WO2003058728A1 - Electroluminescent device - Google Patents

Electroluminescent device Download PDF

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Publication number
WO2003058728A1
WO2003058728A1 PCT/IB2002/005543 IB0205543W WO03058728A1 WO 2003058728 A1 WO2003058728 A1 WO 2003058728A1 IB 0205543 W IB0205543 W IB 0205543W WO 03058728 A1 WO03058728 A1 WO 03058728A1
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Prior art keywords
layer
metallic
luminescent
percolated
substrate
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PCT/IB2002/005543
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German (de)
French (fr)
Italian (it)
Inventor
Piero Perlo
Nello Li Pira
Rossella Monferino
Piermario Repetto
Vito Lambertini
Marzia Paderi
Original Assignee
C.R.F. Società Consortile Per Azioni
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Application filed by C.R.F. Società Consortile Per Azioni filed Critical C.R.F. Società Consortile Per Azioni
Priority to AU2002349687A priority Critical patent/AU2002349687A1/en
Priority to DE60219690T priority patent/DE60219690T2/en
Priority to JP2003558938A priority patent/JP2005514744A/en
Priority to US10/470,310 priority patent/US6861674B2/en
Priority to KR1020047007492A priority patent/KR100905376B1/en
Priority to EP02781692A priority patent/EP1464088B1/en
Publication of WO2003058728A1 publication Critical patent/WO2003058728A1/en

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    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • H05B33/12Light sources with substantially two-dimensional radiating surfaces
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • H05B33/12Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • H05B33/145Arrangements of the electroluminescent material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L28/00Passive two-terminal components without a potential-jump or surface barrier for integrated circuits; Details thereof; Multistep manufacturing processes therefor
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • H05B33/12Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source

