Patent Application
20180127604
Electronic devices containing active organic materials are attracting increasing attention for use in devices such as organic light emitting diodes (OLEDs), organic light-emitting electrochemical cells (LECs), organic photoresponsive devices (in particular organic photovoltaic devices and organic photosensors), organic transistors and memory array devices. Devices containing active organic materials offer benefits such as low weight, low power consumption and flexibility. Moreover, use of soluble organic materials allows use of solution processing in device manufacture, for example inkjet printing, slot die coating or spin-coating.
An OLED comprises a substrate carrying an anode, a cathode and one or more organic light-emitting layers between the anode and cathode.
An organic LEC comprises a substrate carrying an anode, a cathode and an organic light-emitting layer between the anode and cathode comprising a light-emitting material, a salt providing mobile ions and an electrolyte, for example a polymer electrolyte (“polyelectrolyte”). LECs are disclosed in, for example, WO 96/00983.
Holes are injected into the device through the anode and electrons are injected through the cathode during operation of the device. Holes in the highest occupied molecular orbital (HOMO) and electrons in the lowest unoccupied molecular orbital (LUMO) of a light-emitting material combine to form an exciton that releases its energy as light. In the case of an organic LEC, the cations and anions of the salt may respectively p- and n-dope the light-emitting material, which may provide for a low drive voltage.
Suitable light-emitting materials include small molecule, polymeric and dendrimeric materials. Suitable light-emitting polymers for use in the light-emitting layer include poly(arylene vinylenes) such as poly(p-phenylene vinylenes) and polyarylenes such as polyfluorenes.
A light emitting layer may comprise a semiconducting host material and a light-emitting dopant wherein energy is transferred from the host material to the light-emitting dopant. The light-emitting dopant may be fluorescent or phosphorescent.
WO 2008/090795 discloses phosphorescent compounds of formula (1):
wherein R1 represents a group; R2-R4 independently represent a substituent; n2 represents a number of 0-4; n4 represents a number of 0-8; and Q represents an atomic group necessary for forming an aromatic hydrocarbon ring or an aromatic heterocyclic ring.
U.S. Pat. No. 7,659,010 describes a blue light-emitting transition metal containing compound having to the following formula:
wherein A can be triazole or tetrazole, B is a five- or six-membered aryl or heteroaryl ring and M is a d-block transition metal.
EP 1083775 discloses compositions comprising a functional material and a solvent comprising at least one benzene derivative having 1 or more substituents, the substituents having 3 or more carbon atoms in total. The functional material may be an organic EL material. The composition may be used in an inkjet method.
It is an object of the invention to provide stable ink compositions comprising phosphorescent light-emitting materials.
In a first aspect the invention provides an ink comprising a first solvent, a stabiliser and a first phosphorescent metal complex wherein the first phosphorescent metal complex comprises at least one aryl-imidazole or heteroaryl-imidazole ligand that may be unsubstituted or substituted with one or more substituents and wherein the first solvent is selected from: linear, branched or cyclic ethers comprising one or more O—CH2 units; solvents comprising a CH2—C(R6)H—CH2 unit wherein R6 is an organic residue and the two CH2 groups may be linked by a divalent group: bicyclic, partially or fully saturated solvents; solvents of formula R8—CR7═CR7—CH2—R8 wherein each R7 is independently H or C1-10 alkyl and R8 in each occurrence is independently an organic residue; and solvents comprising a benzyl group.
In a second aspect the invention provides a method of forming an organic light-emitting device comprising an anode, a cathode and a light-emitting layer between the anode and cathode, the method comprising the steps of forming the light-emitting layer by depositing the ink of the first aspect over one of the anode and cathode; evaporating the solvent; and forming the other of the anode and cathode over the light-emitting layer.
In a third aspect the invention provides an ink comprising a first solvent, an antioxidant and a first phosphorescent metal complex wherein the first phosphorescent metal complex comprises at least one aryl-imidazole or heteroaryl-imidazole ligand that may be unsubstituted or substituted with one or more substituents.
