Summary of the Invention

The present invention relates to organic light-emitting devices and methods of making the same.

Background

Electronic devices comprising active organic materials are attracting increasing attention for use in devices such as organic light emitting diodes (OLEDs), organic

photoresponsive devices (in particular organic photovoltaic devices and organic photosensors), organic transistors and memory array devices. Devices comprising 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 or spin-coating.

An OLED may comprise a substrate carrying an anode, a cathode and one or more organic light-emitting layers between the anode and cathode.

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.

Suitable light-emitting materials include small molecule, polymeric and dendrimeric materials. Suitable light-emitting polymers include poly(arylene vinylenes) such as poly(p-phenylene vinylenes) and polyarylenes such as polyfiuorenes.

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. For example, J. Appl. Phys. 65, 3610, 1989 discloses a host material doped with a fluorescent light-emitting dopant (that is, a light-emitting material in which light is emitted via decay of a singlet exciton) and Appl. Phys. Lett., 2000, 77, 904 discloses a host material doped with a phosphorescent light emitting dopant (that is, a light-emitting material in which light is emitted via decay of a triplet exciton). Emission from more than one layer of an OLED, in particular to achieve white light emission, is disclosed in, for example, WO 2008/131750, DE 102007020644 and EP 1390962 and SPIE (2004), 5519, 42-47.

Summary of the Invention

In a first aspect the invention provides an organic light-emitting device comprising a first electrode, a second electrode and a first, a second and a third light-emitting layer between the first and second electrodes wherein the second light-emitting layer is disposed between the first and third light emitting layers and has a thickness of at least 10 nm.

Optionally, the second light-emitting layer has a thickness of no more than 40 nm, optionally no more than 30 nm.

Optionally, the first electrode is an anode; the second electrode is a cathode; the first light-emitting layer is disposed between the anode and the second light-emitting layer; and the third light-emitting layer is disposed between the cathode and the second light- emitting layer.

Optionally, the first light-emitting layer comprises a first phosphorescent light-emitting dopant, optionally a green phosphorescent light-emitting dopant.

Optionally, the first light-emitting layer comprises a first host material that is blended with or covalently bound to the first phosphorescent light-emitting dopant.

Optionally, the second light-emitting layer comprises a second phosphorescent light- emitting dopant, optionally a dopant having a longer peak emission wavelength than the first phosphorescent light-emitting dopant, optionally a red phosphorescent light-emitting dopant.

Optionally, the second light-emitting layer comprises a second host material that is blended with or covalently bound to the second phosphorescent light-emitting dopant.

Optionally, the third light-emitting layer comprises a fluorescent light-emitting material, optionally a fluorescent blue light-emitting material.

Optionally, the first and second host materials have a higher triplet energy level than the fluorescent light-emitting material. Optionally, the fluorescent blue light-emitting material is a polymer.

Optionally, the fluorescent light-emitting material has a triplet excited state energy level that is lower than the triplet excited state energy level of the first phosphorescent light- emitting dopant.

Optionally, the triplet excited state energy level of the first phosphorescent dopant is higher than that of the second phosphorescent dopant.

Optionally, the second phosphorescent light-emitting dopant is present in an amount of no more than 1 mol% relative to the other components of the second light-emitting layer.

Optionally, the device emits white light.

In a second aspect the invention provides a method of forming an organic light-emitting device according to the first aspect, the method comprising the steps of: depositing a first light-emitting layer over a first electrode; depositing a second light-emitting layer over the first light-emitting layer; depositing a third light-emitting layer over the second light- emitting layer; and depositing a cathode over the third light-emitting layer.

Optionally according to the second aspect at least one of the first, second and third light- emitting layers is formed by a solution processing method comprising the steps of depositing a composition comprising a solvent and the component or components of the light-emitting layer and evaporating the solvent.

Optionally according to the second aspect the first light-emitting layer is crosslinked prior to formation of the second light-emitting layer by the solution processing method.

Optionally according to the second aspect the second light-emitting layer is crosslinked prior to formation of the third light-emitting layer by the solution processing method.

In a third aspect the invention provides a method of tuning the colour of emission of an organic light emitting device comprising a first electrode, a second electrode and a first and a second light-emitting layer between the first and second electrodes, the method comprising the steps of: selecting a target colour range for emission of the OLED;

determining a thickness of one or more of the light-emitting layers to obtain an OLED emission colour within the selected colour range; and forming the OLED with the selected light-emitting layer thickness or thicknesses. Optionally according to the third aspect the OLED comprises a third light-emitting layer.

Optionally according to the third aspect the OLED is a white light-emitting OLED and the colour range is selected from a range of colour rendering index vales, a range of CIE(x) and CIE(y) values and a range of temperatures of a black body emitter.

The OLED formed by the method of the third aspect of the invention may comprise any of the features of the OLED described with respect to the first aspect of the invention, and may be formed using any of the method steps described with reference to the second aspect of the invention.

Description of the Drawings

The invention will now be described in more detail with reference to the drawings, in which:

Figure 1 illustrates schematically an OLED according to an embodiment of the invention; and

Figure 2 illustrates energy levels for the OLED of Figure 1.

