P-TYPE DOPANT AND ORGANIC LIGHT EMITTING DIODE

Abstract

A P-type dopant is provided, which is a planar aromatic compound having different numbers of fluorine atoms and cyano groups connected at a periphery thereof, and allows adjustment of highest occupied molecular orbital (HOMO) energy levels and lowest unoccupied molecular orbital (LUMO) energy levels and effectively increases luminous efficiency of a light emitting layer. Moreover, an organic light emitting diode is disclosed, including an anode, a cathode, and a light emitting structure located between the anode and the cathode, wherein a hole injecting layer of the light emitting structure is a hole injecting layer including the P-type dopant described above.

Claims

1. A P-type dopant, wherein the P-type dopant is a planar aromatic compound comprising different numbers of fluorine atoms and cyano groups connected at a periphery, and has a following structural formula: ##STR00017##

2. The P-type dopant according to claim 1, wherein the P-type dopant has a following structural formula: ##STR00018##

3. The P-type dopant according to claim 2, wherein the P-type dopant has the following structural formula: ##STR00019## and is synthesized by a following synthesis route: ##STR00020##

4. The P-type dopant according to claim 2, wherein the P-type dopant has the following structural formula: ##STR00021## and is synthesized by a following synthesis route: ##STR00022##

5. The P-type dopant according to claim 2, wherein the P-type dopant has the following structural formula: ##STR00023## and is synthesized by a following synthesis route: ##STR00024##

6. An organic light emitting diode, wherein a material of a hole injecting layer in the organic light emitting diode is a hole injecting material comprising a P-type dopant, and the P-type dopant is a planar aromatic compound comprising different numbers of fluorine atoms and cyano groups connected at a periphery, and has a following structural formula: ##STR00025##

7. The organic light emitting diode according to claim 6, wherein the P-type dopant has the following structural formula: ##STR00026##

8. The organic light emitting diode according to claim 7, wherein the P-type dopant has the following structural formula: ##STR00027## and is synthesized by a following synthesis route: ##STR00028##

9. The organic light emitting diode according to claim 7, wherein the P-type dopant has the following structural formula: ##STR00029## and is synthesized by a following synthesis route: ##STR00030##

10. The organic light emitting diode according to claim 7, wherein the P-type dopant has the following structural formula: ##STR00031## and is synthesized by a following synthesis route: ##STR00032##

11. The organic light emitting diode according to claim 6, wherein the organic light emitting diode further comprises an anode, a cathode, and a light emitting structure located between the anode and the cathode, wherein the light emitting structure comprises the hole injecting layer according to claim 6.

12. The organic light emitting diode according to claim 11, wherein the light emitting structure comprises the hole injecting layer, a hole transporting layer, an electron blocking layer, a light emitting layer, a hole blocking layer, an electron transporting layer, and an electron injecting layer which are sequentially formed.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0013] FIG. 1 is a schematic diagram of an organic light emitting diode according to an embodiment of the present invention.

DETAILED DESCRIPTION

[0014] In response to urgent needs of high-performance P-type dopants, the present invention provides multiple embodiments of a novel P-type dopant having different numbers of fluorine atoms and cyano groups connected at the periphery of a planar aromatic compound. They have the function of adjusting the lowest unoccupied molecular orbital (LUMO) energy levels and effectively increasing the luminous efficiency of a light emitting layer. The synthesis route thereof also has improved material synthesis efficiency, which is conducive to achieving long lifespan and fabrication of high efficiency organic light emitting diodes. In order to achieve the above-mentioned effects, the present invention provides a P-type dopant, which is a planar aromatic compound comprising different numbers of fluorine atoms and cyano groups connected at the periphery, and has the following structural formula:

##STR00009##

[0015] In one embodiment of the present invention, the P-type dopant has the following structural formula:

##STR00010##

[0016] The following further describes the present invention in detail with reference to the embodiments and drawings for purposes of better understanding of the content of the present invention, but the protection scope of the present invention is not limited to these embodiments.

EMBODIMENT 1

[0017] Fabrication of a P-type dopant having the following structural formula:

##STR00011##

and is synthesized by the following synthesis route:

##STR00012##

[0018] Synthesis of Compound 1

[0019] First, 2.82 grams or 5 mmol of raw material 1, 2.3 grams or 25 mmol of cuprous cyanide, and 4.98 grams or 30 mmol of potassium iodide were added to a 100 mL two-necked flask. The two-necked flask were next placed into a glove box and suction and ventilation were performed for three times. Next, 100 mL of N,N′-dimethylformamide (DMF) which were previously dehydrated and deoxygenated were injected under an argon atmosphere and were then reacted at 140° C. for 12 hours. After cooling to room temperature, a hydrochloric acid solution comprising contents of the raw material 1 and ferric chloride (5 mol/L and 100 mL) was added to the two-necked flask, and the mixture was stirred at room temperature for 2 hours to obtain a reaction solution. Subsequently, the reaction solution was introduced into 200 mL of ice water and extracted three times with dichloromethane. The organic phases obtained in each extraction were collected and combined to spin thereof into silica gel, and the silica gel was then subjected to column chromatography (using dichloromethane:n-hexane, v:v, 3:1) for isolation and purification. Finally, 1.1 grams of compound 1 (orange-red powder) were obtained with a yield of 63% and MS (EI) m/z:[M]+: 351.97.