Definitions

  • the present invention relates to an electroluminescent device.
  • the present invention proposes the production of an electroluminescent device of novel conception, which is particularly susceptible to be applied to the field of photonics and is on a competitive level with traditional electroluminescent devices, such as LED and O-LED, both in terms of costs and attainable performances.
  • figure 1 is a graphic representation of the potential barrier between a generic metal and the vacuum, in different conditions
  • figure 2 is a schematic representation of an electroluminescent device produced in accordance with the present invention
  • FIG. 3 is a schematic representation of an electroluminescent device produced in accordance with a first possible variant of the present invention
  • FIG. 4 is a schematic representation of an electroluminescent device produced in accordance with a second possible variant of the present invention.
  • the electroluminescent device is based on the tunneling effect in a three- dimensional percolated layer.
  • a three-dimensional percolated layer is a metallic mesoporous structure, composed of metallic nanoparticles interconnected with one another or dielectric metallic interconnections connected in such a way as to guarantee electrical conduction; the interconnection or connection may be produced by tunneling, as will be explained hereunder.
  • the cavities of micrometric or nanometric dimensions which are found in the mesoporous structure house luminescent nanoparticles or macromolecules; as will be seen, these emit light when they are energized by the electrons which, as a result of tunneling, pass through the percolated layer.
  • mesoporous materials comprises inorganic materials with pores with dimensions below 50 nm. Porous materials with pores of nanometric dimensions are the most difficult to produce.
  • "supramolecular templating" techniques are generally utilized, which use asymmetrical organic molecules as templates, to be removed once the nanoporous structure has been established.
  • Metallic mesoporous materials can instead be grown using evaporation techniques, such as thermal evaporation or electron beam evaporation.
  • the metal-insulator interface is a typical situation inside a metallic system at percolation level, which occurs at each discontinuity of the system.
  • Field emission also called Fowler-Nordheim electron tunneling, consists in transporting electrons through a metal-insulator interface due to the passage, by tunneling effect, of the electrons from the Fermi level of the metal to the conduction band of the insulator means .
  • This tunnel effect occurs when there are strong electric fields (hence the term “emission for field effect”) which are able to bend the energy bands of the insulator means to form a narrow triangular potential barrier between the metal and the insulator.
  • Figure 1 provides for this object a schematic representation of the potential barrier between a generic metal and the vacuum in three different possible situations.
  • the phenomenon of field effect emission or electron tunneling also occurs.
  • the potential barrier that is created at the metal- insulator surface becomes so thin that the electrons of the metal can pass through it by quantum tunneling.
  • the potential barrier becomes thin enough and the electrons that are on the Fermi level of the metal acquire a finite probability of passing through it.
  • the even thinner thickness of the potential barrier allows electrons with even lower energies to pass through by tunnel effect .
  • the current density of emission for field effect is strictly dependent on the intensity of the electric field, while it is substantially independent from the temperature :
  • E represents the intensity of the electric field
  • represents the height of the potential barrier
  • b is a constant of proportionality
  • the percolated metallic system should have a voltage- current characteristic with non-ohmic trend: the increase in the current with the voltage applied, thanks to the contributions of thermal emission and field effect emission, should be faster than it is in an ohmic conductor with linear characteristics.
  • the numeral 1 indicates as a whole an electroluminescent device produced according to the precepts of the present invention, the operation of which is based on the concepts set forth above.
  • the device 1 has a "Current In Plane” architecture and is formed of several parts, namely:
  • the substrate 2 may be transparent and produced in common glass, prepared for example with an ultrasound cleaning process, or may be opaque and produced in plastic material. According to the invention, transparent substrates covered with special costly coatings, such as glass covered with ITO, used in IDLED, P-LED and liquid crystal device technology, are not in any case required.
  • the lateral electrodes 3 are positioned on the glass substrate 2 at the same level and are composed of a continuous metallic layer, deposited by evaporation; the metallic material utilized for the purpose may be copper, silver, gold, aluminum or similar.
  • the electrodes 3 At the ends of the layer 4 , the electrodes 3 generate a difference of potential that induces tunneling of electric charge through this layer. If the voltage applied is high enough to create very intense local electric fields (E «10 7 V/cm) , electron conduction by tunneling as previously described occurs inside the metallic layer 4 at percolation.
  • the percolation point of a discontinuous metallic system is defined as the point in which the film changes from acting as an insulator, typical of the situation in which the film has a great number of discontinuities in relation to the metallic islands, to act as a conductor, typical of the situation in which as the metallic islands are predominant over the discontinuities in the film, direct "links" between its two ends are formed, in which conduction of electric current can take place .
  • electron emission by the metallic islands by electron tunneling effect is used to energize the luminescent particles 5, for instance in the form of semiconductor nanocrystals, metallic nanoparticles or molecules with phosphorescent properties, included in the cavities of the percolated metallic layer 4.
  • the electrons extracted by the metallic islands by electron tunneling have sufficient energy to energize luminescence in the luminescent nanoparticles enclosed in the matrix composed of the percolated metallic structure.
  • the centers of luminescence with nanometric dimensions may be of various types. In particular they may be produced by:
  • organic phosphoruses that is luminescent organic molecules, evaporated together with the metallic structure, among which: Coumarin 7, Alumnium-8- hydroxyquinoline, Spiro compounds, electroluminescent polymers;
  • inorganic semi conductors Si , CdSe, CdTe, "core- shell " CdSe/ZnS and CdSe/CdS structures
  • nanostructures of this type may, if energized by incident electrons with a certain amount of energy, emit photons in the visible field and the near-infrared;
  • - metallic nanocrystals Au, Ag , Co, Ni , Pt, ...) , prepared for example chemically by reduction of metallic ions in solution or physically by evaporation of the metal at high temperature; on the nanometric scale, these metals behave similarly to a semiconductor and are capable of emitting, if energized, visible photons or in the near-infrared; luminescent rare earths, such as metalorganic compounds of europium, terbium (emission in the visible) , erbium, ytterbium (emission in the infrared) .
  • the transparent protective layer 6 of the device 1 according to the invention may finally be composed of very thin transparent glass (about 0.5 mm), produced with sol-gel process and deposited on the percolated metallic layer 4 by spin-coating, dip-coating, evaporation or sputtering, or may be produced with another transparent plastic dielectric.
  • This protective layer 6 does not require the introduction of a polarization film, as required in 0- LED technology, for which it is essential to increase the contrast of the output light.
  • the protective layer 6 of the device 1 according to the invention in addition to being easy to prepare and deposit, thus reduces the total cost of the production process.
  • the metallic mesoporous material 4 at percolation level is in the form of a single layer.
  • the effect of extracting the electrons by the metallic islands which constitute the percolated layer may be increased by replacing the single layer 4 of figure 2 with a multilayer percolated system.
  • the different layers may made of different metals or alternately metal/dielectric.
  • all the layers of the system, indicated with 4A must be at percolation level, to guarantee the same performances of electron transport obtained in the single layer, and must be distributed so as to be in direct contact with metals with different work functions (or extraction potentials) .
  • the various layers 4A of metal at percolation level must be alternated with discontinuous layers of dielectric material, one of which is indicated with 4B.
  • the discontinuity of the dielectric layers 4B is essential to guarantee electric conduction throughout the multilayer system (and not through each single metallic layer) .
  • ElectronVolts applied to continuous electrodes are: Ca-Al, Ca-Ag, Ca- Cu, Ca-Au, Al-Au, Ag-Au.
  • the advantages the new electroluminescent device draws from the characteristics of the percolated metallic layer include :

