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  • Y10S428/917—Electroluminescent

Definitions

• This invention relates to an electroluminescent device comprising a cathode and an anode and, located therebetween, a light-emitting layer (LEL) comprising a phosphorescent guest material, a hole- and electron-transporting host material, and an efficiency-enhancing material having an ionization potential lower than that of the host material and a triplet energy level that is lower than that of the phosphorescent guest material by no more than 0.2 eV.
• LEL light-emitting layer
• an organic EL device is comprised of an anode for hole injection, a cathode for electron injection, and an organic medium sandwiched between these electrodes to support charge recombination that yields emission of light. These devices are also commonly referred to as organic light-emitting diodes, or OLEDs.
• organic EL devices are Gurnee et al. U.S. Pat. No. 3,172,862, issued Mar. 9, 1965; Gurnee U.S. Pat. No. 3,173,050, issued Mar.
• organic EL elements consisting of extremely thin layers (e.g. ⁇ 1.0 ⁇ m ) between the anode and the cathode.
• organic EL element encompasses the layers between the anode and cathode.
• the light-emitting layer commonly consists of a host material doped with a guest material, also known as a dopant.
• a host material doped with a guest material, also known as a dopant.
• HIL hole-injecting layer
• HTL hole-transporting layer
• LEL light- emitting layer
• ETL electron transport/injection layer
• the excited singlet state can be created when excitons formed in an OLED device transfer their energy to the singlet excited state of the dopant. However, it is generally believed that only 25% of the excitons created in an EL device are singlet excitons. The remaining excitons are triplet, which cannot readily transfer their energy to the dopant to produce the singlet excited state of a dopant. This results in a large loss in efficiency since 75% of the excitons are not used in the light emission process. Triplet excitons can transfer their energy to a dopant if it has a triplet excited state that is low enough in energy. If the triplet state of the dopant is emissive it can produce light by phosphorescence.
• singlet excitons can also transfer their energy to lowest singlet excited state of the same dopant.
• the singlet excited state can often relax, by an intersystem crossing process, to the emissive triplet excited state.
• electrophosphorescence is sometimes used to denote electroluminescence wherein the mechanism of luminescence is phosphorescence.
• Another process by which excited states of a dopant can be created is a sequential process in which a hole is trapped by the dopant and subsequently recombines with an electron, or an electron is trapped and subsequently recombines with a hole, in either case producing an excited state of the dopant directly.
• Singlet and triplet states, and fluorescence, phosphorescence, and intersystem crossing are discussed in J. G. Calvert and J. N. Pitts, Jr., Photochemistry (Wiley, New York, 1966) and further discussed in publications by S. R. Forrest and coworkers such as M. A. Baldo, D. F. O'Brien, M. E. Thompson, and S. R. Forrest, Phys. Rev. B, 60, 14422 (1999).
• triplet state is often used to refer to a set of three electronically excited states of spin 1 that have nearly identical electronic structure and nearly identical energy and differ primarily in the orientation of the net magnetic moment of each state.
• a molecule typically has many such triplet states with widely differing energies.
• the term "triplet state” of a molecule will refer specifically to the set of three spin-1 excited states with the lowest energy, and the term “triplet energy” will refer to the energy of these states relative to the energy of the ground state of the molecule.
• the te ⁇ n spacinglet energy will refer to the energy of the lowest excited singlet state relative to that of the ground state of the molecule.
• One class of useful phosphorescent materials is the transition metal complexes having singlet ground states and triplet excited states.
• ⁇ c-tris(2-phenylpyridinato-N,C 2 )iridium(III) (Ir(ppy) 3 ) strongly emits green light from a triplet excited state owing to, first, the large spin-orbit coupling of the heavy atom and, second, the lowest excited state, which is a charge transfer state, having a Laporte allowed (orbital-symmetry-allowed) transition to the ground state (FLA. King, P.J. Spellane, and R.J. Watts, J. Am. Chem. Soc, 107, 1431 (1985), M.G. Colombo, T.C.
• DCJTB 4-(dicyanomethylene)-2-t-butyl-6-(l, 1,7,7- tetramethyljulolidyl-9-enyl)-4H-pyran
• DCJTB suffers from having singlet emission in the red region of the spectrum and therefore can affect the color of the emission of a triplet OLED device. In particular, if an OLED device with blue or green emission is desired, a red contribution from DCJTB emission would be undesirable.
• the invention provides an electroluminescent device comprising a cathode and an anode and, located therebetween, a light-emitting layer (LEL) comprising a phosphorescent guest material, a hole- and electron-transporting host material, and an efficiency-enhancing material having an ionization potential lower than that of the host material and a triplet energy level that is lower than that of the phosphorescent guest material by no more than 0.2 eV.
• LEL light-emitting layer
• the invention also provides a display and an area lighting device employing the device and a process for emitting light using the device.
• FIG. 1 shows a schematic cross-section of a typical OLED device in which this invention may be used.
• DETAILED DESCRIPTION OF THE INVENTION The electroluminescent device is summarized above. It includes a cathode, an anode, and a light-emitting layer comprising a phosphorescent light- emitting material, a hole- and electron-transporting host material, and an efficiency-enhancing material having an ionization potential lower than that of the host material and a triplet energy that is lower than that of the phosphorescent guest material by no more than 0.2 eV.
• the triplet energy of the efficiency-enhancing material is higher than that of the phosphorescent guest material.
• the device can also include layers such as a hole- injecting layer, a hole-transporting layer, a hole-blocking layer, an electron- transporting layer, or more than one of these optional layers.
• the light-emitting layer 109 of the EL device comprises a host material, one or more guest materials for emitting light, and an efficiency-enhancing material whose nature will become evident.
• At least one of the guest materials is a phosphorescent complex such as one comprising an organometallic compound including a 5th-row transition element, e.g. platinum or iridium.
• the light-emitting guest material(s) is typically present in an amount of from 1 to 20 by weight% of the light-emitting layer, and conveniently from 3 to 7 % by weight of the light-emitting layer.
• the phosphorescent complex guest material may be referred to herein as a phosphorescent material.
• the phosphorescent material typically includes one or more ligands, for example, monoanionic ligands that can be coordinated to a metal through an sp 2 carbon and a heteroatom.
• the ligand can be a N- heterocylcic compound such as phenylpyridine (ppy) or phenylisoquiolin (piq) or derivatives or analogs thereof.
• Examples of some useful phosphorescent organometallic materials include tris(2-phenylpyridinato-N,C 2 )iridium(II ⁇ ) and 9* bis(2-phenylpyridinato-N,C )platinum(II).