Detailed Description of the Invention

Figure 1 , which is not drawn to any scale, illustrates schematically an OLED according to an embodiment of the invention. The OLED is carried on substrate 107 and comprises an anode 101, a cathode 105 and three light emitting layers 103G, 103R and 103B between the anode and the cathode. Light-emitting layer 103G comprises a host and a green phosphorescent light-emitting dopant, light-emitting layer 103R comprises a host and a red phosphorescent light-emitting dopant, and light-emitting layer 103B comprises a blue fluorescent light-emitting material.

In operation, holes injected from the anode and electrons injected from the cathode combine in at least the first light-emitting layer 103G and the third light-emitting layer 103B to form excitons. Singlet excitons formed in the third light-emitting layer 103B may decay directly from a singlet excited state Sm of the blue light-emitting material to provide blue light hvB. With reference to Figure 2, triplet excitons formed in layer 103G may be transferred from the triplet excited state energy level T _I G _H of the host to the lower triplet excited state energy level T _IG of the green dopant. This transfer is illustrated in Figure 2 by a dotted line between T _IGH and T _IG . The triplet exciton may then undergo radiative decay to produce green phosphorescence. Light-emitting layer 103G may further be provided with more than one light-emitting dopant, for example a green phosphorescent dopant and a further dopant that also has a triplet excited state lower than T _IG , for example a red phosphorescent dopant.

Light emission from layer 103R may occur by a mechanism similar to that described above with reference to emission from layer 103G. In addition to, or as an alternative to, recombination of holes and electrons to form excitons in light emitting layer 103R, triplet excitons may migrate from layer 103G and / or layer 103B into layer 103R where they may be absorbed by the red phosphorescent dopant.

Light emitted from each of these three layers may combine to provide white light. The white light may have CIE x coordinate equivalent to that emitted by a black body at a temperature in the range of 2500-9000K and a CIE y coordinate within 0.05 or 0.025 of the CIE y co-ordinate of said light emitted by a black body, optionally a CIE x coordinate equivalent to that emitted by a black body at a temperature in the range of 2700-4500K.

Figure 2, which is not drawn to any scale, illustrates schematically the energy levels of layers 103G, 103R and 103B the device of Figure 1.

The blue fluorescent material of layer 103B has a triplet energy level Ti _B that is higher than, or at least no more than 0.2 or 0.1 eV below, the triplet energy level T _IR of the red phosphorescent dopant in order to at least partially prevent quenching of red

phosphorescence by the blue fluorescent material. Moreover, these relative energy levels may allow triplet excitons generated in layer 103B to be absorbed by the red

phosphorescent dopant and undergo radiative decay.

Triplet excitons may have a relatively long lifetime, and as such it may be possible for triplet excitons generated in layer 103G to migrate through layer 103R into layer 103B, which may be more likely at lower concentrations of red phosphorescent dopant in layer 103R, where they may be quenched by the blue fluorescent material which has triplet excited state T _IB that is lower than T _IG . Accordingly, the layer 103R has a thickness of at least 10 nm, which may prevent at least some triplet excitons generated in layer 103G from migrating through layer 103R and reaching layer 103B.

The host material of layer 103R has a triplet energy level T _IRH that is no less than 0.1 eV below the triplet energy level T _IG of the green phosphorescent dopant, and optionally the same as or higher than T _IG in order to at least partially prevent quenching of green phosphorescence by transfer of triplet excitons from T _IG to T _IRH . Moreover, use of a host material for layer 103R having a T _IRH energy level that is the same as or higher than T _IG , for example at least kT higher than T _IG , may cause triplet excitons generated in layer 103G to be confined to that layer. Some triplet excitons may still be absorbed by the red- emitting dopant of layer 103R, however the red-emitting dopant of layer 103R may be provided in an amount that is sufficiently high to generate red emission but sufficiently low to at least partially avoid quenching of green phosphorescence from layer 103G by the red-emitting dopant. The red-emitting dopant may be provided in an amount less than 2.5 mol %, less than 2 mol %, less than 1 mol %, less than 0.5 mol % or less than 0.25 mol % relative to other components of this layer. The red-emitting dopant may be provided in an amount in the range of 0.1-1 mol %.

It has been postulated that degradation of OLEDs may be caused by exciton-exciton interactions, such as triplet-triplet interactions that form highly energetic "super-excited" states. However, the presence of a phosphorescent dopant in both layers 103G and 103R provides a radiative decay pathway for triplet excitons that may at least partially avoid such triplet-triplet interactions.

The thickness of one or more of layers 103R, 103G and 103B may be selected in order to obtain a selected colour output of the OLED, such as a selected colour rendering index (CRI) or selected CIE(x) and CIE(y) co-ordinates. These layer thicknesses may affect the overall OLED colour by modifying the cavity defined by the organic stack of the OLED so as to increase the proportion of light of one colour emitted by the OLED relative to all colours light emitted by the OLED. Furthermore, adjusting layer thicknesses may cause one layer to emit a greater proportion of light by moving part or all of that layer into a recombination zone of the device. For example, increasing thickness of layer 103G may increase green emission of the device, even if the ratio of green emitter to other emitters is unchanged, by moving more of the green layer into a recombination zone.

Accordingly, colour emitted by the OLED may be tuned not only by selection of the emitters but also by thickness of the OLED layers.