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  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Electroluminescent Light Sources (AREA)
  • Luminescent Compositions (AREA)
  • Massaging Devices (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
  • Glass Melting And Manufacturing (AREA)
  • Electrodes Of Semiconductors (AREA)
  • Led Device Packages (AREA)

Abstract

An elecroluminescent device (1) comprises: a supporting substrate (2); at least two electrodes (3) positioned on the substrate (2); at least a three-dimensional percolated layer (4), positioned on the substrate (2) between the two electrodes (3), having a metallic mesoporous structure defining a multitude of cavities of micrometric or nanometric dimensions. Present in the cavities of the three-dimensional percolated layer (4) are a multitude of luminescent inclusions (5), which operate to emit light when energized by elections which, as a result of electron tunneling effect, pass through the three-dimensional percolated layer (4).

Description

TRANSLATION (RULE 12.3)
"Electroluminescent device" * * *
TEXT OF DESCRIPTION
The present invention relates to an electroluminescent device.
More specifically, the present invention proposes the production of an electroluminescent device of novel conception, which is particularly susceptible to be applied to the field of photonics and is on a competitive level with traditional electroluminescent devices, such as LED and O-LED, both in terms of costs and attainable performances.
The object is attained, according to the present invention, by an electroluminescent device having the characteristics of the attached claims, which are an integral part of the present description.
Further objects, characteristics and advantages of the present invention shall become apparent from the description hereunder and the attached drawings, provided purely as a non-limitative example in which: figure 1 is a graphic representation of the potential barrier between a generic metal and the vacuum, in different conditions; figure 2 is a schematic representation of an electroluminescent device produced in accordance with the present invention;
- figure 3 is a schematic representation of an electroluminescent device produced in accordance with a first possible variant of the present invention;
- figure 4 is a schematic representation of an electroluminescent device produced in accordance with a second possible variant of the present invention.
The electroluminescent device according to the invention is based on the tunneling effect in a three- dimensional percolated layer. A three-dimensional percolated layer is a metallic mesoporous structure, composed of metallic nanoparticles interconnected with one another or dielectric metallic interconnections connected in such a way as to guarantee electrical conduction; the interconnection or connection may be produced by tunneling, as will be explained hereunder. According to the invention, the cavities of micrometric or nanometric dimensions which are found in the mesoporous structure house luminescent nanoparticles or macromolecules; as will be seen, these emit light when they are energized by the electrons which, as a result of tunneling, pass through the percolated layer.
The commonly accepted definition for mesoporous materials comprises inorganic materials with pores with dimensions below 50 nm. Porous materials with pores of nanometric dimensions are the most difficult to produce. In particular, for orderly mesoporous materials "supramolecular templating" techniques are generally utilized, which use asymmetrical organic molecules as templates, to be removed once the nanoporous structure has been established. Metallic mesoporous materials can instead be grown using evaporation techniques, such as thermal evaporation or electron beam evaporation.
With regard to tunneling effect, it must here be considered that the metal-insulator interface is a typical situation inside a metallic system at percolation level, which occurs at each discontinuity of the system.
There are various electron transport mechanisms through the metal-insulator interface, such as ohmic conduction, ionic conduction, thermal emission and field effect emission. In a given material, each of the aforesaid mechanisms prevails in a certain temperature and voltage range (electric field) and has a characteristic dependence on the current, the voltage and the temperature. These different processes are not necessarily independent from one another.
Field emission, also called Fowler-Nordheim electron tunneling, consists in transporting electrons through a metal-insulator interface due to the passage, by tunneling effect, of the electrons from the Fermi level of the metal to the conduction band of the insulator means .
This tunnel effect occurs when there are strong electric fields (hence the term "emission for field effect") which are able to bend the energy bands of the insulator means to form a narrow triangular potential barrier between the metal and the insulator.
Figure 1 provides for this object a schematic representation of the potential barrier between a generic metal and the vacuum in three different possible situations.
Generally, it is assumed that the potential energy of an electron passes from zero inside the metal to the value EF+Φ immediately outside the surface of the metal . In figure 1 this case is represented by the curve (a) .
The potential barrier which an electron moving away from the metal encounters has instead a more gradual trend, as it is reasonable to think that initially the potential increases linearly with the distance from the surface of the metal; when an electron reaches the distance of a few A from this surface it should feel the effect of an attractive force equivalent to the force due to a charge -e, in the presence of which the potential energy of the electron may be represented with a function of the type:
Figure imgf000005_0001
where x represents the distance of the electron from the surface of the metal . In figure 1 this case is represented by the curve (b) .
Finally, if an electric field is applied in the direction X in the vacuum region surrounding the heated metal, the potential energy of the electron becomes of the type :
Figure imgf000006_0001
where E represents the electric field applied. By performing the derivative of this expression the presence of a maximum of the potential barrier is found, represented in figure 1 by the curve (c) , which is found at :
Figure imgf000006_0002