The first solvent, antioxidant and first phosphorescent material may be as described anywhere herein. The ink of the third aspect may be used to form an organic light-emitting device as described with reference to the second aspect.
The invention will now be described in more detail with reference to the Figures, in which:
Light-emitting layer 105 comprises a phosphorescent light-emitting material of formula (I) and may comprise one or more further light-emitting materials. Preferably, light-emitting layer 105 comprises at least one further light-emitting material that produces light during operation of the device 100. Preferably, any further light-emitting material of the light-emitting layer 105 is a phosphorescent material.
The phosphorescent material of formula (I) of the light-emitting layer 105 and, if present, any further phosphorescent materials of this layer, may be doped in a host material. The lowest excited state triplet energy (T1) level of the host material is preferably no more than 0.1 eV below that of the phosphorescent light-emitting material of formula (I), and is more preferably about the same or higher than that of the phosphorescent light-emitting material of formula (I) in order to avoid quenching of phosphorescence.
One or more further layers may be provided between the anode 103 and cathode 107, for example hole-transporting layers, electron transporting layers, hole blocking layers and electron blocking layers. The device may contain more than one light-emitting layer.
Preferred device structures include:
Anode/Hole-injection layer/Light-emitting layer/Cathode
Anode/Hole transporting layer/Light-emitting layer/Cathode
Anode/Hole-injection layer/Hole-transporting layer/Light-emitting layer/Cathode
Anode/Hole-injection layer/Hole-transporting layer/Light-emitting layer/Electron-transporting layer/Cathode.
Preferably, at least one of a hole-transporting layer and a hole injection layer is present. Preferably, both a hole injection layer and a hole-transporting layer are present.
The light-emitting layer 105 is deposited by solution processing an ink comprising a phosphorescent compound, a first solvent and a stabiliser, followed by evaporation of the first solvent, the stabiliser and any other solvents present in the ink.
The ink may contain one or more further components that form part of the light-emitting layer, for example one or more further light-emitting materials and one or more host materials.
Preferably, the components of the light-emitting layer are provided in an amount of 0.1-5 wt % of the solvent or solvents of the ink, optionally 1-5 wt %, optionally 1-3 wt %.
The viscosity of the ink is selected according to the solution processing method to be used. For ink-jet printing, the ink preferably has a viscosity of less than 15 cP, preferably less than 10 cP and preferably greater than 2 cP at room temperature.. For slot die coating, the ink preferably has a viscosity of greater than 2 cP at room temperature.
First Phosphorescent Material
Preferably, the first phosphorescent material has formula (I):
wherein:
Ar5 is an aryl or heteroaryl group that may be unsubstituted or substituted with one or more substituents;
R2 is a substituent;
each R3 is independently H or R2;
each R4 is independent H or R2;
M is a transition metal or metal ion;
x is a positive integer of at least 1;
y is 0 or a positive integer; and
each L1 is independently a mono- or polydentate ligand different from ligands of formula
Optionally, substituents R2 are selected from:
alkyl, optionally C1-20 alkyl, wherein one or more non-adjacent C atoms of the alkyl may be replaced with unsubstituted or substituted aryl or heteroaryl, O, S, NR5, C═O or —COO— wherein R5 is a substituent, optionally C1-20 hydrocarbyl, and one or more H atoms of the alkyl may be replaced with F; and
(Ar9)w wherein Ar9 is independently in each occurrence an aryl or heteroaryl group, optionally an aryl group, optionally phenyl, that may be unsubstituted or substituted with one or more substituents, and w is at least 1, optionally 1, 2 or 3
Substituents for groups Ar9 may be selected from F; CN; NO2; and C1-20 alkyl wherein one or more non-adjacent carbon atoms may be replaced with O, S, NR5, C═O or —COO—, and one or more H atoms may be replaced with F, wherein R5 is substituent, optionally a C1-40 hydrocarbyl group, optionally a group selected from C1-20 alkyl and phenyl that may be unsubstituted or substituted with one or more C1-20 alkyl groups
Preferably, each R2 is independently a C1-40 hydrocarbyl group, more preferably C1-20 alkyl or a C1-40 hydrocarbyl group of formula —(Ar9)w wherein each Ar9 group is independently unsubstituted or substituted with one or more C1-20 alkyl groups.
