Electroluminescent materials

Details Electroluminescent materials Electroluminescent materials

2001-06-01

2003-05-20

Yamnitzky, Marie (Department: 1774)

Stock material or miscellaneous articles

Composite

Of inorganic material

C428S917000, C313S503000, C313S504000, C313S506000

Reexamination Certificate

active

06565995

ABSTRACT:

This application is a national stage application of PCT/GB99/04028 filed Dec. 1, 1999. PCT/GB99/04028 was published in English under publication number WO 00/32718 on Jun. 8, 2000.
The present invention relates to electroluminescent materials and to devices incorporating them.
Materials, which emit light when an electric current is passed through them, are well known and used in a wide range of display applications. Liquid crystal devices and devices which are based on inorganic semiconductor systems are widely used, however these suffer from the disadvantages of high energy consumption, high cost of manufacture, low quantum-efficiency and the inability to make flat panel displays, reflectance problems, i.e. low visibility in bright conditions and a narrow viewing angle e.g. +/−45°.
Organic polymers have been proposed as useful in electroluminescent devices, but it is not possible to obtain pure colours, they are expensive to make and have a relatively low efficiency.
Another compound, which has been proposed, is aluminium quinolate, but this requires dopants to be used to obtain a range of colours and has a relatively low efficiency.
In an article in Chemistry letters pp 657-660, 1990 Kido et al disclosed that a terbium (III) acetyl acetonate complex was green electroluminescent and in an article in Applied Physics letters 65 (17) Oct. 24, 1994 Kido et al disclosed that a europium (III) triphenylene diamine complexes was red electroluminescent but these were unstable in atmospheric conditions and difficult to produce as films.
The complexes disclosed in these articles had a relatively low photoluminescent efficiency and were only able to produce green or red light and other colours could not be produced.
Production of white light by electroluminescence is difficult to achieve and has required the use of a plurality of different electroluminescent materials either mixed or in sequential layers. Another method of modifying the colour of emitted light is by use of fluorescent dye or dyes mixed with the electroluminescent material or in sequential layers.
In an article by Takco Wakimoto et al in Applied Surface Science 113/114(1997) pages 698-704 electroluminescent cells are disclosed in which aluminium quinolate is used as the emitter and which is doped by quinacrodine derivatives, which are fluorescent dyes, to change the colour of the emitted light.
We have now discovered electroluminescent compounds in which the emitted light can be varied by varying the applied voltage and which can emit white light.
According to the invention there is provided an electroluminescent device in which the electroluminescent compound is Tb(TMHD)
3
OPNP.
Where TMHD is 2,2,6,6-tetramethyl-3,5-heptanedionato and OPNP is diphenylphosphonimide triphenyl phosphorane.
The colour of light is subjective and colours can be defined by co-ordinates on a two dimensional chart in which colours are areas on the chart and, in the present invention, as well as being observed to be white, white light can be defined as an area in the colour chart CIE 1931.
The electroluminescent compound can be mixed with other transition metal, lanthanide or actinide organic complexes which may change the colour of the emitted light
The electroluminescent device comprises a conductive substrate which acts as the anode, a layer of the electroluminescent material and a metal contact connected to the electroluminescent layer which acts as the cathode. When a current is passed through the electroluminescent layer the layer emits light.
The electroluminescent devices of the invention preferably comprise a transparent substrate which is a conductive glass or plastic material which acts as the anode, preferred substrates are conductive glasses such as indium tin oxide coated glass, but any glass which is conductive or has a conductive layer can be used. Conductive polymers and conductive polymer coated glass or plastics materials can also be used as the substrate. The Tb(TMHD)
3
OPNP can be deposited on the substrate directly by evaporation from a solution in an organic solvent. The solvent which is used can be for example alcohols such as ethanol, ketones such as acetone and methyl acetylacetonate and chlorinated hydrocarbons such as dichloromethane.
Alternatively the material can be deposited by spin coating or by vacuum deposition from the solid state e.g. by sputtering or any other conventional method can be used.
Preferably the Tb(TMHD)
3
OPNP film is made by mixing Tb(TMHD)
3
and OPNP, heating the mixture formed under a vacuum so that the mixture is vaporised and condensing the vapour on to a substrate to form a film or layer of the organo-metallic complex on the substrate. Alternatively the Tb(TMHD)
3
and the OPNP can be deposited sequentially on to the substrate.
In one embodiment of the invention there is a hole transporting layer deposited on the transparent substrate and the Tb(TMHD)
3
OPNP is deposited on the hole transporting layer. The hole transporting layer serves to transport holes and to block the electrons, thus preventing electrons from moving into the electrode without recombining with holes. The recombination of carriers therefore mainly takes place in the emitter layer.
Hole transporting layers are used in polymer electroluminescent devices and any of the known hole transporting materials in film form can be used.
The hole transporting layer can be made of a film of an aromatic amine complex such as poly(vinylcarbazole), N,N′-diphenyl-N,N′-bis(3-methylphenyl)-I,I′-biphenyl-4,4′-diamine (TPD), polyaniline etc.
Optionally dyes such as fluorescent laser dyes, luminescent laser dyes can be included to modify the colour spectrum of the emitted light and also enhance the photoluminescent and electroluminescent efficiencies.
In one embodiment the Tb(TMHD)
3
OPNP is mixed with a polymeric material such as a polyolefin e.g. polyethylene, polypropylene etc. and preferably polystyrene. Preferred amounts of active material in the mixture is from 95% to 5% by weight of active material and more preferably 25 to 20% by weight.
The hole transporting material can optionally be mixed with the Tb(TMHD)
3
OPNP in a ratio of 5-95% of the Tb(TMHD)
3
OPNP to 95 to 5% of the hole transporting compound.
In another embodiment of the invention there is a layer of an electron transporting material between the cathode and the Tb(TMHD)
3
OPNP layer, this electron transporting layer is preferably a metal complex such as a metal quinolate e.g. an aluminium quinolate which will transport electrons when an electric current is passed through it. Alternatively the electron transporting material can be mixed with the Tb(TMHD)
3
OPNP and co-deposited with it.
In a preferred structure there is a substrate formed of a transparent conductive material which is the anode on which is successively deposited a hole transportation layer, the Tb(TMHD)
3
OPNP layer and an electron transporting layer which is connected to the cathode. The cathode can be any low work function metal e.g. aluminium, calcium, lithium, silver/magnesium alloys etc.
At lower voltages e.g. below 10 volts the emitted light principally is yellowish green and corresponds to the typical colour of emitted light of terbium III complexes and, as the voltage is increased, the emitted light becomes nearer a white colour and at a voltage of over 12 volts it appears white to the eye.
Possibly the wavelength of the emitted light changes due to an increase in the strength of the radiation due to the ligands which emit light of a shorter wavelength with increase of voltage so the overall effect is a combination of the contributions from the various moieties in the complex and its interaction with the hole transporting layer.
It is very surprising that this effect can give rise to white light.


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patent: 4455364 (1984-06-01), Sasa
patent: 4720432 (1988-01-01), VanSlyke et al.
patent: 4885211 (1989-12-01), Tang et al.
patent: 5128587 (1992-07-01), Skotheim et al.
patent: 5281489 (1994-01-01), Mori et al.
patent: 5435937

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