rm = V(x) = (EF +Φ)-(e3E/4πε0f2
As can be seen in figure 1, the presence of an external electric field produces a slight decrease in the effective work function. The decrease in the value of the typical work function of the metal in the vacuum is small if the external electric field is not very intense (up to the value of a few thousands of volts/meter) : in this case the maximum potential is found at many A of distance from the external surface of the metal . Even a small decrease in the value of Φ makes the phenomenon of thermal emission possible for many electrons without sufficient energy to pass over the potential barrier in the absence of the external electric field.
When the electric field becomes very intense, around 109 volts/meter, in addition to the decrease in the typical work function of the metal, the phenomenon of field effect emission or electron tunneling also occurs. The potential barrier that is created at the metal- insulator surface becomes so thin that the electrons of the metal can pass through it by quantum tunneling. At a critical value of the electric field the potential barrier becomes thin enough and the electrons that are on the Fermi level of the metal acquire a finite probability of passing through it. For higher values of the electric field, the even thinner thickness of the potential barrier allows electrons with even lower energies to pass through by tunnel effect .
The current density of emission for field effect is strictly dependent on the intensity of the electric field, while it is substantially independent from the temperature :
Figure imgf000007_0001
where E represents the intensity of the electric field, Φ represents the height of the potential barrier and b is a constant of proportionality.
It is important to observe that, in the case of emission through electron tunneling, the electrons do not require thermal energizing (and this explains the fact that j does not depend on the temperature) , but an intense electric field that reduces the thickness of the potential barrier bending the conduction and valence bands of the insulator means . This explains the strict dependence of j on the intensity of the electric field: in fact, in this case, the electrons do not pass over the potential barrier but tunnel through it.
There should only be a slight probability of tunneling for Fermi level electrons unless the barrier is thinner than 10A. Therefore, it is reasonable to expect that the critical value of the electric field above which the phenomenon of emission through field effect will occur is about 3-109 volts/meter. However, this type of emission also occurs with macroscopic electric fields up to 30 times less intense. It is probable that local roughness in the surface of the metal is the cause of the presence of extremely intense electric fields, although only on a local scale, and that the majority of the emission by field effect comes from these zones .
Inside a percolated metallic system, and specifically at each metal-vacuum interface, there are local increases in the electric field that make it possible to reach the values of intensity of the electric field required for electron tunneling to take place. It is important to stress that the smaller the dimensions involved in the field emission phenomenon are, the greater the local increase in the electric field is. At each discontinuity of the percolated metallic system, where there is a local increase in the electric field and electron emission takes place by field effect, a local increase in the current density should occur. In fact, just as those deriving from thermal emission, the electrons emitted by field effect contribute to the total electric current. Due to this, the percolated metallic system should have a voltage- current characteristic with non-ohmic trend: the increase in the current with the voltage applied, thanks to the contributions of thermal emission and field effect emission, should be faster than it is in an ohmic conductor with linear characteristics.
In figure 2 , the numeral 1 indicates as a whole an electroluminescent device produced according to the precepts of the present invention, the operation of which is based on the concepts set forth above.
The device 1 has a "Current In Plane" architecture and is formed of several parts, namely:
- a substrate, indicated with 2; - two lateral electrodes, indicated with 3 ; a layer of metallic mesoporous material at percolation level, indicated with 4;
- luminescent nanometric inclusions 5 in the layer of percolated material 4;
- a transparent protective layer, indicated with 6. The substrate 2 may be transparent and produced in common glass, prepared for example with an ultrasound cleaning process, or may be opaque and produced in plastic material. According to the invention, transparent substrates covered with special costly coatings, such as glass covered with ITO, used in IDLED, P-LED and liquid crystal device technology, are not in any case required.
The lateral electrodes 3 are positioned on the glass substrate 2 at the same level and are composed of a continuous metallic layer, deposited by evaporation; the metallic material utilized for the purpose may be copper, silver, gold, aluminum or similar.
The electric contact between the power generator, indicated schematically with "Low VDC" , of the electroluminescent device 1 and the active layer of the device, composed by the layer 4 of metallic mesoporous material at percolation level, is established through the electrodes 3.
At the ends of the layer 4 , the electrodes 3 generate a difference of potential that induces tunneling of electric charge through this layer. If the voltage applied is high enough to create very intense local electric fields (E «107 V/cm) , electron conduction by tunneling as previously described occurs inside the metallic layer 4 at percolation.
The percolation point of a discontinuous metallic system is defined as the point in which the film changes from acting as an insulator, typical of the situation in which the film has a great number of discontinuities in relation to the metallic islands, to act as a conductor, typical of the situation in which as the metallic islands are predominant over the discontinuities in the film, direct "links" between its two ends are formed, in which conduction of electric current can take place .
In a discontinuous metallic film at percolation level there are different electron transport mechanisms. As mentioned, in addition to normal ohmic conduction of the current, other transport mechanisms occur which involve the interface zones between the metal and the discontinuities, in particular thermal emission and electron tunneling.