Preferably, Ar5 is phenyl that may be unsubstituted or substituted with one or more substituents.
The or each substituent of Ar5, if present, may independently in each occurrence be selected from substituents R2 described above, more preferably selected from a C1-40 hydrocarbyl group, more preferably a C1-40 hydrocarbyl group.
Preferably, R3 is H or a C1-40 hydrocarbyl group as described with reference to R2.
Preferably, R4 is H or a C1-40 hydrocarbyl group as described with reference to R2. More preferably, R4 is H.
M of compounds of formula (I) may be selected from heavy metal transition metal complexes, optionally ruthenium, rhodium, palladium, rhenium, osmium, iridium, platinum and gold. Iridium is particularly preferred.
In one optional arrangement, x is 3 and y is 0.
In another optional arrangement, y is a positive integer, optionally 1 or 2, and each L1 is independently a monodentate or polydentate ligand. Exemplary ligands L1 include tetrakis-(pyrazol-1-yl)borate, 2-carboxypyridyl and diketonates, for example acetylacetonate.
Exemplary compounds of formula (I) are illustrated below:
Preferably, the first phosphorescent compound emits blue light. A blue emitting material may have a photoluminescent spectrum with a peak in the range of no more than 490 nm, optionally in the range of 420-480 nm.
The ink may contain one or more further light-emitting materials, preferably one or more further phosphorescent materials. Optionally, the further light-emitting material or materials emit green or red light.
A green emitting material may have a photoluminescent spectrum with a peak in the range of more than 490 nm up to 580 nm, optionally more than 490 nm up to 540 nm.
A red emitting material may optionally have a peak in its photoluminescent spectrum of more than 580 nm up to 630 nm, optionally 585-625 nm.
The photoluminescence spectrum of a light-emitting material may be measured by casting 5 wt % of the material in a PMMA film onto a quartz substrate to achieve transmittance values of 0.3-0.4 and measuring the spectrum in a nitrogen environment using apparatus C9920-02 supplied by Hamamatsu.
Host
Preferably, the ink comprises a host material. The host material may be a polymeric or non-polymeric material. Preferably, the host is non-polymeric.
The host material preferably has a lowest excited state triplet energy level that is the same as or higher than the lowest excited state triplet energy level of the first phosphorescent compound.
Exemplary non-polymeric hosts have formula (XV):
wherein each R15 and R16 is independently a substituent; X is O or S; each c is independently 0, 1, 2, 3 or 4; and each d is independently 0, 1, 2 or 3.
The host of formula (XV) may have formula (XVa):
Each R15 and R16, where present, may independently in each occurrence be selected from the group consisting of alkyl, optionally C1-20 alkyl, wherein one or more non-adjacent C atoms may be replaced with optionally substituted aryl or heteroaryl, O, S, substituted N, C═O or —COO—, and one or more H atoms may be replaced with F; aryl and heteroaryl groups that may be unsubstituted or substituted with one or more substituents; and a branched or linear chain of aryl or heteroaryl groups. Exemplary aryl or heteroaryl groups are unsubstituted phenyl and phenyl substituted with one or more C1-20 alkyl groups; F; CN and NO2.
X is preferably S.
Host polymers include polymers having a non-conjugated backbone with charge-transporting groups pendant from the polymer backbone, and polymers having a conjugated backbone in which adjacent repeat units of the polymer backbone are conjugated together. A conjugated host polymer may comprise, without limitation, repeat units selected from optionally substituted arylene or heteroarylene repeat units.
Exemplary arylene repeat units include, without limitation, fluorene, phenylene, phenanthrene naphthalene and anthracene repeat units, each of which may independently be unsubstituted or substituted with one or more substituents, optionally one or more C1-40 hydrocarbyl substituents.