Highest occupied molecular orbital (HOMO) levels of the components of layers 103G, 103R and 103B may be selected by appropriate choice of host and / or dopants in order that holes injected from the anode may efficiently reach the light-emitting layer 103B. Likewise, the lowest unoccupied molecular orbital (LUMO) levels of these components may be selected in order that electrons injected from the cathode may efficiently reach the light-emitting layer 103G.

The HOMO level of the host and / or dopant of layer 103R is optionally no more than 0.5 eV, optionally no more than 0.3 eV, deeper (further from vacuum level) than the HOMO level of layer 103G and / or layer 103B. This may at least partially prevent trapping of holes at layer 103R.

The LUMO level of the host and / or dopant of layer 103R is optionally no more than 1.0 eV, optionally no more than 0.5 eV, optionally no more than 0.3 eV, shallower (closer to vacuum level) than the LUMO level of layer 103G and / or layer 103B. This may at least partially prevent trapping of electrons at layer 103R.

HOMO and LUMO levels may be measured by cyclic voltammetry, for example.

Blue fluorescent materials

Exemplary blue fluorescent materials optionally have a peak photo luminescence wavelength less than or equal to 480 nm, such as in the range of 400-480 nm.

The blue fluorescent material may be any form of material, including small molecule, polymeric and dendrimeric materials. Blue fluorescent polymeric materials include materials that have a partially conjugated, fully conjugated or non-conjugated polymer backbone.

An exemplary blue emitter is an at least partially conjugated polymeric emitter comprising optionally substituted (hetero)arylene repeat units, for example optionally substituted fluorene, phenylene and / or indenofiuorene repeat units, and / or

(hetero)arylamine repeat units.

An exemplary blue emitter comprises at least 50 mol % of fluorene repeat units and up to 50 mol %, up to 30 mol % or up to 15 mol % of (hetero)arylamine repeat units.

Exemplary (hetero)arylamine repeat units include repeat units of formula (V):

(V)

wherein Ar ¹ and Ar ² in each occurrence are independently selected from optionally substituted aryl or heteroaryl groups, n is greater than or equal to 1 , preferably 1 or 2, R is H or a substituent, preferably a substituent, and x and y are each independently 1 , 2 or 3.

3 3

R is preferably alkyl, for example C _1-20 alkyl, Ar , or a branched or linear chain of Ar groups, for example -(Ar ³ ) _r , wherein Ar ³ in each occurrence is independently selected from aryl or heteroaryl and r is at least 1 , optionally 1 , 2 or 3.

Any of Ar ¹ , Ar ² and Ar ³ may independently be substituted with one or more substituents. Preferred substituents are selected from the group R consisting of:

alkyl, for example C _1-20 alkyl, wherein one or more non-adjacent C atoms may be replaced with O, S, substituted N, C=0 and -COO- and one or more H atoms of the alkyl group may be replaced with F or aryl or heteroaryl optionally substituted with one or more groups R ⁴ ,

aryl or heteroaryl optionally substituted with one or more groups R ⁴ ,

NR ⁵ 2, OR ⁵ , SR ⁵ ,

fluorine, nitro and cyano;

wherein each R ⁴ is independently alkyl, for example C _1-20 alkyl, in which one or more non-adjacent C atoms may be replaced with O, S, substituted N, C=0 and -COO- and one or more H atoms of the alkyl group may be replaced with F, and each R ⁵ is independently selected from the group consisting of alkyl and aryl or heteroaryl optionally substituted with one or more alkyl groups.

R may comprise a crosslinkable-group, for example a group comprising a polymerisable double bond such and a vinyl or acrylate group, or a benzocyclobutane group.

Any of the aryl or heteroaryl groups in the repeat unit of Formula (V) may be linked by a direct bond or a divalent linking atom or group. Preferred divalent linking atoms and groups include O, S; substituted N; and substituted C.

Where present, substituted N or substituted C of R ³ , R ⁴ or of the divalent linking group may independently in each occurrence be NR ⁶ or CR ⁶ ₂ respectively wherein R ⁶ is alkyl or optionally substituted aryl or heteroaryl. Optional substituents for aryl or heteroaryl groups R ⁶ may be selected from R ⁴ or R ⁵ .

In one preferred arrangement, R is Ar 3 and each of Ar 1 , Ar2 and Ar 3 are i·ndependently and optionally substituted with one or more C _1-20 alkyl groups.

Particularly preferred units satisfying Formula 1 include units of Formulae 1-3:

wherein Ar ¹ and Ar ² are as defined above; and Ar ³ is optionally substituted aryl or heteroaryl. Where present, preferred substituents for Ar include substituents as

1 2

described forAr and Ar , in particular alkyl and alkoxy groups.

Ar 1 , Ar2 and Ar 3 are preferably phenyl, each of which may independently be substituted with one or more substituents as described above.

In another preferred arrangement, aryl or heteroaryl groups of formula (V) are phenyl, each phenyl group being optionally substituted with one or more alkyl groups. In another preferred arrangement, Ar 1 , Ar2 and Ar 3 are phenyl, each of which may be substituted with one or more C _1-20 alkyl groups, and r = 1.

In another preferred arrangement, Ar 1 and Ar 2 are phenyl, each of which may be substituted with one or more C _1-20 alkyl groups, and R is 3,5-diphenylbenzene wherein each phenyl may be substituted with one or more alkyl groups.