Thermal emission only occurs in discontinuous films for sufficiently high temperature values, while electron tunneling occurs prevalently in films characterized by a large number of discontinuities of extremely small size, where sufficiently intense local electric fields form.
Evidence of the electron tunneling phenomenon is given by the non-linear trend of the voltage-current characteristic shown by percolated metallic systems. These show a current discharge that occurs at a critical value of the applied voltage. The current discharge proves that the conductibility of the system increases suddenly at the critical voltage value: this means that by applying suitable voltage, at the discontinuities where sufficiently intense electric fields have been created, electron tunneling effect is obtained. The electrons extracted by the metallic islands towards the discontinuity zones contribute to the total current that passes through the system, thus becoming responsible for the current discharge which can be observed at macroscopic level . It is this very phenomenon which makes the percolated metallic system very interesting for the applications in an electroluminescent device. In fact, electron emission by the metallic islands by electron tunneling effect is used to energize the luminescent particles 5, for instance in the form of semiconductor nanocrystals, metallic nanoparticles or molecules with phosphorescent properties, included in the cavities of the percolated metallic layer 4.
The electrons extracted by the metallic islands by electron tunneling have sufficient energy to energize luminescence in the luminescent nanoparticles enclosed in the matrix composed of the percolated metallic structure. The centers of luminescence with nanometric dimensions may be of various types. In particular they may be produced by:
- organic phosphoruses , that is luminescent organic molecules, evaporated together with the metallic structure, among which: Coumarin 7, Alumnium-8- hydroxyquinoline, Spiro compounds, electroluminescent polymers;
- inorganic semi conductors (Si , CdSe, CdTe, "core- shell " CdSe/ZnS and CdSe/CdS structures) , prepared with self-assembly techniques (which allow control over the diameter of the particles) , electrochemical deposition, Langmuir-Blodgett techniques; nanostructures of this type may, if energized by incident electrons with a certain amount of energy, emit photons in the visible field and the near-infrared;
- metallic nanocrystals (Au, Ag , Co, Ni , Pt, ...) , prepared for example chemically by reduction of metallic ions in solution or physically by evaporation of the metal at high temperature; on the nanometric scale, these metals behave similarly to a semiconductor and are capable of emitting, if energized, visible photons or in the near-infrared; luminescent rare earths, such as metalorganic compounds of europium, terbium (emission in the visible) , erbium, ytterbium (emission in the infrared) .
The transparent protective layer 6 of the device 1 according to the invention may finally be composed of very thin transparent glass (about 0.5 mm), produced with sol-gel process and deposited on the percolated metallic layer 4 by spin-coating, dip-coating, evaporation or sputtering, or may be produced with another transparent plastic dielectric.
This protective layer 6 does not require the introduction of a polarization film, as required in 0- LED technology, for which it is essential to increase the contrast of the output light. The protective layer 6 of the device 1 according to the invention, in addition to being easy to prepare and deposit, thus reduces the total cost of the production process.
In the case shown in figure 2, the metallic mesoporous material 4 at percolation level is in the form of a single layer. In accordance with a possible variant, shown schematically in figure 3, the effect of extracting the electrons by the metallic islands which constitute the percolated layer may be increased by replacing the single layer 4 of figure 2 with a multilayer percolated system.
The different layers may made of different metals or alternately metal/dielectric. In the first case, as shown in figure 3, all the layers of the system, indicated with 4A, must be at percolation level, to guarantee the same performances of electron transport obtained in the single layer, and must be distributed so as to be in direct contact with metals with different work functions (or extraction potentials) . In the second case, as shown in figure 4, the various layers 4A of metal at percolation level must be alternated with discontinuous layers of dielectric material, one of which is indicated with 4B. The discontinuity of the dielectric layers 4B is essential to guarantee electric conduction throughout the multilayer system (and not through each single metallic layer) .
It is known that phenomena of electron emission by a metal, either due to thermal emission or electron tunneling, increase in intensity when atoms of an element characterized by a low work function are distributed on the surface of a metal characterized by a high work function value, and vice versa. The multilayer solution ensures the electroluminescent device has an extremely vast contact area, which increases the possibilities of contact between metallic islands of different elements and contributes towards increasing the number of electrons extracted by tunneling effect . Combinations of metals for which electron emission by tunneling effect is possible for a few ElectronVolts applied to continuous electrodes are: Ca-Al, Ca-Ag, Ca- Cu, Ca-Au, Al-Au, Ag-Au.
The characteristics of the invention are clear from the description given. As well as increased stability, the advantages the new electroluminescent device draws from the characteristics of the percolated metallic layer include :
- the possibility of obtaining light emission in both directions, as a metallic system at percolation level is almost completely transparent; the use of solutions with multi-layer of different layers of discontinuous films has the advantage of increasing the total volume from which light is emitted.
It is clear to those skilled in the art that there are numerous possible variants to the electroluminescent device described as an example, without however departing from the scopes of intrinsic novelty of the invention.
* * * * * * * * * *