The host polymer may contain triazine-containing repeat units. Exemplary triazine-containing repeat units have formula (IV):
wherein Ar12, Ar13 and Ar14 are independently selected from substituted or unsubstituted aryl or heteroaryl, and z in each occurrence is independently at least 1, optionally 1, 2 or 3, preferably 1.
Polymers comprising repeat units of formula (IV) may be copolymers comprising repeat units of formula (IV) and one or more co-repeat units, and may comprise repeat units of formula (IV) and one or more arylene repeat units as described above.
Any of Ar12, Ar13 and Ar14 may be substituted with one or more substituents. Exemplary w substituents are substituents R10, wherein each R10 may independently be selected from the group consisting of:
Substituted N, where present, may be —NR17— wherein R17 is a substituent, optionally a C1-20 hydrocarbyl group.
Preferably, Ar12, Ar13 and Ar14 of formula (IV) are each phenyl, each phenyl independently being unsubstituted or substituted with one or more C1-20 alkyl groups.
Ar14 of formula (IV) is preferably phenyl, and is optionally substituted with one or more C1-20 alkyl groups or a crosslinkable unit.
A particularly preferred repeat unit of formula (IV) has formula (IVa).
The phenyl groups of the repeat unit of formula (IVa) may each independently be unsubstituted or substituted with one or more substituents R10 as described above with respect to formula (IV), preferably one or more C1-20 alkyl groups.
The compound of formula (I) and/or any other phosphorescent material of light-emitting layer 105, may be blended with or covalently bound to a host polymer.
The first phosphorescent material, and/or another phosphorescent material of the ink, if present, may be covalently bound to a host polymer as a repeat unit in the polymer backbone, as an end-group of the polymer, or as a side-chain of the polymer. If the phosphorescent material is provided in a side-chain then it may be directly bound to a repeat unit in the backbone of the polymer or it may be spaced apart from the polymer backbone by a spacer group. Exemplary spacer groups include C1-20 alkyl and aryl-C1-20 alkyl, for example phenyl-C1-20 alkyl. One or more carbon atoms of an alkyl group of a spacer group may be replaced with O, S, C═O or COO.
The first phosphorescent compound mixed with a host material may form 0.1-50 weight %, optionally 0.1-40 weight % of the weight of the components of the layer containing the phosphorescent material.
If the first phosphorescent compound is covalently bound to a host polymer then repeat units comprising the phosphorescent material, or an end unit comprising the phosphorescent material, may form 0.1-20 mol of the polymer.
If two or more phosphorescent materials are provided in light-emitting layer 105 then the phosphorescent material with the highest triplet energy level is preferably provided in a larger weight percentage than the lower triplet energy level phosphorescent material or materials.
Solvents
The ink may comprise one or more first solvents selected from:
(i) Linear, branched or cyclic ether comprising one or more O—CH2— units, for example diethyl ether, tetrahydrofuran, dioxane and diglyme;
(ii) Solvents comprising a CH2—C(R6)H—CH2 unit wherein R6 is an organic residue and the two CH2 groups may be linked by a divalent group.
Optionally, R6 is a C1-30 hydrocarbyl group, optionally phenyl that may be unsubstituted or substituted with one or more C1-10alkyl groups.
Optionally, the two CH2 groups may be linked by ethylene or propylene.
Optionally, the solvent has formula CH3—C(R6)H—CH3.
Exemplary solvents comprising a CH2—C(R6)H—CH2 unit are cyclohexylbenzene and cumene.
(iii) Bicyclic, partially or fully saturated solvents, optionally solvents comprising a secondary carbon atom, optionally partially or fully saturated naphthalenes, for example tetralin and decalin.
(iv) Solvents of formula R8—CR7═CR7—CH2—R8 wherein R7 is H or C1-10 alkyl; and R8 in each occurrence is independently an organic residue, optionally a C1-20 hydrocarbyl group.
(v) Solvents comprising a benzyl group.
Optionally, the or each first solvent consists of 4-20 carbon atoms, optionally 10-20 C atoms, and 0, 1, 2 or 3 oxygen atoms only.