Exemplary fiuorene repeat units include repeat units of formula IV:

(IV)

wherein R ¹ and R ² are independently H or a substituent and wherein R ¹ and R ² may be linked to form a ring.

R ¹ and R ² are optionally selected from the group consisting of hydrogen; optionally

3 3 3

substituted Ar or a linear or branched chain of Ar groups, wherein Ar is as described above; and optionally substituted alkyl, for example C _1-20 alkyl, wherein one or more non- adjacent C atoms of the alkyl group may be replaced with O, S, substituted N, C=0 and - COO-.

In the case where R ¹ or R ² comprises alkyl, optional substituents of the alkyl group include F, CN, nitro, and aryl or heteroaryl optionally substituted with one or more groups R ⁴ wherein R ⁴ is as described above.

In the case where R ¹ or R ² comprises aryl or heteroaryl, each aryl or heteroaryl group may independently be substituted. Preferred optional substituents for the aryl or heteroaryl groups include one or more substituents R .

1 2

Optional substituents for the fiuorene unit, other than substituents R and R , are preferably selected from the group consisting of alkyl wherein one or more non-adjacent C atoms may be replaced with O, S, substituted N, C=0 and -COO-, optionally substituted aryl, optionally substituted heteroaryl, fluorine, cyano and nitro. Where present, substituted N in repeat units of formula (IV) may independently in each occurrence be NR ⁵ or NR ⁶ .

In one preferred arrangement, at least one of R 1 and R2 compri·ses an optionally substituted C1-C20 alkyl or an optionally substituted aryl group, in particular phenyl substituted with one or more C _1-20 alkyl groups.

Host / dopant systems

Phosphorescent light-emitting dopants include metal complexes comprising optionally substituted complexes of formula (II):

ML'qlAlA

(II)

wherein M is a metal; each of L 1 , L2 and L 3 is a coordinating group; q is an integer; r and s are each independently 0 or an integer; and the sum of (a. q) + (b. r) + (c.s) is equal to the number of coordination sites available on M, wherein a is the number of coordination sites on L ¹ , b is the number of coordination sites on L ² and c is the number of coordination sites on L .

Heavy elements M induce strong spin-orbit coupling to allow rapid intersystem crossing and emission from triplet or higher states (phosphorescence). Suitable heavy metals M include d-block metals, in particular those in rows 2 and 3 i.e. elements 39 to 48 and 72 to 80, in particular ruthenium, rhodium, palladium, rhenium, osmium, iridium, platinum and gold. Iridium is particularly preferred.

Suitable coordinating groups for the f-block metals include oxygen or nitrogen donor systems such as carboxylic acids, 1 ,3-diketonates, hydroxy carboxylic acids,

Schiff bases including acyl phenols and iminoacyl groups. As is known, luminescent lanthanide metal complexes require sensitizing group(s) which have the triplet excited energy level higher than the first excited state of the metal ion. Emission is from an f-f transition of the metal and so the emission colour is determined by the choice of the metal. The sharp emission is generally narrow, resulting in a pure colour emission useful for display applications. The d-block metals are particularly suitable for emission from triplet excited states. These metals form organometallic complexes with carbon or nitrogen donors such as porphyrin or bidentate ligands of formula (III):

wherein Ar ⁴ and Ar ⁵ may be the same or different and are independently selected from optionally substituted aryl or heteroaryl; X ¹ and Y ¹ may be the same or different and are independently selected from carbon or nitrogen; and Ar ⁴ and Ar ⁵ may be fused together. Ligands wherein X ¹ is carbon and Y ¹ is nitrogen are particularly preferred.

Examples of bidentate ligands are illustrated below:

Each of Ar ⁴ and Ar ⁵ may carry one or more substituents. Two or more of these substituents may be linked to form a ring, for example an aromatic ring. Particularly preferred substituents include fluorine or trifluoromethyl which may be used to blue-shift the emission of the complex as disclosed in WO 02/45466, WO 02/44189, US 2002- 1 17662 and US 2002-182441 ; alkyl or alkoxy groups as disclosed in JP 2002-324679; carbazole which may be used to assist hole transport to the complex when used as an emissive material as disclosed in WO 02/81448; bromine, chlorine or iodine which can serve to functionalise the ligand for attachment of further groups as disclosed in WO 02/68435 and EP 1245659; and dendrons which may be used to obtain or enhance solution processability of the metal complex as disclosed in WO 02/6655.

A dendron may have optionally substituted formula (VIII)

(VIII)

wherein BP represents a branching point for attachment to a core and Gi represents first generation branching groups.

The dendron may be a first, second, third or higher generation dendron. Gi may be substituted with two or more second generation branching groups G ₂ , and so on, as in optionally substituted formula (Villa):

(Via)

wherein u is 0 or 1 ; v is 0 if u is 0 or may be 0 or 1 if u is 1 ; BP represents a branching point for attachment to a core and Gi, G ₂ and G ₃ represent first, second and third generation dendron branching groups.

Preferably, each group G is selected from the group consisting of aryl and heteroaryl groups. Preferably, at least some or all of the G groups are optionally substituted phenyl.

