Adhesion promoter, electroactive layer and electroactive device comprising same, and method
In one embodiment the present invention discloses a method for making a first layer in an electroactive device comprising the steps of (i) preparing a composition by mixing at least one adhesion promoter material and at least one electroactive material; and (ii) depositing said composition onto a second electroactive layer of said electroactive device; and (iii) optionally further depositing a third electroactive layer onto the surface of said first layer opposite the second layer, wherein said composition enables adhesion between said first layer and said second layer or between said first layer and said third layer, or between said first layer and both said second layer and said third layer. In another embodiment the present invention discloses a method for improving adhesion between layers in an electroactive device comprising the steps of (i) depositing a surface treatment composition comprising at least one adhesion promoter material on at least one surface of a first electroactive layer, and (ii) depositing a second electroactive layer onto the surface of said first layer comprising said adhesion promoter; wherein said composition enables adhesion between said first layer and said second layer of said electroactive device. Electroactive layers and electroactive devices comprising said layers are also disclosed, as well as methods to make said electroactive devices. In another embodiment adhesion promoters comprising 9,9-disubstituted fluorenyl compounds are disclosed, as well as methods for making the same.
1. A method for making a first layer in an electroactive device comprising the steps of (i) preparing a first layer composition by mixing at least one adhesion promoter material and at least one organic electroactive material; wherein the adhesion promoter material comprises 9,9-disubstituted fluorenyl compound of formula (l):
wherein each R is independently alkyl, aryl, halogen, cyano, alkoxide, carboxylate, or hydroxy; each “x” independently has a value of from 0 to the number of positions which can be substituted on the aromatic ring; each R 1 is independently a C 1 -C 16 alkyl group or an aryl group; each R 2 is independently a C 1 -C 16 alkyl group; and the geometry about each double bond is independently either cis or trans, and combination thereof; and (ii) depositing said composition on a second electroactive layer of said electroactive device to form said first layer; and (iii) optionally further depositing a third layer of electroactive material onto the surface of said first layer opposite the second layer, wherein said first layer composition enables adhesion between said first layer and said second layer or between said first layer and said third layer, or between said first layer and both said second layer and said third layer.
2. The method of claim 1 , wherein said depositing is selected from the group consisting of reverse roll coating, wire-wound or Mayer rod coating, direct and offset gravure coating, slot die coating, blade coating, hot melt coating, curtain coating, knife over roll coating, extrusion, air knife coating, spray, rotary screen coating, multilayer slide coating, coextrusion, meniscus coating, comma and microgravure coating, spin coating, dip coating, lithographic process, langmuir process and flash evaporation, vapor deposition, plasma-enhanced chemical-vapor deposition, radio-frequency plasma-enhanced chemical-vapor deposition, expanding thermal-plasma chemical-vapor deposition, sputtering, reactive sputtering, electron-cyclotron-resonance plasma-enhanced chemical-vapor deposition, inductively coupled plasma-enhanced chemical-vapor deposition, and combinations thereof.
3. The method of claim 1 wherein the electroactive material is selected from the group consisting of an organic light emitting material, a hole transport material, a hole injection material, a hole blocking material, an electron injection material, an electron transport material and combinations thereof.
4. The method of claim 3 wherein the light emitting material is selected from the group consisting of poly(N-vinylcarbazole), polyfluorene, poly(alkylfluorene), poly(para-phenylene), poly(p-phenylene vinylene), polythiophene, poly(pyridine vinylene), polyquinoxaline, polyquinoline, polysilanes, 1,3,5-tris{n-(4-diphenylaminophenyl)phenylamino}benzene, phenylanthracene, tetraarylethene, coumarin, rubrene, tetraphenylbutadiene, anthracene, perylene, coronene, tris(8-quinolinolato) aluminum; derivatives of the foregoing, 8-hydroxyquinoline aluminum acetylacetonate, gallium acetylacetonate, indium acetylacetonate, aluminum-(picolylmethylketone)-bis{2,6-di(t-butyl)phenoxide}, scandium-(4-methoxy-picolylmethylketone)-bis(acetylacetonate), and combinations thereof.