EMBODIMENT 2

[0020] Fabrication of a P-type dopant having the following structural formula

##STR00013##

and is synthesized by the following synthesis route:

##STR00014##

[0021] Synthesis of Compound 2

[0022] First, 2.82 grams or 5 mmol of raw material 2, 2.3 grams or 25 mmol of cuprous cyanide, and 4.98 grams or 30 mmol of potassium iodide were added to a 100 mL two-necked flask. The two-necked flask were next placed into a glove box and suction and ventilation were performed for three times. Next, 100 mL of N,N′ -dimethylformamide (DMF) which were previously dehydrated and deoxygenated were injected under an argon atmosphere and were then reacted at 140° C. for 12 hours. After cooling to room temperature, a hydrochloric acid solution comprising contents of the raw material 2 and ferric chloride (5 mol/L and 100 mL) was added to the two-necked flask, and the mixture was stirred at room temperature for 2 hours to obtain a reaction solution. Subsequently, the reaction solution was introduced into 200 mL of ice water and extracted three times with dichloromethane. The organic phases obtained in each extraction were collected and combined to spin thereof into silica gel, and the silica gel is then subjected to column chromatography (using dichloromethane:n-hexane, v:v, 3:1) for isolation and purification. Finally, 1.2 grams of compound 2(orange-red powder) were obtained with a yield of 63% and MS (EI) m/z: [M]+: 381.89.

Embodiment 3

[0023] Fabrication of a P-type dopant having the following structural formula

##STR00015##

and is synthesized by the following synthesis route:

##STR00016##

[0024] Synthesis of Compound 3

[0025] First, 1.40 grams or 5 mmol of raw material 1, 2.3 grams or 25 mmol of cuprous cyanide, and 4.98 grams or 30 mmol of potassium iodide were added to a 100 mL two-necked flask. The two-necked flask were next placed into a glove box and suction and ventilation were performed for three times. Next, 100 mL of N,N′ -dimethylformamide (DMF) which was previously dehydrated and deoxygenated were injected under an argon atmosphere and were then reacted at 140° C. for 12 hours. After cooling to room temperature, a hydrochloric acid solution comprising contents of the raw material 3 and ferric chloride (5 mol/L and 100 mL) was added to the two-necked flask, and the mixture was stirred at room temperature for 2 hours to obtain a reaction solution. Subsequently, the reaction solution was introduced into 200 mL of ice water and extracted three times with dichloromethane. The organic phases obtained in each extraction were collected and combined to spin thereof into silica gel, and the silica gel was then subjected to column chromatography (using dichloromethane:n-hexane, v:v, 3:1) for isolation and purification. Finally, 0.8 grams of compound 3 (orange-red powder) were obtained with a yield of 42% and MS (EI) m/z:[M]+: 378.18.

[0026] Physical Properties of Compounds 1-3:

[0027] The highest occupied molecular orbital (HOMO) energy levels and the lowest unoccupied molecular orbital (LUMO) energy levels of the above compounds 1-3 are shown in the following Table 1:

TABLE-US-00001 TABLE 1 HOMO (eV) LUMO (eV) Compound 1 −9.13 −5.43 Compound 2 −9.11 −5.61 Compound 3 −9.07 −5.64

[0028] The HOMO and LUMO energy levels of the above compounds 1-3 were estimated using cyclic voltammetry combined with optical energy gap (Eg) of molecule in a thin film state according to the following calculation formula:

HOMO=−([Eonset]ox+4.8)eV,

Eg=LUMO−HOMO,

[0029] wherein [Eonset] ox refers to the redox starting potential value of ferrocene under testing.