BP and / or any group G may be substituted with one or more substituents, for example one or more C _1-20 alkyl or alkoxy groups. A light-emitting dendrimer typically comprises a light-emitting core bound to one or more dendrons, wherein each dendron comprises a branching point and two or more dendritic branches. Preferably, the dendron is at least partially conjugated, and at least one of the core and dendritic branches comprises an aryl or heteroaryl group.

Other ligands suitable for use with d-block elements include diketonates, in particular acetylacetonate (acac); triarylphosphines and pyridine, each of which may be substituted.

A green emitting dopant may optionally have a photoluminescent spectrum with a peak in the range of 490-560 nm.

An exemplary green emitter is optionally substituted tris-phenylpyridine iridium (III).

A red emitting dopant may optionally have a peak in its photoluminescent emission spectrum at around 570-630 nm.

An exemplary red emitter is tris-phenylpyridine iridium (III) wherein each pyridine ligand is substituted with 1,3-diphenyltriazine.

The host may be any material having an excited state energy level that is higher than that of the dopant it is used with. Preferably, the gap between the host and dopant excited state energy levels is at least kT in order to avoid back transfer of excitons from the dopant to the host material. The host material is optionally solution processable.

Further phosphorescent dopants may be used, for example a dopant having a wavelength in the range 540-600 nm.

The host materials used for layers 103R and 103G may be the same or different. If they are the same then it will be appreciated that the host material has a triplet energy level that is higher than that of both the red and green phosphorescent dopants.

Suitable hosts for green or red phosphorescent dopants include optionally substituted diaryltriazines or triaryltriazines. Triazine-containing host materials are described in more detail in WO 2008/025997 and include, for example, optionally substituted triphenyltriazine. Optional substituents of the phenyl groups include one or more alkyl groups, for example C _1-20 alkyl groups. The host may be a polymer comprising triazine repeat units, in particular an optionally substituted di-or tri-aryltriazine repeat unit attached as a side group through one of the aryl groups, or a repeat unit attached in the polymer main chain through two of the aryl groups. A host polymer comprising triazine repeat units may comprise further repeat units selected from (hetero) arylene co-repeat units, such as phenyl, fluorene or indeno fluorene repeat units as described above, wherein each of said (hetero)arylene repeat units may optionally be substituted with one or more substituents such as alkyl or alkoxy groups. One class of co-repeat units is fluorene repeat units of formula (IV) as described above.

An exemplary triazine repeat unit of a host polymer has formula (VI):

(VI)

wherein Ar ¹ , Ar ² and Ar ³ are as described with reference to formula (V) above, and may each independently be substituted with one or more substituents described with reference to Ar ¹ , Ar ² and Ar ³ , and z in each occurrence is independently at least 1, optionally 1, 2 or 3. Preferably, Ar ¹ , Ar ² and Ar ³ of formula (VI) are each phenyl, each phenyl being optionally and independently substituted with one or more C _1-20 alkyl groups.

A host polymer comprising aromatic repeat units may form conjugated chains of aromatic units. This conjugation may be interrupted or reduced by inclusion of suitable repeat units in the polymer backbone, such as repeat units that form a twist in the polymer backbone and repeat units that break conjugation.

An example of a repeat unit that may cause a twist in the polymer backbone (for example by steric hindrance) is 1 ,4-phenylene substituted with one or more groups such as one or more alkyl or alkoxy groups, e.g. C _1-20 alkyl or alkoxy groups, in particular 2,5- disubstituted-l ,4-phenylene repeat units.

A class of repeat units that may break conjugation include arylene or heteroarylene repeat units that are linked to adjacent repeat units through non-conjugating positions.

Exemplary units of this kind include 1,2-phenylene repeat units and 1 ,3-phenylene repeat units, each of which may optionally be substituted with one or more substituents such as one or more substituents R ¹ as described above, in particular or more alkyl or alkoxy groups, e.g. C _1-20 alkyl or alkoxy groups, and fiuorene repeat units linked through 2- and / or 6-positions which again may optionally be substituted with one or more substituents such as one or more substituents R ¹ as described above.

Exemplary phenylene repeat units have formula (VII):

(VII)

wherein R ¹ is as described above with reference to formula (IV) and p is 1, 2, 3 or 4, optionally 1 or 2.

Another class of repeat units that may break conjugation include repeat units having formula -Ar-Sp-Ar- wherein each Ar is an optionally substituted aryl or heteroaryl group and Sp is a spacer atom or chain comprising at least one non-conjugating atom between the two Ar groups. Exemplary Ar groups include optionally substituted phenyl. Optional substituents may be one or more substituents R ¹ as described above, in particular or more alkyl or alkoxy groups, e.g. C _1-20 alkyl or alkoxy groups. Exemplary groups Sp include groups of formula -(CH2) _m - wherein m is at least 1 , for example an integer between 1-10, and wherein each H may independently be replaced with a substituent, for example an alkyl group, and wherein one or more carbon atoms may be replaced with a heteroatom, for example O or S.