• Phosphorescent and related materials are also described in WO 00/57676, WO 00/70655, WO 01/41512 Al, WO 02/15645 Al, US 2003/0017361 Al, WO 01/93642 Al, WO 01/39234 A2, US 6,458,475 Bl, WO 02/071813 Al, US 6,573,651 B2, US 2002/0197511 Al, WO 02/074015 A2, US 6,451,455 Bl, US 2003/ 0072964 Al, US 2003 / 0068528 Al, US 6,413,656 Bl, US 6,515,298 B2, US 6,451,415 Bl, US 6,097,147, US 2003/0124381 Al, US 2003/0059646 Al, US 2003/0054198 Al, EP 1 239 526 A2, EP 1 238 981 A2, EP 1 244 155 A2, US 2002/0100906 Al, US 2003 / 0068526 Al, US 2003/0068535 Al, J
• the emission wavelengths of cyclometallated Ir(III) complexes of the type IrL 3 and IrL 2 L0 such as the green-emitting ac-tris(2-phenylpyridinato- N,C 2 )iridium(III) and bis(2-phenylpyridinato-N,C 2 )iridium(III)(acetylacetonate) may be shifted by substitution of electron donating or withdrawing groups at appropriate positions on the cyclometallating ligand L, or by choice of different heterocycles for the cyclometallating ligand L.
• red emitters are the bis(2-(2'-benzothienyl)pyridinato-N,C 3 )iridium(III)(acetylacetonate) and tris(l -phenylisoquinolinato-N,C,C 2 )iridium(III), tris(2-phenylquinolinato-N,C 2 ) iridium(III), and tris(l-phenylisoquinolinato-N,C 2 )iridium(III), and tris(3- phenylisoquinolinato-N,C 2 )iridium(III).
• a blue-emitting example is bis(2-(4,6- difluorophenyl)-pyridinato-N,C )iridium(III)( ⁇ icolinate). Red electrophosphorescence has been reported, using bis(2-(2'- benzo[4,5-a]thienyl)pyridinato-N, C 3 ) iridium (acetylacetonate) [btp 2 lr(acac)] as the phosphorescent material (C. Adachi, S. Lamansky, M. A. Baldo, R. C. Kwong,, M. E. Thompson,, and S. R. Forrest, App. Phys. Lett., 78, 1622-1624 (2001)).
• phosphorescent materials include cyclometallated Pt(II) complexes such as cis-bis(2-phenylpyridinato-N,C 2 )platinum(II), cis-bis(2- (2'-thienyl)pyridinato-N,C 3 ) platinum(II), cis-bis(2-(2'-thienyl)quinolinato-N,C 5 ) platinum(II), or (2-(4,6-difluorophenyl)pyridinato-N,C 2 ') platinum (II) (acetylacetonate).
• cyclometallated Pt(II) complexes such as cis-bis(2-phenylpyridinato-N,C 2 )platinum(II), cis-bis(2- (2'-thienyl)pyridinato-N,C 3 ) platinum(II), cis-bis(2-(2'-thienyl)quinolina
• Pt(II) porphyrin complexes such as 2,3,7,8,12,13,17,18- octaethyl-21H, 23H-porphine platinum(II) are also useful phosphorescent materials. Still other examples of useful phosphorescent materials include coordination complexes of the trivalent lanthanides such as Tb 3+ and Eu 3+ (J. Kido et al., Appl. Phys. Lett, 65, 2124 (1994)). Suitable host materials should preferably be selected so that transfer of a triplet exciton can occur efficiently from the host material to the phosphorescent guest material but cannot occur efficiently from the phosphorescent material to the host material.
• the triplet energy of the phosphorescent material be lower than the triplet energy of the host.
• a large triplet energy implies a large optical bandgap.
• the band gap of the host should not be chosen so large as to cause an unacceptable barrier to injection of charge carriers into the light-emitting layer and an unacceptable increase in the drive voltage of the OLED.
• Suitable host materials are described in WO 00/70655 A2; 01/39234 A2; 01/ 93642 Al ; 02/074015 A2; 02/15645 Al; and US 20020117662.
• Suitable hosts include certain aryl amines, triazoles, indoles and carbazole compounds.
• Desirable host materials are capable of forming a continuous film.
• desirable host materials may be hole- and electron-transporting, that is, they may allow the transport of both holes and electrons.
• Carbazole containing compounds such as CBP (see C. Adachi et al., Organic Electronics, 2, 37-43 (2001)) can serve as both hole- and electron-transporting host materials.
• Suitable host materials include carbazole derivatives such as those represented by Formula 1.
• W independently represents hydrogen or an independently selected substituent, such as a methyl group
• p independently is 0-4
• L A represents a linking group.
• Suitable linking groups include arylene groups such as phenylene or biphenylene groups, or aliphatic or alicyclic groups such as 1,3-propyl or 1,3-cyclobutyl.
• Particularly suitable are compounds of Formula 1 wherein W and L A do not contain additional fused rings such as naphthalene rings. Examples include the following:
• the light-emitting layer may contain more than one host material in order to improve the device's film morphology, electrical properties, light emission efficiency, and lifetime.
• the light-emitting layer may contain a first host material that has good hole-transporting properties, and a second host material that has good electron-transporting properties, which together can form a hole- and electron-transporting host material.
• the efficiency-enhancing material suitable for use in the LEL is selected to have the following two useful properties: an ionization potential that is less than that of the host material and a triplet energy that is not lower than the triplet energy of the phosphorescent guest material by more than about 0.2 eV.
• TAPC 1,1 -Bis(4-di-/?-tolylaminophenyl)cyclohexane
• TAPC 1,1 -Bis(4-di-p-tolylaminophenyl)-4-phenylcyclohexane
• a preferred efficiency enhancing material is 4,4',4" ⁇ tris[(3-methylphenyl)phenylamino]triphenylamine (MTDATA) when used in combination with a host material such as 4,4'-bis(carbazol-9-yl)-biphenyl (CBP) and a phosphorescent light-emitting material such as fac tris(2-phenylpyridinato- N,C 2' ) iridium (III) (Ir(ppy) 3 ).
• MTDATA 4,4',4" ⁇ tris[(3-methylphenyl)phenylamino]triphenylamine
• CBP 4,4'-bis(carbazol-9-yl)-biphenyl
• a phosphorescent light-emitting material such as fac tris(2-phenylpyridinato- N,C 2' ) iridium (III) (Ir(ppy) 3 ).