5. The method of claim 3 wherein the hole injection and hole transport material is selected from the group consisting of poly(3,4-ethylenedioxythiophene), polyaniline, triaryldiamine, tetraphenyldiamine, aromatic tertiary amines, hydrazone derivatives, carbazole derivatives, triazole derivatives, imidazole derivatives, oxadiazole derivatives having an amino group, polythiophenes and combinations thereof.
6. The method of claim 3 wherein the electron injection and hole transport material is selected from the group consisting of tris(8-quinolinolato)aluminum, oxadiazole derivatives, perylene derivatives, pyridine derivatives, pyrimidine derivatives, quinoline derivatives, quinoxaline derivatives, diphenylquinone derivatives, nitro-substituted fluorene derivatives and combinations thereof.
7. The method of claim 3 wherein the hole blocking material is selected from the group consisting of poly(N-vinyl carbazole), bathocurpoine, bis(2-methyl-8-quinolinato)triphenylsilanolate aluminum (III), bis(2-methyl-8-quinolinato)4-phenolate aluminum (III), bis(2-methyl-8-quinolinato)4-phenylphenolate aluminum (III) and combinations thereof.
8. The method of claim 1 wherein x is zero; each R 1 is the same and is a C 1 -C 16 alkyl group; and each R 2 is the same.
9. The method of claim 1 wherein x is zero; each R 1 is the same and is selected from the group consisting of methyl, ethyl, and n-propyl; and each R 2 is the same and is selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, n-pentyl, iso-pentyl, methylpentyl, n-hexyl, and iso-hexyl.
10. A method for improving adhesion between layers in an electroactive device comprising the steps of (i) depositing a surface treatment composition comprising at least one adhesion promoter material on at least one surface of a first electroactive layer, wherein the adhesion promoter material comprises 9,9-disubstituted fluorenyl compound of formula (I):
wherein each R is independently alkyl, aryl, halogen, cyano, alkoxide, carboxylate, or hydroxy: each “x” independently has a value of from 0 to the number of positions which can be substituted on the aromatic ring; each R 1 is independently a C 1 -C 16 alkyl group or an aryl group; each R 2 is independently a C 1 -C 16 alkyl group; and the geometry about each double bond is independently either cis or trans, and combination thereof; and (ii) depositing a second electroactive layer onto the surface of said surface treatment composition comprising said adhesion promoter; wherein said composition enables adhesion between said first layer and said second layer of said electroactive device, wherein said first layer is an organic light emitting layer.
11. The method of claim 10 , wherein said depositing is selected from the group consisting of reverse roll coating, wire-wound or Mayer rod coating, direct and offset gravure coating, slot die coating, blade coating, hot melt coating, curtain coating, knife over roll coating, extrusion, air knife coating, spray, rotary screen coating, multilayer slide coating, coextrusion, meniscus coating, comma and microgravure coating, spin coating, dip coating, lithographic process, langmuir process and flash evaporation, vapor deposition, plasma-enhanced chemical-vapor deposition, radio-frequency plasma-enhanced chemical-vapor deposition, expanding thermal-plasma chemical-vapor deposition, sputtering, reactive sputtering, electron-cyclotron-resonance plasma-enhanced chemical-vapor deposition, inductively coupled plasma-enhanced chemical-vapor deposition, and combinations thereof.
12. The method of claim 10 wherein the light emitting material is selected from the group consisting of poly(N-vinylcarbazole), polyfluorene, poly(alkylfluorene), poly(para-phenylene), poly(p-phenylene vinylene), polythiophene, poly(pyridine vinylene), polyquinoxaline, polyquinoline, polysilanes, 1,3,5-tris{n-(4-diphenylaminophenyl) phenylamino}benzene, phenylanthracene, tetraarylethene, coumarin, rubrene, tetraphenylbutadiene, anthracene, perylene, coronene, tris(8-quinolinolato) aluminum; derivatives of the foregoing, 8-hydroxyquinoline aluminum acetylacetonate, gallium acetylacetonate, indium acetylacetonate, aluminum-(picolylmethylketone)-bis{2,6-di(t-butyl)phenoxide}, scandium-(4-methoxy-picolylmethylketone)-bis(acetylacetonate), and combinations thereof.