Peng et al., 2001 - Google Patents
Efficient light harvesting by sequential energy transfer across aggregates in polymers of finite conjugational segments with short aliphatic linkagesPeng et al., 2001
- Document ID
- 8090385197901562149
- Author
- Peng K
- Chen S
- Fann W
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
Interactions between lumophores have a critical influence on the photophysical properties of conjugated polymers. We synthesized a new series of light-harvesting polymers (poly-DSBs, I− IV) of dialkyloxy-or dialkyl-substituted distyrylbenzene (the substituents being methoxy, 2 …
- 229920000642 polymer 0 title abstract description 329
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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/54—Material technologies
- Y02E10/549—Material technologies organic PV cells
-
- 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
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
-
- 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];
- H01L51/5012—Electroluminescent [EL] layer
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Peng et al. | Efficient light harvesting by sequential energy transfer across aggregates in polymers of finite conjugational segments with short aliphatic linkages | |
Lee et al. | Oxidative stability and its effect on the photoluminescence of poly (fluorene) derivatives: end group effects | |
Liu et al. | Effect of cyano substituents on electron affinity and electron-transporting properties of conjugated polymers | |
Shu et al. | Highly efficient blue-light-emitting diodes from polyfluorene containing bipolar pendant groups | |
Wu et al. | Highly efficient light-emitting diodes based on fluorene copolymer consisting of triarylamine units in the main chain and oxadiazole pendent groups | |
Zhou et al. | Polyfluorenes with phosphonate groups in the side chains as chemosensors and electroluminescent materials | |
Liu et al. | Blue-light-emitting fluorene-based polymers with tunable electronic properties | |
Jacob et al. | Ladder-type pentaphenylenes and their polymers: efficient blue-light emitters and electron-accepting materials via a common intermediate | |
Huang et al. | Novel electroluminescent polymers derived from carbazole and benzothiadiazole | |
Pei et al. | Efficient photoluminescence and electroluminescence from a soluble polyfluorene | |
Ego et al. | Attaching perylene dyes to polyfluorene: three simple, efficient methods for facile color tuning of light-emitting polymers | |
Li et al. | Synthesis and properties of random and alternating fluorene/carbazole copolymers for use in blue light-emitting devices | |
Blouin et al. | Poly (2, 7-carbazole) s: structure− property relationships | |
Remmers et al. | The optical, electronic, and electroluminescent properties of novel poly (p-phenylene)-related polymers | |
Chen et al. | High-efficiency red-light emission from polyfluorenes grafted with cyclometalated iridium complexes and charge transport moiety | |
Lu et al. | Pure deep blue light-emitting diodes from alternating fluorene/carbazole copolymers by using suitable hole-blocking materials | |
Zhang et al. | Electroluminescence of multicomponent conjugated polymers. 2. Photophysics and enhancement of electroluminescence from blends of polyquinolines | |
Deng et al. | Living radical polymerization of bipolar transport materials for highly efficient light emitting diodes | |
Hsu et al. | Fluorescence from conjugated polymer aggregates in dilute poor solution | |
Lu et al. | Polyfluorene-based light-emitting rod− coil block copolymers | |
Zhang et al. | Synthesis and properties of carbazole main chain copolymers with oxadiazole pendant toward bipolar polymer host: tuning the HOMO/LUMO level and triplet energy | |
Wong et al. | Synthesis and characterization of blue-light-emitting alternating copolymers of 9, 9-dihexylfluorene and 9-arylcarbazole | |
Bazan et al. | Fluorescence quantum yield of poly (p-phenylenevinylene) prepared via the paracyclophene route: effect of chain length and interchain contacts | |
Zhou et al. | Effect of Fluorenone Units on the Property of Polyfluorene and Oligofluorene Derivatives: Synthesis, Structure− Properties Relationship, and Electroluminescence | |
Egbe et al. | Investigation of the Photophysical and Electrochemical Properties of Alkoxy-Substituted Arylene− Ethynylene/Arylene− Vinylene Hybrid Polymers |