• the role of ionization potential is not completely understood, but it is believed that the efficiency-enhancing material functions by a sequential process wherein a hole is trapped by the efficiency-enhancing material and subsequently recombines with an electron in the host material, resulting in an excited state of one material or the other. It is further believed that the energy of this excited state is transferred to the phosphorescent guest material, which emits it as phosphorescent light.
• the ionization potential is defined as the energy required to remove an electron from the highest occupied molecular orbital (HOMO) of a substance. It can be measured, for instance, by photoelectron spectroscopy. For example, C.
• the same electrochemical method, solvent, and reference electrode or reference material should be used to evaluate the oxidation potentials of the efficiency-enhancing material and the host material.
• An example of the use of both photoelectron spectroscopic and electrochemical methods to determine ionization and oxidation potentials is given by L.-B. Lin et al, Appl. Physics Lett, 72, 864 (1998).
• the ionization energy of the efficiency-enhancing material must be less than that of the host material. However, if that ionization energy is too low, there may exist an "exciplex" state at sufficiently low energy that transfer of its energy to the phosphorescent guest material is impeded.
• Such an "exciplex" state typically would involve partial or complete transfer of an electron from a molecule of the intended efficiency-enhancing material to a molecule of the host material.
• the efficiency- enhancing material it is desirable, though not absolutely required, that the efficiency- enhancing material not be too good an electron donor.
• the difference in ionization energy between the efficiency-enhancing material and the host material be less than about 1 eV and more desirable that it be less than about 0.5 eV.
• triplet energy values are also not completely understood, but it is believed to be approximately as follows. If the triplet energy of the efficiency-enhancing material satisfies the second criterion, the barrier to transfer of triplet energy from the efficiency-enhancing material directly to the phosphorescent guest material, if any, is not insurmountably large. To facilitate such energy transfer, it is desirable that the triplet energy of the efficiency- enhancing material also not be lower than that of the host material by more than 0.2 eV. This requirement is also stated in equation (1):
• T E represents the triplet energy level of the efficiency-enhancing material
• T H represents the triplet energy level of the host material. If the efficiency-enhancing material has this property, any barrier to transfer of triplet energy from it to the host material, with subsequent transfer to the phosphorescent guest material, is not insurmountably large.
• the triplet energy of the efficiency-enhancing material is higher than that of the phosphorescent material.
• Triplet energy is conveniently measured by any of several methods, as discussed for instance in the book by Murov et al., cited above.
• One convenient method, well known to those skilled in the art, is to record the phosphorescence spectrum at low temperature. Typically, that spectrum has several partially- resolved peaks or shoulders.
• the intensity of phosphorescence reaches half of the intensity at the shortest- wavelength peak or shoulder.
• the energy corresponding to ⁇ 0 is considered to be the triplet energy.
• Adachi et al., in Organic Electronics, 2, 37-43 (2001) show the spectrum of MTDATA in their Fig. 4(b). From the caption, and from previously published data (Baldo et al., Phys. Rev. B 62, 10958 (2000)), it is clear that the dashed line in that figure is the phosphorescence spectrum of MTDATA.
• Fig. 3 in the same paper by Baldo et al. shows a phosphorescence spectrum of Ir(ppy) 3 .
• the value of ⁇ 0 evaluated from that figure is about 490 nm and corresponds to a triplet energy of 2.53 eV.
• the triplet energy of MTDATA is below that of Ir(ppy) 3 , but by less than 0.2 eV, and MTDATA satisfies the second requirement for an efficiency-enhancing material to be used with Ir(ppy) 3 as the phosphorescent material.
• a phosphorescent material with red emission would have a triplet energy below 2.1 eV.
• the triplet energy of MTDATA would exceed that of such a phosphorescent material.
• the triplet state of a compound can also be calculated.
• the triplet state energy for a molecule is obtained as the difference between the ground state energy (E(gs)) of the molecule and the energy of the lowest triplet state (E(ts)) of the molecule, both given in eV.
• the basis set for use with the B3LYP method is defined as follows: MIDI! for all atoms for which MIDI! is defined, 6-31G* for all atoms defined in 6-31G* but not in MIDI!, and either the LACV3P or the LANL2DZ basis set and pseudopotential for atoms not defined in MIDI! or 6-31G*, with LACV3P being the preferred method. For any remaining atoms, any published basis set and pseudopotential may be used.
• E(t) 0.84*(E(ts)-E(gs))+0.35 (eq. 2).
• the triplet energy For polymeric or oligomeric materials, it is sufficient to compute the triplet energy over a monomer or oligomer of sufficient size so that additional units do not substantially change the computed triplet energy.
• the calculated values for the triplet state energy of a given compound may typically show some deviation from the experimental values. Thus, the calculations should be used only as a rough guide in the selection of appropriate materials.
• the efficiency- enhancing material be substantially non-emissive, by which we mean that it does not emit light when used together with the phosphorescent material in the host material.
• the efficiency-enhancing material may not be capable of emitting light when it is present in the host material, regardless of whether the phosphorescent material is present.
• the efficiency-enhancing material may emit light when it is present in the host material without the phosphorescent material, but the energy of the emitting excited state(s) may exceed that of the phosphorescent material, and that energy may be transferred efficiently to the phosphorescent material instead of being emitted by the efficiency-enhancing material.
• a material with blue emission can be used as an efficiency-enhancing material together with a phosphorescent material that emits green light, if the energy of excitation of the former material is efficiently transferred to the phosphorescent material rather than being emitted as blue light.
• a material is termed non-emissive if no more than about half of its singlet energy on average, and no more than about 10% of its triplet energy on average are emitted as light when the material is present together with the phosphorescent material in the host material.
• a material intended for use as an efficiency-enhancing material may be emissive when the phosphorescent material is present at sufficiently low concentration, but it is often desirable that an efficiency-enhancing material be non-emissive when the phosphorescent material is present at the desired concentration.
• the non-emissive property is advantageous when the emission color of the phosphorescent dopant is already optimized, because it prevents contamination of that color by the emission color of the efficiency-enhancing material.
• tertiary aromatic amines including triarylamines, diarylalkyla ines, and aryldialkylamine fulfill the requirements for efficiency enhancing materials, when used together with a host such as CBP and a phosphorescent material whose phosphorescence is in the visible region of the spectrum, for example the blue region of the spectrum or at longer wavelengths, such as green, yellow, orange, or red.
• a host such as CBP
• a phosphorescent material whose phosphorescence is in the visible region of the spectrum, for example the blue region of the spectrum or at longer wavelengths, such as green, yellow, orange, or red.