Claims

* * * CLAIMS
1. An electroluminescent device (1) comprising:
- a glass or plastic supporting substrate (2) ;
- at least two electrodes (3) positioned on said substrate (2) ; at least a three-dimensional percolated layer (4;4A) positioned on said substrate (2) between said electrodes (3) , said three-dimensional percolated layer (4;4A) having a metallic mesoporous structure defining a multitude of cavities with micrometric or nanometric dimensions, said structure being in particular composed of metallic interconnections or metallic dielectrics interconnections connected so as to guarantee electric conduction;
- a multitude of luminescent inclusions (5) , in particular in the form of nanoparticles or macromolecules, housed in respective cavities of said three-dimensional percolated layer (4;4A), where said luminescent inclusions (5) are operative to emit light when energized by electrons which, as a result of electron tunneling effect, pass through said three-dimensional percolated layer (4;4A) .
2. Device according to claim 1, characterized in that said electrodes (3) are operative to establish the electric contact between an external power generator (Low VDC) and said three-dimensional percolated layer (4;4A), in order to generate to the ends of the latter a potential difference which induces transport of electric charge through the layer.
3. Device according to claim 1, characterized in that it is provided with a protective layer (6) of said three-dimensional percolated layer (4;4A).
4. Device according to claim 1, characterized in that said substrate (2) is produced in glass or plastic material .
5. Device according to claim 1, characterized in that said electrodes (3) are composed of a respective continuous metallic layer.
6. Device according to the preceding claim, characterized in that said continuous metallic layer is deposited by evaporation on said substrate (2) .
7. Device according to claim 5, characterized in that said metallic layer is composed of a material selected in the group comprising copper, silver, gold, aluminum, platinum and nickel .
8. Device according to claim 1, characterized in that said luminescent inclusions (5) are in the form of semiconductor nanocrystals, metallic nanoparticles or molecules with phosphorescent properties.
9. Device according to claim 1, characterized in that said luminescent inclusions (5) are in the form of organic phosphoruses, such as Coumarin 7, Alumnium-8- hydroxyquinoline, Spiro compounds, electroluminescent polymers .
10. Device according to claim 1, characterized in that said luminescent inclusions (5) are in the form of inorganic semiconductors, such as Si, CdSe, CdTe, "core-shell" CdSe/ZnS and CdSe/CdS structures.
11. Device according to claim 1, wherein said luminescent inclusions (5) are in the form of metallic nanocrystals .
12. Device according to claim 1, characterized in that said luminescent inclusions (5) are in the form of luminescent rare earths, such as metalorganic compounds of europium, terbium, erbium and ytterbium.
13. Device according to claim 3, characterized in that said protective layer (6) is made of glass or another transparent plastic dielectric.
14. Device according to the preceding claim, characterized in that said glass is produced with sol- gel process and deposited on said percolated metallic layer (4;4A) by spin-coating, by dip-coating, by evaporation or by sputtering.
15. Device according to claim 1, characterized in that it is provided with a plurality of three- dimensional percolated layers (4A) .
16. Device according to the preceding claim, characterized in that said layers (4A) are made of metals differing from one another or according to a repeated layout of the type metal-dielectric-metal - dielectric.
17. Device according to claim 15, characterized in that said layers (4A) are made of one metal alternated with discontinuous layers of dielectric material (4B) .
The foregoing substantially as described and illustrated and for the purposes herein specified.
