. for 12 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M029 may be obtained through column chromatography.
Through the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS (m/z)), the structure of the target product M029 may be obtained as C43H26N4O3 with a calculated value of 646.2 and a test value of 646.3.
Elemental analysis: theoretical value C, 79.86, H, 4.05, N, 8.66; test value C, 79.87, H, 4.05, N, 8.66.
A synthetic route of compound M039 and detailed preparation method may include following:
(1) M001-3 (0.5 mmol), M039-1 (1.5 mmol), KO(t-Bu) (0.75 mmol), [Pd(cinnamyl)Cl]2 (2 mol %), Ligand (1.5 mol %) may be added into 3 mL toluene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 110° C. for 12 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M039 may be obtained through column chromatography.
Through the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS (m/z)), the structure of the target product M039 may be obtained as C49H32N2O with a calculated value of 664.2 and a test value of 664.3.
Elemental analysis: theoretical value C, 88.53, H, 4.85, N, 4.21; test value C, 88.53, H, 4.86, N, 4.21.
A synthetic route of compound M265 and detailed preparation method may include following:
(1) The M265-1 (0.5 mmol), M001-2 (0.75 mmol), K2CO3 (0.5 mmol), PdCl2 (5×104 mmol), TPPDA (5×104 mmol) may be added into 3 mL o-xylene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 100° C. for 24 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M265-2 may be obtained through column chromatography.
(2) M265-2 (0.5 mmol), M029-1 (1.5 mmol), KO(t-Bu) (0.75 mmol), [Pd(cinnamyl)Cl]2 (2 mol %), Ligand (1.5 mol %) may be added into 3 mL toluene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 110° C. for 12 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M265 may be obtained through column chromatography.
Through the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS (m/z)), the structure of the target product M265 may be obtained as C42H25N5O2S with a calculated value of 663.2 and a test value of 663.1.
Elemental analysis: theoretical value C, 76.00, H, 3.80, N, 10.55; test value C, 76.01, H, 3.80, N, 10.55.
A synthetic route of compound M382 and detailed preparation method may include following:
(1) The M001-1 (0.5 mmol), M382-1 (0.75 mmol), K2CO3 (0.5 mmol), PdCl2 (5×104 mmol), TPPDA (5×104 mmol) may be added into 3 mL o-xylene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 100° C. for 24 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M382-2 may be obtained through column chromatography.
(2) The M382-2 (0.5 mmol), M382-3 (1.5 mmol), KO(t-Bu) (0.75 mmol), [Pd(cinnamyl)Cl]2 (2 mol %), Ligand (1.5 mol %) may be added into 3 mL toluene solution and then may be mixed. The mixed solution may be loaded into a 50 mL flask, and may react at 110° C. for 12 hours. After cooling to room temperature, saturated MgSO4 aqueous and ethyl acetate may be slowly added into the mixed solution for extraction three times. Then, solvent may be removed through a rotary evaporator, and a crude product M382 may be obtained through column chromatography.
Through the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS (m/z)), the structure of the target product M382 may be obtained as C47H28N4OS2 with a calculated value of 728.2 and a test value of 728.1.
Elemental analysis: theoretical value C, 77.45, H, 3.87, N, 7.69; test value C, 77.44,
The preparation method of the disclosed compounds in the present disclosure used in the specific embodiments may be similar to the above-mentioned method, and may not be repeated herein. The characterization results, such as the results of mass spectrometry and elemental analysis, may be provided and shown in Table 1.
The refractive indices of the compounds may be detected, and the results may be shown in Table 2.
According to the data in Table 1, compared with a commonly used capping layer material Ref 1 in the industry, the compounds in the present disclosure may have higher refractive indices in the entire visible wavelength range. Therefore, when the above compounds are used as capping layer materials in an OLED device of the blue, green and red light-emitting devices, a substantially high light-emitting efficiency may be expected.
The present application embodiment provides an OLED device.
The structure of the OLED blue-light device may include: ITO (10 nm)/compound 1:compound 2 (3:97 mass ratio) (5 nm)/compound 3 (100 nm)/compound 4 (5 nm)/compound 5:compound 6 (97:3 mass ratio) (30 nm)/compound 7 (5 nm)/compound 8:compound 9 (1:1 mass ratio) (30 nm)/Mg:Ag (10:90 mass ratio) (10 nm)/M001 (70 nm).
The preparation method of the OLED device may include following.
1) A glass substrate having a size of 50 mm×50 mm×0.7 mm may be provided. The glass substrate may be sonicated in isopropanol and deionized water for 30 minutes, respectively, and then may be exposed to ozone for approximately 10 minutes for cleaning, to obtain the substrate 1. The obtained glass substrate with a 10 nm indium tin oxide (ITO) anode may be mounted on a vacuum deposition apparatus.
2) The hole injection layer material compound 2 and the p-doped material compound 1 may be co-evaporated on the ITO anode 2 through a vacuum evaporation, to form the hole injection layer 3 with a doping ratio of approximately 3% (mass ratio) and a thickness of approximately 5 nm.
3) The hole transport layer material compound 3 may be evaporated on the hole injection layer 3 through a vacuum evaporation, to form the first hole transport layer 4 with a thickness of approximately 100 nm.
4) The hole transport layer material compound 4 may be evaporated on the first hole transport layer 4 through a vacuum evaporation, to form the second hole transport layer 5 with a thickness of approximately 5 nm.
5) The compound 5 as a host material and the compound 6 as a doping material may be co-evaporated on the second hole transport layer 5 through a vacuum evaporation, to form the light-emitting layer 6 with a doping ratio of approximately 3% (mass ratio) and a thickness of approximately 30 nm.