• the amine groups can be linked with alkylene or, in some instances, arylene groups.
• the triplet energy of TAPC is approximately equal to that of the structurally related compound, triphenylamine, namely 3.0 eV, which exceeds that of both the typical host material CBP and a typical phosphorescent material, Ir(ppy) .
• the ionization potential of TAPC is about 5.4 eV, which is smaller than the ionization potential of CBP. (See the book by Murov et al. and the article by Lin et al., both cited above).
• TAPC is suitable for use as an efficiency-enhancing material with CBP as the host material and Ir(ppy) 3 as the phosphorescent material.
• the efficiency enhancing material comprises two or more triaryl amines linked together, such as a material of Formula (2a).
• R 1 and R 2 represent H or substituents, provided R 1 and R 2 can join to form a ring.
• R 1 and R 2 can be methyl groups or join to form a cyclohexyl ring group.
• Ar ! -Ar 4 represent independently selected aromatic groups, for example phenyl groups or tolyl groups.
• R a represents hydrogen or an independently selected substituent, such as a methyl group, and n is independently selected as 0-4.
• R 1 , R 2 , R a , and Ar'-Ar 4 do not contain fused aromatic rings. Examples of materials of formula 2a are:
• the efficiency enhancing material comprises a material represented by Fonnula 2b:
• Ar 5 -Ar 10 independently represent aromatic groups, for example phenyl groups and tolyl groups.
• R b independently represents hydrogen or an independently selected substituent, for example a methyl group, h ⁇ and m is independently selected as 0-4.
• R and Ar - Ar 10 do not contain fused aromatic rings. Examples of suitable materials of fonnula 2a are:
• the efficiency-enhancing material is conveniently present at a concentration of from 1 to 30% by weight of the light-emitting layer, and suitably 3 to 10%. Two or more efficiency-enhancing materials can also be used in combination with one another.
• the thickness of the light-emitting layer can be between 2 and 100 nm and is suitably between 5 and 50 nm.
• the addition of an efficiency-enhancing material provides an electroluminescent device with improved luminous yield and power efficiency. Unless otherwise specifically stated, use of the term "substituted" or "substituent” means any group or atom other than hydrogen.
• a substituent group may be halogen or may be bonded to the remainder of the molecule by an atom of carbon, silicon, oxygen, nitrogen, phosphorous, sulfur, selenium, or boron.
• the substituent may be, for example, halogen, such as chloro, bromo or fluoro; nitro; hydroxyl; cyano; carboxyl; or groups which may be further substituted, such as alkyl, including straight or branched chain or cyclic alkyl, such as methyl, trifluoromethyl, ethyl, t-butyl, 3-(2,4-di-t-pentylphenoxy) propyl, and tetradecyl; alkenyl, such as ethylene, 2-butene; alkoxy, such as methoxy, ethoxy, propoxy, butoxy, 2-methoxyethoxy, sec-butoxy, hexyloxy, 2-ethylhexyloxy, tetradecyloxy, 2-(2,4-di-t-pentylphenoxy)ethoxy, and 2-dodecyloxyethoxy; aryl such as phenyl, 4-t-butylphenyl
• the substituents may themselves be further substituted one or more times with the described substituent groups.
• the particular substituents used may be selected by those skilled in the art to attain the desired desirable properties for a specific application and can include, for example, electron-withdrawing groups, electron-donating groups, and steric groups.
• the substituents may be joined together to form a ring such as a fused ring unless otherwise provided.
• the above groups and substituents thereof may include those having up to 48 carbon atoms, typically 1 to 36 carbon atoms and usually less than 24 carbon atoms, but greater numbers are possible depending on the particular substituents selected.
• the present invention can be employed in many OLED device configurations using small molecule materials, oligomeric materials, polymeric materials, or combinations thereof. These range from very simple structures comprising a single anode and cathode to more complex devices, such as passive matrix displays comprised of orthogonal anays of anodes and cathodes to fonn pixels, and active-matrix displays where each pixel is controlled independently, for example, with thin film transistors (TFTs).
• TFTs thin film transistors
• the essential requirements of an OLED are an anode, a cathode, and an organic light-emitting layer located between the anode and cathode. Additional layers may be employed as more fully described hereafter.
• FIG. 1 A typical structure according to the present invention and especially useful for a small molecule device, is shown in FIG. 1 and is comprised of a substrate 101, an anode 103, a hole-injecting layer 105, a hole-transporting layer 107, a light-emitting layer 109, a hole-blocking layer 110, an electron- transporting layer 111, and a cathode 113. These layers are described in detail below. Note that the substrate 101 may alternatively be located adjacent to the cathode 113, or the substrate 101 may actually constitute the anode 103 or cathode 113.
• the organic layers between the anode 103 and cathode 113 are conveniently referred to as the organic EL element.
• the total combined thickness of the organic layers is desirably less than 500 nm.
• the anode 103 and cathode 113 of the OLED are connected to a voltage/cunent source through electrical conductors.
• the OLED is operated by applying a potential between the anode 103 and cathode 113 such that the anode 103 is at a more positive potential than the cathode 113. Holes are injected into the organic EL element from the anode 103 and electrons are injected into the organic EL element from the cathode 113.
• Enhanced device stability can sometimes be achieved when the OLED is operated in an AC mode where, for some time period in the AC cycle, the potential bias is reversed and no cunent flows.
• An example of an AC driven OLED is described in US 5,552,678.
• the OLED device of this invention is typically provided over a supporting substrate 101 where either the cathode 113 or anode 103 can be in contact with the substrate.
• the electrode in contact with the substrate 101 is conveniently refened to as the bottom electrode.
• the bottom electrode is the anode 103, but this invention is not limited to that configuration.
• the substrate 101 can either be light transmissive or opaque, depending on the intended direction of light emission. The light transmissive property is desirable for viewing the EL emission through the substrate 101. Transparent glass or plastic is commonly employed in such cases.
• the substrate 101 can be a complex structure comprising multiple layers of materials. This is typically the case for active matrix substrates wherein TFTs are provided below the OLED layers.
• the substrate 101 at least in the emissive pixelated areas, be comprised of largely transparent materials such as glass or polymers.
• the transmissive characteristic of the bottom support is immaterial, and therefore the substrate can be light transmissive, light absorbing or light reflective.
• Substrates for use in this case include, but are not limited to, glass, plastic, semiconductor materials, such as silicon, ceramics, and circuit board materials.