Exemplary repeat units of a host polymer may include one or more of:

(i) (hetero)arylene co-repeat units, such as phenyl, fiuorene or indenofiuorene repeat units as described above, each of which may optionally be substituted, in particular fiuorene repeat units of formula (IV) and / or phenylene repeat units as described above;

(ii) optionally substituted arylamine repeat units, in particular repeat units of formula (V) as described above; and / or

(iii) optionally substituted triazine repeat units, in particular repeat units of

formula (VI) as described above. Each light-emitting layer may be crosslinkable, in particular if a further layer, such as a further light-emitting layer, is to be deposited onto that layer

The host and the light-emitting dopant may be physically mixed. Alternatively, the light- emitting dopant may be chemically bound to the host. In the case of a polymer host, the light-emitting dopant may be chemically bound as a substituent attached to the polymer backbone, incorporated as a repeat unit in the polymer backbone or provided as an end- group of the polymer as disclosed in, for example, EP 1245659, WO 02/31896, WO 03/18653 and WO 03/22908.

The light-emitting dopant may be attached as a side-chain or end group of a host polymer by providing a reactive group on the light-emitting dopant capable of reacting with the host polymer to form a covalent bond with the polymer.

The light-emitting dopant may be provided in the main chain of a host polymer by providing the light-emitting dopant with two reactive polymerisable groups capable of undergoing polymerization with the reactive groups of the other monomers used to form the polymer. In the case of a metal complex light-emitting dopant comprising one or more ligands of formula (III), the reactive group or groups may be provided as substituents on one or more of Ar ⁴ and / or Ar ⁵ . In another arrangement, Ar ⁴ and / or Ar ⁵ may be substituted, for example substituted with phenyl, and the substituent may in turn be substituted with one or more reactive groups for binding to the host polymer or polymerization into the host polymer main chain.

This binding may result in more efficient transfer of excitons from the host polymer to the light emitting dopant because it may provide intramolecular exciton transfer pathways unavailable to a corresponding mixed system.

Moreover, binding may be beneficial for processing reasons. For example, if the light emitting dopant has low solubility then binding it to a soluble polymer allows the light emitting dopant to be carried in solution by the charge transporting material, enabling device fabrication using solution processing techniques. Furthermore, binding the light emitting dopant to the polymer may prevent phase separation effects in solution- processed devices that may be detrimental to device performance. More than one light-emitting dopant may be used in layers 103R and 103G.

Charge transporting layers

A hole transporting layer may be provided between the anode and the light-emitting layers. Likewise, an electron transporting layer may be provided between the cathode and the light-emitting layers.

Similarly, an electron blocking layer may be provided between the anode and the light- emitting layer and a hole blocking layer may be provided between the cathode and the light-emitting layer. Transporting and blocking layers may be used in combination. Depending on its HOMO and LUMO levels, a single layer may both transport one of holes and electrons and block the other of holes and electrons.

If present, a hole transporting layer located between the anode and the light-emitting layers preferably has a HOMO level of less than or equal to 5.5 eV, more preferably around 4.8-5.5 eV. 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.

If present, an electron transporting layer located between the light-emitting layers and cathode preferably has a LUMO level of around 3-3.5 eV. For example, a layer of a silicon monoxide or silicon dioxide or other thin dielectric layer having thickness in the range of 0.2-2nm may be provided between the light-emitting layer nearest the cathode and the cathode. HOMO and LUMO levels may be measured by cyclic voltammetry.

A hole transporting layer may contain a hole -transporting (hetero)arylamine, such as a homopolymer or copolymer comprising hole transporting repeat units of formula (V). Exemplary copolymers comprise repeat units of formula (V) and optionally substituted (hetero)arylene co-repeat units, such as phenyl, fluorene or indenofiuorene repeat units as described above, wherein each of said (hetero)arylene repeat units may optionally be substituted with one or more substituents such as alkyl or alkoxy groups. Specific co- repeat units include fluorene repeat units of formula (IV) and optionally substituted phenylene repeat units as described above. The hole -transporting layer may be crosslinkable, in particular if it is formed by depositing a hole transporting material from a solution in a solvent. For example a polymer comprising a repeat unit of formula (V), optionally with one or more arylene co- repeat units, may be provided with crosslinkable substituents on one or more of the arylene repeat units and repeat units of formula (V).

Likewise, an electron transporting layer may contain a polymer comprising a chain of optionally substituted arylene repeat units, such as a chain of fluorene repeat units.

Polymer synthesis

Preferred methods for preparation of conjugated polymers, such as polymers comprising repeat units of formula (IV) and / or (V) as described above, comprise a "metal insertion" wherein the metal atom of a metal complex catalyst is inserted between an aryl or heteroaryl group and a leaving group of a monomer. Exemplary metal insertion methods are Suzuki polymerisation as described in, for example, WO 00/53656 and Yamamoto polymerisation as described in, for example, T. Yamamoto, "Electrically Conducting And Thermally Stable π - Conjugated Poly(arylene)s Prepared by Organometallic Processes", Progress in Polymer Science 1993, 17, 1153-1205. In the case of Yamamoto polymerisation, a nickel complex catalyst is used; in the case of Suzuki polymerisation, a palladium complex catalyst is used.

For example, in the synthesis of a linear polymer by Yamamoto polymerisation, a monomer having two reactive halogen groups is used. Similarly, according to the method of Suzuki polymerisation, at least one reactive group is a boron derivative group such as a boronic acid or boronic ester and the other reactive group is a halogen. Preferred halogens are chlorine, bromine and iodine, most preferably bromine.

It will therefore be appreciated that repeat units illustrated throughout this application may be derived from a monomer carrying suitable leaving groups. Likewise, an end group or side group may be bound to the polymer by reaction of a suitable leaving group.