Preferably, the solvent is a liquid at 20° C. and has a boiling point of below 300° C., optionally no more than 250° C., at 1 atmosphere.
Preferably, the first solvent is cyclohexylbenzene. The ink may contain one or more further solvents that are miscible with the one or more first solvents. Exemplary further solvents may be selected from benzene substituted with one or more substituents selected from straight chain or branched C1-10alkyl or alkoxy groups.
Without wishing to be bound by any theory, it is believed that first solvents as described herein may be susceptible to oxidation, and that oxidised first solvents may react with the compounds of formula (I).
Stabiliser
Optionally, the stabiliser is an antioxidant. Without wishing to be bound by any theory, antioxidant stabilisers may prevent oxidation of the first solvent.
Optionally, the stabiliser is a phenol wherein one or more C atoms of the phenol are unsubstituted or substituted with one or more substituents, preferably one or more substituents selected from C1-10alkyl groups; C1-10alkoxy groups; and hydroxyl groups.
Optionally, the stabiliser is an arylamine (primary amine) or diarylamine (secondary amine) wherein the or each aryl group may be unsubstituted or substituted with one or more substituents, optionally one or more substituents selected from C1-10alkyl groups; C1-10alkoxy groups; and hydroxyl groups. Optionally, the or each aryl group is phenyl.
Exemplary stabilisers are butylated hydroxytoluene; polyhydroxyphenols; hydroquinone; aminophenols; and diphenylamine.
Preferably, the stabiliser is butylated hydroxytoluene (BHT):
Optionally, the stabiliser is provided in an amount in the range of 0.5-100 mg per 100 ml of ink, optionally 1-50 or 5-20 mg per 100 ml of ink.
Inkjet Printing
A device may be inkjet printed by providing a patterned insulating layer over the anode to define wells for printing of one colour (in the case of a monochrome device) or multiple colours (in the case of a multicolour, in particular full colour device). The patterned layer is typically a layer of photoresist that is patterned to define wells as described in, for example, EP 0880303.
As an alternative to wells, the ink may be printed into channels defined within a patterned layer. In particular, the insulating layer may be patterned to form channels which, unlike wells, extend over a plurality of pixels and which may be closed or open at the channel ends.
Other solution deposition techniques include spin-coating, slot die coating, dip-coating, flexographic printing, nozzle printing, and screen printing.
Charge Transporting and Charge Blocking Layers
A hole transporting layer may be provided between the anode 103 and the light-emitting layer 105.
An electron transporting layer may be provided between the cathode 107 and the light-emitting layer 105.
A charge-transporting layer or charge-blocking layer may be cross-linked. The crosslinkable group used for this crosslinking may be a crosslinkable group comprising a reactive double bond such and a vinyl or acrylate group, or a benzocyclobutane group. Crosslinking may be performed by thermal treatment, preferably at a temperature of less than about 250° C., optionally in the range of about 100-250° C.
A hole transporting layer may comprise or may consist of a hole-transporting polymer, which may be a homopolymer or copolymer comprising two or more different repeat units. The hole-transporting polymer may be conjugated or non-conjugated. Exemplary conjugated hole-transporting polymers are polymers comprising arylamine repeat units, for example as described in WO 99/54385 or WO 2005/049546 the contents of which are incorporated herein by reference. Conjugated hole-transporting copolymers comprising arylamine repeat units may have one or more co-repeat units selected from arylene repeat units, for example one or more repeat units selected from fluorene, phenylene, phenanthrene naphthalene and anthracene repeat units, each of which may independently be unsubstituted or substituted with one or more substituents, optionally one or more C1-40 hydrocarbyl substituents.
If present, a hole transporting layer located between the anode and the light-emitting layer 105 preferably has a HOMO level of less than or equal to 5.5 eV, more preferably around 4.8-5.5 eV or 5.1-5.3 eV as measured by cyclic voltammetry. The HOMO level of the hole transport layer may be selected so as to be within 0.2 eV, optionally within 0.1 eV, of an adjacent layer (such as a light-emitting layer) in order to provide a small barrier to hole transport between these layers.