• the substrate 101 can be a complex structure comprising multiple layers of materials such as found in active matrix TFT designs. It is necessary to provide in these device configurations a light-transparent top electrode.
• the anode 103 should be transparent or substantially transparent to the emission of interest.
• Common transparent anode materials used in this invention are indium-tin oxide (ITO), indium-zinc oxide (IZO) and tin oxide, but other metal oxides can work including, but not limited to, aluminum- or indium-doped zinc oxide, magnesium-indium oxide, and nickel-tungsten oxide.
• ITO indium-tin oxide
• IZO indium-zinc oxide
• tin oxide other metal oxides can work including, but not limited to, aluminum- or indium-doped zinc oxide, magnesium-indium oxide, and nickel-tungsten oxide.
• metal nitrides such as gallium nitride
• metal selenides such as zinc selenide
• metal sulfides such as zinc sulfide
• the transmissive characteristics of the anode 103 are immaterial and any conductive material can be used, transparent, opaque or reflective.
• Example conductors for this application include, but are not limited to, gold, iridium, molybdenum, palladium, and platinum.
• Typical anode materials, transmissive or otherwise, have a work function of 4.1 eV or greater. Desired anode materials are commonly deposited by any suitable means such as evaporation, sputtering, chemical vapor deposition, or electrochemical means.
• Anodes can be patterned using well-known photolithographic processes. Optionally, anodes may be polished prior to application of other layers to reduce surface roughness so as to minimize short circuits or enhance reflectivity.
• the cathode 113 used in this invention can be comprised of nearly any conductive material. Desirable materials have good film-forming properties to ensure good contact with the underlying organic layer, promote electron injection at low voltage, and have good stability. Useful cathode materials often contain a low work function metal ( ⁇ 4.0 eV) or metal alloy.
• One useful cathode material is comprised of a Mg:Ag alloy wherein the percentage of silver is in the range of 1 to 20 %, as described in U.S. Patent No. 4,885,221.
• cathode materials include bilayers comprising the cathode and a thin electron-injection layer (EIL) in contact with an organic layer (e.g., an electron transporting layer (ETL)), the cathode being capped with a thicker layer of a conductive metal.
• EIL electron-injection layer
• the EIL preferably includes a low work function metal or a salt of a low- work- function metal, and if so, the thicker capping layer does not need to have a low work function.
• One such cathode is comprised of a thin layer of LiF followed by a thicker layer of Al as described in U.S. Patent No. 5,677,572.
• An ETL material doped with an alkali metal for example, Li-doped Alq
• an alkali metal for example, Li-doped Alq
• Other useful cathode material sets include, but are not limited to, those disclosed in U.S. Patent Nos. 5,059,861, 5,059,862, and 6,140,763.
• the cathode 113 When light emission is viewed through the cathode, the cathode 113 must be transparent or nearly transparent. For such applications, metals must be thin or one must use transparent conductive oxides, or a combination of these materials.
• Cathode materials are typically deposited by any suitable method such as evaporation, sputtering, or chemical vapor deposition. When needed, patterning can be achieved through many well known methods including, but not limited to, through-mask deposition, integral shadow masking as described in US 5,276,380 and EP 0 732 868, laser ablation, and selective chemical vapor deposition.
• a hole-injecting layer 105 maybe provided between anode 103 and hole-transporting layer 107.
• the hole-injecting material can serve to improve the film formation property of subsequent organic layers and to facilitate injection of holes into the hole-transporting layer 107.
• Suitable materials for use in the hole- injecting layer 105 include, but are not limited to, porphyrinic compounds as described in US 4,720,432, plasma-deposited fluorocarbon polymers as described in US 6,208,075, and some aromatic amines, for example, MTDATA (4,4',4 M - tris[(3-methylphenyl)phenylamino]triphenylamine).
• a hole-injection layer is conveniently used in the present invention, and is desirably a plasma-deposited fluorocarbon polymer.
• the thickness of a hole-injection layer containing a plasma-deposited fluorocarbon polymer can be in the range of 0.2 to 200 nm and suitably in the range of 0.3 to 1.5 nm.
• the hole-transporting layer 107 of the organic EL device contains at least one hole-transporting compound such as an aromatic tertiary amine, where the latter is understood to be a compound containing at least one trivalent nitrogen atom that is bonded only to carbon atoms, at least one of which is a member of an aromatic ring.
• the aromatic tertiary amine can be an arylamine, such as a monoarylamine, diarylamine, triarylamine, or a polymeric arylamine. Exemplary monomeric triarylamines are illustrated by Klupfel et al. US 3,180,730.
• triarylamines substituted with one or more vinyl radicals and/or comprising at least one active hydrogen containing group are disclosed by Brantley et al US 3,567,450 and US 3,658,520.
• a more prefened class of aromatic tertiary amines is those which include at least two aromatic tertiary amine moieties as described in US 4,720,432 and US 5,061,569.
• Such compounds include those represented by structural fonnula (A).
• Qi and Q 2 are independently selected aromatic tertiary amine moieties and G is a linking group such as an arylene, cycloalkylene, or alkylene group of a carbon to carbon bond.
• G is a linking group such as an arylene, cycloalkylene, or alkylene group of a carbon to carbon bond.
• at least one of Qi or Q 2 contains a polycyclic fused ring structure, e.g., a naphthalene.
• G is an aryl group, it is conveniently a phenylene, biphenylene, or naphthalene moiety.
• a useful class of triarylamines satisfying structural formula (A) and containing two triarylamine moieties is represented by structural formula (B):
• Ri and R 2 each independently represents a hydrogen atom, an aryl group, or an alkyl group or Rj and R 2 together represent the atoms completing a cycloalkyl group; and R 3 and j each independently represents an aryl group, which is in turn substituted with a diaryl substituted amino group, as indicated by structural formula (C): R5 ⁇ participate N C
• R 5 and R 6 are independently selected aryl groups.
• at least one of R 5 or R 6 contains a polycyclic fused ring structure, e.g., a naphthalene.
• Another class of aromatic tertiary amines is the tetraaryldiamines. Desirable tetraaryldiamines include two diarylamino groups, such as indicated by formula (C), linked through an arylene group.
• Useful tetraaryldiamines include those represented by formula (D).
• each Are is an independently selected arylene group, such as a phenylene or anthracene moiety
• n is an integer of from 1 to 4
• Ar, R 7 , R 8 , and R 9 are independently selected aryl groups.
