Li et al., 2010 - Google Patents
Polythiophenes with carbazole side chains: design, synthesis and their application in organic solar cellsLi et al., 2010
- Document ID
- 3367996693375882454
- Author
- Li W
- Han Y
- Chen Y
- Li C
- Li B
- Bo Z
- Publication year
- Publication venue
- Macromolecular Chemistry and Physics
External Links
Snippet
A series of polythiophene derivatives P1‐P5 containing carbazole side chains were designed and synthesized via the Stille polymerization. All carbazole containing polymers showed broad absorption in the visible region. The power conversion efficiencies of solar …
- 229920000123 polythiophene 0 title abstract description 13
Classifications
-
- 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
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
-
- 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
- H01L51/0034—Organic polymers or oligomers
- H01L51/0043—Copolymers
-
- 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
- H01L51/0045—Carbon containing materials, e.g. carbon nanotubes, fullerenes
- H01L51/0046—Fullerenes, e.g. C60, C70
- H01L51/0047—Fullerenes, e.g. C60, C70 comprising substituents, e.g. PCBM
-
- 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
- H01L51/42—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 sensing infra-red radiation, light, electro-magnetic radiation of shorter wavelength or corpuscular radiation and adapted for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation using organic materials as the active part, or using a combination of organic materials with other material as the active part; Multistep processes for their manufacture
- H01L51/4253—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 sensing infra-red radiation, light, electro-magnetic radiation of shorter wavelength or corpuscular radiation and adapted for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation using organic materials as the active part, or using a combination of organic materials with other material as the active part; Multistep processes for their manufacture comprising bulk hetero-junctions, e.g. interpenetrating networks
-
- 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
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
-
- 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
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/34—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
- C08G2261/344—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
-
- 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
- C08G2261/90—Applications
- C08G2261/91—Photovoltaic applications
-
- 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
- C08G2261/40—Polymerisation processes
- C08G2261/41—Organometallic coupling reactions
- C08G2261/411—Suzuki reactions
-
- 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
- C08G2261/10—Definition of the polymer structure
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Najari et al. | Synthesis and characterization of new thieno [3, 4‐c] pyrrole‐4, 6‐dione derivatives for photovoltaic applications | |
Wang et al. | Extending π-conjugation system with benzene: an effective method to improve the properties of benzodithiophene-based polymer for highly efficient organic solar cells | |
Zhou et al. | Tuning energy levels of low bandgap semi-random two acceptor copolymers | |
Huo et al. | Alkylthio‐substituted polythiophene: absorption and photovoltaic properties | |
Chen et al. | Synthesis and characterization of a narrow‐bandgap polymer containing alternating cyclopentadithiophene and diketo‐pyrrolo‐pyrrole units for solar cell applications | |
Wen et al. | Synthesis of 4, 7-diphenyl-2, 1, 3-benzothiadiazole-based copolymers and their photovoltaic applications | |
Zhou et al. | Low band gap copolymers consisting of porphyrins, thiophenes, and 2, 1, 3‐benzothiadiazole moieties for bulk heterojunction solar cells | |
Agneeswari et al. | Synthesis of polymers containing 1, 2, 4‐oxadiazole as an electron‐acceptor moiety in their main chain and their solar cell applications | |
Hu et al. | Synthesis and photovoltaic properties of ester group functionalized polythiophene derivatives | |
Wang et al. | Very‐Low‐Bandgap Metallopolyynes of Platinum with a Cyclopentadithiophenone Ring for Organic Solar Cells Absorbing Down to the Near‐Infrared Spectral Region | |
Song et al. | Synthesis of the 2H-benzimidazole-based conjugated polymers with various thiophene units and their application in photovoltaic | |
Karakawa et al. | Near‐Infrared Photovoltaic Performance of Conjugated Polymers Containing Thienoisoindigo Acceptor Units | |
Zhang et al. | Synthesis and photovoltaic properties of copolymers based on bithiophene and bithiazole | |
Kim et al. | Low-bandgap poly (4H-cyclopenta [def] phenanthrene) derivatives with 4, 7-dithienyl-2, 1, 3-benzothiadiazole unit for photovoltaic cells | |
Du et al. | Ethynylene‐containing donor–acceptor alternating conjugated polymers: Synthesis and photovoltaic properties | |
KR101142206B1 (en) | Conducting polymer incorporating with dithiophene-thiazolothiazole derivatives, organic photoelectric device using it and organic solar cell | |
Baek et al. | Synthesis of new alternating conjugated copolymers consisting of tetrazine/carbazole or tetrazine/fluorene derivatives along with thiophene spacers for photovoltaic applications | |
Zhou et al. | Synthesis and Photovoltaic Properties of a Poly (2, 7‐carbazole) Derivative Based on Dithienosilole and Benzothiadiazole | |
Kim et al. | Effect of side chains on phenanthrene based DA type copolymers for polymer solar cells | |
Tamilavan et al. | Synthesis of three new 1‐(2, 6‐diisopropylphenyl)‐2, 5‐di (2‐thienyl) pyrrole‐based donor polymers and their bulk heterojunction solar cell applications | |
Jang et al. | Synthesis and characterization of low-band-gap poly (thienylenevinylene) derivatives for polymer solar cells | |
Alqurashy et al. | Pyrene–benzothiadiazole‐based copolymers for application in photovoltaic devices | |
Tamilavan et al. | Benzodithiophene‐Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo [3, 4‐c] pyrrole Derivatives for Polymer Solar Cells | |
Zhang et al. | Synthesis and Photovoltaic Properties of Conjugated Copolymers with Benzo [1, 2‐b: 4, 5‐b′] dithiophene and Bis (thiophene) phthalimide Units | |
Lee et al. | Random copolymers based on 3‐hexylthiophene and benzothiadiazole with induced π‐conjugation length and enhanced open‐circuit voltage property for organic photovoltaics |