PCT/IB2002/005543 2002-01-11 2002-12-18 Electroluminescent device WO2003058728A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
AU2002349687A AU2002349687A1 (en) 2002-01-11 2002-12-18 Electroluminescent device
DE60219690T DE60219690T2 (en) 2002-01-11 2002-12-18 Electroluminescent device
JP2003558938A JP2005514744A (en) 2002-01-11 2002-12-18 Electroluminescence device
US10/470,310 US6861674B2 (en) 2002-01-11 2002-12-18 Electroluminescent device
KR1020047007492A KR100905376B1 (en) 2002-01-11 2002-12-18 Electroluminescent device
EP02781692A EP1464088B1 (en) 2002-01-11 2002-12-18 Electroluminescent device

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004079056A2 (en) * 2003-03-06 2004-09-16 C.R.F. Società Consortile Per Azioni Process to make nano-structurated components
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DE102004063030A1 (en) * 2004-12-28 2006-08-17 Johannes-Gutenberg-Universität Mainz Multilayer system, process for its production and its use in electro-optical components
US7108802B2 (en) * 2002-07-01 2006-09-19 Consejo Superior De Investigaciones Cientificas Electroluminescent material containing a conjugated polymer or metal complexes inside zeolites and porous materials and the preparation method thereof
WO2008046058A2 (en) * 2006-10-12 2008-04-17 Cambrios Technologies Corporation Nanowire-based transparent conductors and applications thereof
WO2009006710A1 (en) * 2007-07-09 2009-01-15 Katholieke Universiteit Leuven K.U. Leuven R & D Light-emitting materials for electroluminescent devices
US7560859B2 (en) 2004-09-14 2009-07-14 Shizuo Fujita Fluorescent material having two layer structure and light emitting apparatus employing the same
US8018568B2 (en) 2006-10-12 2011-09-13 Cambrios Technologies Corporation Nanowire-based transparent conductors and applications thereof
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Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004027877A1 (en) * 2002-09-19 2004-04-01 Sharp Kabushiki Kaisha Variable resistance functional body and its manufacturing method
US7259443B2 (en) * 2003-06-26 2007-08-21 E.I. Du Pont De Nemours And Company Methods for forming patterns on a filled dielectric material on substrates
EP1655785A1 (en) * 2004-11-09 2006-05-10 C.R.F. Società Consortile per Azioni Light emitting ambipolar device
DE102005047609A1 (en) * 2005-10-05 2007-04-12 Giesecke & Devrient Gmbh Assurance of authenticity of value documents by means of feature substances
WO2007092606A2 (en) * 2006-02-09 2007-08-16 Qd Vision, Inc. Displays including semiconductor nanocrystals and methods of making same
JP2010508620A (en) * 2006-09-12 2010-03-18 キユーデイー・ビジヨン・インコーポレーテツド Electroluminescent display useful for displaying a predetermined pattern
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RU2480967C2 (en) * 2008-02-27 2013-04-27 Конинклейке Филипс Электроникс Н.В. Hidden organic optoelectronic devices having light-scattering layer
KR101995370B1 (en) 2008-04-03 2019-07-02 삼성 리서치 아메리카 인코포레이티드 Light-emitting device including quantum dots
US9525148B2 (en) 2008-04-03 2016-12-20 Qd Vision, Inc. Device including quantum dots
JP5414258B2 (en) * 2008-12-10 2014-02-12 キヤノン株式会社 Benzoindenochrysene compound and organic light-emitting device using the same
US8343575B2 (en) 2008-12-30 2013-01-01 Nanosys, Inc. Methods for encapsulating nanocrystals and resulting compositions
JP2012514071A (en) * 2008-12-30 2012-06-21 ナノシス・インク. Method for encapsulating nanocrystals and the resulting composition
US10214686B2 (en) 2008-12-30 2019-02-26 Nanosys, Inc. Methods for encapsulating nanocrystals and resulting compositions
US11198270B2 (en) 2008-12-30 2021-12-14 Nanosys, Inc. Quantum dot films, lighting devices, and lighting methods
US9574134B2 (en) * 2009-05-07 2017-02-21 Massachusetts Institute Of Technology Light emitting device including semiconductor nanocrystals
CN102762690A (en) * 2009-11-16 2012-10-31 爱默蕾大学 Lattice-mismatched core-shell quantum dots
EP3839335A1 (en) 2010-11-10 2021-06-23 Nanosys, Inc. Quantum dot films, lighting devices, and lighting methods