• at least one of Ar, R , R 8 , and R 9 is a polycyclic fused ring structure, e.g., a naphthalene
• the various alkyl, alkylene, aryl, and arylene moieties of the foregoing structural formulae (A), (B), (C), (D), can each in turn be substituted.
• Typical substituents include alkyl groups, alkoxy groups, aryl groups, aryloxy groups, and halogen such as fluoride, chloride, and bromide.
• the various alkyl and alkylene moieties typically contain from about 1 to 6 carbon atoms.
• the cycloalkyl moieties can contain from 3 to about 10 carbon atoms, but typically contain five, six, or seven ring carbon atoms ⁇ e.g., cyclopentyl, cyclohexyl, and cycloheptyl ring structures.
• the aryl and arylene moieties are usually phenyl and phenylene moieties.
• the hole-transporting layer can be formed of a single aromatic tertiary amine compound or a mixture of such compounds. Specifically, one may employ a triarylamine, such as a triarylamine satisfying the formula (B), in combination with a tetraaryldiamine, such as indicated by formula (D).
• a triarylamine such as a triarylamine satisfying the formula (B)
• a tetraaryldiamine such as indicated by formula (D).
• aromatic tertiary amines are the following: 1,1 -Bis(4-di-p-tolylaminophenyl)cyclohexane 1 , 1 -Bis(4-di-p-tolylaminophenyl)-4-phenylcyclohexane N,N,N',N'-tetraphenyl-4,4" , -diamino- 1 , l':4', 1 " :4", 1 '"-quaterphenyl Bis(4-dimethylamino-2-methylphenyl)phenylmethane l,4-bis[2-[4-[N,N-di(p-toly)amino] ⁇ henyl]vinyl]benzene (BDTAPVB) N,N,N',N'-Tetra-p-tolyl-4,4'-diaminobiphenyl JS[,N,N',N , -T
• Tertiary aromatic amines with more than two amine groups may be used, including oligomeric materials.
• polymeric hole-transporting materials can be used such as poly(N-vinylcarbazole) (PVK), polythiophenes, polypyrrole, polyaniline, and copolymers such as poly(3,4-ethylenedioxythiophene) / poly(4-styrenesulfonate) also called PEDOT/PSS.
• the hole-transporting layer can comprise two or more sublayers of differing compositions.
• the thickness of the hole-transporting layer can be between 10 and about 500 nm and suitably between 50 and 300 nm.
• LEL Light-Emitting Layer
• the light-emitting layer of the invention comprising a phosphorescent light emitting material, a host and an efficiency enhancing material has been described previously.
• Fluorescent Light-Emitting Materials and Layers LEL
• other light emitting materials may be used in the OLED device in the same or separate layers, including fluorescent materials.
• fluorescent is commonly used to describe any light emitting material, in this case we are referring to a material that emits light from a singlet excited state. Fluorescent materials may be used in the same layer as the phosphorescent material, in adjacent layers, in adjacent pixels, or any combination.
• the light-emitting layer (LEL) of the organic EL element includes a luminescent fluorescent or phosphorescent material where electroluminescence is produced as a result of electron-hole pair recombination.
• the light-emitting layer can be comprised of a single material, but more commonly consists of a host material doped with a guest emitting material or materials where light emission comes primarily from the guest emitting material(s) and can be of any color.
• the host materials in the light-emitting layer can be an electron-transporting material, as defined below, a hole-transporting material, as defined above, or another material or combination of materials that support hole-electron recombination.
• Fluorescent emitting materials are typically incorporated at 0.01 to 10 % by weight of the host material.
• the host and emitting materials can be small non-polymeric molecules or polymeric materials such as polyfluorenes and polyvinylarylenes (e.g., poly(p-phenylenevinylene), PPV).
• small molecule emitting materials can be molecularly dispersed into a polymeric host, or the emitting materials can be added by copolymerizing a minor constituent into a host polymer.
• Host materials may be mixed together in order to improve film fonnation, electrical properties, light emission efficiency, operating lifetime, or manufacturability.
• the host may comprise a material that has good hole- transporting properties and a material that has good electron-transporting properties.
• a fluorescent material as a guest emitting material is a comparison of the singlet energies of the host and the fluorescent material. It is highly desirable that the singlet energy of the fluorescent material be lower than that of the host material.
• Host and emitting materials known to be of use include, but are not limited to, those disclosed in US 4,768,292, US 5,141,671, US 5,150,006, US 5,151,629, US 5,405,709, US 5,484,922, US 5,593,788, US 5,645,948, US 5,683,823, US 5,755,999, US 5,928,802, US 5,935,720, US 5,935,721, and US 6,020,078.
• Metal complexes of 8-hydroxyquinoline and similar derivatives also known as metal-chelated oxinoid compounds (Formula E), constitute one class of useful host compounds capable of supporting electroluminescence, and are particularly suitable for light emission of wavelengths longer than 500 nm, e.g., green, yellow, orange, and red.
• the metal can be monovalent, divalent, trivalent, or tetravalent metal.
• the metal can, for example, be an alkali metal, such as lithium, sodium, or potassium; an alkaline earth metal, such as magnesium or calcium; a trivalent metal, such aluminum or gallium, or another metal such as zinc or zirconium.
• alkali metal such as lithium, sodium, or potassium
• alkaline earth metal such as magnesium or calcium
• trivalent metal such aluminum or gallium, or another metal such as zinc or zirconium.
• any monovalent, divalent, trivalent, or tetravalent metal known to be a useful chelating metal can be employed.
• Z completes a heterocyclic nucleus containing at least two fused aromatic rings, at least one of which is an azole or azine ring. Additional rings, including both aliphatic and aromatic rings, can be fused with the two required rings, if required. To avoid adding molecular bulk without improving on function the number of ring atoms is usually maintained at 18 or less.
• CO-1 Aluminum trisoxine [alias, tris(8-quinolinolato)aluminum(III)]
• CO-2 Magnesium bisoxine [alias, bis(8-quinolinolato)magnesium(II)]
• CO-3 Bis[benzo ⁇ f ⁇ -8-quinolinolato]zinc (II)
• CO-4 Bis(2-methyl-8-quinolinolato)aluminum(III)- ⁇ -oxo-bis(2-methyl-8- quinolinolato) aluminum(III)
• CO-6 Aluminum tris(5-methyloxine) [alias, tris(5-methyl-8-quinolinolato) aluminum(III)]
• CO-7 Lithium oxine [alias, (8-quinolinolato)lithium(I)]
• R , R , R , R , and R represent one or more substituents on each nng where each substituent is individually selected from the following groups: Group 1: hydrogen, or alkyl of from 1 to 24 carbon atoms; Group 2: aryl or substituted aryl of from 5 to 20 carbon atoms; Group 3: carbon atoms from 4 to 24 necessary to complete a fused aromatic ring of anthracenyl; pyrenyl, or perylenyl; Group 4: heteroaryl or substituted heteroaryl of from 5 to 24 carbon atoms as necessary to complete a fused heteroaromatic ring of furyl, thienyl, pyridyl, quinolinyl or other heterocyclic systems; Group 5: alkoxylamino, alkylamino, or arylamino of from 1 to 24 carbon atoms; and Group 6: fluorine, chlorine, bromine or cyano.