Suzuki polymerisation may be used to prepare regioregular, block and random copolymers. In particular, homopolymers or random copolymers may be prepared when one reactive group is a halogen and the other reactive group is a boron derivative group. Alternatively, block or regioregular copolymers may be prepared when both reactive groups of a first monomer are boron and both reactive groups of a second monomer are halogen.

As alternatives to halides, other leaving groups capable of participating in metal insertion include sulfonic acids and sulfonic acid esters such as tosylate, mesylate and trifiate.

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 and the light-emitting layers to assist hole injection from the anode into the layer or layers of semiconducting polymer. A hole transporting layer may be used in combination with a hole injection layer.

Examples of doped organic hole injection materials include optionally substituted, doped poly(ethylene dioxythiophene) (PEDT), in particular PEDT doped with a charge- balancing polyacid such as polystyrene sulfonate (PSS) as disclosed in EP 0901176 and EP 0947123, polyacrylic acid or a fiuorinated sulfonic acid, for example Nafion ®;

polyaniline as disclosed in US 5723873 and US 5798170; and optionally substituted polythiophene or poly(thienothiophene). Examples of conductive inorganic materials include transition metal oxides such as VOx MoOx and RuOx as disclosed in Journal of Physics D: Applied Physics (1996), 29(11), 2750-2753.

Cathode

The cathode is selected from materials that have a workfunction allowing injection of electrons into the light-emitting layer. Other factors influence the selection of the cathode such as the possibility of adverse interactions between the cathode and the light- emitting materials. The cathode may consist of a single material such as a layer of aluminium. Alternatively, it may comprise a plurality of metals, for example a bilayer of a low workfunction material and a high workfunction material such as calcium and aluminium as disclosed in WO 98/10621 ; elemental barium as disclosed in WO

98/57381, Appl. Phys. Lett. 2002, 81(4), 634 and WO 02/84759; or a thin layer of metal compound, in particular an oxide or fluoride of an alkali or alkali earth metal, to assist electron injection, for example lithium fluoride as disclosed in WO 00/48258; 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(1 1), 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, of course, 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 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 a plastic as in US 6268695 which discloses a substrate of alternating plastic and barrier layers or a laminate of thin glass and plastic as disclosed in EP 0949850.

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 as disclosed in, for example, WO 01/81649 or an airtight container as disclosed in, for example, WO 01/19142. 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.

Solution processing

Suitable solvents for forming compositions of the polymer for solution processing include many common organic solvents, such as mono- or poly-alkylbenzenes such as toluene and xylene.

Exemplary solution deposition techniques including printing and coating techniques such spin-coating, dip-coating, roll-to-roll coating or roll-to-roll printing, doctor blade coating, slot die coating, gravure printing, screen printing and inkjet printing.

Coating methods, such as those described above, are particularly suitable for devices wherein patterning of the electroluminescent material is unnecessary - for example for lighting applications or simple monochrome segmented displays.

Printing is particularly suitable for high information content displays, in particular full colour displays. A device may be inkjet printed by providing a patterned layer over the first electrode and defining 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 photoresist 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.

A number of methods may be used to at least partially avoid dissolution of an underlying organic layer during solution deposition of one or more further organic layers on the underlying organic layer. The underlying organic layer may be rendered insoluble by crosslinking prior to solution deposition of a further layer. Crosslinking may be provided by substituents on the materials forming the underlying layer, such as crosslinking substituents on the host and / or dopant material of a light-emitting layer. Alternatively or additionally, a crosslinkable additive may be included in the composition used to form the underlying layer. Alternatively or additionally, the further layer may be formed from a solution comprising a solvent in which the underlying organic layer is insoluble.

Applications

OLEDs as described herein may be used in a wide range of applications, including but not limited to use as display backlights, for example LCD backlights, area illumination and displays. White light-emitting OLEDs may comprise uniform emissive layers. OLEDs for use in displays may comprise a patterned emissive layer or layers and / or a patterned electrode to provide individual display pixels.

Device Example 1

An organic light-emitting device having the following structure was formed on a glass substrate:

ITO / HIL (50 nm) / HTL (21 nm) / ELG (31 nm) / ELR ( 10 nm) / ELB (49 nm) / Cathode

wherein ITO is an indium-tin oxide anode; HIL is a layer of hole-injection material available from Plextronics Inc., a HTL is a hole transporting layer; ELG is a light- emitting layer including a green phosphorescent light-emitting material; ELR is a red phosphorescent light-emitting layer; ELB is a blue fluorescent light-emitting layer; and Cathode is a cathode comprising a trilayer of a metal fluoride, aluminium and silver.

HIL, HTL, ELG, ELR and ELB were each formed by spin-coating a solution comprising the components of that layer and a solvent, and evaporating the solvent. HTL, ELG and ELR comprise crosslinkable groups that were cross-linked prior to spin-coating of the overlying layer.

HTL was formed by spin-coating Hole Transporting Polymer 1 formed by Suzuki polymerisation, as described in WO 00/53656, of the following monomers:

7.5 mol %

ELG was formed by spin-coating a polymer formed by Suzuki polymerisation, as described in WO 00/53656, of monomers and a red phosphorescent end-capping unit in the following molar percentages:

ELG includes both a green phosphorescent repeat unit and a red phosphorescent end- capping group.

