Huang et al., 2015 - Google Patents
A solvent-resistant azide-based hole injection/transporting conjugated polymer for fluorescent and phosphorescent light-emitting diodesHuang et al., 2015
View PDF- Document ID
- 14548265505378535072
- Author
- Huang C
- Chang F
- Chu Y
- Lai C
- Lin T
- Zhu C
- Kuo S
- Publication year
- Publication venue
- Journal of Materials Chemistry C
External Links
Snippet
Interfacial mixing of polymers is a critical issue when attempting to improve the charge transport and stabilize the operation of solution-processed organic light-emitting diodes (OLEDs). Herein, we describe a simple methodology for overcoming interfacial mixing …
- 238000002347 injection 0 title abstract description 18
Classifications
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
- H01L51/0036—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
- H01L51/0038—Poly-phenylenevinylene and derivatives
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
- H01L51/0039—Polyeflurorene and derivatives
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0034—Organic polymers or oligomers
- H01L51/0043—Copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
- H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
- H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/50—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0059—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H01L51/0061—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/50—Physical properties
- C08G2261/51—Charge transport
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L2251/00—Indexing scheme relating to organic semiconductor devices covered by group H01L51/00
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Huang et al. | A solvent-resistant azide-based hole injection/transporting conjugated polymer for fluorescent and phosphorescent light-emitting diodes | |
Wu et al. | Synthesis and characterization of new fluorene-acceptor alternating and random copolymers for light-emitting applications | |
Cho et al. | Saturated and efficient red light-emitting fluorene-based alternating polymers containing phenothiazine derivatives | |
KR101605213B1 (en) | Planarizing agents and devices | |
JP6551238B2 (en) | Polymer or oligomer, hole transport material composition, and organic electronic device using the same | |
Tamilavan et al. | Synthesis and characterization of indenofluorene‐based copolymers containing 2, 5‐bis (2‐thienyl)‐N‐arylpyrrole for bulk heterojunction solar cells and polymer light‐emitting diodes | |
JP2022123002A (en) | Charge transporting material, organic electronic element and organic electroluminescent element | |
Song et al. | White polymer light emitting diode materials introducing dendritic quinoxaline derivative: Synthesis, optical and electroluminescent properties | |
Huang et al. | Synthesis and optical and electroluminescent properties of novel conjugated polyelectrolytes and their neutral precursors derived from fluorene and benzoselenadiazole | |
JP6582786B2 (en) | Composition, charge transport material, and ink and use thereof | |
KR20190082209A (en) | Organic electronic materials, organic layers, organic electronic devices, organic electroluminescence devices, display devices, lighting devices, and display devices | |
JP6782418B2 (en) | Organic electronics materials and their use | |
Su et al. | Thermally crosslinkable hole‐transporting poly (fluorene‐co‐triphenylamine) for multilayer polymer light‐emitting diodes | |
Su et al. | Synthesis and optoelectronic properties of thermally cross-linkable hole-transporting poly (fluorene-co-triphenylamine) | |
JP6827654B2 (en) | Organic Electronics Materials, Ink Compositions, Organic Layers, and Organic Electronics Devices | |
Han et al. | White polymer light-emitting diode materials with efficient electron injection backbone containing polyfluorene, oxadiazole and quinoxaline derivatives | |
JP6641792B2 (en) | Hole transporting polymer, ink composition, and organic electronic device | |
JP6094058B2 (en) | Organic electronic material, ink composition, organic electronic element, organic electroluminescent element, and photoelectric conversion element | |
Jin et al. | Enhancement of electroluminescence properties of red diketopyrrolopyrrole-doped copolymers by oxadiazole and carbazole units as pendants | |
JP6733737B2 (en) | Organic electronic material, ink composition, organic electronic element, and method for manufacturing organic electronic element | |
JP6657702B2 (en) | Organic electronic material, ink composition containing the same, organic electronic device and organic electroluminescent device | |
Lee et al. | Synthesis and characterization of naphthyl‐substituted poly (p‐phenylenevinylene) s with few structural defects for polymer light‐emitting diodes | |
Song et al. | Synthesis and characterization of a fluorene–quinoxaline copolymer for light-emitting applications | |
Palai et al. | Polyalkylthiophene-containing electron donor and acceptor heteroaromatic bicycles: synthesis, photo-physical, and electroluminescent properties | |
JP2024085535A (en) | Ink composition and organic electronics element |