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5796120A (en) * 1995-12-28 1998-08-18 Georgia Tech Research Corporation Tunnel thin film electroluminescent device

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5432015A (en) 1992-05-08 1995-07-11 Westaim Technologies, Inc. Electroluminescent laminate with thick film dielectric
JP4532634B2 (en) * 1998-12-25 2010-08-25 キヤノン株式会社 Method for producing pores
US6771019B1 (en) * 1999-05-14 2004-08-03 Ifire Technology, Inc. Electroluminescent laminate with patterned phosphor structure and thick film dielectric with improved dielectric properties

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5796120A (en) * 1995-12-28 1998-08-18 Georgia Tech Research Corporation Tunnel thin film electroluminescent device

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
BAGRAEV N T ET AL: "Light emission from erbium-doped nanostructures embedded in silicon microcavities", TENTH INTERNATIONAL CONFERENCE ON MODULATED SEMICONDUCTOR STRUCTURES. MSS 10, LINZ, AUSTRIA, 23-27 JULY 2001, vol. 13, no. 2-4, Physica E, March 2002, Elsevier, Netherlands, pages 1059 - 1062, XP002240658, ISSN: 1386-9477 *
LI PIRA N ET AL: "MODELLING AND EXPERIMENTAL EVIDENCE OF QUANTUM PHENOMENA IN METALLIC NON-CONTINUOUS FILMS (METAL QUANTUM WIRE NETWORK - MQWN -)", PROCEEDINGS OF THE EUSPEN. INTERNATIONAL CONFERENCE, XX, XX, vol. 1, 27 May 2001 (2001-05-27), Turin, Italy, pages 212 - 215, XP008014567 *
YAMAMOTO NAOKATSU ET AL: "Inverse-percolation model for investigating a mechanism of formation and photoluminescence of porous silicon", J LUMIN;JOURNAL OF LUMINESCENCE 1999 ELSEVIER SCIENCE PUBLISHERS B.V., AMSTERDAM, NETHERLANDS, vol. 82, no. 1, 1999, pages 85 - 90, XP002240659, ISSN: 0022-2313 *

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CN100483770C (en) 2009-04-29
EP1464088B1 (en) 2007-04-18
KR100905376B1 (en) 2009-07-01
EP1464088A1 (en) 2004-10-06
ITTO20020033A0 (en) 2002-01-11
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AU2002349687A1 (en) 2003-07-24
US6861674B2 (en) 2005-03-01
JP2005514744A (en) 2005-05-19
CN1599963A (en) 2005-03-23
KR20040074986A (en) 2004-08-26
ATE360263T1 (en) 2007-05-15
US20040245647A1 (en) 2004-12-09

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