Preferably a hole-transporting layer, more preferably a crosslinked hole-transporting layer, is adjacent to the light-emitting layer containing the compound of formula (I).
A hole-transporting layer may consist essentially of a hole-transporting material or may comprise one or more further materials. A light-emitting material, optionally a phosphorescent material, may be provided in the hole-transporting layer. A light-emitting material may be blended with or covalently bound to the hole-transporting material.
The light-emitting layer 105 may be adjacent to the cathode 107. In other embodiments, an electron-transporting layer may be provided between the light-emitting layer 105 and the cathode 107.
If present, an electron transporting layer located between the light-emitting layer and cathode preferably has a LUMO level of around 1.8-2.7 eV as measured by square wave voltammetry. An electron-transporting layer may have a thickness in the range of about 5-50 nm, optionally 5-20 nm.
Electron-transporting materials for forming an electron-transporting layer may be non-polymeric or polymeric compounds and may be deposited from a solution in a solvent that the components of the light-emitting layer 105 are substantially insoluble in. The electron transporting materials may be substituted with polar groups and may be soluble in polar solvents.
Exemplary electron transporting polymers suitable for forming an electron-transporting layer are described in WO 2012/133229, the contents of which are incorporated herein by reference.
Hole Injection Layers
A conductive hole injection layer, which may be formed from a conductive organic or inorganic material, may be provided between the anode 103 and the light-emitting layer 105 of an OLED as illustrated in
Cathode
The cathode 107 is selected from materials that have a work function allowing injection of electrons into the light-emitting layer of the OLED. Other factors influence the selection of the cathode such as the possibility of adverse interactions between the cathode and the light-emitting material. The cathode may consist of a single material such as a layer of aluminium. Alternatively, it may comprise a plurality of conductive materials such as metals, for example a bilayer of a low work function material and a high work function material such as calcium and aluminium, for example as disclosed in WO 98/10621. The cathode may comprise elemental barium, for example as disclosed in WO 98/57381, Appl. Phys. Lett. 2002, 81(4), 634 and WO 02/84759. The cathode may comprise a thin (e.g. 0.5-5 nm) layer of metal compound, in particular an oxide or fluoride of an alkali or alkali earth metal, between the organic layers of the device and one or more conductive cathode layers to assist electron injection, for example lithium fluoride as disclosed in WO 00/48258; sodium fluoride; barium fluoride as disclosed in Appl. Phys. Lett. 2001, 79(5), 2001; and barium oxide. In order to provide efficient injection of electrons into the device, the cathode preferably has a workfunction of less than 3.5 eV, more preferably less than 3.2 eV, most preferably less than 3 eV. Work functions of metals can be found in, for example, Michaelson, J. Appl. Phys. 48(11), 4729, 1977.
The cathode may be opaque or transparent. Transparent cathodes are particularly advantageous for active matrix devices because emission through a transparent anode in such devices is at least partially blocked by drive circuitry located underneath the emissive pixels. A transparent cathode comprises a layer of an electron injecting material that is sufficiently thin to be transparent. Typically, the lateral conductivity of this layer will be low as a result of its thinness. In this case, the layer of electron injecting material is used in combination with a thicker layer of transparent conducting material such as indium tin oxide.
It will be appreciated that a transparent cathode device need not have a transparent anode (unless a fully transparent device is desired), and so the transparent anode used for bottom-emitting devices may be replaced or supplemented with a layer of reflective material such as a layer of aluminium. Examples of transparent cathode devices are disclosed in, for example, GB 2348316.
Encapsulation
Organic optoelectronic devices tend to be sensitive to moisture and oxygen. Accordingly, the substrate 101 preferably has good barrier properties for prevention of ingress of moisture and oxygen into the device. The substrate is commonly glass, however alternative substrates may be used, in particular where flexibility of the device is desirable. For example, the substrate may comprise one or more plastic layers, for example a substrate of alternating plastic and dielectric barrier layers or a laminate of thin glass and plastic.