• Illustrative examples include 9, 10-di-(2-naphthyl)anthracene and 2- t-butyl-9,10-di-(2-naphthyl)anthracene.
• Other anthracene derivatives can be useful as a host in the LEL, including derivatives of 9,10-bis[4-(2,2- diphenylethenyl)phenyl]anthracene.
• Benzazole derivatives constitute another class of useful host materials capable of supporting electroluminescence, and are particularly suitable for light emission of wavelengths longer than 400 nm, e.g., blue, green, yellow, orange or red, wherein: n is an integer of 3 to 8; Z is O, NR or S; and R and R' are individually hydrogen; alkyl of from 1 to 24 carbon atoms, for example, propyl, t-butyl, heptyl, and the like; aryl or hetero-atom substituted aryl of from 5 to 20 carbon atoms for example phenyl and naphthyl, furyl, thienyl, pyridyl, quinolinyl and other heterocyclic systems; or halo such as chloro, fluoro; or atoms necessary to complete a fused aromatic ring; and L is a linkage unit consisting of alkyl, aryl, substituted alkyl, or substituted aryl, which connects the multiple
• L may be either conjugated with the multiple benzazoles or not in conjugation with them.
• An example of a useful benzazole is 2,2',2"-(l,3,5-phenylene)tris[l-phenyl-lH-benzimidazole].
• Styrylarylene derivatives as described in U.S. Patent 5,121,029 and JP 08333569 are also useful hosts for blue emission.
• 9,10-bis[4-(2,2- diphenylethenyl)phenyl] anthracene and 4,4'-bis(2,2-diphenylethenyl)- 1 , 1 '-biphenyl (DPVBi) are useful hosts for blue emission.
• Useful fluorescent emitting materials include, but are not limited to, derivatives of anthracene, tetracene, xanthene, perylene, rubrene, coumarin, rhodamine, and quinacridone, dicyanomethylenepyran compounds, thiopyran compounds, polymethine compounds, pyrylium and thiapyrylium compounds, fluorene derivatives, periflanthene derivatives, indenoperylene derivatives, bis(azinyl)amine boron compounds, bis(azinyl)methane compounds, and carbostyryl compounds.
• Illustrative examples of useful materials include, but are not limited to, the following:
• HBL Hole-Blocking Layer
• an OLED device employing a phosphorescent material often requires at least one hole-blocking layer 110 placed between the electron-transporting layer 111 and the light-emitting layer 109 to help confine the excitons or recombination events to the light-emitting layer comprising the host and phosphorescent material.
• there should be an energy barrier for hole migration from the host into the hole-blocking layer while electrons should pass readily from the hole-blocking layer into the light-emitting layer comprising a host and a phosphorescent material.
• the first requirement entails that the ionization potential of the hole-blocking layer 110 be larger than that of the light-emitting layer 109, preferably by 0.2 eV or more.
• the second requirement entails that the electron affinity of the hole-blocking layer 110 not greatly exceed that of the light-emitting layer 109, and preferably be either less than that of light-emitting layer or not exceed that of the light-emitting layer by more than about 0.2 eV. It is further desirable, but not absolutely required, that the triplet energy of the hole-blocking material be greater than that of the phosphorescent material and yet more desirable that the triplet energy of the hole-blocking material be greater than that of the host material.
• Suitable hole-blocking materials are described in WO 00/70655A2 and WO 01/93642 Al.
• Two examples of useful hole-blocking materials are bathocuproine (BCP) and bis(2-methyl-8- quinolinolato)(4-phenylphenolato)aluminum(III) (BAlq).
• BCP bathocuproine
• BAlq bis(2-methyl-8- quinolinolato)(4-phenylphenolato)aluminum(III)
• Metal complexes other than BAlq are also known to block holes and excitons as described in US
• US 20030175553 Al describes the use of ⁇ c-tris(l- 9* phenylpyrazolato-N,C )iridium(III) (Irppz) for this purpose.
• a hole-blocking layer When a hole-blocking layer is used, its thickness can be between 2 and 100 nm and preferably between 5 and 10 nm.
• Electron-Transporting Layer Prefened thin film-forming materials for use in constructing the electron-transporting layer 111 of the organic EL devices of this invention are metal-chelated oxinoid compounds, including chelates of oxine itself (also commonly refereed to as 8-quinolinol or 8-hydroxyquinoline). Such compounds help to inject and transport electrons, exhibiting high levels of performance, and are readily fabricated in the form of thin films.
• Exemplary of contemplated oxinoid compounds are those satisfying structural formula (E), previously described.
• Other electron-transporting materials suitable for use in the electron-transporting layer 111 include various butadiene derivatives as disclosed in US 4,356,429 and various heterocyclic optical brighteners as described in US 4,539,507. Benzazoles satisfying structural formula (G) are also useful electron transporting materials. Triazines are also known to be useful as electron transporting materials. If both a hole-blocking layer 110 and an electron-transporting layer
• the electron affinity of the electron-transporting layer 111 should not greatly exceed that of the hole-blocking layer 110.
• the electron affinity of the electron-transporting layer should be less than that of the hole-blocking layer or not exceed it by more than about 0.2 eV. If an electron-transporting layer is used, its thickness maybe between 2 and 100 nm and preferably between 5 and 20 nm.
• An OLED device employing a phosphorescent material can include an exciton-blocking layer, placed adjacent to light-emitting layer 109 on the anode side, to help confine electron-hole recombination events and the resulting excitons to the light-emitting layer 109 comprising the host and phosphorescent material.
• the exciton-blocking layer may contain a compound having a hole mobility of at least lxl 0 "3 cm 2 V "1 s "1 and a triplet energy exceeding that of the light-emitting material of the LEL, as described in the copending application identified in the first paragraph of this application, the contents of which are incorporated herein.