EMBODIMENTS 4-6

Fabrication of an Organic Light Emitting Diode

[0030] Referring to FIG. 1, an organic light emitting diode of the present invention comprises a conductive anode glass layer S, a semi-transparent cathode layer 8 and a light coupling output layer 9, and a light emitting structure formed between the conductive anode glass layer S and the semi-transparent cathode layer 8. Specifically, the light emitting structure comprises a hole injecting layer 1, a hole transporting layer 2, an electron blocking layer 3, a light emitting layer 4, a hole blocking layer 5, and an electron transporting layer 6, and an electron injection layer 7, which are sequentially formed on the conductive anode glass layer S. Specifically, the conductive anode glass layer S was formed by plating a glass substrate with a total reflection substrate layer made of a conductive reflective indium tin oxide (ITO)/silver (Ag)/indium tin oxide (ITO). The hole injecting layer 1 was composed of 4,4′,4″-tris(carbazol-9-yl) triphenylamine(4,4′,4″-tris(carbazol-9-yl)triphenylamine, TCTA) and the P-type dopants of the present invention, which were, for example, compounds 1-3. The hole transport layer 2 is composed of TCTA. The electron blocking layer 3 was composed of 4-[1-[4-[bis(4-methylphenyl)amino]phenyl]cyclohexyl]-N-(3-methylphenyl)-N-(4-methylphenyl)aniline (TAPC). The light emitting layer 4 was composed of bis [2-((oxo)diphenylphosphino)phenyl]ether (DPEPO) and tris(2-phenylpyridine)iridium (III) (Ir(PPy) 3). The hole blocking layer 5 is composed of 3,3′-[5′-[3-(3-pyridyl)phenyl][1,1′:3′,1″-terphenyl]-3,3″-diyl]dipyridine (TMPyPb). The electron transport layer 6 is composed of 1,3,5-tris[3-(3-pyridyl)phenyl]benzene (TmPyPB) and lithium octahydroxyquinoline (LiQ). The electron injection layer 7 is composed of lithium fluoride (LiF). The semi-transparent cathode layer 8 is composed of magnesium and silver. The light-coupling output layer 9 is composed of 4,4′,4″-tris(carbazole-9-yl)triphenylamine (TCTA). The hole injecting layer 1, the hole transport layer 2, the electron blocking layer 3, the light emitting layer 4, the hole blocking layer 5, the electron transport layer 6, and the electron injection layer 7 constitute the light emitting structure of the organic light emitting diode of the present invention. The organic light emitting diode can be completed according to a method known in the technical field of the present invention, for example, the method disclosed in the reference “Adv. Mater. 2003, 15, 277”. The specific method is described as follows: under high vacuum conditions, the aforementioned materials containing the P-type dopants (compounds 1-3) of the present invention were sequentially formed on a conductive glass by evaporation to complete the process. Here, the compounds 1-3 of the present invention were used to prepare the organic light emitting diodes I-III of Examples 4-6. The structure of the organic light emitting diode I-III from the conductive glass anode layer S to the light coupling output layer 9 are provided as follows:

[0031] Organic light emitting diode (OLED) I: ITO/Ag/ITO (15 nm/140 nm/15 nm)/Compound 1: TCTA (doped with 3% Compound 1, 10 nm)/TCTA (135 nm)/TAPC (5 nm)/DPEPO: ADN (doped with 2% AND, 20 nm)/TMPyPb (5 nm)/Tm3PyPB:LIQ (15:15 nm)/LiF (1 nm)/Mg:Ag (0.9:9 nm)/TCTA (85 nm).

[0032] OLED II: ITO/Ag/ITO (15nm/140nm/15nm)/Compound 2: TCTA (doped with 3% Compound 2, 10 nm)/TCTA (135 nm)/TAPC (5 nm)/DPEPO: ADN (doped with 2% AND, 20 nm)/TMPyPb (5 nm)/Tm3PyPB: LIQ (15:15 nm)/LiF (1 nm)/Mg:Ag (0.9:9 nm)/TCTA (85 nm).

[0033] OLED III: ITO/Ag/ITO (15 nm/140 nm/15 nm)/Compound 3: TCTA (doped with 3% Compound 3, 10 nm)/TCTA (135 nm)/TAPC (5 nm)/DPEPO: ADN (doped with 2% AND, 20 nm)/TMPyPb (5 nm)/Tm3PyPB: LIQ (15:15 nm)/LiF (1 nm)/Mg: Ag (0.9:9 nm)/TCTA (85 nm).

[0034] Data of performance the organic light emitting diodes I-III of Examples 4-6 are shown in the following Table 2. Current, brightness, and voltage of the organic light emitting diodes were measured by a Keithley source measurement system (Keithley 2400 Source-meter, Keithley 2000 Current-meter) with a calibrated silicon photodiode. The electroluminescence spectrum of the organic light emitting diodes were measured by SPEX CCD3000 spectrometer of the French company JY. All measurements were made and done at room temperature.

TABLE-US-00002 TABLE 2 Max current chromaticity Max external P-type efficiency coordinate quantum OLED dopant (cd/A) (CIEx, CIEy) efficiency (%) I Compound 1 4.8 (0.13, 0.046) 12.3% II Compound 2 5.7 (0.13, 0.045) 13.1% III Compound 3 5.2 (0.13, 0.046) 12.9%

[0035] In the P-type dopant of the present invention, different numbers of fluorine atoms and cyano groups are connected at the periphery of a planar aromatic compound, thereby having the function of adjusting the lowest unoccupied molecular orbital (LUMO) energy levels and effectively increasing the luminous efficiency of a light emitting layer. Furthermore, the synthesis route thereof also has improved material synthesis efficiency. At last, an organic light emitting diode using the P-type dopant of the embodiment of the present invention as a light emitting layer has high light emitting efficiency, which is conducive to achieving long lifespan and fabrication of high efficiency organic light emitting diodes, and can be applied and used in various display devices and electronic devices.

[0036] While the present disclosure has been described with the aforementioned preferred embodiments, it is preferable that the above embodiments should not be construed as limiting of the present disclosure. Anyone having ordinary skill in the art can make a variety of modifications and variations without departing from the spirit and scope of the present disclosure as defined by the following claims.