The device may be encapsulated with an encapsulant (not shown) to prevent ingress of moisture and oxygen. Suitable encapsulants include a sheet of glass, films having suitable barrier properties such as silicon dioxide, silicon monoxide, silicon nitride or alternating stacks of polymer and dielectric or an airtight container. In the case of a transparent cathode device, a transparent encapsulating layer such as silicon monoxide or silicon dioxide may be deposited to micron levels of thickness, although in one preferred embodiment the thickness of such a layer is in the range of 20-300 nm. A getter material for absorption of any atmospheric moisture and/or oxygen that may permeate through the substrate or encapsulant may be disposed between the substrate and the encapsulant.
Ink stability
Inks were prepared as set out in Table 1.
Comparative Inks 1 and 2 of a phenylimidazole emitter dissolved in cyclohexylbenzene were found to undergo a colour change over a period of 24 hours, indicating degradation of the ink.
In contrast
A white organic light-emitting device having the following structure was prepared:
ITO (45 nm)/HIL (65 nm)/LE (R) (22 nm)/LE (G, B) (75 nm)/Cathode
wherein ITO is an indium-tin oxide anode; HIL is a hole-injecting layer; LE (R) is a red light-emitting layer; LE (G, B) is a green and blue light-emitting layer; ETL is a electron-transporting layer; and the cathode comprises a layer of sodium fluoride in contact with the light-emitting layer, a layer of aluminium and a layer of silver.
To form the device, a substrate carrying ITO was cleaned using UV/Ozone. The hole injection layer was formed by spin-coating an aqueous formulation of a hole-injection material from Plextronics, Inc. and heating the resultant layer. The red light-emitting layer was formed by spin-coating Red Polymer 1 and crosslinking the polymer by heating. The green and blue light-emitting layer was formed by spin-coating an ink of containing 2 wt % of Host 1 (74 wt %), Green Emitter 1 (1 wt %) and Blue Emitter 1 (25 wt %) dissolved in cyclohexylbenzene and containing 12.5 mg of BHT per 100 ml of ink. The cathode was formed by evaporation of a first layer of sodium fluoride to a thickness of about 2 nm, a second layer of aluminium to a thickness of about 100 nm and a third layer of silver to a thickness of about 100 nm.
Red Polymer 1 was formed by Suzuki polymerisation as described in WO 00/53656 of monomers for forming a phenylene repeat unit, an amine repeat unit and a fluorene repeat unit substituted with crosslinkable group. The polymer was end-capped with a red-emitting end-capping group of formula:
Comparative Device 1
A device was prepared as described for White Device Example 1 except toluene was used in place of cyclohexylbenzene and BHT stabiliser was not included in the ink.
Comparative Device 2
A device was prepared as described for White Device Example 1 except that BHT stabiliser was not included in the ink.
Device Results
In contrast to Comparative Inks 1 and 2 that do not contain a stabiliser, the ink used in White Device Example 1 did not change colour indicating stabilisation by BHT.
The toluene-based ink used in formation of Comparative Device 1 did not show a colour change indicating that little or no degradation of this ink occurs.
Devices were tested at a brightness of 1000 cd/m2. Attempts to test Comparative Device 2 at this brightness failed due to degradation of the device at this brightness. Without wishing to be bound by any theory, it is believed that the poor performance of
Comparative Device 2 is due to degradation of the materials in the ink used in manufacture of this device.
Data for White Device Example 1 and Comparative Device 1 are provided in Table 2. Performance of the devices is similar. Without wishing to be bound by any theory, it is believed that degradation of the cyclohexylbenzene ink of Comparative Device 2 has is at least partially eliminated by the presence of the stabiliser.
Although the present invention has been described in terms of specific exemplary embodiments, it will be appreciated that various modifications, alterations and/or combinations of features disclosed herein will be apparent to those skilled in the art without departing from the scope of the invention as set forth in the following claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1503400.2 | Feb 2015 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/053599 | 2/19/2016 | WO | 00 |