ELR was formed by spin-coating Red Polymer 1 formed by Suzuki polymerisation, as described in WO 00/53656, of monomers and a red phosphorescent end-capping unit in the following molar percentages:

10 % 0.15 %

ELB was formed by spin-coating Blue Polymer 1 formed by Suzuki polymerisation, as described in WO 00/53656, of monomers in the following molar percentages:

Device Example 2

A device was made as described with respect to Example 1 except that layer ELR was formed to a thickness of 15 nm.

Device Example 3 A device was made as described with respect to Example 1 except that layer ELR was formed to a thickness of 20 nm.

Device Example 4

A device was made as described with respect to Example 1 except that layer ELR was formed to a thickness of 40 nm.

Comparative Device 1

A device was made as described with respect to Example 1 except that layer ELR was formed to thicknesses of 5 nm.

With reference to Table 1 below, it can be seen that external quantum efficiency (EQE) is higher at thicknesses at or above 10 nm. Moreover, efficiency measured in lumens / Watt is also higher at thicknesses above 10 nm despite a small increase in drive voltage at higher thicknesses.

Table 1

Without wishing to be bound by any theory, it is believed that increasing thickness of the layer ELR reduces the probability of quenching of a triplet exciton generated in the green phosphorescent layer by the material of the blue fluorescent layer.

Comparative Example 2

A device was made as described with respect to Example 1 except that Red Polymer 1 of emitting layer ELR was replaced with non-emissive Comparative Polymer 1 in which the red phosphorescent emitter is absent to provide a non-emissive layer.

Device Example 5

A device was made as described with respect to Example 1 except that the red phosphorescent material was Red Polymer 2, as illustrated below.

Device Example 6

A device was made as described with respect to Example 1 except that the red phosphorescent material was Red Polymer 3, as illustrated below.

The compositions of the polymers used to form ELR in the devices of Device Example 1 , Comparative Device 2 and Device Example 5 are shown in Table 2 below.

Table 2

Lifetime of devices, that is the time taken for luminance of the device to decay by 50% at constant current, was measured from a starting luminance of 1000 cd/m ² .

The lifetime of the device of Device Example 5 containining light-emitting layer ELR is a factor of 3 higher than Comparative Device 2 in which emissive layer ELR has been replaced with a non-emissive layer. Lifetime of light-emitting layer ELR of Device Example 5 is 5 times higher than that of Comparative Device 2.

Without wishing to be bound by any theory, it is believed that the presence of a phosphorescent dopant in the layer between ELG and ELB provides a pathway for radiative decay of triplet excitons in this layer (either by exciton migration from ELG or ELB, or by recombination of holes and electrons in this layer), thus reducing the probability of triplet-triplet interactions as compared to a device in which this layer does not comprise a phosphorescent dopant. Red emission from this layer may contribute to overall white light emission from the OLED.

Device Example 7

A device having the following structure was prepared as described with reference to Device Example 1 :

ITO / HIL (16 nm) / HTL (22 nm) / ELG (30 nm) / ELR (20 nm) / ELB (51 nm) / Cathode

wherein: HTL was formed by spin-coating Hole Transporting Polymer 1;

ELG is a green light-emitting layer formed by spin-coating a polymer formed by Suzuki polymerisation as described in WO 00/53656 of the following monomers:

7.8 % ELR is a red light-emitting layer formed by spin-coating a polymer formed by Suzuki polymerisation as described in WO 00/53656 of the following monomers and red phosphorescent end-capping group:

ELB is a blue light-emitting layer formed by spin-coating a polymer formed by Suzuki polymerisation as described in WO 00/53656 of the following monomers:

1 %

The device produced white light having CIE coordinates (0.476, 0.419). The time taken for the device to fall to 70% of a starting luminance of 1000 cd / m ² was 706 hours. The device had an external quantum efficiency of 1 1.47 %.

Device Examples 8-10

Organic light-emitting device having the following structure were formed on a glass substrate, according to the method described in Device Example 1 :

ITO / HIL (15 nm) / HTL (23 nm) / ELG (29 nm) / ELR (21 nm) / ELB (51 nm) / Cathode HTL was formed by spin-coating Hole Transporting Polymer 1 as described in Device Example 1.

ELG was formed by spin-coating the polymer used to form ELG as described in Device Example 1.

ELB was formed by spin-coating Blue Polymer 1 as described in Device Example 1.

ELR was formed by spin coating a red polymer containing the repeat units of Red Polymer 1 but with variation of the amount of red phosphorescent end-capping material as set out in Table 3 (increased amount of the end-capping material was provided for by a corresponding reduction in amount of the 2,7-dibromo-9,9-di(3-hexylphenyl)fiuorene monomer).

Table 3

Performance of the devices is set out in Tables 4 and 5. Data in Table 4 is at a brightness of 1 ,000 cd/m 2. Data in Table 5 is at a starting brightness of 2,000 cd/m 2.

Table 4

Table 5

As shown in Table 5, increasing the concentration of the red phosphorescent material increases the lifetime of the devices. Without wishing to be bound by any theory, it is believed that the concentrations of red emitters in these examples provide a pathway for radiative decay of excitons in the red-emitting layer without being high enough to cause substantial quenching of green phosphorescence from adjacent layer ELG.

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.