6) The electron transport material compound 7 may be evaporated on the light-emitting layer 6 through a vacuum evaporation, to form the electron transport layer 7 with a thickness of approximately 5 nm.
7) The electron transport material compound 8 and the compound 9 may be co-evaporated on the electron transport layer 7 through a vacuum evaporation, to form the electron injection layer 8 with a doping mass ratio of approximately 1:1 and a thickness of approximately 30 nm.
8) Magnesium-silver electrode may be evaporated on the electron injection layer 8 through a vacuum evaporation, to form the cathode 9 with a Mg:Ag mass ratio of approximately 1:9 and a thickness of approximately 10 nm.
9) The compound M001 may be evaporated on the cathode 9 through a vacuum evaporation, to form the capping layer 10 with a thickness of approximately 70 nm.
The structure of the compounds used in the OLED device may have the following structures.
The present application embodiment provides an OLED device. The preparation method of the OLED device in the present application embodiment may be the same as the preparation method of the OLED device in the application embodiment 1A, while the OLED device in the present embodiment may have the following device structure.
The structure of the OLED green-light device may include: ITO (10 nm)/compound 1: compound 2 (3:97 mass ratio) (5 nm)/compound 3 (140 nm)/compound 4 (5 nm)/CBP:Ir (ppy)3 (9:1 mass ratio) (40 nm)/compound 7 (5 nm)/compound 8:compound 9 (1:1 mass ratio) (30 nm)/Mg:Ag (10:90 mass ratio) (10 nm)/M001 (70 nm).
The present application embodiment provides an OLED device. The preparation method of the OLED device in the present application embodiment may be the same as the preparation method of the OLED device in the application embodiment 1A, while the OLED device in the present embodiment may have the following device structure.
The structure of the OLED red-light device may include: ITO (10 nm)/compound 1: compound 2 (3:97 mass ratio) (5 nm)/compound 3 (190 nm)/compound 4 (5 nm)/CBP: Ir(piq)2(acac) (96:4 mass ratio) (40 nm)/compound 7 (5 nm)/compound 8:compound 9 (1:1 mass ratio) (30 nm)/Mg:Ag (10:90 mass ratio) (10 nm)/M001 (70 nm).
The difference between application embodiments 2 (A,B,C)-72 (A,B,C) and application embodiments 1(A,B,C) may include that the compound M001 may be replaced with the compounds in Table 3.
The difference between the present comparative embodiment and application embodiments 1(A,B,C) may include that the organic compound M001 in step (9) may be replaced with an equivalent amount of the comparative compound Ref 1. The other preparation steps in the present comparative embodiment may be the same as the preparation steps in the application embodiment 1A.
The difference between the present comparative embodiment and application embodiments 1(A,B,C) may include that the organic compound M001 in step (9) may be replaced with an equivalent amount of the comparative compound Ref 2. The other preparation steps in the present comparative embodiment may be the same as the preparation steps in the application embodiment 1A.
The difference between the present comparative embodiment and application embodiments 1(A,B,C) may include that the organic compound M001 in step (9) may be replaced with an equivalent amount of the comparative compound Ref 3. The other preparation steps in the present comparative embodiment may be the same as the preparation steps in the application embodiment 1A.
The difference between the present comparative embodiment and application embodiments 1(A,B,C) may include that the organic compound M001 in step (9) may be replaced with an equivalent amount of the comparative compound Ref 4. The other preparation steps in the present comparative embodiment may be the same as the preparation steps in the application embodiment 1A.
Performance evaluation of the OLED device
A Keithley 2365A digital nano-voltmeter may be used to test the current of the OLED device at a different voltage, and then the current may be divided by the light-emitting area to obtain a current density of the OLED device at the different voltage. The brightness and radiant energy flux density of the OLED device at the different voltage may be tested using a Konicaminolta CS-2000 spectroradiometer. According to the current density and brightness of the OLED device at the different voltage, the operating driving voltage and current efficiency (Cd/A) under a same current density (10 mA/cm2) may be obtained. The service lifetime of the OLED device may be obtained by measuring the duration when the brightness of the OLED device reaches 95% of the initial brightness (under a test condition of 50 mA/cm2). The specific data may be shown in Table 3.
As can be seen from the above-disclosed embodiments and comparative embodiments, compared with the conventional commercial capping layer material compound Ref1, the compounds in the present disclosure may realize substantially high luminescence when being applied to blue-light, green-light and red-light devices. The light-emitting efficiency of blue-light device is increased by 4%-7%, the light-emitting efficiency of green-light device is increased by 6%-14%, and the light-emitting efficiency of red-light device is increased by 5%-15%. Therefore, the compounds in the present disclosure may have excellent light extraction ability when being used as capping layer materials, and may effectively improve the light-emitting efficiency of the OLED device.
Compared with Ref2, Ref3, and Ref4, M001, M029, M032, and M192 in the present disclosure may improve the refractive indices of the capping layer for the blue-light, green-light, and red-light wavelength regions merely by replacing carbon atoms with nitrogen atoms, thereby effectively improving the blue-light, green-light and red-light light-emitting efficiency of the OLED device. Further, the synthesis of the nitrogen heterocycle may be simple, and the cost may be low, which may be suitable for mass production.
The description of the disclosed embodiments is provided to illustrate the present disclosure to those skilled in the art. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the disclosure. Thus, the present disclosure is not intended to be limited to the embodiments illustrated herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202111452323.0 | Nov 2021 | CN | national |