• layers 109 through 111 can optionally be collapsed into a single layer that serves the function of supporting both light emission and electron transportation. Layers 110 and 111 may also be collapsed into a single layer that functions to block holes or excitons, and supports electron transport. It also known in the art that emitting materials may be included in the hole-transporting layer 107. In that case, the hole-transporting material may serve as a host. Multiple materials may be added to one or more layers in order to create a white-emitting OLED, for example, by combining blue- and yellow-emitting materials, cyan- and red-emitting materials, or red-, green-, and blue-emitting materials.
• White-emitting devices are described, for example, in EP 1 187 235, US 20020025419, EP 1 182 244, US 5,683,823, US 5,503,910, US 5,405,709, and US 5,283,182 and can be equipped with a suitable filter arrangement to produce a color emission.
• This invention may be used in so-called stacked device architecture, for example, as taught in US 5,703,436 and US 6,337,492.
• the organic materials mentioned above are suitably deposited by any means suitable for the form of the organic materials. In the case of small molecules, they are conveniently deposited through sublimation or evaporation, but can be deposited by other means such as coating from a solvent together with an optional binder to improve film formation. If the material is a polymer, coating from a solvent is usually prefened.
• the material to be deposited by sublimation can be vaporized from a sublimator "boat" often comprised of a tantalum material, e.g., as described in US 6,237,529, or can be first coated onto a donor sheet and then sublimed in closer proximity to the substrate.
• Layers with a mixture of materials can utilize separate sublimator boats or the materials can be pre-mixed and coated from a single boat or donor sheet.
• Patterned deposition can be achieved using shadow masks, integral shadow masks (US 5,294,870), spatially-defined thermal dye transfer from a donor sheet (US 5,688,551, US 5,851,709 and US 6,066,357) or an inkjet method (US 6,066,357).
• OLED devices are sensitive to moisture or oxygen, or both, so they are commonly sealed in an inert atmosphere such as nitrogen or argon, along with a desiccant such as alumina, bauxite, calcium sulfate, clays, silica gel, zeolites, alkaline metal oxides, alkaline earth metal oxides, sulfates, or metal halides and perchlorates.
• a desiccant such as alumina, bauxite, calcium sulfate, clays, silica gel, zeolites, alkaline metal oxides, alkaline earth metal oxides, sulfates, or metal halides and perchlorates.
• Methods for encapsulation and desiccation include, but are not limited to, those described in U.S. Patent No. 6,226,890.
• barrier layers such as SiO x , Teflon, and alternating inorganic/polymeric layers are known in the art for encapsulation. Any
• Optical Optimization OLED devices of this invention can employ various well-known optical effects in order to enhance their emissive properties if desired. Included are optimizing layer thicknesses to yield maximum light transmission, providing dielectric minor structures, replacing reflective electrodes with light-absorbing electrodes, providing anti-glare or anti-reflection coatings over the display, providing a polarizing medium over the display, or providing colored, neutral density, or color-conversion filters over the display. Filters, polarizers, and anti- glare or anti-reflection coatings may be specifically provided over the EL device or as part of the EL device. Embodiments of the invention can provide advantageous features such as higher luminous yield and power efficiency.
• Embodiments of the organometallic compounds useful in the invention can provide a wide range of hues including those useful in the emission of white light (directly or through filters to provide multicolor displays). Embodiments of the invention can also provide an area lighting device. The invention and its advantages can be better appreciated by the following examples.
• An EL device (Device 1) satisfying the requirements of the invention was constructed in the following manner: 1. A glass substrate coated with an approximately 85 nm layer of indium-tin oxide (ITO) as the anode was sequentially ultrasonicated in a commercial detergent, rinsed in deionized water, degreased in toluene vapor and exposed to an oxygen plasma for about 1 min. 2. Over the ITO was deposited a 1 nm fluorocarbon (CF X ) hole- injecting layer (HIL) by plasma-assisted deposition of CHF 3 . 3.
• ITO indium-tin oxide
• HIL hole- injecting layer
• a hole-transporting layer (HTL) of NN'-di- 1 -naphthyl-NN'- diphenyl-4, 4'-diaminobiphenyl ( ⁇ PB) having a thickness of 75 nm was then evaporated from a resistance-heated tantalum boat.
• a 35 nm light-emitting layer (LEL) consisted of mixture of 4,4'- ⁇ , ⁇ '-dicarbazole-biphenyl (CBP) as a host, fac tris(2-phenylpyridinato) iridium (III) [i.e., Ir( ⁇ py) 3 ] at 6 wt.
• HBL hole-blocking layer of bis(2-methyl-quinolinolato)(4- phenylphenolato) aluminum(III) (BAlq) having a thickness of 10 nm was then evaporated from another tantalum boat. 6.
• a 40 nm electron-transporting layer (ETL) of tris(8-quinolinolato) aluminum (III) (Alq) was then deposited onto the light-emitting layer. This material was also evaporated from a tantalum boat. 7. On top of the Alq layer was deposited a 220 nm cathode formed of a 10:1 volume ratio of Mg and Ag. The above sequence completed the deposition of the EL device. The device, together with a desiccant, was then hennetically packaged in a dry glove box for protection against ambient environment.
• Device Example 2-5 Devices 2-4 satisfying the requirements of the invention were fabricated in an identical manner to a Device 1 except that the concentration of MTDATA in the LEL, represented as percentage by weight of the light-emitting layer, was as indicated below in Table 1.
• a comparative Device 5 not satisfying the requirements of the invention was fabricated in an identical manner to Device 1 except that MTDATA was not included in the LEL.
• the devices thus formed were tested for efficiency and color at an operating cunent density of 6 mA/cm 2 .
• the results, including 1931 CIE (Commission Internationale de 1' Eclairage) coordinates, CIEx and CIEy, are reported in Table 1. The perceived emission color was green.
• MTDATA satisfies the criteria for an efficiency-enhancing material to be used with Ir(ppy) 3 as the phosphorescent material and CBP as the host material according to the present invention.
• Devices 1-4 incorporating MTDATA as an efficiency-enhancing material in the LEL, are constructed according to the present invention. As can be seen from Table 1 , they show superior luminous yield and power efficiency relative to Device 5, which lacks the efficiency-enhancing material and, therefore, is not constructed according to the curcent invention. Moreover, the efficiency was greatest for Device 3, which contained the efficiency-enhancing material within the suitable range of 3 - 10 by weight.
• HIL Hole-Injecting layer
• HTL Hole-Transporting layer
• HBL Hole-blocking layer
• Electron-Transporting layer (ETL) 113 Cathode

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